UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Form 10-K
[X] Annual Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
For the fiscal year ended: March 31, 2013
[ ] Transition Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
or
Commission file number: 000-54014
VISTAGEN THERAPEUTICS, INC.
(Exact name of registrant as specified in its charter)
Nevada
(State or other jurisdiction of
incorporation or organization)
20-5093315
(I.R.S. Employer
Identification No.)
384 Oyster Point Boulevard, No. 8
South San Francisco, California 94080
(650) 244-9990
(Address, including zip code, and telephone number, including area code, of registrant’s principal executive office)
Securities registered pursuant to Section 12(b) of the Act:
None
Securities registered pursuant to Section 12(g) of the Act:
Common Stock, par value $0.001 per share
Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes [ ] No [X]
Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or 15(d) of the Act. Yes [ ] No [X]
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act
of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject
to such filing requirements for the past 90 days. Yes [X] No [ ]
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data
File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or
for such shorter period that the registrant was required to submit and post such files). Yes [X] No [ ]
Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be
contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of this
Form 10-K or any amendment to this Form 10-K. [ ]
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting
company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange
Act.
Large accelerated filer [ ]
Accelerated filer [ ]
Non-accelerated filer [ ]
(Do not check if a smaller
reporting company)
Smaller reporting company [ ]
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act). Yes [ ] No [X]
The aggregate market value of the common stock of the registrant held by non-affiliates of the registrant on September 30, 2012, the last
business day of the registrant’s second fiscal quarter was: $8,317,414.
As of July 12, 2013 there were 21,265,967 shares of the registrant’s common stock outstanding.
TABLE OF CONTENTS
Business
Risk Factors
Unresolved Staff Comments
Properties
Legal Proceedings
Mine Safety Disclosures
Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity
Securities
Selected Financial Data
Management’s Discussion and Analysis of Financial Condition and Results of Operations
Quantitative and Qualitative Disclosures About Market Risk
Financial Statements and Supplementary Data
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
Controls and Procedures
Other Information
Directors, Executive Officers and Corporate Governance
Executive Compensation
Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters
Certain Relationships and Related Transactions, and Director Independence
Principal Accountant Fees and Services
Item No.
PART I
PART II
PART III
1.
1A.
1B.
2.
3.
4.
5.
6.
7.
7A.
8.
9.
9A.
9B.
10.
11.
12.
13.
14.
PART IV
15.
SIGNATURES
EXHIBIT INDEX
Exhibits and Financial Statement Schedules
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Page No.
2
20
38
38
38
38
38
44
44
57
57
111
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112
112
118
126
130
132
134
135
136
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Cautionary Note Regarding Forward-Looking Statements
This Annual Report on Form 10-K report contains forward-looking statements within the meaning of Section 21E of the Securities Exchange
Act of 1934, as Amended (the “ Exchange Act”) and Section 27A of the Securities Act of 1933 (the “ Securities Act”) which involve risk and
uncertainties . All statements other than statements of historical information provided herein may be deemed to be forward-looking
statements. VistaGen Therapeutics, Inc. (the “Company”) intends that such statements be protected by the safe harbor created under the
Exchange Act and the Securities Act. Forward-looking statements involve risks and uncertainties and the Company’s actual results and the
timing of events may differ significantly from the results or timing discussed in the forward-looking statements. Statements about our current
and future plans, expectations and intentions, results, levels of activity, performance, goals or achievements or any other future events or
developments constitute forward-looking statements. Without limiting the foregoing, the words “may”, “will”, “would”, “should”, “could”,
“expect”, “plan”, “intend”, “trend”, “indication”, “anticipate”, “believe”, “estimate”, “predict”, “likely” or “potential”, or the negative or other
variations of these words or other comparable words or expressions, are intended to identify forward-looking statements. Discussions containing
forward-looking statements in this report may be found, among other places, under “Business”, “Risk Factors” and “Management’s Discussion
and Analysis of Financial Condition and Results of Operations”. Forward-looking statements are based on estimates and assumptions we make
in light of our experience and perception of historical trends, current conditions and expected future developments, as well as other factors that
we believe are appropriate and reasonable in the circumstances.
Many factors could cause our actual results, level of activity, performance or future events to differ materially from those expressed in or
implied by the forward-looking statements, including, but not limited to, the factors which are discussed in greater detail in this report under the
section entitled “Risk Factors”. However, these factors are not intended to represent a complete list of the factors that could affect us. The
purpose of the forward-looking statements is to provide the reader with a description of management’s expectations regarding, among other
things, our financial performance and research and development activities and may not be appropriate for other purposes. Readers are cautioned
not to place undue reliance on these forward-looking statements, which, unless otherwise stated, are made only as of the date of this report. We
have no intention and undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new
information, future events or otherwise after the date of this report, except as required by applicable law. The forward-looking statements
contained in this report are expressly qualified by this cautionary statement. New factors emerge from time to time, and it is not possible for us to
predict which factors may arise. In addition, we cannot assess the impact of each factor on our business or the extent to which any factor, or
combination of factors, may cause our actual results to differ materially from those contained in any forward-looking statements.
EXPLANATORY BACKGROUND INFORMATION
VistaGen Therapeutics, Inc. (“VistaGen” or the “Company” or “we”) is a biotechnology company with expertise in human pluripotent stem cell
technology (“hPSC technology”). We are currently applying our hPSC technology for drug rescue, predictive toxicology and drug metabolism
screening.
VistaGen Therapeutics, Inc., a California corporation (“VistaGen California ”) is a wholly-owned subsidiary of the Company. VistaGen
California was incorporated in California on May 26, 1998. Excaliber Enterprises, Ltd. (“Excaliber”), a publicly-held company (formerly
OTCBB:EXCA), was incorporated under the laws of the State of Nevada on October 6, 2005. After being unable to generate material revenues
based on its original business plan, Excaliber became inactive in 2007. In May 2011, after assessing the prospects associated with its original
business plan and the business opportunities associated with a strategic merger with an established, privately-held biotechnology company
seeking the potential advantages of being a publicly-held company, Excaliber’s Board of Directors agreed to pursue a strategic merger with
VistaGen California, as described in more detail below.
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On May 11, 2011, pursuant to a strategic merger transaction with VistaGen California, Excaliber acquired all outstanding shares of VistaGen
California in exchange for 6,836,452 restricted shares of Excaliber’s common stock (the “Merger”), and Excaliber assumed all of VistaGen
California’s pre-Merger obligations to contingently issue restricted shares of common stock in accordance with VistaGen California’s stock
option agreements, warrant agreements, and a convertible promissory note. In connection with the Merger, Excaliber repurchased 5,064,207
shares of Excaliber common stock from two of its stockholders for a nominal amount, resulting in a total of 784,500 shares of Excaliber common
stock outstanding at the date of the Merger. The 6,836,452 restricted shares of common stock issued to VistaGen California stockholders in
connection with the Merger represented approximately 90% of Excaliber’s outstanding shares of common stock after the closing of the
Merger. As a result of the Merger, the biotechnology business of VistaGen California became the operating business of Excaliber. Shortly after
the Merger:
●
●
●
●
●
●
●
Each of the pre-Merger directors of VistaGen California was appointed as a director of Excaliber;
The pre-Merger directors and officers of Excaliber resigned as officers and directors of Excaliber;
Each of VistaGen California’s pre-Merger officers was appointed an officer of like tenor of Excaliber;
The post-Merger directors of Excaliber (consisting of the pre-Merger directors of VistaGen California) approved a two-for-one (2:1)
stock split of Excaliber’s common stock;
The post-Merger directors of Excaliber approved an increase in the number of shares of common stock Excaliber was authorized to
issue from 200 million to 400 million shares, (see Note 9, Capital Stock, to the Consolidated Financial Statements included in Item 8
of this Annual Report on Form 10-K);
Excaliber’s name was changed to “VistaGen Therapeutics, Inc.”; and
VistaGen California's fiscal year-end of March 31 was adopted as Excaliber’s fiscal year-end.
VistaGen California, as the accounting acquirer in the Merger, recorded the Merger as the issuance of stock for the net monetary assets of
Excaliber, accompanied by a recapitalization. This accounting for the Merger was identical to that resulting from a reverse acquisition, except
that no goodwill or other intangible assets were recorded. Since June 21, 2011, VistaGen’s common stock has traded on the OTC Bulletin
Board under the symbol VSTA.
Item 1.
Business
PART I
We are a biotechnology company with expertise in human pluripotent stem cell technology (“ hPSC technology”). We are applying our hPSC
technology for drug rescue, predictive toxicology and drug metabolism screening. Our primary goal is to generate novel, proprietary, safer
variants of once-promising small molecule drug candidates discovered, developed and ultimately discontinued by pharmaceutical and
biotechnology companies prior to regulatory approval due to unexpected safety concerns relating to the heart and/or liver. We refer to these
new, safer variants as Drug Rescue Variants. Our strategy leverages our hPSC technology platform, Human Clinical Trials in a Test Tube™, our
next generation hPSC-based bioassay systems, CardioSafe 3D™ and LiverSafe 3D™, our network of strategic relationships, and the substantial
prior third-party investment in drug discovery and development of the once-promising drug candidates we plan to include in our drug rescue
programs.
We believe the U.S. pharmaceutical industry is facing a drug discovery and development crisis. In 2012, the U.S. pharmaceutical industry
invested nearly $49 billion in research and development and the Center for Drug Evaluation and Research (CDER) of the U.S. Food and Drug
Administration (FDA) approved a total of only 39 novel drugs, known as New Molecular Entities (NMEs). Despite this investment by the
pharmaceutical industry, since 2003, the FDA has approved an average of approximately 26 NMEs per year. We believe the high cost of drug
development and relatively low annual number of FDA-approved NMEs over the past decade is attributable in large part to the cost of failure
due to unexpected safety issues related to the heart and/or liver. In turn, we believe the unexpected safety issues related to the heart and liver
result from limitations of the major toxicological testing systems currently used in the pharmaceutical industry, namely animal models involving
live animals or animal cells and cellular assays based on transformed cell lines and human cadaver cells, all of which, at best, are capable only of
approximating human biology. We believe better cells, human cells derived from our hPSC technology, can help develop better medicine by
providing clinically relevant human biological information about a new drug candidate early in the drug development process, long before
costly and time-consuming clinical trials.
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With our mature human heart cells derived from pluripotent stem cells, we have developed CardioSafe 3D™, a novel three-dimensional (3D) in
vitro bioassay system for predicting in vivo cardiac effects, both toxic and non-toxic, of small molecule drug candidates long before they are
tested in animals or humans. With our mature human liver cells derived from pluripotent stem cells, we are developing and now validating
LiverSafe 3D™, a novel three-dimensional (3D) in vitro bioassay system for assessing liver toxicity and drug metabolism issues. Our primary
near term goal is to use CardioSafe 3D™, and eventually LiverSafe 3D™, for drug rescue, to recapture substantial potential value associated
with the pharmaceutical industry’s prior investment in drug discovery and development of once-promising small molecule drug candidates
discontinued due to safety issues related to unexpected heart or liver toxicity or drug metabolism issues.
Our drug rescue activities involve the combination of our human pluripotent stem cell technology with third-party modern medicinal
chemistry. Our principal drug rescue goal is to generate new, safe, proprietary chemical variants of once-promising small molecule drug
candidates that were initially discovered and developed by pharmaceutical and biotechnology companies but ultimately discontinued before
receiving FDA or foreign market approval due to heart toxicity, liver toxicity or drug metabolism issues. We refer to these new, safe, proprietary
chemical variants as “Drug Rescue Variants” or “DRVs.” With human heart cells and liver cells derived from pluripotent stem cells, we
believe that CardioSafe 3D™ and, when developed and validated, LiverSafe 3D™, will allow us to assess the heart toxicity, liver toxicity and/or
metabolism profile of new drug candidates with greater speed and precision than traditional animal testing models and cellular assays used in the
drug development process.
We plan to monetize Drug Rescue Variants we develop by licensing them to pharmaceutical companies pursuant to development and marketing
agreements. Through these agreements, for each lead Drug Rescue Variant we develop, anticipate receiving up front license fees, development
and regulatory milestone payments and royalties on commercial sales.
In addition to drug rescue, we are exploring a range of emerging opportunities to advance nonclinical development of selected pilot regenerative
cell therapy programs focused on blood, cartilage, heart, liver and pancreas cells, each based on the proprietary stem cell differentiation and
production capabilities of our Human Clinical Trials in a Test Tube™.
AV-101 is our orally available small molecule prodrug candidate aimed at the multi-billion dollar neurological disease and disorders market.
AV-101 has successfully completed Phase I development in the U.S. for treatment of neuropathic pain, a serious and chronic condition causing
pain after an injury or disease of the peripheral or central nervous system. Neuropathic pain affects approximately 1.8 million people in the U.S.
alone. To date, we have been awarded over $8.3 million of grant funding from the National Institutes of Health (“NIH”) to support preclinical
and Phase I clinical development of AV-101. We believe AV-101 may also be a candidate for development as a therapeutic alternative for
depression, epilepsy and Parkinson’s disease. To advance further clinical development, manufacturing and commercialization of AV-101, we
plan to pursue a strategic licensing arrangement with a pharmaceutical or biotechnology company.
Stem Cell Basics
Human stem cells have the potential to develop into mature cells in the human body. Human pluripotent stem cells (“ hPSCs”) can differentiate
into any of the more than 200 types of cells in the human body. In addition, hPSCs can be expanded readily and have diverse medical research,
drug development and therapeutic applications. We believe hPSCs can be used to develop numerous cell types and tissues that can mimic
complex human biology, including heart and liver biology, for our proposed drug rescue applications.
Pluripotent stem cells are either embryonic stem cells (“ES Cells”) or induced pluripotent stem cells (“iPS Cells”). Both ES Cells and iPS Cells
can be maintained and expanded in an undifferentiated (undeveloped) state indefinitely. We believe these features make them useful research
tools and a reliable source of normal cell populations for creating bioassays to test potential efficacy and toxicity of drug candidates. In addition,
these normal human cells have a wide range of potential applications for regenerative cell therapy.
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Embryonic Stem Cells (ES Cells)
ES Cells are derived from excess fertilized eggs produced during clinical in vitro fertilization (“IVF”) procedures. The excess fertilized eggs are
donated for research purposes with the informed consent of the donors after a successful IVF procedure. ES Cells are not derived from eggs
fertilized in a woman’s body. Such donated fertilized eggs are cultured in vitro and ES Cells are isolated when the embryo is approximately 100
cells, thus long before organs, tissues or nerves have developed.
ES Cells have the most documented potential to both self-renew (create large numbers of cells identical to themselves) and differentiate
(develop) into any of the over 200 types of cells in the body. ES Cells undergo increasingly restrictive developmental decisions during their
differentiation. These “fate decisions” commit the ES Cells to becoming only certain types of mature cells and tissues. At one of the first fate
decision points, ES Cells differentiate into epiblasts. Although epiblasts cannot self-renew, they can differentiate into the major tissues of the
body. This epiblast stage can be used as the starting population of cells that develop into millions of blood, heart, muscle, liver and pancreas
cells, as well as neurons. In the next step, the presence or absence of certain growth factors, together with the differentiation signals resulting
from the physical attributes of the culture techniques, induce the epiblasts to differentiate into neuroectoderm or mesendoderm cells.
Neuroectoderm cells are committed to developing into cells of the skin and cells of the nervous system. Mesendoderm cells are precursor cells
that differentiate into mesoderm and endoderm. Mesoderm cells develop into muscle, bone and blood, among other cell types. Endoderm cells
develop into the internal organs such as the heart, liver, pancreas and intestines, among other cell types.
Induced Pluripotent Stem Cells (iPS Cells)
Over the past several years, Nobel prize-winning developments in stem cell research by third parties have made it possible to obtain pluripotent
stem cell lines from individuals without the use of embryos. Induced pluripotent stem cells (“iPS Cells”) are adult cells, typically human skin or
fat cells, that have been genetically “reprogrammed” to behave like ES Cells by being forced to express genes necessary for maintaining the
pluripotential property of ES Cells. Although researchers are exploring non-viral methods, most iPS Cells are produced by using various viruses
to activate and/or express three or four genes required for the immature pluripotential property similar to ES Cells. It is not yet precisely known,
however, how each gene actually functions to induce cellular pluripotency, nor whether each of the three or four genes is essential for this
reprogramming. Although ES Cells and iPS Cells are believed to be similar in many respects, including their ability to form all cells in the body
and to self-renew, scientists do not yet know whether they differ in clinically significant ways or have the same ability to self-renew and make
more of themselves.
Although there are remaining questions in the field about the lifespan, clinical utility and safety of iPS Cells, we believe that the biology and
differentiation capabilities of ES Cells and iPS Cells are likely to be comparable. There are, however, specific situations in which we may prefer
to use iPS technologies based on the relative ease of generating pluripotent stem cells from:
•
•
individuals with specific inheritable diseases and conditions that predispose the individual to respond differently to drugs; or
individuals with specific variations in genes that directly affect drug levels in the body or alter the manner or efficiency of their
metabolism, breakdown or elimination of drugs.
Because they can significantly affect the therapeutic and/or toxic effects of drugs, these genetic variations have an impact on drug development
and the ultimate success of the drug. We believe that iPS Cell technologies may allow the rapid and efficient generation of pluripotent stem
cells from individuals with the desired specific genetic variation. These stem cells might then be used to develop stem cell-based bioassays, for
both efficacy and toxicity screening, which reflect the effects of these genetic variations, as well as for cell therapy applications.
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Current Drug Development Process
The current drug development paradigm is designed to assess whether a drug candidate is both safe and effective at treating the disease to which
it is targeted. A major challenge in that process is that conventional animal and in vitro testing can, at best, only approximate human biology. A
pharmaceutical company can spend millions of dollars to discover, optimize and validate the potential efficacy of a promising small molecule
drug candidate and advance it through nonclinical development, only to see it fail due to unexpected safety issues relating to heart or liver
toxicity or adverse drug-drug interactions. The pharmaceutical company then often discontinues the development program for the once-
promising drug candidate, despite positive efficacy data indicating its potential therapeutic and commercial benefits. If discontinued, the
pharmaceutical company’s significant prior drug discovery and development investment in the drug candidate is lost.
Taking into account the cost of failures, it has been estimated that the drug discovery and development programs of major pharmaceutical
companies have required an average investment of approximately $1 billion for each new drug candidate that reaches the market. It is also
estimated that about one-third of all potential new drugs candidates fail in preclinical or clinical trials due to safety concerns. In a 2004 white
paper entitled “Stagnation or Innovation”, the FDA noted that even a 10% improvement in predicting the failure of a drug due to toxicity before
the drug enters clinical trials could, when averaged over a pharmaceutical company’s drug development efforts, avoid $100 million in
development costs per marketed drug.
We believe there is an unmet need for more predictive human cell-based toxicology and drug discovery screening assays that more closely
approximate human biology than do current testing systems used in the pharmaceutical industry. By differentiating pluripotent stem cells into
mature, functional human cells that can then be used as the basis for our customized in vitro toxicology screening bioassay systems, we have the
potential to identify human heart and liver toxicity of new drug candidates early in the drug development process, resulting in efficient focusing
of resources on those candidates with the highest probability of success. We believe this has the potential to substantially reduce development
costs and substantially improve the economics of our current healthcare system, while enabling us to generate effective and safer drugs.
Our Human Clinical Trials in a Test Tube TM Platform for Drug Rescue
We are focused on leveraging the substantial prior investment by pharmaceutical companies in discovery and development of new drug
candidates that ultimately were discontinued due to unexpected safety issues relating to the heart and liver toxicity. By combining our stem cell
technology platform, which we refer to as Human Clinical Trials in a Test TubeTM, with modern medicinal chemistry and 3D “micro-organ”
culture systems, we are focused on generating, together with our collaborators, new, safer, proprietary chemical variants of failed drug
candidates. Our primary drug rescue goal is to use our stem cell technology platform to generate Drug Rescue Variants that retain the efficacy
of a large pharmaceutical company’s once-promising drug candidate, but with reduced heart and/or liver toxicity or adverse drug-drug
interactions. We believe our Drug Rescue Variants will offer to pharmaceutical companies a potential opportunity to rescue substantial value
from their prior drug discovery and development investment in once-promising drug candidates which they discontinued due to heart or liver
safety concerns.
Proprietary Pluripotent Stem Cell Differentiation Protocols
Through several years of research, together with our co-founder, Dr. Gordon Keller, we have developed proprietary differentiation protocols
covering key conditions involved in the differentiation of pluripotent stem cells into multiple types of human cells. The human cells generated
by following these proprietary differentiation protocols are integral to our Human Clinical Trials in a Test TubeTM platform. We believe they
support more clinically predictive in vitro bioassay systems than animal testing or cellular assays currently used in drug discovery and
development. Our exclusive licenses with National Jewish Health and Mount Sinai School of Medicine and University Health Network relate to
proprietary stem cell differentiation protocols developed by Dr. Keller and cover, among other things, the following:
•
specific growth and differentiation factors used in the tissue culture medium, applied in specific combinations, at critical concentrations,
and at critical times unique to each desired cell type;
• modified developmental genes and the experimentally controlled regulation of developmental genes, which is critical for determining
what differentiation path a cell will take; and
•
biological markers characteristic of precursor cells, which are committed to becoming specific cells and tissues, and which can be used
to identify, enrich and purify the desired mature cell type.
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We believe our Human Clinical Trials in a Test Tube TM platform will allow us to assess the heart and liver toxicity profile of new, small
molecule drug candidates for a wide range of diseases and conditions, with greater speed and precision than animal testing and cellular assays
currently used by pharmaceutical companies in the drug development.
Growth Factors that Direct and Stimulate the Differentiation Process
The proprietary and licensed technologies underlying our Human Clinical Trials in a Test TubeTM platform allow us to direct and stimulate the
differentiation process of human pluripotent stem cells. As an example, for pluripotent ES Cells, the epiblast is the first stage in differentiation.
One biological factor that controls the first fate decision of the epiblast is the relative concentrations of serum growth factors and activin, a
protein involved in early differentiation and many cell fate decisions. Eliminating serum growth factors and adding the optimal amount of
activin is an important step in inducing the reproducible development of functional cells and, in our view, is essential for the development of a
robust, efficient, and reproducible model of human biological systems suitable for drug rescue applications. The use of activin in these
applications is core to many of the claims in the patent applications underlying our licensed technology. Replacing activin with continuous
exposure to serum factors results in an inefficient and variable differentiation into cells of the heart, liver, blood and other internal organs. See
“Intellectual Property – Mount Sinai School of Medicine Exclusive Licenses.”
In addition to activin, Dr. Keller’s studies have identified a number of other growth and serum-derived factors that play important roles in the
differentiation of ES Cells. Some of the patents and patent applications underlying our licensed technology are directed to the use of a variety of
specific growth factors that increase the efficiency and reproducibility of the pluripotent stem cell differentiation process. We have exclusive
rights to certain patents and patent applications for the use of growth factor concentrations for ES Cell differentiation that we believe are core
and essential for our drug rescue and development applications. See “Intellectual Property - Licenses - Mount Sinai School of Medicine
Exclusive Licenses,” “National Jewish Health Exclusive Licenses” and “University Health Network Exclusive License.”
Developmental Genes that Direct and Stimulate the Differentiation Process
For the purpose of creating our Human Clinical Trials in a Test TubeTM platform, we further control the differentiation process by controlling
regulation of key developmental genes. By studying natural organ and tissue development, researchers have identified many genes that are
critical to the normal differentiation, growth and functioning of tissues of the body. We engineer ES Cells in a way that enables us to regulate
genes that have been identified as critical to control and direct the normal development of specific types of cells. We can then mimic human
biology in a way that allows us to turn on and off the expression of a selected gene by the addition of a specific compound to a culture medium.
By adding specific compounds, we have the ability to influence the expression of key genes that are critically important to the normal biology of
the cell.
Cell Purification Approaches
The proprietary protocols we have licensed for our Human Clinical Trials in a Test TubeTM platform also establish specific marker genes and
proteins which can be used to identify, enrich, purify, and study important populations of intermediate precursor cells that have made specific
fate decisions and are on a specific developmental pathway towards a mature functional cell. These protocols enable a significant increase in the
efficiency, reproducibility, and purity of final cell populations. For example, we are able to isolate millions of purified specific precursor cells
which, together with a specific combination of growth factors, develop full culture wells of functional, beating human heart cells. Due to their
functionality and purity, we believe these cell cultures are ideal for supporting our drug rescue activities.
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3D “Micro-Organ” Culture Systems
In addition to standard two-dimensional (“2D”) cultures which work well for some cell types and cellular assays, the proprietary stem cell
technologies underlying our Human Clinical Trials in a Test TubeTM platform enable us to grow large numbers of normal, non-transformed,
human cells to produce novel in vitro 3D “micro-organ” culture systems. For example, for CardioSafe 3DTM, we grow large numbers of normal,
non-transformed, human heart cells in vitro in 3D micro-organ culture systems. The 3D micro-organ cultures induce the cells to grow, mature,
and develop 3D cell networks and tissue structures. We believe these 3D cell networks and structures more accurately reflect the structures and
biology inside the human body than traditional flat, 2D, single cell layers grown on plastic, that are widely used by pharmaceutical companies
today. We believe that the more representative human biology afforded by the 3D system will yield responses to drug candidates that are more
predictive of human drug responses.
Medicinal Chemistry
Medicinal chemistry involves designing, synthesizing, modifying and developing small molecule drugs suitable for therapeutic use. It is a highly
interdisciplinary science combining organic chemistry, biochemistry, physical chemistry, computational chemistry, pharmacology, and statistics.
The combination of medicinal chemistry with the proprietary and licensed stem cell technologies underlying our Human Clinical Trials in a Test
TubeTM platform are core components of our drug rescue business model. Working with our strategic medicinal chemistry partner, Synterys,
Inc., we are focused on using our stem cell biology to generate a pipeline of effective and safe Drug Rescue Variants of once-promising
pharmaceutical company drug candidates in a more efficient and cost-effective manner than the processes currently used for drug development.
Application of Stem Cell Technology to Drug Rescue
By using CardioSafe 3DTM, we are focused on identifying and optimizing a lead Drug Rescue Variant (generated in collaboration with our
medicinal chemistry partner) with reduced heart toxicity compared to the once-promising pharmaceutical company drug candidate. We believe
each lead Drug Rescue Variant will be a new drug candidate (to which we expect to have certain intellectual property and commercialization
rights) that preserves the therapeutic potential of the original pharmaceutical company drug candidate, and thus retains its potential commercial
value to a pharmaceutical company, but substantially reduces or eliminates its heart toxicity risks. We believe that focusing on failed drug
candidates that generated positive efficacy data will allow us to leverage a pharmaceutical company’s substantial prior investment in discovery
and development of the original drug candidate to develop our new lead Drug Rescue Variant. We anticipate that the positive efficacy data
relating to the pharmaceutical company’s original drug candidate will give us and our medicinal chemistry partner a significant “head start” in
our efforts to generate a lead Drug Rescue Variant, resulting in faster, less expensive development of our Drug Rescue Variants than drug
candidates discovered and developed using only conventional animal testing and cellular testing systems.
CardioSafe 3DTM
We have used the proprietary pluripotent stem cell technology underlying our Human Clinical Trials in a Test Tube TM platform to develop and
validate CardioSafe 3DTM, a human heart cell-based toxicity screening system that we believe is stable, reproducible and capable of generating
data to allow our scientists to more accurately predict the in vivo cardiac effects, both toxic and non-toxic, of drug candidates. A single
CardioSafe 3DTM assay is stable for many weeks and can be used for evaluating the heart toxicity of numerous drug candidates.
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Our initial internal validation study was designed to test the ability of CardioSafe 3DTM to generate data to allow our scientists to predict the in
vivo cardiac effects of drug candidates. This study included 10 drugs previously approved for human use by the FDA and one experimental
research compound widely accepted for studying cardiac electrophysiological effects. We selected these drugs and the research compound
because of their known toxic or non-toxic cardiac effects on human hearts that we believe represent the testing characteristics we expect to
encounter during our drug rescue programs. More specifically:
•
•
•
five of the FDA-approved drugs (astemizole, sotalol, cisapride, terfenadine and sertindole) were withdrawn from the market due to
heart toxicity concerns;
the other five FDA-approved drugs (fexofenadine, nifedipine, verapamil, lidocaine and propranolol) are currently available in the U.S.
market and demonstrate certain measurable clinical non-toxic cardiac effects, one of which (fexofenadine) is a non-cardiotoxic drug
variant (similar in concept to our planned rescued drug variants) of terfenadine (one of the FDA-approved drugs withdrawn from the
market due to heart safety concerns); and
the research compound (E-4031) failed in a small Phase I human clinical study before being discontinued due to heart toxicity
concerns.
In our study analysis, we found that results obtained with CardioSafe 3DTM were consistent with the known human cardiac effects of all 10
FDA-approved drugs and the experimental research compound. By using CardioSafe 3DTM, we were also able to distinguish between the
cardiac effects of terfenadine (SeldaneTM), withdrawn by the FDA due to cardiotoxicity, and the cardiac effects of the closely related
fexofenadine (AllegraTM), the safe and effective chemical variant of terfenadine, which remains on the market.
The results obtained with CardioSafe 3DTM were consistent with the cardiac effects of all five FDA-approved drugs that were later withdrawn
from the market due to concerns of heart toxicity. With respect to the results for sertindole, CardioSafe 3DTM indicated the same cardiac effects
found in clinical testing that caused it to be withdrawn from the market. However, additional clinical studies have been conducted since the
withdrawal of sertindole that have indicated lower incidence of severe cardiac effects than those originally predicted when the drug was
withdrawn. As of the date of this report, sertindole has been approved for limited use by humans in the U.S. for the treatment of schizophrenia,
but the cardiac effects of sertindole are still being researched.
We believe the results of our initial internal CardioSafe 3DTM validation study, as well as the results of our subsequent internal validation
studies involving additional drugs previously approved for human use by the FDA, indicate that CardioSafe 3DTM may be effectively used to
identify Drug Rescue Variants with reduced heart toxicity by providing more accurate and timely indications of direct heart toxicity of drug
candidates than animal models or cellular assay systems currently used by pharmaceutical companies.
We also believe that the results of our internal validation studies support a central premise of our drug rescue business model, which is that by
using our stem cell-derived human heart and liver bioassay systems at the front end of the drug development process, we have the opportunity to
recapture substantial value from prior investment by pharmaceutical companies in discovery and development of drug candidates that have been
put on the shelf due to toxicity concerns. This internal validation study has not been subject to peer review or third party validation. See “Risk
Factors”.
LiverSafe 3DTM
Current human stem cell-based liver cell cultures produce proteins produced by and characteristic of immature and adult liver cells, including
albumin and liver-specific enzymes important for normal drug metabolism. In addition, these liver cells have biochemical pathways and
subcellular structures that are characteristic of normal human liver cells. Although they express many of the mature adult liver proteins and drug
processing enzymes, they do not yet express certain essential enzymes at levels typically seen in mature adult liver cells.
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Working with Dr. Keller, we have produced pluripotent stem cell-derived normal, non-transformed, fully mature, human liver cells. We expect
these mature liver cells to support our ongoing development and validation of LiverSafe 3DTM as our follow-on bioassay system suitable for use
in predicting liver toxicity and metabolism of drug rescue candidates in a manner similar to the way we believe CardioSafe 3DTM can predict
heart toxicity. Our early liver cell research project was funded in part through a grant from the California Institute of Regenerative Medicine
(“CIRM”). We anticipate that our future research and development will focus on the improvement of techniques and production of engineered
human ES Cell and iPS Cell lines used to develop mature functional liver cells as a biological system for testing drugs and, potentially,
regenerative cell therapy for liver disease.
One of the pitfalls of many pluripotent stem cell differentiation protocols is the extremely poor efficiency of producing mature hepatocytes. The
cytochrome P450 3A (CYP3A) subfamily of enzymes is the most predominant in the human liver. In the fetal liver CYP3A7 is the predominant
isoform, whereas there is an almost exclusive shift to the CYP3A4 isoform in the adult liver. Furthermore, CYP3A4 is responsible for the
metabolism of half of the pharmaceuticals currently available, as well as playing a central role in steroid homeostasis. Most published stem cell
differentiation reports demonstrate CPY3A7 expression, but little to no CYP3A4 expression or activity, indicating the lack of maturity of the
hepatocyte-like cells being studied. In an effort to address this problem, we generated a human embryonic stem cell (hESC) reporter line
containing a humanized version of the beta-lactamase reporter gene (hBLA) targeted to the 3’ untranslated region of the CYP3A4 locus. We
have shown the use of this cell line as a semi-quantitative tool for analyzing the expression of CYP3A4 in individual cells and for the selection
of mature hepatocytes by fluorescence activated cell sorting. We have demonstrated that this assay can be used to monitor the induction of
CYP3A4, its expression level over time, and to measure experimental effects on the maturation of hepatocytes. Using an optimized protocol for
the differentiation of hepatocyte-like cells, we have demonstrated adult CYP3A4-hBLA expression in 25-60% of the unsorted differentiated cell
population. Furthermore these cells showed expected adult responses: 1) rifampicin induction, 2) metabolism of known CYP3A4 substrates, 3)
albumin production and 4) phase II enzyme activities. Sorted CYP3A4-hBLA cells express levels of CYP3A4 mRNA approaching that in
human adult liver on a per cell basis. We believe these data suggest that these cells have many of the functional properties of mature
hepatocytes. This system allows us to measure the expression of CYP3A4-hBLA on a per cell basis in response to experimental conditions, and
treatments with drugs, and corroborate those data with cytochromes P450 enzyme activities, Phase II enzyme activities, and secretion of hepatic
factors, such as albumin and urea. These multiple functional analyses provide a powerful system to evaluate the effects of test compounds on
CYP3A4 expression and hepatocyte function, offering a valuable aid for assessing potential drug candidates for toxicity.
Our Drug Rescue Business Model
Our current drug rescue programs are focused on heart toxicity using our CardioSafe 3DTM human heart cell-based bioassay system. We are
focused on rescuing once-promising drug candidates that have positive efficacy data indicating their potential therapeutic and commercial
benefits but that have been discontinued in development by a large pharmaceutical company due to heart toxicity. The initial goal of our drug
rescue program for each drug rescue candidate will be to design and generate, with our medicinal chemistry collaborator, a portfolio of Drug
Rescue Variants. We plan to use CardioSafe 3DTM to identify a lead Drug Rescue Variant that demonstrates an improved therapeutic index
compared to the pharmaceutical company’s original drug candidate (that is, equal or improved efficacy with reduced heart toxicity). We intend
to validate that each lead Drug Rescue Variant demonstrates reduced heart toxicity in both CardioSafe 3DTM and in the same nonclinical testing
model that the pharmaceutical company used to determine heart toxicity for its original drug candidate. We anticipate that the results of these
confirmatory nonclinical safety studies will be drug rescue collaboration milestones demonstrating to a pharmaceutical company the
improvement of our lead Drug Rescue Variant compared to its original once-promising drug candidate.
Our Human Clinical Trials in a Test TubeTM Platform for Stem Cell Therapy
Although we believe the best near term commercial application of our pluripotent stem cell technology platform is for small molecule drug
rescue and development, we also believe the biotechnology industry is now at the beginning of a new era in medicine in which stem cell
technology can be applied to harness the body’s own formidable healing capacity to repair, replace or regenerate organs and tissue damaged by
disease and injury. Over the next two decades, we believe stem cell technology-based regenerative cell therapy has the potential to transform
healthcare in the U.S. by altering the fundamental mechanisms of disease, particularly diseases and conditions associated with aging, and help
slow rapidly rising healthcare costs in the U.S.
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In addition to our drug rescue and development activities, we are exploring emerging regenerative cell therapy opportunities, with emphasis on
potential pilot, nonclinical, proof-of-concept studies focused on blood, cartilage, heart, liver and pancreas cells.
Strategic Transactions and Relationships
Strategic collaborations are a cornerstone of our corporate development strategy. We believe that our strategic outsourcing and sponsoring of
application-focused research gives us flexible access to leading-edge expertise in certain areas at a lower overall cost than attempting to develop
such expertise internally. In particular, we collaborate with the types of third parties identified below for the following functions:
•
•
academic research institutions, such as University Health Network (“UHN”), for stem cell research collaborations;
CROs, such as Cato Research Ltd., for regulatory and drug development expertise and to identify and assess potential drug rescue
candidates; and
• medicinal chemistry companies, such as Synterys, Inc., to analyze drug rescue candidates and generate drug rescue variants.
Dr. Gordon Keller, UHN and McEwen Centre for Regenerative Medicine
UHN in Ontario, Canada is a major landmark in Canada’s healthcare system. UHN is one of the world’s largest research hospitals, with major
research in transplantation, cardiology, neurosciences, oncology, surgical innovation, infectious diseases and genomic medicine. Providing care
to the community for more than two centuries, UHN brings together the talent and resources needed to achieve global impact and provide
exemplary patient care, research and education.
The McEwen Centre for Regenerative Medicine (“McEwen Centre”) is a world-renowned center for stem cell biology and regenerative medicine
and a world-class stem cell research facility affiliated with UHN. Our co-founder, Dr. Gordon Keller, is Director of the McEwen Centre. Dr.
Keller’s lab is one of the world leaders in successfully applying principles from the study of developmental biology of many animal systems to
the differentiation of pluripotent stem cell systems, resulting in reproducible, high-yield production of human heart, liver, blood and vascular
cells. The results and procedures developed in Dr. Keller’s lab are often quoted and used by academic scientists worldwide.
In September 2007, we entered into a long-term sponsored stem cell research and development collaboration with UHN. In December 2010, we
extended the collaboration to September 2017. The primary goal of this ten-year collaboration is to leverage the stem cell research, technology
and expertise of Dr. Gordon Keller to develop and commercialize industry-leading human pluripotent stem cell differentiation technology and
bioassay systems for drug rescue and development and regenerative cell therapy applications. This sponsored research collaboration builds on
our existing strategic licenses from National Jewish Health and Mount Sinai School of Medicine to certain stem cell technologies developed by
Dr. Keller, and is directed to multiple stem cell-based research projects, including advancing use of human pluripotent stem cell-derived heart
and liver to screen new drugs for potential heart and liver toxicity and for potential regenerative cell therapy applications involving blood,
cartilage, heart, liver and pancreas cells. In April 2011, we further expanded the scope of the collaboration to include potential regenerative cell
therapy applications of iPS Cells and cells derived from iPS Cells, to create additional options to fund research and development with respect to
future research projects relating to therapeutic applications of iPS Cells and certain cells derived from iPS Cells and to extend the period that we
have to exercise our options under the agreement. In October 2011, we amended the collaboration agreement to identify five key programs that
will further support our core drug rescue initiatives and potential regenerative cell therapy applications. In October 2012, we amended the
collaboration agreement to direct our focus on heart, liver and blood cell programs supporting our primary bioassay system development and
drug rescue activities and three key potential regenerative cell therapy programs. Under the terms of October 2012 amendment, we are
committed to make quarterly payments of $75,000 from October 2012 through September 2013 to fund these programs. See “Sponsored
Research Collaborations and Intellectual Property Rights – University Health Network, McEwen Centre for Regenerative Medicine, Toronto,
Ontario”, “Intellectual Property – National Jewish Health Exclusive Licenses” and “Intellectual Property – Mount Sinai School of Medicine
Exclusive Licenses.”
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Centre for Commercialization of Regenerative Medicine
The Toronto-based Centre for Commercialization of Regenerative Medicine (“CCRM”) is a not-for-profit, public-private consortium funded by
the Government of Canada, six Ontario-based institutional partners and more than 20 companies representing the key sectors of the regenerative
medicine industry. CCRM supports the development of foundational technologies that accelerate the commercialization of stem cell- and
biomaterials-based products and therapies.
In December 2012, we formalized our membership in the CCRM’s Industry Consortium. Other members of CCRM’s Industry Consortium
include such leading global companies as Pfizer, GE Healthcare and Lonza. The industry leaders that comprise the CCRM consortium benefit
from proprietary access to certain licensing opportunities, academic rates on fee-for-service contracts at CCRM and opportunities to participate
in large collaborative projects, among other advantages. Our CCRM membership reflects our strong association with CCRM and its core
programs and objectives, both directly and through our strategic relationships with Dr. Gordon Keller and UHN. We believe our long-term
sponsored research agreement with Dr. Keller, UHN and UHN’s McEwen Centre for Regenerative Medicine offers a solid foundation and
unique opportunities for expanding the commercial applications of our Human Clinical Trials in a Test Tube ™ platform by building multi-party
collaborations with CCRM and members of its Industry Consortium. We believe these collaborations have the potential to transform medicine
and accelerate significant advances in human health and wellness that stem cell technologies and regenerative medicine promise.
Duke University
In November 2011, we entered into a strategic collaboration with Duke University, one of the premier academic research institutions in the
U.S., aimed at combining our complementary expertise in cardiac stem cell technology, electrophysiology and tissue engineering. The initial
goal of the collaboration is to explore the potential development of novel, engineered, stem cell-derived cardiac tissues to expand the scope of
our drug rescue capabilities focused on heart toxicity. We expect that this collaboration, employing our human stem cell-derived heart cells
combined with Duke’s technology relating to cardiac electrophysiology and cardiac tissue engineering, will permit us to use micro-patterned
cardiac tissue to expand the approaches available to us in our drug rescue programs to quantify drug effects on functional human cardiac tissue.
In May 2013, we announced that researchers at Duke University combined our human stem cell-derived heart cells with innovative tissue
engineering and cardiac electrophysiology technologies to grow what is being called a “heart patch,” which mimics the natural functions of
native human heart tissue. We believe this is the closest man-made approximation of natural human heart muscle to date. This heart patch
technology is being developed to aid in a better understanding of the biology critical to cardiac tissue engineering, for applications in
regenerative cell therapy for heart disease, and as predictive in vitro assays for drug rescue and development. We believe the developed
contractile forces and other functional properties of these cardiac tissues are remarkable and are significantly higher than any previous reports.
The achievement of successfully growing a human heart muscle from cardiomyocytes derived from human pluripotent stem cells expands the
scope of our drug rescue capabilities and reflects the advanced nature and potential of our collaboration with Duke University.
Achieving this capability represents a potentially significant breakthrough in heart cell-based therapies and in testing new medicines for
potential heart toxicity and potential therapeutic benefits impacting heart disease.
The following are among several key development points from the study:
·
The optimized 3D environment of a cardiac tissue patch yields advanced levels of structural and functional maturation of human
cardiomyocytes that produce expected responses to drugs;
· Human cardiomyocyte maturation in an optimized 3D patch environment is enhanced relative to that found in industry standard 2D
cultures;
· No genetic modifications were used to produce, purify, or mature cardiomyocytes, suggesting potential for future therapeutic
·
applications;
Cardiac tissue patches generated using VistaGen’s cardiomyocytes exhibited 2.2-180 fold higher contractile force generation
compared to previous studies;
· Based on a force per cardiomyocyte metric, cardiac tissue engineering methodology that used VistaGen’s cardiomyocytes exhibited 4-
700-fold higher efficiency than previously reported; and
· Cardiac tissue patches generated using VistaGen’s cardiomyocytes exhibited velocities of electrical signal propagation 5-fold higher
compared to previous reports in human engineered cardiac tissues.
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Cato Research and Cato BioVentures
Cato Research
Cato Research is a contract research and development organization (“CRO”), with international resources dedicated to helping a network of
biotechnology and pharmaceutical companies navigate the regulatory approval process in order to bring new biologics, drugs, and medical
devices to markets throughout the world. Cato Research has in-house capabilities to assist its sponsors with aspects of the drug development
process including regulatory strategy, nonclinical and toxicology development, clinical development, data processing, data management,
statistical analysis, regulatory applications, including INDs and NDAs, chemistry, manufacturing, and control programs, cGCP, cGLP and cGMP
audit and compliance activities, and due diligence review of emerging technologies. Cato Research’s senior management team, including co-
founders Allen Cato, M.D., Ph.D. and Lynda Sutton, has over 20 years of experience interacting with the FDA and international regulatory
agencies and a successful track record of product approvals.
Cato BioVentures
Cato Holding Company, doing business as Cato BioVentures (“ Cato BioVentures”), is the venture capital affiliate of Cato Research. Through
strategic CRO service agreements with Cato Research, Cato BioVentures invests in therapeutics and medical devices, as well as platform
technologies such as our Human Clinical Trials in a Test Tube TM platform, which its principals believe are capable of improving the drug
development process and the research and development productivity of a pharmaceutical company.
Our Relationship with Cato Research and Cato BioVentures
Cato Research currently serves as the primary CRO providing strategic development and regulatory expertise and services with respect to our
development of AV-101. See “Business – AV-101.” Cato BioVentures is among our largest institutional investors.
As a result of the access Cato Research has to drug rescue candidates from its biotechnology and pharmaceutical industry network, as well as
Cato BioVentures’ equity interest in VistaGen, we believe that our long-term strategic relationship with Cato BioVentures and Cato Research
may provide us with unique opportunities relating to our drug rescue activities that will permit us to leverage the CRO resources of Cato
Research to assist our efforts to develop lead Drug Rescue Variants internally, should we elect to do so.
United States National Institutes of Health
Since our inception in 1998, the U.S. National Institutes of Health ("NIH") has awarded us a total of $11.3 million in non-dilutive research and
development grants, including $2.3 million to support research and development of our Human Clinical Trials in a Test Tube™ platform and a
total of $8.8 million for nonclinical and Phase 1 clinical development of AV-101 (also referred to in scientific literature as “4-Cl-KYN”). AV-
101, our lead small molecule drug candidate, has completed Phase 1 clinical development in the U.S.
California Institute for Regenerative Medicine — Stem Cell Initiative (Proposition 71)
The California Institute for Regenerative Medicine (“CIRM”) funds stem cell research at academic research institutions and companies
throughout California. CIRM was established in 2004 with the passage of Stem Cell Initiative (Proposition 71) by California voters. As a stem
cell company based in California since 1998, we are eligible to apply for and receive grant funding under the Stem Cell Initiative. To date we
have been awarded approximately $1.0 million of non-dilutive grant funding from CIRM for stem cell research and development related to liver
cells. This research and development focused on the improvement of techniques and the production of engineered human ES Cell lines used to
develop mature functional liver cells as a biological system for testing drugs.
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Celsis In Vitro Technologies, Inc.
In March 2013, we entered into a strategic collaboration with Celsis In Vitro Technologies (“Celsis IVT”), the premier global provider of
specialized in vitro products for drug metabolism, drug-drug interaction and toxicity screening, focused on characterizing and functionally
benchmarking our human liver cell platform, LiverSafe 3D™ with Celsis IVT products for studying and predicting human liver drug
metabolism. We intend to utilize Celsis IVT’s experience and expertise in in vitro drug metabolism to help validate our stem cell-derived human
liver cell platform. We anticipate that Celsis IVT will not only validate our stem cell-derived liver cells in traditional pharmaceutical metabolism
assays, but will also determine genetic variations in our pluripotent stem cell lines that are important to drug development. In addition, we plan
to utilize Celsis IVT’s large inventory of cryopreserved primary human liver cells, currently used throughout the pharmaceutical industry for
traditional and high-throughput liver toxicology and other bioassays, as reference controls with which to monitor and benchmark the functional
properties of our LiverSafe 3D™ platform.
Collaborating with Celsis IVT scientists, we aim to achieve four key objectives:
·
·
·
·
Optimize techniques to handle and maintain primary human cryopreserved primary liver cells as reference controls for various drug
development assays;
Develop a stable supply of characterized and validated human cryopreserved primary liver cells to serve as internal controls and
provide benchmark comparisons for the characterization of our pluripotent stem cell-derived liver cells;
Characterize our stem cell derived liver cells using many of the same industry-standardized assays used to characterize primary
human liver cells; and
Produce a joint publication of the characterization of our stem cell-derived human liver cells.
As an industry leader in the development of in vitro primary hepatocyte technology, we believe Celsis IVT has extensive resources to aid us in
the benchmarking LiverSafe 3D™ to industry standards. We anticipate this collaboration will lead to the further validation of our LiverSafe
3D™ system for predicting liver toxicity and drug metabolism issues long before costly human clinical trials.
Synterys, Inc.
In December 2011, we entered into a strategic medicinal chemistry collaboration agreement with Synterys, Inc. (“Synterys”), a medicinal
chemistry and collaborative drug discovery company. We believe this important collaboration will further our stem cell technology-based drug
rescue initiatives with the support of Synterys’ leading-edge medicinal chemistry expertise. In addition to providing flexible, real-time
medicinal chemistry services in support of our projected drug rescue programs, we anticipate potential collaborative opportunities with
Synterys wherein we jointly identify and develop novel drug rescue opportunities and advance them in preclinical development.
Vala Sciences, Inc.
In October 2011, we entered into an exploratory drug screening collaboration with Vala Sciences, Inc. (“Vala”), a biotechnology company
developing and selling next-generation cell image-based instruments, reagents and analysis software tools. The goal of the collaboration is to
advance drug safety screening methodologies in the most clinically relevant human in vitro bioassay systems currently available to
researchers. Through the collaboration, Vala will use its Kinetic Image Cytometer platform to demonstrate both the suitability and utility of
our human pluripotent stem cell derived-cardiomyocytes for screening new drug candidates for potential cardiotoxicity over conventional in
vitro screening systems and animal models. Cardiomyocytes are the muscle cells of the heart that provide the force necessary to pump blood
throughout the body, and, as such, are the targets of most of the drug toxicities that directly affect the heart. Many of these drug toxicities
result in either arrhythmia (irregular, often fatal, beating of the heart) or reduced ability of the heart to pump the blood necessary to maintain
normal health and vigor. Accurate, sensitive and reproducible measurement of electrophysiological responses of stem cell-derived
cardiomyocytes to new drug candidates is a key element of our CardioSafe 3D™ drug rescue programs.
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AV-101
We have successfully completed our Phase I development of AV-101, also known as “L-4-chlorokynurenine” and “4-Cl-KYN”. AV-101 is a
prodrug candidate for the treatment of neuropathic pain. Our AV-101 IND application on file at the FDA covers our initial Phase I clinical
development of the drug candidate for neuropathic pain. Neuropathic pain is a serious and chronic condition causing pain after an injury or
disease of the peripheral or central nervous system. The neuropathic pain market is large, including approximately 1.8 million people in the U.S.
alone.
We believe the safety studies done in the initial Phase I clinical study of AV-101 will support development of AV-101 for other indications,
including epilepsy and neurodegenerative diseases, such as Huntington’s and Parkinson’s. To date, the NIH has provided us with grant funding
for substantially all of our AV-101 development expenses, including $8.2 million for preclinical and clinical development. We plan to seek a
strategic partner for development and commercialization of AV-101 for neuropathic pain, depression and potentially other neurodegenerative
diseases related to aging.
AV-101 is an orally available prodrug that is converted in the brain into an active metabolite, 7-chlorokynurenic acid (“ 7-Cl-KYNA”), which
regulates the N-methyl-D-aspartate (“NMDA”) receptors. 7-Cl-KYNA is a synthetic analogue of kynurenic acid, a naturally occurring neural
regulatory compound, and is one of the most potent and selective blockers of the regulatory GlyB-site of the NMDA receptor. In preclinical
studies, AV-101 has very good oral bioavailability, is rapidly and efficiently transported across the blood-brain barrier, and is converted into 7-
Cl-KYNA in the brain and spinal cord, preferentially, at the site of seizures and potential neural damage.
The effect of AV-101 on chronic neuropathic pain due to inflammation and nerve damage was assessed in rats by using the Chung nerve ligation
model. AV-101 effects were compared to either saline and MK-801, or gabapentin (Neurontin TM) as positive controls. Similarly to the
therapeutic effects seen in the acute formalin and thermal pain models, AV-101 had a positive effect on chronic neuropathic pain in the Chung
model that were greater than two (2) standard deviations of the control, with no adverse behavioral observations. As expected, MK-801 and
gabapentin also demonstrated reduced pain readouts in the Chung model. The effects observed by AV-101 in both the acute and chronic
neuropathic pain model systems was dose dependent, and was not associated with any side effects at the range of doses administered. Preclinical
AV-101 data demonstrated the potential clinical utility of AV-101 as an analgesic.
Intellectual Property
Intellectual Property Rights Underlying our Human Clinical Trials in a Test TubeTM Platform
We have established our intellectual property rights to the technology underlying our Human Clinical Trials in a Test TubeTM platform through a
combination of exclusive and non-exclusive licenses, patent, and trade secret laws. To our knowledge, we are the first stem cell company
focused primarily on stem cell technology-based drug rescue. We have assembled an intellectual property portfolio around the use of pluripotent
stem cell technologies in drug discovery and development and with specific application to drug rescue. The differentiation protocols we have
licensed direct the differentiation of pluripotent stem cells through:
•
a combination of growth factors (molecules that stimulate the growth of cells);
• modified developmental genes; and
•
precise selection of immature cell populations for further growth and development.
By influencing key branch points in the cellular differentiation process, our pluripotent stem cell technologies can produce fully-differentiated,
non-transformed, highly functional human cells in vitro in an efficient, highly pure and reproducible process.
As of the date of this report, we either own or have licensed 43 issued U.S. patents and 12 U.S. patent applications and certain foreign
counterparts relating to the stem cell technologies that underlie our Human Clinical Trials in a Test TubeTM platform. Our material rights and
obligations with respect to these patents and patent applications are summarized below:
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Licenses
National Jewish Health Exclusive Licenses
We have exclusive licenses to seven issued U.S. patents held by NJH. No foreign counterparts to these U.S. patents and patent application have
been obtained. These U.S. patents contain claims covering composition of matter relating to specific populations of cells and precursors,
methods to produce such cells, and applications of such cells for ES Cell-derived immature pluripotent precursors of all the cells of the
mesoderm and endoderm lineages. Among other cell types, this covers cells of the heart, liver, pancreas, blood, connective tissues, vascular
system, gut and lung cells.
Under this license agreement, we must pay to NJH 1% of our total revenues up to $30 million in each calendar year and 0.5% of all revenues for
amounts greater than $30 million, with minimum annual payments of $25,000. Additionally, we are obligated under the agreement to make
certain royalty payments on sales of products based on NJH’s patents or the sublicensing of such technology. The royalty payments are subject
to anti-stacking provisions which reduce our payments by a percentage of any royalty payments and fees paid to third parties who have licensed
necessary intellectual property to us. This agreement remains in force for the life of the patents so long as neither party elects to terminate the
agreement upon the other party’s uncured breach or default of an obligation under the agreement. We also have the right to terminate the
agreement at any time without cause.
Mount Sinai School of Medicine Exclusive Licenses
We have an exclusive, field restricted, license to two U.S. patents and two U.S. patent applications, and their foreign counterparts filed by
MSSM. Foreign counterparts have been filed in Australia (two), Canada (two), Europe (two), Japan (two), Hong Kong and Singapore. Two of
the U.S. applications have been issued and the foreign counterparts in Australia and Singapore have been issued, while the two counterparts in
Europe are pending. These patent applications have claims covering composition of matter relating to specific populations of cells and
precursors, methods to produce such cells, and applications of such cells, including:
•
•
•
the use of certain growth factors to generate mesoderm (that is, the precursors capable of developing into cells of the heart, blood
system, connective tissues, and vascular system) from human ES Cells;
the use of certain growth factors to generate endoderm (that is, the precursors capable of developing into cells of the liver, pancreas,
lungs, gut, intestines, thymus, thyroid gland, bladder, and parts of the auditory system) from human ES Cells; and
applications of cells derived from mesoderm and endoderm precursors, especially those relating to drug discovery and testing for
applications in the field of in vitro drug discovery and development applications.
This license agreement requires us to pay annual maintenance fees, a patent issue fee and royalty payments based on product sales and services
that are covered by the MSSM patent applications, as well as for any revenues received from sublicensing. Any drug candidates that we develop
will only require royalty payments to the extent they require the practice of the licensed technology. To the extent we incur royalty payment
obligations from other business activities, the royalty payments are subject to anti-stacking provisions which reduce our payments by a
percentage of any royalty payments or fees paid to third parties who have licensed necessary intellectual property to us. The license agreement
will remain in force for the life of the patents so long as neither party terminates the agreement for cause (i) due to a material breach or default in
performance of any provision of the agreement that is not cured within 60 days or (ii) in the case of failure to pay amounts due within 30 days.
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Wisconsin Alumni Research Foundation (“WARF”) Non-Exclusive License
We have non-exclusive licenses to 28 issued stem cell-related U.S. patents, 14 stem cell-related U.S. patent applications, of which two have been
allowed, and certain foreign counterparts held by WARF, for applications in the field of in vitro drug discovery and development. Foreign
counterparts have been filed in Australia, Canada, Europe, China, India, Hong Kong, Israel, Brazil, South Korea, India, Mexico, and New
Zealand. The subject matter of these patents includes specific human ES Cell lines and composition of matter and use claims relating to human
ES Cells important to drug discovery, and drug rescue screening. We have rights to:
•
•
use the technology for internal research and drug development;
provide discovery and screening services to third parties; and
• market and sell research products (that is, cellular assays incorporating the licensed technology).
This license agreement requires us to make royalty payments based on product sales and services that incorporate the licensed technology. We
do not believe that any drug rescue candidates to be developed by us will incorporate the licensed technology and, therefore, no royalty
payments will be payable. Nevertheless, there is a minimum royalty of $20,000 per calendar year. There are also milestone fees related to the
discovery of therapeutic molecules, though no royalties are owed on such molecules. The royalty payments are subject to anti-stacking
provisions which reduce our payments by a percentage of any royalty payments paid to third parties who have licensed necessary intellectual
property to us. The agreement remains in force for the life of the patents so long as we pay all monies due and do not breach any covenants, and
such breach or default is uncured for 90 days. We may also terminate the agreement at any time upon 60 days’ notice. There are no reach
through royalties on customer-owned small molecule or biologic drug products developed using the licensed technologies.
Our Patents
We have filed two U.S. patent applications on liver stem cells and their applications in drug development relating to toxicity testing; one patent
has issued and a second patent application is pending. Of the related international filings, European, Canadian and Korean patents were issued.
The European patent has been validated in 11 European countries. We have filed a U.S. patent application, with foreign counterpart filing in
Canada and Europe, directed to methods for producing human pluripotent stem cell-derived endocrine cells of the pancreas, with a specific focus
on beta-islet cells, the cells that produce insulin, and their uses in diabetes drug discovery and screening.
The material patents currently related to the generation of human heart and liver cells for use in connection with our drug rescue activities are set
forth below:
Territory
US
US
US
Patent No.
7,763,466 Method to produce endoderm cells
7,955,849 Method of enriching population of mesoderm cells
8,143,009 Toxicity typing using liver stem cells
General Subject Matter
Expiration
May 2025
May 2023
June 2023
With respect to AV-101, we recently filed three new U.S. patent applications.
Trade Secrets
We rely, in part, on trade secrets for protection of some of our intellectual property. We attempt to protect trade secrets by entering into
confidentiality agreements with third parties, employees and consultants. Our employees and consultants also sign agreements requiring that
they assign to us their interests in patents and copyrights arising from their work for us.
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Sponsored Research Collaborations and Intellectual Property Rights
University Health Network, McEwen Centre for Regenerative Medicine, Toronto, Ontario
We are currently sponsoring stem cell research by our co-founder, Dr. Gordon Keller, Director of the UHN’s McEwen Centre, focused on
developing improved methods for differentiation of cardiomyocytes (heart cells) from pluripotent stem cells, and their uses as biological systems
for drug discovery and drug rescue, as well as cell therapy. Pursuant to our sponsored research collaboration agreement with UHN, we have the
right to acquire exclusive worldwide rights to any inventions arising from these studies under pre-negotiated terms. Such pre-negotiated terms
provide for royalty payments based on product sales that incorporate the licensed technology and milestone payments based on the achievement
of certain events. Any Drug Rescue Variants that we develop will not incorporate the licensed technology and, therefore, will not require any
royalty payments. To the extent we incur royalty payment obligations from other business activities, the royalty payments will be subject to anti-
stacking provisions which reduce our payments by a percentage of any royalty payments paid to third parties who have licensed necessary
intellectual property to us. These licenses will remain in force for so long as we have an obligation to make royalty or milestone payments to
UHN, but may be terminated earlier upon mutual consent, by us at any time, or by UHN for our breach of any material provision of the license
agreement that is not cured within 90 days. We also have the exclusive option to sponsor research for similar cartilage, liver, pancreas and blood
cell projects with similar licensing rights.
The sponsored research collaboration agreement with UHN, as amended, has a term of ten years, ending on September 18, 2017. The agreement
is subject to renewal upon mutual agreement of the parties. The agreement may be terminated earlier upon a material breach by either party that
is not cured within 30 days. UHN may elect to terminate the agreement if we become insolvent or if any license granted pursuant to the
agreement is prematurely terminated. We have the option to terminate the agreement if Dr. Keller stops conducting his research or ceases to
work for UHN.
UHN License for Stem Cell Culture Technology
In April 2012, we licensed breakthrough stem cell culture technology from the McEwen Centre for Regenerative Medicine (“McEwen Centre”)
located at the University Health Network (“UHN”) in Toronto, Canada. We are utilizing the licensed technology to develop hematopoietic
precursor stem cells from human pluripotent stem cells, with the goal of developing drug screening and cell therapy applications for human
blood system disorders. The breakthrough technology is included in a new United States patent application. We believe this stem cell
technology dramatically advances our ability to produce and purify this important blood stem cell precursor for both in vitro drug screening and
in vivo cell therapy applications. In addition to defining new cell culture methods for our use, the technology describes the surface
characteristics of stem cell-derived adult hematopoietic stem cells. Most groups study embryonic blood development from stem cells, but, for the
first time, we are now able to not only purify the stem cell-derived precursor of all adult hematopoietic cells, but also pinpoint the precise timing
when adult blood cell differentiation takes place in these cultures. We believe these early cells have the potential to be the precursors of the
ultimate adult, bone marrow-repopulating hematopoietic stem cells to repopulate the blood and immune system when transplanted into patients
prepared for bone marrow transplantation. These cells have important potential therapeutic applications for the restoration of healthy blood and
immune systems in individuals undergoing transplantation therapies for cancer, organ grafts, HIV infections or for acquired or genetic blood and
immune deficiencies.
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AV-101-Related Intellectual Property
We have exclusive licenses to issued U.S. patents related to the use and function of AV-101, and various CNS-active molecules related to AV-
101. These patents are held by the University of Maryland, Baltimore, the Cornell Research Foundation, Inc. and Aventis, Inc. The principle
U.S. method of use patent related to AV-101 expired in February 2011. Foreign counterparts to that U.S. patent expired in February
2012. However, through the date of this report, in 2013, we have filed three new U.S. patent applications relating to AV-101. In addition,
among the key components of our commercial protection strategy with respect to AV-101 is the New Drug Product Exclusivity provided by the
FDA under section 505(c)(3)(E) and 505(j)(5)(F) of the Federal Food, Drug, and Cosmetic Act (“ FDCA”). The FDA’s New Drug Product
Exclusivity is available for new chemical entities (“NCEs”) such as AV-101, which, by definition, are innovative and have not been approved
previously by the FDA, either alone or in combination. The FDA’s New Drug Product Exclusivity protection provides the holder of an FDA-
approved new drug application (“NDA”) five years of protection from new competition in the U.S. marketplace for the innovation represented by
its approved new drug product. This protection precludes FDA approval of certain generic drug applications under section 505(b)(2) of the
FDCA, as well certain abbreviated new drug applications (“ANDAs”), during the five year exclusivity period, except that such applications may
be submitted after four years if they contain a certification of patent invalidity or non-infringement.
Under the terms of our license agreement, we may be obligated to make royalty payments on 2% of net sales of products using the unexpired
patent rights, if any, including products containing compounds covered by the patent rights. Additionally, we may be required to pay a 1%
royalty on net sales of combination products that use unexpired patent rights, if any, or contain compounds covered by the patent rights.
Consequently, future sales of AV-101 may be subject to a 2% royalty obligation. There are no license, milestone or maintenance fees under the
agreement. The agreement remains in force until the later of: (i) the expiration or invalidation of the last patent right; and (ii) 10 years after the
first commercial sale of the first product that uses the patent rights or contains a compound covered by the patent rights. This agreement may
also be terminated earlier at the election of the licensor upon our failure to pay any monies due, our failure to provide updates and reports to the
licensor, our failure to provide the necessary financial and other resources required to develop the products, or our failure to cure within 90 days
any breach of any provision of the agreement. We may also terminate the agreement at any time upon 90 days’ written notice so long as we
make all payments due through the effective date of termination.
Competition
We believe that our stem cell technology platform, Human Clinical Trials in a Test Tube TM, is capable of being competitive in growing markets
for pluripotent stem cell technology-based drug discovery, development and rescue, as well as regenerative cell therapy and other commercial
applications in the rapidly growing stem cell and regenerative medicine sector. We have elected to focus a substantial portion of our resources on
stem cell technology-based drug rescue.
We believe that the stem cell technologies underlying our Human Clinical Trials in a Test TubeTM platform and our primary focus on drug
rescue opportunities provide us substantial competitive advantages associated with application of human biology at the front end of the drug
development process, long before animal and human testing. Although we believe that our model for the application of pluripotent stem cell
technology for drug rescue is novel, competition may arise or otherwise increase considerably as the use of stem cell technology for drug
discovery, development and rescue, as well as cell therapy or regenerative medicine continues to become more widespread throughout the
academic research community and pharmaceutical and biotechnology industries.
Competition may arise from academic research institutions, contract research organizations, pharmaceutical companies and biotechnology
companies that seek to apply stem cell technology, including hPSC trechnology, to produce, sell and/or use human heart cells, liver cells, other
cell populations, and in vitro cellular assays including such cells, for internal or third-party research and development purposes, predictive
toxicology screening, assessment of adverse drug-drug interactions, and regenerative cell therapy. A representative list of such companies
includes the following: Acea Biosciences, Advanced Cell Technology, BioTime, Cellectis Bioresearch, Cellular Dynamics, California Stem
Cell, Cellerant Therapeutics, Cytori Therapeutics, HemoGenix, International Stem Cell, iPierian, Neuralstem, Organovo Holdings, PluriStem
Therapeutics, Stem Cells, and Stemina BioMarker Discovery. Pharmaceutical companies and other established corporations such as GE
Healthcare Life Sciences, GlaxoSmithKline, Life Technologies, Novartis, Pfizer, Roche Holdings and others have been and are expected to
continue developing internally stem cell-based research and development programs. We anticipate that acceptance and use of hPSC technology,
including our Human Clinical Trials in a Test TubeTM platform, will continue to occur and increase at pharmaceutical and biotechnology
companies in the future.
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With respect to AV-101, we believe that a range of pharmaceutical and biotechnology companies have programs to develop small molecule drug
candidates for the treatment of neuropathic pain, depression, epilepsy, Parkinson’s disease and other neurological conditions and diseases,
including Abbott Laboratories, GlaxoSmithKline, Johnson & Johnson, Novartis, and Pfizer. We expect that AV-101 will have to compete with a
variety of therapeutic products and procedures.
Government Regulation
United States
With respect to our stem cell research and development in the U.S., the U.S. government has established requirements and procedures relating to
the isolation and derivation of certain stem cell lines and the availability of federal funds for research and development programs involving those
lines. All of the stem cell lines that we are using were either isolated under procedures that meet U.S. government requirements and are approved
for funding from the U.S. government, or were isolated under procedures that meet U.S. government requirements and are approved for use by
regulatory bodies associated with the CIRM.
With respect to drug development, government authorities at the federal, state and local levels in the U.S. and other countries extensively
regulate, among other things, the research, development, testing, manufacture, labeling, promotion, advertising, distribution, marketing, pricing
and export and import of pharmaceutical products such as those we are developing. In the U.S., pharmaceuticals, biologics and medical devices
are subject to rigorous FDA regulation. Federal and state statutes and regulations in the United States govern, among other things, the testing,
manufacture, safety, efficacy, labeling, storage, export, record keeping, approval, marketing, advertising and promotion of our potential drug
rescue variants. The information that must be submitted to the FDA in order to obtain approval to market a new drug varies depending on
whether the drug is a new product whose safety and effectiveness has not previously been demonstrated in humans, or a drug whose active
ingredient(s) and certain other properties are the same as those of a previously approved drug. Product development and approval within this
regulatory framework takes a number of years and involves significant uncertainty combined with the expenditure of substantial resources.
Canada
In Canada, stem cell research and development is governed by two policy documents and by one legislative statute: the Guidelines for Human
Pluripotent Stem Cell Research (the “Guidelines”) issued by the Canadian Institutes of Health Research; the Tri-Council Statement: Ethical
Conduct for Research Involving Humans (the “TCPS”); and the Assisted Human Reproduction Act (the “ Act”). The Guidelines and the TCPS
govern stem cell research conducted by, or under the auspices of, institutions funded by the federal government. Should we seek funding from
Canadian government agencies or should we conduct research under the auspices of an institution so funded, we may have to ensure the
compliance of such research with the ethical rules prescribed by the Guidelines and the TCPS.
The Act subjects all research conducted in Canada involving the human embryo, including ES Cell derivation (but not the stem cells once
derived), to a licensing process overseen by a federal licensing agency. However, as of the date of this report, the provisions of the Act
regarding the licensing of ES Cell derivation were not in force
We are not currently conducting stem cell research in Canada. We are, however, sponsoring stem cell research by Dr. Gordon Keller at UHN’s
McEwen Centre. We anticipate conducting stem cell research (with both ES Cells and iPS Cells), in collaboration with Dr. Keller and is
research team, at UHN during 2013 and beyond pursuant to our long term sponsored research collaboration with Dr. Keller and UHN. Should
the provisions of the Act come into force, we may have to apply for a license for all ES Cell research we may sponsor or conduct in Canada and
ensure compliance of such research with the provisions of the Act.
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Foreign
In addition to regulations in the U.S., we may be subject to a variety of foreign regulations governing clinical trials and commercial sales and
distribution of our products outside of the U.S. Whether or not we obtain FDA approval for a product, we must obtain approval of a product by
the comparable regulatory authorities of foreign countries before we can commence clinical trials or marketing of the product in those countries.
The approval process varies from country to country, and the time may be longer or shorter than that required for FDA approval. The
requirements governing the conduct of clinical trials, product licensing, pricing and reimbursement vary greatly from country to country.
Subsidiaries and Inter-Corporate Relationships
VistaGen Therapeutics. Inc., a California corporation, is our wholly-owned subsidiary and has the following two wholly-owned subsidiaries:
VistaStem Canada Inc., a corporation incorporated pursuant to the laws of the Province of Ontario, intended to facilitate our stem cell-based
research and development and drug rescue activities in Ontario, Canada including our collaboration with Dr. Keller and UHN should we elect to
expand our U.S. operations into Canada; and Artemis Neuroscience, Inc., a corporation incorporated pursuant to the laws of the State of
Maryland and focused on development of AV-101. The operations of VistaGen Therapeutics, Inc., a California corporation, and each of its two
wholly-owned subsidiaries are managed by our senior management team based in South San Francisco, California.
Item 1A. Risk Factors
Risks Related to Our Financial Position and Need for Additional Capital
We have incurred significant losses since inception. We expect to incur losses for the foreseeable future and may never achieve or maintain
profitability.
We have incurred significant operating losses in each fiscal year since our inception, including net losses of $12.9 million and $12.2 million for
the fiscal years ending March 31, 2013 and 2012, respectively. Our accumulated deficit was $67.7 million and $54.8 million, and our
stockholders’ deficit was $12.6 million and $5.7 million as of March 31, 2013 and 2012, respectively. These losses have resulted principally
from costs incurred in our research and development programs and general and administrative expenses.
To date, we have generated approximately $16.4 million of revenue from grant awards and strategic collaborations. We have financed our
operations primarily through grant awards and private placements of our securities. We have devoted substantially all of our efforts to research
and development. We expect to continue to incur significant expenses, operating and net losses and negative cash flow from operations, which
may increase, for the foreseeable future due primarily to anticipated increases in expenses for research and product development and increases in
general and administrative expenses related to operating and reporting as a public company, particularly in the event we are able to achieve our
goal of listing on the NASDAQ Global Market or a similar national exchange. The net losses we incur may fluctuate from quarter to
quarter. We anticipate that our business will generate operating losses until we successfully implement our commercial development strategy
relating to drug rescue and generate significant revenue to support our level of operating expenses related to:
Research and development of our hPSC technology platform;
Drug rescue activities;
Acquisition and/or in-license of products and technologies;
·
·
·
· Maintainence, expasion and protection of our intellectual property portfolio;
·
·
Hiring additional scientific and technical personnel; and
Adding operational, financial and management information systems and personnel to support our drug rescue activities and regulatory
compliance requirements relating to being a reporting company.
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To become and remain profitable we must develop and commercialize, either directly or, more likely, through collaborative arrangements with
pharmaceutical and biotechnology companies, a product or products with significant market potential. This will require us or our partners to be
successful in a range of challenging activities, including nonclinical testing and clinical trials of our Drug Rescue Variants, obtaining marketing
approval for these product candidates and manufacturing, marketing and selling those products for which we or our prospective partners may
obtain marketing approval. We and our collaborators may never succeed in these activities and, even if we do, may never generate revenues
that are significant or large enough to achieve profitability. If we do achieve profitability, we may not be able to sustain or increase profitability
on a quarterly or annual basis. Our failure to become or remain profitable would decrease the value of the company and could impair our ability
to raise capital, maintain our research, development and drug rescue efforts, expand our business or continue our operations. A decline in the
value of the company could also cause you to lose all or part of your investment.
We need to raise substantial additional capital to continue our research and drug rescue programs, and continue as a going concern
To fund our current and proposed hPSC technology research and development and drug rescue programs, and continue as a going concern,
we will need to raise substantial additional capital. The amount of additional capital we will need will depend on many factors, including:
•
•
•
•
revenues, if any, generated from collaborations with pharmaceutical and biotechnology companies involving the discovery,
development or licensing of customized cellular bioassays and new chemical entities, including Drug Rescue Variants, AV-101 or
other drug or biologic candidates or regenerative cell therapy product candidates;
expenses we incur in discovering, developing and licensing Drug Rescue Variants or other drug or biologic candidates;
the commercial success of our hPSC technology-based research and development efforts and AV-101; and
the emergence of competing scientific and technological developments and the extent to which we acquire or in-license other
products and technologies.
Other than the Autilion Financing, as defined below, we do not currently have any contractually committed sources of additional capital.
As of the date of this report, we have completed a nominal initial closing of the Autilion Financing. In the event the remaining portion of
the Autilion Financing is not completed as provided for in our financing agreement with Autilion, we will require substantial additional
financing through strategic collaborations, public or private equity financings, capital lease transactions or other financing sources and such
additional financing may not be available to us on a timely basis or on acceptable terms, or at all. If we are unable to complete the
Autilion Financing in full, or secure additional funding, or adequate funds are not available on a timely basis, we may be required to delay,
reduce or eliminate research and development programs, including drug rescue programs, license to third parties the rights to
commercialize products or technologies that we would otherwise seek to commercialize, or any combination of these activities. Any of
these results would materially harm our business, financial condition, and results of operations, and may cause our stock price to decline
and result in our inability to continue as a going concern.
We have entered into a strategic financing agreement to provide us with $36.0 million in working capital. An initial closing under the
agreement resulting in nominal proceeds has occurred. However, the second closing under the agreement, in the amount of $475,000
and scheduled for July 11, 2013, has not yet occurred. In the event the second closing, or any subsequently scheduled closing, does
not occur in a timely manner, we will need to secure alternative sources of capital, which may not be available on acceptable terms, or
at all, potentially resulting in our inability to continue as a going concern.
In April 2013, we entered into a Securities Purchase Agreement (as amended, the “Purchase Agreement”) providing for the issuance to
Autilion AG, a corporation organized and existing under the laws of Switzerland (“ Autilion), of 72 million shares of our common stock
for total gross proceeds of $36 million (the “AutilionFinancing”). As amended, the Purchase Agreement provides for a series of closings
between June 27, 2013 and September 30, 2013. As of the date of this report, a closing resulting in nominal proceeds from the Autilion
Financing has occurred. However, the second closing under the agreement, in the amount of $475,000 and scheduled for July 11, 2013,
has not yet occurred. This, we are informed by Autilion, is due to administrative delays involving Autilion and its international affiliates
and investment partners. Because the closing did not occur, the Purchase Agreement is currently in default. We have been informed by
Autilion that we will receive the total $36 million of proceeds contemplated by the Purchase Agreement. However, we can give no
assurances as to whether we will receive any additional funding in connection with the Autilion Financing. In the event we are not able to
close with respect to at least a significant portion of the proceeds anticipated from the Autilion Financing, we will need to obtain
substantial additional financing. Substantial additional financing may not be available on a timely basis, on terms acceptable to us, or at
all. In the event we are unable to obtain additional financing, our business, financial condition, and results of operations may be harmed,
the price of our stock may decline, and we may not be able to continue as a going concern.
In the event the Autilion Financing is completed in an amount exceeding $11.0 million, and we issue over 22 million shares of our
restricted common stock in connection with such funding, Autilion will control in excess of 50% of our issued and outstanding common
stock, resulting in a change in control of the Company. In addition, substantial dilution to existing stockholders will occur upon
completion of the Autilion Financing in part or in full.
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Some of our programs have been supported by government grants, which may not be available in the future. If we cannot continue to obtain
grant funding from government entities or private research foundations or research, drug rescue and development funding from
pharmaceutical or biotechnology companies, or if we fail to replace these sources of funding, our ability to continue operations will be
harmed.
We have received, and in the future, may receive, funds under research and economic development grant programs funded by state and federal
governmental agencies. and private grant funding and funding from pharmaceutical companies with which we have collaborative relationships.
In order to fund a substantial portion of future operations, particularly future operations related to our proposed drug rescue activities, we may
need to apply for and receive additional grant funding from governments and governmental organizations such as NIH, the NIH’s National
Institute of Neurological Disease and Stroke, and the California Institute for Regenerative Medicine. However, we may not secure any
additional funding from any governmental organization or private research foundation or otherwise. We cannot assure you that we will receive
grant funding in the future. If grant funds are required and are no longer available, or if the funds no longer meet our needs, some of our current
and future operations may be delayed or terminated. In addition, our business, financial condition and results of operations may be adversely
affected if we are unable to obtain future grants or alternative sources of funding.
Our independent auditors have expressed substantial doubt about our ability to continue as a going concern.
Our consolidated financial statements for the year ended March 31, 2013 included in Item 8 of this Report on Form 10-K, have been prepared
assuming that we will continue to operate as a going concern. The report of our independent registered public accounting firm on our
consolidated financial statements includes an explanatory paragraph discussing conditions that raise a substantial doubt about our ability to
continue as a going concern.
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Risks Related to Identification, Access, and Development of Our Drug Rescue Variants
We have not yet developed a Drug Rescue Variant and we cannot be certain that we will be able to do so in the future. Our prospective
customers, the pharmaceutical and biotechnology companies of the world, may not perceive value in our drug rescue efforts or otherwise
may choose not to collaborate with us.
Our ability to develop a Drug Rescue Variant is highly dependent upon the accuracy and efficiency of our Human Clinical Trials in a Test
TubeTM platform, particularly our CardioSafe 3D™ bioassay system. We have no operating history with respect to the development of Drug
Rescue Variants and we cannot be certain we will be able to develop and license one or more Drug Rescue Variants in the future. There are a
number of factors that may impact our ability to develop a Drug Rescue Variant, including:
•
•
•
•
•
Our ability to identify and access the potential for drug rescue of once-promising small molecule drug candidates that
pharmaceutical or biotechnology companies have discontinued in development due to unexpected safety concerns relating to
the heart or liver. If we cannot identify once-promising drug candidates that can be rescued in an efficient and cost-effective
manner, our business will be adversely affected. And, we may choose to focus our resources on a potential drug rescue
candidate the rescue of which ultimately proves to be unsuccessful. If we are unable to identify and access suitable drug
candidates for our drug rescue programs, we will not be able to generate product revenues in future periods, which likely will
result in significant harm to our financial position and adversely impact our stock price.
To the extent we seek to rescue once-promising but discontinued drug candidates that are not otherwise available for research
and development based on information available in the public domain, our ability to license from third-parties drug candidates
that have been discontinued in development due to unexpected heart or liver safety concerns. Because we may seek to leverage
prior third-party investment in drug discovery and development of a small molecule compounds with proprietary rights held by
third parties, the success of our business may depend, in significant part, on our ability to acquire or license such discontinued
compounds from third-parties. However, such third parties might be reluctant to enter into product acquisition or license
agreements with us on commercially reasonable terms, if at all. The licensing and acquisition of proprietary small molecule
compounds, even compounds that have failed in development due to heart or liver safety concerns, is a highly competitive
area, and a number of more established companies are also pursuing strategies to license or acquire compounds that we may
consider attractive as drug rescue candidates. These established companies have a competitive advantage over us due to their
size, cash resources and greater clinical development and commercialization capabilities. In addition, companies that perceive
us to be a competitor may be unwilling to sell or license drug candidate rights to us. We have no experience in negotiating
these licenses and there can be no assurances that we will be able to acquire or obtain licenses to discontinued drug rescue
candidates on commercially reasonable terms, if at all. If we are unable to acquire or obtain licenses to drug candidates we
seek to rescue, our business may be adversely affected.
Our medicinal chemistry collaborator’s ability to design and produce Drug Rescue Variants that are structurally related to the
drug candidate that was discontinued in development due to heart or liver safety concerns. If our medicinal chemistry
collaborator is unsuccessful for any reason in designing and producing Drug Rescue Variants, our business will be adversely
affected.
Our ability to execute our drug rescue programs in a timely and cost-effective manner. If our drug rescue programs are less
efficient and more expensive than we expect, our business will be adversely affected.
Our ability to develop Drug Rescue Variants and license them to pharmaceutical and biotechnology companies. The time
necessary to rescue any individual pharmaceutical product is long and can be uncertain. Only a small number of research and
development programs ultimately result in commercially successful drugs. We cannot assure you that toxicity results indicated
by our drug rescue testing models are indicative of results that would be achieved in future animal studies, in in vitro testing,
or in clinical studies, all or some of which will be required in order to obtain regulatory approval of our Drug Rescue Variants.
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Our internal validation studies of CardioSafe 3D TM have not been subject to peer review or third party validation.
Our internal validation studies, conducted to validate the ability of our CardioSafe 3DT M bioassay system to predict the cardiac effects of
prospective drug rescue candidates referred to under “Business – Application of Stem Cell Technology to Drug Rescue – CardioSafe 3D TM”,
have not been subject to peer review or third party validation. It is possible that the results we obtained from our internal validation studies may
not be able to be replicated by third parties. If we elect to license drug rescue candidates from pharmaceutical or biotechnology companies rather
than accessing information available in the public domain, and such companies cannot replicate our results, it will be difficult to negotiate and
obtain licenses from such companies to drug candidates we may seek to rescue. Even if such results can be replicated, pharmaceutical and
biotechnology companies may nevertheless conclude that their current drug testing models are better than our human heart cell-based bioassay
system, CardioSafe 3DTM, and that it does not merit a license to the drug candidate we seek to rescue. Our business model is predicated on our
ability to identify and, if information is not otherwise available in the public domain, obtain licenses from pharmaceutical and biotechnology
companies to promising drug rescue candidates. If licenses are required, and if we cannot obtain licenses to suitable drug rescue candidates, our
business will be adversely affected.
We cannot say with certainty that our in vitro toxicological testing systems, including CardioSafe 3DTM, and, when developed and validated,
LiverSafe 3DTM, will be more efficient or accurate at predicting the toxicity adverse drug-drug interactions of new drug candidates and Drug
Rescue Variants than the nonclinical testing models currently used by pharmaceutical companies.
The success of our drug rescue model is dependent upon the human heart and liver cell-based bioassay systems we develop being more accurate,
efficient and clinically predictive than animal and cellular testing models currently used in the pharmaceutical and biotechnology industries. The
accuracy and efficiency of our human heart and liver cell-based bioassay systems is central to our ability to generate Drug Rescue Variants. If
our bioassay systems are less accurate and less efficient than currently-used animal and cellular testing models, our business will be adversely
affected.
If we cannot enter into and successfully manage a sufficient number of strategic collaborations with pharmaceutical and biotechnology
companies, our ability to generate Drug Rescue Variants and fund our future operations will be harmed.
A future element of our drug rescue business model is to enter into strategic development and marketing collaborations with established
pharmaceutical and biotechnology companies to finance or otherwise assist in the development, marketing and manufacture of Drug Rescue
Variants utilizing our hPSC technology-based bioassay systems for screening heart toxicity, liver toxicity and adverse drug-drug interactions.
Our goal in such collaborations will be to generate a recurring stream of revenues from upfront license fees, research and development milestone
payments and royalties on commercial sales of Drug Rescue Variants. Our prospects, therefore, will depend in large part upon our ability to
attract and retain pharmaceutical and biotechnology collaborators and to generate Drug Rescue Variants that meet the requirements of our
prospective collaborators. In addition, our collaborators will generally have the right to abandon research and development projects and
terminate applicable agreements, including funding obligations, prior to or upon the expiration of the agreed-upon research and development
terms. There can be no assurance that we will be successful in establishing multiple future collaborations with pharmaceutical and biotechnology
companies on acceptable terms or at all, that current or future collaborations will not terminate funding before completion of projects, that our
existing or future collaborative arrangements will result in successful development and commercialization of Drug Rescue Variants or that we
will derive any revenues from such arrangements. To the extent that we are unable to maintain existing or establish new strategic collaborations
with pharmaceutical and biotechnology companies, it would require substantial additional capital for us to undertake research, development and
commercialization activities on our own.
In varying degrees for each of the drug candidates we may seek to include in our drug rescue programs , following internal studies to establish in
vitro proof of concept of the safety and efficacy of each lead Drug Rescue Variant, we expect to rely on our pharmaceutical or biotechnology
company collaborators to develop, conduct Investigational New Drug-enabling studies and human clinical trials on, obtain regulatory approvals
for, manufacture, market and/or commercialize the Drug Rescue Variant(s) we license to them. Such collaborators’ diligence and dedication of
resources in conducting these activities will depend on, among other things, their own competitive, marketing and strategic considerations,
including the relative advantages of competitive products. The failure of our collaborators to conduct, successfully and diligently, their
collaborative activities relating to Drug Rescue Variants we license to them would have a material adverse effect on us.
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Some of our competitors or pharmaceutical or biotechnology companies may develop technologies that are superior to or more cost-effective
than ours, which may impact the commercial viability of our technologies and which may significantly damage our ability to sustain
operations.
The pharmaceutical and biotechnology industries are intensely competitive. Other hPSC biology-based bioassay systems and drug candidates
that could compete directly with the bioassay technologies and product candidates that we seek to discover, develop and commercialize
currently exist and are being developed by pharmaceutical and biotechnology companies and by academic and other research-oriented
organizations.
Many of the pharmaceutical and biotechnology companies developing and marketing these competing products and technologies have
significantly greater financial resources and expertise than we do in research and development, manufacturing, preclinical and clinical testing,
obtaining regulatory approvals and marketing and distribution of new drug candidates. Pharmaceutical and biotechnology companies with whom
we seek to collaborate also have or may develop their own competing internal programs.
Small companies may also prove to be significant competitors, particularly through collaborative arrangements with large and established
companies. Academic institutions, government agencies and other public and private research organizations are conducting research, seeking
patent protection and establishing collaborative arrangements for research, clinical development and marketing of products similar to ours. These
companies and institutions compete with us in recruiting and retaining qualified scientific and management personnel, obtaining collaborators
and licensees, as well as in acquiring technologies complementary to our programs.
In addition to the above factors, we expect to face competition in the areas of evaluation of product efficacy and safety, the timing and scope of
regulatory consents, availability of resources, reimbursement coverage, price and patent position, including potentially dominant patent positions
of others.
As a result of the foregoing, our competitors may develop more effective or more affordable products, or achieve earlier patent protection or
product commercialization than we do. Most significantly, competitive products may render any technologies and product candidates that we
develop obsolete, which would negatively impact our business and ability to sustain operations.
Restrictions on the use of Embryonic Stem Cells (“ES Cells”), political commentary and the ethical and social implications of research
involving ES Cells could prevent us from developing or gaining acceptance for commercially viable products based upon such stem cells and
adversely affect the market price of our Common Stock.
Some of our most important programs involve the use of ES Cells. Some believe the use of ES Cells gives rise to ethical and social issues
regarding the appropriate use of these cells. Our research related to ES Cells may become the subject of adverse commentary or publicity, which
could significantly harm the market price of our Common Stock.
Although substantially less than in years past, certain political and religious groups in the United States voice opposition to ES Cell technology
and practices. All procedures we use to obtain clinical samples, and the procedures we use to isolate ES Cells, are consistent with the informed
consent and ethical guidelines promulgated by the U.S. National Academy of Science, the International Society of Stem Cell Research
(“ISSCR”), and the NIH. These procedures and documentation have been reviewed by an external Stem Cell Research Oversight Committee, and
all cell lines we use have been approved under these guidelines. We use stem cells derived from excess fertilized eggs that have been created for
clinical use in in vitro fertilization (“IVF”) procedures and have been donated for research purposes with the informed consent of the donors
after a successful IVF procedure because they are no longer desired or suitable for IVF. Many research institutions, including some of our
scientific collaborators, have adopted policies regarding the ethical use of human embryonic tissue. These policies may have the effect of
limiting the scope of research conducted using ES Cells, thereby impairing our ability to conduct research in this field.
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The U.S. government and its agencies on July 7, 2009 published guidelines for the ethical derivation of human ES Cells required for receiving
federal funding for ES Cell research. All of the ES Cell lines we use meet these guidelines for NIH funding. In the U.S., the President’s Council
on Bioethics monitors stem cell research, and may make recommendations from time to time that could place restrictions on the scope of
research using human embryonic or fetal tissue. Although numerous states in the U.S. are considering, or have in place, legislation relating to
stem cell research, including California whose voters approved Proposition 71 to provide up to $3 billion of state funding for stem cell research
in California, it is not yet clear what affect, if any, state actions may have on our ability to commercialize stem cell technologies. The use of
embryonic or fetal tissue in research (including the derivation of ES Cells) in other countries is regulated by the government, and varies widely
from country to country. These regulations may affect our ability to commercialize ES Cell-based bioassay systems.
Government-imposed restrictions with respect to use of ES Cells in research and development could have a material adverse effect on us by
harming our ability to establish critical collaborations, delaying or preventing progress in our research and development, and causing a decrease
in the market interest in our stock. These potential ethical concerns do not apply to iPS Cells because their derivation does not involve the use of
embryonic tissues.
We have assumed that the biological capabilities of Induced Pluripotent Stem Cells (“iPS Cells”) and ES Cells for in vitro bioassay systems
are likely to be comparable. If it is discovered that this assumption is incorrect, our ability to develop our Human Clinical Trials in a Test
TubeTM platform could be harmed.
We use both ES Cells and iPS Cells as the basis for the continuing development of our Human Clinical Trials in a Test Tube TM platform. With
respect to iPS Cells, scientists are still unsure about the clinical utility, life span, and safety of such cells, and whether such cells differ in any
clinically significant ways from ES Cells. If we discover that iPS Cells will not be useful for whatever reason for our Human Clinical Trials in a
Test TubeTM platform, we could be limited to using only ES Cells. This could negatively affect our ability to develop our Human Clinical Trials
in a Test Tube TM platform, particularly in circumstances where it would be preferable to produce iPS Cells to reflect the effects of desired
specific genetic variations.
Risks Related to the Regulation of Biological Products
Some of our products, including our or our prospective collaborators’ potential regenerative cell therapy products, may be subject to biological
product regulations. During their clinical development, biological products are regulated pursuant to Investigational New Drug (“IND”)
requirements. Product development and approval takes a number of years, involves the expenditure of substantial resources and is uncertain.
Many biological products that appear promising ultimately do not reach the market because they cannot meet FDA or other regulatory
requirements. In addition, there can be no assurance that the current regulatory framework will not change through regulatory, legislative or
judicial actions or that additional regulation will not arise during our product development that may affect approval, delay the submission or
review of an application, if required, or require additional expenditures by us.
The activities required before a new biological product may be approved for marketing in the U.S. primarily begin with preclinical testing,
which includes laboratory evaluation and animal studies to assess the potential safety and efficacy of the product as formulated. Results of
preclinical studies are summarized in an IND application to the FDA. Human clinical trials may begin 30 days following submission of an IND
application, unless the FDA requires additional time to review the application or raise questions.
Clinical testing involves the administration of the drug or biological product to healthy human volunteers or to patients under the supervision of
a qualified principal investigator, usually a physician, pursuant to an FDA-reviewed protocol. Each clinical study is conducted under the
auspices of an institutional review board (“IRB”) at each of the institutions at which the study will be conducted. A clinical plan, or “protocol,”
accompanied by the approval of an IRB, must be submitted to the FDA as part of the IND application prior to commencement of each clinical
trial. Human clinical trials are conducted typically in three sequential phases. Phase I trials consist of, primarily, testing the product’s safety in a
small number of patients or healthy volunteers. In Phase II, the safety and efficacy of the product candidate is evaluated in a specific patient
population. Phase III trials typically involve additional testing for safety and clinical efficacy in an expanded patient population at geographically
dispersed sites. The FDA may order the temporary or permanent discontinuance of a preclinical or clinical trial at any time for a variety of
reasons, particularly if safety concerns exist.
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A company seeking FDA approval to market a biological product must file a Biologics License Application (“BLA”). In addition to reports of the
preclinical and human clinical trials conducted under the IND application, the BLA includes evidence of the product’s safety, purity, potency
and efficacy, as well as manufacturing, product identification and other information. Submission of a BLA does not assure FDA approval for
marketing. The application review process generally takes one to three years to complete, although reviews of drugs and biological products for
life-threatening diseases may be accelerated or expedited. However, the process may take substantially longer.
The FDA requires at least one and often two properly conducted, adequate and well-controlled clinical studies demonstrating efficacy with
sufficient levels of statistical assurance. However, additional information may be required. Notwithstanding the submission of such data, the
FDA ultimately may decide that the BLA does not satisfy the regulatory criteria for approval and not approve the application. The FDA may
impose post-approval obligations, such as additional clinical tests following BLA approval to confirm safety and efficacy (Phase IV human
clinical trials). The FDA may, in some circumstances, also impose restrictions on the use of the biological product that may be difficult and
expensive to administer. Further, the FDA requires reporting of certain safety and other information that becomes known to a manufacturer of an
approved biological product. Product approvals may be withdrawn if compliance with regulatory requirements is not maintained or if problems
occur after the product reaches the market.
Prior to approving an application, the FDA will inspect the prospective manufacturer to ensure that the manufacturer conforms to the FDA’s
current good manufacturing practice (“cGMP”) regulations that apply to biologics. To comply with the cGMP regulations, manufacturers must
expend time, money and effort in product recordkeeping and quality control to assure that the product meets applicable specifications and other
requirements. The FDA periodically inspects manufacturing facilities in the U.S. and abroad in order to assure compliance with applicable cGMP
requirements. Our failure to comply with the FDA’s cGMP regulations or other FDA regulatory requirements could have a significant adverse
effect on us.
After a product is approved for a given indication in a BLA, subsequent new indications or dosage levels for the same product are reviewed by
the FDA via the filing and approval of a BLA supplement. The BLA supplement is more focused than the BLA and deals primarily with safety
and effectiveness data related to the new indication or dosage. Applicants are required to comply with certain post-approval obligations, such as
compliance with cGMPs.
Risks Related to Our Intellectual Property
If we fail to meet our obligations under license agreements, we may lose our rights to key technologies on which our business depends.
Our business depends on several critical technologies that are based in part on patents licensed from third parties. Those third-party license
agreements impose obligations on us, such as payment obligations and obligations to diligently pursue development of commercial products
under the licensed patents. If a licensor believes that we have failed to meet our obligations under a license agreement, the licensor could seek to
limit or terminate our license rights, which could lead to costly and time-consuming litigation and, potentially, a loss of the licensed rights.
During the period of any such litigation our ability to carry out the development and commercialization of potential products could be
significantly and negatively affected. If our license rights were restricted or ultimately lost, our ability to continue our business based on the
affected technology would be severely adversely affected.
If we elect to leverage prior discovery and development of drug candidates under license arrangements with third-party pharmaceutical or
biotechnology companies, or other third parties, it is uncertain what ownership rights, if any, we will obtain over intellectual property we
derive from such licenses to lead Drug Descue Variants we develop in connection with any such third-party licenses.
If, instead of identifying drug candidates for our drug rescue programs based on information available to us in the public domain, we elect to
negotiate and obtain licenses from pharmaceutical and biotechnology companies, or other third-parties, to drug candidates that these third-parties
have discontinued in development because of unexpected heart or liver safety concerns, there can be no assurances that we will obtain
ownership rights over intellectual property we derive from our licenses to the failed drug candidates or rights to Drug Rescue Variants we
generate and develop as new, safer and effective alternatives to the original failed drug candidates. If we are unable to obtain ownership rights
over intellectual property related to Drug Rescue Variants we generate, or economic participation rights relating to the successful development
and commercialization of such Drug Rescue Variants by potential collaborators, our business will be adversely affected.
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If we are not able to obtain and enforce patent protection or other commercial protection for AV-101 or our pluripotent stem cell
technologies, the value of AV-101 and our stem cell technologies and product candidates will be harmed.
Commercial protection of AV-101 and our proprietary pluripotent stem cell technologies is critically important to our business. Our success will
depend in large part on our ability to obtain and enforce our patents and maintain trade secrets, both in the U.S. and in other countries, and, with
respect to AV-101, secure New Drug Product Exclusivity provided by the FDA under section 505(c)(3)(E) and 505(j)(5)(F) of the Federal Food,
Drug, and Cosmetic Act.
Additional patents may not be granted, and our existing U.S. and foreign patents might not provide us with commercial benefit or might be
infringed upon, invalidated or circumvented by others. In addition, the availability of patents in foreign markets, and the nature of any protection
against competition that may be afforded by those patents, is often difficult to predict and vary significantly from country to country. With
respect to AV-101. the principle U.S. method of use patent and its foreign counterparts have expired. Although recently we have filed three new
U.S. patent applications relating to AV-101, we or others with whom we may collaborate for the development and commercialization of AV-101
may choose not to seek, or may be unable to obtain, patent protection in a country that could potentially be an important market for AV-101.
The patent positions of pharmaceutical and biopharmaceutical companies, including ours, are highly uncertain and involve complex legal and
technical questions. In particular, legal principles for biotechnology patents in the U.S. and in other countries are evolving, and the extent to
which we will be able to obtain patent coverage to protect our technology, or enforce issued patents, is uncertain.
For example, the European Patent Convention prohibits the granting of European patents for inventions that concern “uses of human embryos
for industrial or commercial purposes”. The European Patent Office is presently interpreting this prohibition broadly, and is applying it to reject
patent claims that pertain to ES Cells. However, this broad interpretation is being challenged through the European Patent Office appeals system.
As a result, we do not yet know whether or to what extent we will be able to obtain European patent protection for our proprietary ES Cell-based
technology and systems.
Publication of discoveries in scientific or patent literature tends to lag behind actual discoveries by at least several months and sometimes several
years. Therefore, the persons or entities that we or our licensors name as inventors in our patents and patent applications may not have been the
first to invent the inventions disclosed in the patent applications or patents, or the first to file patent applications for these inventions. As a result,
we may not be able to obtain patents for discoveries that we otherwise would consider patentable and that we consider to be extremely
significant to our future success.
Where several parties seek U.S. patent protection for the same technology, the U.S. Patent and Trademark Office (“ U.S. PTO”) may declare an
interference proceeding in order to ascertain the party to which the patent should be issued. Patent interferences are typically complex, highly
contested legal proceedings, subject to appeal. They are usually expensive and prolonged, and can cause significant delay in the issuance of
patents. Moreover, parties that receive an adverse decision in interference can lose patent rights. Our pending patent applications, or our issued
patents, may be drawn into interference proceedings, which may delay or prevent the issuance of patents or result in the loss of issued patent
rights. If more groups become engaged in scientific research related to ES Cells, the number of patent filings by such groups and therefore the
risk of our patents or applications being drawn into interference proceedings may increase. The interference process can also be used to
challenge a patent that has been issued to another party.
Outside of the U.S., certain jurisdictions, such as Europe, Japan, New Zealand and Australia, permit oppositions to be filed against the granting
of patents. Because our intent is to commercialize our products internationally, securing both proprietary protection and freedom to operate
outside of the U.S. is important to our business.
Patent opposition proceedings are not currently available in the U.S. patent system, but legislation is pending to introduce them. However, issued
U.S. patents can be re-examined by the U.S. PTO at the request of a third party. Patents owned or licensed by us may therefore be subject to re-
examination. As in any legal proceeding, the outcome of patent re-examinations is uncertain, and a decision adverse to our interests could result
in the loss of valuable patent rights.
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Successful challenges to our patents through interference, opposition or re-examination proceedings could result in a loss of patent rights in the
relevant jurisdiction(s). As more groups become engaged in scientific research and product development areas of hES Cells, the risk of our
patents being challenged through patent interferences, oppositions, re-examinations or other means will likely increase. If we institute such
proceedings against the patents of other parties and we are unsuccessful, we may be subject to litigation, or otherwise prevented from
commercializing potential products in the relevant jurisdiction, or may be required to obtain licenses to those patents or develop or obtain
alternative technologies, any of which could harm our business.
Furthermore, if such challenges to our patent rights are not resolved promptly in our favor, our existing business relationships may be
jeopardized and we could be delayed or prevented from entering into new collaborations or from commercializing certain products, which could
materially harm our business.
The confidentiality agreements that are designed to protect our trade secrets could be breached, and we might not have adequate remedies for the
breach. Additionally, our trade secrets and proprietary know-how might otherwise become known or be independently discovered by others, all
of which could materially harm our business.
We may have to engage in costly litigation to enforce or protect our proprietary technology, particularly our pluripotent stem cell technology
and human heart and liver cell-based bioassay systems, or to defend challenges to our proprietary technology by our competitors, which may
harm our business, results of operations, financial condition and cash flow.
Litigation may be necessary to protect our proprietary rights, especially our rights to our pluripotent stem cell technology and human heart and
liver cell-based bioassay systems. Such litigation is expensive and would divert material resources and the time and attention of our management.
We cannot be certain that we will have the required resources to pursue litigation or otherwise to protect our proprietary rights. In the event that
we are unsuccessful in obtaining and enforcing patents, our business would be negatively impacted and th price of our Common Stock could
decline. Further, our patents may be challenged, invalidated or circumvented, and our patent rights may not provide proprietary protection or
competitive advantages to us.
Patent litigation may also be necessary to enforce patents issued or licensed to us or to determine the scope and validity of our proprietary rights
or the proprietary rights of others. We may not be successful in any patent litigation. An adverse outcome in a patent litigation, patent opposition,
patent interference, or any other proceeding in a court or patent office could subject our business to significant liabilities to other parties, require
disputed rights to be licensed from other parties or require us to cease using the disputed technology, any of which could severely harm our
business and could cause the price of our Common Stock to decline.
We may be subject to litigation that will be costly to defend or pursue and uncertain in its outcome.
Our business may bring us into conflict with our institutional investors, licensees, licensors, or others with whom we have contractual or other
business relationships, or with our competitors or others whose interests differ from ours. If we are unable to resolve such conflicts on terms that
are satisfactory to all parties, we may become involved in litigation brought by or against us. Any such litigation is likely to be expensive and
may require a significant amount of management’s time and attention, at the expense of other aspects of our business. The outcome of litigation
is always uncertain, and in some cases could include judgments against us that require us to pay damages, enjoin us from certain activities, or
otherwise affect our legal or contractual rights, which could have a significant adverse effect on our business.
Much of the information and know-how that is critical to our business is not patentable and we may not be able to prevent others from
obtaining this information and establishing competitive enterprises.
We rely, in significant part, on trade secrets to protect our proprietary technologies, especially in circumstances that we believe patent protection
is not appropriate or available. We attempt to protect our proprietary technologies in part by confidentiality agreements with our advisors,
collaborators, consultants, contractors and employees. We cannot assure you that these agreements will not be breached, that we would have
adequate remedies for any breach, or that our trade secrets will not otherwise become known or be independently discovered by competitors, any
of which would harm our business significantly.
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We may be subject to infringement claims that are costly to defend, and which may limit our ability to use disputed technologies and prevents
us from pursuing research and development or commercialization of potential products.
Our commercial success depends significantly on our ability to operate without infringing patents and the proprietary rights of others. Our
technologies may infringe on the patents or proprietary rights of others. In addition, we may become aware of discoveries and technology
controlled by third parties that are advantageous to our programs. In the event our technologies infringe the rights of others or we require the use
of discoveries and technologies controlled by third parties, we may be prevented from pursuing research, development or commercialization of
potential products or may be required to obtain licenses to those patents or other proprietary rights or develop or obtain alternative technologies.
We have obtained licenses from several universities and companies for technologies that we anticipate incorporating into our Human Clinical
Trials in a Test Tube TM platform. We may not be able to obtain a license to patented technology on commercially favorable terms, or at all. If
we do not obtain a necessary license, we may need to redesign our technologies or obtain rights to alternate technologies, the research and
adoption of which could cause delays in product development. In cases where we are unable to license necessary technologies, we could be
prevented from developing certain potential products. Our failure to obtain alternative technologies or a license to any technology that we may
require to research, develop or commercialize our product candidates would significantly and negatively affect our business and the price of our
Common Stock could decline.
Risks Related to Development, Clinical Testing and Regulatory Approval of Drug Rescue Variants and other Drug Candidates, Biologic
Candidates and Regenerative Cell Therapy Product Candidates
We have limited experience as a corporation conducting clinical trials, or in other areas required for the successful commercialization and
marketing of Drug Rescue Variants and other drug candidates, biologic candidates or regenerative cell therapy product candidates.
We will need to receive regulatory approval for any product candidate before it may be marketed and distributed. Such approval will require,
among other things, completing carefully controlled and well-designed clinical trials demonstrating the safety and efficacy of each product
candidate. This process is lengthy, expensive and uncertain. As a company, we have limited experience in conducting clinical trials. Such trials
will require additional financial and management resources, collaborators with the requisite clinical experience or reliance on third party clinical
investigators, contract research organizations and consultants. Relying on third parties may force us to encounter delays that are outside of our
control, which could materially harm our business.
We also do not currently have marketing and distribution capabilities for product candidates. Developing an internal sales and distribution
capability would be an expensive and time-consuming process. To market and distribute any Drug Rescue Variant and other drug candidate,
biologic candidate or regenerative cell therapy product candidate we develop, we plan to enter into strategic a agreement with a third-party
collaborator that would be responsible for marketing and distribution. However, these third-party collaborators may not be capable of
successfully selling any of our product candidates.
Because we and our collaborators must complete lengthy and complex development and regulatory approval processes required to market
drug products in the U.S. and other countries, we cannot predict whether or when we or our collaborators will be permitted to commercialize
Drug Rescue Variants or other drug candidates, biologic candidates or regenerative cell therapy product candidates to which we have
commercial rights.
Federal, state and local governments in the U.S. and governments in other countries have significant regulations in place that govern many of our
activities and may prevent us from creating commercially viable products derived from our drug rescue, drug development and regenerative cell
therapy programs.
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The regulatory process, particularly for drug and biologic candidates, is uncertain, can take many years and requires the expenditure of
substantial resources. Any Drug Rescue Variant or other drug candidate, biologic candidate or regenerative cell therapy product candidate that
we or our collaborators develop must receive all relevant regulatory agency approvals before it may be marketed in the U.S. or other countries.
Biological drugs and non-biological drugs are rigorously regulated. In particular, human pharmaceutical therapeutic product candidates are
subject to rigorous preclinical and clinical testing and other requirements by the FDA in the U.S. and similar health authorities in other countries
in order to demonstrate safety and efficacy. Because any Drug Rescue Variant or other drug candidate, biologic candidate or regenerative cell
therapy product candidate we develop, or collaborate with others to develop, are expected to involve the application of new technologies or are
based upon new therapeutic approaches, they may be subject to substantial additional review by various government regulatory authorities, and,
as a result, the process of obtaining regulatory approvals for them may proceed more slowly than for drug or biologic candidates based upon
more conventional technologies. We may never obtain regulatory approval to market a Drug Rescue Variant or other drug candidate, biologic
candidate or regenerative cell therapy product candidate.
Data obtained from preclinical and clinical activities is susceptible to varying interpretations that could delay, limit or prevent regulatory agency
approvals. In addition, delays or rejections may be encountered as a result of changes in regulatory agency policy during the period of product
development and/or the period of review of any application for regulatory agency approval for a drug or biologic candidate. Delays in obtaining
regulatory agency approvals could significantly harm the marketing of any product that we or our collaborators develop, impose costly
procedures upon our activities or the activities of our collaborators, diminish any competitive advantages that we or our collaborators may attain,
or adversely affect our ability to receive royalties and generate revenues and profits.
If we obtain regulatory agency approval for a new drug, biologic or regenerative cell therapy product, this approval may entail limitations on the
indicated uses for which it can be marketed that could limit the potential commercial use of the product. Additionally, approved products and
their manufacturers are subject to continual review, and discovery of previously unknown problems with a product or its manufacturer may
result in restrictions on the product or manufacturer, including withdrawal of the product from the market. The sale by us or our collaborators of
any commercially viable product will be subject to government regulation from several standpoints, including the processes of manufacturing,
advertising and promoting, selling and marketing, labeling and distribution. Failure to comply with regulatory requirements can result in severe
civil and criminal penalties, including but not limited to product recall or seizure, injunction against product manufacture, distribution, sales and
marketing and criminal prosecution. The imposition of any of these penalties could significantly impair our business, financial condition and
results of operations.
Entry into clinical trials with one or more drug candidates, biologic candidates or regenerative cell therapy product candidates may not result
in any commercially viable products.
We may never generate revenues from product sales because of a variety of risks inherent in our business, including the following risks:
•
•
clinical trials may not demonstrate the safety and efficacy of our Drug Rescue Variants or other drug candidates, biologic candidates or
regenerative cell therapy product candidates;;
completion of clinical trials may be delayed, or costs of clinical trials may exceed anticipated amounts;
• we may not be able to obtain regulatory approval of our Drug Rescue Variants or other drug candidates, biologic candidates or
regenerative cell therapy product candidates; or may experience delays in obtaining such approval;
• we may not be able to manufacture our Drug Rescue Variants or other drug candidates, biologic candidates or regenerative cell therapy
product candidates economically on a commercial scale;
• we and any licensees of ours may not be able to successfully market our Drug Rescue Variants or other drug candidates, biologic
candidates or regenerative cell therapy product candidates;
•
•
•
physicians may not prescribe our products, or patients or third party payors may not accept our Drug Rescue Variants or other drug
candidates, biologic candidates or regenerative cell therapy product candidates;
others may have proprietary rights which prevent us from marketing our Drug Rescue Variants or other drug candidates, biologic
candidates or regenerative cell therapy product candidates; and
competitors may sell similar, superior or lower-cost products.
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To be successful, our Drug Rescue Variants, drug candidates, biologic candidates and regenerative cell therapy product candidates must be
accepted by the healthcare community, which can be very slow to adopt or unreceptive to new technologies and products.
Our Drug Rescue Variants, drug candidates, biologic candidates and regenerative cell therapy product candidates, if developed and approved for
marketing, may not achieve market acceptance because hospitals, physicians, patients or the medical community in general may decide not to
accept and utilize these products. The Drug Rescue Variants, drug candidates, biologic candidates and regenerative cell therapy product
candidates that we may attempt to develop may represent substantial departures from established treatment methods and will compete with a
number of conventional drugs and therapies manufactured and marketed by major pharmaceutical and biotechnology companies. The degree of
market acceptance of any of our product candidates will depend on a number of factors, including:
•
•
•
•
our establishment and demonstration to the medical community of the clinical efficacy and safety of our Drug Rescue Variants, drug
candidates, biologic candidates and regenerative cell therapy product candidates;
our ability to create product candidates that are superior to alternatives currently on the market;
our ability to establish in the medical community the potential advantage of our treatments over alternative treatment methods; and
reimbursement policies of government and third-party payors.
If the healthcare community does not accept our developed Drug Rescue Variants, drug candidates, biologic candidates or regenerative cell
therapy product candidates for any of the foregoing reasons, or for any other reason, our business would be materially harmed.
Risks Related to Our Dependence on Third Parties
Our reliance on the activities of our non-employee advisors, consultants, research institutions and scientific contractors, whose activities are
not wholly within our control, may lead to delays in development of our product candidates.
We rely upon and have relationships with scientific consultants at academic and other institutions, some of whom conduct research at our
request, and other advisors, including former pharmaceutical company executives, contractors and consultants with expertise in drug discovery,
drug development, medicinal chemistry, regulatory strategy, corporate development or other matters. These parties are not our employees and
may have commitments to, or consulting or advisory contracts with, other entities that may limit their availability to us. We have limited control
over the activities of our advisors, consultants and contractors and, except as otherwise required by our collaboration and consulting agreements,
can expect only limited amounts of their time to be dedicated to our activities.
In addition, we have formed, and anticipate forming additional, sponsored research collaborations with academic and other research institutions
throughout the world. We are highly dependent on these sponsored research collaborations for the development of our intellectual property.
These research facilities may have commitments to other commercial and non-commercial entities. There can also be no assurances that any
intellectual property will be created from our sponsored research collaborations and, even if it is created, that the intellectual property will have
any value or application to our business. We have limited control over the operations of these laboratories and can expect only limited amounts
of their time to be dedicated to our research goals.
If any third party with whom we have or enter into a relationship is unable or refuses to contribute to projects on which we need their help, our
ability to advance our technologies and develop our product candidates could be significantly harmed.
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Our stem cell technology-based drug rescue business model involves reliance on strategic collaborations with third parties.
Our stem cell technology-based business model contemplates making arrangements with third parties:
•
•
•
to identify, in the public domain or elsewhere, and access failed drug candidates to rescue and develop;
to license lead Drug Rescue Variants that we develop; and
to perform stem cell research and development and supply contract services, such as medicinal chemistry, that is our key to our future
success.
A key component of our strategy is developing a “drug rescue ecosystem” by entering into collaborative arrangements with pharmaceutical and
biotechnology companies, academic institutions, contract research and development and regulatory service organizations and others for certain
aspects of ourresearch and development programs. There can be no assurance, however, that we will be able to maintain our current
collaborations or establish additional collaborations on favorable terms, if at all, or that our current or future collaborative arrangements will be
successful.
Should any collaborator fail to develop or commercialize successfully any Drug Rescue Variant, drug candidate or biologic candidate to which it
has rights from us, or any of the collaborator’s drug candidate or biologic candidate to which we may have rights, our business may be adversely
affected. In addition, while we believe that collaborators will have sufficient economic motivation to continue their funding, there can be no
assurance that any of these collaborations will be continued or result in successfully commercialized product candidates. Failure of a
collaborator to continue funding any particular program, or our inability to provide our collaborator with required funding, could delay or halt
the development or commercialization of any technology or product candidates arising out of such programs. In addition, there can be no
assurance that the collaborators will not pursue alternative technologies, change strategy, re-allocate resources, terminate our agreement, develop
alternative product candidates either on their own or in collaboration with others, including our competitors.
If a conflict of interest arises between us and one or more of our collaborators, they may act in their own self-interest and not in our interest or in
the interest of our shareholders. Some of our collaborators are conducting, and any of our future collaborators may conduct, multiple product
candidate development efforts within the disease area that is the subject of collaboration with us.
Given these risks, our current and future collaborative efforts with third parties may not be successful. Failure of these efforts could require us to
devote additional internal resources to the activities currently performed, or to be performed, by third parties, to seek alternative third-party
collaborators, or to delay product candidate development or commercialization, which could have a material adverse effect on our business,
financial conditions or results of operations.
Risks Related to Our Operations
We depend on key scientific and management personnel and collaborators for the implementation of our business plan, the loss of whom
would slow our ability to conduct research and develop and impair our ability to compete.
Our future success depends to a significant extent on the skills, experience and efforts of our executive officers and key employees on our
scientific staff. Competition for personnel, especially scientific personnel, is intense and we may be unable to retain our current personnel, attract
or assimilate other highly qualified management and scientific personnel in the future. The loss of any or all of these individuals would result in
a significant loss in the knowledge and experience that we, as an organization, possess and could harm our business and might significantly
delay or prevent the achievement of research, development or business objectives. Our management and key employees can terminate their
employment with us at any time.
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We also rely on numerous consultants, strategic advisors and strategic collaborators, especially our long-term strategic collaboration with
Dr. Gordon Keller, who assists us in formulating our stem cell research and development strategies. We face intense competition for qualified
individuals from numerous pharmaceutical, biopharmaceutical and biotechnology companies, as well as academic and other research institutions.
We may not be able to attract and retain these individuals on acceptable terms. Failure to do so could materially harm our business.
Although the current term of our sponsored research collaboration agreement with UHN and our co-founder, Dr. Gordon Keller, does not expire
until September 2017, and our intention is to renew and extend the agreement beyond 2017, there can be no assurances that we will be able to
renew or extend the agreement beyond 2017 on mutually agreeable terms, if at all. Additionally, there can be no assurances that we will receive
any invention notices or secure a license to any intellectual property resulting from such sponsored research.
We will need to hire additional highly specialized, skilled personnel to achieve our business plan. Our inability to hire qualified personnel in
a timely manner will harm our business.
Our ability to execute on our business plan will depend on the talents and efforts of highly skilled individuals with specialized training in the
field of stem cell research and bioassay development, as well as in vitro drug candidate screening and nonclinical and clinical development. Our
future success depends on our ability to identify, hire and retain these highly skilled personnel during our early stages of development.
Competition in our industry for qualified employees with the specialized training we require is intense. In addition, our compensation
arrangements may not always be successful in attracting the new employees we require. Our ability to execute our drug rescue business model
effectively depends on our ability to attract these new employees.
Our research and development activities involve the controlled use of hazardous materials, and improper handling of these materials by our
employees or agents could expose us to significant legal and financial penalties.
Our research and development activities involve the controlled use of hazardous materials, chemicals and various radioactive compounds. As a
consequence, we are subject to numerous environmental and safety laws and regulations, including those governing laboratory procedures
exposure to blood-borne pathogens and the handling of bio-hazardous materials. We may be required to incur significant costs to comply with
current or future environmental laws and regulations and may be adversely affected by the cost of compliance with these laws and regulations.
Although we believe that our safety procedures for using, handling, storing and disposing of hazardous materials comply with the standards
prescribed by state and federal regulations, the risk of accidental contamination or injury from these materials cannot be eliminated. In the event
of such an accident, state or federal authorities could curtail our use of these materials and we could be liable for any civil damages that result,
the cost of which could be substantial. Further, any failure by us to control the use, disposal, removal or storage, or to adequately restrict the
discharge, or assist in the cleanup, of hazardous chemicals or hazardous, infectious or toxic substances could subject us to significant liabilities,
including joint and several liability under certain statutes. Any such liability could exceed our resources and could have a material adverse effect
on our business, financial condition and results of operations. Additionally, an accident could damage our research and manufacturing facilities
and operations.
Additional federal, state and local laws and regulations affecting us may be adopted in the future. We may incur substantial costs to comply with
these laws and regulations and substantial fines or penalties if we violate any of these laws or regulations.
We may not be able to obtain or maintain sufficient insurance on commercially reasonable terms or with adequate coverage against
potential liabilities in order to protect ourselves against product liability claims.
Our business exposes us to potential product liability risks that are inherent in the testing, manufacturing and marketing of human therapeutic
products and testing technologies. We may become subject to product liability claims if the use of our potential products is alleged to have
injured subjects or patients. This risk exists for product candidates tested in human clinical trials as well as potential products that are sold
commercially. In addition, product liability insurance is becoming increasingly expensive. As a result, we may not be able to obtain or maintain
product liability insurance in the future on acceptable terms or with adequate coverage against potential liabilities that could have a material
adverse effect on our business.
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Our business is subject to the risks of earthquakes, fire, floods and other natural catastrophic events, and to interruption by man-made
problems such as computer viruses or terrorism.
Our corporate headquarters are located in the San Francisco Bay Area, a region known for seismic activity. A significant natural disaster, such
as an earthquake, fire or a flood, could harm our business. In addition, our servers are vulnerable to computer viruses, break-ins and similar
disruptions from unauthorized tampering with our computer systems. In addition, acts of terrorism or war could cause disruptions in our business
or the economy as a whole.
We may select and develop product candidates that fail.
We may select for development and expend considerable resources including time and money on product candidates that fail to complete trials,
obtain regulatory approval or achieve sufficient sales, if any, to be profitable.
Additional Risks
Our principal institutional stockholders own a significant percentage of our stock and will be able to exercise significant influence.
Our current principal institutional stockholders, Platinum Long Term Growth Fund, Cato BioVentures and their respective affiliates own, and
Autilion AG is anticipated to own, a significant percentage of our outstanding capital stock. Accordingly, these stockholders may be able to
determine the composition of a majority of our Board of Directors, retain the voting power to approve certain matters requiring stockholder
approval, and continue to have significant influence over our affairs. This concentration of ownership could have the effect of delaying or
preventing a change in our control. See Item 12, “Security Ownership of Certain Beneficial Owners and Management and Related Stockholder
Matters,” for further information about the ownership of our capital stock by our executive officers, directors, and principal shareholders.
When we require future capital, we may not be able to secure additional funding in order to expand our operations and develop new
products.
We expect to seek opportunities to raise additional funds from public and private stock offerings, issuance of promissory notes or debentures,
borrowings under lease lines of credit, corporate partnering arrangements, or other sources. This additional financing may not be available on a
timely basis on terms acceptable to us, or at all. Additional financing may be dilutive to stockholders or may require us to grant a lender a
security interest in our assets. The amount of money we will need will depend on many factors, including:
• revenues generated, if any;
• development expenses incurred;
• the commercial success of our drug rescue and other research and development efforts; and
• the emergence of competing scientific and technological developments.
If adequate funds are not available, we may have to delay or reduce the scope of our drug rescue and development of our product candidates and
technologies or license to third parties the rights to commercialize products or technologies that we would otherwise seek to commercialize
ourselves. We may also have to reduce collaboration efforts, including sponsored research collaborations. Any of these results would materially
harm our business, financial condition and results of operations.
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The market price of our common stock has been volatile and may fluctuate significantly in response to many factors, some of which are
beyond our control and may be unrelated to our performance.
We anticipate that the market price of our common stock will fluctuate significantly in response to many factors, some of which are
unpredictable, beyond our control and unrelated to our performance, including specific factors such as the announcement of new products or
product enhancements by us or our competitors, developments concerning intellectual property rights and regulatory approvals, quarterly
variations in our and our competitors’ results of operations, changes in earnings estimates or recommendations by any securities analysts,
developments in our industry, strategic actions by us or our competitors, such as acquisitions or restructurings, new laws or regulations or new
interpretations of existing laws or regulations applicable to our business, the public’s reaction to our press releases, our other public
announcements and our filings with the SEC, changes in accounting standards, policies, guidance, interpretations or principles, our inability to
raise additional capital as needed, substantial sales of common stock underlying warrants or preferred stock, sales of common stock or other
securities by us or our management team, and general market conditions and other factors, including factors unrelated to our own operating
performance or the condition or prospects of the biotechnology industry.
Further, the stock market in general, and securities of micro-cap and small-cap companies in particular, frequently experience extreme price and
volume fluctuations. Continued broad market fluctuations could result in extreme volatility in the price of our common stock, which could cause
a decline in the value of our common stock. You should also be aware that price volatility is likely to be worse if the trading volume of our
common stock is low.
There may not ever be an active market for our common stock.
Although our common stock is quoted on the OTC Bulletin Board, the trading of our common stock may be extremely sporadic. For example,
several days may pass before any shares are traded. There can be no assurance that an active market for our common stock will develop.
Accordingly, investors must bear the economic risk of an investment in our common stock for an indefinite period of time.
Because we became a public company by means of a strategic reverse merger, we may not be able to attract the attention of investors or
major brokerage firms.
Because we became a public company by means of a strategic reverse merger transaction in May 2011 rather than through a traditional firmly-
underwritten initial public offering involving an investment banking or brokerage firm, securities analysts or major brokerage firms may not
provide coverage of us because there may be limited incentive to recommend the purchase of our common stock.
Because we became a public company as a result of a strategic reverse merger with a public shell, unknown liabilities may adversely affect
our financial condition.
We became a public company by means of a strategic reverse merger with a public shell. While management conducted extensive due diligence
prior to consummating our strategic reverse merger in May 2011, in the event the public shell contained undisclosed liabilities, and management
was unable to address or otherwise offset such liabilities, such liabilities may materially, and adversely affect our financial condition. As a
result of the risks associated with unknown liabilities, potential investors may be unsure or unwilling to invest in our common stock.
We will incur significant costs to ensure compliance with corporate governance, federal securities law and accounting requirements.
Since becoming a public company by means of a strategic reverse merger in May 2011, we are subject to the periodic reporting and other
requirements of the federal securities laws, rules and regulations. We have incurred and will incur significant costs to comply with such
requirements, including accounting and related auditing costs, and costs to comply with corporate governance and other costs of operating a
public company. The filing and internal control reporting requirements imposed by federal securities laws, rules and regulations are rigorous and
we may not be able to meet them, resulting in a possible decline in the price of our common stock and our inability to obtain future
financing. Any failure to comply or adequately comply with federal securities laws, rules or regulations could subject us to fines or regulatory
actions, which may materially adversely affect our business, results of operations and financial condition.
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Our compliance with the Sarbanes-Oxley Act and SEC rules concerning internal controls may be time consuming, difficult and costly.
Our management team has limited experience as officers of a publicly-traded company, and prior to May 2011, we did not operate as a publicly-
traded company. It may be time consuming, difficult and costly for us to implement and maintain the internal controls and reporting procedures
required by the Sarbanes-Oxley Act. If we are unable to comply with the Sarbanes-Oxley Act’s internal controls and disclosure requirements, we
may not be able to obtain the independent registered public accounting firm attestations that the Sarbanes-Oxley Act requires certain publicly-
traded companies to obtain. If it is determined that we have a material weakness in our internal control over financial reporting, or if our
independent registered accounting firm is unable to provide an unqualified attestation report on our internal controls when required, we could
incur additional costs and suffer adverse publicity and other consequences of any such determination, investors could lose confidence in our
financial information and the price of our common stock could decline.
We cannot assure you that our common stock will be liquid or that our common stock will become listed on the New York Stock Exchange, a
NASDAQ OMX market, or other similar exchanges.
We do not yet meet the initial listing standards of the New York Stock Exchange, the NASDAQ Global Market, or other similar exchanges.
Until our common stock is listed on a broader exchange, we anticipate that it will remain quoted on the OTC Bulletin Board, another over-the-
counter quotation system, or in the “pink sheets.” In those venues, however, investors may find it difficult to obtain accurate quotations as to the
market value of our common stock. In addition, if we failed to meet the criteria set forth in SEC regulations, various requirements would be
imposed by law on broker-dealers who sell our securities to persons other than established customers and accredited investors. Consequently,
such regulations may deter broker-dealers from recommending or selling our common stock, which may further affect liquidity. This would also
make it more difficult to raise additional capital.
There may be additional issuances of shares of preferred stock in the future.
Following approval by our stockholders in October 2011, our Articles of Incorporation now permit us to issue up to 10.0 million shares of
preferred stock and our Board has authorized the issuance of 500,000 shares of Series A Convertible Preferred Stock, all of which shares are
outstanding at March 31, 2013. Our Board of Directors could authorize the issuance of additional series of preferred stock in the future and such
preferred stock could grant holders preferred rights to our assets upon liquidation, the right to receive dividends before dividends would be
declared to holders of our common stock, and the right to the redemption of such shares, possibly together with a premium, prior to the
redemption of the common stock. In the event and to the extent that we do issue additional preferred stock in the future, the rights of holders of
our common stock could be impaired thereby, including without limitation, with respect to liquidation.
Our common stock may be considered a “penny stock.”
Since we became a publicly-traded company in May 2011, our common stock has traded on the OTC Bulletin Board at a price of less than $5.00
per share. The Securities and Exchange Commission (“SEC”) has adopted regulations which generally define a “penny stock” as an equity
security that has a market price of less than $5.00 per share, subject to specific exemptions. To the extent that the market price of our common
stock is less than $5.00 per share and, therefore, may be considered a “penny stock,” brokers and dealers effecting transactions in our common
stock must disclose certain information concerning the transaction, obtain a written agreement from the purchaser and determine that the
purchaser is reasonably suitable to purchase the securities. These rules may restrict the ability of brokers or dealers to sell our common stock and
may affect your ability to sell shares of our common stock. In addition, as long as our common stock remains listed on the OTC Bulletin Board,
investors may find it difficult to obtain accurate quotations of the stock, and may find few buyers to purchase such stock and few market makers
to support its price.
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We do not intend to pay cash dividends on our common stock in the foreseeable future.
We have never declared or paid any dividends on our shares of common stock and we do not currently anticipate paying any such dividends in
the foreseeable future. Any payment of cash dividends will depend upon our financial condition, contractual restrictions, financing agreement
covenants, solvency tests imposed by corporate law, results of operations, anticipated cash requirements and other factors and will be at the
discretion of our Board of Directors. Furthermore, we may incur indebtedness that may severely restrict or prohibit the payment of dividends.
We may be at risk of securities class action litigation that could result in substantial costs and divert management’s attention and resources.
In the past, securities class action litigation has been brought against a company following periods of volatility in the market place of its
securities. Due to the potential volatility of our stock price, we may be the target of securities litigation in the future. Securities litigation could
result in substantial costs and divert management’s attention and resources.
Item 1B. Unresolved Staff Comments
The disclosures in this section are not required since we qualify as a smaller reporting company.
Item 2. Properties
Our headquarters are located at 384 Oyster Point Boulevard, No. 8, South San Francisco, California 94080-1967, where we occupy
approximately 6,900 square feet of office and lab space under a lease expiring on June 30, 2013. In April 2013, we entered into a four-year
lease of laboratory and headquarters office space at 343 Allerton Avenue, South San Francisco, California 94080. Our occupancy at that
location is anticipated to commence in August 2013. We believe our new facilities at 343 Allerton Avenue, South San Francisco, California
will be suitable and adequate for our current and future needs.
Item 3. Legal Proceedings
From time to time, we may become involved in claims and other legal matters arising in the ordinary course of business. We are not presently
involved in any legal proceedings nor do we know of any legal proceedings which are threatened or contemplated.
Item 4. Mine Safety Disclosures
Not applicable.
PART II
Item 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities
Market Information
On June 21, 2011 our common stock began trading on the OTC Bulletin Board under the symbol “VSTA.” There was no established trading
market for our common stock prior to that date. On May 23, 2011 our directors approved a 2-for-1 stock split. The stock split became effective
on the OTC Bulletin Board on June 21, 2011.
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Shown below is the range of high and low closing prices for our common stock for the periods indicated as reported by the OTC Bulletin
Board. The market quotations reflect inter-dealer prices, without retail mark-up, mark-down or commissions and may not necessarily represent
actual transactions.
Year Ending March 31, 2013
First quarter ending June 30, 2012
Second quarter ending September 30, 2012
Third quarter ending December 31, 2012
Fourth quarter ending March 31, 2013
Year Ending March 31, 2012
First quarter ending June 30, 2011 (from June 21, 2011)
Second quarter ending September 30, 2011
Third quarter ending December 31, 2011
Fourth quarter ending March 31, 2012
High
Low
$
$
$
$
$
$
$
$
2.80 $
1.50 $
0.95 $
0.90 $
2.60 $
2.60 $
3.10 $
3.15 $
0.50
0.51
0.55
0.60
2.45
1.80
2.57
2.55
On July 10, 2013 the closing price of our common stock on the OTC Bulletin Board was $0.60 per share.
As of July 10, 2013, we had 21,265,967 shares of common stock outstanding and 350 stockholders of record. On the same date, one stockholder
held all 500,000 outstanding restricted shares of our Series A Preferred Stock.
Dividend Policy
We have not paid any dividends in the past and we do not anticipate that we will pay dividends in the foreseeable future. Covenants in certain
of our debt agreements prohibit us from paying dividends while the debt remains outstanding.
Issuer Purchase of Equity Securities
There were no repurchases of our common stock during the fiscal year ended March 31, 2013
Securities Authorized for Issuance Under Equity Compensation Plans
Equity Grants
As of March 31, 2013, options to purchase a total of 4,912,604 restricted shares of our common stock are outstanding at a weighted average
exercise price of $1.32 per share, of which 4,227,436 options are vested and exercisable at a weighted average exercise price of $1.35 per share
and 687,168 are unvested and not exercisable at a weighted average exercise price of $1.12 per share. These options were issued under our 2008
Plan and our 1999 Plan, each as described below. At March 31, 2013, an additional 257,867 shares remain available for future equity grants
under our 2008 Plan.
Plan category
Equity compensation plans approved by security holders
Equity compensation plans not approved by security holders
Total
Number of securities
to be issued upon
exercise of
outstanding options,
warrants and rights
(a)
Weighted-average
exercise price of
outstanding
options, warrants
and rights
(b)
Number of securities
remaining available
for future issuance
under equity
compensation plans
(excluding securities
reflected in column
(a))
(c)
4,442,133 $
470,471
4,912,604 $
1.33
1.21
1.32
257,867
--
257,867
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2008 Stock Incentive Plan
Shareholders of VistaGen California adopted our 2008 Plan on December 19, 2008. We assumed the 2008 Plan in connection with the
Merger. The maximum number of shares of our common stock that may be granted pursuant to the 2008 Plan is currently 5,000,000. In all
cases, the maximum number of shares of common stock under the 2008 Plan will be subject to adjustments for stock splits, stock dividends or
other similar changes in our common stock or our capital structure. Notwithstanding the foregoing, the maximum number of shares of common
stock available for grant of options intended to qualify as “incentive stock options” under the provisions of Section 422 of the Internal Revenue
Code of 1986 (the “Code”), is 5,000,000.
Our 2008 Plan provides for the grant of stock options, restricted shares of common stock, stock appreciation rights and dividend equivalent
rights, collectively referred to as “awards”. Stock options granted under the 2008 Plan may be either incentive stock options under the provisions
of Section 422 of the Code, or non-qualified stock options. We may grant incentive stock options only to employees of VistaGen or any parent or
subsidiary of VistaGen. Awards other than incentive stock options may be granted to employees, directors and consultants.
Our Board of Directors or the Compensation Committee of the Board of Directors, referred to as the “Administrator”, administers our 2008 Plan,
including selecting the award recipients, determining the number of shares to be subject to each award, determining the exercise or purchase
price of each award and determining the vesting and exercise periods of each award.
The exercise price of all incentive stock options granted under our 2008 Plan must be at least equal to 100% of the fair market value of the shares
on the date of grant. If, however, incentive stock options are granted to an employee who owns stock possessing more than 10% of the voting
power of all classes of our stock or the stock of any parent or subsidiary of us, the exercise price of any incentive stock option granted must not
be less than 110% of the fair market value on the grant date. The maximum term of these incentive stock options granted to employees who own
stock possessing more than 10% of the voting power of all classes of our stock or the stock of any parent or subsidiary of us must not exceed five
years. The maximum term of an incentive stock option granted to any other participant must not exceed ten years. The Administrator will
determine the term and exercise or purchase price of all other awards granted under our 2008 Plan.
Under the 2008 Plan, incentive stock options may not be sold, pledged, assigned, hypothecated, transferred or disposed of in any manner other
than by will or by the laws of descent or distribution and may be exercised, during the lifetime of the participant, only by the participant. Other
awards shall be transferable:
•
•
by will and by the laws of descent and distribution; and
during the lifetime of the participant, to the extent and in the manner authorized by the Administrator by gift or pursuant to a domestic
relations order to members of the participant’s immediate family.
The 2008 Plan permits the designation of beneficiaries by holders of awards, including incentive stock options.
In the event of termination of a participant’s service for any reason other than disability or death, such participant may, but only during the
period specified in the award agreement of not less than 30 days (generally 90 days) commencing on the date of termination (but in no event
later than the expiration date of the term of such award as set forth in the award agreement), exercise the portion of the participant’s award that
was vested at the date of such termination or such other portion of the participant’s award as may be determined by the Administrator. The
participant’s award agreement may provide that upon the termination of the participant’s service for cause, the participant’s right to exercise the
award shall terminate concurrently with the termination of the participant’s service. In the event of a participant’s change of status from
employee to consultant, an employee’s incentive stock option shall convert automatically into a non-qualified stock option on the day three
months and one day following such change in status. To the extent that the participant’s award was unvested at the date of termination, or if the
participant does not exercise the vested portion of the participant’s award within the period specified in the award agreement of not less than
30 days commencing on the date of termination, the award shall terminate. If termination was caused by death or disability, any options which
have become exercisable prior to the time of termination, will remain exercisable for twelve months from the date of termination (unless a
shorter or longer period of time is determined by the Administrator).
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Following the date that the exemption from application of Section 162(m) of the Code ceases to apply to awards, the maximum number of
shares with respect to which options and stock appreciation rights may be granted to any participant in any calendar year will be 2,500,000 shares
of common stock. In connection with a participant’s commencement of service with us, a participant may be granted options and stock
appreciation rights for up to an additional 500,000 shares that will not count against the foregoing limitation. In addition, following the date that
the exemption from application of Section 162(m) of the Code ceases to apply to awards, for awards of restricted stock and restricted shares of
common stock that are intended to be “performance-based compensation” (within the meaning of Section 162(m)), the maximum number of
shares with respect to which such awards may be granted to any participant in any calendar year will be 2,500,000 shares of common stock. The
limits described in this paragraph are subject to adjustment in the event of any change in our capital structure as described below.
The terms and conditions of awards shall be determined by the Administrator, including the vesting schedule and any forfeiture provisions.
Awards under the plan may vest upon the passage of time or upon the attainment of certain performance criteria. The performance criteria
established by the Administrator may be based on any one of, or combination of, the following:
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
increase in share price;
earnings per share;
total shareholder return;
operating margin;
gross margin;
return on equity;
return on assets;
return on investment;
operating income;
net operating income;
pre-tax profit;
cash flow;
revenue;
expenses;
earnings before interest, taxes and depreciation;
economic value added; and
market share.
Subject to any required action by our shareholders, the number of shares of common stock covered by outstanding awards, the number of shares
of common stock that have been authorized for issuance under the 2008 Plan, the exercise or purchase price of each outstanding award, the
maximum number of shares of common stock that may be granted subject to awards to any participant in a calendar year, and the like, shall be
proportionally adjusted by the Administrator in the event of any increase or decrease in the number of issued shares of common stock resulting
from certain changes in our capital structure as described in the 2008 Plan.
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Effective upon the consummation of a Corporate Transaction (as defined below), all outstanding awards under the 2008 Plan will terminate
unless the acquirer assumes or replaces such awards. The Administrator has the authority, exercisable either in advance of any actual or
anticipated Corporate Transaction or Change in Control (as defined below) or at the time of an actual Corporate Transaction or Change in
Control and exercisable at the time of the grant of an award under the 2008 Plan or any time while an award remains outstanding, to provide for
the full or partial automatic vesting and exercisability of one or more outstanding unvested awards under the 2008 Plan and the release from
restrictions on transfer and repurchase or forfeiture rights of such awards in connection with a Corporate Transaction or Change in Control, on
such terms and conditions as the Administrator may specify. The Administrator also shall have the authority to condition any such award vesting
and exercisability or release from such limitations upon the subsequent termination of the service of the grantee within a specified period
following the effective date of the Corporate Transaction or Change in Control. The Administrator may provide that any awards so vested or
released from such limitations in connection with a Change in Control, shall remain fully exercisable until the expiration or sooner termination
of the award.
Under our 2008 Plan, a Corporate Transaction is generally defined as:
•
•
•
•
•
an acquisition of securities possessing more than fifty percent (50%) of the total combined voting power of our outstanding securities
but excluding any such transaction or series of related transactions that the Administrator determines shall not be a Corporate
Transaction;
a reverse merger in which we remain the surviving entity but: (i) the shares of common stock outstanding immediately prior to such
merger are converted or exchanged by virtue of the merger into other property, whether in the form of securities, cash or otherwise; or
(ii) in which securities possessing more than fifty percent (50%) of the total combined voting power of our outstanding securities are
transferred to a person or persons different from those who held such securities immediately prior to such merger;
a sale, transfer or other disposition of all or substantially all of the assets of our Corporation;
a merger or consolidation in which our Corporation is not the surviving entity; or
a complete liquidation or dissolution.
Under our 2008 Plan, a Change in Control is generally defined as: (i) the acquisition of more than 50% of the total combined voting power of
our stock by any individual or entity which a majority of our Board of Directors (who have served on our board for at least 12 months) do not
recommend our shareholders accept; (ii) or a change in the composition of our Board of Directors over a period of 12 months or less.
Unless terminated sooner, our 2008 Plan will automatically terminate in 2017. Our Board of Directors may at any time amend, suspend or
terminate our 2008 Plan. To the extent necessary to comply with applicable provisions of U.S. federal securities laws, state corporate and
securities laws, the Internal Revenue Code, the rules of any applicable stock exchange or national market system, and the rules of any non-U.S.
jurisdiction applicable to awards granted to residents therein, we shall obtain shareholder approval of any such amendment to the 2008 Stock
Plan in such a manner and to such a degree as required.
As of March 31, 2013, we have options to purchase an aggregate of 4,442,133 restricted shares of common stock outstanding under our 2008
Plan.
1999 Stock Incentive Plan
VistaGen California’s Board of Directors adopted the 1999 Plan on December 6, 1999. The 1999 Plan has terminated under its own terms, and
as a result, no awards may currently be granted under the 1999 Plan. However, the options and awards that have already been granted pursuant to
the 1999 Plan remain operative.
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The 1999 Plan permitted VistaGen California to make grants of incentive stock options, non-qualified stock options and restricted stock awards.
VistaGen California initially reserved 450,000 restricted shares of its common stock for the issuance of awards under the 1999 Plan, which
number was subject to adjustment in the event of a stock split, stock dividend or other change in our capitalization. Generally, shares that were
forfeited or cancelled from awards under the 1999 Plan also were available for future awards.
The 1999 Plan could be administered by either VistaGen California’s Board of Directors or a committee designated by its Board of Directors.
VistaGen California’s Board of Directors designated its Compensation Committee as the committee with full power and authority to select the
participants to whom awards were granted, to make any combination of awards to participants, to accelerate the exercisability or vesting of any
award and to determine the specific terms and conditions of each award, subject to the provisions of the 1999 Plan. All directors, executive
officers, and certain other key persons (including employees, consultants and advisors) of VistaGen California were eligible to participate in the
1999 Plan.
The exercise price of incentive stock options awarded under the 1999 Plan could not be less than the fair market value of the common stock on
the date of the option grant and could not be less than 110% of the fair market value of the common stock to persons owning stock representing
more than 10% of the voting power of all classes of our stock. The exercise price of non-qualified stock options could not be less than 85% of
the fair market value of the common stock. The term of each option granted under the 1999 Plan could not exceed ten years (or five years, in the
case of an incentive stock option granted to a 10% shareholder) from the date of grant. VistaGen California’s Compensation Committee
determined at what time or times each option might be exercised (provided that in no event could it exceed ten years from the date of grant) and,
subject to the provisions of the 1999 Plan, the period of time, if any, after retirement, death, disability or other termination of employment during
which options could be exercised.
The 1999 Plan also permitted the issuance of restricted stock awards. Restricted stock awards issued by VistaGen California were shares of
common stock that vest in accordance with terms and conditions established by VistaGen California’s Compensation Committee. The
Compensation Committee could impose conditions to vesting that it determined to be appropriate. Shares of restricted stock that did not vest
were subject to our right of repurchase or forfeiture. VistaGen California’s Compensation Committee determined the number of shares of
restricted stock granted to any employee. Our 1999 Plan also gave VistaGen California’s Compensation Committee discretion to grant stock
awards free of any restrictions.
Unless the Compensation Committee provided otherwise, the 1999 Plan did not generally allow for the transfer of incentive stock options and
other awards and only the recipient of an award could exercise an award during his or her lifetime. Non-qualified stock options were transferable
only to the extent provided in the award agreement, in a manner consistent with the applicable law, and by will and by the laws of descent and
distribution. In the event of a change in control of the Company, as defined in the 1999 Plan, the outstanding options will automatically vest
unless our Board of Directors and the Board of Directors of the surviving or acquiring entity make appropriate provisions for the continuation or
assumption of any outstanding awards under the 1999 Plan.
As of March 31, 2013, we have options outstanding under our 1999 Plan to purchase an aggregate of 470,471 restricted shares of our common
stock.
Recent Sales of Unregistered Securities
During the three years preceding the date of this report, we issued the following securities which were not registered under the Securities Act of
1933, as amended (the “Securities Act”) and that have not been previously reported in a Quarterly Report on Form 10-Q or a Current Report on
Form 8-K:
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2012 Private Placement of Units
Between January 2013 and March 2013, we sold 1,415,074 Units in a private placement to 25 accredited investors and received cash proceeds of
$657,537 and settled outstanding amounts payable for professional fees in lieu of cash payment for services in the amount of $50,000. We sold
the Units for $0.50 per Unit, with each Unit consisting of one restricted share of our common stock and a five-year warrant to purchase one half
(1/2) of one restricted share of our common stock at an exercise price of $1.50 per share. We have used the proceeds from the sale of the Units
for general corporate purposes. We offered and sold the Units in transactions exempt from registration under the Securities Act, in reliance on
Section 4(2) thereof and Rule 506 of Regulation D thereunder.
Item 6. Selected Financial Data
The disclosures in this section are not required since we qualify as a smaller reporting company.
Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations
Cautionary Note Regarding Forward-Looking Statements
The following discussion contains forward-looking statements that are based on the current beliefs of our management, as well as current
assumptions made by, and information currently available to, our management. All statements contained in the discussion below, other than
statements that are purely historical, are forward-looking statements. These forward-looking statements are subject to risks and uncertainties
that could cause our future actual results, performance or achievements to differ materially from those expressed in, or implied by, any such
forward-looking statements as a result of certain factors, including, but not limited to, those risks and uncertainties discussed in this section, as
well as in the section entitled “Risk Factors,” and elsewhere in our other filings with the SEC. Forward-looking statements are based on
estimates and assumptions we make in light of our experience and perception of historical trends, current conditions and expected future
developments, as well as other factors that we believe are appropriate and reasonable in the circumstances. See “Cautionary Note Regarding
Forward-Looking Statements” elsewhere in this Annual Report on Form 10-K.
Our business is subject to significant risks including, but not limited to, our ability to obtain additional financing, the results of our research and
development efforts, the results of non-clinical and clinical testing, the effect of regulation by the United States Food and Drug Administration
(“FDA”) and other agencies, the impact of competitive products, product development, commercialization and technological difficulties, the
effect of our accounting policies, and other risks as detailed in the section entitled “Risk Factors” and in our other filings with the Securities
and Exchange Commission. Further, even if our product candidates appear promising at various stages of development, our share price may
decrease such that we are unable to raise additional capital without dilution or other terms that may be unacceptable to our management, Board
of Directors and stockholders.
Investors are cautioned not to place undue reliance on the forward-looking statements contained herein. Additionally, unless otherwise stated,
the forward-looking statements contained in this report are made as of the date of this report, and we have no intention and undertake no
obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as
required by applicable law. The forward-looking statements contained in this report are expressly qualified by this cautionary statement. New
factors emerge from time to time, and it is not possible for us to predict which factors may arise. In addition, we cannot assess the impact of
each factor on our business or the extent to which any factor, or combination of factors, may cause our actual results to differ materially from
those contained in any forward-looking statements.
Business Overview
We are a biotechnology company applying human pluripotent stem cell technology for drug rescue and regenerative cell therapy.
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Drug rescue involves the combination of human pluripotent stem cell technology with modern medicinal chemistry to generate new chemical
variants (“Drug Rescue Variants”) of promising small molecule drug candidates that pharmaceutical or biotechnology companies have
discontinued during development due to unexpected safety concerns involving the heart and/or liver. We anticipate that our stem cell technology
platform, Human Clinical Trials in a Test Tube tm, will allow us to assess the heart and liver toxicity profile of new drug candidates with greater
speed and precision than in vitro techniques and technologies currently used in the drug development process. Our drug rescue model is
designed to leverage both substantial prior third-party investment in discovery and development of once-promising drug candidates which
ultimately were discontinued prior to market approval and the predictive toxicology and other drug development capabilities of our Human
Clinical Trials in a Test Tubetm platform.
Our Human Clinical Trials in a Test Tube tm platform is based on a combination of proprietary and exclusively licensed stem cell technologies,
including technologies developed over the last 20 years by VistaGen California’s co-founder and Canadian scientist, Dr. Gordon Keller, and
Dr. Ralph Snodgrass, VistaGen California’s co-founder, and our President and Chief Scientific Officer. Dr. Keller is currently the Director of the
University Health Network’s McEwen Centre for Regenerative Medicine in Toronto. Dr. Keller’s research is focused on understanding and
controlling stem cell differentiation (development) and production of multiple types of mature, functional, human cells from pluripotent stem
cells, including heart cells and liver cells that can be used in our biological assay systems for drug rescue and development. Dr. Snodgrass has
over 20 years of experience in both academia and industry in the development and application of stem cell differentiation systems for drug
discovery and development.
With mature heart cells produced from stem cells, we have developed CardioSafe 3D ™, a three-dimensional (“3D”) bioassay system. We
believe CardioSafe 3D ™ is capable of predicting the in vivo cardiac effects, both toxic and non-toxic, of small molecule drug candidates before
they are tested in humans. Our immediate goal is to leverage CardioSafe 3D ™ to generate and monetize a pipeline of small molecule drug
candidates through drug rescue collaborations. We intend to expand our drug rescue capabilities by developing LiverSafe 3D ™, a human liver
cell-based bioassay system for assessing potential liver toxicity and adverse drug-drug interactions.
In parallel with our drug rescue activities, we plan to advance pilot nonclinical development of regenerative cell therapy programs focused on
blood, cartilage, heart, liver and pancreas cells. Each of these regenerative cell therapy programs is based on the proprietary differentiation and
production capabilities of our Human Clinical Trials in a Test Tube tm platform.
With grant funding from the U.S. National Institutes of Health (“NIH”), we have successfully completed Phase 1 development of AV-101 during
calendar 2012. AV-101 is an orally available small molecule prodrug candidate aimed at the multi-billion dollar neurological disease and
disorders market, including neuropathic pain, a serious and chronic condition causing pain after an injury or disease of the peripheral or central
nervous system. Neuropathic pain affects approximately 1.8 million people in the U.S. alone. To date, we have been awarded over $8.8 million
of grant funding from the NIH for non-clinical and Phase I clinical development of AV-101.
Our immediate plan is to utilize the vast amount of information available in the public domain with respect to potential small molecule drug
candidates for inclusion in our drug rescue programs. We may also seek to acquire rights to drug rescue candidates that third-parties, including
academic research institutions and biotechnology, medicinal chemistry and pharmaceutical companies have discontinued due to unexpected
safety concerns involving the heart and/or liver. In connection with our drug rescue programs, we will collaborate with contract medicinal
chemistry and other third parties to generate and assess the therapeutics and commercial potential of each Drug Rescue Variant we generate. We
plan to have economic participation rights in each Drug Rescue Variant we are able to generate in connection with our projected drug rescue
programs.
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The Merger
VistaGen Therapeutics, Inc., a California corporation (“VistaGen California ”) is a wholly-owned subsidiary of the Company. VistaGen
California was incorporated in California on May 26, 1998 . Excaliber Enterprises, Ltd. (Excaliber), a publicly-held company (formerly
OTCBB:EXCA), was incorporated under the laws of the State of Nevada on October 6, 2005. After being unable to generate material revenues
based on its original business plan, Excaliber became inactive in 2007. In May 2011, after assessing the prospects associated with its original
business plan and the business opportunities associated with a strategic merger with an established, privately-held, biotechnology company
seeking the potential advantages of being a publicly-held company, Excaliber’s Board of Directors agreed to pursue a strategic merger with
VistaGen California.
On May 11, 2011, pursuant to a strategic merger transaction with VistaGen California, Excaliber acquired all outstanding shares of VistaGen
California in exchange for 6,836,452 restricted shares of Excaliber’s common stock (the “Merger”), and Excaliber assumed all of VistaGen
California’s pre-Merger obligations to contingently issue restricted shares of common stock in accordance with VistaGen California’s stock
option agreements, warrant agreements, and a convertible promissory note. In connection with the Merger, Excaliber repurchased 5,064,207
shares of Excaliber common stock from two of its stockholders for a nominal amount, resulting in a total of 784,500 shares of Excaliber common
stock outstanding at the date of the Merger. The 6,836,452 restricted shares issued to VistaGen California stockholders in connection with the
Merger represented approximately 90% of Excaliber’s outstanding shares of common stock after the closing of the Merger. As a result of the
Merger, the biotechnology business of VistaGen California became the operating business of Excaliber. Shortly after the Merger:
·
·
·
·
·
·
·
Each of the pre-Merger directors of VistaGen California was appointed as a director of Excaliber;
The pre-Merger directors and officers of Excaliber resigned as officers and directors of Excaliber;
Each of VistaGen California’s pre-Merger officers was appointed an officer of like tenor of Excaliber;
The post-Merger directors of Excaliber (consisting of the pre-Merger directors of VistaGen California) approved a two-for-one (2:1)
stock split of Excaliber’s common stock;
The post-Merger directors of Excaliber approved an increase in the number of shares of common stock Excaliber was authorized to
issue from 200 million to 400 million shares, (see Note 9, Capital Stock, to the Consolidated Financial Statements included in Item 8
of this Annual Report on Form 10-K);
Excaliber’s name was changed to “VistaGen Therapeutics, Inc.”; and
VistaGen California's fiscal year-end of March 31 was adopted as Excaliber’s fiscal year-end.
VistaGen California, as the accounting acquirer in the Merger, recorded the Merger as the issuance of stock for the net monetary assets of
Excaliber, accompanied by a recapitalization. This accounting for the Merger was identical to that resulting from a reverse acquisition, except
that no goodwill or other intangible assets were recorded. A total of 1,569,000 shares of common stock, representing the 784,500 shares held by
stockholders of Excaliber immediately prior to the Merger and effected for the post-Merger two-for-one (2:1) stock split mentioned above, have
been retroactively reflected as outstanding for the period prior to the Merger in the fiscal year ended March 31, 2012 for purposes of
determining basic and diluted loss per common share in the Consolidated Statements of Operations and Comprehensive Income of the Company
included in Item 8 of this Form 10-K. Additionally, the accompanying Consolidated Balance Sheets of the Company retroactively reflect the
authorized capital stock and $0.001 par value of Excaliber’s common stock and the two-for one (2:1) stock split after the Merger.
The financial statements included in this discussion and in the Consolidated Financial Statements of the Company included in Item 8 of this
Form 10-K represent the activity of VistaGen California for the pre-Merger portion of fiscal 2012 and the consolidated activity of VistaGen
California and Excaliber from May 11, 2011 (the date of the Merger) through March 31, 2013. The activities and results of operations of
Excaliber in the pre-Merger period presented were not material.
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Primary Merger-Related Transactions
Immediately preceding and concurrent with the Merger:
●
●
●
VistaGen California sold 2,216,106 Units, consisting of one restricted share of VistaGen's common stock and a three-year warrant
to purchase one-fourth (1/4) of one restricted share of VistaGen common stock at an exercise price of $2.50 per share, at a price of
$1.75 per Unit in a private placement for aggregate gross offering proceeds of $3,878,197, including $2,369,194 in cash (“2011
Private Placement”). The restricted shares and warrants issued in the 2011 Private Placement became restricted shares and warrants
of the Company upon consummation of the Merger;
Holders of certain promissory notes issued by VistaGen California from 2006 through 2010 converted their notes totaling
$6,174,793, including principal and accrued but unpaid interest, into 3,528,290 Units at $1.75 per Unit. These Units were the same
Units issued in connection with the 2011 Private Placement. The restricted shares and warrants issued upon the conversion of such
promissory notes became restricted shares and warrants of the Company upon consummation of the Merger; and
All holders of VistaGen California's then-outstanding preferred stock converted all 2,884,655 of their restricted shares of VistaGen
California preferred stock into 2,884,655 restricted shares of VistaGen California common stock, all of which shares became
restricted shares of the Company upon consummation of the Merger. See Note 8, Convertible Promissory Notes and other Notes
Payable and Note 9, Capital Stock, to the Consolidated Financial Statements included in Item 8 of this Form 10-K for a further
description of these transactions.
Financial Operations Overview
Net Loss
We are in the development stage and, since inception, have devoted substantially all of our time and efforts to hPSC research and bioassay
development, small molecule drug development, creating, protecting and patenting intellectual property, recruiting personnel and raising
working capital. As of March 31, 2013, we had an accumulated deficit of $67.7 million. Our net loss for the years ended March 31, 2013 and
2012 was $12.9 million and $12.2 million, respectively. We expect these conditions to continue for the foreseeable future as we expand our drug
rescue activities and the capabilities of our Human Clinical Trials in a Test Tube™ platform.
Summary of Fiscal Year 2013
During the fiscal year ending March 31, 2013, we have continued to expand the capabilities of CardioSafe 3D™ and develop and validate
LiverSafe 3D™. Additionally, we have continued to advance our review of prospective drug rescue candidates and successfully completed
Phase 1 clinical development of AV-101. We also directed concentrated effort to finalizing and analyzing the AV-101 Phase 1b clinical trial
results and preparing final clinical study reports required under the terms of our NIH grant awards. Our executive management has been
significantly focused on providing sufficient operating capital to advance our research and development objectives while meeting our continuing
operational needs. To that end, in June 2012 and October 2012 we entered into agreements with Platinum Long Term Growth VII, LLC
(“Platinum”) pursuant to which we received an aggregate of $3.25 million in cash proceeds from the issuance of senior secured convertible
promissory notes and related warrants to purchase 3.25 million restricted shares of our common stock. Subject to certain adjustments, these notes
are convertible into restricted shares of our common stock at a conversion price of $0.50 per share and the warrants are exercisable at an exercise
price of $0.50 per share. Further, we modified Platinum’s exchange rights with respect to the 500,000 restricted shares of our Series A preferred
stock that it holds. Additionally, we entered into strategic debt restructuring agreements with certain long-term service providers and research
and development collaborators to modify the payment requirements of our liabilities to them by significantly reducing the monthly cash payment
requirements or, in several cases, to entirely restructure the liability so that it is now payable only in restricted shares of our common stock.
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In August 2012, we entered into such a strategic debt restructuring agreement with Morrison & Foerster (“M&F”), our former general
corporate counsel and continuing intellectual property counsel. Pursuant to the M&F strategic debt restructuring agreement, we converted
approximately $1.4 million of our then-existing promissory note debt to M&F into a new unsecured promissory note payable only in restricted
shares of our common stock in connection with M&F’s future exercise of a warrant to purchase approximately 1.4 million shares of our common
stock at $1.00 per share, provided, however, that M&F has the option to require us to repay the note in cash upon a change of control or event of
default, as both are defined in the agreement.
In October 2012, we entered into similar strategic debt restructuring agreements with Cato Research Ltd. (“ CRL”), our CRO collaborator for
development of AV-101, and University Health Network (“ UHN”), our long-term stem cell research and development collaborator in Canada, in
which we converted approximately $1.0 million of existing accounts payable debt owed to CRL and approximately $0.55 million of existing
accounts payable debt owed to UHN into new notes payable only in restricted shares of our common stock in connection with future warrant
exercises by CRL and UHN to purchase approximately 1,000,000 and 550,000 restricted shares of our common stock, respectively, at $1.00 per
share. Additionally, we reduced the current monthly unsecured promissory note payment requirements with respect to existing debt of $1.0
million owed to M&F and $0.3 million owed to Cato Holding Company. The Platinum, M&F, CRL and UHN debt restructuring transactions are
described in greater detail in Note 8, Convertible Promissory Notes and Other Notes Payable and Note 9, Capital Stock, in the Consolidated
Financial Statements included in Item 8 of this Annual Report on Form 10-K. The accounting for these transactions resulted in the recognition
in the financial statements for fiscal 2013 of (i) non-cash losses attributable to certain of the debt modifications (loss on early extinguishment of
debt); (ii) liabilities related to certain of the warrants issued and potentially issuable to Platinum and the related non-cash expense attributable to
the change in the fair value of the warrant liability during the period; (iii) non-cash interest expense attributable to the discounts recorded with
respect to the Platinum, M&F, CRL and UHN promissory notes; and (iv) a deemed dividend with respect to the modification of the exchange
rights for the shares of our Series A Preferred stock held by Platinum and the related prospective issuance of a five-year warrant to purchase
restricted shares of our common stock upon Platinum's exercise of its Series A Preferred Stock exchange rights. These transactions and
agreements, including the conversion of certain promissory notes into shares of restricted common stock, the exercise of warrants to purchase
restricted common stock or Platinum’s exercise of its exchange rights with respect to the shares of our Series A Preferred stock it holds, will
potentially require the issuance of a significant number of restricted shares of our common stock at various points in the future, which may be
substantially dilutive to our existing stockholders.
The following table summarizes the results of our operations for the fiscal years ended March 31, 2013 and 2012 (amounts in $000):
Revenues:
Grant revenue
Operating expenses:
Research and development
General and administrative
Total operating expenses
Loss from operations
Other expenses, net:
Interest expense, net
Change in warrant and put and note extension option liabilities
Loss on early extinguishment of debt
Other income
Loss before income taxes
Income taxes
Net loss
Deemed dividend on Series A Preferred Stock
Net loss attributable to common stockholders
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Fiscal Year Ended March
31,
2013
2012
$
200
$
1,342
3,431
3,562
6,993
(6,793)
(921)
(1,636)
(3,568)
35
(12,883)
(4)
(12,887) $
(10,193)
(23,080) $
5,389
4,997
10,386
(9,044)
(1,893)
(78)
(1,193)
-
(12,208)
(2)
(12,210)
-
(12,210)
$
$
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Revenue
Our primary sources of revenue for the fiscal years ended March 31, 2013 and 2012 were government grant awards from the NIH to pursue the
development of AV-101 and from California Institute of Regenerative Medicine (“ CIRM”) to develop our bioassay system for predictive liver
toxicology and drug metabolism drug screening, and from a strategic research contract with third parties. Our AV-101 grant from NIH
accounted for 94% and 87% of our total revenue for fiscal year 2013 and 2012, respectively. The NIH grant expired in its normal course on June
30, 2012 and has not been extended or renewed. Our CIRM grant terminated in September 2011 and accounted for 6% of our total revenue in
fiscal year 2012. Government grant revenue typically reimburses us for expenses incurred in the subject research area plus a nominal allocation
or fee to cover our related administrative and infrastructure costs.
Research and Development Expense
Research and development expense represented approximately 49% and 52% of our operating expenses for the years ended March 31, 2013 and
2012, respectively. Research and development costs are expensed as incurred. Research and development expense consists of both internal and
external expenses incurred in sponsored stem cell research and drug development activities, costs associated with the development of AV-101
and costs related to the licensing, application and prosecution of our intellectual property. These expenses primarily consist of the following:
•
•
•
•
•
•
salaries, benefits, including stock-based compensation costs, travel and related expense for personnel associated with research and
development activities;
fees paid to contract research organizations and other professional service providers for services related to the conduct and analysis of
clinical trials and other development activities;
fees paid to third parties for access to licensed technology and costs associated with securing and maintaining patents related to our
internally generated inventions:
laboratory supplies and materials;
leasing and depreciation of laboratory equipment; and
allocated costs of facilities and infrastructure.
General and Administrative Expense
General and administrative expense consists primarily of salaries and related expense, including stock-based compensation expense, for
personnel in executive, finance and accounting, and other support functions. Other costs include professional fees for legal, investor relations and
accounting services and other strategic consulting and public company expenses as well as facility costs not otherwise included in research and
development expense. Following the Merger in May 2011, we increased our administrative headcount and engaged certain consulting services
to meet our obligations as a public reporting company.
Other Expenses, Net
We incurred interest expense on the outstanding balance of our convertible promissory notes issued beginning in 2006, substantially all of which
were converted into Units consisting of restricted common stock and warrants in May 2011 at a price of $1.75 per Unit in connection with the
Merger. We also incurred interest expense on the May 2011 Platinum Note prior to its exchange into our Series A Preferred Stock in December
2011, on the Senior Secured Convertible Promissory Notes issued to Platinum in October 2012 and in February 2013 and March 2013, and on
various notes issued to certain service providers during the years ended March 31, 2011 and 2012 and on the new and modified notes issued to
M&F, CRL and UHN during the year ended March 31, 2013.
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We recorded non-cash expense in fiscal 2013 and 2012 related to the change in the fair values of the derivatives associated with various
promissory notes issued to Platinum prior to fiscal 2012 and during fiscal 2013. In fiscal 2013, we recorded non-cash losses on early
extinguishment of debt in connection with the modification of certain promissory notes issued to Platinum, Morrison & Foerster, Cato Holding
Company and to investors in convertible promissory notes issued in February 2012 as well as in connection with the settlement of accounts
payable by issuing promissory notes to Cato Research Ltd and University Health Network, In fiscal 2012, we recorded a non-cash loss on early
extinguishment of debt related to the exchange of the Platinum Note into shares of our Series A Preferred Stock under the terms of a note and
warrant exchange agreement. In fiscal 2013, we also recorded a non-cash deemed dividend related to the modification of the exchange rights of
our Series A Preferred Stock held by Platinum, including the impact of the prospective issuance of a five-year warrant to purchase restricted
shares of our common stock upon Platinum's exercise of its Series A Preferred Stock exchange rights.
Critical Accounting Policies and Estimates
We consider certain accounting policies related to revenue recognition, impairment of long-lived assets, research and development, stock-based
compensation, and income taxes to be critical accounting policies that require the use of significant judgments and estimates relating to matters
that are inherently uncertain and may result in materially different results under different assumptions and conditions. The preparation of
financial statements in conformity with United States generally accepted accounting principles (“GAAP”) requires us to make estimates and
assumptions that affect the amounts reported in the financial statements and accompanying notes to the consolidated financial statements. These
estimates include useful lives for property and equipment and related depreciation calculations, and assumptions for valuing options, warrants
and other stock-based compensation. Our actual results could differ from these estimates.
Revenue Recognition
Our revenues consist primarily of revenues from government grant awards and strategic collaborations. We recognize revenue under the
provisions of the Securities and Exchange Commission issued Staff Accounting Bulletin 104, Topic 13, Revenue Recognition Revised and
Updated (“SAB 104”) and Accounting Standards Codification (“ASC”) 605-25, Revenue Arrangements-Multiple Element Arrangements (“ASC
605-25”). Revenue for arrangements not having multiple deliverables, as outlined in ASC 605-25, is recognized once costs are incurred and
collectability is reasonably assured.
Revenue arrangements with multiple components are divided into separate units of accounting if certain criteria are met, including whether the
delivered component has stand-alone value to the customer. Consideration received is allocated among the separate units of accounting based on
their respective selling prices. The selling price for each unit is based on vendor-specific objective evidence, or VSOE, if available, third party
evidence if VSOE is not available, or estimated selling price if neither VSOE nor third party evidence is available. The applicable revenue
recognition criteria are then applied to each of the units.
We recognize revenue when the four basic criteria of revenue recognition are met: (1) a contractual agreement exists; (2) the transfer of
technology has been completed or services have been rendered; (3) the fee is fixed or determinable; and (4) collectability is reasonably assured.
For each source of revenue, we comply with the above revenue recognition criteria in the following manner:
•
Collaborative arrangements typically consist of non-refundable and/or exclusive technology access fees, cost reimbursements for
specific research and development spending, and various milestone and future product royalty payments. If the delivered technology
does not have stand-alone value, the amount of revenue allocable to the delivered technology is deferred. Non-refundable upfront fees
with stand-alone value that are not dependent on future performance under these agreements are recognized as revenue when received,
and are deferred if we have continuing performance obligations and have no objective and reliable evidence of the fair value of those
obligations. We recognize non-refundable upfront technology access fees under agreements in which we have a continuing
performance obligation ratably, on a straight-line basis, over the period in which we are obligated to provide services. Cost
reimbursements for research and development spending are recognized when the related costs are incurred and when collectability is
reasonably assured. Payments received related to substantive, performance-based “at-risk” milestones are recognized as revenue upon
achievement of the milestone event specified in the underlying contracts, which represent the culmination of the earnings
process. Amounts received in advance are recorded as deferred revenue until the technology is transferred, costs are incurred, or a
milestone is reached.
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•
Technology license agreements typically consist of non-refundable upfront license fees, annual minimum access fees and/or royalty
payments. Non-refundable upfront license fees and annual minimum payments received with separable stand-alone values are
recognized when the technology is transferred or accessed, provided that the technology transferred or accessed is not dependent on the
outcome of the continuing research and development efforts. Otherwise, revenue is recognized over the period of our continuing
involvement.
• Government grant awards, which support our research efforts on specific projects, generally provide for reimbursement of approved
costs as defined in the terms of grant awards. We recognize grant revenue when associated project costs are incurred.
Impairment of Long-Lived Assets
In accordance with ASC 360-10, Property, Plant & Equipment—Overall , we review for impairment whenever events or changes in
circumstances indicate that the carrying amount of property and equipment may not be recoverable. Determination of recoverability is based on
an estimate of undiscounted future cash flows resulting from the use of the asset and its eventual disposition. In the event that such cash flows
are not expected to be sufficient to recover the carrying amount of the assets, we write down the assets to their estimated fair values and
recognize the loss in the statements of operations.
Research and Development Expenses
Research and development expenses include internal and external costs. Internal costs include salaries and employment related expenses of
scientific personnel and direct project costs. External research and development expenses consist of sponsored stem cell research and
development costs, costs associated with clinical and non-clinical development of AV-101, our lead drug candidate, and costs related to
application and prosecution of patents related to our stem cell technology platform, Human Clinical Trials in a Test Tube ™, and AV-101. All
such costs are charged to expense as incurred.
Stock-Based Compensation
We account for stock-based payment arrangements in accordance with ASC 718, Compensation-Stock Compensation and ASC 505-50, Equity-
Equity Based Payments to Non-Employees which requires the recognition of compensation expense, using a fair-value based method, for all
costs related to stock-based payments including stock options and restricted stock awards. We recognize compensation cost for all share-based
awards to employees based on their grant date fair value. Share-based compensation expense is recognized over the period during which the
employee is required to perform service in exchange for the award, which generally represents the scheduled vesting period. We have no awards
with market or performance conditions. For equity awards to non-employees, we re-measure the fair value of the awards as they vest and the
resulting value is recognized as an expense during the period over which the services are performed.
We use the Black-Scholes option pricing model to estimate the fair value of stock-based awards as of the grant date. The Black-Scholes model is
complex and dependent upon key data input estimates. The primary data inputs with the greatest degree of judgment are the expected terms of
the stock options and the estimated volatility of our stock price. The Black-Scholes model is highly sensitive to changes in these two inputs. The
expected term of the options represents the period of time that options granted are expected to be outstanding. We use the simplified method to
estimate the expected term as an input into the Black-Scholes option pricing model. We determine expected volatility using the historical
method, which, because of the limited period during which our stock has been publicly traded, is based on the historical daily trading data of the
common stock of a peer group of public companies over the expected term of the option.
Income Taxes
We account for income taxes using the asset and liability approach for financial reporting purposes. We recognize deferred tax assets and
liabilities for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and
liabilities and their respective tax bases and operating loss and tax credit carryforwards. Deferred tax assets and liabilities are measured using
enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled.
The effect on deferred tax assets and liabilities of a change in tax rates is recognized in income in the period that includes the enactment date.
Valuation allowances are established, when necessary, to reduce the deferred tax assets to an amount expected to be realized.
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Recent Accounting Pronouncements
See Note 3 to the consolidated financial statements included in Item 8 in this Annual Report on Form 10-K for information on recent accounting
pronouncements.
Results of Operations
Comparison of Years Ended March 31, 2013 and 2012
Revenue
The following table compares our primary revenue sources between the periods (in $000):
NIH - AV-101 grant
CIRM grant
Subcontract revenue
Total Revenue
Fiscal Year Ended March 31,
2013
2012
$
$
$
187
-
13
1,163
79
100
200
$
1,342
Although limited project work on AV-101 continued through fiscal 2013, we reported no grant revenue from the NIH grant after the first quarter
of fiscal 2013, as the grant expired in its normal course at June 30, 2012. We had drawn the maximum amount available under the grant award
prior to its expiration. Our work under the California Institute of Regenerative Medicine ("CIRM") grant was completed in the quarter ended
September 30, 2011. Revenue associated with our subcontract research arrangement terminated in May 2012.
Research and Development Expense
Research and development expense decreased by 36% to $3.4 million in fiscal 2013 compared to $5.4 million in fiscal 2012. The following
table compares the primary components of research and development expense between the periods (in $000):
Salaries and benefits
Stock-based compensation
UHN research under SRCA
Consulting services
Technology licenses and royalties
Project-related third-party research and supplies:
AV-101
CIRM
All other including CardioSafe and LiverSafe
Rent
Depreciation
Total Research and Development Expense
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Fiscal Years Ended March 31,
2013
2012
$
$
$
792
510
466
14
136
1,079
-
293
1,372
115
26
-
$
3,431
862
477
830
-
340
2,191
37
410
2,638
104
37
101
5,389
Table of Contents
Salary and benefits expense decreased primarily as a result of salary reductions taken voluntarily by the Company’s senior management during
the last three quarters of fiscal 2013 and the absence in fiscal 2013 of a compensation bonus granted in fiscal 2012, partially offset by the costs
attributable to new scientific personnel added since June 2011. Stock-based compensation increased in fiscal 2013 compared to fiscal 2012
primarily as a result of recognizing (i) the expense resulting from the October 2012 modification of certain stock option grants having exercise
prices between $1.13 per share and $2.58 per share made to certain scientific employees and consultants in prior years to reduce the exercise
price to $0.75 per share and (ii) the March 2013 grant to our Chief Scientific Officer of a ten-year warrant to purchase 1,000,000 shares of our
common stock at an exercise price of $0.64 per share. Partially offsetting this increase was the expense impact of certain option grants made in
prior years that became fully-vested late in fiscal year 2012 or in the first quarter of fiscal 2013, requiring little, if any, expense during fiscal
2013. Sponsored research in both fiscal 2013 and fiscal 2012 reflects the continuation of our long-term stem cell research collaboration with Dr.
Gordon Keller’s laboratory in accordance with modifications to our collaboration agreement with UHN made in the third and fourth quarters of
fiscal 2012 and in a further modification effective beginning in the third quarter of fiscal 2013. Additionally, fiscal 2012 expense for sponsored
research at UHN included a non-cash grant of our common stock valued at $175,000 made in May 2011. Technology license expense decreased
in fiscal 2013 reflecting reduced costs for patent prosecution and protection that we are required to fund under the terms of certain of our license
agreements. We recognize these costs as they are passed on to us by the licensors and they do not occur ratably throughout the year or between
years. We began a Phase 1b clinical trial of AV-101 early in calendar 2012 and completed it late in calendar 2012, with expenses during the
second half of fiscal 2013 primarily reflecting the costs associated with finalizing and analyzing the Phase 1b clinical trial results and preparing
final clinical study reports required under the terms of the NIH grant, primarily through third-party collaborators, including Cato Research
Ltd. AV-101 expenses in fiscal 2012 included the costs of preparing for the clinical trial and other primarily grant-reimbursable efforts
conducted by Cato Research Ltd. and other third-party collaborators. The CIRM grant expired at the end of September 2011 and grant-related
effort on that project has ceased. We do not track internal research and development expenses, including compensation costs, by project as we
do not currently believe that such project accounting is required given the level and overlap of project resources, including staffing, that are
dedicated to our research and development projects. Warrant modification expense in fiscal 2012 relates to the non-cash expense we recorded as
a result of the December 2011 Agreement Regarding Payment of Invoices and Warrant Exercises between the Company and Cato Holding
Company (“CHC”), Cato Research Ltd. (“CRL”) and certain CHC affiliates pursuant to which CHC and the CHC affiliates exercised warrants at
discounted exercise prices to purchase an aggregate of 492,541 restricted shares of our common stock and we received $60,200 cash, and, in lieu
of cash payment for certain of the warrant exercises, settled outstanding liabilities of $245,300 for past services received from CRL and prepaid
$226,400 for future services that were received from CRL.
General and Administrative Expense
General and administrative expense decreased by 29% to $3.6 million in fiscal 2013 compared to $5.0 million in fiscal 2012. The following
table compares the primary components of general and administrative expense between the periods (in $000):
Salaries and benefits
Stock-based compensation
Consulting services
Legal, accounting and other professional fees
Investor relations
Insurance
Travel and entertainment
Rent and utilities
Warrant modification expense
All other
Total general and administrative expense
-53-
Fiscal Years Ended March 31,
2013
2012
$
$
617
731
157
554
622
122
37
85
507
130
875
1,114
558
1,033
343
101
68
89
641
175
$
3,562
$
4,997
Table of Contents
The decrease in salaries and benefits expense in fiscal 2013 compared with fiscal 2012 results primarily from our May 2011 forgiveness, in
conjunction with our going-public transaction, of notes receivable from certain officers in the aggregate amount of $185,000, plus an accrual for
related tax gross-ups aggregating $136,000 to which they remain entitled, which we recorded as compensation expense. Partially offsetting that
decrease is the impact of converting certain current employees from consulting status during fiscal 2012 to employee status in fiscal
2013. Stock-based compensation expense decreased in fiscal 2013 as option grants of significant size and expense made in prior years became
fully-vested in the second half of fiscal 2012, requiring no additional expense in fiscal 2013. Partially offsetting that decrease is the impact of
recognizing (i) the expense resulting from the October 2012 modification of certain stock option grants having exercise prices between $1.13 per
share and $2.58 per share made to certain administrative employees and business consultants in prior years to reduce the exercise price to $0.75
per share and (ii) the March 2013 grant to our senior management and independent members of our Board of Directors of ten-year warrants to
purchase an aggregate of 2,000,000 restricted shares of our common stock at an exercise price of $0.64 per share. Legal, accounting and other
professional fees in fiscal 2012 included significant one-time charges related to the Merger and going-public transaction and positioning the
Company for its initial public and SEC reporting status. Expense recorded in the current year reflects more normalized levels. Since becoming
a public reporting and publicly-traded company, we have engaged certain third parties to provide us with investor relations services and to
conduct market awareness initiatives that were not necessary as a private company. A portion of the compensation that we have provided to
certain of these providers has been in the form of grants of restricted common stock or warrants to purchase restricted common stock. In those
situations, we have expensed the grant date fair value of the restricted stock or warrants ratably over the term of the underlying contract, all of
which have been completed at March 31, 2013. Additionally, we incurred non-cash warrant modification expense totaling $507,000 in fiscal
2013 related to reducing the exercise price of certain outstanding warrants to purchase our common stock, as described in Note 9 to the
Consolidated Financial Statements included in Item 8 of this report. In fiscal 2012, we incurred non-cash warrant modification expense of
$641,000 related to reducing the exercise price and, in some cases, extending the term, of certain outstanding warrants to purchase our common
stock.
Other Expenses, Net
Other expenses, net includes interest expense, net of interest income, in both years, and the non-cash impact of changes in the fair value of the
warrant liabilities related to warrants issued or issuable to Platinum as a result of the October 2012 Agreement in fiscal 2013 and of the
derivatives treated as liabilities resulting from the issuance of prior notes and warrants to Platinum in fiscal 2012. Other expenses, net also
includes the non-cash loss on extinguishment of debt resulting from the modification of indebtedness to Platinum, Morrison & Foerster, Cato
Research Ltd., and University Health Network, as well as the conversion by the holders of our 12% Convertible Promissory Notes issued in
February 2012 into restricted shares of our common stock and warrants during fiscal 2013, and the cancellation of a $4.0 million note issued to
Platinum and Platinum’s related exercise of warrants and exchange of restricted shares of our common stock into restricted shares of our Series
A preferred stock during fiscal 2012.
The following table compares the primary components of net interest expense between the periods (in $000):
Interest expense on promissory notes, including discount amortization
Charge for fair value of replacement warrants issued in connection
with exercise of modified warrants
Charge related to losses on accounts payable settled by issuance
of common stock or notes payable
Charge for investment banker warrants related to February 2012 Convertible
promissory notes
Charge for legal fees related to issuance of Senior Secured Promissory
Notes to Platinum under June and October 2012 agreements
Other interest expense, including on capital leases and premium financing
Effect of foreign currency fluctuations on notes payable
Interest Income
Fiscal Year Ended
March 31,
2013
2012
$
796
$
1,887
36
80
28
59
5
1,004
(53)
(30)
-
-
-
-
7
1,894
-
(1)
Interest Expense, net
$
921
$
1,893
-54-
Table of Contents
The reduction of interest expense applicable to promissory notes and amortization of the related discounts primarily reflects the effect of the
December 2011 conversion to equity of $4.0 million principal amount of 10% convertible notes plus accrued interest issued to Platinum prior to
fiscal 2012, including the amortization of related note discounts. Further, in April and May 2011, other convertible notes and accrued interest
outstanding prior to the Merger were converted into restricted common stock at the time of the Merger. Offsetting these reductions is the accrued
interest and discount amortization recorded for the July 2012 through March 2013 issuance and restructuring of an aggregate of $3.3 million of
10% senior secured convertible notes to Platinum and the restructuring of an additional $3.9 million of debt into new convertible notes to other
service providers including Morrison & Foerster, Cato Research Ltd., and University Health Network. Additionally, during the quarter ended
September 30, 2012, we issued restricted shares of our common stock and a note payable in settlement of certain past due accounts payable
liabilities and recognized losses aggregating $80,000 based on the fair value of the restricted stock and note issued compared to the recorded
liability. In fiscal 2013, we recognized interest income related to the restructuring of the May 2011 note receivable we accepted for the purchase
of shares of our common stock.
In conjunction with the issuance, pursuant to the October 2012 Agreement, of the Senior Secured Convertible Promissory Notes and related
Exchange Warrant and Investment Warrants to Platinum in October 2012, February 2013 and March 2013 (as described more completely in
Note 8, Convertible Promissory Notes and Other Notes Payable in the Consolidated Financial Statements included in Item 8 of this Annual
Report on Form 10-K), and the potential issuance of the Series A Exchange Warrant to Platinum (as described in Note 9, Capital Stock in the
Consolidated Financial Statements included in Item 8 of this Annual Report on Form 10-K), we determined that the warrants included certain
exercise price adjustment features requiring the warrants to be treated as liabilities. We recorded the warrant liability at its estimated fair value
as of the date of warrant issuance or contract execution. During fiscal 2013, we recognized non-cash expense of $1.6 million related to the
increase in the estimated fair value of these liabilities, which resulted primarily from the increase in the market price of our common stock
related to the anticipated exercise price of the warrants. The $78,000 of non-cash expense recognized in fiscal year 2012 related to the
termination of liability treatment for certain derivatives associated with earlier notes and warrants issued to Platinum as a result of our going-
public transaction.
We recognized non-cash losses on the early extinguishment of debt in the aggregate amount of $3.6 million in fiscal 2013 as a result of the
restructuring of notes payable to Platinum and Cato Holding Company, and the restructuring of accounts payable to Cato Research, Ltd. and
University Health Network that were converted in to notes payable, as well as upon the conversion by the holders of our 12% Convertible
Promissory notes issued in February 2012 into restricted shares of our common stock and warrants, all of which were treated as extinguishment
of debt for accounting purposes, all as described more completely in Note 8, Convertible Promissory Notes and Other Notes Payable, in the
Consolidated Financial Statements included in Item 8 of this report. In fiscal 2012, we recognized a non-cash loss of $1.2 million on the early
extinguishment of debt in connection with the cancellation of a $4.0 million note and related accrued interest issued to Platinum and Platinum’s
related exercise of warrants and exchange of shares of our common stock into shares of our Series A preferred stock.
In October 2012, in connection with the Note and Exchange Agreement we entered with Platinum, as described in Note 8, Convertible
Promissory Notes and Other Notes Payable, and Note 9, Capital Stock, in the Consolidated Financial Statements included in this report, we
recorded a non-cash deemed dividend of $10.2 million as a result of the modification of the exchange rights for the Series A Preferred Stock
held by Platinum and the related prospective issuance of a five-year warrant to purchase restricted shares of our common stock upon Platinum’s
exercise of its Series A Preferred Stock exchange rights.
-55-
Table of Contents
Liquidity and Capital Resources
At March 31, 2013, we had cash and cash equivalents of $638,100 and our current liabilities exceeded our current assets by $1.7 million.
However, in April 2013, we entered into a Securities Purchase Agreement pursuant to which, as amended, we have agreed to sell, and Autilion,
AG, a company organized and existing under the laws of Switzerland (“Autilion”), has agreed to purchase, 72.0 million restricted shares of our
common stock for $0.50 per share resulting in aggregate gross proceeds to us of $36.0 million, in a series of tranches scheduled to close between
June 27, 2013 and September 30, 2013 (the “Autilion Financing”). The Autilion Financing also provides for the election to our Board of
Directors of a designee of Autilion. Through the date of this report, we have completed a nominal initial closing of the Autilion
Financing. During our fiscal year ended March 31, 2013, we financed our operations primarily through the issuance of $3.3 million of 10%
Senior Secured Convertible Promissory Notes to Platinum, the sale of Units consisting of common stock and five-year warrants to purchase
common stock that generated approximately $1.1 million of cash proceeds, and the exercise of warrants, most of which were modified to reduce
their original exercise prices, that generated approximately $0.3 million of cash proceeds.
Since inception in May 1998, we have financed our operations, technology development and technology acquisitions primarily through the
issuance and sale of equity and equity-linked securities for cash consideration and convertible promissory notes and short-term promissory notes,
as well as from government research grant awards and strategic collaboration payments.
We anticipate that our cash expenditures during the next twelve months will be approximately $4.0 million to $6.0 million. We believe that our
current cash and cash equivalents, combined with the expected cash proceeds from the Autilion Financing, will enable us to fund our operations
well beyond the next twelve months. Additionally, we may supplement those funds to meet our cash needs and fund our working capital
requirements through a combination of additional private placements of our securities, which may include both debt and equity securities, stem
cell technology-based research and development collaborations, stem cell technology and drug candidate license fees and government grant
awards. Since our inception, we have demonstrated the ability to manage our costs aggressively and increase our operating efficiencies while
advancing our stem cell technology platform and AV-101 development programs. To further advance drug rescue applications of our stem cell
technology platform, as well as support our operating activities, we plan to continue to manage our monthly operating costs associated with
salaries and benefits, regulatory and public company consulting, contract research and development, legal, accounting and other working capital
costs carefully.
Although we have been successful since May 1998 with raising sufficient capital, and we will continue to pursue additional financing
opportunities, as and when required, to meet our business objectives, there can be no assurance that additional capital will be available to us in
sufficient amounts, on terms favorable to us, and without substantial dilution to our current stockholders, if at all. If we are unable to complete
the Autilion Financing or one or more private placements, or otherwise obtain sufficient financing through strategic collaborations or
government grant awards, we will be required to delay, scale back or discontinue certain drug rescue and/or research and development activities,
and this will adversely affect our ability to operate as a going concern and could cause our stock price to decline. If we obtain additional strategic
financing by selling our equity or debt securities, including sales of our common stock pursuant to the completion of the Autilion Financing,
substantial dilution to our existing stockholders will result. Our future working capital requirements will depend on many factors, including,
without limitation, the scope and nature of our strategic opportunities related to our stem cell technology platform, including drug rescue and cell
therapy research and development efforts, the success of such programs, our ability to obtain government grant awards and our ability to enter
into strategic collaborations with institutions on terms acceptable to us.
-56-
Table of Contents
Cash and Cash Equivalents
The following table summarizes changes in cash and cash equivalents for the periods stated (in thousands):
Fiscal Year Ended
March 31,
2013
2012
Net cash used in operating activities
Net cash used in investing activities
Net cash provided by financing activities, including warrant exercises and sale of Units in 2012 and sale of
Units in 2011
$
$
$
(3,463) $
(135) $
(3,566)
(32)
4,156
$
3,540
Off-Balance Sheet Arrangements
Other than contractual obligations incurred in the normal course of business, we do not have any off-balance sheet financing arrangements or
liabilities, guarantee contracts, retained or contingent interests in transferred assets or any obligation arising out of a material variable interest in
an unconsolidated entity. VistaGen California has two inactive, wholly-owned subsidiaries, Artemis Neuroscience, Inc., a Maryland corporation,
and VistaStem Canada, Inc., an Ontario corporation.
Item 7A. Quantitative and Qualitative Disclosures About Market Risk
The disclosures in this section are not required since we qualify as a smaller reporting company.
Item 8. Financial Statements and Supplementary Data
INDEX TO CONSOLIDATED FINANCIAL STATEMENTS
Report of Independent Registered Public Accounting Firm
Consolidated Balance Sheets
Consolidated Statements of Operations and Comprehensive Loss
Consolidated Statements of Cash Flows
Consolidated Statements of Preferred Stock
Consolidated Statements of Stockholders' Deficit
Notes to Consolidated Financial Statements
-57-
Page
58
59
60
61
63
64
68
Table of Contents
REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
To the Board of Directors and Stockholders
VistaGen Therapeutics, Inc.
(a development stage company)
We have audited the accompanying consolidated balance sheets of VistaGen Therapeutics, Inc. (a development stage company) as of
March 31, 2013 and 2012 and the related consolidated statements of operations and comprehensive loss, cash flows, preferred stock, and
stockholders’ deficit for the years then ended, and for the period from May 26, 1998 (inception) through March 31, 2013. These financial
statements are the responsibility of the Company's management. Our responsibility is to express an opinion on these consolidated financial
statements based on our audits.
We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those
standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material
misstatement. We were not engaged to perform an audit of the Company's internal control over financial reporting. Our audits included
consideration of internal control over financial reporting as a basis for designing audit procedures that are appropriate in the circumstances, but
not for the purpose of expressing an opinion on the effectiveness of the Company's internal control over financial reporting. Accordingly, we
express no such opinion. An audit also includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial
statements, assessing the accounting principles used and significant estimates made by management, and evaluating the overall financial
statement presentation. We believe that our audits provide a reasonable basis for our opinion.
In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the consolidated financial
position of VistaGen Therapeutics, Inc. (a development stage company) at March 31, 2013 and 2012, and the consolidated results of its
operations and its cash flows for the years then ended, and for the period from May 26, 1998 (inception) through March 31, 2013, in conformity
with U.S. generally accepted accounting principles.
The accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going concern.
As discussed in Note 2 to the consolidated financial statements, the Company is a development stage company, has not yet generated sustainable
revenues, has suffered recurring losses from operations and has a stockholders’ deficit, all of which raise substantial doubt about its ability to
continue as a going concern. The consolidated financial statements do not include any adjustments that might result from the outcome of this
uncertainty.
/s/ OUM & CO. LLP
San Francisco, California
July 17, 2013
-58-
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED BALANCE SHEETS
(Amounts in $100’s, except share amounts)
ASSETS
Table of Contents
Current assets:
Cash and cash equivalents
Unbilled contract payments receivable
Prepaid expenses
Total current assets
Property and equipment, net
Security deposits and other assets
Total assets
LIABILITIES AND STOCKHOLDERS’ DEFICIT
Current liabilities:
Accounts payable
Accrued expenses
Notes payable and accrued interest
Notes payable and accrued interest to related parties
Capital lease obligations
Deferred revenue
Total current liabilities
Non-current liabilities:
Senior secured convertible promissory notes, net of discount of $1,963,100 at March 31, 2013
and accrued interest
Convertible promissory notes, net of discount of $499,300 at March 31, 2012 and accrued interest
Notes payable, net of discount of $1,142,600 at March 31, 2013 and $228,900 at March 31, 2012
Notes payable to related parties, net of discount of $147,200 at March 31, 2013 and $24,300 at
March 31, 2012 and accrued interest
Warrant liability
Accrued officers’ compensation
Capital lease obligations
Total non-current liabilities
Total liabilities
Commitments and contingencies
Stockholders’ deficit:
Preferred stock, $0.001 par value; 10,000,000 shares, including 500,000 Series A shares, authorized
at March 31, 2013 and 2012; 500,000 and 437,055 Series A shares issued and outstanding at
March 31, 2013 and 2012, respectively
Common stock, $0.001 par value; 200,000,000 shares authorized at March 31, 2013 and 2012;
23,480,169 and 18,704,267 shares issued at March 31, 2013 and March 31, 2012, respectively
Additional paid-in capital
Treasury stock, at cost, 2,713,308 and 2,083,858 shares of common stock held at March 31, 2013
and March 31, 2012, respectively
Notes receivable from sale of common stock
Deficit accumulated during development stage
Total stockholders’ deficit
Total liabilities and stockholders’ deficit
See accompanying notes to consolidated financial statements.
-59-
March 31,
March 31,
2013
2012
$
$
$
$
$
$
638,100
-
33,700
671,800
180,700
29,000
881,500
1,353,700
342,900
617,100
93,000
7,600
-
2,414,300
1,425,700
-
2,091,800
1,106,000
6,394,000
-
6,100
11,023,600
13,437,900
81,000
106,200
50,900
238,100
74,500
29,000
341,600
1,750,800
657,300
582,500
168,200
10,500
13,200
3,182,500
-
6,000
2,684,300
107,700
-
57,000
9,700
2,864,700
6,047,200
500
400
23,500
59,266,000
18,700
52,539,500
(3,968,100)
(209,100)
(3,231,700)
(250,000)
(67,669,200) (54,782,500)
(5,705,600)
(12,556,400)
341,600
$
881,500
$
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(Amounts in $100’s, except share and per share amounts)
Revenues:
Grant revenue
Collaboration revenue
Other
Total revenues
Operating expenses:
Research and development
Acquired in-process research and development
General and administrative
Total operating expenses
Loss from operations
Other expenses, net:
Interest expense, net
Change in warrant and put and note extension option liabilities
Loss on early extinguishment of debt
Other income
Loss before income taxes
Income taxes
Net loss
May 26,
1998
(Inception)
Through
Fiscal Years Ended March 31, March 31,
2013
2012
2013
$
$
200,400
-
-
200,400
1,342,200
-
-
1,342,200
$ 12,963,100
2,283,600
1,123,500
16,370,200
3,430,800
-
3,562,700
6,993,500
(6,793,100)
29,555,700
5,388,600
7,523,200
-
30,681,100
4,997,000
10,385,600
67,760,000
(9,043,400) (51,389,800)
(920,700)
(1,635,800)
(3,567,800)
34,400
(12,883,000)
(3,700)
(12,886,700)
(78,000)
(1,193,500)
(1,893,200) (10,362,200)
(1,217,300)
(4,761,300)
81,900
(12,207,900) (67,648,700)
(20,500)
(12,209,500) (67,669,200)
(1,600)
200
Deemed dividend on Series A Preferred stock
(10,193,200)
-
(10,193,200)
Net loss attributable to common stockholders
$ (23,079,900) $ (12,209,500) $ (77,862,400)
Basic and diluted net loss attributable to common stockholders per common share
Weighted average shares used in computing basic and diluted net
loss attributable to common stockholders per common share
$
(1.27) $
(0.83)
18,108,444
14,736,651
Comprehensive loss
$ (12,886,700) $ (12,209,500) $ (67,669,200)
See accompanying notes to consolidated financial statements.
-60-
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF CASH FLOWS
(Amounts in $100’s)
Cash flows from operating activities:
Net loss
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
Acquired in-process research and development
Amortization of imputed discount on non-interest bearing notes
Amortization of discounts on 7%, 7.5% and 10% notes
Amortization of discounts on Platinum notes
Amortization of discounts on August 2010 short-term notes
Amortization of discounts on February 2012 12% convertible notes
Loss on early extinguishment of debt
Loss on settlements of accounts payable
Change in warrant and put and note term extension option liabilities
Stock-based compensation
Expense related to modification of warrants
Fair value of Series C preferred stock, common stock, and warrants
granted for services
Fair value of common stock granted for services prior to the Merger
Fair value of common stock granted for services following the Merger
Fair value of warrants granted for services and interest following the Merger
Fair value of additional warrants granted pursuant to exercises of modified
warrants (fiscal year 2013) and under Discounted Warrant Exercise
Program (fiscal year 2012)
Fair value of common stock issued for note term modification
Interest income on note receivable for stock purchase
Consulting services by related parties settled by issuing promissory notes
Gain on sale of assets
Changes in operating assets and liabilities:
Unbilled contract payments receivable
Prepaid expenses and other current assets
Security deposits and other assets
Accounts payable and accrued expenses
Deferred revenues
Net cash used in operating activities
Cash flows from investing activities:
Purchases of equipment, net
Net cash used in investing activities
Cash flows from financing activities:
Net proceeds from issuance of common stock and warrants, including units
Net proceeds from issuance of preferred stock and warrants
Proceeds from exercise of modified warrants (fiscal 2013) and under
Discounted Warrant Exercise Program (fiscal 2012)
Proceeds from issuance of notes under line of credit
Proceeds from issuance of 7% note payable to founding stockholder
Net proceeds from issuance of 7% convertible notes
Net proceeds from issuance of 10% convertible notes and warrants
Net proceeds from issuance of Platinum notes and warrants
Net proceeds from issuance of 2008/2010 notes and warrants
Net proceeds from issuance of 2006/2007 notes and warrants
Net proceeds from issuance of 7% notes payable
Net proceeds from issuance of August 2010 short-term notes and warrants
Net proceeds from issuance of February 2012 12% convertible notes and warrants
Repayment of capital lease obligations
Repayment of notes
Net cash provided by financing activities
Net increase (decrease) in cash and cash equivalents
Cash and cash equivalents at beginning of period
Cash and cash equivalents at end of period
Period
From
May 26,
1998
(Inception)
Through
March 31,
2013
Fiscal Years Ended
March 31,
2013
2012
$ (12,886,700) $ (12,209,500) $ (67,669,200)
33,800
-
-
214,500
13,400
-
26,900
3,567,800
78,300
1,635,800
1,241,300
508,200
-
-
340,000
183,800
45,600
-
-
57,200
909,000
14,300
(4,200)
1,193,500
77,900
1,591,300
741,700
-
2,225,500
452,000
564,500
35,900
-
(27,600)
-
-
138,100
22,400
-
-
-
777,500
7,523,200
45,000
473,700
3,562,100
572,000
22,700
4,761,300
78,300
1,217,200
5,595,600
1,249,900
925,400
2,225,500
792,000
748,300
174,000
22,400
(27,600)
44,600
(16,800)
106,200
46,200
-
1,432,200
(13,200)
(3,463,200)
(64,000)
(1,900)
2,100
744,300
(65,600)
-
41,700
(29,000)
15,918,500
-
(3,565,800) (20,971,700)
(135,400)
(135,400)
(32,400)
(32,400)
(816,200)
(816,200)
1,185,100
-
2,679,200
-
3,985,100
4,198,600
262,100
-
-
-
-
3,222,100
-
-
-
-
-
(16,900)
(496,700)
4,155,700
557,100
81,000
638,100
$
$
1,166,300
-
-
-
-
-
-
-
-
-
466,500
(14,500)
(757,600)
3,539,900
(58,300)
139,300
81,000
1,428,400
200,000
90,000
575,000
1,655,000
6,922,100
2,971,800
1,025,000
55,000
800,000
466,500
(117,400)
(1,829,100)
22,426,000
638,100
-
638,100
$
Supplemental disclosure of cash flow activities:
Cash paid for interest
Cash paid for income taxes
$
$
225,900
3,681
$
$
265,400
1,600
$
$
665,600
20,481
-61-
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF CASH FLOWS (continued)
(Amounts in $100s, except share amounts)
Supplemental disclosure of noncash activities:
Forgiveness of accrued compensation and accrued interest
payable to officers transferred to equity
Exercise of warrants and options in exchange for debt cancellation
Settlement of accrued and prepaid interest by issuance of
Series C Preferred Stock
Conversion of 10% notes payable, net of discount, and
related accrued interest of $408,600 into Series C Preferred stock
Issuance of Series B-1 Preferred stock for acquired in-process
research and development
Conversion of 7% notes payable, net of discount, and
related accrued interest of $3,800 into Series B Preferred stock
Conversion of accounts payable into convertible promissory notes
Conversion of accounts payable into note payable
Conversion of accounts payable into common stock
Conversion of accrued interest on convertible promissory
notes into common stock
Notes receivable from sale of common stock to related parties
upon exercise of options and warrants
Capital lease obligations
Recognition of put option and note term extension option liabilities upon
issuance of Original Platinum Notes
Incremental fair value of put option and note term extension
option liabilities from debt modifications
Incremental fair value of note conversion option from debt modification
Incremental fair value of warrant from debt modifications
Recognition of warrant liability upon adoption of new accounting standard
Fair value of warrants issued with August 2010 short term notes
Note discount upon issuance of August 2010 short term notes
Fair value of warrants issued with February 2012 12 % convertible notes
Note discount upon issuance of February 2012 12% convertible notes
Conversion of 2006/2007 and 2008/2010 Notes into Units,
including accrued interest of $1,365,600
Conversion of all series of pre-Merger preferred stock into Units
Conversion of 2011 Platinum Note into Series A Preferred stock,
including accrued interest of $611,100 and conversion premium
Conversion of 7% note payable and accrued interest of $11,500 into common stock and
warrants
Conversion of accounts payable to Morrison & Foerster, McCarthy Tetrault
and Desjardins into notes payable
Accounts payable and cancellation premium converted into 2011 Private
Placement Units
Accrued interest on Cato Holding Company note converted to note payable
Accounts payable settled in December 2011 and May/June 2012 warrant exercises
Insurance premiums settled by issuing note payable
Conversion of accrued interest and fees on February 2012 Notes into 2012
Private Placement Units
Accrued interest on July and August 2012 Notes to Platinum converted into
Exchange Note
Accounts payable settled by issuance of stock or notes payable and stock
Accounts payable converted into 2012 Private Placement Units
Recognition of warrant liability upon issuance to Platinum of October 2012
Exchange Note and October 2012, February 2013 and March 2013
Investment Notes
Recognition of warrant liability for potential issuance to Platinum of Series A
Exchange Warrant under the terms of the October 2012 Agreement
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
Period From
May 26,
1998
(Inception)
Through
March 31,
Fiscal Years Ended
March 31,
2013
2012
2013
-
-
$
$
-
$
-
$
-
$
-
-
$
$
800,000
112,800
-
$
35,300
-
$
2,050,300
-
$
7,523,200
-
-
1,558,500
103,200
$
$
$
$
-
-
-
275,400
$
$
$
$
508,000
893,700
4,368,800
1,927,300
-
$
-
-
$
$
-
$
-
-
-
-
-
-
-
-
$
$
$
$
$
$
$
$
-
$
921,400
-
19,000
-
-
-
-
-
-
-
542,000
495,200
$
$
$
$
$
$
$
$
$
$
$
$
149,800
139,700
-
141,200
479,400
1,891,200
276,700
151,300
130,900
320,000
542,000
495,200
$
6,174,800
-
6,174,800
- $ 14,534,800 $ 14,534,800
$
-
$
5,763,900
$
5,763,900
$
19,500
$
19,500
-
$
1,603,400
$
1,603,400
-
-
12,500
110,100
$
$
$
$
169,000
90,800
267,600
88,500
$
$
$
$
169,000
90,800
280,100
198,600
92,900
$
-
$
92,900
22,600
104,900
50,000
$
$
$
-
-
-
$
$
$
22,600
104,900
50,000
1,690,000
$
-
$
1,690,000
3,068,200
$
-
$
3,068,200
See accompanying notes to consolidated financial statements.
-62-
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF PREFERRED STOCK
Period from May 26, 1998 (inception) through March 31, 2013
(Amounts in $100s, except share and per share amounts)
Preferred
Stock
(Shares)
Series A
Series B Series B-1
Series C
Total
Preferred Preferred Preferred Preferred Preferred
Stock
Stock
Stock
Stock
Stock
Balances at May 26, 1998 (inception)
Issuance of Series A preferred stock
at $2.302 per share for cash, net of
issuance costs of $24,000
Balances at March 31, 2000
Issuance of Series A preferred stock
at $2.302 per share for cash, net of
issuance costs of $5,500
Issuance of Series B preferred stock
at $5.545 per share for cash,
including conversion of $575,000 face
value of 7% convertible notes plus
accrued interest of $3,800, net of
unamortized discount of $70,800 and
issuance costs of $39,800
Balances at March 31, 2001
Issuance of Series B preferred stock
at $5.545 per share for cash, net of
issuance costs of $97,200
Balances at March 31, 2002 and 2003
Issuance of Series B-1 preferred stock
at $5.545 for acquired in-process
research and development
Balances at March 31, 2004
Issuance of Series C preferred stock
at $6.00 per share for cash, including
conversion of $1,655,000 face value of
10% convertible notes plus accrued
interest of $408,600, net of unamortized
note discount of $13,200
and issuance costs of $27,200
Proceeds allocated to warrants issued in
connection with Series C preferred
stock
Balances at March 31, 2005
Issuance of Series C preferred stock
at $6.00 per share for cash, net of
issuance costs of $20,700
Issuance of Series C preferred stock
at $6.00 per share for services and in
payment of interest on line of credit
Balances at March 31, 2006 through
March 31, 2011
Conversion of all series of preferred
stock into VistaGen common stock in
connection with the Merger
Balances at March 31, 2012 and 2013
-
$
-
$
-
$
-
$
-
$
-
429,350
429,350
964,200
964,200
2,580
500
-
-
-
316,282
748,212
-
964,700
1,643,300
1,643,300
199,286
947,498
-
964,700
1,007,800
2,651,100
-
-
-
-
-
-
-
-
-
-
-
-
-
-
964,200
964,200
500
1,643,300
2,608,000
1,007,800
3,615,800
1,356,750
2,304,248
-
964,700
-
2,651,100
7,523,200
7,523,200
-
-
7,523,200
11,139,000
390,327
-
-
-
2,301,500
2,301,500
-
2,694,575
-
964,700
-
2,651,100
-
7,523,200
(25,500)
2,276,000
(25,500)
13,415,000
143,331
46,749
-
-
-
-
-
-
839,300
839,300
280,500
280,500
2,884,655
964,700
2,651,100
7,523,200
3,395,800
14,534,800
(2,884,655)
$
-
(964,700)
$
-
(2,651,100)
$
-
(7,523,200)
$
-
(3,395,800) (14,534,800)
-
$
-
See accompanying notes to consolidated financial statements.
-63-
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ DEFICIT
Period from May 26, 1998 (inception) through March 31, 2013
(Amounts in $100s, except share and per share amounts)
Notes
Deficit
Series A Preferred
Stock
Shares Amount
Common Stock
Shares
Amount
Additional
Paid-in Treasury
Capital
Stock
from
Sale of
Stock
Receivable
Accumulated
During the
Development Stockholders’
Total
Stage
Deficit
Balances at
May 26,
1998
(inception)
Initial sale
of common
stock for
cash to
Founder
Fair value
of common
stock issued
for services
Effect of the
Merger
Net loss for
fiscal year
1999
Balances at
March 31,
1999
Sale of
common
stock for
cash
Fair value
of common
stock issued
for services
Fair value
of warrants
issued for
services
Net loss for
fiscal year
2000
Balances at
March 31,
2000
- $
- $
- $
- $
- $
- $
-
-
- 1,000,000
1,000
4,000
-
-
-
5,000
-
-
4,000
-
400
1,569,000
1,600
(1,600)
-
-
-
-
-
-
-
-
-
-
-
-
400
-
-
(230,900)
(230,900)
-
- 2,573,000
2,600
2,800
-
-
(230,900)
(225,500)
-
- 200,000
200
19,800
-
-
-
20,000
-
- 104,375
100
21,800
-
-
-
21,900
-
-
-
-
-
-
-
39,500
-
-
-
-
-
-
39,500
-
(700,000)
(700,000)
-
- 2,877,375
2,900
83,900
-
-
(930,900)
(844,100)
-
Common stock issued
upon exercise of
options
from 1999
Stock
Incentive
Plan
Fair value
of common
stock issued
for services
Fair value
of warrants
issued for
services
Proceeds allocated to warrants
issued in connection with
7% convertible
notes
Net loss for
-
-
-
-
14,000
-
4,600
-
-
-
4,600
- 100,000
100
32,900
-
-
-
33,000
-
-
-
13,100
-
-
-
13,100
-
-
-
91,200
-
-
-
91,200
fiscal year
2001
Balances at
March 31,
2001
-
-
-
-
-
-
-
(1,809,000)
(1,809,000)
-
- 2,991,375
3,000
225,700
-
-
(2,739,900)
(2,511,200)
-
Common stock issued upon
exercise of options from 1999
Stock Incentive
Plan
Fair value
of warrants
issued for
services
Proceeds allocated to warrants
issued in connection with
10% convertible
notes
Net loss for
fiscal year 2002
-
-
-
-
1,511
-
500
-
-
-
500
-
-
-
33,100
-
-
-
33,100
-
-
-
-
-
-
7,300
-
-
-
-
-
7,300
-
(2,113,000)
(2,113,000)
Balances at
March 31,
2002
-
- 2,992,886
3,000
266,600
-
-
(4,852,900)
(4,583,300)
-
Common stock issued upon
exercise of options from 1999
Stock Incentive
Plan
Fair value
of warrants
issued for
services
Proceeds allocated to warrants
issued in connection with
10%
convertible
notes
Net loss for
fiscal year
2003
-
-
-
-
15,000
-
5,000
-
-
-
5,000
-
-
-
46,500
-
-
-
46,500
-
-
-
-
-
86,800
-
-
-
-
-
-
86,800
-
(502,600)
(502,600)
Balances at
March 31,
2003
-
- 3,007,886
3,000
404,900
-
-
(5,355,500)
(4,947,600)
-
Common stock issued upon
exercise of options from 1999
Stock
Incentive
Plan
Fair value
of warrants
issued for
services
Proceeds allocated to warrants
issued in connection with
10% convertible
notes
Net loss for
fiscal year
2004
-
-
-
-
2,925
-
600
-
-
-
600
-
-
-
2,200
-
-
-
2,200
-
-
-
-
-
11,400
-
-
-
-
-
-
11,400
-
(8,755,500)
(8,755,500)
Balances at
March 31,
2004
-
- 3,010,811
3,000
419,100
-
- (14,111,000)
(13,688,900)
Common stock issued upon
exercise of options from 1999
Stock
Incentive
Plan
-
-
10,708
-
4,800
-
-
-
4,800
-
Proceeds allocated to warrants
issued in connection with
Series C
preferred stock
Fair value
of warrants
issued for
services
Net loss for
fiscal year
2005
-
-
-
-
-
25,500
-
-
-
25,500
-
-
-
-
-
1,500
-
-
-
-
-
-
1,500
-
(1,082,800)
(1,082,800)
Balances at
March 31,
2005
-
- 3,021,519
3,000
450,900
-
- (15,193,800)
(14,739,900)
-
Common stock issued upon
exercise of options from 1999
Stock
Incentive
Plan
Fair value
of warrants
issued for
services
Net loss for
fiscal year
2006
-
-
-
14,604
-
6,600
-
-
-
6,600
-
-
-
-
-
3,300
-
-
-
-
-
-
3,300
-
(1,772,100)
(1,772,100)
Balances at
March 31,
2006
(continued)
- $
- 3,036,123 $
3,000 $ 460,800 $
- $
- $ (16,965,900) $ (16,502,100)
-64-
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ DEFICIT (continued)
Period from May 26, 1998 (inception) through March 31, 2013
(Amounts in $100s, except share and per share amounts)
Series A Preferred
Stock
Common Stock
Paid-in Treasury
Additional
Shares Amount
Shares
Amount
Capital
Stock
from
Sale of
Stock
the
Development
Stage
Total
Stockholders’
Deficit
Deficit
Notes
Accumulated
Receivable During
- $
-
-
-
Balances at
March 31,
2006
Common stock issued
upon exercise of options
from 1999 Stock
Incentive Plan and
warrants for:
Cash
Debt
cancellation
Notes
receivable
Sale of
common
stock for cash
Share-based
compensation
expense
Fair value of
warrants
issued for
services
Forgiveness of accrued
compensation and
accrued interest
payable to
officers
Net loss for
fiscal year
2007
-
-
-
-
-
- 3,036,123 $
3,000 $ 460,800 $
- $
- $ (16,965,900) $ (16,502,100)
-
33,465
100
27,600
- 108,418
100
112,700
-
-
-
-
- 204,498
200
149,600
-
(149,800)
-
10,000
-
1,000
-
-
-
109,800
-
-
-
-
-
-
-
27,700
112,800
-
-
1,000
-
109,800
-
-
-
3,100
-
-
-
3,100
-
-
-
-
799,900
-
-
-
-
-
-
-
799,900
-
(1,999,800)
(1,999,800)
Balances at
March 31,
2007
-
- 3,392,504
3,400 1,664,500
-
(149,800) (18,965,700)
(17,447,600)
-
-
Common stock issued upon
exercise of options from 1999
Stock Incentive
Plan
-
Common stock issued upon
settlement of employment
contract
Share-based
compensation
expense
Proceeds allocated to warrants
issued in connection with
Original Platinum
Notes
Fair value of
warrants
issued for
services
Accrued
interest on
notes
receivable
Net loss for
fiscal year
2008
-
-
-
-
-
2,234
-
1,900
-
20,000
-
42,000
-
-
-
247,600
-
-
-
221,000
-
-
-
-
-
-
-
-
-
1,900
-
42,000
-
247,600
-
-
221,000
-
-
-
224,000
-
-
-
224,000
-
-
-
-
-
-
-
-
-
(9,200)
-
(9,200)
-
-
(5,446,700)
(5,446,700)
Balances at
March 31,
2008
-
- 3,414,738
3,400 2,401,000
-
(159,000) (24,412,400)
(22,167,000)
-
-
Common stock issued upon
exercise of options from 2008
Stock Incentive
Plan and
Scientific
Advisory Plan
Share-based
compensation
expense
Proceeds allocated to warrants
issued in connection
with Platinum Notes and
incremental fair value
of warrant
modification
Fair value of
warrants
issued for
services
Accrued
interest on
notes
receivable
Effect of
reverse stock
split
Net loss for
fiscal year
2009
-
-
-
-
-
-
3,500
-
1,000
-
-
-
108,200
-
-
-
-
-
1,000
-
108,200
-
-
-
72,700
-
-
-
72,700
-
-
-
5,300
-
-
-
5,300
-
-
-
(6)
-
-
-
-
-
-
-
-
-
(7,900)
-
(7,900)
-
-
-
-
-
-
(4,696,200)
(4,696,200)
Balances at
March 31,
2009
-
- 3,418,232
3,400 2,588,200
-
(166,900) (29,108,600)
(26,683,900)
-
-
-
-
Cumulative
effect of
adopting new
accounting
standard
Common
stock issued
upon exercise
of warrant
Common stock issued for
cancellation of accounts payable
and accrued
interest
Incremental fair value of note
conversion options from
debt
modification
Common
stock issued
for services
Share-based
compensation
expense
Fair value of warrants issued for
services and incremental
fair value of
warrant
modification
Fair value of
warrants issued in
connection with
7.5% Notes
Accrued
interest on
notes
receivable
-
-
-
-
-
-
-
(293,700)
-
-
142,300
(151,400)
-
1,086
-
100
-
-
-
100
- 1,646,792
1,600 2,468,600
-
-
-
2,470,200
-
-
-
828,500
- 175,000
200
262,300
-
-
-
668,500
-
-
-
-
-
-
-
828,500
-
262,500
-
668,500
-
-
-
110,100
-
-
-
110,100
-
-
-
291,200
-
-
-
291,200
Net loss for
fiscal year
2010
Balances at
March 31,
2010
(continued)
-
-
-
-
-
-
-
-
-
-
-
(8,400)
-
(8,400)
-
-
(4,124,500)
(4,124,500)
- $
- 5,241,110 $
5,200 $6,923,800 $
- $ (175,300) $ (33,090,800) $ (26,337,100)
-65-
Table of Contents
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ DEFICIT (continued)
Period from May 26, 1998 (inception) through March 31, 2013
(Amounts in $100s, except share and per share amounts)
Series A
Additional
Preferred Stock Common Stock
Paid-in Treasury
Shares Amount Shares
Amount Capital
Stock
Notes
Receivable
from
Sale of
Stock
Deficit
Accumulated
During the
Development Stockholders’
Total
Stage
Deficit
Balances at March
31, 2010
Share-based
compensation
expense
Accrued interest on
notes receivable
Fair value of warrants
issued in connection with the
August 2010 Short-
Term Notes
Incremental fair value of note
conversion options from
debt modification
Net loss for fiscal
year 2011
- $
-
-
-
-
-
- 5,241,110 $
5,200 $ 6,923,800 $
- $ (175,300) $ (33,090,800) $ (26,337,100)
-
-
-
-
-
-
-
-
-
-
- 1,628,800
-
-
-
1,628,800
-
-
-
(8,800)
-
(8,800)
-
252,000
- 1,062,800
-
-
-
-
-
-
-
-
252,000
-
1,062,800
-
(9,482,200)
(9,482,200)
Balances at March
31, 2011
Share-based
compensation
expense
Accrued interest on
notes receivable
Reclassification of
warrant liability to
equity
Incremental value
of Platinum note
modification
Incremental value of
Morrison & Foerster
warrant modification
Stock issued in May 2011
Private Placement, net of
$202,000
placement fees
Payments on note
receivable for sale
of stock
Stock issued upon
conversion of convertible
promissory notes
Stock issued upon
conversion of all series of
preferred stock
Fair value of stock
issued for services
prior to the Merger
Forgiveness of
notes at the Merger
Stock issued upon exercise
of modified warrants
(includes Platinum
exercises)
Incremental value of
warrant modifications
(including
modification of
Platinum warrants)
Fair value of bonus warrants
under Discounted Warrant
-
- 5,241,110
5,200 9,867,400
-
(184,100) (42,573,000)
(32,884,500)
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
- 1,591,300
-
-
-
1,591,300
-
-
(1,000)
-
(1,000)
-
424,100
- 1,070,600
-
58,700
-
-
-
-
-
-
-
424,100
-
1,070,600
-
58,700
- 2,216,106
2,200 3,674,000
-
(500,000)
-
3,176,200
-
250,000
250,000
- 3,528,290
3,500 6,171,300
- 2,884,655
2,900 14,531,900
- 1,371,743
1,400 2,224,100
-
-
-
-
-
-
-
6,174,800
-
14,534,800
-
2,225,500
-
-
-
-
-
185,100
-
185,100
-
- 3,121,259
3,100 3,426,200
-
-
-
3,429,300
-
-
-
- 1,028,900
-
-
-
1,028,900
-
-
-
-
-
Exercise Program
Stock issued in Fall
2011 Follow-on
Offering
Stock issued upon exercise of
options from the 1999
Stock Incentive
Plan
Fair value of stock
issued for services
following the
Merger
Fair value of
warrants issued for
services
Proceeds allocated to warrants
issued and beneficial
conversion feature in connection
with 12% convertible
notes
Stock issued in
connection with
note term extension
Stock issued upon
conversion of
Platinum Note to
equity
(net of Platinum
warrant exercise
reflected above)
Common stock exchanged for
Series A Preferred under
agreements with
Platinum:
231,090
-
-
-
-
-
-
138,100
-
63,570
100
111,200
-
-
-
-
-
138,100
-
111,300
-
113,979
100
102,100
-
-
-
102,200
-
155,555
200
451,800
-
-
-
564,500
-
-
-
461,700
-
8,000
-
22,400
-
-
-
-
-
-
-
-
-
-
452,000
-
564,500
-
461,700
-
22,400
200
-
- 3,387,700
-
-
-
3,387,900
Common Stock
Exchange
Agreement
Note and Warrant
Exchange
Agreement
Net loss for fiscal
year 2012
45,980
-
159,985
200
-
-
-
-
-
-
750,600
(750,600)
-
-
2,480,900 (2,481,100)
-
-
-
-
-
- (12,209,500)
(12,209,500)
Balances at March
31, 2012
(continued)
437,055 $
400 18,704,267 $ 18,700 $52,539,500 $(3,231,700) $ (250,000) $ (54,782,500) $
(5,705,600)
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Table of Contents
Balances at
March 31,
2012
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ DEFICIT (continued)
Period from May 26, 1998 (inception) through March 31, 2013
(Amounts in $100s, except share and per share amounts)
Series A Preferred
Stock
Shares Amount
Additional
Common Stock
Paid-in Treasury
Shares
Amount Capital
Stock
Notes
Receivable
from
Sale of
Stock
Deficit
Accumulated
During the
Development
Stage
Total
Stockholders’
Deficit
437,055 $
400 18,704,267 $ 18,700 $52,539,500 $(3,231,700) $ (250,000) $ (54,782,500) $
(5,705,600)
-
-
-
-
-
-
-
Share-based
compensation
expense
Fair value of
common stock
issued for
services
Fair value of
warrants
issued for
services
Shares issued
upon exercise of
modified
warrants
Incremental fair
value of
modified
warrants
Fair value of warrants
issued upon exercise of
modified
warrants
Fair value of shares
issued in settlement of
accounts payable
Common stock
exchanged for
Series A
Preferred under
2012 Exchange
Agreement with
Platinum
Payment on note
receivable from
sale of stock
Modification of
note receivable
from sale of
stock
Incremental fair value of
modified warrant and
fair
value of warrant issued
in connection with
Morrison &
Foerster note
payable
restructuring
-
Fair value of warrant issued
to Cato Holding Company
in connection
with note
payable
restructure
Fair value of warrant
issued to Cato Research,
Ltd. in connection
62,945
-
-
-
with accounts
-
-
- 1,241,300
-
-
-
1,241,300
-
400,000
400
339,600
-
-
-
340,000
-
-
-
106,200
-
-
-
106,200
-
549,056
500
274,000
-
-
-
274,500
-
-
-
440,700
-
-
-
440,700
-
-
-
35,900
-
103,235
100
103,100
-
-
-
-
-
35,900
-
103,200
100
-
-
736,300
(736,400)
-
-
-
-
-
-
-
-
66,900
-
66,900
-
-
-
-
-
(26,000)
-
(26,000)
-
-
-
998,500
-
-
-
998,500
-
-
-
120,500
-
-
-
120,500
-
-
-
payable
restructure
Fair value of warrant issued to
University Health Network
in connection
with accounts
payable
restructure
-
Fair value of warrants issued
to Morrison & Foerster,
Cato Research Ltd. and
University Health Network
in connection
with accrued
interest on
underlying notes
Sale of Units in
Winter 2012
Private
Placement, net
Exchange of
February 2012
convertible notes
for Units
-
Fair value of warrants issued
to banker in connection with
exchange of
February 2012
convertible notes
Premium of fair value over face
value of Exchange Note
issued to
Platinum
Fair value of Series A Exchange
Warrant issuable to
Platinum
recorded as a
Warrant
Liability
Proceeds allocated to beneficial
conversion feature of
Investment Notes issued to
Platinum in October 2012,
February 2013
and March
2013
Incremental fair value of
warrant modifications in
February 2013
-
Net loss for
fiscal year
2013
-
-
-
-
-
-
-
-
486,200
-
-
-
486,200
-
-
-
264,800
-
-
-
264,800
-
-
-
49,400
-
-
-
49,400
- 2,366,330
2,400 1,246,600
-
-
-
1,249,000
- 1,357,281
1,400 1,214,200
-
-
-
1,215,600
-
-
-
28,200
-
-
-
28,200
-
-
- 1,083,200
-
-
-
1,083,200
-
-
- (3,068,200)
-
-
-
(3,068,200)
-
-
-
-
-
958,500
-
-
67,500
-
-
-
-
-
-
-
-
-
958,500
-
67,500
- (12,886,700)
(12,886,700)
Balances at
March 31,
2013
500,000 $
500 23,480,169 $ 23,500 $59,266,000 $(3,968,100) $ (209,100) $ (67,669,200) $ (12,556,400)
See accompanying notes to consolidated financial statements.
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Table of Contents
1. Description of Business
VISTAGEN THERAPEUTICS, INC.
(a development stage company)
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
VistaGen Therapeutics, Inc., a Nevada corporation (“VistaGen” or the “Company”), is a biotechnology company with expertise in human
pluripotent stem cell technology (“hPSC technology”). The Company is currently applying its hPSC technology for drug rescue, predictive
toxicology and drug metabolism screening. The Company’s primary goal is to use its hPSC technology platform, which it also refers to as
Human Clinical Trials in a Test Tube ™, and the novel pharmaceutical assay systems developed using its hPSC technology expertise and
network of strategic relationships, to generate novel, proprietary, safer variants (Drug Rescue Variants) of once-promising small molecule drug
candidates originally discovered, developed and ultimately discontinued by large pharmaceutical or biotechnology companies prior to market
approval due to unexpected safety concerns relating to heart toxicity, liver toxicity or adverse drug-drug interactions. The Company’s strategy
is to leverage substantial prior third-party investment in drug discovery and drug development and to generate early indications, or predictions,
of how humans will ultimately respond to new drug candidates, including Drug Rescue Variants, before they are ever tested in humans, bringing
human biology to the front end of the drug development process..
VistaGen's orally-available, small molecule drug candidate, AV-101, has successfully completed Phase 1 development in the Unites States for
treatment of neuropathic pain. Neuropathic pain, a serious and chronic condition causing pain after an injury or disease of the peripheral or
central nervous system, affects millions of people worldwide. The NIH awarded VistaGen approximately $8.8 million for preclinical and clinical
development of AV-101.
VistaGen is in the development stage and, since inception, has devoted substantially all of its time and efforts to hPSC research and bioassay
development, small molecule drug development, creating, protecting and patenting intellectual property, recruiting personnel and raising
working capital.
The Merger
VistaGen Therapeutics, Inc., a California corporation (“VistaGen California ”) is a wholly-owned subsidiary of the Company. VistaGen
California was incorporated in California on May 26, 1998. Excaliber Enterprises, Ltd. (“Excaliber”), a publicly-held company (formerly
OTCBB: EXCA) was incorporated under the laws of the State of Nevada on October 6, 2005. After being unable to generate material revenues
based on its original business plan, Excaliber became inactive in 2007. In May 2011, after assessing the prospects associated with its original
business plan and the business opportunities associated with a strategic merger with an established, privately-held, biotechnology company
seeking the potential advantages of being a publicly-held company, Excaliber’s Board of Directors agreed to pursue a strategic merger with
VistaGen California, as described below.
On May 11, 2011, pursuant to a strategic merger transaction with VistaGen California, Excaliber acquired all outstanding shares of VistaGen
California in exchange for 6,836,452 shares of Excaliber common stock (the “Merger”), and Excaliber assumed all of VistaGen California’s pre-
Merger obligations to contingently issue shares of common stock in accordance with VistaGen California’s stock option agreements, warrant
agreements, and a convertible promissory note. In connection with the Merger, Excaliber repurchased 5,064,207 shares of its common stock
from two of its stockholders for a nominal amount, resulting in a total of 784,500 shares of Excaliber common stock outstanding at the date of
the Merger. The 6,836,452 shares issued to VistaGen California stockholders in connection with the Merger represented approximately ninety
percent (90%) of the outstanding shares of Excaliber’s common stock after the closing of the Merger. As a result of the Merger, the business of
VistaGen California became the operating business of Excaliber.
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Table of Contents
Immediately preceding and concurrent with the Merger:
VistaGen California sold 2,216,106 Units, consisting of one share of VistaGen California restricted common stock and a three-year
warrant to purchase one-fourth (1/4) of one share of VistaGen California restricted common stock at an exercise price of $2.50 per share,
at a price of $1.75 per Unit in a private placement for aggregate gross offering proceeds of $3,878,200, including $2,369,200 in cash (the
“2011 Private Placement”). See Note 9, Capital Stock, for a further description;
Holders of certain promissory notes issued by VistaGen California from 2006 through 2010 converted notes totaling $6,174,793,
including principal and accrued but unpaid interest, into 3,528,290 Units at $1.75 per Unit. These Units were the same Units issued in
connection with the 2011 Private Placement. See Note 8, Convertible Promissory Notes and Other Notes Payable; and
All holders of VistaGen California's then-outstanding 2,884,655 shares of restricted preferred stock converted all of their preferred shares
into 2,884,655 shares of VistaGen California restricted common stock. See Note 9, Capital Stock.
●
●
●
Shortly after the Merger:
● Each of VistaGen California's pre-Merger directors was appointed as a director of Excaliber;
● The pre-Merger directors and officers of Excaliber resigned as officers and directors of Excaliber;
● Each of VistaGen California’s pre-Merger officers was appointed an officer of like tenor of Excalber;
●
●
The post-Merger directors of Excaliber (consisting of the pre-Merger directors of VistaGen California) approved a two-for-one (2:1)
forward stock split of Excaliber’s common stock;
The post-Merger directors of Excaliber approved an increase in the number of shares of common stock Excaliber was authorized to issue
from 200 million to 400 million shares (see Note 9, Capital Stock);
● Excaliber’s name was changed to “VistaGen Therapeutics, Inc.”;
● VistaGen’s common stock began trading on the OTC Bulletin Board under the symbol “VSTA” effective on June 21, 2011; and
● VistaGen adopted VistaGen California's fiscal year-end of March 31st.
VistaGen California, as the accounting acquirer in the Merger, recorded the Merger as the issuance of common stock for the net monetary assets
of Excaliber, accompanied by a recapitalization. This accounting for the Merger was identical to that resulting from a reverse acquisition, except
that no goodwill or other intangible assets were recorded. A total of 1,569,000 shares of common stock, representing the shares held by
stockholders of Excaliber immediately prior to the Merger and effected for the post-Merger two-for-one (2:1) stock split noted above, have been
retroactively reflected as outstanding for all periods presented in the accompanying Consolidated Financial Statements of the
Company. Additionally, the accompanying Consolidated Balance Sheets of the Company retroactively reflect the $0.001 par value of
Excaliber’s common stock and the two-for one (2:1) stock split after the Merger.
In October 2011, the Company’s stockholders amended the Company’s Articles of Incorporation to (1) reduce the number of shares of common
stock the Company is authorized to issue from 400 million shares to 200 million shares; (2) authorize the Company to issue up to 10 million
shares of preferred stock; and (3) authorize the Company’s Board of Directors to prescribe the classes, series and the number of each class or
series of preferred stock and the voting powers, designations, preferences, limitations, restrictions and relative rights of each class or series of
preferred stock. In December 2011, the Company’s Board of Directors authorized the creation of a series of up to 500,000 shares of Series A
Preferred Stock, par value $0.001 (“Series A Preferred”). Pursuant to the Note Exchange and Purchase Agreement of October 11, 2012 (the
“October 2012 Agreement”), as amended, between the Company and Platinum Long Term Growth VII, LLC (“ Platinum”), currently the
Company’s largest institutional security holder, Platinum has the right and option to exchange 500,000 shares of the Company’s Series A
Preferred held by Platinum for (i) a total of 15,000,000 restricted shares of the Company’s common stock, and (ii) a five-year warrant to
purchase 7,500,000 restricted shares of the Company’s common stock at an exercise price of $1.50 per share (see Note 9, Capital Stock).
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Table of Contents
The Consolidated Financial Statements of the Company in this Report represent the activity of VistaGen California from May 26, 1998, and the
consolidated activity of VistaGen California and Excaliber (now VistaGen Therapeutics, Inc., a Nevada corporation) from May 11, 2011 (the
date of the Merger). The Consolidated Financial Statements of the Company also include the accounts of VistaGen California’s two wholly-
owned subsidiaries, Artemis Neuroscience, Inc., a Maryland corporation (“Artemis”), and VistaStem Canada, Inc., an Ontario corporation
(“VistaStem Canada”).
2. Basis of Presentation and Going Concern
The accompanying Consolidated Financial Statements of the Company have been prepared assuming the Company will continue as a going
concern. As a development stage company without sustainable revenues, VistaGen has experienced recurring losses and negative cash flows
from operations. From inception through March 31, 2013, VistaGen has a deficit accumulated during its development stage of $67.7
million. The Company expects these conditions to continue for the foreseeable future as it expands its Human Clinical Trials in a Test Tube ™
platform and executes its drug rescue and regenerative cell therapy business programs.
At March 31, 2013, the Company had approximately $638,100 in cash and cash equivalents. Such cash and cash equivalents are not sufficient to
enable the Company to fund its operations, including expected cash expenditures of approximately $5 million, through the next twelve months.
However, in April 2013, the Company entered into a securities purchase agreement, as amended, with an institutional investor involving the
Company’s private issuance and sale of its restricted common stock in a transaction involving a series of closings scheduled to occur between
June 27, 2013 and September 30, 2013, which financing transaction is expected to generate aggregate cash proceeds to the Company of $36.0
million (see Note 16, Subsequent Events, for a further description of this private placement). Additionally, the Company expects that its
participation in strategic collaborations, including licensing transactions, may provide additional cash in support of its future working capital
requirements.
3. Summary of Significant Accounting Policies
Use of Estimates
The preparation of financial statements in conformity with U.S. generally accepted accounting principles (“U.S. GAAP”) requires management
to make estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at
the date of the financial statements, and the reported amounts of revenues and expenses during the reporting period. Actual results could differ
from those estimates. Significant estimates include those relating to revenue recognition, share-based compensation, and the assumptions used
to value warrants, warrant modifications and put option, note term extension, and warrant liabilities.
Principles of Consolidation
The accompanying consolidated financial statements include the Company’s accounts, and the accounts of VistaGen California’s wholly-owned
inactive subsidiaries, Artemis, and VistaStem Canada.
Change in Authorized Number of Shares
Effective with the Merger, the Company was authorized to issue up to 400,000,000 shares of common stock, $0.001 par value and no shares of
preferred stock. On October 28, 2011, the Company held a special meeting of its stockholders at which the stockholders approved a proposal to
amend the Company’s Articles of Incorporation to (1) reduce the number of authorized shares of the Company’s common stock from
400,000,000 shares to 200,000,000 shares; (2) authorize the Company to issue up to 10,000,000 shares of preferred stock; and (3) authorize the
Company’s Board of Directors to prescribe the classes, series and the number of each class or series of preferred stock and the voting powers,
designations, preferences, limitations, restrictions and relative rights of each class or series of preferred stock. In December 2011, the
Company’s Board of Directors authorized the creation of a series of up to 500,000 shares of Series A Preferred Stock. See Note 9, Capital Stock.
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Table of Contents
Cash and Cash Equivalents
Cash and cash equivalents are considered to be highly liquid investments with maturities of three months or less at the date of purchase.
Property and Equipment
Property and equipment is stated at cost. Repairs and maintenance costs are expensed in the period incurred. Depreciation is calculated using the
straight-line method over the estimated useful lives of the assets. The estimated useful lives of property and equipment range from five to seven
years.
Impairment or Disposal of Long-Lived Assets
The Company evaluates its long-lived assets, primarily property and equipment, for impairment whenever events or changes in circumstances
indicate that their carrying value may not be recoverable from the estimated future cash flows expected to result from their use or eventual
disposition. If the estimates of future undiscounted net cash flows are insufficient to recover the carrying value of the assets, the Company
records an impairment loss in the amount by which the carrying value of the assets exceeds their fair value. If the assets are determined to be
recoverable, but the useful lives are shorter than originally estimated, the Company depreciates or amortizes the net book value of the assets
over the newly determined remaining useful lives. The Company has not recorded any impairment charges to date.
Revenue Recognition
The Company generates revenue principally from collaborative research and development arrangements, technology transfer agreements,
including strategic licenses, and government grants. Revenue arrangements with multiple components are divided into separate units of
accounting if certain criteria are met, including whether the delivered component has stand-alone value to the customer. Consideration received
is allocated among the separate units of accounting based on their respective selling prices. The selling price for each unit is based on vendor-
specific objective evidence, or VSOE, if available, third party evidence if VSOE is not available, or estimated selling price if neither VSOE nor
third party evidence is available. The applicable revenue recognition criteria are then applied to each of the units.
The Company recognizes revenue when the four basic criteria of revenue recognition are met: (1) a contractual agreement exists; (2) the transfer
of technology has been completed or services have been rendered; (3) the fee is fixed or determinable; and (4) collectability is reasonably
assured. For each source of revenue, the Company complies with the above revenue recognition criteria in the following manner:
•
Collaborative arrangements typically consist of non-refundable and/or exclusive up front technology access fees, cost reimbursements
for specific research and development spending, and various milestone and future product royalty payments. If the delivered technology
does not have stand-alone value, the amount of revenue allocable to the delivered technology is deferred. Non-refundable upfront fees
with stand-alone value that are not dependent on future performance under these agreements are recognized as revenue when received,
and are deferred if the Company has continuing performance obligations and has no objective and reliable evidence of the fair value of
those obligations. The Company recognizes non-refundable upfront technology access fees under agreements in which it has a
continuing performance obligation ratably, on a straight-line basis, over the period in which the Company is obligated to provide
services. Cost reimbursements for research and development spending are recognized when the related costs are incurred and when
collectability is reasonably assured. Payments received related to substantive, performance-based “at-risk” milestones are recognized as
revenue upon achievement of the milestone event specified in the underlying contracts, which represent the culmination of the earnings
process. Amounts received in advance are recorded as deferred revenue until the technology is transferred, costs are incurred, or a
milestone is reached.
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Table of Contents
•
•
Technology license agreements typically consist of non-refundable upfront license fees, annual minimum access fees, development
and/or regulatory milestone payments and/or royalty payments. Non-refundable upfront license fees and annual minimum payments
received with separable stand-alone values are recognized when the technology is transferred or accessed, provided that the technology
transferred or accessed is not dependent on the outcome of the continuing research and development efforts. Otherwise, revenue is
recognized over the period of the Company’s continuing involvement, and, in the case of development and/or regulatory milestone
payments, when the applicable event triggering such a payment has occurred.
Government grants, which support the Company’s research efforts on specific projects, generally provide for reimbursement of
approved costs as defined in the terms of grant awards. Grant revenue is recognized when associated project costs are incurred.
Research and Development Expenses
Research and development expenses include internal and external costs. Internal costs include salaries and employment related expenses of the
Company’s internal scientific personnel and direct project costs. External research and development expenses consist of sponsored stem cell
research and development costs, costs associated with non-clinical and clinical drug rescue and development activities, including development of
AV-101, the Company’s drug development candidate which has successfully completed Phase 1 development, and costs related to protection of
the Company’s intellectual property, including, but not limited to, application and prosecution of patents related to the Company’s stem cell
technology platform, Human Clinical Trials in a Test Tube ™, and AV-101. All such research and development costs are charged to expense as
incurred.
Share-Based Compensation
The Company recognizes compensation cost for all share-based awards to employees in its financial statements based on their grant date fair
value. Share-based compensation expense is recognized over the period during which the employee is required to perform service in exchange
for the award, which generally represents the scheduled vesting period of options and warrants to purchase common stock of the Company. The
Company has no awards with market or performance conditions. For share-based awards to non-employees, the Company re-measures the fair
value of such awards as they vest and the resulting value is recognized as an expense during the period over which applicable services are
performed by the recipient.
Income Taxes
The Company accounts for income taxes using the asset and liability approach for financial reporting purposes. Deferred tax assets and
liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing
assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. Deferred tax assets and liabilities are
measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be
recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in income in the period that includes
the enactment date. Valuation allowances are established, when necessary, to reduce the deferred tax assets to an amount expected to be realized.
Concentrations of Credit Risk
Financial instruments, which potentially subject the Company to concentrations of credit risk, consist principally of cash and cash equivalents.
The Company’s investment policies limit any such investments to short-term, low-risk investments. The Company deposits cash and cash
equivalents with quality financial institutions and is insured to the maximum of federal limitations. Balances in these accounts may exceed
federally insured limits at times.
Comprehensive Loss
The Company has no components of other comprehensive loss other than net loss, and accordingly the Company’s comprehensive loss is
equivalent to its net loss for the periods presented.
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Table of Contents
Loss per Common Share
Basic loss per share of common stock excludes dilution and is computed by dividing the net loss by the weighted-average number of shares of
common stock outstanding for the period. Diluted loss per share of common stock reflects the potential dilution that could occur if securities or
other contracts to issue shares of common stock were exercised or converted into shares of common stock. For all periods presented, potentially
dilutive securities are excluded from the computation in loss periods, as their effect would be antidilutive. A total of 1,569,000 shares of
common stock, representing the 784,500 shares held by stockholders of Excaliber immediately prior to the Merger and effected for the post-
Merger two-for-one (2:1) stock split described in Note 1, Description of Business, have been retroactively reflected as outstanding for the period
prior to the Merger in the fiscal year ended March 31, 2012 for purposes of determining basic and diluted loss per common share in the
accompanying Consolidated Statements of Operations.
Potentially dilutive securities excluded in determining diluted net loss per common share are as follows:
Series A preferred stock issued and outstanding (1)
Common stock warants issuable to Platinum upon exchange of Series A preferred stock under the terms of
the October 11, 2012 Note Purchase and Exchange Agreement
Outstanding options under the 2008 and 1999 Stock Incentive Plans
Outstanding warrants to purchase common stock
10% convertible Exchange Note and Investment Notes issued to Platinum in October 2012, February 2013
and March 2013, including accrued interest through March 31, 2013 (2)
Total
March 31,
2013
2012
15,000,000
4,370,550
7,500,000
4,912,604
14,660,335
-
4,805,771
4,126,589
6,775,682
-
48,848,621
13,302,910
(1) at March 31, 2013, assumes exchange under the terms of the October 11, 2012 Note Exchange and Purchase Agreement with Platinum
(2) assumes conversion under the terms of the October 11, 2012 Note Exchange and Purchase Agreement with Platinum and the terms of the
individual notes
Recently Adopted Accounting Standards
In June 2011, the FASB issued ASU No. 2011-05, Presentation of Comprehensive Income, which was issued to enhance comparability between
entities that report under U.S. GAAP and International Financial Reporting Standards (“IFRS”), and to provide a more consistent method of
presenting non-owner transactions that affect an entity’s equity. ASU 2011-05 eliminates the option to report other comprehensive income and
its components in the statement of changes in stockholders’ equity and requires an entity to present the total of comprehensive income, the
components of net income and the components of other comprehensive income either in a single continuous statement or in two separate but
consecutive statements. This pronouncement became effective for fiscal years beginning after December 15, 2011. The Company’s adoption of
this ASU effective April 1, 2012 did not have any impact on its consolidated results of operations or financial position; however it required
modification of the format of the former “Consolidated Statements of Operations” to include total comprehensive loss and changing the title of
the statements to “Consolidated Statements of Operations and Comprehensive Loss.”
In May 2011, the FASB issued ASU No. 2011-04, Amendments to Achieve Common Fair Value Measurement and Disclosure Requirements in
U.S. GAAP and International Financial Reporting Standards (“IFRS”). This pronouncement was issued to provide a consistent definition of
fair value and ensure that the fair value measurement and disclosure requirements are similar between U.S. GAAP and IFRS. ASU 2011-04
changes certain fair value measurement principles and enhances the disclosure requirements particularly for Level 3 fair value measurements.
The Company’s adoption of ASU No. 2011-04 effective April 1, 2012 did not have a material impact on its consolidated results of operations or
financial condition.
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Recent Accounting Pronouncements
There have been no recent accounting pronouncements or changes in accounting pronouncements during the fiscal year ended March 31, 2013
that are of significance, or of potential significance, to the Company.
4. Fair Value Measurements
The Company follows the principles of fair value accounting as they relate to its financial assets and financial liabilities. Fair value is defined as
the estimated exit price received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the
measurement date, rather than an entry price that represents the purchase price of an asset or liability. Where available, fair value is based on
observable market prices or parameters, or derived from such prices or parameters. Where observable prices or inputs are not available,
valuation models are applied. These valuation techniques involve some level of management estimation and judgment, the degree of which is
dependent on several factors, including the instrument’s complexity. The required fair value hierarchy that prioritizes observable and
unobservable inputs used to measure fair value into three broad levels is described as follows:
•
•
•
Level 1 — Quoted prices (unadjusted) in active markets that are accessible at the measurement date for assets or liabilities. The fair
value hierarchy gives the highest priority to Level 1 inputs.
Level 2 — Inputs other than Level 1 that are observable, either directly or indirectly, such as quoted prices for similar assets or
liabilities; quoted prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market
data for substantially the full term of the assets or liabilities.
Level 3 — Unobservable inputs (i.e., inputs that reflect the reporting entity’s own assumptions about the assumptions that market
participants would use in estimating the fair value of an asset or liability) are used when little or no market data is available. The fair
value hierarchy gives the lowest priority to Level 3 inputs.
A financial instrument’s categorization within the valuation hierarchy is based upon the lowest level of input that is significant to the fair value
measurement. Where quoted prices are available in an active market, securities are classified as Level 1 of the valuation hierarchy. If quoted
market prices are not available for the specific financial instrument, then the Company estimates fair value by using pricing models, quoted
prices of financial instruments with similar characteristics or discounted cash flows. In certain cases where there is limited activity or less
transparency around inputs to valuation, financial assets or liabilities are classified as Level 3 within the valuation hierarchy.
The Company does not use derivative instruments for hedging of market risks or for trading or speculative purposes. In conjunction with the
issuance of the Senior Secured Convertible Promissory Notes and related Exchange Warrant and Investment Warrants to Platinum in October
2012, February 2013 and March 2013 (see Note 8, Convertible Promissory Notes and Other Notes Payable), and the potential issuance of the
Series A Exchange Warrant (see Note 9, Capital Stock), all pursuant to the October 2012 Agreement, the Company determined that the warrants
included certain exercise price adjustment features requiring the warrants to be treated as liabilities, which were recorded at their estimated fair
value. The Company determined the fair value of the warrant liability using a Monte Carlo simulation model with Level 3 inputs. Inputs used to
determine fair value include the remaining contractual term of the warrants, risk-free interest rates, expected volatility of the price of the
underlying common stock, and the probability of a financing transaction that would trigger a reset in the warrant exercise price, and, in the case
of the Series A Exchange Warrant, the probability of Platinum’s exchange of the shares of Series A Preferred it holds into shares of common
stock. Changes in the fair value of these warrant liabilities have been recognized as non-cash expense in other income (expense) in the
Consolidated Statements of Operations and Comprehensive Loss for the year ended March 31, 2013.
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During 2007 and 2008, the Company issued three convertible promissory notes with an aggregate principal balance of $4.0 million (the
“Original Platinum Notes”) to Platinum Long Term Growth VII, LLC (“Platinum”). On May 5, 2011, the Original Platinum Notes were
amended, restated and consolidated into a single note (the “May 2011 Platinum Note”) with a principal balance of $4.0 million (“May 2011
Amendment”). In conjunction with the issuance of the Original Platinum Notes, the Company determined that (i) the cash payment option or put
option, which provided Platinum with the right to require the Company to repay part of the debt in cash at a 25% premium, and (ii) the note term
extension option, which provided Platinum with the right to extend the maturity date by one year, were embedded derivatives that should be
bifurcated and accounted for separately as liabilities. In conjunction with the issuance of the Original Platinum Notes, the Company also issued
warrants to purchase 560,000 shares of its common stock. These warrants included certain exercise price adjustment features and, as a result, the
Company determined that the warrants were liabilities, which were recorded at their estimated fair value. The Company determined the fair
value of the (i) put option and note term extension option using an internal valuation model with Level 3 inputs and (ii) the warrant liability
using a lattice model with Level 3 inputs. Inputs used to determine fair value included estimated value of the underlying common stock at the
valuation measurement date, the remaining contractual term of the notes, risk-free interest rates, expected volatility of the price of the
underlying common stock, and the probability of a qualified financing. Changes in the fair value of these liabilities prior to the May 2011
Amendment were recognized as a non-cash charge or income in other income (expense) in the Consolidated Statements of Operations and
Comprehensive Loss for the year ended March 31, 2012.
As a result of the May 2011 Amendment, Platinum’s cash payment or put option was eliminated. Further, concurrent with the Merger
transaction described in Note 1 above, the warrants were determined not to be liabilities, since the exercise price adjustment feature terminated
upon the Company becoming a public company as a result of the Merger. The increase in fair value of the warrant liability of $7,000 and the
increase in the put option and note term extension option liabilities of $71,000 were recognized in other expense, net in the statement of
operations for the first quarter of the fiscal year ended March 31, 2012. The remaining put option and note term extension option liabilities, in
the amount of $161,800, were reclassified to note discount in connection with the May 2011 Amendment. The aggregate fair value of the
warrants at May 11, 2011, $424,100, was reclassified from a liability to additional paid-in capital, a component of stockholders’ deficit.
In December 2011, the Company and Platinum entered into a Note and Warrant Exchange Agreement pursuant to which the May 2011 Platinum
Note and the warrants issued to Platinum were cancelled in exchange for shares of the Company’s Series A Preferred stock.
The fair value hierarchy for liabilities measured at fair value on a recurring basis is as follows:
Fair Value Measurements at
Reporting Date Using
Quoted Prices
in Active
Markets for
Identical
Assets
(Level 1)
Significant
Other
Observable
Inputs
(Level 2)
Significant
Unobservable
Inputs
(Level 3)
Total
Carrying
Value
March
31, 2013:
Warrant
liability
March
31, 2012:
Put
option
and note
term
extension
option
liabilities
Warrant
liability
$
6,394,000
$
-
$
-
$
6,394,000
$
$
-
-
$
$
-
-
$
$
-
-
$
$
-
-
During the fiscal years ended March 31, 2013 and 2012, there were no significant changes to the valuation models used for purposes of
determining the fair value of the Level 3 warrant liability or the put option and note term extension liabilities.
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The changes in Level 3 liabilities measured at fair value on a recurring basis are as follows:
Fair Value Measurements Using Significant
Unobservable Inputs (Level 3)
Balance at March 31, 2011
Put Option
and
Note Term
Extension Warrant
Liability
Liabilities
$
90,800
$
417,100
$
507,900
Total
Mark to market loss included in net loss
Reclassification of liability to note discount on Original Platinum Notes upon Merger
Reclassification of remaining warrant liability to equity upon Merger
71,000
(161,800)
7,000
-
-
(424,100)
78,000
(161,800)
(424,100)
Balance at March 31, 2012
$
-
$
-
$
-
Recognition of warrant liability upon issuance of Exchange and Investment Warrants
to Platinum under October 2012 Agreement
Recognition of warrant liability in connection with Series A Exchange Warrant
potentially issuable to Platinum under October 2012 Agreement
Mark to market loss included in net loss
-
-
-
1,690,000
1,690,000
3,068,200
1,635,800
3,068,200
1,635,800
Balance at March 31, 2013
$
-
$
6,394,000
$
6,394,000
No assets or other liabilities were measured on a recurring basis at fair value at March 31, 2013 or 2012.
5. Property and Equipment
Property and equipment consists of the following:
Laboratory equipment
Computers and network equipment
Office furniture and equipment
Accumulated depreciation and amortization
Property and equipment, net
March 31,
2013
2012
$
$
649,500
12,900
69,600
732,000
515,800
12,900
75,600
604,300
(551,300)
(529,800)
$
180,700
$
74,500
In connection with the issuance of Senior Secured Convertible Promissory Notes to Platinum in July and August 2012 and with the October
2012 Agreement with Platinum, the Company entered into a Security Agreement with Platinum under which the repayment of all amounts due
under the terms of the various notes issued to Platinum are secured by the Company’s assets, including its tangible and intangible personal
property, licenses, patent licenses, trademarks and trademark licenses (see Note 8, Convertible Promissory Notes and Other Notes Payable). In
February 2004, the Company granted a security interest covering its laboratory and computer equipment in conjunction with notes payable under
a line of credit agreement. The security interest was released in April 2011 in connection with the consolidation of certain notes payable.
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6. AV-101 Acquisition
In November 2003, pursuant to an Agreement and Plan of Merger (the “Artemis Agreement”), the Company acquired Artemis, a private company
also in the development stage, for the purpose of acquiring exclusive licenses to patents and other intellectual property related to the use and
function of AV-101, a new drug candidate then in nonclinical development, with the potential to treat neuropathic pain, depression, and other
neurological diseases and disorders, epilepsy, Huntington’s disease and Parkinson’s disease. Pursuant to the Artemis Agreement, each share of
common stock of Artemis was converted into the right to receive 0.9045 shares of VistaGen California’s Series B-1 Preferred Stock, resulting in
VistaGen California’s pre-Merger issuance of 1,356,750 shares of its Series B-1 Preferred Stock. The shares of Series B-1 Preferred Stock were
valued, pre-Merger, at $5.545 per share, and accordingly the pre-Merger purchase price of all outstanding shares of Artemis in 2003 was
$7,523,200. The total purchase price was allocated to AV-101 acquired in-process research and development and was expensed subsequent to
the acquisition, since AV-101 required further research and development before the Company could commence clinical trials and did not have
any proven alternative future uses.
The NIH awarded the Company an aggregate of $4.2 million to support nonclinical development of AV-101 during fiscal years 2006 through
2008, culminating in the submission in November 2008 of its Investigational New Drug ("IND") application to conduct Phase 1 human clinical
testing of AV-101 for neuropathic pain. In April 2009, the NIH awarded the Company an aggregate of $4.2 million grant to support the Phase 1
clinical development of AV-101, and subsequently increased the grant to an aggregate of $4.6 million in July 2010. The Company completed the
Phase 1a clinical trial of AV-101 during the third calendar quarter of 2011 and completed the Phase 1b clinical testing in the last half of calendar
2012. To date, VistaGen has received an aggregate of $8.8 million from the NIH for non-clinical and clinical development of AV-101.
7. Accrued Expenses
Accrued expenses consist of:
Accrued professional services
Accrued research and development expenses
Accrued vacation pay and other compensation
Accrued placement agent fees
Accrued royalties and license fees
All other
March 31,
March 31,
2013
2012
$
$
67,800
-
219,300
-
25,000
30,800
107,400
237,500
229,900
50,000
5,000
27,500
$
342,900
$
657,300
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8. Convertible Promissory Notes and Other Notes Payable
The following table summarizes the components of the Company’s convertible promissory notes and other notes payable:
Principal
Balance
Senior Secured 10% Convertible Promissory Notes
issued to Platinum:
Exchange Note issued on October 11,
2012
Investment Note issued on October 11,
2012
Investment Note issued on October 19,
2012
Investment Note issued on February 22,
2013
Investment Note issued on March 12,
2013
$
500,000
500,000
250,000
1,272,600
March 31, 2013
Accrued
Interest
Total
Principal
Balance
March 31, 2012
Accrued
Interest
Total
$
61,700
$
1,334,300
$
-
$
-
$
24,200
524,200
23,000
523,000
2,600
252,600
4,700
116,200
-
116,200
$
754,700
3,388,800
(1,963,100)
$
1,425,700
-
-
-
-
-
-
-
$
-
-
-
-
-
-
-
$
750,000
3,272,600
(1,963,100)
$
1,309,500
-
-
-
-
-
-
-
-
Aggregate note discount
Total Senior notes (non-current)
Convertible Promissory Notes:
February 2012 12% convertible
promissory notes
Note discount
Total 12% convertible notes, net
(non-current)
Notes Payable to unrelated parties:
7.0% Notes payable (April 2011)
7.0% Notes payable (August 2012)
less: current portion
7.0% Notes payable - non-current
portion
$
$
$
$
$
7.5% Notes payable to service
providers for
accounts payable converted to notes
payable:
Burr, Pilger, Mayer
Desjardins
McCarthy Tetrault
May 2011 Morrison Foerster
August 2012 Morrison & Foerster
Note A
August 2012 Morrison & Foerster Note
B, payable solely in restricted shares of
the Company's common stock (1)
University Health Network, payable
solely in restricted shares of the
Company's common stock (1)
Note discount
less: current portion
non-current portion and discount
5.8% and 8% Notes payable to
insurance
premium financing company (current)
10% Notes payable to vendors for
accounts
payable converted to notes payable
less: current portion
non-current portion
$
$
$
$
$
-
-
-
$
$
-
59,400
59,400
$
(8,100)
$
-
-
-
$
$
$
-
-
-
-
$
-
-
-
$
500,000
$
(499,300)
$
5,300
-
505,300
(499,300)
700
$
5,300
$
6,000
$
-
59,400
59,400
(8,100)
$
63,800
-
$
63,800
(63,800)
$
400
-
400
$
(400)
64,200
-
64,200
(64,200)
$
51,300
$
-
$
51,300
$
-
$
-
$
-
$
90,400
194,100
403,100
-
937,400
$
-
800
1,700
-
$
90,400
194,900
404,800
-
$
93,400
224,300
459,400
2,420,100
$
1,100
2,800
5,700
37,900
94,500
227,100
465,100
2,458,000
1,379,400
60,100
1,439,500
-
937,400
-
-
-
-
-
-
549,500
3,553,900
(1,142,600)
2,411,300
(450,300)
$
1,961,000
19,400
82,000
-
82,000
(2,500)
$
79,500
568,900
3,635,900
(1,142,600)
2,493,300
(452,800)
$
2,040,500
-
3,197,200
(228,900)
2,968,300
(367,700)
$
2,600,600
-
47,500
-
47,500
-
47,500
$
-
3,244,700
(228,900)
3,015,800
(367,700)
2,648,100
4,200
$
-
$
4,200
$
4,600
$
-
$
4,600
128,800
$
(128,800)
$
-
23,300
$
(23,300)
$
-
152,100
$
(152,100)
$
-
165,400
$
(146,000)
$
19,400
16,800
-
16,800
$
$
182,200
(146,000)
36,200
$
$
$
Total notes payable to unrelated
parties
less: current portion
non-current portion and discount
Notes payable to related parties:
April 2011 7 % Note to Cato Holding
Co.
October 2012 7.5% Note to Cato
Holding Co.
October 2012 7.5% Note to Cato
Research Ltd., payable solely in
restricted shares of the Company's
common stock (1)
Note discount
Total notes payable to related parties
less: current portion
non-current portion and discount
$
2,603,700
$
(591,400)
$
2,012,300
105,300
$
(25,800)
$
79,500
2,709,000
$
(617,200)
$
2,091,800
3,202,100
$
(582,100)
$
2,620,000
64,700
$
(400)
$
64,300
3,266,800
(582,500)
2,684,300
-
$
-
$
-
$
293,300
$
6,900
$
300,200
293,600
7,400
301,000
-
-
-
1,009,000
1,302,600
(147,200)
1,155,400
(85,600)
$
1,069,800
36,200
43,600
-
43,600
(7,400)
$
36,200
1,045,200
1,346,200
(147,200)
1,199,000
(93,000)
$
1,106,000
-
293,300
(24,300)
269,000
(168,200)
$
100,800
-
6,900
-
6,900
-
6,900
$
-
300,200
(24,300)
275,900
(168,200)
107,700
(1) See description of debt restructuring in Note 8.
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Senior Secured Convertible Promissory Notes issued to Platinum
On July 2, 2012 and on August 31, 2012, the Company issued to Platinum senior secured convertible promissory notes in the principal amount
of $500,000 (the “July 2012 Platinum Note”) and $750,000 (the "August 2012 Platinum Note"), respectively. The July 2012 Platinum Note and
the August 2012 Platinum Note each accrued interest at the rate of 10% per annum and were due and payable on July 2, 2015. The July 2012
Platinum Note and the August 2012 Platinum Note were each mandatorily convertible into securities that may be issued by the Company in an
equity, equity-based, or debt financing, or series of financings, subsequent to the issuance of the note resulting in gross proceeds to the Company
of at least $3,000,000, excluding any additional investment by Platinum.
On October 11, 2012, the Company and Platinum entered into a Note Exchange and Purchase Agreement (the “October 2012 Agreement”) in
which the July 2012 Platinum Note and the August 2012 Platinum Note (together, the “Existing Notes”), as well as the related accrued interest,
were consolidated into and exchanged for a single senior secured convertible note in the amount of $1,272,577 (the “Exchange Note”) and
Platinum agreed to purchase four additional 10% senior secured convertible promissory notes in the aggregate principal amount of $2.0 million
(the “Investment Notes”), issuable over four separate $500,000 tranches between October 2012 and December 2012. The first and second
$500,000 Investment Notes, in the aggregate principal amount of $1.0 million, were purchased by Platinum on October 11, 2012 and October
19, 2012, respectively. The Company and Platinum also entered into an amended and restated Security Agreement to secure repayment of all
obligations due and payable under the terms of the Investment Notes and Exchange Note.
On November 14, 2012 and January 31, 2013, the Company and Platinum entered into amendments to the October 2012 Agreement (the “ NEPA
Amendments”), pursuant to which the final two $500,000 tranches contemplated by the October 2012 Agreement were combined into a single
Investment Note in the aggregate principal amount of $1.0 million (the “$1.0 Million Note”). Under the terms and conditions of the NEPA
Amendment, Platinum agreed to purchase the $1.0 Million Note within five business days of the Company's notice to Platinum of the
consummation of a debt or equity financing, or combination of financings, prior to February 15, 2013, resulting in gross proceeds to the
Company of at least $1.0 million (the “Additional Financing Requirement”). The Company satisfied the Additional Financing Requirement on
February 12, 2013 (See Note 9, Capital Stock). Effective February 22, 2013, the Company and Platinum entered into an additional amendment
to the October 2012 Agreement pursuant to which Platinum agreed to purchase an Investment Note in the face amount of $250,000 on February
22, 2013 and an additional Investment Note in the face amount of $750,000 on or before March 12, 2013, which Investment Note was issued by
the Company and purchased by Platinum on March 12, 2013.
The Exchange Note and each Investment Note (together, the “Notes”) accrue interest at a rate of 10% per annum and, subject to certain
limitations and exceptions set forth in the Notes, unless converted earlier and voluntarily by Platinum, will be due and payable in restricted shares
of the Company’s common stock on October 11, 2015, or three years from the date of issuance, as determined by the terms of the Investment
Notes. At maturity, all principal and accrued interest under the Notes shall be payable by the Company through the issuance of restricted shares
of common stock to Platinum. Subject to certain potential adjustments set forth in the Notes, the number of restricted shares of common stock
issuable as payment in full for each of the Notes at maturity will be calculated by dividing the outstanding Note balance plus accrued interest by
$0.50 per share. Prior to maturity, the outstanding principal and any accrued interest on the Exchange Note and each of the Investment Notes is
convertible, in whole or in part, at Platinum’s option into shares of the Company’s common stock at a conversion price of $0.50 per share,
subject to certain adjustments. The conversion feature in each of the Notes constituted a beneficial conversion feature at the date of issuance.
As additional consideration for the purchase of the Investment Notes, the Company agreed to issue to Platinum warrants to purchase an
aggregate of 2,000,000 shares of the Company’s common stock, issuable in separate tranches together with each Investment Note, of which a
warrant to purchase 500,000 shares was issued to Platinum on October 11, 2012 and on October 19, 2012, a warrant to purchase 250,000 shares
was issued to Platinum on February 22, 2013 and a warrant to purchase 750,000 shares was issued to Platinum on March 12, 2013 (each an
“Investment Warrant”). In addition, the Company issued Platinum a warrant to purchase 1,272,577 shares of the Company’s common stock in
connection with the issuance of the Exchange Note (the “Exchange Warrant”). At issuance, the Platinum Exchange Warrant and each
Investment Warrant has a term of 5 years and an exercise price of $1.50 per share, subject to certain adjustments. See Note 16, Subsequent
Events, regarding a modification of the exercise price of the Exchange Warrant and the Investment Warrants. The Company and Platinum also
executed and subsequently amended a security agreement to secure repayment of all obligations due and payable under the terms of the
Exchange Note and all of the Investment Notes.
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As a result of the beneficial conversion feature in the Exchange Note and the issuance of the Exchange Warrant, the Company determined that
the cancellation of the Existing Notes and the issuance of the Exchange Note should be accounted for as an extinguishment of debt. The
Company determined that the fair value of the Exchange Note, including the beneficial conversion feature, was $2,355,800 using a Monte Carlo
simulation model and inception-date assumptions including market price of common stock of $0.75 per share; stock price volatility of 85%; risk-
free interest rate of 0.67%; conversion price of $0.50 per share; note term of 3 years; 75% probability that conversion would occur at or
immediately prior to maturity; and 25% probability that an event requiring either the repayment of the Exchange Note or its conversion into
common stock would occur prior to maturity. The fair value of the Exchange Note at inception represented a substantial premium over its face
value. In accordance with the provisions of ASC 470-20, Debt with Conversion and Other Options, the Company recognized the premium in
excess of the face value, $1,083,200, as a non-cash charge to loss on early extinguishment of debt in the accompanying Consolidated Statement
of Operations and Comprehensive Income for the year ended March 31, 2013 and as a credit to additional paid-in capital and recorded the
liability for the Exchange Note at its face value.
Subject to limited exceptions, which include issuances of common stock pursuant to the 2012 Private Placement of Units (see Note 9, Capital
Stock), the Exchange Warrant and each of the Investment Warrants include certain exercise price reset and anti-dilution protection features in the
event that the Company issues other shares of common stock during the five-year term of the warrants at a price less than their initial $1.50 per
share exercise price. As a result of these provisions, the Exchange Warrant and the Investment Warrants do not meet the criteria set forth in ASC
815, Derivatives and Hedging, to be considered indexed to the Company’s own stock and treated as equity instruments. Consequently, the
Company recorded the Exchange Warrant and each of the Investment Warrants as liabilities at their fair value, which was estimated at the
issuance date using a Monte Carlo simulation model and the following assumptions:
Market price of common stock
Exercise price
Risk-free interest rate
Volatility
Term (years)
Dividend rate
Fair value per share
Number of shares
Fair value at date of issuance
Exchange
Warrant
10/11/2012
Investment Warrants Issued on:
2/22/2013
10/19/2012
3/12/2013
$
$
$
0.75
1.50
$
0.67%
85.0%
5.0
0%
$
0.75
1.50
$
0.67%
85.0%
5.0
0%
$
0.75
1.50
$
0.67%
85.0%
5.0
0%
$
0.60
1.50
$
0.84%
85.0%
5.0
0%
0.80
1.50
0.88%
85.0%
5.0
0%
$
$
0.53
1,272,577
672,000
$
$
0.53
500,000
264,000
$
$
0.53
500,000
264,000
$
$
0.39
250,000
97,000
$
$
0.52
750,000
393,000
The fair value of the Exchange Warrant at the date of issuance was recorded as a liability and as a corresponding charge to loss on early
extinguishment of debt in the accompanying Consolidated Statement of Operations and Comprehensive Income for the year ended March 31,
2013. The fair value of each Investment Warrant at the date of issuance was recorded as a liability and as a corresponding discount to the
related Investment Note. Subject to limitations of the absolute amount of discount attributable to each Investment Note, the Company treated
the issuance-date intrinsic value of the beneficial conversion feature embedded in each Investment Note as an additional component of the
discount attributable to each Investment Note and recorded a discount attributable to the beneficial conversion feature for each Investment
Note. The Company amortizes the aggregate discount attributable to each of the Investment Notes using the interest method over the respective
term of each note. The table below summarizes the components of the discount and the effective interest rate at inception for the Exchange Note
and each of the Investment Notes.
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Table of Contents
Face value
Discount attributable to:
Fair value of warrant
Beneficial conversion feature
Inception Date Carrying Value of
Exchange
Investment Notes Issued on:
Note
10/11/2012
10/19/2012
2/22/2013
3/12/2013
$
1,272,600
$
500,000
$
500,000
$
250,000
$
750,000
-
-
(264,000)
(231,000)
(264,000)
(231,000)
(97,000)
(147,000)
(393,000)
(349,500)
Inception date carrying value
$
1,272,600
$
5,000
$
5,000
$
6,000
$
7,500
Effective Interest Rate
10.00%
159.05%
159.05%
127.27%
159.05%
The fair value of the Exchange Warrant and Investment Warrants was re-measured as of March 31, 2013 at an aggregate of $1,988,000 and the
$298,000 increase in fair value since inception was reflected in the accompanying Consolidated Statement of Operations and Comprehensive
Income for the year ended March 31, 2013.
May 2011 Platinum Note
During 2007 and 2008, the Company issued three convertible promissory notes with an aggregate principal balance of $4.0 million to Platinum
(the “Original Platinum Notes”). In conjunction with the issuance of the Original Platinum Notes, the Company also issued warrants to
Platinum to purchase an aggregate of 560,000 shares of the Company’s common stock. On May 5, 2011, the Original Platinum Notes were
amended, restated and consolidated into a single note (the “May 2011Platinum Note”) with a principal balance of $4.0 million and an extended
maturity date of June 30, 2012, a one year extension from the June 30, 2011 maturity date of the Original Platinum Notes (the “May 2011
Amendment”). The May 2011 Platinum Note continued to bear interest at an annual rate of 10%. Platinum retained the right, in its sole
discretion, to extend the maturity date of the May 2011 Platinum Note by one year to June 30, 2013. The May 2011 Platinum Note would have
been automatically converted, subject to certain conditions, upon the last to occur of (i) the closing of an equity or equity-based financing or
series of equity or equity-based financings after May 1, 2011 resulting in gross proceeds to the Company totaling at least $5.0 million, including
the 2011 Private Placement (see Note 9, Capital Stock) and cancellation of debt not otherwise convertible; and (ii) the Company becoming a
publicly traded company ("Amended Qualified Financing"). The number of shares issuable to Platinum upon the automatic conversion of the
May 2011 Platinum Note would have been determined in accordance with one of the following three formulas, as selected by Platinum in its sole
discretion: (i) the outstanding principal plus accrued but unpaid interest ("Outstanding Balance") as of the closing of the Amended Qualified
Financing multiplied by 1.25 and divided by $1.75 per share; (ii) the Outstanding Balance as of the closing of the Amended Qualified Financing
multiplied by 1.25 and divided by the per share price of shares sold in the Amended Qualified Financing; or (iii) the Outstanding Balance as of
the closing of the Amended Qualified Financing divided by the Company's per share price assuming a pre-Amended Qualified Financing
valuation of the Company of $30 million on a fully-diluted basis, subject to certain exclusions. Under the May 2011 Platinum Note, the cash
payment option previously included in the Original Platinum Notes was eliminated. In the event the Company had completed an Amended
Qualified Financing prior to December 31, 2011, interest accrued on the May 2011 Platinum Note from May 5, 2011 through the date of the
closing of the Amended Qualified Financing would have been forgiven.
The May 2011 Platinum Note would have been voluntarily convertible, at the option of Platinum, at any time prior to an Amended Qualified
Financing or its maturity date into restricted shares of common stock determined by multiplying the Outstanding Balance being converted by
1.25 and dividing by the lesser of (i) $1.75 per share; (ii) the per share price in any subsequent equity financing; or (iii) the per share price
assuming a $30 million valuation of the Company on a fully diluted basis (subject to certain exclusions). Platinum could have elected to convert
the May 2011 Platinum Note at any time, but was not obligated to convert the May 2011 Platinum Note until the restricted shares issuable upon
conversion of the note were freely tradable pursuant to an effective registration statement or could have been sold in any ninety day period
without registration under the Securities Act of 1933, as amended (“Securities Act”), in compliance with Rule 144. Additionally, Platinum could
not have converted the May 2011 Platinum Note if the shares issuable upon conversion would result in it beneficially owning in excess of 9.99%
of the then outstanding shares of the Company's common stock. However, Platinum could have waived this condition upon giving 61 days’
notice to the Company.
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In connection with the issuance of the May 2011 Platinum Note, the Company issued to Platinum a three-year warrant to purchase 825,574
restricted shares of the Company’s common stock at an exercise price of $2.50 per share. The warrant would have expired on May 5, 2014, and
become exercisable upon Platinum’s conversion of the May 2011 Platinum Note and would have been exercisable for one-fourth (1/4) of the
number of shares issued in the conversion.
In December 2011, the Company and Platinum entered into a Note and Warrant Exchange Agreement pursuant to which the May 2011 Platinum
Note was cancelled and all warrants issued to Platinum were exercised in exchange for restricted shares of the Company’s new Series A
Preferred stock. See Note and Warrant Exchange Agreement below.
The Company evaluated the extension of the maturity date of the Original Platinum Notes along with the issuance of the new three-year warrant
and determined that the modifications were to be accounted for as a troubled debt restructuring on a prospective basis. The Company recorded a
discount to the May 2011 Platinum Note of $908,900, which amount was equal to the incremental fair value of the note conversion feature and
the cash payment or put option liability, and the fair value of the new warrant. The note discount was to be amortized as non-cash interest
expense over the remaining term of the May 2011 Platinum Note using the effective interest method. The effective annual interest rate of the
May 2011 Platinum Note was determined to be 17.3%, based on the amount of the note discount, the stated interest rate, and the note term.
Warrant Liability related to Original Platinum Notes
The warrants issued with the Original Platinum Notes included certain exercise price adjustment features and accordingly were not deemed to be
indexed to the Company’s common stock. At issuance, the Company recorded the estimated fair value of the warrant liability of $151,300 as a
non-current liability in the consolidated balance sheet. Changes in the estimated fair value of the warrant liability were recorded in other income
(expense) in the Consolidated Statement of Operations and Comprehensive Loss until the closing of the Merger on May 11, 2011, when the
amended warrants no longer contained the exercise price adjustment features, at which time the warrants were deemed to be indexed to the
Company’s common stock and therefore no longer treated as a liability. The warrant liability was recorded at its fair value of $424,100 at May
11, 2011, which resulted in non-cash expense of $7,000 that was charged to other income (expense) in the first quarter of the fiscal year ended
March 31, 2012. As of May 11, 2011, $424,100, the then-current aggregate fair value of these warrants, was reclassified from warrant liability
to additional paid-in capital, a component of stockholders’ deficit.
December 2011 Note and Warrant Exchange Agreement with Platinum
On December 29, 2011, the Company and Platinum entered into a Note and Warrant Exchange Agreement pursuant to which the May 2011
Platinum Note and all outstanding warrants issued to Platinum to purchase an aggregate of 1,599,858 restricted shares of the Company’s
common stock were cancelled in exchange for 391,075 restricted shares of the Company’s newly-created Series A Preferred Stock (“ Series A
Preferred”). Each share of Series A Preferred was initially convertible into ten shares of the Company’s common stock (see Note 9, Capital
Stock). The Company issued 231,090 restricted shares of Series A Preferred to Platinum in connection with the note cancellation based on the
sum of the $4,000,000 principal balance of the Platinum Note plus accrued but unpaid interest through May 11, 2011 adjusted for a 125%
conversion premium, net of the $1,719,800 aggregate exercise price of the outstanding 1,599,858 warrants held by Platinum, and a contractual
conversion basis of $1.75 per common share, all adjusted for the stated 1:10 Series A Preferred to common exchange ratio. An additional
159,985 restricted shares of Series A Preferred were issued to Platinum in connection with the warrant exercise and exchange to acquire the
common shares issued upon the warrant exercise.
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The Company determined that the cancellation of the Platinum Note and exercise of the warrants pursuant to the Note and Warrant Exchange
Agreement should be accounted for as a debt extinguishment. The Company estimated the fair value of the restricted shares of Series A
Preferred stock tendered to Platinum for the cancellation of the Platinum Note under the terms of the agreement at $15.51 per share ($1.55 on a
per common share equivalent basis). The Company recorded a loss of $1,193,500 attributable to the early debt extinguishment, reported in
Other expenses, net in the accompanying Consolidated Statements of Operations and Comprehensive Loss for the year ended March 31,
2012. The loss includes $287,278, calculated using the Black-Scholes Option Pricing Model, representing the incremental fair value of the
warrants exercised by Platinum as modified to reduce their exercise price. (See Discounted Warrant Exercise Program in Note 9, Capital Stock,
for a description of the modification of warrant exercise prices and the resulting valuation that occurred during the quarter ended December 31,
2011.) The restricted common shares issued in connection with the warrant exercise that were exchanged for shares of Series A Preferred Stock
are treated as Treasury Stock in the accompanying Consolidated Balance Sheets at March 31, 2013 and 2012.
February 2012 Convertible Promissory Notes
On February 28, 2012, the Company completed a private placement of convertible promissory notes to certain accredited investors in the
aggregate principal amount of $500,000 (the "Notes"). Each Note accrued interest at the rate of 12% per annum and was to mature on the earlier
of (i) twenty-four months from the date of issuance, or (ii) the consummation of an equity, equity-based, or series of equity-based financings
resulting in gross proceeds to the Company of at least $4.0 million (the “Qualified Financing Threshold”). The holders of the Notes had the
right to voluntarily convert the outstanding principal amount of the Notes and all accrued and unpaid interest (the “Outstanding Balance”) at any
time prior to maturity into that number of restricted shares of the Company’s common stock equal to the Outstanding Balance, divided by $3.00
(the "Conversion Shares"). In addition, in the event the Company consummated a financing equal to or exceeding the Qualified Financing
Threshold, and the price per unit of the securities sold, or price per share of common stock issuable in connection with such financing, was at
least $2.00 (a “Qualified Financing”), the Outstanding Balance would have automatically converted into such securities, including warrants, that
were issued in the Qualified Financing, the amount of which would have been determined according to the following formula: (Outstanding
Balance at the closing date of the Qualified Financing) x (1.25) / (the per security price of the securities sold in the Qualified Financing). The
purchaser of each Note was issued a five-year warrant to purchase, for $2.75 per share, the number of restricted shares of the Company’s
common stock equal to 150% of the total principal amount of the Notes purchased by such purchaser, divided by $2.75, resulting in the potential
issuance of an aggregate of 272,724 restricted shares of the Company’s common stock upon exercise of the warrants (the “Warrant
Shares”). The warrants terminate, if not exercised, five years from the date of issuance. The Company valued the warrants at a fair value of
$1.99 per share on the date of issuance using the Black-Scholes option pricing model and the following assumptions: fair value of common
stock - $2.85; risk-free interest rate – 0.84%; volatility – 89.9%; contractual term – 5.00 years; dividend rate – 0%.
The Company allocated the proceeds from the Notes and associated warrants based on their relative fair values. The relative fair value
attributable to the warrants was $260,076, which the Company recorded as a discount to the Notes and a corresponding credit to additional paid-
in capital. The Company recorded an additional note discount of $235,084 for the fair value of the non-contingent beneficial conversion feature
of the Notes. The note discounts totaling $495,160 were to be amortized to interest expense using the effective interest method over the term of
the Notes. The effective interest rate on the Notes at the date of issuance was 268.9% based on the stated interest rate, the amount of discount,
and the term of the Notes.
The Company entered into a Registration Rights Agreement with the purchasers of the February 2012 Notes pursuant to which the Company
agreed to register for resale the Conversion Shares and the Warrant Shares. The Company agreed to file a registration statement no later than
ninety days from the February 28, 2012 closing date, or by May 28, 2012 (the “Filing Deadline”). Should the Company not have filed the
registration statement by the Filing Deadline or if the registration statement had not been declared effective by the agreed upon effectiveness
deadline, the Company was required to make aggregate payments to the purchasers in an amount equal to 1% of the $500,000 aggregate face
amount of the February 2012 Notes for each 30-day period following the Filing Deadline, or pro-rata portion thereof, with an aggregate
limitation of $50,000.
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On November 15, 2012, the holders of the February 2012 Notes entered into an Exchange Agreement with the Company (the " Exchange
Agreement"). Under the terms of the Exchange Agreement, (i) the current amount due under the terms of the February 2012 Notes, $678,600,
which amount included all accrued interest as well as additional consideration for the conversion, was exchanged for a total of 1,357,281
restricted shares of the Company's common stock and five-year warrants to purchase 678,641 restricted shares of the Company's common stock
at an exercise price of $1.50 per share (the "Note Exchange Securities"); and (ii)
the Registration Rights Agreement was
terminated. Additionally, the Company issued a five-year warrant to purchase 72,000 restricted shares of the Company’s common stock at an
exercise price of $1.50 per share as partial compensation to an investment bank that had placed certain of the Notes. The Company recorded the
issuance of the warrants with a charge to interest expense of $28,200 and a corresponding credit to additional paid-in capital.
The Company determined that the exchange of the Notes into restricted shares of its common stock should be accounted for as an
extinguishment of debt. The Company recognized as consideration in the exchange the sum of (i) the fair value of the restricted common stock
issued in the exchange at the quoted market price of $0.70 per share on the date of the exchange, or $950,100, and (ii) the fair value of the
warrants, which was determined to be $0.39 per share, or $265,500, using the Black Scholes Option Pricing Model and the following
assumptions: market price per share: $0.70; exercise price per share: $1.50; risk-free interest rate: 0.62%; contractual term: 5 years; volatility:
89.5%; expected dividend rate: 0%. The aggregate consideration less the net carrying value of the Notes, including accrued interest, resulted in
the recognition of $1,145,100 as a non-cash loss on early extinguishment of debt in the accompanying Consolidated Statements of Operations
and Comprehensive Income for the year ended March 31, 2013. The warrants issued to the investment bank were valued using the same
assumptions as used for the warrants issued to the exchanging note holders.
Restructuring of Note Payable to Morrison & Foerster
On May 5, 2011, the Company and Morrison & Foerster LLP (“Morrison & Foerster”), then the Company’s general corporate and and
intellectual property counsel, amended a previously outstanding note (the “Original Note”) issued by the Company in payment of legal services
(the “Amended Note”). Under the Amended Note, the principal balance of the Original Note was increased to $2,200,000, interest accrued at the
rate of 7.5% per annum, and the Company was required to make an additional payment of $100,000 within three business days of the date of the
Amended Note. The Company made the required $100,000 payment in a timely manner.
On August 31, 2012, the Company restructured the Amended Note (the “ Restructuring Agreement”). Pursuant to the Restructuring Agreement,
the Company issued to Morrison & Foerster two new unsecured promissory notes to replace the Amended Note, one in the principal amount of
$1,000,000 ("Replacement Note A") and the other in the principal amount of $1,379,400 ("Replacement Note B") (together, the "Replacement
Notes"); amended an outstanding warrant to purchase restricted shares of the Company’s common stock (the “Amended M&F Warrant”); and
issued a new warrant to purchase restricted shares of the Company’s common stock (the “New M&F Warrant”). Under the terms of the
Restructuring Agreement, the Amended Note was cancelled and all of the Company's past due payment obligations under the Amended Note
were satisfied. The Company made a payment of $155,000 to Morrison & Foerster on August 31, 2012 pursuant to the terms of the Amended
Note, and issued the Replacement Notes, each dated as of August 31, 2012. Both Replacement Notes accrue interest at the rate of 7.5% per
annum and are due and payable on March 31, 2016. Replacement Note A requires monthly payments of $15,000 per month through March 31,
2013, and $25,000 per month thereafter until maturity. Payment of the principal and interest on Replacement Note B will be made solely in
restricted shares of the Company’s common stock pursuant to Morrison & Foerster’s surrender from time to time of all or a portion of the
principal and interest balance due on Replacement Note B in connection with its exercise of the New M&F Warrant, at an exercise price of $1.00
per share, and concurrent cancellation of indebtedness and surrender of Replacement Note B; provided, however, that Morrison & Foerster shall
have the option to require payment of Replacement Note B in cash upon the occurrence of a change in control of the Company or an event of
default, and only in such circumstances.
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The Company treated the aggregate of the incremental value of the Amended M&F Warrant and the fair value of the New M&F Warrant as a
discount to the Replacement Notes. Under the terms of the Amended M&F Warrant, the Company amended the warrant to purchase 425,000
restricted shares of its common stock originally issued to Morrison & Foerster on March 15, 2010 to extend the expiration date of the warrant
from December 31, 2014 to September 15, 2017 and to provide for exercise by paying cash or by the cancellation in whole or in part of the
Company’s indebtedness under either of the Replacement Notes. The Company determined that the incremental value of the Amended M&F
Warrant was $121,650 at the modification date using the Black-Scholes Option Pricing Model and the following assumptions:
Assumption:
Market price per share
Exercise price per share
Risk-free interest rate
Expected term in years
Volatility
Dividend rate
Weighted Average Fair Value per share
Pre-modification
Post-modification
0.94
$
0.94
2.00
2.00
$
0.60 %
0.25 %
5.04
2.33
88.8 %
77.9 %
0.0 %
0.0 %
0.24
$
0.52
$
$
$
The New M&F Warrant is exercisable for the number of restricted shares of the Company’s common stock equal to the principal and accrued
interest due under the terms of Replacement Note B divided by the warrant exercise price of $1.00 per share. At the August 31, 2012 date of
grant, the New M&F Warrant was exercisable to purchase 1,379,376 restricted shares of the Company’s common stock. The New M&F
Warrant effectively permits exercise only by the cancellation in whole or in part of the Company’s indebtedness under either of the Replacement
Notes. The New M&F Warrant expires on September 15, 2017. The Company determined the fair value of the New M&F Warrant to be $0.64
per share, or $876,800, at the date of grant using the Black Scholes Option Pricing Model and the following assumptions: market price per
share: $0.94; exercise price per share: $1.00; risk-free interest rate: 0.61%; contractual term: 5.04 years; volatility: 88.8%; expected dividend
rate: 0%. The note discounts totaling $1,197,900, including the $199,500 remaining unamortized discount recorded prior to the modification,
will be amortized to interest expense using the effective interest method over the term of the Replacement Notes. The aggregate amount of the
incremental fair value of the Amended M&F Warrant and the fair value of the New M&F Warrant, $998,450, was recognized as equity and was
credited to additional paid-in capital in the accompanying Consolidated Balance Sheets. The effective interest rate on the Replacement Notes at
the date of issuance was 32.3%, based on the stated interest rate, the amount of discount, and the term of the Replacement Notes. Through
March 31, 2013, the Company has adjusted the New M&F Warrant to increase the number of restricted shares available for purchase by 60,088
shares, based on interest accrued on Replacement Note B through that date. The Company has recorded the fair value of the additional shares as
a charge to interest expense and a corresponding credit to additional paid-in capital.
Restructuring of Accounts Payable to Cato Research Ltd. (“CRL”)
On October 10, 2012, the Company issued to CRL, a contract research and development partner and a related party: (i) an unsecured promissory
note in the initial principal amount of $1,009,000, which is payable solely in restricted shares of the Company’s common stock and which
accrues interest at the rate of 7.5% per annum, compounded monthly (the “CRL Note”), as payment in full for all contract research and
development services and regulatory advice (“CRO Services”) rendered by CRL to the Company and its affiliates through December 31, 2012
with respect to the non-clinical and clinical development of AV-101, and (ii) a five-year warrant to purchase, at a price of $1.00 per share,
1,009,000 restricted shares of the Company’s common stock, the amount equal to the sum of the principal amount of the CRL Note, plus all
accrued interest thereon, divided by $1.00 per share (the “CRL Warrant”). The principal amount of the CRL Note may, at the Company’s option,
be automatically increased as a result of future CRO Services rendered by CRL to the Company and its affiliates from January 1, 2013 to June
30, 2013. The CRL Note is due and payable on March 31, 2016 and is payable solely by CRL's surrender from time to time of all or a portion of
the principal and interest balance due on the CRL Note in connection with its concurrent exercise of the CRL Warrant, provided, however, that
CRL will have the option to require payment of the CRL Note in cash upon the occurrence of a change in control of the Company or an event of
default, and only in such circumstances.
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The Company determined that the cancellation of the accounts payable to CRL for CRO Services and the related issuance of the CRL Note
should be accounted for as an extinguishment of debt. Accordingly, the Company recorded the CRL Note at its fair value of $857,900 based on
the present value of its scheduled cash flows and assumptions regarding market interest rates for unsecured debt of similar quality. The
Company determined the fair value of the CRL Warrant to be $0.48 per share, or $486,164, using the Black Scholes Option Pricing Model and
the following assumptions: market price per share: $0.75; exercise price per share: $1.00; risk-free interest rate: 0.66%; contractual term: 5 years;
volatility: 89.9%; expected dividend rate: 0%. The Company recognized the difference between the sum of the fair values of the CRL Note and
the CRL Warrant less the accounts payable balance due to CRL, $335,100, as a non-cash loss on early extinguishment of debt in the
accompanying Consolidated Statements of Operations and Comprehensive Income for the year ended March 31, 2013. The fair value of the
warrant, $486,164, which is treated as an equity instrument, was credited to additional paid in capital at the issuance date. The difference
between the face value of the CRL Note and its fair value, $151,100, has been treated as a discount to the note and is being amortized over the
term of the note using the interest method, resulting in an effective interest rate of 12.1% on the CRL Note. Through March 31, 2013, the
Company has adjusted the CRL Warrant to increase the number of restricted shares available for purchase by 36,188 shares, based on interest
accrued on the CRL Note through that date. The Company has recorded the fair value of the additional shares as a charge to interest expense and
a corresponding credit to additional paid-in capital.
Issuance and Restructuring of Long-Term Promissory Note to Cato Holding Company
In April 2011, all amounts owed by the Company to Cato Holding Company (" CHC") and its affiliates, which included the $105,000 balance of
an August 2010 Short-Term Note issued to Cato BioVentures, were consolidated into a single note, in the principal amount of $352,273 (the
“2011 CHC Note”). Concurrently, CHC released all of its security interests in certain of the Company’s personal property. The 2011 CHC note
accrued interest at 7% per annum, compounded monthly. Under the terms of the note, the Company was to make six monthly payments of
$10,000 each beginning June 1, 2011, and thereafter to make payments of $12,500 monthly until the note was repaid in full. The Company had
the option to prepay the outstanding balance under this note in full or in part at any time during its term without penalty.
On October 10, 2012, the Company and CHC restructured the 2011 CHC Note. The 2011 CHC Note was cancelled and exchanged for a new
unsecured promissory note in the principal amount of $310,443 (the “2012 CHC Note”) and a five-year warrant to purchase 250,000 restricted
shares of the Company’s common stock at a price of $1.50 per share (the “CHC Warrant”). The 2012 CHC Note accrues interest at a rate of
7.5% per annum and is due and payable in monthly installments of $10,000, beginning November 1, 2012 and continuing until the outstanding
balance is paid in full.
The Company determined that the cancellation of the 2011 CHC Note and the issuance of the 2012 CHC Note should be accounted for as an
extinguishment of debt. Accordingly, the Company recorded the 2012 CHC Note at its fair value of $291,100 based on the present value of its
scheduled cash flows and assumptions regarding market interest rates for unsecured debt of similar quality. The Company determined the fair
value of the CHC Warrant to be $0.48 per share, or $120,462, using the Black Scholes Option Pricing Model and the following assumptions:
market price per share: $0.75; exercise price per share: $1.50; risk-free interest rate: 0.66%; contractual term: 5 years; volatility: 89.9%; expected
dividend rate: 0%. The Company recognized the difference between the sum of the fair values of the 2012 CHC Note and the CHC Warrant less
the carrying value of the 2011 CHC Note, $119,100, as a non-cash loss on early extinguishment of debt in the accompanying Consolidated
Statements of Operations and Comprehensive Income for the year ended March 31, 2013. The fair value of the warrant, $120,462, which is
treated as an equity instrument, was credited to additional paid in capital at the issuance date. The difference between the face value of the 2012
CHC Note and its fair value, $19,343, has been treated as a discount to the note and is being amortized over the term of the note using the
interest method, resulting in an effective interest rate of 11.9% on the CHC 2012 Note.
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Restructuring of Accounts Payable to University Health Network (“UHN”)
On October 10, 2012, the Company issued to UHN: (i) an unsecured promissory note in the principal amount of $549,500, which is
payable solely in restricted shares of the Company’s common stock and which accrues interest at the rate of 7.5% per annum, as payment in full
for all sponsored stem cell research and development activities by UHN and Gordon Keller, Ph.D. under the SCRA through September 30, 2012
(the “UHN Note”), and (ii) a five-year warrant to purchase, at a price of $1.00 per share, 549,500 restricted shares of the Company’s common
stock, the amount equal to the sum of the principal amount of the UHN Note, plus all accrued interest thereon, divided by $1.00 per share (the
“UHN Warrant”). The UHN Note is due and payable on March 31, 2016 and is payable solely by UHN's surrender from time to time of all or a
portion of the principal and interest balance due on the UHN Note in connection with its concurrent exercise of the UHN Warrant, provided,
however, that UHN will have the option to require payment of the UHN Note in cash upon the occurrence of a change in control of the
Company or an event of default, and only in such circumstances.
The Company determined that the restructuring of the accounts payable to UHN under the SRCA, defined below, and the related issuance of the
UHN Note should be accounted for as an extinguishment of debt. Accordingly, the Company recorded the UHN Note at its fair value of
$467,211 based on the present value of its scheduled cash flows and assumptions regarding market interest rates for unsecured debt of similar
quality. The Company determined the fair value of the UHN Warrant to be $0.48 per share, or $264,775, using the Black Scholes Option Pricing
Model and the following assumptions: market price per share: $0.75; exercise price per share: $1.00; risk-free interest rate: 0.66%; contractual
term: 5 years; volatility: 89.9%; expected dividend rate: 0%. The Company recognized the difference between the sum of the fair values of the
UHN Note and the UHN Warrant less the accounts payable balance due to UHN, $182,500, as a non-cash loss on early extinguishment of debt in
the accompanying Consolidated Statements of Operations and Comprehensive Income for the year ended March 31, 2013. The fair value of the
warrant, $264,775, which is treated as an equity instrument, was credited to additional paid in capital at the issuance date. The difference
between the face value of the UHN Note and its fair value has been treated as a discount to the note and is being amortized over the term of the
note using the interest method, resulting in an effective interest rate of 11.3% on the UHN Note. Through March 31, 2013, the Company has
adjusted the UHN Warrant to increase the number of restricted shares available for purchase by 19,421 shares, based on interest accrued on the
UHN Note through that date. The Company has recorded the fair value of the additional shares as a charge to interest expense and a
corresponding credit to additional paid-in capital.
Issuance of Long-Term Notes and Cancellation of Amounts Payable
On February 25, 2011, the Company issued to Burr, Pilger, and Mayer, LLC (“BPM”) an unsecured promissory note in the principal amount of
$98,674 for amounts payable in connection with valuation services provided to the Company by BPM. The BPM note bears interest at the rate
of 7.5% per annum and has payment terms of $1,000 per month, beginning March 1, 2011 and continuing until all principal and interest are paid
in full. In addition, a payment of $25,000 shall be due upon the sale of the Company or upon the Company completing a financing transaction
of at least $5.0 million during any three-month period, with the payment increasing to $50,000 (or the amount then owed under the note, if less)
upon the Company completing a financing of over $10.0 million.
On April 29, 2011, the Company issued to Desjardins Securities, Inc. (“Desjardins”) an unsecured promissory note in the principal amount of
CDN $236,000 for amounts payable for legal fees incurred by Desjardins in connection with investment banking services provided to the
Company by Desjardins. The Desjardins note bears interest at 7.5% and will be due, along with all accrued but unpaid interest on the earliest of
(i) June 30, 2014, (ii) the consummation of a Change of Control, as defined in the Desjardins note, and (iii) any failure to pay principal or
interest when due. The Company was required to make payments of CDN $4,000 per month beginning May 31, 2011, increasing to CDN
$6,000 per month on January 31, 2012. Beginning on January 1, 2012, the Company is also required to make payments equal to one-half of one
percent (0.5%) of the net proceeds of all private or public equity financings closed during the term of the note.
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On May 5, 2011, the Company issued to McCarthy Tetrault LLP (“ McCarthy”) an unsecured promissory note in the principal amount of CDN
$502,797 for the amounts payable in connection with Canadian legal services provided to the Company. The McCarthy note bears interest at
7.5% and will be due, along with all accrued but unpaid interest on the earliest of (i) June 30, 2014, (ii) the consummation of a Change of
Control, as defined in the McCarthy note, and (iii) any failure to pay principal or interest when due. The Company was required to make
payments of CDN $10,000 per month beginning May 31, 2011, which payment amounts increased to CDN $15,000 per month on January 31,
2012. Beginning on January 1, 2012, the Company is also required to make payments equal to one percent (1%) of the net proceeds of all private
or public equity financings closed during the term of the note.
On August 30, 2012, the Company issued a promissory note in the principal amount of $60,000 and 15,000 restricted shares of its common
stock valued at a market price of $0.94 per share to Progressive Medical Research in settlement of past due obligations for clinical research
services in the amount of $79,900. Under the terms of the settlement, the Company also agreed to make monthly cash payments of $5,000 in
August 2012 through December 2012. The promissory note bears interest at 7% per annum and requires payments of $1,000 per month
beginning January 15, 2013 until all principal and interest is paid in full. The note requires payment in full upon the sale of all or substantially
all of the Company’s assets or upon the Company completing a financing transaction, or series of transactions, resulting in gross proceeds to the
Company of at least $4.0 million in any three-month period, excluding proceeds from stock option or warrant exercises. The Company charged
the loss on the settlement to interest expense.
August 2010 Short-Term Note Converted to 7% Note Payable
In August 2010, the Company issued short-term, (the “ August 2010 Short-Term Notes”) having an aggregate principal amount, as adjusted, of
$1,120,000. In May 2011, a total of $840,000 of the aggregate principal amount of the August 2010 Short-Term Notes were converted into
Units consisting of restricted shares of the Company’s common stock and three-year warrants to purchase restricted shares of the Company’s
common stock at an exercise price of $2.50 per share. Of the remaining balance of the August 2010 Short Term Notes; $105,000 of such
amount was converted into a long-term note issued to Cato Holding Company, doing business as Cato BioVentures; and $175,000 of such
amount was amended into a note bearing interest at 7% per annum, as described below.
In April 2011, the Company and the holder of a non-interest bearing, unsecured promissory note issued in August 2010 in the face amount
of $175,000 amended the note, whereby the Company paid $50,000 of the note balance in May 2011 and was to make four monthly payments
of $5,000 between May 2011 and August 2011, an additional nine monthly payments of $11,125 per month for the period from September 1,
2011 through May 1, 2012, plus a final payment on May 2, 2012 equal to any remaining balance. In September 2011, the Company and the
holder agreed to modify the payment schedule to require payments of $5,000 per month through November 1, 2011, six monthly payments of
$11,125 for the period from December 1, 2011 through May 1, 2012, an additional payment of $11,125 on May 2, 2012, plus a final payment on
June 30, 2012 equal to any remaining balance. For strategic purposes, the Company did not make the February 2012 and March 2012 payments
as scheduled. In March 2012, the Company and the note holder again agreed to modify the payment schedule to require seven monthly payments
of $9,171 beginning June 1, 2012 with the final payment due on December 1, 2012 to include interest accrued after March 2012. The Company
repaid the note and accrued interest in installments through March 2013.
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Notes Payable Issued for the Cancellation of Accounts Payable
On October 12, 2009, the Company issued a promissory note payable to the Regents of the University of California (“ UC”) with a principal
balance of $90,000 in exchange for the cancellation of certain amounts payable under a research collaboration agreement (the “UC Note 1”). UC
Note 1 was payable in monthly principal installments of $15,000 through May 30, 2010. Interest on UC Note 1 at 10% per annum was payable
on May 30, 2010. If the Company had completed an initial public offering of its stock prior to May 30, 2010, the remaining balance of UC Note
1 would have been payable within 10 business days after the initial public offering was consummated. The Company made the first two
monthly installments totaling an aggregate of $30,000. On February 25, 2010, the Company issued a promissory note payable to UC having a
principal balance of $170,000 in exchange for the cancellation of the remaining $60,000 principal balance of UC Note 1 and certain amounts
payable under a research collaboration agreement (“UC Note 2”). UC Note 2 was payable in monthly principal installments of $15,000 through
May 31, 2010, with the remaining $125,000 plus all accrued and unpaid interest due on or before June 30, 2010. If the Company had completed
an initial public offering of its stock prior to June 30, 2010, the remaining balance of the Note would have been payable within 10 business days
after the initial public offering was consummated. On June 28, 2010, the Company amended UC Note 2 to extend the payment terms as follows:
monthly installments of $15,000 payable through May 31, 2010, $10,000 due on June 30, 2010 and $115,000 plus all accrued and unpaid interest
due and payable on or before August 30, 2010. On August 25, 2010 and again on October 30, 2010, the Company amended UC Note 2 to
extend the date of the final installment payment to be made under UC Note 2 to December 31, 2010 while adding a strategic premium to
preserve license rights under the research collaboration agreement in exchange for an increase in the then-outstanding principal amount of UC
Note 2 by $15,000 to $125,000. On December 22, 2010, the Company amended UC Note 2 a fourth time and decreased the monthly payment
amount to $5,000 with payments continuing until the outstanding balance of principal and interest is paid in full. The provision requiring the
payment of the outstanding balance within 10 business days following the closing of an initial public offering remains unchanged.
On March 1, 2010, the Company issued a 10% promissory note with a principal balance of $75,000 to National Jewish Health in exchange for
the cancellation of certain amounts payable for accrued royalties. The principal balance plus all accrued and unpaid interest was initially due on
or before December 31, 2010 (“March 2010 Note”). If the Company had completed an initial public offering of its stock prior to any installment
dates, $25,000 of the remaining balance of the March 2010 Note would have been due on June 30, 2010, and any remaining principal balance
and all accrued and unpaid interest would have been payable within 90 business days after the initial public offering was consummated. On
December 28, 2010, the Company amended the March 2010 Note and extended its maturity date to the first to occur of April 30, 2011 or 30 days
following the closing of a financing with gross proceeds of $5,000,000 or more. The Company has been in extended discussions with the holder
of the March 2010 Note and expects the Note will be cancelled in favor of certain amounts payable to the Company equal to or greater than the
outstanding balance of the Note. At March 31, 2013, the Company has made no payments on the March 2010 Note.
On August 13, 2010, the Company issued a 10% promissory note with a principal balance of $40,962 to MicroConstants, Inc. in exchange for
the cancellation of certain amounts payable for services rendered. Under the terms of this note, the Company is to make payments of $1,000 per
month with any unpaid principal or accrued interest due and payable upon the first to occur of (i) August 1, 2013, (ii) the issuance and sale of
equity securities whereby the Company raises at least $5,000,000 or (iii) the sale or acquisition of all or substantially all of the Company’s stock
or assets.
9. Capital Stock
Changes in Amounts of Capital Stock Authorized
At March 31, 2011 and prior to the Merger, Excaliber was authorized to issue up to 200,000,000 shares of common stock, $0.001 par value, and
no shares of preferred stock. Effective with the Merger, the Company was authorized to issue up to 400,000,000 shares of common stock,
$0.001 par value and no shares of preferred stock. On October 28, 2011, the Company held a special meeting of its stockholders at which the
stockholders approved a proposal to amend its Articles of Incorporation to (1) reduce the number of shares of common stock the Company is
authorized to issue from 400,000,000 shares to 200,000,000 shares; (2) authorize the Company to issue up to 10,000,000 shares of preferred
stock; and (3) authorize the Company’s Board of Directors to prescribe the classes, series and the number of each class or series of preferred
stock and the voting powers, designations, preferences, limitations, restrictions and relative rights of each class or series of preferred stock.
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Series A Preferred Stock
In December 2011, the Company’s Board of Directors authorized the creation of a series of up to 500,000 shares of Series A Preferred Stock, par
value $0.001 (“Series A Preferred”). Each restricted share of Series A Preferred is convertible at the option of the holder into ten restricted
shares of the Company's common stock. The Series A Preferred ranks prior to the common stock for purposes of liquidation preference.
The Series A Preferred has no separate dividend rights, however, whenever the Board of Directors declares a dividend on the common stock,
each holder of record of a share of Series A Preferred shall be entitled to receive an amount equal to such dividend declared on one share of
common stock multiplied by the number of shares of common stock into which such share of Series A Preferred could be converted on the
Record Date.
Except with respect to transactions upon which the Series A Preferred shall be entitled to vote separately as a class, the Series A Preferred has no
voting rights. The restricted common stock into which the Series A Preferred is convertible shall, upon issuance, have all of the same voting
rights as other issued and outstanding shares of the Company’s common stock.
In the event of the liquidation, dissolution or winding up of the affairs of the Company, after payment or provision for payment of the debts and
other liabilities of the Company, the holders of Series A Preferred then outstanding shall be entitled to receive an amount per share of Series A
Preferred calculated by taking the total amount available for distribution to holders of all the Company's outstanding common stock before
deduction of any preference payments for the Series A Preferred, divided by the total of (x), all of the then outstanding shares of the Company's
common stock, plus (y) all of the shares of the Company's common stock into which all of the outstanding shares of the Series A Preferred can
be converted before any payment shall be made or any assets distributed to the holders of the common stock or any other junior stock.
At March 31, 2013, there were 500,000 restricted shares of Series A Preferred outstanding, all issued to Platinum under the terms of the Note
and Warrant Exchange Agreement described in Note 8, Convertible Promissory Notes and Other Notes Payable, and the December 2011
Common Stock Exchange Agreement, described below. Platinum’s exchange rights with respect to the Series A Preferred have been modified
as described in the section entitled 2012 Exchange Agreement with Platinum and Deemed Dividend, below.
2011 Private Placement of Units
On May 11, 2011, and immediately preceding the closing of the Merger, VistaGen California sold 2,216,106 Units in a private placement for
aggregate gross proceeds of $3,878,200, including $2,369,200 in cash, a $500,000 short-term note receivable due on September 6, 2011,
cancellation of $840,000 of short-term notes maturing on April 30, 2011, a note cancellation premium of $94,500, and cancellation of $74,500 of
accounts payable (the “2011 Private Placement”). The Units were sold for $1.75 per Unit and consisted of one restricted share of common stock
and a three-year warrant to purchase one-fourth (1/4) of one restricted share of common stock at an exercise price of $2.50 per share. Warrants
to purchase a total of 554,013 restricted shares of common stock were issued to the purchasers of the Units. Concurrently, VistaGen California
issued to its placement agent three-year warrants to purchase 114,284 restricted shares of its common stock at $2.50 per share, and agreed to pay
$200,000 in placement agent fees, $150,000 of which amount was paid on May 11, 2011.
In October 2011, VistaGen restructured the terms of a $500,000 short term promissory note received from an investor in conjunction with the
2011 Private Placement. The Company modified the note to extend the repayment term through September 1, 2012 and to increase the interest
rate to 5% per annum. On November 8, 2012 the Company and the investor again amended the note to require payment of the outstanding
balance of $256,000, reflecting unpaid principal and accrued interest, in twenty-four monthly payments of $11,000 beginning in December 2012
and continuing through November 2014, with a final payment of the remaining unpaid principal and interest due in December 2014. The
outstanding principal balance of the note receivable at March 31, 2013 is $209,100.
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Conversion of Convertible Promissory Notes
On May 11, 2011, concurrent with the Merger, holders of certain promissory notes issued by VistaGen California from 2006 through 2010
converted their notes totaling aggregate principal and interest of $6,174,793 into 3,528,290 Units, at a price of $1.75 per Unit. These Units were
the same Units issued in connection with the 2011 Private Placement.
Conversion of Pre-Merger Preferred Stock
On May 11, 2011, concurrent with the Merger, all holders of VistaGen California's then-outstanding preferred stock converted all of their
preferred shares into 2,884,655 restricted shares of VistaGen California common stock so that, at the completion of the Merger, VistaGen
California had no shares of preferred stock outstanding.
Fall 2011 Follow-On Unit Offering
Beginning in October 2011, the Company initiated a follow-on private placement of Units. These Units were essentially the same as the Units
issued in connection with the 2011 Private Placement, namely, each Unit was priced at $1.75 and consisted of one restricted share of the
Company’s common stock and a three-year warrant to purchase one-fourth (1/4) of one restricted share of the Company’s common stock at an
exercise price of $2.50 per share. The Company sold a total of 63,570 Units and received aggregate cash proceeds of $111,300.
Discounted Warrant Exercise Program
During the quarter ended December 31, 2011, certain warrant holders exercised warrants to purchase an aggregate of 3,121,259 restricted shares
of the Company’s common stock at reduced exercise prices, including warrants to purchase 1,599,858 restricted shares of common stock
exercised by Platinum under the terms of the Note and Warrant Exchange Agreement, as described in Note 8, Convertible Promissory Notes and
Other Notes Payable. The warrants exercised by Platinum were exercised at reduced prices ranging from $0.75 per share to $1.25 per share,
resulting in proceeds of $1,719,800 which was applied to reduce the outstanding balance of the Platinum Note and accrued interest under the
terms of the Note and Exchange Agreement.
Other investors and service providers exercised warrants to purchase an aggregate of 1,028,860 restricted shares of the Company’s common
stock at reduced exercise prices ranging from $0.75 per share to $1.31 per share. In conjunction with these exercises, the Company:
·
·
·
issued 965,734 restricted shares of its common stock and received cash proceeds of $1,106,100;
issued 29,426 restricted shares of its common stock to warrant holders who elected to exercise their warrants in lieu of payment by the
Company in satisfaction of outstanding indebtedness to such holders totaling an aggregate of $30,100; and
issued 33,700 restricted shares of its common stock to warrant holders who elected to exercise their warrants in lieu of payment by the
Company in satisfaction of payment for services in the aggregate amount of $41,400 to be performed in the future by such holders.
Additionally, in December 2011, the Company entered into an Agreement Regarding Payment of Invoices and Warrant Exercises with Cato
Holding Company (“CHC”), CRL, and certain individual warrant holders affiliated with CHC and CRL (collectively, the “CHC Affiliates”)
under the terms of which CHC and the CHC Affiliates exercised warrants to purchase an aggregate of 492,541 restricted shares of the
Company’s common stock at reduced exercise prices ranging from $0.88 per share to $1.25 per share. As a result of these warrant exercises, the
Company received cash payments of $60,200 in connection with the exercise of warrants to purchase 68,417 restricted shares and, in lieu of cash
payments for the remainder of the warrants to purchase 424,124 restricted shares, CHC and CRL agreed to the satisfaction of outstanding
indebtedness to CRL in the amount of $245,300 and pre-payment for future services in the amount of $226,400.
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The Company determined that the increase in the fair value of the warrants exercised as a result of the Discounted Warrant Exercise Program
was $618,400, of which $287,300 is a component of the loss on debt extinguishment related to the conversion of the Platinum Note, as described
in Note 8, Convertible Promissory Notes and Other Notes Payable, $101,200 is attributable to the modifications of the CHC and CHC Affiliates
warrants and reflected in research and development expense, and $229,800 is reflected in general and administrative expense for the fiscal year
ended March 31, 2012 in the accompanying Consolidated Statements of Operations and Comprehensive Loss. The warrants subject to the
exercise price modifications were valued at the inception of the Discounted Warrant Exercise Program using the Black-Scholes Option Pricing
Model and using the following assumptions:
Assumption:
Market price per share
Exercise price per share
Risk-free interest rate
Expected term in years
Volatility
Dividend rate
Post-modification
Pre-modification
$
2.60
2.60
$
1.50 - $2.625
0.75 - $1.31
$
$
0.18% - 0.45 %
0.90 – 3.25
65.7% - 82.8 %
0.0 %
0.02 %
0.25
41.1 %
0.0 %
Weighted Average Fair Value per share
$
1.30
$
1.50
With respect to use of the Black-Scholes Option Pricing Model for determining the fair value of warrants issued or modified, the Company
employs the following in determining its valuation input assumptions. The market price per share is based on the quoted market price of the
Company’s common stock on the Over-the-Counter Bulletin Board on the date of the issuance or modification. Because of its short history as a
public company, the Company estimates volatility based on the historical volatilities of a peer group of public companies over the expected term
of the warrants. The risk-free rate of interest is based on the quoted constant maturity rate for U.S Treasury Bills on the date of issuance or
modification for the term corresponding with the expected term of the warrant. The expected dividend rate is zero as the Company has not paid
and does not expect to pay dividends in the near future.
December 2011 Common Stock Exchange Agreement with Platinum
On December 22, 2011, the Company entered into a Common Stock Exchange Agreement (the " Exchange Agreement") with Platinum, pursuant
to which Platinum converted 484,000 restricted shares of the Company’s common stock into 45,980 restricted shares of the then newly created
Series A Preferred (the " Exchange"). Each restricted share of Series A Preferred issued to Platinum is convertible into ten restricted shares of
the Company’s common stock. In consideration for the Exchange, the Series A Preferred received by Platinum in connection with the Exchange
is convertible into the equivalent of 0.95 restricted shares of common stock surrendered in connection with the Exchange. The Company
determined the fair value of the common stock subject to the Exchange to be $1.55 per share and has reflected the 484,000 restricted common
shares as treasury stock on that basis in the accompanying Consolidated Balance Sheet at March 31, 2012 and 2013.
2012 Exchange Agreement with Platinum and Deemed Dividend
On June 29, 2012, the Company and Platinum entered into an Exchange Agreement (the “2012 Platinum Exchange Agreement”) pursuant to
which the Company agreed to issue Platinum 62,945 restricted shares of Series A Preferred in exchange for 629,450 restricted shares of common
stock then owned by Platinum, in consideration for Platinum’s agreement to purchase from the Company the July 2012 Platinum Note, as
described in Note 8, Convertible Promissory Notes and Other Notes Payable. Under the terms of the 2012 Platinum Exchange Agreement,
Platinum, at its option, could have exchanged all or a portion of its Series A Preferred for the securities issued in connection with a qualified
financing, an equity or equity-based financing, or series of financing transactions resulting in gross proceeds to the Company of at least $3.0
million, based on the stated value of $15.00 per share of Series A Preferred. The Company estimated the fair value of the Series A Preferred
shares tendered to Platinum under the terms of the 2012 Platinum Exchange Agreement at $736,400 ($1.17 per share on a common share
equivalent basis). Following the issuance of the Series A Preferred pursuant to the 2012 Platinum Exchange Agreement, Platinum owns all
500,000 authorized and outstanding restricted shares of the Company’s Series A Preferred, each share of which, in accordance with the
certificate of designations, is convertible into ten shares of the Company’s common stock. The common shares exchanged for shares of Series A
Preferred are treated as treasury stock in the accompanying Consolidated Balance Sheet at March 31, 2013.
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Pursuant to the October 2012 Agreement described in Note 8, Convertible Promissory Notes and Other Notes Payable, Platinum’s exchange
rights in the Series A Preferred were modified such that Platinum now has the right and option to exchange 500,000 restricted shares of the
Company’s Series A Preferred that it holds for (i) a total of 15,000,000 restricted shares of the Company’s common stock, and (ii) a five-year
warrant to purchase 7,500,000 restricted shares of the Company’s common stock at an initial exercise price of $1.50 per share (the “ Series A
Exchange Warrant”). The modification of the exchange ratio resulted in a deemed dividend of $7,125,000 to Platinum for accounting purposes,
which has been reflected in the accompanying Consolidated Statement of Operations and Comprehensive Loss for the fiscal year ended March
31, 2013. The amount of the deemed dividend was determined based on the value of the 10 million incremental shares to which Platinum is
entitled pursuant to the October 2012 Agreement valued at the $0.75 per share quoted market price for the Company’s common stock on the date
of the agreement, an aggregate of $7.5 million, adjusted for an expected 95% probability of exercise of the exchange rights by Platinum. The fair
value of the Series A Exchange Warrant, determined to be $0.43 per share, or $3,228,700, on the date of the agreement using the Black Scholes
Option Pricing Model and the following assumptions: market price per share: $0.75; exercise price per share: $1.50; risk-free interest rate:
0.67%; contractual term: 5 years; volatility: 89.9%; expected dividend rate: 0%; and adjusted for an expected 95% probability of exercise of the
exchange rights by Platinum, was recognized as a liability in the amount of $3,068,200 at the date of the October 2012 Agreement, with a
corresponding charge to Additional paid-in capital in the accompanying Consolidated Balance Sheet. The fair value of the Series A Exchange
Warrant was treated as an additional component of the deemed dividend in the accompanying Consolidated Statement of Operations and
Comprehensive Loss for the fiscal year ended March 31, 2013.
The fair value of the Series A Exchange Warrant was re-measured as of March 31, 2013 at $4,406,000 and the $1,337,800 increase in fair value
since the date of the October 2012 Agreement was reflected in the accompanying Consolidated Statement of Operations and Comprehensive
Loss for the year ended March 31, 2013.
2012 Private Placement of Units
Between September 2012 and March 2013, the Company sold 2,366,330 Units in a private placement to accredited investors and received cash
proceeds of $1,133,200 and settled outstanding amounts payable for legal fees in lieu of cash payment for services in the amount of $50,000. The
Units were sold for $0.50 per Unit and each Unit consisted of one restricted share of the Company’s common stock and a five year warrant to
purchase one half (1/2) of one restricted share of the Company’s common stock at an exercise price of $1.50 per share. In addition, in November
2012, pursuant to an Exchange Agreement, the holders of the February 2012 Notes exchanged the aggregate amount of $678,600 due under the
terms of such notes for a total of 678,641 Units, consisting of 1,357,281 restricted shares of the Company's common stock and five-year warrants
to purchase 678,641 restricted shares of the Company's common stock at an exercise price of $1.50 per share. The gross cash proceeds from this
private placement of Units satisfied the Additional Financing Requirement under the October 2012 Agreement with Platinum, as amended,
described in Note 8, Convertible Promissory Notes and Other Notes Payable, entitling the Company to sell and requiring Platinum to purchase
senior secured convertible promissory notes in the aggregate face amount of $1.0 million in February and March 2013. In connection with the
settlement of legal fees payable by issuing Units, the Company recorded a loss on extinguishment of debt of $30,800 based on the fair market
value of the common shares and the warrant comprising the Unit on the effective date of the settlement.
Common Stock and Warrant Grants
On April 29, 2011, VistaGen California issued 157,143 restricted shares of its common stock at a per share price of $1.75 as a prepayment for
CRO services to be performed by Cato Research Ltd., a related party, during 2011. The prepayment of $275,000 was recognized in research
and development expense in the Consolidated Statement of Operations and Comprehensive Loss as the services were performed by Cato
Research, Ltd. during the fiscal year ended March 31, 2012.
In December 2010, VistaGen California agreed to issue 700,000 restricted shares of its common stock, valued at $1.50 per share, related to its
execution of the second amendment to its Sponsored Research Collaboration Agreement (“SRCA”) with UHN as described in Note 12,
Licensing and Collaborative Agreements , and recorded $1,050,000 of research and development expense in the Consolidated Statements of
Operations for the fiscal year ended March 31, 2011. Such shares were issued in May 2011. In April 2011, VistaGen California agreed to issue
to UHN an additional 100,000 restricted shares of its common stock valued at $1.75 per share in conjunction with its execution of the third
amendment to the SRCA, as also described in Note 12, and recorded $175,000 of research and development expense in the Consolidated
Statements of Operations and Comprehensive Loss for the fiscal year ended March 31, 2012. Such shares were issued in May 2011.
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On May 10, 2011, VistaGen California issued 75,000 restricted shares of common stock, valued at $1.75 per share, to a strategic consultant for
services rendered and recorded $131,250 in general and administrative expense in the Consolidated Statements of Operations and
Comprehensive Loss for the fiscal year ended March 31, 2012.
In January 2012, the Company issued an aggregate of 50,000 restricted shares of its common stock, valued at $3.15 per share, and three-year
warrants to purchase an aggregate of 50,000 restricted shares of its common stock at an exercise price of $3.00 per share to two service providers
as compensation for services. The Company recorded $157,500 in general and administrative expense in the Consolidated Statements of
Operations for the fiscal year ended March 31, 2012 related to the restricted stock grants. The Company valued the warrants at a fair value of
$1.73 per share on the date of issuance using the Black-Scholes option pricing model and the following assumptions: fair value of common
stock - $3.15; risk-free interest rate – 0.40%; volatility – 84.6%; contractual term – 3.00 years; dividend rate – 0%, and recorded $86,700 in
general and administrative expense in the Consolidated Statements of Operations and Comprehensive Loss for the fiscal year ended March 31,
2012 related to the warrant grants.
In February 2012, the Company granted four-year warrants to non-employee members of its Board of Directors and Scientific Advisory Board
and to certain strategic consultants to purchase an aggregate of 280,000 restricted shares of its common stock at an exercise price of $3.00 per
share. The Company valued the warrants at a fair value of $1.71 per share on the date of issuance using the Black-Scholes option pricing model
and the following assumptions: fair value of common stock - $2.75; risk-free interest rate – 0.63%; volatility – 90.0%; contractual term – 4.00
years; dividend rate – 0%, and recorded $179,200 in research and development expense and $298,600 in general and administrative expense in
the Consolidated Statements of Operations and Comprehensive Loss for the fiscal year ended March 31, 2012.
In March 2012, the Company granted three-year warrants to purchase an aggregate of 100,000 restricted shares of its common stock at an
exercise price of $3.00 per share to investors who had exercised warrants generating more than $100,000 in cash proceeds to the Company
during the Discounted Warrant Exercise Program. The Company valued the warrants at a fair value of $1.38 per share on the date of issuance
using the Black-Scholes option pricing model and the following assumptions: fair value of common stock - $2.79; risk-free interest rate –
0.54%; volatility – 79.5%; contractual term – 3.00 years; dividend rate – 0%, and recorded $138,100 in interest expense in the Consolidated
Statements of Operations and Comprehensive Loss for the fiscal year ended March 31, 2012.
During March 2012, the Company issued 50,000 restricted shares of its common stock, valued at $2.79 per share, to a strategic consultant for
services rendered and recorded $139,500 in general and administrative expense in expense in the Consolidated Statements of Operations and
Comprehensive Loss for the fiscal year ended March 31, 2012. The Company also issued 55,555 restricted shares of its common stock, valued
at $2.79 per share, to University Health Network, a related party, in connection with the execution of License Agreement No. 2, and recorded
$155,000 in research and development expense in the Consolidated Statements of Operations and Comprehensive Loss for the fiscal year ended
March 31, 2012. The Company also issued 8,000 restricted shares of its common stock, valued at $2.80 per share, in connection with the
extension of the term of a promissory note, and recorded $22,400 in interest expense in the Consolidated Statements of Operations and
Comprehensive Loss for the fiscal year ended March 31, 2012.
In April 2012, the Company entered into a contract for investor relations consulting services pursuant to which it granted three-year warrants to
purchase 50,000 restricted shares of the Company’s common stock at an exercise price of $2.80 per share. The Company valued the warrant at
$69,200 using the Black Scholes Option Pricing Model and the following assumptions: market price per share: $2.74; exercise price per share:
$2.80; risk-free interest rate: 0.50%; contractual term: 3 years; volatility: 79.09%; expected dividend rate: 0%. The fair value of the warrant was
initially recorded as a prepaid expense and was to be expensed over one year in accordance with the terms of the contract. The contract and
related warrant were cancelled in October 2012 and the remaining amount attributable to the fair value of the warrant was expensed.
In June 2012, the Company entered into a contract for investor relations and public company support services through December 31, 2012
pursuant to which it granted 280,000 restricted shares of its common stock valued at $238,000 based on the grant date quoted market price of
$0.85 per share and warrants to purchase 100,000 restricted shares of its common stock at an exercise price of $3.00 per share through December
31, 2015. The Company valued the warrant at $25,800 using the Black Scholes Option Pricing Model and the following assumptions: market
price per share: $0.85; exercise price per share: $3.00; risk-free interest rate: 0.46%; contractual term: 3.53 years; volatility: 84.279%; expected
dividend rate: 0%. The fair value of the stock and the warrant was recorded as a prepaid expense and is being expensed over the approximately
six-month term of the contract.
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In June 2012, the Company entered into a contract for investor relations consulting services pursuant to which it granted 120,000 restricted
shares of its common stock valued at $102,000 based on the grant date quoted market price of $0.85 per share. The fair value of the stock was
recorded as a prepaid expense and is being expensed over the approximately six-month term of the contract.
In August 2012, the Company modified an existing warrant and issued a new warrant to Morrison & Foerster as additional consideration for the
Restructuring Agreement, as disclosed in Note 8, Convertible Promissory Notes and Other Notes Payable. As described in Note 8, the Company
has treated the aggregate of the incremental value of the Amended M&F Warrant and the fair value of the New M&F Warrant as a discount to
the Replacement Notes, which discount is being amortized to interest expense using the effective interest rate method over the term of the
Replacement Notes.
During August 2012, the Company issued 88,235 restricted shares of its common stock valued at a market price of $1.01 per share in settlement
of a past-due obligation for business development consulting services in the amount of $25,000. The Company charged the loss on the
settlement to interest expense. As disclosed in Note 8, Convertible Promissory Notes and Other Notes Payable, in August 2012, the Company
issued a promissory note in the principal amount of $60,000 and 15,000 restricted shares of its common stock valued at $0.94 per share in
settlement of its past due obligation for AV-101 clinical development services.
In February 2013, the Company entered into a contract for various strategic consulting services pursuant to which it granted a five-year warrant
to purchase 25,000 shares of the Company’s common stock at an exercise price of $1.50 per share. The Company valued the warrant at $11,200
using the Black Scholes Option Pricing Model and the following assumptions: market price per share: $0.79; exercise price per share: $1.50;
risk-free interest rate: 0.84%; contractual term: 5 years; volatility: 87.14%; expected dividend rate: 0%, and expensed the fair value of the
warrant during the fourth quarter of the fiscal year ended March 31, 2013.
On March 3, 2013, the Company granted ten-year warrants to purchase an aggregate of 3,000,000 restricted shares of the Company’s
unregistered common stock at an exercise price of $0.64 per share to the independent members of its Board of Directors and certain of its
officers. The warrants become exercisable for 50% of the shares on April 1, 2013, 25% of the shares on April 1, 2014 and 25% of the shares on
April 1, 2015, provided that the warrant will become fully vested upon a change in control of the Company, as defined, or the consummation by
the Company and a third party of a license or sale transaction involving at least one new drug rescue variant. The Company valued the warrants
at $1,604,800 using the Black Scholes Option Pricing Model and the following assumptions: market price per share: $0.64; exercise price per
share: $0.64; risk-free interest rate: 1.86%; contractual term: 10 years; volatility: 84.73%; expected dividend rate: 0%. The Company recognized
stock compensation expense of $802,400 related to the grants in the fourth quarter of the fiscal year ended March 31, 2013.
Warrant Modifications
Between May and June 30, 2012, the Company offered certain warrant holders the opportunity to exercise their warrants to purchase restricted
shares of the Company’s common stock at reduced exercise prices. The Company subsequently extended the offer through August 2012.
Warrant holders exercised warrants to purchase an aggregate of 524,056 restricted shares of the Company’s common stock and the Company
received cash proceeds of $262,000. In addition, certain warrant holders exercised warrants to purchase 25,000 restricted shares of the
Company’s common stock in lieu of payment by the Company in satisfaction of amounts due for services in the aggregate amount of
$12,500. For every three discounted warrant shares exercised by the warrant holders, the Company granted a three-year warrant to purchase one
share of its common stock at an exercise price of $3.00 per share.
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The Company calculated the fair value of the warrants exercised immediately before and after the May 18, 2012 Board of Directors approval of
the modification offer, and on the exercise date for the exercises occurring after June 30, 2012, and determined that the increase in the fair value
of the warrants exercised was $440,700, which is reflected in general and administrative expense in the accompanying Consolidated Statements
of Operations and Comprehensive Loss for the year ended March 31, 2013. The warrants subject to the exercise price modifications were
valued using the Black-Scholes Option Pricing Model and the following assumptions:
Assumption:
Market price per share (weighted average)
Exercise price per share (weighted average)
Risk-free interest rate (weighted average)
Expected term in years (weighted average)
Volatility (weighted average)
Dividend rate
Weighted Average Fair Value per share
$
$
$
Pre-modification
Post-modification
1.95
0.50
0.06%
0.12
85.7%
0.0%
1.95 $
2.75 $
0.29%
1.93
78.0%
0.0%
0.64 $
1.45
In connection with the foregoing exercises, the Company issued three-year warrants to purchase 183,025 restricted shares of the Company’s
common stock at an exercise price of $3.00 per share. The Company valued these warrants at $35,900 using the Black Scholes Option Pricing
Model and the following assumptions: weighted average market price per share: $0.89; exercise price per share: $3.00; risk-free interest rate:
0.42%; contractual term: 3.0 years; volatility: 78.04%; expected dividend rate: 0%. The fair value of the warrants was charged to interest
expense.
In February 2013, the Company modified certain outstanding warrants to purchase an aggregate of 1,706,709 restricted shares of the Company’s
common stock at exercise prices in excess of $1.50 per share to reduce the exercise price to $1.50 per share. The Company determined that the
increase in the fair value of the warrants exercised was $67,500, which is reflected in general and administrative expense in the accompanying
Consolidated Statements of Operations and Comprehensive Loss for the year ended March 31, 2013. The warrants subject to the exercise price
modification were valued using the Black-Scholes Option Pricing Model and the following assumptions:
Assumption:
Market price per share (weighted average)
Exercise price per share (weighted average)
Risk-free interest rate (weighted average)
Expected term in years (weighted average)
Volatility (weighted average)
Dividend rate
Weighted Average Fair Value per share
$
$
$
-96-
Pre-modification
Post-modification
0.60
1.50
0.21%
1.38
80.8%
0.0%
0.60 $
2.51 $
0.21%
1.38
80.8%
0.0%
0.03 $
0.07
Table of Contents
Other Warrant Modifications
In December 2011, the Company entered into a consulting agreement with a strategic consultant for general and capital markets advisory
services. As consideration for the services to be provided under this agreement, the Company modified the term and exercise price of certain
previously-issued warrants to purchase an aggregate of 384,184 restricted shares of its common stock. The Company determined that the
increase in the fair value of the modified warrants was $397,500, which is reflected in general and administrative expense for the fiscal year
ended March 31, 2012 in the accompanying Consolidated Statements of Operations and Comprehensive Loss. The warrants modified were
valued using the Black-Scholes Option Pricing Model and using the following assumptions:
Assumption:
Market price per share
Exercise price per share
Risk-free interest rate
Expected term in years
Volatility
Dividend rate
Post-modification
Pre-modification
$
2.99
2.99
$
2.25 - $3.00
1.125 - $1.50
$
$
0.02% - 0.29 %
0.53 – 2.39
69.4% – 81.0 %
0.0 %
0.29 %
2.39
81.0 %
0.0 %
Weighted Average Fair Value per share
$
1.00
$
2.03
In December 2011, the Company also entered into a consulting agreement with an individual for strategic consulting services. As consideration
for the services to be provided under this agreement, the Company modified the term and exercise price of certain previously-issued warrants to
purchase an aggregate of 23,138 restricted shares of its common stock and will pay the consultant $1,000 per month for the period June 2012
through December 2012. The Company determined that the increase in the fair value of the modified warrants was $13,100, which is reflected
in general and administrative expense for the fiscal year ended March 31, 2012 in the accompanying Consolidated Statements of Operations and
Comprehensive Loss. The warrants modified were valued using the Black-Scholes Option Pricing Model and using the following assumptions:
Assumption:
Market price per share
Exercise price per share
Risk-free interest rate
Expected term in years
Volatility
Dividend rate
Post-modification
Pre-modification
$3.05
$
3.05
$
1.75 - $2.50
$0.88 - $1.25
$
$
0.25% - 0.29 %
2.00 – 2.36
74.8% – 78.3 %
0.0 %
0.29 %
2.36
78.3 %
0.0 %
Weighted Average Fair Value per share
$
1.69
$
2.25
Warrants Outstanding
The following table summarizes outstanding warrants to purchase restricted shares of the Company’s common stock as of March 31, 2013 and
2012. The weighted average exercise price of outstanding warrants at March 31, 2013 and 2012 was $1.26 and $2.16 per share, respectively.
Exercise
Price
$0.64
$0.88
$1.00
$1.125
$1.25
$1.50
$1.75
$2.00
$2.50
$2.625
$2.75
$3.00
$6.00
Expiration
Date
3/3/2023
5/11/2014
9/15/2017 to 9/30/2017
12/28/2012
5/11/2014 to 12/31/2014
12/31/2012 to 3/14/2018
12/31/2013
8/3/2013 to 9/15/2017
5/11/2014
12/31/2013
2/28/2017
5/11/2015 to 2/13/2016
6/28/2012 to 12/31/2013
-97-
Shares Subject to Purchase
March 31,
2013
March 31,
2012
3,000,000
15,428
3,053,573
-
120,280
7,460,816
349,235
425,000
42,443
68,560
-
125,000
-
14,660,335
-
314,328
1,500
97,679
120,280
375,000
643,184
609,000
617,394
588,200
272,724
430,000
57,300
4,126,589
Table of Contents
Reserved Shares
At March 31, 2013, the Company has reserved shares of its common stock for future issuance as follows:
Upon exchange of all shares of Series A Preferred Stock currently issued and outstanding (1)
15,000,000
Warrant shares issuable to Platinum upon exercise of common stock warrant upon exchange of Series A preferred stock
under the terms of the October 11, 2012 Note Purchase and Exchange Agreement
110% of shares issuable upon conversion of 10% convertible Exchange Note and Investment Notes issued to Platinum in
October 2012, February 2013 and March 2013, including interest accrued through maturity (2)
Pursuant to warrants to purchase common stock:
Subject to outstanding warrants
Issuable pursuant to accrued interest through maturity on outstanding promissory notes
issued to Morrison & Foerster, Cato Research Ltd., and University Health Network
Pursuant to stock incentive plans:
Subject to outstanding options under the 2008 and 1999 Stock Incentive Plans
Available for future grants
Upon sales of additional Units pursuant to the 2012 Private Placement of Units
Total
7,500,000
9,747,422
14,660,335
1,196,427
15,856,762
4,912,604
257,867
5,170,471
15,414,583
68,689,238
(1) assumes exchange under the terms of the October 11, 2012 Note Exchange and Purchase Agreement with Platinum
(2) assumes conversion under the terms of the October 11, 2012 Note Exchange and Purchase Agreement with Platinum and the terms of the
individual notes
10. Research and Development Expenses
The Company recorded research and development expenses of approximately $3.4 million and $5.4 million in the fiscal years ended March 31,
2013 and 2012, respectively. Research and development expense is composed primarily of employee compensation expenses, including stock–
based compensation, and direct project expenses, including costs incurred by third-party research collaborators, some of which may be
reimbursed under the terms of grant or collaboration agreements.
11. Income Taxes
The provision for income taxes for the periods presented in the consolidated statements of operations represents minimum California franchise
taxes. Income tax expense differed from the amounts computed by applying the U.S. federal income tax rate of 34% to pretax losses as a result
of the following:
Computed expected tax benefit
Losses not benefitted
Other
Income tax expense
-98-
Fiscal Years Ended March 31,
2013
2012
(34.0)%
34.0%
0.1%
0.1%
(34.0)%
34.0%
0.1%
0.1%
Table of Contents
Deferred income taxes reflect the net tax effect of temporary differences between the carrying amounts of assets and liabilities for financial
reporting purposes and the amounts used for income tax purposes. Significant components of the Company’s deferred tax assets are as follows
(in thousands):
Deferred tax assets:
Net operating loss carryovers
Basis differences in fixed assets
Accruals and reserves
Total deferred tax assets
Valuation allowance
Net deferred tax assets
2013
2012
March 31,
$
$
19,010
9
8
19,027
(19,027
)
-
$
$
16,191
13
9
16,213
(16,213
)
-
Realization of deferred tax assets is dependent upon future earnings, if any, the timing and amount of which are uncertain. Accordingly, the
deferred tax assets have been fully offset by a valuation allowance. The valuation allowance increased by $2,814,000 and $2,991,000 during the
fiscal years ended March 31, 2013 and 2012, respectively. When realized, deferred tax assets related to employee stock options will be credited
to additional paid-in capital.
As of March 31, 2013, the Company had U.S. federal net operating loss carryforwards of $47.9 million, which will expire in fiscal years 2019
through 2033. As of March 31, 2013, the Company had state net operating loss carryforwards of $34.8 million, which will expire in fiscal
years 2013 through 2033.
U.S. federal and state tax laws include substantial restrictions on the utilization of net operating loss carryforwards in the event of an ownership
change of a corporation. The Company has not performed a change in ownership analysis since its inception in 1998 and accordingly some or all
of its net operating loss carryforwards may not be available to offset future taxable income, if any. Even if the loss carryforwards are available
they may be subject to substantial annual limitations resulting from past ownership changes, and ownership changes occurring after March 31,
2013, that could result in the expiration of the loss carryforwards before they are utilized.
The Company files income tax returns in the U.S. federal and Canadian jurisdictions and California and Maryland state jurisdictions. The
Company is subject to U.S. federal and state income tax examinations by tax authorities for tax years 1999 through 2013 due to net operating
losses that are being carried forward for tax purposes.
The Company does not have any uncertain tax positions or unrecognized tax benefits at March 31, 2013 and 2012. The Company’s policy is to
recognize interest and penalties related to income taxes as components of interest expense and other expense, respectively.
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12. Licensing and Collaborative Agreements
University Health Network
On September 17, 2007, the Company and UHN entered into a Sponsored Research Collaboration Agreement (“ SRCA”) to develop certain stem
cell technologies for drug discovery and drug rescue technologies. The SRCA was amended on April 19, 2010 to extend the term to five years
and give the Company various options to extend the term for an additional three years. On December 15, 2010, the Company and UHN entered
into a second amendment to expand the scope of work to include induced pluripotent stem cell technology and to further expand the scope of
research and term extension options. On April 25, 2011, the Company and UHN amended the SRCA a third time to expand the scope to include
therapeutic and stem cell therapy applications of induced pluripotent cells and to extend the date during which the Company elected to fund
additional projects through April 30, 2012. On October 24, 2011, the Company and UHN amended the SRCA a fourth time to identify five key
programs that will further support the Company’s core drug rescue initiatives and potential cell therapy applications. Under the terms of the
fourth amendment, the Company committed to making monthly payments of $50,000 per month from October 2011 through September 2012 to
fund these programs. As disclosed in Note 8, Convertible Notes and Other Notes Payable, in October 2012, the Company issued to UHN a
promissory note in the principal amount of $549,500 and a warrant to purchase 549,500 restricted shares of the Company’s common stock as
payment in full for services rendered under the fourth amendment. Additionally, the Company and UHN entered into Amendment No. 5 to the
SRCA establishing the sponsored research projects and the sponsored research budgets under the SRCA from October 1, 2012 to September 30,
2013, as well as a schedule of the Company’s sponsored research payments for such period totaling $309,000, including payments aggregating
$150,000 applicable to services for the period from October 1, 2012 through March 31, 2013.
Concurrent with the execution of the fourth amendment to the SRCA, the Company and UHN entered into a License Agreement under the terms
of which UHN granted the Company exclusive rights to the use of a novel molecule that can be employed in the identification and isolation of
mature and immature human cardiomyocytes from pluripotent stem cells, as well as methods for the production of cardiomyocytes from
pluripotent stem cells that express this marker. In consideration for the grant of the license, the Company has agreed to make payments to UHN
totaling $3.9 million, if, and when, it achieves certain commercial milestones set forth in the License Agreement, and to pay UHN royalties based
on the receipt of revenue, if any, by the Company attributable to the licensed patents.
In March 2012, the Company and UHN entered into License Agreement No. 2 under the terms of which UHN granted the Company exclusive
rights to the use of technology included in a new U.S. patent application to develop hematopoietic precursor stem cells from human pluripotent
stem cells. Hematopoietic precursor stem cells give rise to all red and white blood cells and platelets in the body. The Company plans to use the
UHN invention to improve the cell culture methods utilized to efficiently produce hematopoietic stem cell populations. In consideration for the
grant of the license, the Company issued to UHN 55,555 restricted shares of its common stock, valued at $155,000 in March 2012 and was
obligated to make a cash payment of $25,000 in July 2012. Under the terms of License Agreement No. 2, the Company has also agreed to make
payments to UHN totaling $3.9 million, if, and when, it achieves certain milestones designated in License Agreement No. 2, and to pay UHN
royalties based on the receipt of revenue, if any, by the Company attributable to the licensed patents.
U.S. National Institutes of Health
From 1998 through 2008, the U.S. National Institutes of Health ("NIH") awarded VistaGen California a total of $11.3 million in non-dilutive
research and development grants, including $2.3 million to support research and development of its stem cell technology-based Human Clinical
Trials in a Test Tube™ platform and, as described below, a total of $8.8 million for nonclinical and Phase 1 clinical development of AV-101
(also referred to in scientific literature as “4-Cl-KYN”). AV-101, the Company’s small molecule drug candidate, has successfully completed
Phase 1 clinical development.
During fiscal years 2006 through 2008, the NIH awarded VistaGen California a $4.2 million grant to support preclinical development of AV-101
for treatment of neuropathic pain and other neurodegenerative diseases such as Huntington’s and Parkinson’s diseases. In April 2009, the NIH
awarded VistaGen California a $4.2 million grant to support the Phase I clinical development of AV-101, which amount was subsequently
increased to a total of $4.6 million in July 2010. The Company recognized $0.2 million and $1.2 million of grant revenue related to AV-101 in
the fiscal years ended March 31, 2013 and 2012, respectively.
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Table of Contents
Cato Research Ltd.
The Company has built a strategic development relationship with Cato Research Ltd. (“ CRL”), a global contract research and development
organization, or CRO, and an affiliate of one of the Company’s largest stockholders. See Note 14, Related Party Transactions . CRL has
provided the Company with access to essential CRO services supporting its nonclinical and Phase 1 clinical development programs. The
Company recorded research and development expenses of $703,800 and $1,461,300 in the fiscal years ended March 31, 2013 and 2012,
respectively, for services provided by CRL. As disclosed in Note 8, Convertible Notes and Other Notes Payable, in October 2012, the Company
issued to CRL a promissory note in the initial principal amount of $1,009,000, which is payable solely in restricted shares of the Company’s
common stock as payment in full for all contract research and development services and regulatory advice rendered by CRL to the Company
and its affiliates through December 31, 2012 with respect to the preclinical and clinical development of AV-101, and a five-year warrant to
purchase 1,009,000 restricted shares of the Company’s common stock.
13. Stock Option Plans and 401(k) Plan
The Company has the following share-based compensation plans.
2008 Stock Incentive Plan
The Company’s 2008 Stock Incentive Plan (the “2008 Plan”) was adopted by the shareholders of VistaGen California on December 19, 2008
and assumed by the Company in connection with the Merger. The maximum number of shares of the Company’s common stock that may be
granted pursuant to the 2008 Plan is 5,000,000 shares. The maximum number of shares that may be granted under the 2008 Plan is subject to
adjustments for stock splits, stock dividends or other similar changes in the common stock or capital structure.
1999 Stock Incentive Plan
The Company’s 1999 Stock Incentive Plan (the “1999 Plan”) was adopted by the shareholders of VistaGen California on December 6, 1999 and
assumed by the Company in connection with the Merger. The Company initially reserved 900,000 shares for the issuance of awards under the
1999 Plan. The 1999 Plan has terminated under its own terms and, as a result, no awards may currently be granted under the 1999 Plan.
However, the unexpired options and awards that have already been granted pursuant to the 1999 Plan remain operative.
Scientific Advisory Board 1998 Stock Incentive Plan
The Company’s Scientific Advisory Board 1998 Stock Incentive Plan (the “ SAB Plan”) was adopted by VistaGen California’s Board of
Directors in July 1998. The VistaGen California Board of Directors authorized 25,000 shares of common stock for awards from the
SAB Plan. No awards have been granted from the SAB Plan since August 2001. The SAB Plan expired in July 2008 and all of the options
granted from the SAB Plan have either been exercised or expired during fiscal 2012.
Description of the 2008 Plan
Under the terms of the 2008 Plan, the Compensation Committee of the Company’s Board of Directors may grant shares, options or similar rights
having either a fixed or variable price related to the fair market value of the shares and with an exercise or conversion privilege related to the
passage of time, the occurrence of one or more events, or the satisfaction of performance criteria or other conditions, or any other security with
the value derived from the value of the shares. Such awards include stock options, restricted stock, restricted stock units, stock appreciation
rights and dividend equivalent rights.
The Compensation Committee may grant nonstatutory stock options under the 2008 Plan at a price of not less than 100% of the fair market
value of the Company’s common stock on the date the option is granted. Incentive stock options under the 2008 Plan may be granted at a price
of not less than 100% of the fair market value of the Company’s common stock on the date the option is granted. Incentive stock options
granted to employees who, on the date of grant, own stock representing more than 10% of the voting power of all of the Company’s classes of
stock are granted at an exercise price of not less than 110% of the fair market value of the Company’s common stock. The maximum term of
these incentive stock options granted to employees who own stock possessing more than 10% of the voting power of all classes of the
Company’s stock may not exceed five years. The maximum term of an incentive stock option granted to any other participant may not exceed
ten years. The Compensation Committee determines the term and exercise or purchase price of all other awards granted under the 2008 Plan.
The Compensation Committee also determines the terms and conditions of awards, including the vesting schedule and any forfeiture
provisions. Awards under the 2008 Plan may vest upon the passage of time or upon the attainment of certain performance criteria established
by the Compensation Committee.
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Table of Contents
Unless terminated sooner, the 2008 Plan will automatically terminate in 2017. The Board of Directors may at any time amend, suspend or
terminate the Company’s 2008 Plan.
During the first quarter of fiscal 2013, when the quoted market price of the Company’s common stock was $0.51, the Company granted options
to purchase an aggregate of 155,000 shares of its common stock at an exercise price of $0.51 per share to certain of its employees, excluding the
Company’s Chief Executive Officer and President and Chief Scientific Officer, and to certain scientific consultants. Options granted during the
first quarter of fiscal 2013 have a contractual term of 10 years and vest over a period of 4 years. During the third quarter of fiscal 2013, when the
quoted market price of the Company’s common stock was $0.71 per share, the Company cancelled outstanding options to purchase an aggregate
of 870,550 shares of its common stock at exercise prices between $1.13 per share and $2.58 per share held by certain employees, excluding the
Company’s Chief Executive Officer and President and Chief Scientific Officer, and by certain consultants and granted those persons new
options to purchase an aggregate of 920,550 shares at an exercise price of $0.75 per share. Options granted during the third quarter of fiscal 2013
have a contractual term of 10 years and options to purchase 604,699 shares were granted as immediately vested, with the remaining option
shares vesting over a period of two years. The cancellation and reissuance was accounted for as a modification of the options. During fiscal
year 2012, the Company granted options to purchase an aggregate of 1,020,000 shares of its common stock at exercise prices ranging from $1.75
per share to $2.99 per share to certain of its employees and scientific and business consultants, including members of the Company's Board of
Directors and Scientific Advisory Board, and one of the Company’s officers exercised options to purchase 113,636 restricted shares of its
common stock at an exercise price of $0.88 per share. Including the impact of the modification of the option grants during fiscal 2013 described
above, the Company recorded share-based compensation costs related to 2008 Plan option grants of $438,800 for the fiscal year ended March
31, 2013 compared with $1,591,300 for the fiscal year ended March 31, 2012.
The following table summarizes share-based compensation expense, including share-based expense related to the March 2013 grant of warrants
to certain of the Company’s officers and to its independent directors as described in Note 9, Capital Stock, included in the accompanying
Consolidated Statement of Operations and Comprehensive Loss for the years ended March 31, 2013 and 2012.
Research and development expense:
related to stock option grants
related to warrant grants to officers and directors
General and administrative expense:
related to stock option grants
related to warrant grants to officers and directors
Total share-based compensation expense
Fiscal Years Ended
March 31,
2013
2012
$
$
$
242,300
267,500
509,800
477,400
-
477,400
196,600
534,900
731,500
1,241,300
$
1,113,900
-
1,113,900
1,591,300
The Company used the Black-Scholes option valuation model with the following assumptions to determine share-based compensation expense
related to option grants during the fiscal years ended March 31, 2013 and 2012:
Exercise price
Market price on date of grant
Risk-free interest rate
Expected term (years)
Volatility
Expected dividend yield
Fiscal Years Ended March 31,
2012
2013
$0.51 and $0.75
$0.51 and $0.71
0.895% to 1.74%
$
$
1.75 to $2.99
1.75 to $2.99
1.19% to 3.39%
6.25 to 10.0
82.9% to 85.4%
0%
6.25 to 10.0
78.9% to 91.3%
0%
Fair value per share at grant date
$
0.36 to $0.59 $
1.08 to $2.48
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Table of Contents
The expected term of options represents the period that the Company’s share-based compensation awards are expected to be outstanding. The
Company has calculated the weighted-average expected term of the options using the simplified method as prescribed by Securities and
Exchange Commission Staff Accounting Bulletins No. 107 and No. 110 (“SAB No. 107 and 110”). The utilization of SAB No. 107 and 110
was based on the lack of relevant historical data due to the Company’s limited historical experience as a publicly traded company as well as
the lack of liquidity resulting from the limited number of freely-tradable shares of its common stock. Limited historical experience and lack
of liquidity in its stock also resulted in the Company’s decision to utilize the historical volatilities of a peer group of public companies’ stock
over the expected term of the option in determining its expected volatility assumptions. The risk-free interest rate for periods related to the
expected life of the options is based on the U.S. Treasury yield curve in effect at the time of grant. The expected dividend yield is zero, as the
Company has not paid any dividends and does not anticipate paying dividends in the near future. The Company calculated the forfeiture rate
based on an analysis of historical data, as it reasonably approximates the currently anticipated rate of forfeitures for granted and outstanding
options that have not vested.
The following table summarizes activity for the fiscal years ended March 31, 2013 and 2012 under the Company’s stock option plans:
Fiscal Years Ended March 31,
Options outstanding at beginning of period
Options granted
Options exercised
Options cancelled
Options forfeited
Options expired
Options outstanding at end of period
Options exercisable at end of period
Weighted average grant-date fair value of
options granted during the period
2013
Weighted
Average
Exercise
Price
2012
Weighted
Average
Exercise
Price
Number of
Number of
Shares
4,805,771
1,075,550
-
$
$
$
(870,550) $
(29,167) $
(69,000) $
4,912,604
4,227,436
$
$
$
Shares
$
3,949,153
$
1,020,000
(113,979) $
$
(30,000) $
(19,403) $
-
4,805,771
3,740,135
$
$
$
1.53
0.72
-
1.72
1.75
1.34
1.32
1.35
0.52
1.42
1.88
0.88
-
1.75
0.80
1.53
1.45
1.36
The following table summarizes information on stock options outstanding and exercisable under the Company’s option plans as of March 31,
2013:
Exercise
Price
0.51 - $0.72
0.75
0.80 - $1.13
1.50
1.65 - $1.925
2.10 - $2.99
$
$
$
$
$
$
Number
Outstanding
267,540
920,550
455,776
2,413,250
695,833
159,655
4,912,604
Options Outstanding
Weighted
Average
Remaining
Years until
Expiration
Weighted
Average
Exercise
Price
7.05
9.58
3.83
6.68
5.99
5.08
6.83
$
$
$
$
$
$
$
Options Exercisable
Number
Exercisable
112,540
670,494
455,776
2,413,250
415,721
159,655
4,227,436
$
$
$
$
$
$
$
0.60
0.75
1.00
1.50
1.76
2.16
1.32
Weighted
Average
Exercise
Price
0.72
0.75
1.00
1.50
1.74
2.16
1.35
At March 31, 2013, there were 257,867 shares of the Company’s common stock remaining available for grant under the 2008 Plan. There were
no option exercises during the year ended March 31, 2013. The Company received cash proceeds of $102,200 as a result of options exercised
during the year ended March 31, 2012.
Aggregate intrinsic value is the sum of the amounts by which the fair value of the stock exceeded the exercise price (“ in-the-money-options”).
Based on the quoted market price of the Company’s common stock of $0.83 per share on March 31, 2013, the aggregate intrinsic value of
outstanding options at that date was $165,000, of which $87,300 related to exercisable options.
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As of March 31, 2013, there was approximately $743,000 of unrecognized compensation cost related to non-vested share-based compensation
awards from the 2008 Plan, which is expected to be recognized through May 2016.
Stock Grants from 2008 Plan
As discussed in Note 8, Convertible Promissory Notes and Other Notes Payable, in April and May 2011, the Company issued an aggregate of
139,600 restricted shares of its common stock from the 2008 Plan to Desjardins and McCarthy as partial compensation for services performed by
the two entities. At the date of issuance, the shares were valued at $1.75 per share and the Company recorded $244,300 in general and
administrative expense in connection with the issuances.
401(k) Plan
The Company, through a third-party agent, maintains a retirement and deferred savings plan for its employees. This plan is intended to qualify as
a tax-qualified plan under Section 401(k) of the Internal Revenue Code. The retirement and deferred savings plan provides that each participant
may contribute a portion of his or her pre-tax compensation, subject to statutory limits. Under the plan, each employee is fully vested in his or
her deferred salary contributions. Employee contributions are held and invested by the plan’s trustee. The retirement and deferred savings plan
also permits the Company to make discretionary contributions, subject to established limits and a vesting schedule. To date, the Company has
not made any discretionary contributions to the retirement and deferred savings plan on behalf of participating employees.
14. Related Party Transactions
Cato Holding Company (“CHC”), doing business as Cato BioVentures ("CBV"), the parent of CRL, is one of the Company’s largest institutional
stockholders at March 31, 2013, holding common stock and warrants to purchase common stock. Prior to the May 11, 2011 conversion of
certain of the Company’s outstanding promissory notes and the conversion of preferred stock into shares of common stock, CBV held various
promissory notes and a majority of the Company's Series B-1 Preferred Stock. Shawn Singh, the Company’s Chief Executive Officer and
member of its Board of Directors, served as Managing Principal of CBV and as an officer of CRL until August 2009. As described in Note 8,
Convertible Promissory Notes and Other Notes Payable, in April 2011, CBV loaned the Company $352,273 under the terms of the 2011 CHC
Note. On October 10, 2012, the Company and CHC cancelled the 2011 CHC Note and exchanged it for a new unsecured promissory note in the
principal amount of $310,443 (the “2012 CHC Note”) and a five-year warrant to purchase 250,000 restricted shares of the Company’s common
stock at a price of $1.50 per share (the “CHC Warrant ”). Additionally, on October 10, 2012, the Company issued to CRL: (i) an unsecured
promissory note in the initial principal amount of $1,009,000, which is payable solely in restricted shares of the Company’s common stock and
which accrues interest at the rate of 7.5% per annum, compounded monthly (the “CRL Note”), as payment in full for all contract research and
development services and regulatory advice rendered by CRL to the Company and its affiliates through December 31, 2012 with respect to the
preclinical and clinical development of AV-101, and (ii) a five-year warrant to purchase, at a price of $1.00 per share, 1,009,000 restricted shares
of the Company’s common stock.
During fiscal year 2007, the Company entered into a contract research organization arrangement with CRL related to the development of AV-
101, under which the Company incurred expenses of $703,800 and $1,461,300 for the fiscal years ended March 31, 2013 and 2012, respectively,
a substantial portion of which were reimbursed under the NIH grant. Total interest expense on notes payable to CHC and CRL was $101,700
and $93,100 for the fiscal years ended March 31, 2013 and 2012, respectively, with the majority of amounts reported for periods prior to May
2011 having been converted to equity. On April 29, 2011, the Company issued 157,143 restricted shares of common stock, valued at $1.75 per
share, as prepayment for research and development services to be performed by CRL during 2011. As described in Note 9, Capital Stock, in
December 2011, the Company entered into an Agreement Regarding Payment of Invoices and Warrant Exercises with CHC, CRL and the CHC
affiliates pursuant to which CHC and the CHC Affiliates exercised warrants at discounted exercise prices to purchase an aggregate of 492,541
restricted shares of the Company’s common stock and the Company received $60,200 cash, and, in lieu of cash payment for certain of the
warrant exercises, settled outstanding liabilities of $245,300 for past services received from CRL and prepaid $226,400 for future services to be
received from CRL, which services had been fully received by March 31, 2012.
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Prior to his April 2003 appointment as one of the Company’s officers (on a part-time basis) and as a director, the Company retained Mr. Singh as
a consultant to provide legal and other consulting services. During the course of the consultancy, as payment for his services, the Company
issued him warrants to purchase 55,898 restricted shares of common stock at $0.80 per share and a 7% promissory note in the principal amount
of $26,400. On May 11, 2011, and concurrent with the Merger, the Company paid the outstanding balance of principal and accrued interest
totaling $36,000 (see Note 8, Convertible Promissory Notes and Other Notes Payable). Upon the approval by the Board of Directors, in
December 2006, VistaGen California accepted a full-recourse promissory note in the amount of $103,400 from Mr. Singh in payment of the
exercise price for options and warrants to purchase an aggregate of 126,389 restricted shares of the Company’s common stock. The note accrued
interest at a rate of 4.90% per annum and was due and payable no later than the earlier of (i) December 1, 2016 or (ii) ten days prior to the
Company becoming subject to the requirements of the Securities Exchange Act of 1934, as amended (“Exchange Act”). On May 11, 2011, in
connection with the Merger, the $128,200 outstanding balance of the principal and accrued interest on this note was cancelled in accordance
with Mr. Singh's employment agreement and recorded as additional compensation. In accordance with his employment agreement, Mr. Singh is
also entitled to an income tax gross-up on the compensation related to the note cancellation. At March 31, 2012 and 2013, the Company had
accrued $101,900 as an estimate of the gross-up amount, but had not yet paid that amount to Mr. Singh.
In March 2007, VistaGen California accepted a full recourse promissory note in the amount of $46,400 from A. Franklin Rice, its former Chief
Financial Officer and a former director of the Company in exchange for his exercise of options to purchase 52,681 restricted shares of the
Company’s common stock. The note accrued interest at a rate of 4.90% per annum and was due and payable no later than the earlier of
(i) March 1, 2017 or (ii) ten days prior to the Company becoming subject to the requirements of the Exchange Act. On May 11, 2011, in
connection with the Merger, the $57,000 outstanding balance of principal and accrued interest on this note was cancelled in accordance with Mr.
Rice's employment agreement and recorded as additional compensation. In accordance with his employment agreement, Mr. Rice is entitled to
an income tax gross-up on the compensation related to the note cancellation. At March 31, 2012 and 2013, the Company had accrued $33,900
as an estimate of the gross-up amount, but had not paid it to Mr. Rice.
Prior to the Merger, VistaGen California engaged Jon A. Saxe, a current director, separately from his duties as a director, as a management
consultant from July 1, 2000 through June 30, 2010 to provide strategic and other business advisory services. As payment for consulting services
rendered through June 30, 2010, Mr. Saxe has been issued warrants and non-qualified options to purchase an aggregate of 250,815 restricted
shares of the Company’s common stock, of which he has exercised warrants to purchase 18,568 restricted shares. Additionally, Mr. Saxe was
issued a 7% promissory note in the amount of $8,000. On May 11, 2011, the $14,400 balance of the note and related accrued interest plus a note
cancellation premium of $5,100 was converted to 11,142 restricted shares of the Company’s common stock and a three-year warrant to purchase
2,784 restricted shares of common stock at an exercise price of $2.50 per share. In lieu of payment from the Company, in December 2011, Mr.
Saxe exercised the warrant as a part of the Discounted Warrant Exercise Program at an exercise price of $1.25 per share in satisfaction of
amounts owed to him in conjunction with his service as a member of the Board of Directors.
15. Commitments, Contingencies, Guarantees and Indemnifications
From time to time, the Company may become involved in claims and other legal matters arising in the ordinary course of business. Management
is not currently aware of any matters that will have a material adverse effect on the Company’s consolidated financial position, results of
operations or its cash flows.
The Company indemnifies its officers and directors for certain events or occurrences while the officer or director is or was serving at the
Company’s request in such capacity. The term of the indemnification period is for the officer’s or director’s lifetime. The Company will
indemnify the officers or directors against any and all expenses incurred by the officers or directors because of their status as one of the
Company’s directors or executive officers to the fullest extent permitted by California law. The Company has never incurred costs to defend
lawsuits or settle claims related to these indemnification agreements. The Company has a director and officer insurance policy which limits the
Company's exposure and may enable it to recover a portion of any future amounts paid. The Company believes the fair value of these
indemnification agreements is minimal. Accordingly, there are no liabilities recorded for these agreements at March 31, 2013 or 2012.
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In the normal course of business, the Company provides indemnifications of varying scopes under agreements with other companies, typically
clinical research organizations, investigators, clinical sites, suppliers and others. Pursuant to these agreements, the Company generally
indemnifies, holds harmless, and agrees to reimburse the indemnified parties for losses suffered or incurred by the indemnified parties in
connection with the use or testing of the Company's product candidates or with any U.S. patents or any copyright or other intellectual property
infringement claims by any third party with respect to the Company's product candidates. The terms of these indemnification agreements are
generally perpetual. The potential future payments the Company could be required to make under these indemnification agreements is
unlimited. The Company maintains liability insurance coverage that limits its exposure. The Company believes the fair value of these
indemnification agreements is minimal. Accordingly, the Company has not recorded any liabilities for these agreements as of March 31, 2013
or 2012.
Leases
As of March 31, 2013 and 2012, the following assets are under capital lease obligations and included in property and equipment:
Leased laboratory and computer equipment
Accumulated amortization
March 31,
)
2013
$
$
133,200
(114,900
18,300
2012
$
$
139,700
(119,200
20,500
)
Amortization expense for assets recorded under capital leases is included in depreciation expense. Future minimum payments, by year and in
the aggregate, required under capital leases are as follows:
Fiscal Years Ending March 31,
2014
2015
2016
2017
2018
Future minimum lease payments
Less imputed interest included in minimum lease payments
Present value of minimum lease payments
Less current portion
Non-current capital lease obligation
Equipment
Capital Leases
$
$
8,600
4,300
1,200
1,200
100
15,400
(1,700
13,700
(7,600
6,100
)
)
At March 31, 2013, future minimum payments under operating leases relate to the Company’s facility lease in South San Francisco, California
through June 30, 2013 and total $45,000 for the fiscal year ended March 31, 2014. See Note 16, Subsequent Events. Total facility rent expense
incurred by the Company for the fiscal years ended March 31, 2013 and 2012 was $179,000 and $166,000, respectively.
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Long-Term Debt Repayment
At March 31, 2013, future minimum principal payments related to long-term debt were as follows:
Fiscal Years Ending March 31,
2014
2015
2016
2017
2018
Thereafter through October 2023
16. Subsequent Events
$
Amount
684,200
609,800
541,700
185,800
18,000
71,600
$
2,111,100
The Company has evaluated subsequent events through July 12, 2013 and has identified the following material events and transactions that
occurred after March 31, 2013.
Autilion AG Securities Purchase Agreement
On April 8, 2013, the Company entered into a Securities Purchase Agreement (the “ Purchase Agreement”) with Autilion AG, a company
organized and existing under the laws of Switzerland (“Autilion”). On April 12, 2013, Autilion assigned the Purchase Agreement to its affiliate,
Bergamo Acquisition Corp. PTE LTD, a corporation organized and existing under the laws of Singapore (“ Bergamo Singapore”). On April 30,
2013, the Company and Bergamo Singapore amended the Purchase Agreement (“ Amendment No. 1”) to modify the investment dates. On June
27, 2013, the Company, Autilion and Bergamo Singapore further amended the Agreement to vacate Autilion’s April 2013 assignment of the
Purchase Agreement to Bergamo Singapore, provide for an initial closing under the Purchase Agreement, and amend certain of the investment
dates under the Purchase Agreement (“Amendment No. 2”, and together with the Agreement and Amendment No. 1, the “Amended
Agreement”). Under the terms of the Amended Agreement, Autilion is contractually obligated to purchase an aggregate of 72.0 million
restricted shares of the Company’s common stock at a purchase price of $0.50 per share for aggregate cash consideration of $36.0 million, in a
series of tranches between June 27, 2013 and September 30, 2013 (cumulatively, the “Autilion Financing”). The Amended Agreement also
provides for the election to the Company’s Board of Directors of a designee of Autilion upon completion of the Autilion Financing. The
Company has completed a nominal initial closing of the Autilion Financing.
The Company and Autilion also entered into a Voting Agreement, pursuant to which Autilion has agreed to vote all shares of capital stock of the
Company held by Autilion consistent with the recommendation of a majority of the members of the Company’s Board of Directors. In addition,
in the event of a Change in Control of the Company, as defined in the Voting Agreement, or an extraordinary transaction outside of the ordinary
course of the Company’s business, in each case approved by a majority of the Company’s Board of Directors, including Autilion's designee, as
well as by the holders of a majority of the outstanding shares of Common Stock held by stockholders unaffiliated with Autilion (an “Approved
Transaction”), Autilion is required to vote all shares of capital stock of the Company held by it for such Approved Transaction.
Modification of Warrants held by Platinum
Effective on May 24, 2013, the Company and Platinum entered into an Amendment and Waiver pursuant to which the Company agreed to
reduce the exercise price of the Exchange Warrant and the Investment Warrants issued to Platinum in October 2012 and February 2013 and
March 2013 (collectively, the “Warrants”) from $1.50 per share to $0.50 per share in consideration for Platinum’s agreement to waive its rights
for any increase in the number of shares of common stock issuable under the adjustment provisions of the Exchange Warrant and the Investment
Warrants that would otherwise occur from (i) the Company’s sale of shares of its common stock at a price of $0.50 per share in connection with
the Bergamo Financing; (ii) the March 2013 grant of warrants to certain of the Company’s officers and independent directors to purchase an
aggregate of 3.0 million restricted shares of common stock at an exercise price of $0.64 per share; and (iii) the Company’s issuance of restricted
shares of its common stock resulting in gross proceeds not to exceed $1.5 million in connection with the exercise by warrant holders, by no later
than June 30, 2013, of previously outstanding warrants for which the Company may reduce the exercise price to not less than $0.50 per share.
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Facility Lease
On April 24, 2013, the Company entered into a four-year facility lease for approximately 10,900 square feet of laboratory and headquarters
office space in South San Francisco, California beginning July 1, 2013. Future minimum payments under the lease are as follows:
Fiscal Years Ending March 31,
2014
2015
2016
2017
2018
Warrant Modifications
Amount
$
$
$
$
$
121,100
252,000
265,100
278,200
70,400
During June and July 2013, the Company offered certain warrant holders the opportunity to exercise their warrants to purchase restricted
shares of the Company’s common stock at an exercise price reduced from $1.50 per share to $0.50 per share. Through the date of this report,
warrant holders exercised warrants to purchase an aggregate of 399,106 restricted shares of the Company’s common stock and the Company
received cash proceeds of $191,200 and settled accounts payable for professional services in the amount of $8,300 in lieu of cash payment by
the Company.
17. Supplemental Financial Information
Quarterly Results of Operations (Unaudited)
The following table presents the unaudited statements of operations data for each of the eight quarters in the period ended March 31, 2013. This
information represents the activity of VistaGen California for the pre-Merger portion of the first quarter of fiscal 2012 and the consolidated
activity of VistaGen California and the Company from May 11, 2011 (the date of the Merger) through March 31, 2013. A total of 1,569,000
shares of common stock, representing the 784,500 shares held by stockholders of Excaliber immediately prior to the Merger and effected for the
post-Merger two-for-one (2:1) stock split described in Note 1, Description of Business, have been retroactively reflected as outstanding for the
entire fiscal year ended March 31, 2012 for purposes of determining basic and diluted loss per common share below.
The information has been presented on the same basis as the audited financial statements and all necessary adjustments, consisting only of
normal recurring adjustments, have been included in the amounts below to present fairly the unaudited quarterly results when read in
conjunction with the audited financial statements and related notes. The operating results for any quarter should not be relied upon as necessarily
indicative of results for any future period.
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Unaudited Quarterly Results of Operations
(in thousands, except share and per share amounts)
Three Months Ended
September
30,
2012
December
31,
2012
June 30,
2012
March 31,
2013
Total Fiscal
Year
2013
Revenues:
Grant revenue
Total revenues
Operating expenses:
Research and development
General and administrative
Total operating expenses
Loss from operations
Other expenses, net:
Interest expense, net
Change in put and note extension option and warrant
liabilities
Loss on early extinguishment of debt
Other income
Loss before income taxes
Income taxes
Net loss
Deemed dividend on Series A Preferred Stock
Net loss attributable to common stockholders
Basic and diluted net loss per common share
Weighted average shares used in computing basic and
diluted net loss per common share
$
$
200
200
$
—
—
$
—
—
$
—
—
866
1,055
1,921
(1,721)
1,106
576
1,682
(1,682)
1,120
799
1,919
(1,919)
339
1,132
1,471
(1,471)
200
200
3,431
3,562
6,993
(6,793)
(103)
(274)
(235)
(309)
(921)
—
—
—
(1,824)
(2)
(1,826)
-
(1,826) $
(0.11) $
—
—
—
(1,956)
—
(1,956)
(1,956) $
(0.11) $
358
(3,537)
-
(5,333)
(2)
(5,335)
(10,193)
(15,528) $
(0.85) $
(1,994)
(31)
35
(3,770)
—
(3,770)
(3,770) $
(0.19) $
(1,636)
(3,568)
35
(12,883)
(4)
(12,887)
(10,193)
(23,080)
(1.27)
$
$
16,842,655
17,094,833
18,292,301
20,236,491
18,108,444
Note: reflects adjustment to amount of deemed dividend on Series A Preferred Stock in the quarter ended December 31, 2012.
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Three Months Ended
September
30,
2011
December
31,
2011
June 30,
2011
March 31,
2012
Total Fiscal
Year
2012
Revenues:
Grant revenue
Total revenues
Operating expenses:
Research and development
General and administrative
Total operating expenses
Loss from operations
Other expenses, net:
Interest expense, net
Change in put and note extension option and warrant
liabilities
Loss on early extinguishment of debt
Loss before income taxes
Income taxes
Net loss
Basic and diluted net loss per common share
Weighted average shares used in computing basic and
diluted net loss per common share
$
$
555
555
$
316
316
$
2
2
$
469
469
1,028
1,127
2,155
(1,600)
(1,227)
894
2,121
(1,805)
1,306
1,548
2,854
(2,852)
1,828
1,428
3,256
(2,787)
1,342
1,342
5,389
4,997
10,386
(9,044)
(731)
(451)
(455)
(256)
(1,893)
(78)
-
(2,409)
(2)
(2,411) $
$
-0.22
—
—
(2,256)
—
(2,256) $
$
-0.15
—
(1,193)
(4,500)
—
(4,500) $
$
-0.28
—
—
(3,043)
—
(3,043) $
$
-0.18
(78)
(1,193)
(12,208)
(2)
(12,210)
-0.83
$
$
11,105,854
15,241,904
16,035,861
16,542,717
14,736,651
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Item 9. Changes in and Disagreements With Accountants on Accounting and Financial Disclosure
On May 13, 2011, in connection with the Merger, we dismissed Weaver & Martin, LLC (“WM”) as Excaliber’s independent registered public
accounting firm. The Company’s Board of directors approved the dismissal of WM.
The reports of WM on the financial statements of Excaliber as of and for the fiscal years ended December 31, 2009 and 2010 contained no
adverse opinion or disclaimer of opinion and were not qualified or modified as to uncertainty, audit scope or accounting principle.
During Excaliber’s fiscal years ended December 31, 2009 and 2010 and through May 13, 2011, (i) there were no disagreements with WM on any
matter of accounting principles or practices, financial statement disclosure, or auditing scope or procedure, which disagreements, if not resolved
to WM satisfaction, would have caused WM to make reference to the subject matter of such disagreements in its reports on Excaliber’s
consolidated financial statements for such years, and (ii) there were no reportable events as defined in Item 304(a)(1)(v) of Regulation S-K.
The Company provided WM with a copy of the above disclosures prior to its filing with the Securities and Exchange Commission (“SEC”) of the
Current Report on Form 8-K describing the Merger on May 16, 2011 and requested WM to furnish the Company with a letter addressed to the
SEC stating whether WM agrees with the above statements and, if not, stating the respects in which it does not agree. A copy of WM’s letter
dated May 13, 2011 is attached as Exhibit 16.1 to the Company’s Current Report on Form 8-K filed on May 16, 2011 and is incorporated herein
by reference.
Based on the Board of Directors’ approval, we engaged OUM & Co. LLP (“OUM”) on May 13, 2011, as our independent registered public
accounting firm for the fiscal year ending March 31, 2012. During Excaliber’s two most recent fiscal years ended December 31, 2009 and 2010
and through May 13, 2011, neither Excaliber nor anyone on its behalf consulted OUM regarding either (i) the application of accounting
principles to a specified transaction, either completed or proposed, or the type of audit opinion that might be rendered on Excaliber’s financial
statements, and no written report or oral advice was provided to Excaliber that OUM concluded was an important factor considered by Excaliber
in reaching a decision as to the accounting, auditing or financial reporting issue; or (ii) any matter that was the subject of a disagreement or
reportable event as defined in Item 304(a)(1)(iv) and Item 304(a)(1)(v), respectively, of Regulation S-K.
OUM was VistaGen California’s auditor prior to the Merger. As such, OUM audited VistaGen California’s financial statements as of March 31,
2010 and 2009, and for the four years in the period ended March 31, 2011, and for the period from May 26, 1998 (inception) through March 31,
2011, which are included in the Company’s Current Report on Form 8-K filed on May 16, 2011, and as subsequently amended, and provided
advice to VistaGen with respect to accounting, auditing, and financial reporting issues related to the Merger.
Item 9A. Controls and Procedures
Evaluation of Disclosure Controls and Procedures
Based on their evaluation as of the end of the period covered by this report, our Chief Executive Officer and Chief Financial Officer have
concluded that our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) were effective as of
the end of the period covered by this report to ensure that information that we are required to disclose in reports that management files or
submits under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in SEC rules and forms.
Our disclosure controls and procedures are designed to provide reasonable assurance of achieving their objectives, and our chief executive
officer and acting chief financial officer have concluded that these controls and procedures are effective at the “reasonable assurance” level. We
believe that a control system, no matter how well designed and operated, cannot provide absolute assurance that the objectives of the control
system are met, and no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, within a
company have been detected.
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Management’s Annual Report on Internal Control Over Financial Reporting
Our management is responsible for establishing and maintaining adequate internal control over financial reporting. A company’s internal control
over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation
of financial statements for external purposes in accordance with U.S. GAAP.
There are inherent limitations in the effectiveness of any system of internal control, including the possibility of human error and the
circumvention or overriding of controls. Accordingly, even effective internal controls can provide only reasonable assurances with respect to
financial statement preparation. Further, because of changes in conditions, the effectiveness of internal control may vary over time.
Our management assessed the effectiveness of our internal control over financial reporting as of March 31, 2013. In making this assessment,
management used the criteria set forth by the Committee of Sponsoring Organizations (COSO) of the Treadway Commission in Internal Control
—Integrated Framework. Based on its assessment using the COSO criteria, management concluded that our internal control over financial
reporting was effective as of March 31, 2013.
As a result of the enactment of the Dodd-Frank Wall Street Reform and Consumer Protection Act of 2010, and the resulting amendment of
Section 404 of the Sarbanes-Oxley Act of 2002, as a non-accelerated filer, we are not required to provide an attestation report by our
independent registered public accounting firm regarding internal control over financial reporting for the fiscal year ended March 31, 2013 or
thereafter, until such time as we are no longer eligible for the exemption for smaller issuers set forth within the Sarbanes-Oxley Act.
Changes in Internal Control Over Financial Reporting
There were no changes in our internal control over financial reporting that occurred during our most recent fiscal quarter that have materially
affected, or are reasonably likely to materially affect, our internal control over financial reporting.
Item 9B. Other Information
None.
Item 10. Directors Officers and Corporate Governance.
PART III
Our senior management is composed of individuals with significant management experience. The following table sets forth specific information
regarding our executive officers and directors as of June 1, 2013:
Name
Shawn K. Singh, J.D.
H. Ralph Snodgrass, Ph.D.
Jerrold D. Dotson
Jon S. Saxe, J.D.
Brian J. Underdown, PhD.
Age
50
63
59
76
72
Position
Chief Executive Officer and Director
President, Chief Scientific Officer and Director
Chief Financial Officer
Director
Director
Mr. Gregory A. Bonfiglio served as a member of VistaGen California’s Board of Directors beginning in February 2007 and as a member of our
Board from shortly following the Merger through January 6, 2013, when he resigned to pursue his venture capital duties on a full-time
basis. The following is a brief summary of the background of each of our current executive officers and directors, including their principal
occupation during the five preceding years. All directors serve until their successors are elected and qualified.
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Shawn K. Singh, J.D. has over 20 years of experience working with biotechnology, medical device and pharmaceutical companies, both private
and public. Mr. Singh became VistaGen California’s Chief Executive Officer in August 2009; he joined VistaGen California’s Board of
Directors in 2000. Upon completion of the Merger in May 2011, Mr. Singh also became Chief Executive Officer and a director of the
Company. Mr. Singh served on VistaGen California’s management team on a part-time basis from late-2003, following VistaGen California’s
acquisition of Artemis Neuroscience, of which he was President, to August 2009. From February 2001 to August 2009, Mr. Singh served as
Managing Principal of Cato BioVentures, a life science venture capital firm, and as Chief Business Officer and General Counsel of Cato
Research, a global contract research organization affiliated with Cato BioVentures. Mr. Singh served as President (part-time) of Echo
Therapeutics (Nasdaq: ECTE), from September 2007 to June 2009, and as a director of the company through December 2012, and as Chief
Executive Officer (part-time) of Hemodynamic Therapeutics from November 2004 to August 2009. From November 2000 to February 2001,
Mr. Singh served as Managing Director of Start-Up Law, a management consulting firm serving early-stage biotechnology companies.
Mr. Singh served as Chief Business Officer of SciClone Pharmaceuticals (Nasdaq: SCLN) from November 1993 to November 2000 and as a
corporate finance associate of Morrison & Foerster LLP, an international law firm, from May 1991 to November 1993. Mr. Singh also currently
serves as a member of the Board of Directors of Armour Therapeutics, a privately-held company focused on prostate cancer. Mr. Singh is a
member of the State Bar of California.
The Corporate Governance and Nominating Committee believes that Mr. Singh possesses substantial expertise in senior leadership roles leading
biotechnology, biopharmaceutical and medical device companies from product introduction through commercialization, and that such expertise
is extremely valuable to the Board of Directors and the Company as we execute our business plan. In addition, the Board of Directors values
the input provided by Mr. Singh given his extensive legal and venture capital experience working with multiple privately- and publicly-held
biotechnology, pharmaceutical and medical device companies.
H. Ralph Snodgrass, Ph.D. co-founded VistaGen California in 1998 with Dr. Gordon Keller, and served continuously as VistaGen California’s
President, Chief Executive Officer and Director until August 2009, when he became President and Chief Scientific Officer. Upon completion of
the Merger in May 2011, Dr. Snodgrass became our President and Chief Scientific Officer. Dr. Snodgrass became a director of the Company in
June 2011, shortly following the Merger. Prior to founding VistaGen California, Dr. Snodgrass was a key member of the executive management
team which lead Progenitor, Inc., a biotechnology company focused on developmental biology, through its initial public offering, and was its
Chief Scientific Officer from June 1994 to May 1998, and its Executive Director from July 1993 to May 1994. He received his Ph.D. in
immunology from the University of Pennsylvania, and has more than 20 years of experience in senior biotechnology management and over
10 years research experience as a professor at the Lineberger Comprehensive Cancer Center, University of North Carolina Chapel Hill School of
Medicine, and as a member of the Institute for Immunology, Basel, Switzerland. Dr. Snodgrass is a past Board Member of the Emerging
Company Section of the Biotechnology Industry Organization (BIO), and past member of the International Society Stem Cell Research Industry
Committee. Dr. Snodgrass has published more than 80 scientific papers, is the inventor on more than 17 patents and a number of patent
applications, is, or has been, the principal investigator on U.S. federal and private foundation sponsored research grants with budgets totaling
more than $14.5 million and is recognized as an expert in stem cell biology with more than 20 years’ experience in the uses of stem cells as
biological tools for drug discovery and development.
The Corporate Governance and Nominating Committee believes that Dr. Snodgrass’ expertise in biotechnology focused on developmental
biology, including stem cell biology, his extensive senior management experience leading biotechnology companies at all stages of development,
as well as his reputation and standing in the fields of biotechnology and stem cell research, allow him to bring to the Company and the Board of
Directors a unique understanding of the challenges and opportunities associated with pluripotent stem cell biology, as well as credibility in the
markets in which we operate.
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Jerrold D. Dotson, CPA has served as VistaGen’s Chief Financial Officer since September 2011; he became a VistaGen employee in September
2012. Prior to joining VistaGen on a consulting basis in September 2011, Mr. Dotson served as Corporate Controller for Discovery Foods
Company, a privately held Asian frozen foods company from January 2009 to September 2011. From February 2007 through September 2008,
Mr. Dotson served as Vice President, Finance and Administration (principal financial and accounting officer) for Calypte Biomedical
Corporation (OTCBB: CBMC), a public biotechnology company. Mr. Dotson served as Calypte’s Corporate Secretary from 2001 through
September 2008. He also served as Calypte’s Director of Finance from January 2000 through July 2005 and was a financial consultant to
Calypte from August 2005 through January 2007. Prior to joining Calypte, from 1988 through 1999, Mr. Dotson worked in various financial
management positions, including Chief Financial Officer, for California & Hawaiian Sugar Company, a privately held company. Mr. Dotson is
licensed as a CPA in California and received his BS degree in Business Administration with a concentration in accounting from Abilene
Christian College.
Jon S. Saxe, J.D. served as the Chairman of VistaGen California’s Board of Directors from 2000 until the Merger. He also served as the
Chairman of VistaGen California’s Audit Committee. Upon completion of the Merger, Mr. Saxe became a director and Chairman of the
Company and retained his role as Chairman of the Audit Committee. He is the retired President and was a director of PDL BioPharma. From
1989 to 1993, he was President, Chief Executive Officer and a director of Synergen, Inc. (acquired by Amgen). Mr. Saxe served as Vice
President, Licensing & Corporate Development for Hoffmann-LaRoche from 1984 through 1989, and Head of Patent Law from 1978 through
1989. Mr. Saxe currently is a director of SciClone Pharmaceuticals, Inc. (Nasdaq: SCLN) and Durect Corporation (Nasdaq: DRRX), and private
biotechnology, medical device and pharmaceutical companies. Mr. Saxe also has served as a director of other biotechnology and pharmaceutical
companies, including ID Biomedical (acquired by GlaxoSmithKline), Sciele Pharmaceuticals, Inc. (acquired by Shionogi), Amalyte (acquired by
Kemin Industries), Cell Pathways (acquired by OSI Pharmaceuticals), and other companies, both public and private. Mr. Saxe has a B.S.Ch.E.
from Carnegie-Mellon University, a J.D. degree from George Washington University and an LL.M. degree from New York University.
The Corporate Governance and Nominating Committee believes that Mr. Saxe’s years of experience as a senior executive with major
biopharmaceutical and biotechnology companies, including Protein Design Labs, Inc., Synergen, Inc. and Hoffmann-Roche, Inc. as well as his
experience serving as a director of numerous private and public biotechnology and pharmaceutical companies, serving as Chairman, and Chair
and member of audit, compensation and governance committees of both private and public companies, provides the Company and the Board of
Directors with highly valuable insight and perspective into the biotechnology and pharmaceutical industries, as well as the strategic
opportunities and challenges that we face.
Brian J. Underdown, Ph.D. joined VistaGen California’s Board of Directors in November 2009 and became a director of the Company shortly
following the completion of the Merger, in June 2011. Since September 1997, Dr. Underdown is a Managing Director of Lumira Capital Corp.,
having started in the venture capital industry in 1997 with MDS Capital Corporation (MDSCC). His investment focus has been on therapeutics
in both new and established companies in both Canada and the United States. Prior to joining MDSCC, Dr. Underdown held a number of senior
management positions in the biopharmaceutical industry and at universities. Dr. Underdown has served on the Board of a number of biologics
companies including: ID Biomedical (acquired by GSK), Trillium Therapeutics (merged with Stem Cell Therapeutics), and Ception
Therapeutics (acquired by Cephalon/Teva). Dr. Underdown’s current board positions include: Argos Therapeutics, Ontario Genomics Institute
(Chair) and the McMaster Innovation Park. He has served on a number of Boards and advisory bodies of government sponsored research
organizations including CANVAC, the Canadian National Centre of Excellence in Vaccines and Allergen, the Canadian National Centre of
Excellence in Allergy and Asthma. Dr. Underdown obtained his Ph.D. in immunology from McGill University and undertook post-doctoral
studies at Washington University School of Medicine.
The Corporate Governance and Nominating Committee believes that Dr. Underdown’s extensive background working in the biotechnology and
pharmaceutical industries, as a director of numerous private and public companies, as well as his venture capital experience funding and advising
start-up and established companies focused on therapeutics, provides the Company and its Board of Directors with an in-depth understanding of
the myriad of issues facing the Company, from funding development to executing its business plan.
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Each of our executive officers is elected by, and serves at the discretion of, the Board of Directors. Each of our executive officers devotes his
full time to our affairs.
Family Relationships
We are not aware of any family relationships between any of our directors or officers.
Board Composition and Committees
Our Board of Directors is currently composed of four members, Jon S. Saxe, Chairman, Shawn K. Singh, H. Ralph Snodgrass, Ph.D., and Brian
J. Underdown, Ph.D. All actions of the Board of Directors require the approval of a majority of the directors in attendance at a meeting at which
a quorum is present. We currently have standing Audit, Compensation and Corporate Governance and Nominating Committees.
Audit Committee
The Audit Committee was established by the Board to oversee our accounting and financial reporting processes and the audits of our financial
statements. In meeting this objective, the Audit Committee evaluates the performance of and assesses the qualifications and independence of our
independent registered public accounting firm. The Committee also approves the engagement of our independent registered public accounting
firm and determines whether to retain or terminate their services or to appoint and engage a new independent registered public accounting firm.
The Committee reviews and approves the retention of the independent registered public accounting firm to perform any proposed permissible
non-audit services and confers with management and our independent registered public accounting firm regarding the effectiveness of internal
controls over financial reporting. The Committee reviews the financial statements to be included in our Annual Report on Form 10-K and in our
Quarterly Reports on Form 10-Q and discusses with management and our independent registered public accounting firm the results of the annual
audit. Currently, our three independent directors (as independence is currently defined in Rule 10A-3(b)(1) under the Securities Exchange Act of
1934, as amended (the “Exchange Act”), Mr. Saxe (Chairman) and Dr. Underdown comprise the Audit Committee. The Audit Committee is
governed by a written charter. Our Board of Directors has made a determination that Mr. Saxe is an audit committee financial expert.
Compensation Committee
The Compensation Committee of the Board reviews and recommends to the Board our overall compensation strategy and policies. The
Compensation Committee reviews and recommends to the Board corporate performance goals and objectives relevant to the compensation of our
executive officers and other senior management; reviews and recommends to the Board the compensation and other terms of employment of our
Chief Executive Officer and other executive officers; and oversees the administration of our incentive and equity-based compensation plans and
other similar programs. Dr. Underdown (Chairman) and Mr. Saxe currently comprise the Compensation Committee: Both members of our
Compensation Committee are independent (as independence is currently defined in Rule 4200(a)(15) of the Nasdaq listing standards). The
Compensation Committee is governed by a written charter.
Corporate Governance and Nominating Committee
The Corporate Governance and Nominating Committee of the Board is primarily responsible for identifying, and recommending candidates to
serve as directors (consistent with criteria approved by the Board), recommending to the Board candidates for election and reelection to the
Board, making recommendations to the Board regarding the size and composition of the Board and its committees; assessing the performance of
the Board and its committees and overseeing compliance with our corporate governance guidelines. Dr. Underdown (Chairman), and Mr. Saxe
currently comprise the Corporate Governance and Nominating Committee. All current members of the Nominating and Corporate Governance
Committee are independent (as independence is currently defined in Rule 4200(a)(15) of the Nasdaq listing standards). The Nominating and
Corporate Governance Committee is governed by a written charter.
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All potential candidates for director nominees, including candidates recommended by our stockholders, are reviewed in the context of the
current composition of the Board, our operating requirements and the long-term interests of our stockholders. In conducting this assessment, the
Committee considers such factors as it deems appropriate given our current needs and those of our Board, to maintain a balance of expertise,
experience and capability. The Corporate Governance and Nominating Committee reviews directors’ overall service during their term, including
the number of meetings attended, their level of participation and quality of performance. The Committee also determines whether the nominee
would be independent, which determination is based upon applicable Nasdaq or other exchange listing standards, applicable SEC rules and
regulations and the advice of counsel, if necessary.
The Corporate Governance and Nominating Committee will consider director candidates recommended by stockholders in the same manner as it
considers recommendations from current directors or other sources. Stockholders who wish to recommend individuals for consideration by the
Corporate Governance and Nominating Committee to become nominees for election to the Board may do so by delivering a written
recommendation to the Company Secretary at the following address: 384 Oyster Point Boulevard, No. 8, South San Francisco, CA 94080 at
least 60 days prior, but no more than 90 days prior, to the anniversary date of the last annual meeting of stockholders. Submissions should
include the full name, address and age of the proposed nominee, a description of the proposed nominee’s business experience for at least the
previous five years, complete biographical information, a description of the proposed nominee’s qualifications as a director, and the number of
shares of our stock beneficially owned by the proposed nominee. The nominating stockholder must also provide his or her name and address of
record and the number of shares of our stock that he or she owns beneficially or of record.
The Corporate Governance and Nominating Committee has not established specific minimum qualifications for recommended nominees or
specific qualities or skills for one or more of our directors to possess, other than as are necessary to meet any requirements under rules and
regulations (including any stock exchange rules) applicable to the Company. The Corporate Governance and Nominating Committee uses a
subjective process for identifying and evaluating nominees for director, based on the information available to, and the subjective judgments of,
the members of the Committee and our then current needs for the Board as a whole. Although it does not have a formal policy regarding the
consideration of diversity, the Corporate Governance and Nominating Committee considers the needs for the Board as a whole when identifying
and evaluating nominees and, among other things, considers diversity in background, age, experience, qualifications, attributes and skills in
identifying nominees.
The Corporate Governance and Nominating Committee’s process for identification and evaluation of director candidates is generally as follows:
(a) In the event of a vacancy or the establishment of a new directorship on the Board, candidate(s) for director nominee(s) shall be presented
to the full Board for consideration and approval upon the recommendation of no less than a majority of the independent members of the
Board (as independence is defined under any stock exchange rules that may be applicable to the Company at such time).
(b) We believe that the continuing service of qualified incumbents promotes stability and continuity in the boardroom, contributing to the
Board's ability to work as a collective body, while giving us the benefit of the familiarity and insight into our affairs that our directors have
accumulated during their tenure. Accordingly, the process for identifying nominees reflects our practice of re-nominating incumbent
directors who continue to satisfy the criteria for membership on the Board, whom the independent members of the Board believe continue to
make important contributions to the Board and who consent to continue their service on the Board. Consistent with this policy, in
considering candidates for election at annual meetings of stockholders, the independent members of the Board will first determine the
incumbent directors whose terms expire at the upcoming meeting and who wish to continue their service on the Board.
(c) The independent members of the Board will evaluate the qualifications and performance of the incumbent directors that desire to
continue their service. In particular, as to each such incumbent director, the independent members of the Board will (i) consider if the
director continues to satisfy the minimum qualifications for director candidates adopted by the independent members of the Board, (ii)
review any assessments of the performance of the director during the preceding term made by the Board, and (iii) determine whether there
exist any special, countervailing considerations against re-nomination of the director.
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(d) If the independent members of the Board determine that an incumbent director consenting to re-nomination continues to be qualified and
has satisfactorily performed his or her duties as director during the preceding term, and there exist no reasons, including considerations
relating to the composition and functional needs of the Board as a whole, why in the view of the independent members of the Board the
incumbent should not be re-nominated, the independent members of the Board will, absent special circumstances, propose the incumbent
director for reelection.
(e) The process by the independent members of the Board for identifying and evaluating nominees for director, including nominees
recommended by a stockholder, involves (with or without the assistance of a retained search firm):
·
·
·
·
·
compiling names of potentially eligible candidates;
conducting background and reference checks;
conducting interviews with candidates and/or others;
meeting to consider and approve final candidates; and, as appropriate,
preparing and presenting to the full Board an analysis with regard to particular recommended candidates.
During the search process, the independent directors shall endeavor to identify director nominees who have the highest personal and
professional integrity, have demonstrated exceptional ability and judgment, and, together with other director nominees and current Board
members, shall effectively serve the long-term interests of our stockholders and contribute to our overall corporate goals.
(f) In considering potential new directors, the independent members of the Board will review individuals from various disciplines and
backgrounds. Among the qualifications to be considered in the selection of candidates are:
·
·
·
·
personal and professional integrity;
broad experience in business, finance or administration;
familiarity with our industry; and
prominence and reputation.
Board Attendance at Board of Directors, Committee and Stockholder Meetings
Our Board of Directors met four times and acted by unanimous written consent ten times during the fiscal year ended March 31, 2013. Our
Audit Committee met four times and our Compensation Committee requested action by the entire Board of Directors for grants of options and
warrants and the modification of certain options on three occasions during the same period. No director serving during fiscal 2013 attended
fewer than 75% of the aggregate of all meetings of the Board and the committees of the Board upon which such director served.
We do not have a formal policy regarding attendance by members of the Board at our annual meeting of stockholders, but directors are
encouraged to attend. We did not hold an annual meeting of stockholders during our fiscal year ended March 31, 2013.
Code of Ethics
We have adopted a Code of Ethics applicable to our directors, officers and all employees. The Code of Ethics is available on our website at
www.vistagen.com.
Compensation Committee Interlocks and Insider Participation
Our Compensation Committee consists of Dr. Underdown and Mr. Saxe, each of whom is a non-employee director. Neither member of the
Compensation Committee has a relationship that would constitute an interlocking relationship with executive officers or directors of another
entity.
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Section 16 Beneficial Ownership Reporting Compliance
Section 16(a) of the Exchange Act requires our officers, directors and persons who beneficially own more than ten percent of our common stock
(collectively, “Reporting Persons”) to file reports of ownership on Form 3 and changes in ownership on Form 4 or Form 5 with the
Commission. The Reporting Persons are also required by SEC rules to furnish us with copies of all reports that they file pursuant to Section
16(a). Except as described below, we believe that during our fiscal year ended March 31, 2013, all of the Reporting Persons complied with all
applicable reporting requirements.
On March 3, 2013, Mr. Saxe was granted a warrant to purchase 150,000 restricted shares of our common stock at an exercise price of $0.64 per
share, but did not report this acquisition of derivative securities until March 6, 2013.
Item 11. Executive Compensation
Our Compensation Objectives
Our compensation practices are designed to attract key employees and to retain, motivate and reward our executive officers for their
performance and contribution to our long-term success. Our Board of Directors, through the Compensation Committee, seeks to compensate our
executive officers by combining short and long-term cash and equity incentives. It also seeks to reward the achievement of corporate and
individual performance objectives, and to align executive officers’ incentives with shareholder value creation. The Compensation Committee
seeks to tie individual goals to the area of the executive officer’s primary responsibility. These goals may include the achievement of specific
financial or business development goals. The Compensation Committee seeks to set performance goals that reach across all business areas and
include achievements in finance/business development and corporate development.
The Compensation Committee makes decisions regarding salaries, annual bonuses, if any, and equity incentive compensation for our executive
officers, approves corporate goals and objectives relevant to the compensation of the Chief Executive Officer and our other executive officers.
The Compensation Committee solicits input from our Chief Executive Officer regarding the performance of our other executive officers.
Finally, the Compensation Committee also administers our incentive compensation and benefit plans.
Although we have no formal policy for a specific allocation between current and long-term compensation, or cash and non-cash compensation,
we have established a pay mix for our officers with a relatively equal balance of both, providing a competitive salary with a significant portion
of compensation awarded on both corporate and personal performance.
Compensation Components
Our compensation consists primarily of three elements: base salary, annual bonus and long-term equity incentives. We describe each element of
compensation in more detail below.
Base Salary
Base salaries for our executive officers are established based on the scope of their responsibilities and their prior relevant experience, taking into
account competitive market compensation paid by other companies in our industry for similar positions and the overall market demand for such
executives at the time of hire. An executive officer’s base salary is also determined by reviewing the executive officer’s other compensation to
ensure that the executive officer’s total compensation is in line with our overall compensation philosophy.
Base salaries are reviewed annually and increased for merit reasons, based on the executive officers’ success in meeting or exceeding individual
objectives. Additionally, we adjust base salaries as warranted throughout the year for promotions or other changes in the scope or breadth of an
executive officer’s role or responsibilities.
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Annual Bonus
The Compensation Committee assesses the level of the executive officer’s achievement of meeting individual goals, as well as that executive
officer’s contribution towards our corporate-wide goals. The amount of the cash bonus depends on the level of achievement of the individual
performance goals, with a target bonus generally set as a percentage of base salary and based on the achievement of pre-determined
milestones. To conserve our cash resources, our management team did not seek, and our Compensation Committee did not award, cash bonuses
to executive officers during fiscal 2012 or 2013.
Long-Term Equity Incentives
The Compensation Committee believes that to attract and retain management, key employees and non-management directors the compensation
paid to these persons should include, in addition to base salary and potential annual cash incentives, equity based compensation that is
competitive with peer companies. The Compensation Committee determines the amount and terms of equity based compensation granted under
our stock option plans.
Summary Compensation Table
The following table sets forth summary information concerning certain compensation awarded, paid to, or earned by the Named Executive
Officers (“NEOs”) for all services rendered in all capacities to us for the fiscal years ended March 31, 2013 and March 31, 2012.
Name and Principal Position
Shawn K. Singh, J.D. (1)
Chief Executive Officer
H. Ralph Snodgrass, Ph.D. (2)
President, Chief Scientific
Officer
Jerrold D. Dotson (3)
Chief Financial Officer
Fiscal
Year
Salary
($)
Bonus
($)
2013
2012
201,646
292,268
2013
203,086
2012
249,428
2013
2012
97,269
-
Option and
Warrant
Awards (4)
($)
All Other
Compensation
($)
Total
($)
-
-
-
-
-
-
802,411(5)
108,056(7)
534,941(5)
-
230,104(8)
1,004,057
630,428
-
738,027
105,618(7)
100,000(9)
455,046
134,316(6)
108,535(7)
62,333(10)
71,293(10)
293,918
179,828
(1) Mr. Singh became VistaGen California’s Chief Executive Officer on August 20, 2009 and the Company’s Chief Executive Officer in
May 2011, in connection with the Merger. In our fiscal years ended March 31, 2013 and 2012, Mr. Singh’s annual base cash salary,
excluding potential cash bonus amounts, pursuant to his January 2010 employment agreement was contractually set at $347,500.
However, to conserve cash for our operations during our fiscal years ended March 31, 2013 and 2012, Mr. Singh voluntarily reduced his
base cash salary in each of such fiscal years to the amounts indicated. In addition, pursuant to his employment agreement, Mr. Singh is
eligible to receive an annual incentive bonus of up to fifty percent (50%) of his base cash salary. However to conserve cash for our
operations during our fiscal years ended March 31, 2013 and 2012, Mr. Singh voluntarily refrained from receiving any cash bonus from
the Company.
(2) Through August 20, 2009, Dr. Snodgrass served as VistaGen California’s President and Chief Executive Officer, at which time he
became its President and Chief Scientific Officer. He became the Company’s President and Chief Scientific Officer in May 2011, in
connection with the Merger. In our fiscal years ended March 31, 2013 and 2012, Dr. Snodgrass’ annual base cash salary, excluding
potential cash bonus amounts, pursuant to his January 2010 employment agreement was contractually set at $305,000. However, to
conserve cash for our operations during our fiscal years ended March 31, 2013 and 2012, Dr. Snodgrass voluntarily reduced his base cash
salary in each of such fiscal years to the amounts indicated. In addition, pursuant to his employment agreement, Dr. Snodgrass is eligible
to receive an annual incentive bonus of up to fifty percent (50%) of his base cash salary. However to conserve cash for our operations
during our fiscal years ended March 31, 2013 and 2012, Dr. Snodgrass voluntarily refrained from receiving any cash bonus from the
Company.
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(3) Mr. Dotson served as Chief Financial Officer on a part-time contract basis from September 19, 2011 through August 2012, at which time
he became our employee.
(4) The amounts in the Option and Warrant Awards column represent only the aggregate grant date fair value of options or warrants to
purchase restricted shares of our common stock awarded to Mr. Singh, Dr. Snodgrass and Mr. Dotson during the fiscal year presented
computed in accordance with the Financial Accounting Standards Board’s Accounting Standards Codification Topic 718, Compensation
– Stock Compensation ("ASC 718”). The amounts in this column do not represent any cash payments actually received by Mr. Singh, Dr.
Snodgrass or Mr. Dotson with respect to any of such options or warrants to purchase restricted shares of our common stock awarded to
them during the periods presented. To date, Mr. Singh, Dr. Snodgrass and Mr. Dotson have not exercised such options or warrants to
purchase common stock, and there can be no assurance that any of them will ever realize any of the ASC 718 grant date fair value
amounts presented in the Option and Warrant Awards column.
(5) We used the Black Scholes Option Pricing Model and the following assumptions for determining the grant date fair value of the warrants
to purchase shares of our common stock granted during the fiscal year ended March 31, 2013:
Market price per share
Exercise price per share
Risk-free interest rate
Expected Term (years)
Volatility
Dividend rate
$
$
0.64
0.64
1.86%
10.0
84.73%
0.0%
Grant date fair value per share
$
0.53
(6)
In October 2012, the Company modified the stock option award granted to Mr. Dotson in September 2011 to reduce the exercise price
of the option from $2.58 per share to $0.75 per share and granted him a new stock option to purchase an additional 50,000 restricted
shares of our common stock. We used the Black Scholes Option Pricing Model and the following assumptions to determine incremental
fair value of the modified option and the grant date fair value of $0.51 per share for the new option: market price per share: $0.71;
exercise price per share: $0.75; risk-free interest rate: 1.00%; expected term: 6.25 years; volatility 85.35%; dividend rate: 0%. The
figure reported includes (i) the grant date fair value of the warrant granted to Mr. Dotson, determined in accordance with the
assumptions described in note 5 above, $106,988; (ii) the fair value of the new option, $25,385; and (iii) the incremental fair value
resulting from the modification of the September 2011 stock option grant, $1,943.
(7)
We used the Black Scholes Option Pricing Model and the following assumptions for determining the grant date fair value of the options
to purchase shares of our common stock granted during the fiscal year ended March 31, 2012:
Market price per share
Exercise price per share
Risk-free interest rate
Expected Term (years)
Volatility
Dividend rate
Singh
$1.58
$1.75
2.43%
6.25
78.9%
0.0%
Snodgrass Dotson
$2.58
$2.58
1.97%
10.0
85.7%
0.0%
$1.58
$1.925
2.43%
6.25
78.9%
0.0%
Grant date fair value per share
$1.08
$1.06
$2.17
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(8)
In December 2006, VistaGen California accepted a full-recourse promissory note in the amount of $103,411 from Mr. Singh in payment
of the exercise price for options and warrants to purchase an aggregate of 126,389 restricted shares of VistaGen California’s common
stock. On May 11, 2011, in connection with the Merger, the $128,168 outstanding balance of the principal and accrued interest on this
note was cancelled in accordance with Mr. Singh's 2010 employment agreement and was treated as additional compensation. In
accordance with his employment agreement, Mr. Singh is entitled to an income tax gross-up on the compensation related to the note
cancellation. At March 31, 2012 and 2013, the Company had accrued $101,936 as an estimate of the gross-up amount payable to Mr.
Singh, but had not yet paid such amount to Mr. Singh.
(9)
In December 2011, Dr. Snodgrass received a non-cash compensation award of $100,000 enabling his cashless exercise of previously
granted options to purchase 113,636 restricted shares of our common stock at an exercise price of $0.88 per share.
(10) Amounts shown represent cash compensation paid to Mr. Dotson under the terms of the consulting agreement between the Company and
Mr. Dotson for the periods April 2012 through August 2012 and September 2011 through March 2012, respectively.
None of the NEOs is entitled to perquisites or other personal benefits which, in the aggregate, are worth over $50,000 or over 10% of their
base salary.
Benefit Plans
401(k) Plan
We maintain, through a registered agent, a retirement and deferred savings plan for our officers and employees. This plan is intended to qualify
as a tax-qualified plan under Section 401(k) of the Internal Revenue Code of 1986, as amended. The retirement and deferred savings plan
provides that each participant may contribute a portion of his or her pre-tax compensation, subject to statutory limits. Under the plan, each
employee is fully vested in his or her deferred salary contributions. Employee contributions are held and invested by the plan’s trustee. The
retirement and deferred savings plan also permits us to make discretionary contributions subject to established limits and a vesting schedule. To
date, we have not made any discretionary contributions to the retirement and deferred savings plan on behalf of participating employees.
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Options and Warrants Granted to NEOs
The following table provides information regarding each compensation-related unexercised stock option and warrant to purchase restricted
shares of our common stock held by each of the NEOs as of March 31, 2013.
Name
Shawn K. Singh, J.D.
Total:
H. Ralph Snodgrass, Ph.D.
Total:
Jerrold D. Dotson
Total:
Number of Securities
Underlying Unexercised
Options (#) Exercisable
Stock Options
Number of Securities
Underlying
Unexercised
Options
(#)Unexercisable
Option
Exercise
Price ($)
20,000
40,000
20,000
20,000
60,000
22,500
1,000,000
425,000
47,916
-
1,655,416
50,000
25,000
150,000
6,362
250,000
47,916
-
529,278
31,533
-
31,353
-
-
-
-
-
-
-
-
52,084
1,500,000 (1)
1,552,084
-
-
-
-
-
52,084
1,000,000 (1)
1,052,084
68,447
200,000 (1)
268,447
0.80
0.72
2.10
2.10
1.13
1.13
1.50
1.50
1.75
0.64
1.13
1.13
1.65
0.88
1.50
1.925
0.64
0.75
0.64
Option
Expiration
Date
12/21/2016
5/17/2017
1/17/2018
1/17/2018
3/24/2019
6/17/2019
11/4/2019
12/30/2019
4/25/2021
3/3/2023
3/24/2014
6/17/2014
11/4/2014
12/20/2016
12/30/2019
4/25/2021
3/3/2023
10/30/2022
3/3/2023
(1)
Represents warrant to purchase restricted shares of our common stock granted on March 3, 2013 at the market price of our common
stock on the grant date. The warrant becomes exercisable for 50% of the shares on April 1, 2013, 25% of the shares on April 1, 2014
and 25% of the shares on April 1, 2015, provided that the warrant will become fully vested upon a change in control of the Company,
as defined, or upon the consummation by the Company and a third party of a license or sale transaction involving at least one new drug
rescue variant.
Employment Agreements
Mr. Singh and Dr. Snodgrass have entered into employment agreements with us that were effective during the fiscal years ended March 31, 2012
and 2013.
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Singh Agreement
Mr. Singh entered into an employment agreement with VistaGen California, dated as of April 28, 2010, as amended on May 9, 2011, (the “ Singh
Agreement”), which we have assumed. Under the Singh Agreement, Mr. Singh’s base salary is $347,500 per year. However, in our fiscal years
ended March 31, 2013 and 2012, Mr. Singh voluntarily reduced his annual base salary to $201,646 and $292,268, respectively, to conserve cash
for our operations. Mr. Singh is eligible to receive an annual incentive bonus of up to 50% of his base salary. Payment of his annual incentive
bonus is at the discretion of the Compensation Committee of our Board of Directors. In the event we terminate Mr. Singh’s employment without
cause, he is entitled to receive severance in an amount equal to:
•
•
•
twelve months of his then-current base salary payable in the form of salary continuation;
a pro-rated portion of the incentive bonus that the Board of Directors determines in good faith that Mr. Singh earned prior to his
termination; and
such amounts required to reimburse him for Consolidated Omnibus Budget Reconciliation Act (“ COBRA”) payments for continuation
of his medical health benefits for such twelve-month period.
In addition, in the event Mr. Singh terminates his employment with good reason following a change of control, he is entitled to twelve months of
his then-current base salary payable in the form of salary continuation.
In addition, the Singh Agreement provides that all of our outstanding stock option agreements with Mr. Singh will provide for:
•
•
acceleration of vesting of 50% of his then unvested options, if any, pursuant to each such stock option agreement in the event we
terminate Mr. Singh’s employment without cause; and
full acceleration of vesting of all of his remaining unvested shares, if any, pursuant to each such stock option agreement in the event
that we terminate Mr. Singh’s employment without cause within twelve months of a “change of control” (as defined below under
“-Change of Control Provisions”).
Finally, pursuant to the Singh Agreement, the principal and accrued interest owed by Mr. Singh pursuant to that certain full recourse promissory
note, dated December 21, 2006, was forgiven and cancelled by VistaGen on May 11, 2011. Within twelve months thereafter, Mr. Singh is
entitled to receive a tax gross-up cash bonus in an amount equal to his U.S. and California income tax liability related to the forgiveness and
cancellation of his note. At March 31, 2013 and 2012, we had accrued $101,936 as an estimate of the gross-up amount payable to Mr. Singh, but
had not yet paid that amount to Mr. Singh. See Notes 8 and 14 to our Consolidated Financial Statements which are included in Item 8 of this
report.
Snodgrass Agreement
Dr. Snodgrass entered into an employment agreement with VistaGen California, dated as of April 28, 2010, as amended on May 9, 2011, (the
“Snodgrass Agreement”), which we have assumed. Under the Snodgrass Agreement, Dr. Snodgrass’s base salary is $305,000 per
year. However, in our fiscal years ended March 31, 2013 and 2012, Dr. Snodgrass voluntarily reduced his annual salary to $203,086 and
$249,428, respectively, to conserve cash for our operations. Dr. Snodgrass is eligible to receive an annual incentive bonus of up to 50% of his
base salary. Payment of his annual incentive bonus is at the discretion of the Board of Directors. In the event we terminate Dr. Snodgrass’s
employment without cause, he is entitled to receive severance in an amount equal to
•
•
•
twelve months of his then-current base salary payable in the form of salary continuation;
a pro-rated portion of the incentive bonus that the Board of Directors determines in good faith that Dr. Snodgrass earned prior to his
termination; and
such amounts required to reimburse him for COBRA payments for continuation of his medical health benefits for such twelve-month
period.
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In addition, in the event Dr. Snodgrass terminates his employment with good reason, he is entitled to twelve months of his then-current base
salary payable in the form of salary continuation.
In addition, the Snodgrass Agreement provides that all of our outstanding stock option agreements with Dr. Snodgrass will be amended to
provide for:
•
•
acceleration of vesting of 50% of his then unvested options, if any, pursuant to each such stock option agreement in the event we
terminate Dr. Snodgrass’s employment without cause; and
full acceleration of vesting of all of his remaining unvested shares, if any, pursuant to each such stock option agreement in the event
that we terminate Dr. Snodgrass’s employment without cause within twelve months of a “change of control” (as defined below under “
Change of Control Provisions”).
Change of Control Provisions
Pursuant to each of their respective employment agreements, Dr. Snodgrass is entitled to severance if he terminates his employment at any time
for “good reason” (as defined below), while Mr. Singh is entitled to severance if he terminates his employment for good reason only after a
change of control. Under their respective agreements, “good reason” means any of the following events if the event is effected by VistaGen
without the executive’s consent (subject to VistaGen’s right to cure):
•
•
a material reduction in the executive’s responsibility; or
a material reduction in the executive’s base salary following the Merger except for reductions that are comparable to reductions
generally applicable to similarly situated executives of VistaGen.
Furthermore, pursuant to their respective employment agreements and their stock option award agreements, in the event we terminate the
executive without cause within twelve months following a change of control, the executive’s remaining unvested shares become fully vested
and exercisable. Upon a change of control in which the successor corporation does not assume the executive’s stock options, the stock options
granted to the executive under the 1999 Plan become fully vested and exercisable.
Pursuant to their respective employment agreements, a change of control occurs when: (i) any “person” as such term is used in Sections 13(d)
and 14(d) of the Securities Exchange Act of 1934, as amended (other than VistaGen, a subsidiary, an affiliate, or a VistaGen employee benefit
plan, including any trustee of such plan acting as trustee) becoming the “beneficial owner” (as defined in Rule 13d-3 under the U.S. Securities
Exchange Act of 1934, as amended), directly or indirectly, of securities of VistaGen representing 50% or more of the combined voting power of
VistaGen’s then outstanding securities; (ii) a sale of substantially all of VistaGen’s assets; or (iii) any merger or reorganization of VistaGen
whether or not another entity is the survivor, pursuant to which the holders of all the shares of capital stock of VistaGen outstanding prior to the
transaction hold, as a group, fewer than 50% of the shares of capital stock of VistaGen outstanding after the transaction.
In the event that, following termination of employment, amounts are payable to an executive pursuant to his employment agreement, the
executive’s eligibility for severance is conditioned on the executive having first signed a release agreement.
Pursuant to their respective employment agreements, the estimated amount that could be paid by VistaGen assuming that a change of control
occurred on the last business day of VistaGen’s current fiscal year is $347,500 for Mr. Singh and $305,000 for Dr. Snodgrass, excluding the
imputed value of accelerated vesting of their stock options or the warrants to purchase restricted shares of our common stock granted in March
2013.
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DIRECTOR COMPENSATION
We do not have a formal compensation plan for our non-employee directors. Our informal plan prescribes that the Chairman of our Board of
Directors, who is an independent director, has, since October 1, 2011, earned $2,500 per quarter. Our other independent directors have earned
$2,000 per quarter since that date. Beginning in July 2011, the Chairman of our Audit Committee and each independent director who serves as a
member of our Audit Committee have also earned $1,000 quarterly. In addition, from time to time, our independent directors may receive non-
qualified stock option, warrants or other equity-based awards. With the exception of Mr. Bonfiglio, who was paid $12,000 for his service as an
independent director and a member of our Audit Committee for the period of January 2012 through December 2012 following his resignation
from the Board in January 2013, we did not pay our independent directors during our 2013 fiscal year.
The following table sets forth a summary of the compensation earned by our non-employee directors in our fiscal year ended March 31, 2013.
Name
Jon S. Saxe (3)
Gregory A. Bonfiglio, J.D. (4)
Brian J. Underdown, Ph.D. (5)
Fees Earned
or Paid in
Cash (1) ($)
Option and
Warrant
Awards (2) ($)
Other
Compensation
($)
Total
($)
14,000
9,000
12,000
80,241
-
80,241
-
-
-
94,241
9,000
92,241
(1)
(2)
(3)
(4)
(5)
With the exception of the amount shown for Mr. Bonfiglio, the amounts shown represent fees earned for service on our Board of
Directors and Audit Committee during the fiscal year which we have accrued but have not paid to the director at March 31, 2013.
The amounts in this column represent the grant date fair value of a warrant to purchase 150,000 restricted shares of our common stock
granted to each of our current independent directors on March 3, 2013, computed in accordance with the Financial Accounting Standards
Board’s Accounting Standards Codification Topic 718, Compensation – Stock Compensation (" ASC 718”). We used the Black Scholes
Option Pricing Model and the assumptions identified in footnote 5 to the Summary Compensation Table earlier in this Item 11 to
determine the $0.53 per share grant date fair value of the warrant awards. The amounts in this column, therefore, do not represent cash
payments actually received by Mr. Saxe or Dr. Underdown with respect to the warrants awarded during the fiscal year. To date, Mr.
Saxe and Dr. Underdown have not exercised such warrants, and there can be no assurance that either of them will ever realize any of the
ASC 718 grant date fair value amounts presented.
Mr. Saxe has served as the Chairman of our Board of Directors and the Chairman of our Audit Committee throughout our fiscal year
ended March 31, 2013. At March 31, 2013, Mr. Saxe holds: (i) 37,492 restricted shares of our common stock; (ii) options to purchase
264,750 restricted shares of our common stock, of which options to purchase 238,708 restricted shares are vested; and (iii) warrants to
purchase 200,000 restricted shares of our common stock, of which 50,000 are exercisable.
Mr. Bonfiglio served as a member of our Board of Directors and a member of our Audit Committee until his resignation on January 6,
2013. At March 31, 2013, Mr. Bonfiglio owned vested options to purchase 175,833 restricted shares of our common stock, all of which
expired on April 6, 2013 as a result of his resignation from the Board of Directors to pursue his venture capital duties on a full-time
basis. Mr. Bonfiglio also holds a currently exercisable warrant to purchase 50,000 restricted shares of our common stock.
Dr. Underdown has served as a member of our Board of Directors and a member of our Audit Committee throughout our fiscal year
ended March 31, 2013. At March 31, 2013, Dr. Underdown holds: (i) options to purchase 185,000 restricted shares of our common
stock, of which options to purchase 158,958 restricted shares are vested; and (ii) warrants to purchase 200,000 restricted shares of our
common stock, of which 50,000 are exercisable.
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Director Independence
Our securities are not currently listed on a national securities exchange or on any inter-dealer quotation system which has a requirement that
directors be independent. We evaluate independence by the standards for director independence established by applicable laws, rules, and listing
standards, including, without limitation, the standards for independent directors established by the New York Stock Exchange, Inc., the
NASDAQ OMX, and the SEC.
Subject to some exceptions, these standards generally provide that a director will not be independent if (a) the director is, or in the past three
years has been, an employee of ours; (b) a member of the director’s immediate family is, or in the past three years has been, an executive officer
of ours; (c) the director or a member of the director’s immediate family has received more than $120,000 per year in direct compensation from
us other than for service as a director (or for a family member, as a non-executive employee); (d) the director or a member of the director’s
immediate family is, or in the past three years has been, employed in a professional capacity by our independent public accountants, or has
worked for such firm in any capacity on our audit; (e) the director or a member of the director’s immediate family is, or in the past three years
has been, employed as an executive officer of a company where one of our executive officers serves on the compensation committee; or (f) the
director or a member of the director’s immediate family is an executive officer of a company that makes payments to, or receives payments from,
us in an amount which, in any twelve-month period during the past three years, exceeds the greater of $1,000,000 or two percent of that other
company’s consolidated gross revenues.
Jon S. Saxe and Brian J. Underdown, Ph.D. each qualify as an independent director under the qualification standards noted above.
Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters.
The following table sets forth the beneficial ownership of our Common Stock as of July 12, 2013 by the following individuals or entities: (i)
each stockholder known to us to beneficially own more than 5% of the outstanding shares of our common stock; (ii) the Chief Executive
Officer, any person serving as Chief Financial Officer during our fiscal year ended March 31, 2013, and the two most highly compensated
executive officers other than the Chief Executive Officer and Chief Financial Officer who were serving as an executive officer as of March 31,
2013 (collectively, the “Named Executive Officers”); (iii) each director; and (iv) current executive officers and directors, as a group.
Beneficial ownership is determined in accordance with Securities and Exchange Commission (“SEC”) rules and includes voting and investment
power with respect to the shares. Under such rules, beneficial ownership includes any shares as to which the individual has sole or shared voting
power or investment power and also any shares which the individual has the right to acquire currently or within 60 days after July 12, 2013
through the exercise of any stock options or other rights, including upon the exercise of warrants to purchase shares of common stock and the
conversion of preferred stock into common stock. Such shares are deemed outstanding for computing the percentage ownership of the person
holding such options or rights, but are not deemed outstanding for computing the percentage ownership of any other person. As of July 12, 2013,
there were 21,265,967 shares of our common stock issued and outstanding.
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Unless otherwise indicated in the footnotes below, we believe that the individuals and entities named in the table have sole voting and
investment powers with respect to all shares shown as beneficially owned by them.
Name and Address
Number of Shares (1)
Percent of Class
Shawn K. Singh, JD (2)
Chief Executive Officer and Director
384 Oyster Point Blvd., No. 8
South San Francisco, CA 94080
H. Ralph Snodgrass, Ph.D. (3)
President, Chief Scientific Officer and Director
384 Oyster Point Blvd., No. 8
South San Francisco, CA 94080
Jerrold D. Dotson (4)
Principal Financial and Accounting Officer
384 Oyster Point Blvd., No. 8
South San Francisco, CA 94080
Jon S. Saxe (5)
Chairman of the Board of Directors
384 Oyster Point Blvd., No. 8
South San Francisco, CA 94080
Brian J. Underdown, Ph.D. (6)
Director
384 Oyster Point Blvd., No. 8
South San Francisco, CA 94080
Cato BioVentures (7)
4364 South Alston Avenue
Durham, NC 27713
Platinum Long Term Growth Fund VII, LLC (8)
152 W 57 St 54th Floor
New York, NY 10019
Morrison & Foerster LLP (9)
555 Market Street
San Francisco, CA 94105
University Health Network (10)
101 College St. Ste. 150
Toronto ON, Canada M5G 1L7
All Officers and Directors as a Group
(7 persons) (11)
* Less than one percent (1%)
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2,834,059
11.91%
2,244,163
10.06%
159,418
*
406,408
1.88%
289,166
1.34%
4,625,690
20.49%
929,412
2,090,256
1,717,251
4.37%
9.03%
7.86%
5,933,214
23.13%
Table of Contents
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
This table is based upon information supplied by officers, directors and principal stockholders and Forms 3, Forms 4, and Schedule
13G filed with the Securities and Exchange Commission. Unless otherwise indicated in the footnotes to this table and subject to
community property laws where applicable, we believe that each of the stockholders named in this table has sole voting and
investment power with respect to the shares indicated as beneficially owned. Applicable percentages are based on 21,265,967 shares
of common stock outstanding on July 12, 2013.
Includes options to purchase 1,665,833 restricted shares of common stock exercisable within 60 days of July 12, 2013 and currently
exercisable warrants to purchase 866,052 restricted shares of common stock.
Includes options to purchase 539,695 restricted shares of common stock exercisable within 60 days of July 12, 2013 and currently
exercisable warrants to purchase 500,000 restricted shares of common stock.
Includes options to purchase 59,418 restricted shares of common stock exercisable within 60 days of July 12, 2013, including options
to purchase 9,853 restricted shares of common stock held by Mr. Dotson’s wife, and currently exercisable warrants to purchase
100,000 restricted shares of common stock.
Includes options to purchase 243,916 restricted shares of common stock exercisable within 60 days of July 12, 2013 and currently
exercisable warrants to purchase 125,000 restricted shares of common stock.
Includes options to purchase 164,166 restricted shares of common stock exercisable within 60 days of July 12, 2013 and currently
exercisable warrants to purchase 125,000 restricted shares of common stock.
Based upon information contained in Form 4 filed on January 9, 2012. Includes currently exercisable warrants to purchase 1,314,854
restricted shares of common stock. Dr. Allen E. Cato, Ph.D., M.D. is deemed to have voting and investment authority over the shares
held by Cato Holding Company.
Based upon information contained in Schedule 13G/A filed on February 15, 2013 reporting transactions through December 31, 2012,
updated for transactions with Platinum occurring thereafter through July 12, 2013. The number of shares beneficially owned at July
12, 2013 includes 929,412 restricted shares of common stock owned by Platinum.
The number of shares beneficially owned excludes 15,000,000 restricted shares of common stock and a warrant to purchase 7,500,000
restricted shares of common stock that may currently be acquired by Platinum upon exchange of 500,000 restricted shares of our
Series A Preferred Stock. Pursuant to that October 11, 2012 Note Exchange and Purchase Agreement by and between the Company
and Platinum, there is a limitation on exchange such that the number of shares of common stock that may be acquired by Platinum
upon exchange of the Series A Preferred Stock is limited to the extent necessary to ensure that, following such exchange, the total
number of shares of common stock then beneficially owned by Platinum does not exceed 9.99% of the total number of our issued and
outstanding shares of common stock without providing us with 61 days’ prior notice thereof.
Further, the number of shares beneficially owned also excludes 10,243,639 restricted shares of Common Stock that may be acquired
by Platinum upon conversion of various Senior Secured Convertible Promissory Notes in the aggregate face amount of $3,272,577
(the “Convertible Notes”) plus accrued but unpaid interest or exercise of various common stock purchase warrants to purchase an
aggregate of 3,272,577 restricted shares of common stock. Pursuant to the terms of the respective Convertible Notes and common
stock purchase warrant agreements, there is a limitation on conversion of the Convertible Notes and exercise of the warrants such that
the number of shares of common stock that Platinum may acquire upon such conversion or exercise is limited to the extent necessary
to ensure that, following such conversion or exercise, the total number of shares of common stock then beneficially owned by
Platinum does not exceed 4.99% or 9.99% of the total number of issued and outstanding shares of our common stock without
providing us with 61 days’ prior notice thereof.
(9)
Includes currently exercisable warrants to purchase 1,890,256 restricted shares of common stock.
(10)
Includes currently exercisable warrants to purchase 579,196 restricted shares of common stock.
(11)
Includes options to purchase an aggregate of 2,673,028 restricted shares of common stock exercisable within 60 days of July 12, 2013,
and currently exercisable warrants to purchase an aggregate of 1,716,052 restricted shares of common stock.
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Securities Authorized for Issuance Under Equity Compensation Plans
Equity Grants
As of March 31, 2013, options to purchase a total of 4,912,604 restricted shares of our common stock are outstanding at a weighted average
exercise price of $1.32 per share, of which 4,227,436 options are vested and exercisable at a weighted average exercise price of $1.35 per share
and 685,168 are unvested and unexercisable at a weighted average exercise price of $1.12 per share. These options were issued under our 2008
Plan, which has been approved by our stockholders, and under our 1999 Plan, which has now expired, but was not approved by our
stockholders. An additional 257,867 shares remain available for future equity grants under our 2008 Plan.
Number of securities
to be issued upon
exercise of
outstanding options,
warrants and rights
(a)
Weighted-average
exercise price of
outstanding
options, warrants
and rights
(b)
Number of securities
remaining available
for future issuance
under equity
compensation plans
(excluding securities
reflected in column
(a))
(c)
4,442,133 $
470,471
4,912,604 $
1.33
1.21
1.32
257,687
--
257,687
Plan category
Equity compensation plans approved by security holders
Equity compensation plans not approved by security holders
Total
1999 Stock Incentive Plan
VistaGen California’s Board of Directors adopted the 1999 Plan on December 6, 1999. The 1999 Plan has terminated under its own terms, and
as a result, no awards may currently be granted under the 1999 Plan. However, the options and awards that have already been granted pursuant to
the 1999 Plan remain operative.
The 1999 Plan permitted VistaGen California to make grants of incentive stock options, non-qualified stock options and restricted stock awards.
VistaGen California initially reserved 450,000 shares of its common stock for the issuance of awards under the 1999 Plan, which number was
subject to adjustment in the event of a stock split, stock dividend or other change in our capitalization. Generally, shares that were forfeited or
cancelled from awards under the 1999 Plan also were available for future awards.
The 1999 Plan could be administered by either VistaGen California’s Board of Directors or a committee designated by its Board of Directors.
VistaGen California’s Board of Directors designated its Compensation Committee as the committee with full power and authority to select the
participants to whom awards were granted, to make any combination of awards to participants, to accelerate the exercisability or vesting of any
award and to determine the specific terms and conditions of each award, subject to the provisions of the 1999 Plan. All directors, executive
officers, and certain other key persons (including employees, consultants and advisors) of VistaGen California were eligible to participate in the
1999 Plan.
The exercise price of incentive stock options awarded under the 1999 Plan could not be less than the fair market value of the common stock on
the date of the option grant and could not be less than 110% of the fair market value of the common stock to persons owning stock representing
more than 10% of the voting power of all classes of our stock. The exercise price of non-qualified stock options could not be less than 85% of
the fair market value of the common stock. The term of each option granted under the 1999 Plan could not exceed ten years (or five years, in the
case of an incentive stock option granted to a 10% shareholder) from the date of grant. VistaGen California’s Compensation Committee
determined at what time or times each option might be exercised (provided that in no event could it exceed ten years from the date of grant) and,
subject to the provisions of the 1999 Plan, the period of time, if any, after retirement, death, disability or other termination of employment during
which options could be exercised.
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The 1999 Plan also permitted the issuance of restricted stock awards. Restricted stock awards issued by VistaGen California were shares of
common stock that vest in accordance with terms and conditions established by VistaGen California’s Compensation Committee. The
Compensation Committee could impose conditions to vesting that it determined to be appropriate. Shares of restricted stock that did not vest
were subject to our right of repurchase or forfeiture. VistaGen California’s Compensation Committee determined the number of shares of
restricted stock granted to any employee. Our 1999 Plan also gave VistaGen California’s Compensation Committee discretion to grant stock
awards free of any restrictions.
Unless the Compensation Committee provided otherwise, the 1999 Plan did not generally allow for the transfer of incentive stock options and
other awards and only the recipient of an award could exercise an award during his or her lifetime. Non-qualified stock options were transferable
only to the extent provided in the award agreement, in a manner consistent with the applicable law, and by will and by the laws of descent and
distribution. In the event of a change in control of the Company, as defined in the 1999 Plan, the outstanding options will automatically vest
unless our Board of Directors and the Board of Directors of the surviving or acquiring entity make appropriate provisions for the continuation or
assumption of any outstanding awards under the 1999 Plan.
As of March 31, 2013, we have options outstanding under the 1999 Plan to purchase an aggregate of 470,471 restricted shares of our common
stock.
Item 13. Certain Relationships and Related Transactions, and Director Independence.
Cato Holding Company (“CHC”), doing business as Cato BioVentures (" CBV"), the parent of Cato Research Ltd. (“CRL”), is one of our largest
institutional stockholders at March 31, 2013, holding common stock and warrants to purchase common stock. Prior to the May 11, 2011
conversion of certain of VistaGen California’s outstanding promissory notes and the conversion of VistaGen California’s preferred stock into
shares of our common stock, CBV held various promissory notes and a majority of VistaGen California’s Series B-1 Preferred Stock. Shawn
Singh, our Chief Executive Officer and member of our Board of Directors, served as Managing Principal of CBV and as an officer of CRL until
August 2009. In April 2011, CBV loaned VistaGen California $352,273 under the terms of a promissory note (the “ 2011 CHC Note ”). On
October 10, 2012, we agreed with CHC to cancel the 2011 CHC Note and exchange it for a new unsecured promissory note in the principal
amount of $310,443 (the “2012 CHC Note”) and a five-year warrant to purchase 250,000 shares of our common stock at a price of $1.50 per
share (the “CHC Warrant ”). Additionally, on October 10, 2012, we issued to CRL: (i) an unsecured promissory note in the initial principal
amount of $1,009,000, which is payable solely in restricted shares of the Company’s common stock and which accrues interest at the rate of
7.5% per annum, compounded monthly (the “CRL Note”), as payment in full for all contract research and development services and regulatory
advice rendered by CRL to us and our affiliates through December 31, 2012 with respect to the preclinical and clinical development of AV-101,
and (ii) a five-year warrant to purchase, at a price of $1.00 per share, 1,009,000 restricted shares of our common stock.
During fiscal year 2007, VistaGen California entered into a contract research organization arrangement with CRL related to the development of
AV-101, under which we Company incurred expenses of $703,800 and $1,461,300 for the fiscal years ended March 31, 2013 and 2012,
respectively, a substantial portion of which were reimbursed under the NIH grant. Total interest expense on notes payable to CHC and CRL was
$101,700 and $93,100 for the fiscal years ended March 31, 2013 and 2012, respectively, with the majority of amounts reported for periods prior
to May 2011 having been converted to equity. On April 29, 2011, VistaGen California issued 157,143 restricted shares of common stock, valued
at $1.75 per share, as prepayment for research and development services to be performed by CRL during 2011. In December 2011, we entered
into an Agreement Regarding Payment of Invoices and Warrant Exercises with CHC, CRL and certain CHC affiliates pursuant to which CHC
and the CHC Affiliates exercised warrants at discounted exercise prices to purchase an aggregate of 492,541 restricted shares of our common
stock and we received $60,200 cash, and, in lieu of cash payment for certain of the warrant exercises, settled outstanding liabilities of $245,300
for past services received from CRL and prepaid $226,400 for future services to be received from CRL, which services had been fully received
by March 31, 2012.
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Prior to his appointment as one of VistaGen California’s officers (on a part-time basis) and directors, in April 2003, VistaGen California retained
Mr. Singh as a consultant to provide legal and other consulting services. During the course of the consultancy, as payment for his services,
VistaGen California issued him warrants to purchase 55,898 restricted shares of common stock at $0.80 per share and a 7% promissory note in
the principal amount of $26,400. On May 11, 2011, and concurrent with the Merger, the Company paid the outstanding balance of principal and
accrued interest totaling $36,000. Upon the approval by the Board of Directors, in December 2006, VistaGen California accepted a full-recourse
promissory note in the amount of $103,400 from Mr. Singh in payment of the exercise price for options and warrants to purchase an aggregate of
126,389 shares of VistaGen California’s common stock. The note accrued interest at a rate of 4.90% per annum and was due and payable no later
than the earlier of (i) December 1, 2016 or (ii) ten days prior to the Company becoming subject to the requirements of the Securities Exchange
Act of 1934, as amended (“Exchange Act”). On May 11, 2011, in connection with the Merger, the $128,200 outstanding balance of the principal
and accrued interest on this note was cancelled in accordance with Mr. Singh's employment agreement and recorded as additional compensation.
In accordance with his employment agreement, Mr. Singh is also entitled to an income tax gross-up on the compensation related to the note
cancellation. At March 31, 2012 and 2013, the Company had accrued $101,900 as an estimate of the gross-up amount payable to Mr. Singh, but
had not yet paid it to Mr. Singh.
In March 2007, VistaGen California accepted a full recourse promissory note in the amount of $46,360 from Franklin Rice, its former Chief
Financial Officer and a former director of VistaGen California in exchange for his exercise of options to purchase 52,681 restricted shares of
VistaGen California’s common stock. The note accrued interest at a rate of 4.90% per annum and was due and payable no later than the earlier
of (i) March 1, 2017 or (ii) ten days prior to VistaGen California becoming subject to the requirements of the Exchange Act. On May 11, 2011,
in connection with the Merger, the $57,000 outstanding balance of principal and accrued interest on this note was cancelled in accordance with
Mr. Rice's employment agreement and recorded as additional compensation. In accordance with his employment agreement, Mr. Rice is entitled
to an income tax gross-up on the compensation related to the note cancellation. At March 31, 2012 and 2013, we had accrued $33,900 as an
estimate of the gross-up amount, but had not paid it to Mr. Rice.
VistaGen California previously engaged Jon A. Saxe, a current director, separately from his duties as a director, as a management consultant
from July 1, 2000 through June 30, 2010 to provide strategic and other business advisory services. As payment for consulting services rendered
through June 30, 2010, Mr. Saxe has been issued warrants and non-qualified options to purchase an aggregate of 250,815 shares of the
Company’s common stock, of which he has exercised warrants to purchase for 18,568 shares. Additionally, Mr. Saxe was issued a 7%
promissory note in the amount of $8,000. On May 11, 2011, the $14,400 balance of the note and related accrued interest plus a note
cancellation premium of $5,100 was converted to 11,142 shares of the Company’s common stock and a three-year warrant to purchase 2,784
shares of common stock at an exercise price of $2.50 per share. In lieu of cash payment from the Company, in December 2011, Mr. Saxe
exercised the warrant as a part of the Discounted Warrant Exercise Program at an exercise price of $1.25 per share in satisfaction for amounts
owed to him in conjunction with his service as a member of the Board of Directors.
Director Independence
Our securities are not currently listed on a national securities exchange or on any inter-dealer quotation system which has a requirement that
directors be independent. We evaluate independence by the standards for director independence established by applicable laws, rules, and listing
standards, including, without limitation, the standards for independent directors established by the New York Stock Exchange, Inc., the
NASDAQ OMX, and the SEC.
Subject to some exceptions, these standards generally provide that a director will not be independent if (a) the director is, or in the past three
years has been, an employee of ours; (b) a member of the director’s immediate family is, or in the past three years has been, an executive officer
of ours; (c) the director or a member of the director’s immediate family has received more than $120,000 per year in direct compensation from
us other than for service as a director (or for a family member, as a non-executive employee); (d) the director or a member of the director’s
immediate family is, or in the past three years has been, employed in a professional capacity by our independent public accountants, or has
worked for such firm in any capacity on our audit; (e) the director or a member of the director’s immediate family is, or in the past three years
has been, employed as an executive officer of a company where one of our executive officers serves on the compensation committee; or (f) the
director or a member of the director’s immediate family is an executive officer of a company that makes payments to, or receives payments from,
us in an amount which, in any twelve-month period during the past three years, exceeds the greater of $1,000,000 or two percent of that other
company’s consolidated gross revenues.
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Table of Contents
Jon S. Saxe and Brian J. Underdown each qualify as an independent director in accordance with the qualification standards noted above.
Item 14. Principal Accounting Fees and Services.
Fees and Services
OUM & Co. LLP (“OUM”) served as our independent registered public accounting firm for the fiscal years ended March 31, 2013 and March
31, 2012. Information provided below includes fees for professional services provided to us by OUM for the fiscal years ended March 31, 2013
and 2012.
Audit fees
Audit-related fees
Tax fees
All other fees
Total fees
Audit Fees:
Fiscal Years Ended March 31,
2013
2012
$
$
$
167,500
-
18,747
-
152,500
-
15,000
-
186,247
$
167,500
Audit fees include fees billed for the annual audit of the Company’s financial statements and quarterly reviews for the fiscal years ended March
31, 2013 and 2012, and for services normally provided by OUM in connection with routine statutory and regulatory filings or engagements.
Audit-Related Fees:
Audit- related fees includes fees billed for assurance and related services that are reasonably related to the performance of the annual audit or
reviews of the Company’s financial statements and are not reported under “Audit Fees.” During the fiscal years ended March 31, 2013 or 2012,
no such fees were billed by OUM.
Tax Fees:
Tax fees include fees for professional services for tax compliance, tax advice and tax planning for the tax years ended March 31, 2013 and 2012.
All Other Fees:
All other fees include fees for products and services other than those described above. During the fiscal years ended March 31, 2013 and 2012,
no such fees were billed by OUM.
Pre-Approval of Audit and Non-Audit Services
All auditing services and non-audit services provided to us by our independent registered public accounting firm are required to be pre-approved
by the Audit Committee. OUM did not provide any audit-related or other services in fiscal 2013 and 2012. The pre-approval of non-audit
services to be provided by OUM includes making a determination that the provision of the services is compatible with maintaining the
independence of OUM as an independent registered public accounting firm and would be approved in accordance with SEC rules for
maintaining auditor independence. None of the fees outlined above were approved using the “de minimis exception” under SEC rules.
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Table of Contents
Report of the Audit Committee of the Board of Directors
The Audit Committee has reviewed and discussed with management and OUM & Co. LLP (“OUM”), our independent registered public
accounting firm, the audited consolidated financial statements in the VistaGen Therapeutics, Inc. Annual Report on Form 10-K for the year
ended March 31, 2013. The Audit Committee has also discussed with OUM those matters required to be discussed by the statement on Auditing
Standards No. 61, as amended (AICPA, Professional Standard, Vol. 1. AU section 380), as adopted by the Public Company Accounting
Oversight Board (the “PCAOB”) in Rule 3200T.
OUM also provided the Audit Committee with the written disclosures and the letter required by the applicable requirements of the PCAOB
regarding the independent auditor’s communication with the Audit Committee concerning independence. The Audit Committee has discussed
with the registered public accounting firm their independence from our company.
Based on its discussions with management and the registered public accounting firm, and its review of the representations and information
provided by management and the registered public accounting firm, including as set forth above, the Audit Committee recommended to our
board of directors that the audited financial statements be included in our Annual Report on Form 10-K for the year ended March 31, 2013.
Respectfully Submitted by:
MEMBERS OF THE AUDIT COMMITTEE
Jon S. Saxe, Audit Committee Chairman
Brian J. Underdown
Dated: July 17, 2013
The information contained above under the caption “Report of the Audit Committee of the Board of Directors” shall not be deemed to be
soliciting material or to be filed with the SEC, nor shall such information be incorporated by reference into any future filing under the Securities
Act of 1933, as amended, or the Securities Exchange Act, as amended, except to the extent that we specifically incorporate it by reference into
such filing.
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Table of Contents
PART IV
Item 15. Exhibits, Financial Statement Schedules
(a)(1) Financial Statements
See Index to Financial Statements under Item 8 on page 57.
(a)(2) Consolidated Financial Statement Schedules
Consolidated financial statement schedules are omitted because they are not applicable or are not required or the information required to be set
forth therein is included in the Consolidated Financial Statements or notes thereto.
(a)(3) Exhibits
The exhibits listed in the Exhibit Index below are filed or incorporated by reference as part of this report.
Exhibit Index
Exhibit No.
2.1 *
3.1 *
3.2
3.3
3.4 *
3.5
4.1 *
10.1 *
10.2 *
10.3 *
10.4 *
10.5 *
10.6 *
10.7 *
10.8 *
10.9 *
10.10 *
10.11 *
10.12 *
10.18 *
10.19 *
10.20 *
10.21 *
10.22 *
10.23 *
10.24 *
10.25 *
10.26 *
10.27 *
10.28 *
10.29 *
Description*
Agreement and Plan of Merger by and among Excaliber Enterprises, Ltd., VistaGen Therapeutics, Inc. and Excaliber Merger
Subsidiary, Inc.
Articles of Incorporation in effect as of May 11, 2011.
Articles of Merger filed with the Nevada Secretary of State on May 24, 2011.
Certificate of Amendment filed with the Nevada Secretary of State on December 6, 2011.
Bylaws in effect.as of May 11, 2011, incorporated by reference from the document filed as Exhibit 3.2 in the Company’s
Current Report on Form 8-K filed on May 16, 2011.
Certificate of Designations Series A Preferred, incorporated by reference from the Company’s Current Report on Form 8-
K/A filed on December 22, 2011.
Fourth Amended and Restated Investors’ Rights Agreement, dated August 1, 2005, by and among VistaGen and certain
(former) holders of Preferred Stock of VistaGen, as amended by that certain Amendment No. 1 to Fourth Amended and
Restated Investors’ Rights Agreement, dated July 10, 2010.
VistaGen’s 1999 Stock Incentive Plan.
Form of Option Agreement under VistaGen’s 1999 Stock Incentive Plan.
VistaGen’s Scientific Advisory Board 1998 Stock Incentive Plan.
Form of Option Agreement under VistaGen’s Scientific Advisory Board 1998 Stock Incentive Plan.
VistaGen’s 2008 Stock Incentive Plan.
Form of Option Agreement under VistaGen’s 2008 Stock Incentive Plan.
Securities Purchase Agreement, dated October 30, 2009, by and between VistaGen and Cato BioVentures.
Securities Purchase Agreement, dated April 27, 2011, by and between VistaGen and Cato BioVentures.
Securities Purchase Agreement, dated November 5, 2009, by and between VistaGen and Platinum Long Term Growth Fund.
Securities Purchase Agreement, dated December 2, 2009, by and between VistaGen and University Health Network.
Securities Purchase Agreement, dated April 25, 2011, by and between VistaGen and University Health Network.
Form of Subscription Agreement, dated May 11, 2011, by and between VistaGen and certain investors.
Industrial Lease, dated March 5, 2007, by and between Oyster Point LLC and VistaGen, as amended by that certain First
Amendment to Lease, dated as of April 24, 2009, and as further amended by that certain Second Amendment to Lease, dated
as of October 19, 2010 and that certain Third Amendment to Lease, dated as of April 1, 2011.
Clinical Study Agreement, dated April 15, 2010, by and between VistaGen and Progressive Medical Concepts, LLC.
Strategic Development Services Agreement, dated February 26, 2007, by and between VistaGen and Cato Research Ltd.
License Agreement by and between National Jewish Medical and Research Center and VistaGen, dated July 12, 1999, as
amended by that certain Amendment to License Agreement dated January 25, 2001, as amended by that certain Second
Amendment to License Agreement dated November 6, 2002, as amended by that certain Third Amendment to License
Agreement dated March 1, 2003, and as amended by that certain Fourth Amendment to License Agreement dated April 15,
2010.
License Agreement by and between Mount Sinai School of Medicine of New York University and the Company, dated
October 1, 2004.
Non-Exclusive License Agreement, dated December 5, 2008, by and between VistaGen and Wisconsin Alumni Research
Foundation, as amended by that certain Wisconsin Materials Addendum, dated February 2, 2009.
Sponsored Research Collaboration Agreement, dated September 18, 2007, between VistaGen and University Health Network,
as amended by that certain Amendment No. 1, Amendment No. 2 and Amendment No. 3 dated April 19, 2010, December 15,
2010 and April, 25, 2011, respectively.
Letter Agreement, dated Feb 12, 2010, by and between VistaGen and The Regents of the University of California.
License Agreement, dated October 24, 2001, by and between the University of Maryland, Baltimore, Cornell Research
Foundation and Artemis Neuroscience, Inc.
Non-exclusive License Agreement, dated September 1, 2010, by and between VistaGen and TET Systems GmbH & Co. KG.
Amended and Restated Senior Convertible Promissory Bridge Note dated June 19, 2007 issued by VistaGen to Platinum Long
Term Growth VII, LLC.
Second Amended and Restated Letter Loan Agreement dated May 16, 2008, by and between VistaGen and Platinum Long
Term Growth VII, LLC, as amended by that certain Amendment No. 1 to Second Amended and Restated Letter Loan
Agreement dated October 16 2009, as further amended by that certain Amendment to Letter Loan Agreement dated May 5,
2011.
10.30 *
Promissory Note dated April 29, 2011 issued by VistaGen to Cato Holding Company.
10.31 *
10.32 *
10.33 *
10.34 *
10.35 *
10.36 *
10.37 *
10.38 *
10.39 *
10.40 *
10.41 *
10.42 *
10.43 *
10.44 *
10.45 *
10.46
10.47
10.48
10.49
10.50
10.51
10.52
10.53
10.54
10.55
10.56
10.57
10.58
10.59
10.60
10.61
10.62
10.63
10.64
Unsecured Promissory Note dated April 28, 2011 issued by VistaGen to Desjardins Securities.
Unsecured Promissory Note dated April 28, 2011 issued by VistaGen to McCarthy Tetrault LLP.
Unsecured Promissory Note dated April 28, 2011 issued by VistaGen to Morrison & Foerster LLP
Promissory Note dated February 25, 2010 issued by VistaGen to The Regents of the University of California.
Note and Warrant Purchase Agreement dated August 4, 2010, by and between VistaGen and certain investors, as amended by
that certain Amendment No. 1 to Note and Warrant Purchase Agreement, dated November 10, 2010.
Conversion Agreement, dated April 29, 2011, by and among VistaGen and certain holders of unsecured promissory notes
issued pursuant to that certain Note and Warrant Purchase Agreement, dated August 4, 2010, by and between VistaGen and
such note holders.
Agreement regarding Conversion of Unsecured Promissory Note, dated April 29, 2011, by and between VistaGen and The
Dillon Family Trust.
Senior Note and Warrant Purchase Agreement dated August 13, 2006, by and between VistaGen and certain investors, as
amended by that certain Amendment No. 1 to Senior Convertible Bridge Note and Warrant Purchase Agreement dated
January 31, 2007, as further amended by that certain Amendment No. 2 to Senior Convertible Bridge Note and Warrant
Purchase Agreement dated June 11, 2007, as further amended by that certain Omnibus Amendment dated April 28, 2011
Senior Note and Warrant Purchase Agreement dated May 16, 2008, by and between VistaGen and certain investors, as
amended by that certain Amendment No. 1 to Senior Convertible Bridge Note and Warrant Purchase Agreement dated
November 2, 2009, as further amended by that certain Omnibus Amendment dated April 28, 2011.
Employment Agreement, by and between, VistaGen and Shawn K. Singh, dated April 28, 2010, as amended May 9, 2011.
Employment Agreement, by and between, VistaGen and H. Ralph Snodgrass, PhD, dated April 28, 2010, as amended May 9,
2011.
Employment Agreement, by and between VistaGen and A. Franklin Rice, dated April 28, 2010, as amended May 9, 2011.
Agreement regarding sale of shares of common stock dated May 9, 2011 by and between Excaliber and Stephanie Y. Jones,
whereby Excaliber purchased from Mrs. Jones 4,982,103 shares of Excaliber common stock for $10.
Agreement regarding sale of shares of common stock dated May 9, 2011 by and between Excaliber and Nicole Jones,
whereby Excaliber purchased from Nicole Jones 82,104 shares of Excaliber common stock for $10.
Joinder Agreement dated May 11, 2011 by and between Excaliber, Platinum Long Term Growth VII, LLC and VistaGen
Notice of Award by National Institutes of Health, Small Business Innovation Research Program, to VistaGen Therapeutics,
Inc. for project, Clinical Development of 4-CI-KYN to Treat Pain dated June 22, 2009, with revisions dated July 19, 2010 and
August 9, 2011, incorporated by reference from the Company’s Current Report on Form 8-K/A filed on December 20, 2011.
Notice of Grant Award by California Institute of Regenerative Medicine and VistaGen Therapeutics, Inc. for
Project: Development of an hES Cell-Based Assay System for Hepatocyte Differentiation Studies and Predictive Toxicology
Drug Screening, dated April 1, 2009, incorporated by reference from the Company’s Current Report on Form 8-K/A filed on
December 20, 2011.
Amendment No. 4, dated October 24, 2011, to Sponsored Research Collaboration Agreement between VistaGen and
University Health Network, incorporated by reference from the Company’s Current Report on Form 8-K/A filed on
November 30, 2011.
License Agreement No. 1, dated as of October 24, 2011 between University Health Network and VistaGen Therapeutics, Inc.,
incorporated by reference from the Company’s Current Report on Form 8-K/A filed on November 30, 2011.
Strategic Medicinal Chemistry Services Agreement, dated as of December 6, 2011, between Synterys, Inc. and VistaGen
Therapeutics, Inc., incorporated by reference from the Company’s Current Report on Form 8-K/A filed on December 7, 2011.
Common Stock Exchange Agreement, dated as of December 22, 2011 between Platinum Long Term Growth VII, LLC and
VistaGen Therapeutics, Inc., incorporated by reference from the Company’s Current Report on Form 8-K/A filed on
December 23, 2011.
Note and Warrant Exchange Agreement, dated as of December 28, 2011 between Platinum Long Term Growth VII, LLC and
VistaGen Therapeutics, Inc., incorporated by reference from the Current Report on Form 8-K/A filed on January 4, 2012.
Form of Convertible Note and Warrant Purchase Agreement, dated as of February 28, 2012, by and between VistaGen
Therapeutics, Inc. and certain investors, incorporated by reference from the Current Report on Form 8-K/A filed on March 2,
2012.
Form of Convertible Promissory Note, dated as of February 28, 2012, incorporated by reference from the Company’s Current
Report on Form 8-K/A filed on March 2, 2012.
Form of Warrant to Purchase Common Stock, dated as of February 28, 2012, incorporated by reference from the Company’s
Current Report on Form 8-K/A filed on March 2, 2012.
Form of Registration Rights Agreement, dated as of February 28, 2012, by and between VistaGen and certain investors,
incorporated by reference from the Company’s Current Report on Form 8-K/A filed on March 2, 2012.
License Agreement No. 2, dated as of March 19, 2012 between University Health Network and VistaGen Therapeutics, Inc. ,
incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Exchange Agreement dated as of June 29, 2012 between Platinum Long Term Growth VII, LLC and VistaGen Therapeutics.
Inc., incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Secured Convertible Promissory Note, Dated as of July 2, 2012, issued to Platinum Long Term Growth VII, LLC.,
incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Security Agreement between Platinum Long Term Growth VII, LLC and VistaGen Therapeutics. Inc., dated as of July 2,
2012, incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Secured Convertible Promissory Note, Dated as of August 30, 2012, issued to Platinum Long Term Growth VII, LLC.,
incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6, 2012.
Amendment to Security Agreement between Platinum Long Term Growth VII, LLC and VistaGen Therapeutics. Inc.as of
August 30, 2012, incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6, 2012.
Unsecured Promissory Note in the face amount of $1,000,000 issued to Morrison & Foerster LLP on August 31, 2012
(Replacement Note A), incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6,
2012.
Unsecured Promissory Note in the face amount of $1,379,376 issued to Morrison & Foerster LLP on August 31, 2012
(Replacement Note B), incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6,
2012.
10.77
10.76
10.74
10.73
10.72
10.71
10.70
10.69
10.68
10.66
10.67
10.75
10.65
Stock Purchase Warrant issued to Morrison & Foerster LLP on August 31, 2012 to purchase 1,379,376 shares of the
Company’s common stock (New Morrison & Foerster Warrant), incorporated by reference from the Company’s Current
Report on Form 8-K filed on September 6, 2012.
Warrant to Purchase Common Stock issued to Morrison & Foerster LLP on August 31, 2012 to purchase 425,000 shares of
the Company’s common stock (Amended Morrison & Foerster Warrant), incorporated by reference from the Company’s
Current Report on Form 8-K filed on September 6, 2012.
Note Exchange and Purchase Agreement dated as of October 11, 2012 by and between VistaGen Therapeutics, Inc. and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on
October 16, 2012.
Form of Senior Secured Convertible Promissory Note issued to Platinum Long Term Growth VII, LLP under the Note
Exchange and Purchase Agreement, incorporated by reference from the Company’s Current Report on Form 8-K filed on
October 16, 2012.
Form of Warrant to Purchase Shares of Common Stock issued to Platinum Long Term Growth VII, LLP under the Note
Exchange and Purchase Agreement, incorporated by reference from the Company’s Current Report on Form 8-K filed on
October 16, 2012.
Amended and Restated Security Agreement as of October 11, 2012 between VistaGen Therapeutics, Inc. and Platinum Long
Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on October 16,
2012.
Intellectual Property Security and Stock Pledge Agreement as of October 11, 2012 between VistaGen California and Platinum
Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on October
16, 2012.
Negative Covenant Agreement dated October 11, 2012 between VistaGen California, Artemis Neuroscience, Inc. and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on
October 16, 2012.
Amendment to Note Exchange and Purchase Agreement as of November 14, 2012 between VistaGen Therapeutics Inc. and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on
November 20, 2012.
Form of Note Exchange Agreement between VistaGen Therapeutics, Inc. and Holders of the Company’s Promissory Notes
dated February 28, 2012, incorporated by reference from the Company’s Current Report on Form 8-K filed on November 20,
2012.
Amendment No. 2 to Note Exchange and Purchase Agreement as of January 31, 2013 between VistaGen Therapeutics Inc.
and Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Quarterly Report on Form 10-Q
filed on February 14, 2013.
Amendment No. 3 to Note Exchange and Purchase Agreement as of February 22, 2013 between VistaGen Therapeutics Inc.
and Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed
on February 28, 2013.
Form of Warrant to Purchase Common Stock issued to independent members of the Company’s Board of Directors and its
executive officers on March 3, 2013, incorporated by reference from the Company’s Current Report on Form 8-K filed on
March 6, 2013.
Securities Purchase Agreement between VistaGen Therapeutics, Inc., and Autilion AG dated April 8, 2013, incorporated by
reference from the Company’s Current Report on Form 8-K filed on April 10, 2013.
Voting Agreement between VistaGen Therapeutics, Inc., and Autilion AG dated April 8, 2013, incorporated by reference
from the Company’s Current Report on Form 8-K filed on April 10, 2013.
Note Conversion Agreement as of April 4, 2013 between VistaGen Therapeutics Inc. and Platinum Long Term Growth VII,
LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on April 10, 2013.
Assignment and Assumption Agreement between Autilion AG and Bergamo Acquisition Corp. PTE LTD dated April 12,
2013.
Amendment No. 1 to Securities Purchase Agreement dated April 30, 2013 between VistaGen Therapeutics, Inc. and Bergamo
Acquisition Corp. PTE LTD, incorporated by reference from the Company’s Current Report on Form 8-K filed on May 1,
2013.
Lease between Bayside Area Development, LLC and VistaGen Therapeutics, Inc. (California) dated April 24, 2013.
Indemnification Agreement effective May 20, 2013 between the Company and Jon S. Saxe.
Indemnification Agreement effective May 20, 2013 between the Company and Shawn K. Singh
Indemnification Agreement effective May 20, 2013 between the Company and H. Ralph Snodgrass.
Indemnification Agreement effective May 20, 2013 between the Company and Brian J. Underdown.
Indemnification Agreement effective May 20, 2013 between the Company and Jerrold D. Dotson.
Amendment and Waiver effective May 24, 2013 between the Company and Platinum Long Term Growth VII, LLC,
incorporated by reference from the Company’s Current Report on Form 8-K filed on June 3, 2013.
Amendment No. 2 to Securities Purchase Agreement dated June 27, 2013 between the Company and Autilion AG and Bergamo
Acquisition Corp. PTE LTD, incorporated by reference from the Company's Current Report on Form 8-K filed on June 28,
2013.
Letter regarding change in certifying accountant
List of Subsidiaries.
Power of Attorney
Certification of the Company’s Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
Certification of the Company’s Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
Certification of the Company’s Chief Executive Officer and Chief Financial Officer pursuant to Section 906 of the Sarbanes-
Oxley Act of 2002.
101.INS **
XBRL Instance Document
101.SCH ** XBRL Taxonomy Schema
101.CAL ** XBRL Taxonomy Extension Calculation Linkbase
101.DEF ** XBRL Taxonomy Extension Definition Linkbase
101.LAB ** XBRL Taxonomy Extension Label Linkbase
101.PRE ** XBRL Taxonomy Extension Presentation Linkbase
10.83
10.84
10.85
10.86
10.87
10.88
10.89
16.1*
21.1*
24.1
31.1
31.2
32.1
10.79
10.78
10.80
10.81
10.82
10.90
* Incorporated by reference from the like-numbered exhibit filed with our Current Report on Form 8-K on May 16, 2011.
** Pursuant to Rule 406T of Regulation S-T, these interactive files are deemed not filed or part of a registration statement or prospectus for
purposes of Sections 11 or 12 of the Securities Act of 1933 or Section 18 of the Securities Exchange Act of 1934 and otherwise are not subject
to liability.
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Table of Contents
SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be
signed on its behalf by the undersigned, thereunto duly authorized, in the City of South San Francisco, State of California, on the 18th day of
July, 2013.
VistaGen Therapeutics, Inc.
By:
/s/ Shawn K. Singh
Shawn K. Singh, J.D.
Chief Executive Officer
POWER OF ATTORNEY
KNOW ALL PERSONS BY THESE PRESENTS , that each person whose signature appears below constitutes and appoints each of Shawn
K. Singh, J.D. and Jerrold D. Dotson his true and lawful attorney-in-fact and agent, with full power of substitution, for him and in his name,
place and stead, in any and all capacities, to sign any and all amendments to this annual report on Form 10-K, and to file the same, with all
exhibits thereto, and other documents in connection therewith, with the Securities and Exchange Commission, granting unto said attorney-in-fact
and agent, full power and authority to do and perform each and every act and thing requisite and necessary to be done in connection therewith, as
fully to all intents and purposes as he might or could do in person, hereby ratifying and confirming all that said attorney-in-fact and agent, or his
substitutes or substitute, may lawfully do or cause to be done by virtue hereof.
IN WITNESS WHEREOF, each of the undersigned has executed this Power of Attorney as of the date indicated opposite his name.
Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed by the following persons on behalf of the
Registrant and in the capacities and on the dates indicated.
Signature
/s/ Shawn K. Singh
Shawn K. Singh, JD
/s/ Jerrold D. Dotson
Jerrold D. Dotson
/s/ H. Ralph Snodgrass
H. Ralph Snodgrass, Ph.D
/s/ Jon S. Saxe
Jon S. Saxe
/s/ Brian J. Underdown
Brian J. Underdown, Ph. D
Title
Chief Executive Officer, and Director
(Principal Executive Officer)
Chief Financial Officer
(Principal Financial and Accounting Officer)
Date
July 18, 2013
July 18, 2013
President, Chief Scientific Officer and Director
July 18, 2013
Chairman of the Board of Directors
July 18, 2013
Director
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July 18, 2013
Table of Contents
Exhibit No.
2.1 *
3.1 *
3.2
3.3
3.4 *
3.5
4.1 *
10.1 *
10.2 *
10.3 *
10.4 *
10.5 *
10.6 *
10.7 *
10.8 *
10.9 *
10.10 *
10.11 *
10.12 *
10.18 *
10.19 *
10.20 *
10.21 *
10.22 *
10.23 *
10.24 *
10.25 *
10.26 *
10.27 *
10.28 *
10.29 *
10.30 *
10.31 *
10.32 *
10.33 *
10.34 *
10.35 *
10.36 *
10.37 *
10.38 *
10.39 *
Exhibit Index
Description*
Agreement and Plan of Merger by and among Excaliber Enterprises, Ltd., VistaGen Therapeutics, Inc. and Excaliber Merger
Subsidiary, Inc.
Articles of Incorporation in effect as of May 11, 2011.
Articles of Merger filed with the Nevada Secretary of State on May 24, 2011.
Certificate of Amendment filed with the Nevada Secretary of State on December 6, 2011.
Bylaws in effect.as of May 11, 2011, incorporated by reference from the document filed as Exhibit 3.2 in the Company’s
Current Report on Form 8-K filed on May 16, 2011.
Certificate of Designations Series A Preferred, incorporated by reference from the Company’s Current Report on Form 8-
K/A filed on December 22, 2011.
Fourth Amended and Restated Investors’ Rights Agreement, dated August 1, 2005, by and among VistaGen and certain
(former) holders of Preferred Stock of VistaGen, as amended by that certain Amendment No. 1 to Fourth Amended and
Restated Investors’ Rights Agreement, dated July 10, 2010.
VistaGen’s 1999 Stock Incentive Plan.
Form of Option Agreement under VistaGen’s 1999 Stock Incentive Plan.
VistaGen’s Scientific Advisory Board 1998 Stock Incentive Plan.
Form of Option Agreement under VistaGen’s Scientific Advisory Board 1998 Stock Incentive Plan.
VistaGen’s 2008 Stock Incentive Plan.
Form of Option Agreement under VistaGen’s 2008 Stock Incentive Plan.
Securities Purchase Agreement, dated October 30, 2009, by and between VistaGen and Cato BioVentures.
Securities Purchase Agreement, dated April 27, 2011, by and between VistaGen and Cato BioVentures.
Securities Purchase Agreement, dated November 5, 2009, by and between VistaGen and Platinum Long Term Growth Fund.
Securities Purchase Agreement, dated December 2, 2009, by and between VistaGen and University Health Network.
Securities Purchase Agreement, dated April 25, 2011, by and between VistaGen and University Health Network.
Form of Subscription Agreement, dated May 11, 2011, by and between VistaGen and certain investors.
Industrial Lease, dated March 5, 2007, by and between Oyster Point LLC and VistaGen, as amended by that certain First
Amendment to Lease, dated as of April 24, 2009, and as further amended by that certain Second Amendment to Lease, dated
as of October 19, 2010 and that certain Third Amendment to Lease, dated as of April 1, 2011.
Clinical Study Agreement, dated April 15, 2010, by and between VistaGen and Progressive Medical Concepts, LLC.
Strategic Development Services Agreement, dated February 26, 2007, by and between VistaGen and Cato Research Ltd.
License Agreement by and between National Jewish Medical and Research Center and VistaGen, dated July 12, 1999, as
amended by that certain Amendment to License Agreement dated January 25, 2001, as amended by that certain Second
Amendment to License Agreement dated November 6, 2002, as amended by that certain Third Amendment to License
Agreement dated March 1, 2003, and as amended by that certain Fourth Amendment to License Agreement dated April 15,
2010.
License Agreement by and between Mount Sinai School of Medicine of New York University and the Company, dated
October 1, 2004.
Non-Exclusive License Agreement, dated December 5, 2008, by and between VistaGen and Wisconsin Alumni Research
Foundation, as amended by that certain Wisconsin Materials Addendum, dated February 2, 2009.
Sponsored Research Collaboration Agreement, dated September 18, 2007, between VistaGen and University Health
Network, as amended by that certain Amendment No. 1, Amendment No. 2 and Amendment No. 3 dated April 19, 2010,
December 15, 2010 and April, 25, 2011, respectively.
Letter Agreement, dated Feb 12, 2010, by and between VistaGen and The Regents of the University of California.
License Agreement, dated October 24, 2001, by and between the University of Maryland, Baltimore, Cornell Research
Foundation and Artemis Neuroscience, Inc.
Non-exclusive License Agreement, dated September 1, 2010, by and between VistaGen and TET Systems GmbH & Co. KG.
Amended and Restated Senior Convertible Promissory Bridge Note dated June 19, 2007 issued by VistaGen to Platinum
Long Term Growth VII, LLC.
Second Amended and Restated Letter Loan Agreement dated May 16, 2008, by and between VistaGen and Platinum Long
Term Growth VII, LLC, as amended by that certain Amendment No. 1 to Second Amended and Restated Letter Loan
Agreement dated October 16 2009, as further amended by that certain Amendment to Letter Loan Agreement dated May 5,
2011.
Promissory Note dated April 29, 2011 issued by VistaGen to Cato Holding Company.
Unsecured Promissory Note dated April 28, 2011 issued by VistaGen to Desjardins Securities.
Unsecured Promissory Note dated April 28, 2011 issued by VistaGen to McCarthy Tetrault LLP.
Unsecured Promissory Note dated April 28, 2011 issued by VistaGen to Morrison & Foerster LLP
Promissory Note dated February 25, 2010 issued by VistaGen to The Regents of the University of California.
Note and Warrant Purchase Agreement dated August 4, 2010, by and between VistaGen and certain investors, as amended
by that certain Amendment No. 1 to Note and Warrant Purchase Agreement, dated November 10, 2010.
Conversion Agreement, dated April 29, 2011, by and among VistaGen and certain holders of unsecured promissory notes
issued pursuant to that certain Note and Warrant Purchase Agreement, dated August 4, 2010, by and between VistaGen and
such note holders.
Agreement regarding Conversion of Unsecured Promissory Note, dated April 29, 2011, by and between VistaGen and The
Dillon Family Trust.
Senior Note and Warrant Purchase Agreement dated August 13, 2006, by and between VistaGen and certain investors, as
amended by that certain Amendment No. 1 to Senior Convertible Bridge Note and Warrant Purchase Agreement dated
January 31, 2007, as further amended by that certain Amendment No. 2 to Senior Convertible Bridge Note and Warrant
Purchase Agreement dated June 11, 2007, as further amended by that certain Omnibus Amendment dated April 28, 2011
Senior Note and Warrant Purchase Agreement dated May 16, 2008, by and between VistaGen and certain investors, as
amended by that certain Amendment No. 1 to Senior Convertible Bridge Note and Warrant Purchase Agreement dated
November 2, 2009, as further amended by that certain Omnibus Amendment dated April 28, 2011.
10.40 *
10.41 *
10.42 *
10.43 *
10.44 *
10.45 *
10.46
10.47
10.48
10.49
10.50
10.51
10.52
10.53
10.54
10.55
10.56
10.57
10.58
10.59
10.60
10.61
10.62
10.63
10.64
10.65
10.66
10.67
10.68
10.69
Employment Agreement, by and between, VistaGen and Shawn K. Singh, dated April 28, 2010, as amended May 9, 2011.
Employment Agreement, by and between, VistaGen and H. Ralph Snodgrass, PhD, dated April 28, 2010, as amended May 9,
2011.
Employment Agreement, by and between VistaGen and A. Franklin Rice, dated April 28, 2010, as amended May 9, 2011.
Agreement regarding sale of shares of common stock dated May 9, 2011 by and between Excaliber and Stephanie Y. Jones,
whereby Excaliber purchased from Mrs. Jones 4,982,103 shares of Excaliber common stock for $10.
Agreement regarding sale of shares of common stock dated May 9, 2011 by and between Excaliber and Nicole Jones,
whereby Excaliber purchased from Nicole Jones 82,104 shares of Excaliber common stock for $10.
Joinder Agreement dated May 11, 2011 by and between Excaliber, Platinum Long Term Growth VII, LLC and VistaGen
Notice of Award by National Institutes of Health, Small Business Innovation Research Program, to VistaGen Therapeutics,
Inc. for project, Clinical Development of 4-CI-KYN to Treat Pain dated June 22, 2009, with revisions dated July 19, 2010
and August 9, 2011, incorporated by reference from the Company’s Current Report on Form 8-K/A filed on December 20,
2011.
Notice of Grant Award by California Institute of Regenerative Medicine and VistaGen Therapeutics, Inc. for Project:
Development of an hES Cell-Based Assay System for Hepatocyte Differentiation Studies and Predictive Toxicology Drug
Screening, dated April 1, 2009, incorporated by reference from the Company’s Current Report on Form 8-K/A filed on
December 20, 2011.
Amendment No. 4, dated October 24, 2011, to Sponsored Research Collaboration Agreement between VistaGen and
University Health Network, incorporated by reference from the Company’s Current Report on Form 8-K/A filed on
November 30, 2011.
License Agreement No. 1, dated as of October 24, 2011 between University Health Network and VistaGen Therapeutics,
Inc., incorporated by reference from the Company’s Current Report on Form 8-K/A filed on November 30, 2011.
Strategic Medicinal Chemistry Services Agreement, dated as of December 6, 2011, between Synterys, Inc. and VistaGen
Therapeutics, Inc., incorporated by reference from the Company’s Current Report on Form 8-K/A filed on December 7,
2011.
Common Stock Exchange Agreement, dated as of December 22, 2011 between Platinum Long Term Growth VII, LLC and
VistaGen Therapeutics, Inc., incorporated by reference from the Company’s Current Report on Form 8-K/A filed on
December 23, 2011.
Note and Warrant Exchange Agreement, dated as of December 28, 2011 between Platinum Long Term Growth VII, LLC
and VistaGen Therapeutics, Inc., incorporated by reference from the Current Report on Form 8-K/A filed on January 4,
2012.
Form of Convertible Note and Warrant Purchase Agreement, dated as of February 28, 2012, by and between VistaGen
Therapeutics, Inc. and certain investors, incorporated by reference from the Current Report on Form 8-K/A filed on March
2, 2012.
Form of Convertible Promissory Note, dated as of February 28, 2012, incorporated by reference from the Company’s
Current Report on Form 8-K/A filed on March 2, 2012.
Form of Warrant to Purchase Common Stock, dated as of February 28, 2012, incorporated by reference from the Company’s
Current Report on Form 8-K/A filed on March 2, 2012.
Form of Registration Rights Agreement, dated as of February 28, 2012, by and between VistaGen and certain investors,
incorporated by reference from the Company’s Current Report on Form 8-K/A filed on March 2, 2012.
License Agreement No. 2, dated as of March 19, 2012 between University Health Network and VistaGen Therapeutics, Inc. ,
incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Exchange Agreement dated as of June 29, 2012 between Platinum Long Term Growth VII, LLC and VistaGen Therapeutics.
Inc., incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Secured Convertible Promissory Note, Dated as of July 2, 2012, issued to Platinum Long Term Growth VII, LLC.,
incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Security Agreement between Platinum Long Term Growth VII, LLC and VistaGen Therapeutics. Inc., dated as of July 2,
2012, incorporated by reference from the Company’s Annual Report on Form 10-K filed on July 2, 2012.
Secured Convertible Promissory Note, Dated as of August 30, 2012, issued to Platinum Long Term Growth VII, LLC.,
incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6, 2012.
Amendment to Security Agreement between Platinum Long Term Growth VII, LLC and VistaGen Therapeutics. Inc.as of
August 30, 2012, incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6, 2012.
Unsecured Promissory Note in the face amount of $1,000,000 issued to Morrison & Foerster LLP on August 31, 2012
(Replacement Note A), incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6,
2012.
Unsecured Promissory Note in the face amount of $1,379,376 issued to Morrison & Foerster LLP on August 31, 2012
(Replacement Note B), incorporated by reference from the Company’s Current Report on Form 8-K filed on September 6,
2012.
Stock Purchase Warrant issued to Morrison & Foerster LLP on August 31, 2012 to purchase 1,379,376 shares of the
Company’s common stock (New Morrison & Foerster Warrant), incorporated by reference from the Company’s Current
Report on Form 8-K filed on September 6, 2012.
Warrant to Purchase Common Stock issued to Morrison & Foerster LLP on August 31, 2012 to purchase 425,000 shares of
the Company’s common stock (Amended Morrison & Foerster Warrant), incorporated by reference from the Company’s
Current Report on Form 8-K filed on September 6, 2012.
Note Exchange and Purchase Agreement dated as of October 11, 2012 by and between VistaGen Therapeutics, Inc. and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed
on October 16, 2012.
Form of Senior Secured Convertible Promissory Note issued to Platinum Long Term Growth VII, LLP under the Note
Exchange and Purchase Agreement, incorporated by reference from the Company’s Current Report on Form 8-K filed on
October 16, 2012.
Form of Warrant to Purchase Shares of Common Stock issued to Platinum Long Term Growth VII, LLP under the Note
Exchange and Purchase Agreement, incorporated by reference from the Company’s Current Report on Form 8-K filed on
October 16, 2012.
10.71
10.76
10.79
10.70
10.78
10.74
10.80
10.73
10.75
10.77
10.72
Amended and Restated Security Agreement as of October 11, 2012 between VistaGen Therapeutics, Inc. and Platinum Long
Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on October 16,
2012.
Intellectual Property Security and Stock Pledge Agreement as of October 11, 2012 between VistaGen California and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed
on October 16, 2012.
Negative Covenant Agreement dated October 11, 2012 between VistaGen California, Artemis Neuroscience, Inc. and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed
on October 16, 2012.
Amendment to Note Exchange and Purchase Agreement as of November 14, 2012 between VistaGen Therapeutics Inc. and
Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed
on November 20, 2012.
Form of Note Exchange Agreement between VistaGen Therapeutics, Inc. and Holders of the Company’s Promissory Notes
dated February 28, 2012, incorporated by reference from the Company’s Current Report on Form 8-K filed on November
20, 2012.
Amendment No. 2 to Note Exchange and Purchase Agreement as of January 31, 2013 between VistaGen Therapeutics Inc.
and Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Quarterly Report on Form 10-Q
filed on February 14, 2013.
Amendment No. 3 to Note Exchange and Purchase Agreement as of February 22, 2013 between VistaGen Therapeutics Inc.
and Platinum Long Term Growth VII, LLP, incorporated by reference from the Company’s Current Report on Form 8-K
filed on February 28, 2013.
Form of Warrant to Purchase Common Stock issued to independent members of the Company’s Board of Directors and its
executive officers on March 3, 2013, incorporated by reference from the Company’s Current Report on Form 8-K filed on
March 6, 2013.
Securities Purchase Agreement between VistaGen Therapeutics, Inc., and Autilion AG dated April 8, 2013, incorporated by
reference from the Company’s Current Report on Form 8-K filed on April 10, 2013.
Voting Agreement between VistaGen Therapeutics, Inc., and Autilion AG dated April 8, 2013, incorporated by reference
from the Company’s Current Report on Form 8-K filed on April 10, 2013.
Note Conversion Agreement as of April 4, 2013 between VistaGen Therapeutics Inc. and Platinum Long Term Growth VII,
LLP, incorporated by reference from the Company’s Current Report on Form 8-K filed on April 10, 2013.
Assignment and Assumption Agreement between Autilion AG and Bergamo Acquisition Corp. PTE LTD dated April 12,
2013.
Amendment No. 1 to Securities Purchase Agreement dated April 30, 2013 between VistaGen Therapeutics, Inc. and
Bergamo Acquisition Corp. PTE LTD, incorporated by reference from the Company’s Current Report on Form 8-K filed on
May 1, 2013.
Lease between Bayside Area Development, LLC and VistaGen Therapeutics, Inc. (California) dated April 24, 2013.
Indemnification Agreement effective May 20, 2013 between the Company and Jon S. Saxe.
Indemnification Agreement effective May 20, 2013 between the Company and Shawn K. Singh
Indemnification Agreement effective May 20, 2013 between the Company and H. Ralph Snodgrass.
Indemnification Agreement effective May 20, 2013 between the Company and Brian J. Underdown.
Indemnification Agreement effective May 20, 2013 between the Company and Jerrold D. Dotson.
Amendment and Waiver effective May 24, 2013 between the Company and Platinum Long Term Growth VII, LLC,
incorporated by reference from the Company’s Current Report on Form 8-K filed on June 3, 2013.
Amendment No. 2 to Securities Purchase Agreement dated June 27, 2013 between the Company and Autilion AG and
Bergamo Acquisition Corp. PTE LTD, incorporated by reference from the Company's Current Report on Form 8-K filed on
June 28, 2013.
Letter regarding change in certifying accountant
List of Subsidiaries.
Power of Attorney
Certification of the Company’s Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
Certification of the Company’s Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
Certification of the Company’s Chief Executive Officer and Chief Financial Officer pursuant to Section 906 of the
Sarbanes-Oxley Act of 2002.
XBRL Instance Document
101.INS **
101.SCH ** XBRL Taxonomy Schema
101.CAL ** XBRL Taxonomy Extension Calculation Linkbase
101.DEF ** XBRL Taxonomy Extension Definition Linkbase
101.LAB ** XBRL Taxonomy Extension Label Linkbase
101.PRE ** XBRL Taxonomy Extension Presentation Linkbase
10.83
10.84
10.85
10.86
10.87
10.88
10.89
16.1*
21.1*
24.1
31.1
31.2
32.1
10.90
10.82
10.81
* Incorporated by reference from the like-numbered exhibit filed with our Current Report on Form 8-K on May 16, 2011.
** Pursuant to Rule 406T of Regulation S-T, these interactive files are deemed not filed or part of a registration statement or prospectus for
purposes of Sections 11 or 12 of the Securities Act of 1933 or Section 18 of the Securities Exchange Act of 1934 and otherwise are not
subject to liability.
ASSIGNMENT AND ASSUMPTION AGREEMENT
Exhibit 10.81
This Assignment and Assumption Agreement (the “ Assignment and Assumption Agreement”) is entered into as of April 12, 2013, by
and between Autilion AG, a company organized under the laws of Switzerland (“ Assignor”), and its affiliate, Bergamo Acquisition Corp PTE,
LTD, a company registered under the laws of the Republic of Singapore (“Assignee”). All terms used, but not defined, herein shall have the
meanings ascribed to them in the Underlying Agreements (defined below).
WHEREAS, Assignor and VistaGen Therapeutics, Inc., a corporation organized under the laws of the State of Nevada (“VistaGen”),
are parties to a Securities Purchase Agreement and Voting Agreement, each dated April 8, 2013, complete copies of which (including all
exhibits, amendments and modifications thereto) are incorporated herein by this reference (the “Underlying Agreements”);
WHEREAS, Assignor has agreed to assign to Assignee all of its rights and obligations under the Underlying Agreements
(collectively, the “Assigned Rights and Obligations”), and Assignee has agreed to assume the Assigned Rights and Obligations.
NOW, THEREFORE, for good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties
hereto agree as follows:
1. Assignment and Assumption. Assignor hereby assigns to Assignee all of Assignor’s rights and obligations under the Underlying
Agreements with respect to the Assigned Rights and Obligations, and Assignee hereby accepts the foregoing assignment and assumes
all of the rights and obligations of Assignor under the Underlying Agreements with respect to the Assigned Rights and Obligations.
2. Effective Date. The date on which the Assignment and Assumption Agreement is effective is April 11, 2013.
3. Successors. All future transfers and assignments of the Assigned Rights and Obligations transferred and assigned hereby are subject to
the transfer and assignment provisions of the Underlying Agreements. This Assignment and Assumption Agreement shall inure to the
benefit of, and be binding upon, the permitted successors and assigns of the parties hereto.
4. Counterparts. This Assignment and Assumption Agreement may be executed in counterparts, each of which shall be an original, but all
of which together constitute one and the same instrument.
IN WITNESS WHEREOF, Assignor and Assignee, by their duly authorized officials, hereby execute and deliver this Assignment and
Assumption Agreement, effective as of the date set forth in Section 2 above.
ASSIGNOR: AUTILION AG
ASSIGNEE: BERGAMO ACQUISITION CORP PTE, LTD
By: /s/ Hillard Herzog
Name: Hillard Herzog
Title: President
By: /s/ Hillard Herzog
Name: Hillard Herzog
Title: President
BRITANNIA MODULAR LABS I
LEASE
Exhibit 10.83
This Lease (the "Lease"), dated as of the date set forth in Section 1 of the Summary of Basic Lease Information (the " Summary"),
below, is made by and between BAYSIDE AREA DEVELOPMENT, LLC, a Delaware limited liability company ("Landlord"), and
VISTAGEN THERAPEUTICS, INC., a California corporation ("Tenant").
SUMMARY OF BASIC LEASE INFORMATION
DESCRIPTION
April 24, 2013
TERMS OF LEASE
1. Date:
2. Premises
(Article 1).
2.1 Building:
333-353 Allerton Avenue
South San Francisco, California
Comprising 67,337 rentable square feet of space ("RSF") in the
aggregate.
Approximately 10,909 RSF consisting of Suite 5 in the Building, with
a street address of 343 Allerton Avenue, as further set forth in
Exhibit A to the Lease.
Forty eight (48) months.
The date that Landlord delivers the Premises to Tenant "Ready for
Occupancy" as that term is defined in Section 3(a) of the Tenant Work
the Lease as Exhibit B, which Lease
Letter attached
Commencement Date
to be June 30, 2013.
Notwithstanding the foregoing and any early access to the Premises
by Tenant pursuant to Section 6 of the Tenant Work Letter, the Lease
Commencement Date shall not be sooner than June 30, 2013.
is anticipated
to
then
the day
If the Lease Commencement Date shall be the first day of a calendar
the 48th month
month,
anniversary of the Lease Commencement Date; or, if the Lease
Commencement Date shall be other than the first day of a calendar
month, then the last day of the month in which the 48th month
anniversary of the Lease Commencement Date occurs.
immediately preceding
2.2 Premises:
3. Lease Term
(Article 2).
3.1 Length of Term:
3.2 Lease Commencement Date:
3.3 Lease Expiration Date:
-1-
4. Base Rent (Article 3):
Lease Year
1*
2
3
4
$
$
$
$
Annual
Base Rent
242,179.80
255,270.60
268,361.40
281,452.20
$
$
$
$
Monthly
Installment
of Base Rent
Monthly Base Rent
per RSF
20,181.65
21,272.55
22,363.45
23,454.35
$
$
$
$
1.85
1.95
2.05
2.15
*Note: Tenant shall have no obligation to pay any Base Rent for the Premises attributable to the first three (3) months of the Lease Term
(the "Rent Abatement Period").
5. Tenant FF&E Allowance (Exhibit B):
An amount equal to $5.00 per RSF (i.e., $54,545.00 based upon
10,909 rentable square feet in the Premises).
6. Tenant's Share
(Article 4):
7. Permitted Use
(Article 5):
8. Security Deposit
(Article 21):
9. Parking
(Article 28):
16.20%.
The Premises shall be used only for general office, biotechnology and
pharmaceutical research and development, engineering, laboratory,
storage and/or warehouse uses, including, but not limited to,
administrative offices and other lawful uses reasonably related to or
incidental to such specified uses, all (i) consistent with first class life
sciences and pharmaceutical projects in the South San Francisco,
California, area ("First Class Life Sciences Projects"), and (ii) in
compliance with, and subject to, applicable federal, state and local
laws, rules and regulations and the terms of this Lease.
$46,908.70
2.8 unreserved parking spaces for every 1,000 RSF of the Premises,
subject to the terms of Article 28 of the Lease.
-2-
10. Address of Tenant
(Section 29.18):
11. Address of Landlord
(Section 29.18):
12. Broker(s)
(Section 29.24):
384 Oyster Point Blvd., Suite #8
South San Francisco, CA 94080
Attention: Shawn K. Singh
(Prior to Lease Commencement Date)
and
343 Allerton Avenue
South San Francisco, California 94080-4816
Attention: Shawn K. Singh
(After Lease Commencement Date)
See Section 29.18 of the Lease.
CBRE, Inc.
950 Tower Lane, Suite 870
Foster City, CA 94404
Attention: Christopher R. Jacobs
-3-
1.
PREMISES, BUILDING, PROJECT, AND COMMON AREAS
1.1 Premises, Building, Project and Common Areas.
1.1.1 The Premises. Landlord hereby leases to Tenant and Tenant hereby leases from Landlord the premises set forth in
Section 2.2 of the Summary (the " Premises"). The outline of the Premises is set forth in Exhibit A attached hereto. The outline of the
"Building" and the "Project," as those terms are defined in Section 1.1.2 below, are further depicted on the Site Plan attached hereto as
Exhibit A-1 . The parties hereto agree that the lease of the Premises is upon and subject to the terms, covenants and conditions herein set
forth, and Tenant covenants as a material part of the consideration for this Lease to keep and perform each and all of such terms, covenants
and conditions by it to be kept and performed and that this Lease is made upon the condition of such performance. The parties hereto hereby
acknowledge that the purpose of Exhibit A is to show the approximate location of the Premises only, and such Exhibit is not meant to
constitute an agreement, representation or warranty as to the construction of the Premises, the precise area thereof or the specific location of
the "Common Areas," as that term is defined in Section 1.1.3, below, or the elements thereof or of the accessways to the Premises or the
"Project," as that term is defined in Section 1.1.2, below. Except as specifically set forth in this Lease and in the Tenant Work Letter attached
hereto as Exhibit B (the "Tenant Work Letter "), Landlord shall not be obligated to provide or pay for any improvement work or services
related to the improvement of the Premises. Tenant also acknowledges that neither Landlord nor any agent of Landlord has made any
representation or warranty regarding the condition of the Premises, the Building or the Project or with respect to the suitability of any of the
foregoing for the conduct of Tenant's business, except as specifically set forth in this Lease and the Tenant Work Letter. The taking of
possession of the Premises by Tenant shall conclusively establish that the Premises and the Building were at such time in good and sanitary
order, condition and repair.
1.1.2 The Building and The Project. The Premises are a part of the building set forth in Section 2.1 of the Summary (the
"Building"). The term "Project," as used in this Lease, shall mean (i) the Building and the Common Areas, (ii) the land (which is improved
with landscaping, parking facilities and other improvements) upon which the Building and the Common Areas are located, (iii) the other
office/laboratory buildings located in the project known as "Britannia Modular Labs I", and the land upon which such adjacent
office/laboratory buildings and associated landscaping and parking facilities are located, and (iv) at Landlord's discretion, any additional real
property, areas, land, buildings or other improvements added thereto outside of the Project.
1.1.3 Common Areas. Tenant shall have the non-exclusive right to use in common with other tenants in the Project, and
subject to the rules and regulations referred to in Article 5 of this Lease, those portions of the Project which are provided, from time to time, for
use in common by Landlord, Tenant and any other tenants of the Project (such areas, together with such other portions of the Project
designated by Landlord, in its discretion, are collectively referred to herein as the "Common Areas"). The manner in which the Common
Areas are maintained and operated shall be at the sole discretion of Landlord and the use thereof shall be subject to such rules, regulations and
restrictions as Landlord may make from time to time. Landlord reserves the right to close temporarily, make alterations or additions to, or
change the location of elements of the Project and the Common Areas; provided, however, that any such closures, alterations, additions or
changes (a) shall not materially interfere with Tenant's use of such Common Area and (b) shall be accomplished in a first-class and
professional manner.
1.2 Rentable Square Feet of Premises. The rentable square footage of the Premises is hereby deemed to be as set forth in Section
2.2 of the Summary, and shall not be subject to measurement or adjustment during the Lease Term.
1.3 Right of First Offer/First Refusal . Landlord hereby grants to the Tenant named in the Summary (the " Original Tenant") a
right of first offer with respect to the suite adjacent to the Premises containing approximately 5,518 RSF, and with the street address of 345
Allerton Avenue as shown on Exhibit A to this Lease (the "First Offer Space"). Tenant's right of first offer shall be on the terms and
conditions set forth in this Section 1.3.
-4-
1.3.1 Procedure for Offer.
1.3.1.1 Through October 31, 2013. During the period prior to and including October 31, 2013, Landlord shall
notify Tenant (the "First Refusal Notice ") from time to time when Landlord receives a bona fide offer to lease the First Offer Space or any
portion thereof from a third party. Pursuant to such First Refusal Notice, Landlord shall offer to lease to Tenant the First Offer Space on the
"Early Exercise Terms", as defined in Section 1.3.2 below.
1.3.1.2 After October 31, 2013. After October 31, 2013, Landlord shall notify Tenant (the " First Offer Notice")
from time to time when the First Offer Space or any portion thereof becomes available for lease to third parties, and in any event prior to
entering into any lease of the First Offer Space with a third party. Pursuant to such First Offer Notice, Landlord shall offer to lease to Tenant
the then available First Offer Space. The First Offer Notice shall describe the space so offered to Tenant and shall set forth the rent and other
economic terms upon which Landlord is willing to lease such space to Tenant (the "First Offer Rent").
1.3.2 Early Exercise of First Offer Right. In the event that Tenant elects to exercise its first offer right prior to October 31,
2013 (the "Early Exercise"), then (i) the "First Offer Rent" payable during the term of Tenant's lease of the First Offer Space shall be equal to
the Base Rent payable under this Lease with respect to the initial Premises (i.e., at the same rate per RSF, and including the increases in such
rate, applicable to the initial Premises as set forth in Section 4 of the Summary), (ii) Landlord shall provide an improvement allowance for the
construction or improvement of the First Offer Space equal to $40.00 per RSF of the First Offer Space, (iii) Landlord shall provide Tenant
with ninety (90) days in which to construct improvements and alterations in the First Offer Space prior to the occurrence of the First Offer
Commencement Date, and (iv) the term of Tenant's lease of the First Offer Space shall expire coterminously with Tenant's lease of the initial
Premises (collectively, the "Early Exercise Terms").
1.3.3 Procedure for Acceptance. If Tenant wishes to exercise Tenant's right of first offer with respect to the space
described in the First Offer Notice, then within five (5) business days of delivery of the First Refusal Notice or First Offer Notice to Tenant,
Tenant shall deliver notice to Landlord of Tenant's election to exercise its right of first offer with respect to the entire space described in the
First Offer Notice on the terms contained in such notice. If Tenant does not so notify Landlord within the five (5) business day period, then
Landlord shall be free to lease the space described in the First Offer Notice to anyone to whom Landlord desires on any terms Landlord
desires. Notwithstanding anything to the contrary contained herein, Tenant must elect to exercise its right of first offer, if at all, with respect to
all of the space offered by Landlord to Tenant at any particular time, and Tenant may not elect to lease only a portion thereof.
1.3.4 Construction In First Offer Space. Tenant shall take the First Offer Space in its "as is" condition, subject to any
improvement allowance granted as a component of the First Offer Rent (or as part of the Early Exercise Terms), and the construction of
improvements in the First Offer Space shall comply with the terms of Article 8 of this Lease.
1.3.5 Amendment to Lease. If Tenant timely exercises Tenant's right to lease the First Offer Space as set forth herein,
Landlord and Tenant shall within ten (10) business days after such exercise, execute an amendment to this Lease for such First Offer Space
upon the terms and conditions as set forth in the First Offer Notice, or upon the Early Exercise Terms, if applicable, and this Section
1.3. Tenant shall commence payment of Rent for the First Offer Space, and the term of the First Offer Space shall commence upon the date
of delivery of the First Offer Space to Tenant (the " First Offer Commencement Date") and terminate on the date set forth in the First Offer
Notice (except in the event of an Early Exercise, in which event Tenant's lease of the First Offer Space shall expire coterminously with
Tenant's lease of the initial Premises).
1.3.6 Termination of Right of First Offer . The rights contained in this Section 1.3 shall be personal to the Original
Tenant, and may only be exercised by the Original Tenant (and not any assignee, sublessee or other transferee of the Original Tenant's interest
in this Lease) if the Original Tenant occupies the entire Premises. The right of first offer granted herein shall terminate upon the failure by
Tenant to exercise its right of first offer with respect to the First Offer Space as offered by Landlord. The terms of this Section 1.3 shall not
apply after the end of the initial Lease Term. Tenant shall not have the right to lease First Offer Space, as provided in this Section 1.3, if, as of
the date of the attempted exercise of any right of first offer by Tenant, Tenant is in default under this Lease, after the expiration of any
applicable notice and cure period, or Tenant has previously been in default, after the expiration of any applicable notice and cure period, under
this Lease more than once.
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2.
LEASE TERM; DELAYED DELIVERY; OPTION TERM
2.1 Lease Term. The terms and provisions of this Lease shall be effective as of the date of this Lease. The term of this Lease (the
"Lease Term") shall be as set forth in Section 3.1 of the Summary, shall commence on the date set forth in Section 3.2 of the Summary (the
"Lease Commencement Date"), and shall terminate on the date set forth in Section 3.3 of the Summary (the " Lease Expiration Date")
unless this Lease is sooner terminated as hereinafter provided. For purposes of this Lease, the term "Lease Year" shall mean each consecutive
twelve (12) month period during the Lease Term. At any time during the Lease Term, Landlord may deliver to Tenant a notice in the form as
set forth in Exhibit C, attached hereto, as a confirmation only of the information set forth therein, which Tenant shall execute and return to
Landlord within five (5) days of receipt thereof.
2.2 Delayed Delivery. Landlord shall use commercially reasonable efforts to cause the Lease Commencement Date to occur on or
before June 30, 2013 (the "Outside Delivery Date"). Subject to the terms of this Lease, if Landlord has not caused the Lease Commencement
Date to have occurred on or before the Outside Delivery Date, then Landlord agrees that Landlord will reimburse Tenant the actual increase in
amounts required to be paid by Tenant with respect to its existing lease of space at 384 Oyster Point Boulevard, in South San Francisco,
California (the "Hold Over Costs"). The Hold Over Costs shall consist of only the amount by which the "base rental" is increased over the
base rental payable during the last month of Tenant's lease, and shall not include any costs for utilities, taxes, insurance or other charges
payable by Tenant under its lease. In no event shall the total amount of Hold Over Costs payable by Landlord hereunder exceed
$10,000.00. Prior to Landlord being obligated to pay any Hold Over Costs, Tenant shall provide Landlord with reasonable evidence of the
amount of such Hold Over Costs, and of Tenant's payment thereof. Landlord's obligation to pay such Hold Over Costs shall be Tenant's sole
remedy for Landlord's failure to cause the Lease Commencement Date to occur on or before the Outside Delivery Date. The Outside Delivery
Date shall be extended to the extent the Lease Commencement Date is delayed by "Tenant Delay", as that term is defined in Section 1(j) of the
Tenant Work Letter.
2.3 Option Term.
2.3.1 Option Right. Landlord hereby grants Original Tenant one (1) option to extend the Lease Term for a period of three
(3) years (the "Option Term"), which option shall be exercisable only by written notice delivered by Tenant to Landlord as provided below,
provided that, as of the date of delivery of such notice, Tenant is not in default under this Lease, beyond any applicable notice and cure period
set forth in this Lease, and Tenant has not previously been in default under this Lease, beyond any applicable notice and cure period set forth in
this Lease, more than two (2) times. Upon the proper exercise of such option to extend, and provided that, at Landlord's option, as of the end
of the initial Lease Term, Tenant is not in default under this Lease, beyond any applicable notice and cure period set forth in this Lease, and
Tenant has not previously been in default under this Lease, beyond any applicable notice and cure period set forth in this Lease, more than two
(2) times, the Lease Term, as it applies to the Premises, shall be extended for a period of three (3) years. The rights contained in this Section
2.3 shall be personal to the Original Tenant, and may only be exercised by the Original Tenant if the Original Tenant occupies the entire
Premises.
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2.3.2 Option Rent. The annual Rent payable by Tenant during the Option Term (the " Option Rent") shall be equal to the
"Fair Rental Value," as that term is defined below, for the Premises as of the commencement date of the Option Term. The " Fair Rental
Value," as used in this Lease, shall be equal to the annual rent per rentable square foot (including additional rent and considering any "base
year" or "expense stop" applicable thereto), including all escalations, at which tenants (pursuant to leases consummated within the twelve (12)
month period preceding the first day of the Option Term), are leasing non-sublease, non-encumbered, non-equity space which is not
significantly greater or smaller in size than the subject space, for a comparable lease term, in an arm's length transaction, which comparable
space is located in the Building or in "Comparable Buildings," as that term is defined in this Section 2.3.2, below (transactions satisfying the
foregoing criteria shall be known as the "Comparable Transactions "), taking into consideration the following concessions (the
"Concessions"): (a) rental abatement concessions, if any, being granted such tenants in connection with such comparable space; (b) tenant
improvements or allowances provided or to be provided for such comparable space, and taking into account the value, if any, of the existing
improvements in the subject space, such value to be based upon the age, condition, design, quality of finishes and layout of the improvements;
and (c) other reasonable monetary concessions being granted such tenants in connection with such comparable space; provided, however, that
in calculating the Fair Rental Value, no consideration shall be given to (i) the fact that Landlord is or is not required to pay a real estate
brokerage commission in connection with Tenant's exercise of its right to extend the Lease Term, or the fact that landlords are or are not
paying real estate brokerage commissions in connection with such comparable space, and (ii) any construction period, if any, granted to
tenants in Comparable Transactions in connection with the design, permitting and construction of tenant improvements in such comparable
spaces. The Fair Rental Value shall additionally include a determination as to whether, and if so to what extent, Tenant must provide Landlord
with financial security, such as a letter of credit or guaranty, for Tenant's Rent obligations in connection with Tenant's lease of the Premises
during the Option Term. Such determination shall be made by reviewing the extent of financial security then generally being imposed in
Comparable Transactions from tenants of comparable financial condition and credit history to the then existing financial condition and credit
history of Tenant (with appropriate adjustments to account for differences in the then-existing financial condition of Tenant and such other
tenants). The Concessions (A) shall be reflected in the effective rental rate (which effective rental rate shall take into consideration the total
dollar value of such Concessions as amortized on a straight-line basis over the applicable term of the Comparable Transaction (in which case
such Concessions evidenced in the effective rental rate shall not be granted to Tenant)) payable by Tenant, or (B) at Landlord’s election, all
such Concessions shall be granted to Tenant in kind. Notwithstanding the foregoing, during the Option Term, the Option Rent shall increase
by three percent (3%) per annum on each anniversary of the first (1st) day of the Option Term. The term “Comparable Buildings” shall mean
other First Class Life Sciences Projects located in the South San Francisco, California, area that are comparable in age (based on the date of
original construction or the latest major renovation) location, quality of construction, services and amenities.
2.3.3 Exercise of Option. The option contained in this Section 2.3 shall be exercised by Tenant, if at all, only in the
following manner: Tenant shall deliver written notice (the " Option Exercise Notice") to Landlord not more than twelve (12) months nor less
than nine (9) months prior to the expiration of the initial Lease Term, stating that Tenant is irrevocably exercising its option.
2.3.4 Determination of Option Rent. In the event Tenant timely and appropriately exercises its option to extend the Lease
Term, Landlord shall notify Tenant of Landlord's determination of the Option Rent on or before the date that is thirty (30) days following
Landlord's receipt of the Option Exercise Notice. If Tenant, on or before the date which is thirty (30) days following the date upon which
Tenant receives Landlord's determination of the Option Rent, in good faith objects to Landlord's determination of the Option Rent, then
Landlord and Tenant shall attempt to agree upon the Option Rent using their good-faith efforts. If Landlord and Tenant fail to reach
agreement within thirty (30) days following Tenant's objection to the Option Rent (the "Outside Agreement Date "), then each party shall
thereafter make a separate determination of the Option Rent, within five (5) business days of the Outside Agreement Date, and such
determinations shall be submitted to arbitration in accordance with Sections 2.3.4.1 through 2.3.4.4, below. If Tenant fails to object to
Landlord's determination of the Option Rent within the time period set forth herein, then Tenant shall be deemed to have rejected Landlord's
determination of the Option Rent, and the matter shall be submitted to arbitration in accordance with the terms hereof.
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2.3.4.1 Landlord and Tenant shall each appoint one arbitrator who shall be, at the option of the appointing party, a
MAI appraiser, a real estate broker, or real estate attorney, who shall have been active over the five (5) year period ending on the date of such
appointment in the leasing or appraisal, as the case may be, of life science properties in San Diego, California. Each such arbitrator shall be
appointed within twenty (20) days after the Outside Agreement Date. Landlord and Tenant may consult with their selected arbitrators prior to
appointment and may select an arbitrator who is favorable to their respective positions. The arbitrators so selected by Landlord and Tenant
shall be deemed "Advocate Arbitrators."
2.3.4.2 The two (2) Advocate Arbitrators so appointed shall be specifically required pursuant to an engagement
letter within ten (10) days of the date of the appointment of the last appointed Advocate Arbitrator to agree upon and appoint a third arbitrator
("Neutral Arbitrator") who shall be qualified under the same criteria set forth hereinabove for qualification of the two Advocate Arbitrators,
except that neither the Landlord or Tenant or either parties' Advocate Arbitrator may, directly or indirectly, consult with the Neutral Arbitrator
prior or subsequent to his or her appointment. The Neutral Arbitrator shall be retained via an engagement letter jointly prepared by Landlord's
counsel and Tenant’s counsel.
2.3.4.3 The three arbitrators shall, within thirty (30) days of the appointment of the Neutral Arbitrator, reach a
decision as to whether the parties shall use Landlord's or Tenant's submitted Option Rent, and shall notify Landlord and Tenant thereof. The
determination of the arbitrators shall be limited solely to the issue of whether Landlord's or Tenant's submitted Option Rent is the closest to
the actual Option Rent, taking into account the requirements of Section 2.3.2 of this Lease, as determined by the arbitrators.
2.3.4.4 The decision of the majority of the three arbitrators shall be binding upon Landlord and Tenant.
2.3.4.5 If either Landlord or Tenant fails to appoint an Advocate Arbitrator within twenty (20) days after the
Outside Agreement Date, then either party may petition the presiding judge of the Superior Court of San Diego County to appoint such
Advocate Arbitrator subject to the criteria in Section 2.3.4.1 of this Lease, or if he or she refuses to act, either party may petition any judge
having jurisdiction over the parties to appoint such Advocate Arbitrator.
2.3.4.6 If the two (2) Advocate Arbitrators fail to agree upon and appoint the Neutral Arbitrator within ten (10)
business days after the appointment of the last appointed Advocate Arbitrator, then either party may petition the presiding judge of the
Superior Court of San Diego County to appoint the Neutral Arbitrator, subject to criteria in Section 2.3.4.2 of this Lease, or if he or she refuses
to act, either party may petition any judge having jurisdiction over the parties to appoint such arbitrator.
2.3.4.7 The cost of the arbitration shall be paid by Landlord and Tenant equally.
2.3.4.8 In the event that the Option Rent shall not have been determined pursuant to the terms hereof prior to the
commencement of the Option Term, Tenant shall be required to pay as Option Rent, an amount equal to 103% of the Base Rent payable by
Tenant as of the expiration of the initial Lease Term, and upon the final determination of the Option Rent, the payments made by Tenant shall
be reconciled with the actual amounts of Option Rent due, and the appropriate party shall make any corresponding payment to the other party.
3.
BASE RENT Tenant shall pay, without prior notice or demand, to Landlord or Landlord's agent at the management office of the
Project, or, at Landlord's option, at such other place as Landlord may from time to time designate in writing, by electronic wire transfer or by a
check for currency which, at the time of payment, is legal tender for private or public debts in the United States of America, base rent ("Base
Rent") as set forth in Section 4 of the Summary, payable in equal monthly installments as set forth in Section 4 of the Summary in advance on
or before the first day of each and every calendar month during the Lease Term, without any setoff or deduction whatsoever. The Base Rent
for the first full month of the Lease Term after the Rent Abatement Period shall be paid at the time of Tenant's execution of this Lease. If any
Rent payment date (including the Lease Commencement Date) falls on a day of the month other than the first day of such month or if any
payment of Rent is for a period which is shorter than one month, the Rent for any fractional month shall accrue on a daily basis for the period
from the date such payment is due to the end of such calendar month or to the end of the Lease Term at a rate per day which is equal to 1/365
of the applicable annual Rent. All other payments or adjustments required to be made under the terms of this Lease that require proration on a
time basis shall be prorated on the same basis.
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4.
ADDITIONAL RENT
4.1 General Terms.
4.1.1 Direct Expenses; Additional Rent . In addition to paying the Base Rent specified in Article 3 of this Lease, Tenant
shall pay "Tenant's Share " of the annual "Direct Expenses," as those terms are defined in Sections 4.2.6 and 4.2.2 of this Lease,
respectively. Such payments by Tenant, together with any and all other amounts payable by Tenant to Landlord pursuant to the terms of this
Lease, are hereinafter collectively referred to as the "Additional Rent", and the Base Rent and the Additional Rent are herein collectively
referred to as "Rent." All amounts due under this Article 4 as Additional Rent shall be payable for the same periods and in the same manner
as the Base Rent. Without limitation on other obligations of Tenant which survive the expiration of the Lease Term, the obligations of Tenant
to pay the Additional Rent provided for in this Article 4 shall survive the expiration of the Lease Term.
4.1.2 Triple Net Lease. Landlord and Tenant acknowledge that, except as otherwise provided to the contrary in this Lease,
it is their intent and agreement that this Lease be a "TRIPLE NET" lease and that as such, the provisions contained in this Lease are intended
to pass on to Tenant or reimburse Landlord for the costs and expenses reasonably associated with this Lease, the Building and the Project, and
Tenant's operation therefrom. To the extent such costs and expenses payable by Tenant cannot be charged directly to, and paid by, Tenant,
such costs and expenses shall be paid by Landlord but reimbursed by Tenant as Additional Rent.
4.2 Definitions of Key Terms Relating to Additional Rent . As used in this Article 4, the following terms shall have the meanings
hereinafter set forth:
4.2.1 Intentionally Deleted.
4.2.2 "Direct Expenses" shall mean "Operating Expenses" and "Tax Expenses."
4.2.3 "Expense Year" shall mean each calendar year in which any portion of the Lease Term falls, through and including
the calendar year in which the Lease Term expires, provided that Landlord, upon notice to Tenant, may change the Expense Year from time to
time to any other twelve (12) consecutive month period, and, in the event of any such change, Tenant's Share of Direct Expenses shall be
equitably adjusted for any Expense Year involved in any such change.
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4.2.4 "Operating Expenses" shall mean all expenses, costs and amounts of every kind and nature which Landlord pays or
accrues during any Expense Year because of or in connection with the ownership, management, maintenance, security, repair, replacement,
restoration or operation of the Project, or any portion thereof. Without limiting the generality of the foregoing, Operating Expenses shall
specifically include any and all of the following: (i) the cost of supplying all utilities, the cost of operating, repairing, maintaining, and
renovating the utility, telephone, mechanical, sanitary, storm drainage, and elevator systems, and the cost of maintenance and service contracts
in connection therewith; (ii) the cost of licenses, certificates, permits and inspections and the cost of contesting any governmental enactments
which may affect Operating Expenses, and the costs incurred in connection with a governmentally mandated transportation system
management program or similar program; (iii) the cost of all insurance carried by Landlord in connection with the Project and Premises as
reasonably determined by Landlord; (iv) the cost of landscaping, relamping, and all supplies, tools, equipment and materials used in the
operation, repair and maintenance of the Project, or any portion thereof; (v) the cost of parking area operation, repair, restoration, and
maintenance; (vi) fees and other costs, including management and/or incentive fees, consulting fees, legal fees and accounting fees, of all
contractors and consultants in connection with the management, operation, maintenance and repair of the Project; (vii) payments under any
equipment rental agreements and the fair rental value of any management office space; (viii) subject to item (f), below, wages, salaries and
other compensation and benefits, including taxes levied thereon, of all persons engaged in the operation, maintenance and security of the
Project; (ix) costs under any instrument pertaining to the sharing of costs by the Project; (x) operation, repair, maintenance and replacement of
all systems and equipment and components thereof of the Project; (xi) the cost of janitorial, alarm, security and other services, replacement of
wall and floor coverings, ceiling tiles and fixtures in common areas, maintenance and replacement of curbs and walkways, repair to roofs and
re-roofing; (xii) amortization (including interest on the unamortized cost) over such period of time as Landlord shall reasonably determine, of
the cost of acquiring or the rental expense of personal property used in the maintenance, operation and repair of the Project, or any portion
thereof; (xiii) the cost of capital improvements or other costs incurred in connection with the Project (A) which are intended to effect
economies in the operation or maintenance of the Project, or any portion thereof, or to reduce current or future Operating Expenses or to
enhance the safety or security of the Project or its occupants, (B) that are required to comply with present or anticipated conservation
programs, (C) which are replacements or modifications of nonstructural items located in the Common Areas required to keep the Common
Areas in good order or condition, or (D) that are required under any governmental law or regulation; provided, however, that any capital
expenditure shall be amortized (including interest on the amortized cost) over such period of time as Landlord shall reasonably determine; and
(xiv) costs, fees, charges or assessments imposed by, or resulting from any mandate imposed on Landlord by, any federal, state or local
government for fire and police protection, trash removal, community services, or other services which do not constitute "Tax Expenses" as
that term is defined in Section 4.2.5, below, (xv) cost of tenant relation programs reasonably established by Landlord, and (xvi) payments
under any easement, license, operating agreement, declaration, restrictive covenant, or instrument pertaining to the sharing of costs by the
Building, including, without limitation, any covenants, conditions and restrictions affecting the property, and reciprocal easement agreements
affecting the property, any parking licenses, and any agreements with transit agencies affecting the Property (collectively, " Underlying
Documents"). Notwithstanding the foregoing, for purposes of this Lease, Operating Expenses shall not, however, include:
(a) costs, including legal fees, space planners' fees, advertising and promotional expenses (except as
otherwise set forth above), and brokerage fees incurred in connection with the original construction or development, or original or
future leasing of the Project, and costs, including permit, license and inspection costs, incurred with respect to the installation of tenant
improvements made for new tenants initially occupying space in the Project after the Lease Commencement Date or incurred in
renovating or otherwise improving, decorating, painting or redecorating vacant space for tenants or other occupants of the Project
(excluding, however, such costs relating to any common areas of the Project or parking facilities);
mortgages and other debt costs, if any, penalties and interest;
(b) except as set forth in items (xii), (xiii), and (xiv) above, depreciation, interest and principal payments on
(c) costs for which the Landlord is reimbursed by any tenant or occupant of the Project or by insurance by
its carrier or any tenant's carrier or by anyone else, and electric power costs for which any tenant directly contracts with the local public
service company;
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(d) any bad debt loss, rent loss, or reserves for bad debts or rent loss;
(e) costs associated with the operation of the business of the partnership or entity which constitutes the
Landlord, as the same are distinguished from the costs of operation of the Project (which shall specifically include, but not be limited
to, accounting costs associated with the operation of the Project). Costs associated with the operation of the business of the partnership
or entity which constitutes the Landlord include costs of partnership accounting and legal matters, costs of defending any lawsuits with
any mortgagee (except as the actions of the Tenant may be in issue), costs of selling, syndicating, financing, mortgaging or
hypothecating any of the Landlord's interest in the Project, and costs incurred in connection with any disputes between Landlord and its
employees, between Landlord and Project management, or between Landlord and other tenants or occupants;
(f) the wages and benefits of any employee who does not devote substantially all of his or her employed
time to the Project unless such wages and benefits are prorated to reflect time spent on operating and managing the Project vis-a-vis
time spent on matters unrelated to operating and managing the Project; provided, that in no event shall Operating Expenses for
purposes of this Lease include wages and/or benefits attributable to personnel above the level of Project manager;
(g) amount paid as ground rental for the Project by the Landlord;
(h) except for a Project management fee to the extent allowed pursuant to item (l) below, overhead and profit
increment paid to the Landlord or to subsidiaries or affiliates of the Landlord for services in the Project to the extent the same exceeds
the costs of such services rendered by qualified, first-class unaffiliated third parties on a competitive basis;
Landlord, provided that any compensation paid to any concierge at the Project shall be includable as an Operating Expense;
(i) any compensation paid to clerks, attendants or other persons in commercial concessions operated by the
(j) rentals and other related expenses incurred in leasing air conditioning systems, elevators or other
equipment which if purchased the cost of which would be excluded from Operating Expenses as a capital cost, except equipment not
affixed to the Project which is used in providing engineering, janitorial or similar services and, further excepting from this exclusion
such equipment rented or leased to remedy or ameliorate an emergency condition in the Project ;
Landlord provides selectively to one or more tenants (other than Tenant) without reimbursement;
(k) all items and services for which Tenant or any other tenant in the Project reimburses Landlord or which
(l) any costs expressly excluded from Operating Expenses elsewhere in this Lease;
(m) rent for any office space occupied by Project management personnel to the extent the size or rental rate
of such office space exceeds the size or fair market rental value of office space occupied by management personnel of the comparable
buildings in the vicinity of the Building, with adjustment where appropriate for the size of the applicable project;
and
(n) costs arising from the gross negligence or willful misconduct of Landlord in connection with this Lease;
(o) costs incurred to comply with laws relating to the removal of hazardous material (as defined under
applicable law) that was in existence in the Building or on the Project prior to the Lease Commencement Date, or that is introduced to
the Project after the Lease Commencement Date by anyone other than Tenant or the contractors, agents, servants, employees, invitees,
guests or licensees of Tenant.
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4.2.5 Taxes.
4.2.5.1 "Tax Expenses" shall mean all federal, state, county, or local governmental or municipal taxes, fees,
charges or other impositions of every kind and nature, whether general, special, ordinary or extraordinary (including, without limitation, real
estate taxes, general and special assessments, transit taxes, leasehold taxes or taxes based upon the receipt of rent, including gross receipts or
sales taxes applicable to the receipt of rent, unless required to be paid by Tenant, personal property taxes imposed upon the fixtures,
machinery, equipment, apparatus, systems and equipment, appurtenances, furniture and other personal property used in connection with the
Project, or any portion thereof), which shall be paid or accrued during any Expense Year (without regard to any different fiscal year used by
such governmental or municipal authority) because of or in connection with the ownership, leasing and operation of the Project, or any portion
thereof.
4.2.5.2 Tax Expenses shall include, without limitation: (i) Any tax on the rent, right to rent or other income from
the Project, or any portion thereof, or as against the business of leasing the Project, or any portion thereof; (ii) Any assessment, tax, fee, levy
or charge in addition to, or in substitution, partially or totally, of any assessment, tax, fee, levy or charge previously included within the
definition of real property tax; (iii) Any assessment, tax, fee, levy, or charge allocable to or measured by the area of the Premises or the Rent
payable hereunder, including, without limitation, any business or gross income tax or excise tax with respect to the receipt of such rent, or
upon or with respect to the possession, leasing, operating, management, maintenance, alteration, repair, use or occupancy by Tenant of the
Premises, or any portion thereof; and (iv) Any assessment, tax, fee, levy or charge, upon this transaction or any document to which Tenant is a
party, creating or transferring an interest or an estate in the Premises or the improvements thereon.
4.2.5.3 Any costs and expenses (including, without limitation, reasonable attorneys' and consultants' fees) incurred
in attempting to protest, reduce or minimize Tax Expenses shall be included in Tax Expenses in the Expense Year such expenses are
incurred. Tax refunds shall be credited against Tax Expenses and refunded to Tenant regardless of when received, based on the Expense Year
to which the refund is applicable, provided that in no event shall the amount to be refunded to Tenant for any such Expense Year exceed the
total amount paid by Tenant as Additional Rent under this Article 4 for such Expense Year. If Tax Expenses for any period during the Lease
Term or any extension thereof are increased after payment thereof for any reason, including, without limitation, error or reassessment by
applicable governmental or municipal authorities, Tenant shall pay Landlord upon demand Tenant's Share of any such increased Tax
Expenses. Notwithstanding anything to the contrary contained in this Section 4.2.5, there shall be excluded from Tax Expenses (i) all excess
profits taxes, franchise taxes, gift taxes, capital stock taxes, inheritance and succession taxes, estate taxes, federal and state income taxes, and
other taxes to the extent applicable to Landlord's net income (as opposed to rents, receipts or income attributable to operations at the Project),
(ii) any items included as Operating Expenses, and (iii) any items paid by Tenant under Section 4.5 of this Lease.
4.2.6 "Tenant's Share" shall mean the percentage set forth in Section 6 of the Summary.
4.3 Allocation of Direct Expenses. The parties acknowledge that the Building is a part of a multi-building project and that the costs
and expenses incurred in connection with the Project (i.e., the Direct Expenses) should be shared between the Building and the other buildings
in the Project. Accordingly, as set forth in Section 4.2 above, Direct Expenses (which consist of Operating Expenses and Tax Expenses) are
determined annually for the Project as a whole, and a portion of the Direct Expenses, which portion shall be determined by Landlord on an
equitable basis, shall be allocated to the Building (as opposed to other buildings in the Project). Such portion of Direct Expenses allocated to
the Building shall include all Direct Expenses attributable solely to the Building and an equitable portion of the Direct Expenses attributable to
the Project as a whole, and shall not include Direct Expenses attributable solely to other buildings in the Project.
4.4 Calculation and Payment of Additional Rent. Tenant shall pay to Landlord, in the manner set forth in Section 4.4.1, below, and
as Additional Rent, Tenant's Share of Direct Expenses for each Expense Year.
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4.4.1 Statement of Actual Direct Expenses and Payment by Tenant. Landlord shall endeavor to give to Tenant following
the end of each Expense Year, a statement (the "Statement") which shall state the Direct Expenses incurred or accrued for such preceding
Expense Year, and which shall indicate the amount of Tenant's Share of Direct Expenses. Upon receipt of the Statement for each Expense
Year commencing or ending during the Lease Term, Tenant shall pay, with its next installment of Base Rent due, the full amount of Tenant's
Share of Direct Expenses for such Expense Year, less the amounts, if any, paid during such Expense Year as " Estimated Direct Expenses,"
as that term is defined in Section 4.4.2, below, and if Tenant paid more as Estimated Direct Expenses than the actual Tenant's Share of Direct
Expenses, Tenant shall receive a credit in the amount of Tenant's overpayment against Rent next due under this Lease. The failure of
Landlord to timely furnish the Statement for any Expense Year shall not prejudice Landlord or Tenant from enforcing its rights under this
Article 4. Even though the Lease Term has expired and Tenant has vacated the Premises, when the final determination is made of Tenant's
Share of Direct Expenses for the Expense Year in which this Lease terminates, Tenant shall immediately pay to Landlord such amount, and if
Tenant paid more as Estimated Direct Expenses than the actual Tenant's Share of Direct Expenses, Landlord shall, within thirty (30) days,
deliver a check payable to Tenant in the amount of the overpayment. The provisions of this Section 4.4.1 shall survive the expiration or earlier
termination of the Lease Term.
4.4.2 Statement of Estimated Direct Expenses. In addition, Landlord shall endeavor to give Tenant a yearly expense
estimate statement (the "Estimate Statement") which shall set forth Landlord's reasonable estimate (the "Estimate") of what the total amount
of Direct Expenses for the then-current Expense Year shall be and the estimated Tenant's Share of Direct Expenses (the " Estimated Direct
Expenses"). The failure of Landlord to timely furnish the Estimate Statement for any Expense Year shall not preclude Landlord from
enforcing its rights to collect any Estimated Direct Expenses under this Article 4, nor shall Landlord be prohibited from revising any Estimate
Statement or Estimated Direct Expenses theretofore delivered to the extent necessary. Thereafter, Tenant shall pay, with its next installment of
Base Rent due, a fraction of the Estimated Direct Expenses for the then-current Expense Year (reduced by any amounts paid pursuant to the
last sentence of this Section 4.4.2). Such fraction shall have as its numerator the number of months which have elapsed in such current
Expense Year, including the month of such payment, and twelve (12) as its denominator. Until a new Estimate Statement is furnished (which
Landlord shall have the right to deliver to Tenant at any time), Tenant shall pay monthly, with the monthly Base Rent installments, an amount
equal to one-twelfth (1/12) of the total Estimated Direct Expenses set forth in the previous Estimate Statement delivered by Landlord to
Tenant.
4.5 Taxes and Other Charges for Which Tenant Is Directly Responsible . Tenant shall be liable for and shall pay ten (10) days
before delinquency, taxes levied against Tenant's equipment, furniture, fixtures and any other personal property located in or about the
Premises. If any such taxes on Tenant's equipment, furniture, fixtures and any other personal property are levied against Landlord or
Landlord's property or if the assessed value of Landlord's property is increased by the inclusion therein of a value placed upon such
equipment, furniture, fixtures or any other personal property and if Landlord pays the taxes based upon such increased assessment, which
Landlord shall have the right to do regardless of the validity thereof but only under proper protest if requested by Tenant, Tenant shall upon
demand repay to Landlord the taxes so levied against Landlord or the proportion of such taxes resulting from such increase in the assessment,
as the case may be.
5.
USE OF PREMISES
5.1 Permitted Use. Tenant shall use the Premises solely for the Permitted Use set forth in Section 7 of the Summary and Tenant
shall not use or permit the Premises or the Project to be used for any other purpose or purposes whatsoever without the prior written consent
of Landlord, which may be withheld in Landlord's sole discretion.
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5.2 Prohibited Uses. Tenant further covenants and agrees that Tenant shall not use, or suffer or permit any person or persons to use,
the Premises or any part thereof for any use or purpose in violation of the laws of the United States of America, the State of California, or the
ordinances, regulations or requirements of the local municipal or county governing body or other lawful authorities having jurisdiction over
the Project) including, without limitation, any such laws, ordinances, regulations or requirements relating to hazardous materials or
substances, as those terms are defined by applicable laws now or hereafter in effect, or any Underlying Documents. Landlord shall have the
right to impose reasonable and customary rule and regulations regarding the use of the Project, as reasonably deemed necessary by Landlord
with respect to the orderly operation of the Project, and Tenant shall comply with such reasonable rules and regulations. Tenant shall not do or
permit anything to be done in or about the Premises which will in any way damage the reputation of the Project or obstruct or interfere with
the rights of other tenants or occupants of the Building, or injure or annoy them or use or allow the Premises to be used for any improper,
unlawful or objectionable purpose, nor shall Tenant cause, maintain or permit any nuisance in, on or about the Premises. Tenant shall comply
with, and Tenant's rights and obligations under the Lease and Tenant's use of the Premises shall be subject and subordinate to, all recorded
easements, covenants, conditions, and restrictions now or hereafter affecting the Project.
5.3 Hazardous Materials.
5.3.1 Tenant's Obligations.
5.3.1.1 Prohibitions. As a material inducement to Landlord to enter into this Lease with Tenant, Tenant has fully
and accurately completed Landlord’s Pre-Leasing Environmental Exposure Questionnaire (the “ Environmental Questionnaire”), which is
attached as Exhibit E. Tenant agrees that except for those chemicals or materials, and their respective quantities, specifically listed on the
Environmental Questionnaire, neither Tenant nor Tenant’s employees, contractors and subcontractors of any tier, entities with a contractual
relationship with Tenant (other than Landlord), or any entity acting as an agent or sub-agent of Tenant (collectively, " Tenant's Agents") will
produce, use, store or generate any "Hazardous Materials," as that term is defined below, on, under or about the Premises, nor cause or permit
any Hazardous Material to be brought upon, placed, stored, manufactured, generated, blended, handled, recycled, used or "Released," as that
term is defined below, on, in, under or about the Premises. If any material information provided to Landlord by Tenant on the Environmental
Questionnaire, or otherwise relating to information concerning Hazardous Materials is false, incomplete, or misleading in any material respect,
the same shall be deemed a default by Tenant under this Lease. Tenant shall deliver to Landlord an updated Environmental Questionnaire at
least once a year. Landlord’s prior written consent shall be required to any material change in Hazardous Materials use for the Premises
described on the initial Environmental Questionnaire, such consent not to be unreasonably withheld. Tenant shall not install or permit any
underground storage tank on the Premises. For purposes of this Lease, "Hazardous Materials" means all flammable explosives, petroleum
and petroleum products, waste oil, radon, radioactive materials, toxic pollutants, asbestos, polychlorinated biphenyls (“PCBs”), medical waste,
chemicals known to cause cancer or reproductive toxicity, pollutants, contaminants, hazardous wastes, toxic substances or related materials,
including without limitation any chemical, element, compound, mixture, solution, substance, object, waste or any combination thereof, which
is or may be hazardous to human health, safety or to the environment due to its radioactivity, ignitability, corrosiveness, reactivity,
explosiveness, toxicity, carcinogenicity, infectiousness or other harmful or potentially harmful properties or effects, or defined as, regulated as
or included in, the definition of “hazardous substances,” “hazardous wastes,” “hazardous materials,” or “toxic substances” under any
Environmental Laws. The term “Hazardous Materials” for purposes of this Lease shall also include any mold, fungus or spores, whether or
not the same is defined, listed, or otherwise classified as a “hazardous material” under any Environmental Laws, if such mold, fungus or
spores may pose a risk to human health or the environment or negatively impact the value of the Premises. For purposes of this Lease,
"Release" or "Released" or "Releases" shall mean any release, deposit, discharge, emission, leaking, spilling, seeping, migrating, injecting,
pumping, pouring, emptying, escaping, dumping, disposing, or other movement of Hazardous Materials into the environment.
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5.3.1.2 Notices to Landlord. Tenant shall notify Landlord in writing as soon as possible but in no event later than
five (5) days after (i) the occurrence of any actual, alleged or threatened Release of any Hazardous Material in, on, under, from, about or in the
vicinity of the Premises (whether past or present), regardless of the source or quantity of any such Release, or (ii) Tenant becomes aware of
any regulatory actions, inquiries, inspections, investigations, directives, or any cleanup, compliance, enforcement or abatement proceedings
(including any threatened or contemplated investigations or proceedings) relating to or potentially affecting the Premises, or (iii) Tenant
becomes aware of any claims by any person or entity relating to any Hazardous Materials in, on, under, from, about or in the vicinity of the
Premises, whether relating to damage, contribution, cost recovery, compensation, loss or injury. Collectively, the matters set forth in
clauses (i), (ii) and (iii) above are hereinafter referred to as “Hazardous Materials Claims”. Tenant shall promptly forward to Landlord
copies of all orders, notices, permits, applications and other communications and reports in connection with any Hazardous Materials
Claims. Additionally, Tenant shall promptly advise Landlord in writing of Tenant’s discovery of any occurrence or condition on, in, under or
about the Premises that could subject Tenant or Landlord to any liability, or restrictions on ownership, occupancy, transferability or use of the
Premises under any "Environmental Laws," as that term is defined below. Tenant shall not enter into any legal proceeding or other action,
settlement, consent decree or other compromise with respect to any Hazardous Materials Claims without first notifying Landlord of Tenant’s
intention to do so and affording Landlord the opportunity to join and participate, as a party if Landlord so elects, in such proceedings and in no
event shall Tenant enter into any agreements which are binding on Landlord or the Premises without Landlord’s prior written
consent. Landlord shall have the right to appear at and participate in, any and all legal or other administrative proceedings concerning any
Hazardous Materials Claim. For purposes of this Lease, “Environmental Laws” means all applicable present and future laws relating to the
protection of human health, safety, wildlife or the environment, including, without limitation, (i) all requirements pertaining to reporting,
licensing, permitting, investigation and/or remediation of emissions, discharges, Releases, or threatened Releases of Hazardous Materials,
whether solid, liquid, or gaseous in nature, into the air, surface water, groundwater, or land, or relating to the manufacture, processing,
distribution, use, treatment, storage, disposal, transport, or handling of Hazardous Materials; and (ii) all requirements pertaining to the health
and safety of employees or the public. Environmental Laws include, but are not limited to, the Comprehensive Environmental Response,
Compensation and Liability Act of 1980, 42 USC § 9601, et seq., the Hazardous Materials Transportation Authorization Act of 1994, 49 USC
§ 5101, et seq., the Solid Waste Disposal Act, as amended by the Resource Conservation and Recovery Act of 1976, and Hazardous and Solid
Waste Amendments of 1984, 42 USC § 6901, et seq., the Federal Water Pollution Control Act, as amended by the Clean Water Act of 1977,
33 USC § 1251, et seq., the Clean Air Act of 1966, 42 USC § 7401, et seq., the Toxic Substances Control Act of 1976, 15 USC § 2601, et
seq., the Safe Drinking Water Act of 1974, 42 USC §§ 300f through 300j, the Occupational Safety and Health Act of 1970, as amended,
29 USC § 651 et seq., the Oil Pollution Act of 1990, 33 USC § 2701 et seq., the Emergency Planning and Community Right-To-Know Act of
1986, 42 USC § 11001 et seq., the National Environmental Policy Act of 1969, 42 USC § 4321 et seq., the Federal Insecticide, Fungicide and
Rodenticide Act of 1947, 7 USC § 136 et seq., California Carpenter-Presley-Tanner Hazardous Substance Account Act, California Health &
Safety Code §§ 25300 et seq., Hazardous Materials Release Response Plans and Inventory Act, California Health & Safety Code, §§ 25500 et
seq., Underground Storage of Hazardous Substances provisions, California Health & Safety Code, §§ 25280 et seq., California Hazardous
Waste Control Law, California Health & Safety Code, §§ 25100 et seq., and any other state or local law counterparts, as amended, as such
applicable laws, are in effect as of the Lease Commencement Date, or thereafter adopted, published, or promulgated.
5.3.1.3 Releases of Hazardous Materials. If any Release of any Hazardous Material in, on, under, from or about
the Premises shall occur at any time during the Lease and/or if any other Hazardous Material condition exists at the Premises that requires
response actions of any kind, and such Release or condition is or was caused by Tenant or an invitee of Tenant, then, in addition to notifying
Landlord as specified above, Tenant, at its own sole cost and expense, shall (i) immediately comply with any and all reporting requirements
imposed pursuant to any and all Environmental Laws, (ii) provide a written certification to Landlord indicating that Tenant has complied with
all applicable reporting requirements, (iii) take any and all necessary investigation, corrective and remedial action in accordance with any and
all applicable Environmental Laws, utilizing an environmental consultant approved by Landlord, all in accordance with the provisions and
requirements of this Section 5.3, including, without limitation, Section 5.3.4, and (iv) take any such additional investigative, remedial and
corrective actions as Landlord shall in its reasonable discretion deem necessary such that the Premises are remediated to the condition existing
prior to such Release.
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5.3.1.4 Indemnification. Without limiting in any way Tenant’s obligations under any other provision of this Lease,
Tenant shall be solely responsible for and shall protect, defend, indemnify and hold the Landlord Parties harmless from and against any and all
claims, judgments, losses, damages, costs, expenses, penalties, enforcement actions, taxes, fines, remedial actions, liabilities (including,
without limitation, actual attorneys’ fees, litigation, arbitration and administrative proceeding costs, expert and consultant fees and laboratory
costs) including, without limitation, consequential damages and sums paid in settlement of claims, which arise during or after the Lease Term,
whether foreseeable or unforeseeable, that arise during or after the Lease Term in whole or in part, foreseeable or unforeseeable, directly or
indirectly arising out of or attributable to the presence, use, generation, manufacture, treatment, handling, refining, production, processing,
storage, Release or presence of Hazardous Materials in, on, under or about the Premises by Tenant or Tenant's Agents. The foregoing
indemnity shall not be applicable to claims based on any Hazardous Materials existing on, in or under the Premises, Building or Project as of
the date of this Lease, except to the extent the actions of Tenant or Tenant's Agents exacerbate any previously existing Hazardous Materials
condition.
5.3.1.5 Compliance with Environmental Laws. Without limiting the generality of Tenant’s obligation to comply
with applicable laws as otherwise provided in this Lease, Tenant shall, at its sole cost and expense, comply with all Environmental
Laws. Tenant shall obtain and maintain any and all necessary permits, licenses, certifications and approvals appropriate or required for the
use, handling, storage, and disposal of any Hazardous Materials used, stored, generated, transported, handled, blended, or recycled by Tenant
on the Premises. Landlord shall have a continuing right, without obligation, to require Tenant to obtain, and to review and inspect any and all
such permits, licenses, certifications and approvals, together with copies of any and all Hazardous Materials management plans and programs,
any and all Hazardous Materials risk management and pollution prevention programs, and any and all Hazardous Materials emergency
response and employee training programs respecting Tenant’s use of Hazardous Materials. Upon request of Landlord, Tenant shall deliver to
Landlord a narrative description explaining the nature and scope of Tenant’s activities involving Hazardous Materials and showing to
Landlord’s satisfaction compliance with all Environmental Laws and the terms of this Lease.
5.3.2 Assurance of Performance.
5.3.2.1 Environmental Assessments In General. Landlord may, but shall not be required to, engage from time to
time such contractors as Landlord determines to be appropriate to perform environmental assessments of a scope reasonably determined by
Landlord (an "Environmental Assessment ") to ensure Tenant’s compliance with the requirements of this Lease with respect to Hazardous
Materials. .
5.3.2.2 Costs of Environmental Assessments. All costs and expenses incurred by Landlord in connection with any
such Environmental Assessment initially shall be paid by Landlord; provided that if any such Environmental Assessment shows that Tenant
has failed to comply with the provisions of this Section 5.3, then all of the costs and expenses of such Environmental Assessment shall be
reimbursed by Tenant as Additional Rent within ten (10) days after receipt of written demand therefor.
5.3.3 Tenant’s Obligations upon Surrender. At the expiration or earlier termination of the Lease Term, Tenant, at
Tenant’s sole cost and expense, shall: (i) cause an Environmental Assessment of the Premises to be conducted in accordance with Section
15.3; (ii) cause all Hazardous Materials to be removed from the Premises and disposed of in accordance with all Environmental Laws and as
necessary to allow the Premises to be used for any purpose; and (iii) cause to be removed all containers installed or used by Tenant or Tenant’s
Agents to store any Hazardous Materials on the Premises, and cause to be repaired any damage to the Premises caused by such removal.
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5.3.4 Clean-up.
5.3.4.1 Environmental Reports; Clean-Up. If any written report, including any report containing results of any
Environmental Assessment (an “Environmental Report”) shall indicate (i) the presence of any Hazardous Materials as to which Tenant has a
removal or remediation obligation under this Section 5.3, and (ii) that as a result of same, the investigation, characterization, monitoring,
assessment, repair, closure, remediation, removal, or other clean-up (the “Clean-up”) of any Hazardous Materials is required, Tenant shall
immediately prepare and submit to Landlord within thirty (30) days after receipt of the Environmental Report a comprehensive plan, subject
to Landlord’s written approval, specifying the actions to be taken by Tenant to perform the Clean-up so that the Premises are restored to the
conditions required by this Lease. Upon Landlord’s approval of the Clean-up plan, Tenant shall, at Tenant’s sole cost and expense, without
limitation on any rights and remedies of Landlord under this Lease, immediately implement such plan with a consultant reasonably acceptable
to Landlord and proceed to Clean-Up Hazardous Materials in accordance with all applicable laws and as required by such plan and this
Lease. If, within thirty (30) days after receiving a copy of such Environmental Report, Tenant fails either (a) to complete such Clean-up, or
(b) with respect to any Clean-up that cannot be completed within such thirty-day period, fails to proceed with diligence to prepare the Clean-
up plan and complete the Clean-up as promptly as practicable, then Landlord shall have the right, but not the obligation, and without waiving
any other rights under this Lease, to carry out any Clean-up recommended by the Environmental Report or required by any governmental
authority having jurisdiction over the Premises, and recover all of the costs and expenses thereof from Tenant as Additional Rent, payable
within ten (10) days after receipt of written demand therefor.
5.3.4.2 No Rent Abatement . Tenant shall continue to pay all Rent due or accruing under this Lease during any
Clean-up, and shall not be entitled to any reduction, offset or deferral of any Base Rent or Additional Rent due or accruing under this Lease
during any such Clean-up.
5.3.4.3 Surrender of Premises. Tenant shall complete any Clean-up prior to surrender of the Premises upon the
expiration or earlier termination of this Lease. Tenant shall obtain and deliver to Landlord a letter or other written determination from the
overseeing governmental authority confirming that the Clean-up has been completed in accordance with all requirements of such
governmental authority and that no further response action of any kind is required for the unrestricted use of the Premises (“Closure
Letter”). Upon the expiration or earlier termination of this Lease, Tenant shall also be obligated to close all permits obtained in connection
with Hazardous Materials in accordance with applicable laws.
5.3.4.4 Failure to Timely Clean-Up. Should any Clean-up for which Tenant is responsible not be completed, or
should Tenant not receive the Closure Letter and any governmental approvals required under Environmental Laws in conjunction with such
Clean-up prior to the expiration or earlier termination of this Lease, then Tenant shall be liable to Landlord as a holdover tenant (as more
particularly provided in Article 16) until Tenant has fully complied with its obligations under this Section 5.3.
5.3.5 Confidentiality. Unless compelled to do so by applicable law, Tenant agrees that Tenant shall not disclose, discuss,
disseminate or copy any information, data, findings, communications, conclusions and reports regarding the environmental condition of the
Premises to any Person (other than Tenant’s consultants, attorneys, property managers and employees that have a need to know such
information), including any governmental authority, without the prior written consent of Landlord. In the event Tenant reasonably believes
that disclosure is compelled by applicable law, it shall provide Landlord ten (10) days’ advance notice of disclosure of confidential
information so that Landlord may attempt to obtain a protective order. Tenant may additionally release such information to bona fide
prospective purchasers or lenders, subject to any such parties’ written agreement to be bound by the terms of this Section 5.3.
5.3.6 Copies of Environmental Reports. Within thirty (30) days of receipt thereof, Tenant shall provide Landlord with a
copy of any and all environmental assessments, audits, studies and reports regarding Tenant’s activities with respect to the Premises, or ground
water beneath the Land, or the environmental condition or Clean-up thereof. Tenant shall be obligated to provide Landlord with a copy of
such materials without regard to whether such materials are generated by Tenant or prepared for Tenant, or how Tenant comes into possession
of such materials.
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5.3.7 Signs, Response Plans, Etc. Tenant shall be responsible for posting on the Premises any signs required under
applicable Environmental Laws. Tenant shall also complete and file any business response plans or inventories required by any applicable
laws. Tenant shall concurrently file a copy of any such business response plan or inventory with Landlord.
5.3.8 Survival. Each covenant, agreement, representation, warranty and indemnification made by Tenant set forth in this
Section 5.3 shall survive the expiration or earlier termination of this Lease and shall remain effective until all of Tenant’s obligations under
this Section 5.3 have been completely performed and satisfied.
6.
SERVICES AND UTILITIES
6.1 In General. Tenant will be responsible, at its sole cost and expense, for the furnishing of all services and utilities to the Premises,
including, but not limited to heating, ventilation and air-conditioning, electricity, water, telephone, janitorial and interior Premises security
services.
the Premises and shall be paid directly by Tenant to the applicable utility provider.
6.1.1 All utilities (including without limitation, electricity, gas, sewer and water) to the Building are separately metered at
6.1.2 Landlord shall not provide janitorial services for the Premises. Tenant shall be solely responsible for performing all
janitorial services and other cleaning of the Premises, all in compliance with applicable laws. The janitorial and cleaning of the Premises shall
be adequate to maintain the Premises in a manner consistent with First Class Life Sciences Projects.
Tenant shall cooperate fully with Landlord at all times and abide by all regulations and requirements that Landlord may reasonably
prescribe for the proper functioning and protection of the HVAC, electrical, mechanical and plumbing systems. Provided that Landlord agrees
to provide and maintain and keep in continuous service utility connections to the Project, including electricity, water and sewage connections,
Landlord shall have no obligation to provide any services or utilities to the Building, including, but not limited to heating, ventilation and air-
conditioning, electricity, water, telephone, janitorial and interior Building security services.
6.2 Interruption of Use. Tenant agrees that Landlord shall not be liable for damages, by abatement of Rent or otherwise, for failure
to furnish or delay in furnishing any service (including telephone and telecommunication services), or for any diminution in the quality or
quantity thereof, when such failure or delay or diminution is occasioned, in whole or in part, by breakage, repairs, replacements, or
improvements, by any strike, lockout or other labor trouble, by inability to secure electricity, gas, water, or other fuel at the Building or
Project after reasonable effort to do so, by any riot or other dangerous condition, emergency, accident or casualty whatsoever, by act or default
of Tenant or other parties, or by any other cause; and such failures or delays or diminution shall never be deemed to constitute an eviction or
disturbance of Tenant's use and possession of the Premises or relieve Tenant from paying Rent or performing any of its obligations under this
Lease. Furthermore, Landlord shall not be liable under any circumstances for a loss of, or injury to, property or for injury to, or interference
with, Tenant's business, including, without limitation, loss of profits, however occurring, through or in connection with or incidental to a
failure to furnish any of the services or utilities as set forth in this Article 6.
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7.
REPAIRS
7.1 Tenant Repair Obligations. Tenant shall, throughout the Term, at its sole cost and expense, maintain, repair, replace and
improve as required, the Premises and every part thereof in a good standard of maintenance, repair and replacement as required, and in good
and sanitary condition, all in accordance with the standards of First Class Life Sciences Projects, except for Landlord Repair Obligations,
whether or not such maintenance, repair, replacement or improvement is required in order to comply with applicable Laws ("Tenant's Repair
Obligations"), including, without limitation, the following: (1) glass, windows, window frames, window casements (including the repairing,
resealing, cleaning and replacing of both interior and exterior windows) and skylights; (2) interior and exterior doors, door frames and door
closers; (3) interior lighting (including, without limitation, light bulbs and ballasts); (4) the plumbing, sewer, drainage, electrical, fire
protection, elevator, escalator, life safety and security systems and equipment, existing heating, ventilation and air-conditioning systems, and
all other mechanical, electrical and communications systems and equipment (collectively, the " Premises Systems"), including without
limitation (i) any specialty or supplemental Premises Systems installed by or for Tenant and (ii) all electrical facilities and equipment,
including lighting fixtures, lamps, fans and any exhaust equipment and systems, electrical motors and all other appliances and equipment of
every kind and nature located in, upon or about the Premises; (5) all communications systems serving the Premises; (6) all of Tenant's security
systems in or about or serving the Premises; (7) Tenant's signage; (8) interior demising walls and partitions (including painting and wall
coverings), equipment, floors, and any roll-up doors, ramps and dock equipment; and (9) the non-structural portions of the roof of the
Building, including the roof membrane and coverings. Tenant’s Repair Obligations also includes the routine maintenance of the load bearing
and exterior walls of the Building within the Premises, including, without limitation, any painting, sealing, patching and waterproofing of such
walls. Tenant shall additionally be responsible, at Tenant’s sole cost and expense, to furnish all expendables, including light bulbs, paper
goods and soaps, used in the Premises, and, to the extent that Landlord notifies Tenant in writing of its intention to no longer arrange for such
monitoring, cause the fire alarm systems serving the Premises to be monitored by a monitoring or protective services firm approved by
Landlord in writing.
7.2 Service Contracts. All Building Systems, including HVAC, elevators, main electrical, plumbing and fire/life-safety systems,
shall be maintained, repaired and replaced by Tenant (i) in a commercially reasonable first-class condition, (ii) in accordance with any
applicable manufacturer specifications relating to any particular component of such Premises Systems, (iii) in accordance with applicable
Laws. Tenant shall contract with a qualified, experienced professional third party service companies (a " Service Contract"). Tenant shall
regularly, in accordance with commercially reasonable standards, generate and maintain preventive maintenance records relating to each
Building’s mechanical and main electrical systems, including life safety, elevators and the central plant (“Preventative Maintenance
Records”). In addition, upon Landlord’s request, Tenant shall deliver a copy of all current Service Contracts to Landlord and/or a copy of the
Preventative Maintenance Records.
7.3 Landlord's Right to Perform Tenant's Repair Obligations . Tenant shall notify Landlord in writing at least thirty (30) days
prior to performing any material Tenant's Repair Obligations, including without limitation, any Tenant's Repair Obligation which affect the
Premises Systems or which is reasonably anticipated to cost more than $100,000.00. Upon receipt of such notice from Tenant, Landlord shall
have the right to either (i) perform such material Tenant's Repair Obligation by delivering notice of such election to Tenant within thirty (30)
days following receipt of Tenant's notice, and Tenant shall pay Landlord the cost thereof (including Landlord's reasonable supervision fee)
within thirty (30) days after receipt of an invoice therefor, or (ii) require Tenant to perform such Tenant's Repair Obligation at Tenant's sole
cost and expense. If Tenant fails to perform any Tenant's Repair Obligation within a reasonable time period, as reasonably determined by
Landlord, then Landlord may, but need not, following delivery of notice to Tenant of such election, make such Tenant Repair Obligation, and
Tenant shall pay Landlord the cost thereof, (including Landlord's reasonable supervision fee) within thirty (30) days after receipt of an invoice
therefor.
7.4 Landlord Repair Obligations. Landlord shall be responsible for repairs to the exterior walls, foundation and roof of the
Building, the structural portions of the floors of the Building, except to the extent that such repairs are required due to the negligence or willful
misconduct of Tenant (the "Landlord Repair Obligation"); provided, however, that if such repairs are due to the negligence or willful
misconduct of Tenant, Landlord shall nevertheless make such repairs at Tenant's expense, or, if covered by Landlord's insurance, Tenant shall
only be obligated to pay any deductible in connection therewith.
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8.
ADDITIONS AND ALTERATIONS
8.1 Landlord's Consent to Alterations . Tenant may not make any improvements, alterations, additions or changes to the Premises
or any mechanical, plumbing or HVAC facilities or systems pertaining to the Premises (collectively, the " Alterations") without first procuring
the prior written consent of Landlord to such Alterations, which consent shall be requested by Tenant not less than ten (10) business days prior
to the commencement thereof, and which consent shall not be unreasonably withheld by Landlord, provided it shall be deemed reasonable for
Landlord to withhold its consent to any Alteration which adversely affects the structural portions or the systems or equipment of the Building
or is visible from the exterior of the Building. Notwithstanding the foregoing, Tenant shall be permitted to make Alterations following ten
(10) business days notice to Landlord, but without Landlord's prior consent, to the extent that such Alterations (i) do not affect the building
systems or equipment, (ii) are not visible from the exterior of the Building, and (iii) cost less than $50,000.00 for a particular job of work. The
construction of the initial improvements to the Premises shall be governed by the terms of the Tenant Work Letter and not the terms of this
Article 8.
8.2 Manner of Construction. Landlord may impose, as a condition of its consent to any and all Alterations or repairs of the
Premises or about the Premises, such requirements as Landlord in its reasonable discretion may deem desirable, including, but not limited to,
the requirement that upon Landlord's request, Tenant shall, at Tenant's expense, remove such Alterations upon the expiration or any early
termination of the Lease Term. Tenant shall construct such Alterations and perform such repairs in a good and workmanlike manner, in
conformance with any and all applicable federal, state, county or municipal laws, rules and regulations and pursuant to a valid building permit,
issued by the city in which the Building is located (or other applicable governmental authority). Tenant shall not use (and upon notice from
Landlord shall cease using) contractors, services, workmen, labor, materials or equipment that, in Landlord's reasonable judgment, would
disturb labor harmony with the workforce or trades engaged in performing other work, labor or services in or about the Building or the
Common Areas. Upon completion of any Alterations (or repairs), Tenant shall deliver to Landlord final lien waivers from all contractors,
subcontractors and materialmen who performed such work. In addition to Tenant's obligations under Article 9 of this Lease, upon completion
of any Alterations, Tenant agrees to cause a Notice of Completion to be recorded in the office of the Recorder of the County of San Francisco
in accordance with Section 3093 of the Civil Code of the State of California or any successor statute, and Tenant shall deliver to the Project
construction manager a reproducible copy of the "as built" drawings of the Alterations as well as all permits, approvals and other documents
issued by any governmental agency in connection with the Alterations.
8.3 Payment for Improvements. If Tenant orders any work directly from Landlord, Tenant shall pay to Landlord an amount equal
to five percent (5%) of the cost of such work to compensate Landlord for all overhead, general conditions, fees and other costs and expenses
arising from Landlord's involvement with such work. If Tenant does not order any work directly from Landlord, Tenant shall reimburse
Landlord for Landlord's reasonable, actual, out-of-pocket costs and expenses actually incurred in connection with Landlord's review of such
work.
8.4 Construction Insurance. In addition to the requirements of Article 10 of this Lease, in the event that Tenant makes any
Alterations, prior to the commencement of such Alterations, Tenant shall provide Landlord with evidence that Tenant carries " Builder's All
Risk" insurance in an amount approved by Landlord covering the construction of such Alterations, and such other insurance as Landlord may
reasonably require, it being understood and agreed that all of such Alterations shall be insured by Tenant pursuant to Article 10 of this Lease
immediately upon completion thereof. In addition, Tenant's contractors and subcontractors shall be required to carry (i) Commercial General
Liability Insurance in an amount approved by Landlord, with Landlord, and, at Landlord's option, Landlord's property manager and project
manager, as additional insureds in an amount approved by Landlord, and otherwise in accordance with the requirements of Article 10 of this
Lease, and (ii) workers compensation insurance with a waiver of subrogation in favor of Landlord . Landlord may, in its discretion, require
Tenant to obtain a lien and completion bond or some alternate form of security satisfactory to Landlord in an amount sufficient to ensure the
lien-free completion of such Alterations and naming Landlord as a co-obligee.
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8.5 Landlord's Property. All Alterations, improvements, fixtures, built-in equipment and/or appurtenances which may be installed
in or about the Premises, from time to time, shall be at the sole cost of Tenant and shall be and become the property of Landlord and remain in
place at the Premises following the expiration or earlier termination of this Lease. Notwithstanding the foregoing, Landlord may, by written
notice to Tenant prior to the end of the Lease Term, or given following any earlier termination of this Lease, require Tenant, at Tenant's
expense, to remove any Alterations and/or improvements and/or systems and equipment within the Premises and to repair any damage to the
Premises and Building caused by such removal and return the affected portion of the Premises to a building standard tenant improved
condition as determined by Landlord. If Tenant fails to complete such removal and/or to repair any damage caused by the removal of any
Alterations and/or improvements and/or systems and equipment in the Premises and return the affected portion of the Premises to a building
standard tenant improved condition as reasonably determined by Landlord, Landlord may do so and may charge the reasonable cost thereof to
Tenant. Tenant hereby protects, defends, indemnifies and holds Landlord harmless from any liability, cost, obligation, expense or claim of
lien in any manner relating to the installation, placement, removal or financing of any such Alterations, improvements, fixtures and/or
equipment in, on or about the Premises, which obligations of Tenant shall survive the expiration or earlier termination of this Lease.
9.
COVENANT AGAINST LIENS Tenant shall keep the Project and Premises free from any liens or encumbrances arising out of
the work performed, materials furnished or obligations incurred by or on behalf of Tenant, and shall protect, defend, indemnify and hold
Landlord harmless from and against any claims, liabilities, judgments or costs (including, without limitation, reasonable attorneys' fees and
costs) arising out of same or in connection therewith. Tenant shall give Landlord notice at least twenty (20) days prior to the commencement
of any such work on the Premises (or such additional time as may be necessary under applicable laws) to afford Landlord the opportunity of
posting and recording appropriate notices of non-responsibility (to the extent applicable pursuant to then applicable laws). Tenant shall
remove any such lien or encumbrance by bond or otherwise within ten (10) business days after notice by Landlord, and if Tenant shall fail to
do so, Landlord may pay the amount necessary to remove such lien or encumbrance, without being responsible for investigating the validity
thereof.
10.
INSURANCE
10.1 Indemnification and Waiver. Tenant hereby assumes all risk of damage to property or injury to persons in, upon or about the
Premises from any cause whatsoever and agrees that Landlord, its partners, subpartners and their respective officers, agents, servants,
employees, lenders, any property manager and independent contractors (collectively, "Landlord Parties") shall not be liable for, and are
hereby released from any responsibility for, any damage either to person or property or resulting from the loss of use thereof, which damage is
sustained by Tenant or by other persons claiming through Tenant. Tenant shall indemnify, defend, protect, and hold harmless the Landlord
Parties from any and all claims, loss, cost, damage, injury, expense and liability (including without limitation court costs and reasonable
attorneys' fees) incurred in connection with or arising from any cause in, on or about the Premises, any acts, omissions or negligence of Tenant
or of any person claiming by, through or under Tenant, or of the contractors, agents, servants, employees, invitees, guests or licensees of
Tenant or any such person, in, on or about the Project or any breach of the terms of this Lease, either prior to, during, or after the expiration of
the Lease Term, provided that the terms of the foregoing indemnity shall not apply to the gross negligence or willful misconduct of
Landlord. Should Landlord be named as a defendant in any suit brought against Tenant in connection with or arising out of Tenant's
occupancy of the Premises, Tenant shall pay to Landlord its costs and expenses incurred in such suit, including without limitation, its actual
professional fees such as reasonable appraisers', accountants' and attorneys' fees. The provisions of this Section 10.1 shall survive the
expiration or sooner termination of this Lease with respect to any claims or liability arising in connection with any event occurring prior to
such expiration or termination.
10.2 Tenant's Compliance With Landlord's Property Insurance . Landlord shall insure the Building during the Lease Term
against loss or damage under an "all risk" property insurance policy. Such coverage shall be in such amounts, from such companies, and on
such other terms and conditions, as Landlord may from time to time reasonably determine. Additionally, at the option of Landlord, such
insurance coverage may include the risks of earthquakes and/or flood damage and additional hazards, a rental loss endorsement and one or
more loss payee endorsements in favor of the holders of any mortgages or deeds of trust encumbering the interest of Landlord in the Building
or the ground or underlying lessors of the Building, or any portion thereof. Tenant shall, at Tenant's expense, comply with all insurance
company requirements pertaining to the use of the Premises. If Tenant's conduct or use of the Premises causes any increase in the premium
for such insurance policies then Tenant shall reimburse Landlord for any such increase. Tenant, at Tenant's expense, shall comply with all
rules, orders, regulations or requirements of the American Insurance Association (formerly the National Board of Fire Underwriters) and with
any similar body.
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10.3 Tenant's Insurance. Tenant shall maintain the following coverages in the following amounts.
10.3.1 Commercial General Liability Insurance on an occurrence form covering the insured against claims of bodily injury,
personal injury and property damage (including loss of use thereof) arising out of Tenant's operations, and contractual liabilities including a
contractual coverage, and including products and completed operations coverage, for limits of liability on a per location basis of not less than:
Bodily Injury and
Property Damage Liability
Personal Injury Liability
$5,000,000 each occurrence
$5,000,000 annual aggregate
$3,000,000 each occurrence
$3,000,000 annual aggregate
10.3.2 Property Insurance covering (i) all office furniture, business and trade fixtures, office equipment, free-standing
cabinet work, movable partitions, merchandise and all other items of Tenant's property on the Premises installed by, for, or at the expense of
Tenant, (ii) the "Tenant Improvements," as that term is defined in the Tenant Work Letter, and any other improvements which exist in the
Premises as of the Lease Commencement Date (excluding the Base Building) (the "Original Improvements"), and (iii) all other
improvements, alterations and additions to the Premises. Such insurance shall be written on an "all risks" of physical loss or damage basis,
for the full replacement cost value (subject to reasonable deductible amounts) new without deduction for depreciation of the covered items and
in amounts that meet any co-insurance clauses of the policies of insurance and shall include coverage for damage or other loss caused by fire
or other peril including, but not limited to, vandalism and malicious mischief, theft, water damage of any type, including sprinkler leakage,
bursting or stoppage of pipes, and explosion.
Tenant for actual direct or indirect loss of earnings attributable to the risks outlined in Section 10.3.2 above.
10.3.3 Business Income Interruption for one (1) year plus Extra Expense insurance in such amounts as will reimburse
10.3.4 Worker's Compensation and Employer's Liability or other similar insurance pursuant to all applicable state and local
statutes and regulations. The policy shall include a waiver of subrogation in favor of Landlord, its employees, Lenders and any property
manager or partners.
10.4 Form of Policies. The minimum limits of policies of insurance required of Tenant under this Lease shall in no event limit the
liability of Tenant under this Lease. Such insurance shall (i) name Landlord, its subsidiaries and affiliates, its property manager (if any) and
any other party the Landlord so specifies, as an additional insured or loss payee, as applicable, including Landlord's managing agent, if any;
(ii) be issued by an insurance company having a rating of not less than A:IX in Best's Insurance Guide or which is otherwise acceptable to
Landlord and licensed to do business in the State of California; (iv) be primary insurance as to all claims thereunder and provide that any
insurance carried by Landlord is excess and is non-contributing with any insurance required of Tenant; (v) be in form and content reasonably
acceptable to Landlord; and (vi) provide that said insurance shall not be canceled or coverage changed unless thirty (30) days' prior written
notice shall have been given to Landlord and any mortgagee of Landlord (unless such cancellation is the result of non-payment of
premiums). Tenant shall deliver said policy or policies or certificates thereof to Landlord on or before the Lease Commencement Date and at
least ten (10) days before the expiration dates thereof. In the event Tenant shall fail to procure such insurance, or to deliver such policies or
certificate, Landlord may, at its option, procure such policies for the account of Tenant, and the cost thereof shall be paid to Landlord within
five (5) days after delivery to Tenant of bills therefor.
10.5 Subrogation. Landlord and Tenant hereby agree to look solely to, and seek recovery only from, their respective insurance
carriers in the event of a property or business interruption loss to the extent that such coverage is agreed to be provided hereunder. The parties
each hereby waive all rights and claims against each other for such losses, and waive all rights of subrogation of their respective insurers,
provided such waiver of subrogation shall not affect the right to the insured to recover thereunder. The parties agree that their respective
insurance policies do now, or shall, contain the waiver of subrogation.
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10.6 Additional Insurance Obligations. Tenant shall carry and maintain during the entire Lease Term, at Tenant's sole cost and
expense, increased amounts of the insurance required to be carried by Tenant pursuant to this Article 10 and such other reasonable types of
insurance coverage and in such reasonable amounts covering the Premises and Tenant's operations therein, as may be reasonably requested by
Landlord or Landlord's lender, but in no event in excess of the amounts and types of insurance then being required by landlords of buildings
comparable to and in the vicinity of the Building.
11.
DAMAGE AND DESTRUCTION
11.1 Repair of Damage to Premises by Landlord. Tenant shall promptly notify Landlord of any damage to the Premises resulting
from fire or any other casualty. If the Premises or any Common Areas serving or providing access to the Premises shall be damaged by fire or
other casualty, Landlord shall promptly and diligently, subject to reasonable delays for insurance adjustment or other matters beyond
Landlord's reasonable control, and subject to all other terms of this Article 11, restore the Base Building and such Common Areas. Such
restoration shall be to substantially the same condition of the Base Building and the Common Areas prior to the casualty, except for
modifications required by zoning and building codes and other laws or by the holder of a mortgage on the Building or Project or any other
modifications to the Common Areas deemed desirable by Landlord, which are consistent with the character of the Project, provided that
access to the Premises shall not be materially impaired. Upon the occurrence of any damage to the Premises, upon notice (the "Landlord
Repair Notice") to Tenant from Landlord, Tenant shall assign to Landlord (or to any party designated by Landlord) all insurance proceeds
payable to Tenant under Tenant's insurance required under Section 10.3 of this Lease, and Landlord shall repair any injury or damage to the
Tenant Improvements and the Original Improvements installed in the Premises and shall return such Tenant Improvements and Original
Improvements to their original condition; provided that if the cost of such repair by Landlord exceeds the amount of insurance proceeds
received by Landlord from Tenant's insurance carrier, as assigned by Tenant, the cost of such repairs shall be paid by Tenant to Landlord prior
to Landlord's commencement of repair of the damage. In the event that Landlord does not deliver the Landlord Repair Notice within sixty
(60) days following the date the casualty becomes known to Landlord, Tenant shall, at its sole cost and expense, repair any injury or damage
to the Tenant Improvements and the Original Improvements installed in the Premises and shall return such Tenant Improvements and Original
Improvements to their original condition. Whether or not Landlord delivers a Landlord Repair Notice, prior to the commencement of
construction, Tenant shall submit to Landlord, for Landlord's review and approval, all plans, specifications and working drawings relating
thereto, and Landlord shall select the contractors to perform such improvement work. Landlord shall not be liable for any inconvenience or
annoyance to Tenant or its visitors, or injury to Tenant's business resulting in any way from such damage or the repair thereof; provided
however, that if such fire or other casualty shall have damaged the Premises or Common Areas necessary to Tenant's occupancy, and the
Premises are not occupied by Tenant as a result thereof, then during the time and to the extent the Premises are unfit for occupancy, the Rent
shall be abated in proportion to the ratio that the amount of rentable square feet of the Premises which is unfit for occupancy for the purposes
permitted under this Lease bears to the total rentable square feet of the Premises. In the event that Landlord shall not deliver the Landlord
Repair Notice, Tenant's right to rent abatement pursuant to the preceding sentence shall terminate as of the date which is reasonably
determined by Landlord to be the date Tenant should have completed repairs to the Premises assuming Tenant used reasonable due diligence
in connection therewith.
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11.2 Landlord's Option to Repair. Notwithstanding the terms of Section 11.1 of this Lease, Landlord may elect not to rebuild
and/or restore the Premises, Building and/or Project, and instead terminate this Lease, by notifying Tenant in writing of such termination
within sixty (60) days after the date of discovery of the damage, such notice to include a termination date giving Tenant sixty (60) days to
vacate the Premises, but Landlord may so elect only if the Building or Project shall be damaged by fire or other casualty or cause, whether or
not the Premises are affected, and one or more of the following conditions is present: (i) in Landlord's reasonable judgment, repairs cannot
reasonably be completed within one hundred eighty (180) days after the date of discovery of the damage (when such repairs are made without
the payment of overtime or other premiums); (ii) the holder of any mortgage on the Building or Project or ground lessor with respect to the
Building or Project shall require that the insurance proceeds or any portion thereof be used to retire the mortgage debt, or shall terminate the
ground lease, as the case may be; (iii) the damage is not fully covered by Landlord's insurance policies; (iv) Landlord decides to rebuild the
Building or Common Areas so that they will be substantially different structurally or architecturally; (v) the damage occurs during the last
twelve (12) months of the Lease Term; or (vi) any owner of any other portion of the Project, other than Landlord, does not intend to repair the
damage to such portion of the Project; provided, however, that if Landlord does not elect to terminate this Lease pursuant to Landlord's
termination right as provided above, and the repairs cannot, in the reasonable opinion of Landlord, be completed within one hundred eighty
(180) days after being commenced, Tenant may elect, no earlier than sixty (60) days after the date of the damage and not later than ninety (90)
days after the date of such damage, to terminate this Lease by written notice to Landlord effective as of the date specified in the notice, which
date shall not be less than thirty (30) days nor more than sixty (60) days after the date such notice is given by Tenant. Notwithstanding the
provisions of this Section 11.2, Tenant shall have the right to terminate this Lease under this Section 11.2 only if each of the following
conditions is satisfied: (a) the damage to the Project by fire or other casualty was not caused by the gross negligence or intentional act of
Tenant or its partners or subpartners and their respective officers, agents, servants, employees, and independent contractors; (b) Tenant is not
then in default under this Lease; (c) as a result of the damage, Tenant cannot reasonably conduct business from the Premises; and, (d) as a
result of the damage to the Project, Tenant does not occupy or use the Premises at all.
11.3 Waiver of Statutory Provisions. The provisions of this Lease, including this Article 11, constitute an express agreement
between Landlord and Tenant with respect to any and all damage to, or destruction of, all or any part of the Premises, the Building or the
Project, and any statute or regulation of the State of California, including, without limitation, Sections 1932(2) and 1933(4) of the California
Civil Code, with respect to any rights or obligations concerning damage or destruction in the absence of an express agreement between the
parties, and any other statute or regulation, now or hereafter in effect, shall have no application to this Lease or any damage or destruction to
all or any part of the Premises, the Building or the Project.
12.
NONWAIVER No provision of this Lease shall be deemed waived by either party hereto unless expressly
waived in a writing signed thereby. The waiver by either party hereto of any breach of any term, covenant or condition herein contained shall
not be deemed to be a waiver of any subsequent breach of same or any other term, covenant or condition herein contained. The subsequent
acceptance of Rent hereunder by Landlord shall not be deemed to be a waiver of any preceding breach by Tenant of any term, covenant or
condition of this Lease, other than the failure of Tenant to pay the particular Rent so accepted, regardless of Landlord's knowledge of such
preceding breach at the time of acceptance of such Rent. No acceptance of a lesser amount than the Rent herein stipulated shall be deemed a
waiver of Landlord's right to receive the full amount due, nor shall any endorsement or statement on any check or payment or any letter
accompanying such check or payment be deemed an accord and satisfaction, and Landlord may accept such check or payment without
prejudice to Landlord's right to recover the full amount due. No receipt of monies by Landlord from Tenant after the termination of this Lease
shall in any way alter the length of the Lease Term or of Tenant's right of possession hereunder, or after the giving of any notice shall
reinstate, continue or extend the Lease Term or affect any notice given Tenant prior to the receipt of such monies, it being agreed that after the
service of notice or the commencement of a suit, or after final judgment for possession of the Premises, Landlord may receive and collect any
Rent due, and the payment of said Rent shall not waive or affect said notice, suit or judgment.
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13.
CONDEMNATION If the whole or any part of the Premises, Building or Project shall be taken by power of eminent domain or
condemned by any competent authority for any public or quasi-public use or purpose, or if any adjacent property or street shall be so taken or
condemned, or reconfigured or vacated by such authority in such manner as to require the use, reconstruction or remodeling of any part of the
Premises, Building or Project, or if Landlord shall grant a deed or other instrument in lieu of such taking by eminent domain or condemnation,
Landlord shall have the option to terminate this Lease effective as of the date possession is required to be surrendered to the authority. Tenant
shall not because of such taking assert any claim against Landlord or the authority for any compensation because of such taking and Landlord
shall be entitled to the entire award or payment in connection therewith, except that Tenant shall have the right to file any separate claim
available to Tenant for any taking of Tenant's personal property and fixtures belonging to Tenant and removable by Tenant upon expiration of
the Lease Term pursuant to the terms of this Lease, and for moving expenses, so long as such claims do not diminish the award available to
Landlord, its ground lessor with respect to the Building or Project or its mortgagee, and such claim is payable separately to Tenant. All Rent
shall be apportioned as of the date of such termination. If any part of the Premises shall be taken, and this Lease shall not be so terminated,
the Rent shall be proportionately abated. Tenant hereby waives any and all rights it might otherwise have pursuant to Section 1265.130 of
The California Code of Civil Procedure. Notwithstanding anything to the contrary contained in this Article 13, in the event of a temporary
taking of all or any portion of the Premises for a period of one hundred and eighty (180) days or less, then this Lease shall not terminate but
the Base Rent and the Additional Rent shall be abated for the period of such taking in proportion to the ratio that the amount of rentable
square feet of the Premises taken bears to the total rentable square feet of the Premises. Landlord shall be entitled to receive the entire award
made in connection with any such temporary taking.
14.
ASSIGNMENT AND SUBLETTING
14.1 Transfers. Tenant shall not, without the prior written consent of Landlord, assign, mortgage, pledge, hypothecate, encumber, or
permit any lien to attach to, or otherwise transfer, this Lease or any interest hereunder, permit any assignment, or other transfer of this Lease or
any interest hereunder by operation of law, sublet the Premises or any part thereof, or enter into any license or concession agreements or
otherwise permit the occupancy or use of the Premises or any part thereof by any persons other than Tenant and its employees and contractors
(all of the foregoing are hereinafter sometimes referred to collectively as "Transfers" and any person to whom any Transfer is made or sought
to be made is hereinafter sometimes referred to as a "Transferee"). If Tenant desires Landlord's consent to any Transfer, Tenant shall notify
Landlord in writing, which notice (the "Transfer Notice") shall include (i) the proposed effective date of the Transfer, which shall not be less
than thirty (30) days nor more than one hundred eighty (180) days after the date of delivery of the Transfer Notice, (ii) a description of the
portion of the Premises to be transferred (the "Subject Space"), (iii) all of the terms of the proposed Transfer and the consideration therefor,
including calculation of the "Transfer Premium", as that term is defined in Section 14.3 below, in connection with such Transfer, the name
and address of the proposed Transferee, and a copy of all existing executed and/or proposed documentation pertaining to the proposed
Transfer, and (iv) current financial statements of the proposed Transferee certified by an officer, partner or owner thereof, business credit and
personal references and history of the proposed Transferee and any other information reasonably required by Landlord which will enable
Landlord to determine the financial responsibility, character, and reputation of the proposed Transferee, nature of such Transferee's business
and proposed use of the Subject Space. Any Transfer made without Landlord's prior written consent shall, at Landlord's option, be null, void
and of no effect, and shall, at Landlord's option, constitute a default by Tenant under this Lease. Whether or not Landlord consents to any
proposed Transfer, Tenant shall pay Landlord's reasonable review and processing fees, as well as any reasonable professional fees (including,
without limitation, attorneys', accountants', architects', engineers' and consultants' fees) incurred by Landlord, within thirty (30) days after
written request by Landlord.
14.2 Landlord's Consent. Landlord shall not unreasonably withhold or delay its consent to any proposed Transfer of the Subject
Space to the Transferee on the terms specified in the Transfer Notice. Without limitation as to other reasonable grounds for withholding
consent, the parties hereby agree that it shall be reasonable under this Lease and under any applicable law for Landlord to withhold consent to
any proposed Transfer where one or more of the following apply:
Building or the Project;
14.2.1 The Transferee is of a character or reputation or engaged in a business which is not consistent with the quality of the
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14.2.2 The Transferee is either a governmental agency or instrumentality thereof;
be undertaken in connection with the Transfer on the date consent is requested; or
14.2.3 The Transferee is not a party of reasonable financial worth and/or financial stability in light of the responsibilities to
the Project a right to cancel its lease.
14.2.4 The proposed Transfer would cause a violation of another lease for space in the Project, or would give an occupant of
If Landlord consents to any Transfer pursuant to the terms of this Section 14.2 (and does not exercise any recapture rights Landlord
may have under Section 14.4 of this Lease), Tenant may within six (6) months after Landlord's consent, but not later than the expiration of
said six-month period, enter into such Transfer of the Premises or portion thereof, upon substantially the same terms and conditions as are set
forth in the Transfer Notice furnished by Tenant to Landlord pursuant to Section 14.1 of this Lease, provided that if there are any changes in
the terms and conditions from those specified in the Transfer Notice such that Landlord would initially have been entitled to refuse its consent
to such Transfer under this Section 14.2, Tenant shall again submit the Transfer to Landlord for its approval and other action under this Article
14 (including Landlord's right of recapture, if any, under Section 14.4 of this Lease). Notwithstanding anything to the contrary in this Lease, if
Tenant or any proposed Transferee claims that Landlord has unreasonably withheld or delayed its consent under Section 14.2 or otherwise has
breached or acted unreasonably under this Article 14, their sole remedies shall be a suit for contract damages (other than damages for injury to,
or interference with, Tenant's business including, without limitation, loss of profits, however occurring) or declaratory judgment and an
injunction for the relief sought, and Tenant hereby waives all other remedies, including, without limitation, any right at law or equity to
terminate this Lease, on its own behalf and, to the extent permitted under all applicable laws, on behalf of the proposed Transferee.
14.3 Transfer Premium. If Landlord consents to a Transfer, as a condition thereto which the parties hereby agree is reasonable,
Tenant shall pay to Landlord fifty percent (50%) of any " Transfer Premium," as that term is defined in this Section 14.3, received by Tenant
from such Transferee. "Transfer Premium" shall mean all rent, additional rent or other consideration payable by such Transferee in
connection with the Transfer in excess of the Rent and Additional Rent payable by Tenant under this Lease during the term of the Transfer on
a per rentable square foot basis if less than all of the Premises is transferred, and after deduction of (i) any costs of improvements made to the
Subject Space in connection with such Transfer, (ii) brokerage commissions paid in connection with such Transfer, and (iii) reasonable legal
fees incurred in connection with such Transfer. "Transfer Premium" shall also include, but not be limited to, key money, bonus money or
other cash consideration paid by Transferee to Tenant in connection with such Transfer, and any payment in excess of fair market value for
services rendered by Tenant to Transferee or for assets, fixtures, inventory, equipment, or furniture transferred by Tenant to Transferee in
connection with such Transfer. The determination of the amount of Landlord's applicable share of the Transfer Premium shall be made on a
monthly basis as rent or other consideration is received by Tenant under the Transfer.
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14.4 Landlord's Option as to Subject Space. Notwithstanding anything to the contrary contained in this Article 14, in the event
Tenant contemplates a Transfer which, together with all prior Transfers then remaining in effect, would cause fifty percent (50%) or more of
the Premises to be Transferred for more than fifty percent (50%) of the then remaining Lease Term (taking into account any extension of the
Lease Term which has irrevocably exercised by Tenant), Tenant shall give Landlord notice (the " Intention to Transfer Notice") of such
contemplated Transfer (whether or not the contemplated Transferee or the terms of such contemplated Transfer have been determined). The
Intention to Transfer Notice shall specify the portion of and amount of rentable square feet of the Premises which Tenant intends to Transfer
(the "Contemplated Transfer Space "), the contemplated date of commencement of the Contemplated Transfer (the " Contemplated
Effective Date"), and the contemplated length of the term of such contemplated Transfer, and shall specify that such Intention to Transfer
Notice is delivered to Landlord pursuant to this Section 14.4 in order to allow Landlord to elect to recapture the Contemplated Transfer
Space. Thereafter, Landlord shall have the option, by giving written notice to Tenant within thirty (30) days after receipt of any Intention to
Transfer Notice, to recapture the Contemplated Transfer Space. Such recapture shall cancel and terminate this Lease with respect to such
Contemplated Transfer Space as of the Contemplated Effective Date. In the event of a recapture by Landlord, if this Lease shall be canceled
with respect to less than the entire Premises, the Rent reserved herein shall be prorated on the basis of the number of rentable square feet
retained by Tenant in proportion to the number of rentable square feet contained in the Premises, and this Lease as so amended shall continue
thereafter in full force and effect, and upon request of either party, the parties shall execute written confirmation of the same. If Landlord
declines, or fails to elect in a timely manner, to recapture such Contemplated Transfer Space under this Section 14.4, then, subject to the other
terms of this Article 14, for a period of nine (9) months (the "Nine Month Period") commencing on the last day of such thirty (30) day
period, Landlord shall not have any right to recapture the Contemplated Transfer Space with respect to any Transfer made during the Nine
Month Period, provided that any such Transfer is substantially on the terms set forth in the Intention to Transfer Notice, and provided further
that any such Transfer shall be subject to the remaining terms of this Article 14. If such a Transfer is not so consummated within the Nine
Month Period (or if a Transfer is so consummated, then upon the expiration of the term of any Transfer of such Contemplated Transfer Space
consummated within such Nine Month Period), Tenant shall again be required to submit a new Intention to Transfer Notice to Landlord with
respect any contemplated Transfer, as provided above in this Section 14.4.
14.5 Effect of Transfer. If Landlord consents to a Transfer, (i) the terms and conditions of this Lease shall in no way be deemed to
have been waived or modified, (ii) such consent shall not be deemed consent to any further Transfer by either Tenant or a Transferee, (iii)
Tenant shall deliver to Landlord, promptly after execution, an original executed copy of all documentation pertaining to the Transfer in form
reasonably acceptable to Landlord, (iv) Tenant shall furnish upon Landlord's request a complete statement, certified by an independent
certified public accountant, or Tenant's chief financial officer, setting forth in detail the computation of any Transfer Premium Tenant has
derived and shall derive from such Transfer, and (v) no Transfer relating to this Lease or agreement entered into with respect thereto, whether
with or without Landlord's consent, shall relieve Tenant or any guarantor of the Lease from any liability under this Lease, including, without
limitation, in connection with the Subject Space. Landlord or its authorized representatives shall have the right at all reasonable times to audit
the books, records and papers of Tenant relating to any Transfer, and shall have the right to make copies thereof. If the Transfer Premium
respecting any Transfer shall be found understated, Tenant shall, within thirty (30) days after demand, pay the deficiency, and if understated
by more than two percent (2%), Tenant shall pay Landlord's costs of such audit.
14.6 Additional Transfers . For purposes of this Lease, the term "Transfer" shall also include (i) if Tenant is a partnership, the
withdrawal or change, voluntary, involuntary or by operation of law, of fifty percent (50%) or more of the partners, or transfer of fifty percent
(50%) or more of partnership interests, within a twelve (12)-month period, or the dissolution of the partnership without immediate
reconstitution thereof, and (ii) if Tenant is a closely held corporation (i.e., whose stock is not publicly held and not traded through an exchange
or over the counter), (A) the dissolution, merger, consolidation or other reorganization of Tenant or (B) the sale or other transfer of an
aggregate of fifty percent (50%) or more of the voting shares of Tenant (other than to immediate family members by reason of gift or death),
within a twelve (12)-month period, or (C) the sale, mortgage, hypothecation or pledge of an aggregate of fifty percent (50%) or more of the
value of the unencumbered assets of Tenant within a twelve (12)-month period.
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14.7 Occurrence of Default. Any Transfer hereunder shall be subordinate and subject to the provisions of this Lease, and if this
Lease shall be terminated during the term of any Transfer, Landlord shall have the right to: (i) treat such Transfer as cancelled and repossess
the Subject Space by any lawful means, or (ii) require that such Transferee attorn to and recognize Landlord as its landlord under any such
Transfer. If Tenant shall be in default under this Lease, Landlord is hereby irrevocably authorized, as Tenant's agent and attorney-in-fact, to
direct any Transferee to make all payments under or in connection with the Transfer directly to Landlord (which Landlord shall apply towards
Tenant's obligations under this Lease) until such default is cured. Such Transferee shall rely on any representation by Landlord that Tenant is
in default hereunder, without any need for confirmation thereof by Tenant. Upon any assignment, the assignee shall assume in writing all
obligations and covenants of Tenant thereafter to be performed or observed under this Lease. No collection or acceptance of rent by Landlord
from any Transferee shall be deemed a waiver of any provision of this Article 14 or the approval of any Transferee or a release of Tenant from
any obligation under this Lease, whether theretofore or thereafter accruing. In no event shall Landlord's enforcement of any provision of this
Lease against any Transferee be deemed a waiver of Landlord's right to enforce any term of this Lease against Tenant or any other person. If
Tenant's obligations hereunder have been guaranteed, Landlord's consent to any Transfer shall not be effective unless the guarantor also
consents to such Transfer.
14.8 Non-Transfers. Notwithstanding anything to the contrary contained in this Article 14, an assignment or subletting of all or a
portion of the Premises to an affiliate of Tenant (an entity which is controlled by, controls, or is under common control with, Tenant), shall not
be deemed a Transfer under this Article 14, provided that Tenant notifies Landlord of any such assignment or sublease and promptly supplies
Landlord with any documents or information requested by Landlord regarding such assignment or sublease or such affiliate, and further
provided that such assignment or sublease is not a subterfuge by Tenant to avoid its obligations under this Lease. " Control," as used in this
Section 14.8, shall mean the ownership, directly or indirectly, of at least fifty-one percent (51%) of the voting securities of, or possession of
the right to vote, in the ordinary direction of its affairs, of at least fifty-one percent (51%) of the voting interest in, any person or entity. No
such permitted assignment or subletting shall serve to release Tenant from any of its obligations under this Lease.
15.
SURRENDER OF PREMISES; OWNERSHIP AND REMOVAL OF TRADE FIXTURES
15.1 Surrender of Premises. No act or thing done by Landlord or any agent or employee of Landlord during the Lease Term shall
be deemed to constitute an acceptance by Landlord of a surrender of the Premises unless such intent is specifically acknowledged in writing by
Landlord. The delivery of keys to the Premises to Landlord or any agent or employee of Landlord shall not constitute a surrender of the
Premises or effect a termination of this Lease, whether or not the keys are thereafter retained by Landlord, and notwithstanding such delivery
Tenant shall be entitled to the return of such keys at any reasonable time upon request until this Lease shall have been properly
terminated. The voluntary or other surrender of this Lease by Tenant, whether accepted by Landlord or not, or a mutual termination hereof,
shall not work a merger, and at the option of Landlord shall operate as an assignment to Landlord of all subleases or subtenancies affecting the
Premises or terminate any or all such sublessees or subtenancies.
15.2 Removal of Tenant Property by Tenant . Upon the expiration of the Lease Term, or upon any earlier termination of this
Lease, Tenant shall, subject to the provisions of this Article 15, quit and surrender possession of the Premises to Landlord in as good order and
condition as when Tenant took possession and as thereafter improved by Landlord and/or Tenant, reasonable wear and tear and repairs which
are specifically made the responsibility of Landlord hereunder excepted. Upon such expiration or termination, Tenant shall, without expense
to Landlord, remove or cause to be removed from the Premises all debris and rubbish, and such items of furniture, equipment, free-standing
cabinet work, movable partitions and other articles of personal property owned by Tenant or installed or placed by Tenant at its expense in the
Premises, and such similar articles of any other persons claiming under Tenant, as Landlord may, in its sole discretion, require to be removed,
and Tenant shall repair at its own expense all damage to the Premises and Building resulting from such removal.
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15.3 Environmental Assessment . In connection with its surrender of the Premises, Tenant shall submit to Landlord, at least one
hundred twenty (120) days prior to the expiration date of this Lease (or in the event of an earlier termination of this Lease, as soon as
reasonably possible following such termination), an environmental Assessment of the Premises by a competent and experienced environmental
engineer or engineering firm reasonably satisfactory to Landlord (pursuant to a contract approved by Landlord and providing that Landlord
can rely on the Environmental Assessment), which (i) evidences that the Premises are in a clean and safe condition and free and clear of any
Hazardous Materials; and (ii) includes a review of the Premises by an environmental consultant for asbestos, mold, fungus, spores, and other
moisture conditions, on-site chemical use, and lead-based paint. If such Environmental Assessment reveals that remediation or Clean-up is
required under any Environmental Laws, Tenant shall submit a remediation plan prepared by a recognized environmental consultant and shall
be responsible for all costs of remediation and Clean-up, as more particularly provided in Section 5.3, above.
15.4 Condition of the Building and Premises Upon Surrender. In addition to the above requirements of this Article 15, upon the
expiration of the Lease Term, or upon any earlier termination of this Lease, Tenant shall, surrender the Premises and Building such that the
same are in compliance with all Applicable Laws and with Tenant having complied with all of Tenant’s obligations under this Lease, including
those relating to improvement, repair, maintenance, compliance with law, testing and other related obligations of Tenant set forth in Article 7
of this Lease. In the event that the Building and Premises shall be surrendered in a condition which does not comply with the terms of this
Section 15.4, because Tenant failed to comply with its obligations set forth in Lease, then following thirty (30) days notice to Tenant, during
which thirty (30) day period Tenant shall have the right to cure such noncompliance, Landlord shall be entitled to expend all reasonable costs
in order to cause the same to comply with the required condition upon surrender and Tenant shall immediately reimburse Landlord for all such
costs upon notice and Tenant shall be deemed during the period that Tenant or Landlord, as the case may be, perform obligations relating to
the Surrender Improvements to be in holdover under Article 16 of this Lease.
HOLDING OVER If Tenant holds over after the expiration of the Lease Term or earlier termination thereof, with the express or
16.
implied consent of Landlord, such tenancy shall be from month-to-month only, and shall not constitute a renewal hereof or an extension for
any further term. If Tenant holds over after the expiration of the Lease Term of earlier termination thereof, without the express or implied
consent of Landlord, such tenancy shall be deemed to be a tenancy by sufferance only, and shall not constitute a renewal hereof or an
extension for any further term. In either case, Rent shall be payable at a monthly rate equal to 150% of the Rent applicable during the last
rental period of the Lease Term under this Lease. Such month-to-month tenancy or tenancy by sufferance, as the case may be, shall be subject
to every other applicable term, covenant and agreement contained herein. Nothing contained in this Article 16 shall be construed as consent
by Landlord to any holding over by Tenant, and Landlord expressly reserves the right to require Tenant to surrender possession of the Premises
to Landlord as provided in this Lease upon the expiration or other termination of this Lease. The provisions of this Article 16 shall not be
deemed to limit or constitute a waiver of any other rights or remedies of Landlord provided herein or at law. If Tenant fails to surrender the
Premises upon the termination or expiration of this Lease, in addition to any other liabilities to Landlord accruing therefrom, Tenant shall
protect, defend, indemnify and hold Landlord harmless from all loss, costs (including reasonable attorneys' fees) and liability resulting from
such failure, including, without limiting the generality of the foregoing, any claims made by any succeeding tenant founded upon such failure
to surrender and any lost profits to Landlord resulting therefrom.
17.
ESTOPPEL CERTIFICATES Within ten (10) business days following a request in writing by Landlord, Tenant shall execute,
acknowledge and deliver to Landlord an estoppel certificate, which, as submitted by Landlord, shall be substantially in the form of Exhibit D,
attached hereto (or such other form as may be required by any prospective mortgagee or purchaser of the Project, or any portion thereof),
indicating therein any exceptions thereto that may exist at that time, and shall also contain any other information reasonably requested by
Landlord or Landlord's mortgagee or prospective mortgagee. Any such certificate may be relied upon by any prospective mortgagee or
purchaser of all or any portion of the Project. Tenant shall execute and deliver whatever other instruments may be reasonably required for
such purposes. At any time during the Lease Term, Landlord may require Tenant to provide Landlord with a current financial statement and
financial statements of the two (2) years prior to the current financial statement year. Such statements shall be prepared in accordance with
generally accepted accounting principles and, if such is the normal practice of Tenant, shall be audited by an independent certified public
accountant. Failure of Tenant to timely execute, acknowledge and deliver such estoppel certificate or other instruments shall constitute an
acceptance of the Premises and an acknowledgment by Tenant that statements included in the estoppel certificate are true and correct, without
exception.
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18.
SUBORDINATION This Lease shall be subject and subordinate to all present and future ground or underlying leases of the
Building or Project and to the lien of any mortgage, trust deed or other encumbrances now or hereafter in force against the Building or Project
or any part thereof, if any, and to all renewals, extensions, modifications, consolidations and replacements thereof, and to all advances made or
hereafter to be made upon the security of such mortgages or trust deeds, unless the holders of such mortgages, trust deeds or other
encumbrances, or the lessors under such ground lease or underlying leases, require in writing that this Lease be superior thereto. Tenant
covenants and agrees in the event any proceedings are brought for the foreclosure of any such mortgage or deed in lieu thereof (or if any
ground lease is terminated), to attorn, without any deductions or set-offs whatsoever, to the lienholder or purchaser or any successors thereto
upon any such foreclosure sale or deed in lieu thereof (or to the ground lessor), if so requested to do so by such purchaser or lienholder or
ground lessor, and to recognize such purchaser or lienholder or ground lessor as the lessor under this Lease, provided such lienholder or
purchaser or ground lessor shall agree to accept this Lease and not disturb Tenant's occupancy, so long as Tenant timely pays the rent and
observes and performs the terms, covenants and conditions of this Lease to be observed and performed by Tenant. Landlord's interest herein
may be assigned as security at any time to any lienholder. Tenant shall, within ten (10) days of request by Landlord, execute such further
instruments or assurances as Landlord may reasonably deem necessary to evidence or confirm the subordination or superiority of this Lease to
any such mortgages, trust deeds, ground leases or underlying leases. Tenant waives the provisions of any current or future statute, rule or law
which may give or purport to give Tenant any right or election to terminate or otherwise adversely affect this Lease and the obligations of the
Tenant hereunder in the event of any foreclosure proceeding or sale.
19.
DEFAULTS; REMEDIES
19.1 Events of Default. The occurrence of any of the following shall constitute a default of this Lease by Tenant:
when due unless such failure is cured within five (5) business days after notice; or
19.1.1 Any failure by Tenant to pay any Rent or any other charge required to be paid under this Lease, or any part thereof,
19.1.2 Except where a specific time period is otherwise set forth for Tenant's performance in this Lease, in which event the
failure to perform by Tenant within such time period shall be a default by Tenant under this Section 19.1.2, any failure by Tenant to observe or
perform any other provision, covenant or condition of this Lease to be observed or performed by Tenant where such failure continues for thirty
(30) days after written notice thereof from Landlord to Tenant; provided that if the nature of such default is such that the same cannot
reasonably be cured within a thirty (30) day period, Tenant shall not be deemed to be in default if it diligently commences such cure within
such period and thereafter diligently proceeds to rectify and cure such default; or
19.1.3 Abandonment or vacation of all or a substantial portion of the Premises by Tenant; or
such failure continues for more than two (2) business days after notice from Landlord; or
19.1.4 The failure by Tenant to observe or perform according to the provisions of Articles 5, 14, 17 or 18 of this Lease where
19.1.5 Tenant's failure to occupy the Premises within ten (10) business days after the Lease Commencement Date.
The notice periods provided herein are in lieu of, and not in addition to, any notice periods provided by law.
19.2 Remedies Upon Default. Upon the occurrence of any event of default by Tenant, Landlord shall have, in addition to any other
remedies available to Landlord at law or in equity (all of which remedies shall be distinct, separate and cumulative), the option to pursue any
one or more of the following remedies, each and all of which shall be cumulative and nonexclusive, without any notice or demand whatsoever.
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19.2.1 Terminate this Lease, in which event Tenant shall immediately surrender the Premises to Landlord, and if Tenant fails
to do so, Landlord may, without prejudice to any other remedy which it may have for possession or arrearages in rent, enter upon and take
possession of the Premises and expel or remove Tenant and any other person who may be occupying the Premises or any part thereof, without
being liable for prosecution or any claim or damages therefor; and Landlord may recover from Tenant the following:
plus
(i) The worth at the time of award of the unpaid rent which has been earned at the time of such termination;
(ii) The worth at the time of award of the amount by which the unpaid rent which would have been earned
after termination until the time of award exceeds the amount of such rental loss that Tenant proves could have been reasonably
avoided; plus
Term after the time of award exceeds the amount of such rental loss that Tenant proves could have been reasonably avoided; plus
(iii) The worth at the time of award of the amount by which the unpaid rent for the balance of the Lease
(iv) Any other amount necessary to compensate Landlord for all the detriment proximately caused by
Tenant's failure to perform its obligations under this Lease or which in the ordinary course of things would be likely to result therefrom;
and
from time to time by applicable law.
(v) At Landlord's election, such other amounts in addition to or in lieu of the foregoing as may be permitted
The term "rent" as used in this Section 19.2 shall be deemed to be and to mean all sums of every nature required to be paid by Tenant
pursuant to the terms of this Lease, whether to Landlord or to others. As used in Sections 19.2.1(i) and (ii), above, the "worth at the time of
award" shall be computed by allowing interest at the rate set forth in Article 25 of this Lease, but in no case greater than the maximum amount
of such interest permitted by law. As used in Section 19.2.1(iii) above, the "worth at the time of award " shall be computed by discounting
such amount at the discount rate of the Federal Reserve Bank of San Francisco at the time of award plus one percent (1%).
19.2.2 Landlord shall have the remedy described in California Civil Code Section 1951.4 (lessor may continue lease in
effect after lessee's breach and abandonment and recover rent as it becomes due, if lessee has the right to sublet or assign, subject only to
reasonable limitations). Accordingly, if Landlord does not elect to terminate this Lease on account of any default by Tenant, Landlord may,
from time to time, without terminating this Lease, enforce all of its rights and remedies under this Lease, including the right to recover all rent
as it becomes due.
19.2.3 Landlord shall at all times have the rights and remedies (which shall be cumulative with each other and cumulative
and in addition to those rights and remedies available under Sections 19.2.1 and 19.2.2, above, or any law or other provision of this Lease),
without prior demand or notice except as required by applicable law, to seek any declaratory, injunctive or other equitable relief, and
specifically enforce this Lease, or restrain or enjoin a violation or breach of any provision hereof.
19.3 Subleases of Tenant. Whether or not Landlord elects to terminate this Lease on account of any default by Tenant, as set forth in
this Article 19, Landlord shall have the right to terminate any and all subleases, licenses, concessions or other consensual arrangements for
possession entered into by Tenant and affecting the Premises or may, in Landlord's sole discretion, succeed to Tenant's interest in such
subleases, licenses, concessions or arrangements. In the event of Landlord's election to succeed to Tenant's interest in any such subleases,
licenses, concessions or arrangements, Tenant shall, as of the date of notice by Landlord of such election, have no further right to or interest in
the rent or other consideration receivable thereunder.
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19.4 Efforts to Relet. No re-entry or repossession, repairs, maintenance, changes, alterations and additions, reletting, appointment
of a receiver to protect Landlord's interests hereunder, or any other action or omission by Landlord shall be construed as an election by
Landlord to terminate this Lease or Tenant's right to possession, or to accept a surrender of the Premises, nor shall same operate to release
Tenant in whole or in part from any of Tenant's obligations hereunder, unless express written notice of such intention is sent by Landlord to
Tenant. Tenant hereby irrevocably waives any right otherwise available under any law to redeem or reinstate this Lease.
20.
COVENANT OF QUIET ENJOYMENT Landlord covenants that Tenant, on paying the Rent, charges for services and other
payments herein reserved and on keeping, observing and performing all the other terms, covenants, conditions, provisions and agreements
herein contained on the part of Tenant to be kept, observed and performed, shall, during the Lease Term, peaceably and quietly have, hold and
enjoy the Premises subject to the terms, covenants, conditions, provisions and agreements hereof without interference by any persons lawfully
claiming by or through Landlord. The foregoing covenant is in lieu of any other covenant express or implied.
SECURITY DEPOSIT On or before the Lease Commencement Date of this Lease, Tenant shall deposit with Landlord a security
21.
deposit (the "Security Deposit") in the amount set forth in Section 8 of the Summary, as security for the faithful performance by Tenant of all
of its obligations under this Lease. If Tenant defaults with respect to any provisions of this Lease, including, but not limited to, the provisions
relating to the payment of Rent, the removal of property and the repair of resultant damage, Landlord may, without notice to Tenant, but shall
not be required to apply all or any part of the Security Deposit for the payment of any Rent or any other sum in default and Tenant shall, upon
demand therefor, restore the Security Deposit to its original amount. Any unapplied portion of the Security Deposit shall be returned to
Tenant, or, at Landlord's option, to the last assignee of Tenant's interest hereunder, within sixty (60) days following the expiration of the
Lease Term. Tenant shall not be entitled to any interest on the Security Deposit. Tenant hereby irrevocably waives and relinquishes any and
all rights, benefits, or protections, if any, Tenant now has, or in the future may have, under Section 1950.7 of the California Civil Code, any
successor statute, and all other provisions of law, now or hereafter in effect, including, but not limited to, any provision of law which
(i) establishes the time frame by which a landlord must refund a security deposit under a lease, and/or (ii) provides that a landlord may claim
from a security deposit only those sums reasonably necessary to remedy defaults in the payment of rent, to repair damage caused by a tenant or
to clean the subject premises. Tenant acknowledges and agrees that (a) any statutory time frames for the return of a security deposit are
superseded by the express period identified in this Article 21, above, and (b) rather than be so limited, Landlord may claim from the Security
Deposit (1) any and all sums expressly identified in this Article 21, above, and (2) any additional sums reasonably necessary to compensate
Landlord for any and all losses or damages caused by Tenant's default of this Lease, including, but not limited to, all damages or rent due upon
termination of Lease pursuant to Section 1951.2 of the California Civil Code.
COMMUNICATIONS AND COMPUTER LINE Tenant may install, maintain, replace, remove or use any communications or
22.
computer wires and cables serving the Premises (collectively, the "Lines"), provided that Tenant shall obtain Landlord's prior written consent,
use an experienced and qualified contractor approved in writing by Landlord, and comply with all of the other provisions of Articles 7 and 8
of this Lease. Tenant shall pay all costs in connection therewith. Landlord reserves the right, upon notice to Tenant prior to the expiration or
earlier termination of this Lease, to require that Tenant, at Tenant's sole cost and expense, remove any Lines located in or serving the Premises
prior to the expiration or earlier termination of this Lease.
23.
SIGNS
23.1 Exterior Signage. Landlord, at Landlord's sole cost and expense, shall install the initial signage identifying Tenant (i) on the
existing monument sign located at the Building, and (ii) at the entrance to the Building (collectively, " Tenant Signage"); provided, however,
in no event shall Tenant's Signage include an "Objectionable Name," as that term is defined in Section 23.3, of this Lease. All such signage
shall be subject to all required governmental approvals. Upon the expiration or earlier termination of this Lease, Tenant shall remove all of its
signs at Tenant's sole cost and expense. The graphics, materials, color, design, lettering, lighting, size, illumination, specifications and exact
location of Tenant's Signage (collectively, the " Sign Specifications") shall be Project standard as determined by Landlord. Any changes to
Tenant's Signage shall be at Tenant's sole cost and expense.
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23.2 Objectionable Name. Tenant's Signage shall not include a name or logo which relates to an entity which is of a character or
reputation, or is associated with a political faction or orientation, which is inconsistent with the quality of the Project, or which would
otherwise reasonably offend a landlord of the Comparable Buildings (an "Objectionable Name"). The parties hereby agree that the
following name, or any reasonable derivation thereof, shall be deemed not to constitute an Objectionable Name: "VistaGen Therapeutics,
Inc."
23.3 Prohibited Signage and Other Items. Any signs, notices, logos, pictures, names or advertisements which are installed and
that have not been separately approved by Landlord may be removed without notice by Landlord at the sole expense of Tenant. Any signs,
window coverings, or blinds (even if the same are located behind the Landlord-approved window coverings for the Building), or other items
visible from the exterior of the Premises or Building, shall be subject to the prior approval of Landlord, in its sole discretion.
24.
COMPLIANCE WITH LAW Tenant shall not do anything or suffer anything to be done in or about the Premises or the Project
which will in any way conflict with any law, statute, ordinance or other governmental rule, regulation or requirement now in force or which
may hereafter be enacted or promulgated. At its sole cost and expense, Tenant shall promptly comply with all such governmental
measures. Should any standard or regulation now or hereafter be imposed on Landlord or Tenant by a state, federal or local governmental
body charged with the establishment, regulation and enforcement of occupational, health or safety standards for employers, employees,
landlords or tenants, then Tenant agrees, at its sole cost and expense, to comply promptly with such standards or regulations. Tenant shall be
responsible, at its sole cost and expense, to make all alterations to the Building and Premises as are required to comply with the governmental
rules, regulations, requirements or standards described in this Article 24. The judgment of any court of competent jurisdiction or the
admission of Tenant in any judicial action, regardless of whether Landlord is a party thereto, that Tenant has violated any of said governmental
measures, shall be conclusive of that fact as between Landlord and Tenant.
25.
LATE CHARGES If any installment of Rent or any other sum due from Tenant shall not be received by Landlord or Landlord's
designee within five (5) business days after Tenant's receipt of written notice from Landlord that said amount is due, then Tenant shall pay to
Landlord a late charge equal to five percent (5%) of the overdue amount plus any reasonable attorneys' fees incurred by Landlord by reason of
Tenant's failure to pay Rent and/or other charges when due hereunder. The late charge shall be deemed Additional Rent and the right to
require it shall be in addition to all of Landlord's other rights and remedies hereunder or at law and shall not be construed as liquidated
damages or as limiting Landlord's remedies in any manner. In addition to the late charge described above, any Rent or other amounts owing
hereunder which are not paid within ten (10) days after the date they are due shall bear interest from the date when due until paid at a rate per
annum equal to the lesser of (i) the annual "Bank Prime Loan" rate cited in the Federal Reserve Statistical Release Publication G.13(415),
published on the first Tuesday of each calendar month (or such other comparable index as Landlord and Tenant shall reasonably agree upon if
such rate ceases to be published) plus four (4) percentage points, and (ii) the highest rate permitted by applicable law.
26.
LANDLORD'S RIGHT TO CURE DEFAULT; PAYMENTS BY TENANT
26.1 Landlord's Cure. All covenants and agreements to be kept or performed by Tenant under this Lease shall be performed by
Tenant at Tenant's sole cost and expense and without any reduction of Rent, except to the extent, if any, otherwise expressly provided
herein. If Tenant shall fail to perform any obligation under this Lease, and such failure shall continue in excess of the time allowed under
Section 19.1.2, above, unless a specific time period is otherwise stated in this Lease, Landlord may, but shall not be obligated to, make any
such payment or perform any such act on Tenant's part without waiving its rights based upon any default of Tenant and without releasing
Tenant from any obligations hereunder.
26.2 Tenant's Reimbursement. Except as may be specifically provided to the contrary in this Lease, Tenant shall pay to Landlord,
upon delivery by Landlord to Tenant of statements therefor: (i) sums equal to expenditures reasonably made and obligations incurred by
Landlord in connection with the remedying by Landlord of Tenant's defaults pursuant to the provisions of Section 26.1; (ii) sums equal to all
losses, costs, liabilities, damages and expenses referred to in Article 10 of this Lease; and (iii) sums equal to all expenditures made and
obligations incurred by Landlord in collecting or attempting to collect the Rent or in enforcing or attempting to enforce any rights of Landlord
under this Lease or pursuant to law, including, without limitation, all reasonable legal fees and other amounts so expended. Tenant's
obligations under this Section 26.2 shall survive the expiration or sooner termination of the Lease Term.
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27.
ENTRY BY LANDLORD Landlord reserves the right at all reasonable times and upon reasonable notice to Tenant (except in the
case of an emergency) to enter the Premises to (i) inspect them; (ii) show the Premises to prospective purchasers, or to current or prospective
mortgagees, ground or underlying lessors or insurers or, during the last twelve (12) months of the Lease Term, to prospective tenants; (iii) post
notices of nonresponsibility (to the extent applicable pursuant to then applicable law); or (iv) alter, improve or repair the Premises or the
Building, or for structural alterations, repairs or improvements to the Building or the Building's systems and equipment. Landlord may make
any such entries without the abatement of Rent, except as otherwise provided in this Lease, and may take such reasonable steps as required to
accomplish the stated purposes. In an emergency, Landlord shall have the right to use any means that Landlord may deem proper to open the
doors in and to the Premises. Any entry into the Premises by Landlord in the manner hereinbefore described shall not be deemed to be a
forcible or unlawful entry into, or a detainer of, the Premises, or an actual or constructive eviction of Tenant from any portion of the Premises.
28.
TENANT PARKING Tenant shall have the right to use the amount of parking set forth in Section 9 of the Summary, in the on-
site and/or off-site, as the case may be, parking facility (or facilities) which serve the Project. Tenant shall abide by all reasonable rules and
regulations which are prescribed from time to time for the orderly operation and use of the parking facility where the parking passes are
located (including any sticker or other identification system established by Landlord and the prohibition of vehicle repair and maintenance
activities in the parking facilities), and shall cooperate in seeing that Tenant's employees and visitors also comply with such rules and
regulations. Tenant's use of the Project parking facility shall be at Tenant's sole risk and Tenant acknowledges and agrees that Landlord shall
have no liability whatsoever for damage to the vehicles of Tenant, its employees and/or visitors, or for other personal injury or property
damage or theft relating to or connected with the parking rights granted herein or any of Tenant's, its employees' and/or visitors' use of the
parking facilities.
29.
MISCELLANEOUS PROVISIONS
29.1 Terms; Captions. The words "Landlord" and "Tenant" as used herein shall include the plural as well as the singular. The
necessary grammatical changes required to make the provisions hereof apply either to corporations or partnerships or individuals, men or
women, as the case may require, shall in all cases be assumed as though in each case fully expressed. The captions of Articles and Sections
are for convenience only and shall not be deemed to limit, construe, affect or alter the meaning of such Articles and Sections.
29.2 Binding Effect. Subject to all other provisions of this Lease, each of the covenants, conditions and provisions of this Lease
shall extend to and shall, as the case may require, bind or inure to the benefit not only of Landlord and of Tenant, but also of their respective
heirs, personal representatives, successors or assigns, provided this clause shall not permit any assignment by Tenant contrary to the
provisions of Article 14 of this Lease.
29.3 No Air Rights. No rights to any view or to light or air over any property, whether belonging to Landlord or any other person,
are granted to Tenant by this Lease. If at any time any windows of the Premises are temporarily darkened or the light or view therefrom is
obstructed by reason of any repairs, improvements, maintenance or cleaning in or about the Project, the same shall be without liability to
Landlord and without any reduction or diminution of Tenant's obligations under this Lease.
29.4 Modification of Lease. Should any current or prospective mortgagee or ground lessor for the Building or Project require a
modification of this Lease, which modification will not cause an increased cost or expense to Tenant or in any other way materially and
adversely change the rights and obligations of Tenant hereunder, then and in such event, Tenant agrees that this Lease may be so modified and
agrees to execute whatever documents are reasonably required therefor and to deliver the same to Landlord within ten (10) business days
following a request therefor. At the request of Landlord or any mortgagee or ground lessor, Tenant agrees to execute a short form of Lease
and deliver the same to Landlord within ten (10) business days following the request therefor.
29.5 Transfer of Landlord's Interest . Tenant acknowledges that Landlord has the right to transfer all or any portion of its interest
in the Project or Building and in this Lease, and Tenant agrees that in the event of any such transfer, Landlord shall automatically be released
from all liability under this Lease and Tenant agrees to look solely to such transferee for the performance of Landlord's obligations hereunder
after the date of transfer and such transferee shall be deemed to have fully assumed and be liable for all obligations of this Lease to be
performed by Landlord, including the return of any Security Deposit, and Tenant shall attorn to such transferee.
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29.6 Prohibition Against Recording. Except as provided in Section 29.4 of this Lease, neither this Lease, nor any memorandum,
affidavit or other writing with respect thereto, shall be recorded by Tenant or by anyone acting through, under or on behalf of Tenant.
29.7 Landlord's Title. Landlord's title is and always shall be paramount to the title of Tenant. Nothing herein contained shall
empower Tenant to do any act which can, shall or may encumber the title of Landlord.
29.8 Relationship of Parties. Nothing contained in this Lease shall be deemed or construed by the parties hereto or by any third
party to create the relationship of principal and agent, partnership, joint venturer or any association between Landlord and Tenant.
29.9 Application of Payments. Landlord shall have the right to apply payments received from Tenant pursuant to this Lease,
regardless of Tenant's designation of such payments, to satisfy any obligations of Tenant hereunder, in such order and amounts as Landlord, in
its sole discretion, may elect.
29.10 Time of Essence. Time is of the essence with respect to the performance of every provision of this Lease in which time of
performance is a factor.
29.11 Partial Invalidity. If any term, provision or condition contained in this Lease shall, to any extent, be invalid or unenforceable,
the remainder of this Lease, or the application of such term, provision or condition to persons or circumstances other than those with respect to
which it is invalid or unenforceable, shall not be affected thereby, and each and every other term, provision and condition of this Lease shall be
valid and enforceable to the fullest extent possible permitted by law.
29.12 No Warranty. In executing and delivering this Lease, Tenant has not relied on any representations, including, but not limited
to, any representation as to the amount of any item comprising Additional Rent or the amount of the Additional Rent in the aggregate or that
Landlord is furnishing the same services to other tenants, at all, on the same level or on the same basis, or any warranty or any statement of
Landlord which is not set forth herein or in one or more of the exhibits attached hereto.
29.13 Landlord Exculpation. The liability of Landlord or the Landlord Parties to Tenant for any default by Landlord under this
Lease or arising in connection herewith or with Landlord's operation, management, leasing, repair, renovation, alteration or any other matter
relating to the Project or the Premises shall be limited solely and exclusively to an amount which is equal to the lesser of (a) the interest of
Landlord in the Building or (b) the equity interest Landlord would have in the Building if the Building were encumbered by third-party debt in
an amount equal to eighty percent (80%) of the value of the Building (as such value is determined by Landlord), provided that in no event
shall such liability extend to any sales or insurance proceeds received by Landlord or the Landlord Parties in connection with the Project,
Building or Premises. Neither Landlord, nor any of the Landlord Parties shall have any personal liability therefor, and Tenant hereby
expressly waives and releases such personal liability on behalf of itself and all persons claiming by, through or under Tenant. The limitations
of liability contained in this Section 29.13 shall inure to the benefit of Landlord's and the Landlord Parties' present and future partners,
beneficiaries, officers, directors, trustees, shareholders, agents and employees, and their respective partners, heirs, successors and
assigns. Under no circumstances shall any present or future partner of Landlord (if Landlord is a partnership), or trustee or beneficiary (if
Landlord or any partner of Landlord is a trust), have any liability for the performance of Landlord's obligations under this
Lease. Notwithstanding any contrary provision herein, neither Landlord nor the Landlord Parties shall be liable under any circumstances for
injury or damage to, or interference with, Tenant's business, including but not limited to, loss of profits, loss of rents or other revenues, loss of
business opportunity, loss of goodwill or loss of use, in each case, however occurring, or loss to inventory, scientific research, scientific
experiments, laboratory animals, products, specimens, samples, and/or scientific, business, accounting and other records of every kind and
description kept at the premises and any and all income derived or derivable therefrom.
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29.14 Entire Agreement. It is understood and acknowledged that there are no oral agreements between the parties hereto affecting
this Lease and this Lease constitutes the parties' entire agreement with respect to the leasing of the Premises and supersedes and cancels any
and all previous negotiations, arrangements, brochures, agreements and understandings, if any, between the parties hereto or displayed by
Landlord to Tenant with respect to the subject matter thereof, and none thereof shall be used to interpret or construe this Lease. None of the
terms, covenants, conditions or provisions of this Lease can be modified, deleted or added to except in writing signed by the parties hereto.
29.15 Right to Lease. Landlord reserves the absolute right to effect such other tenancies in the Project as Landlord in the exercise of
its sole business judgment shall determine to best promote the interests of the Building or Project. Tenant does not rely on the fact, nor does
Landlord represent, that any specific tenant or type or number of tenants shall, during the Lease Term, occupy any space in the Building or
Project.
29.16 Force Majeure. Any prevention, delay or stoppage due to strikes, lockouts, labor disputes, acts of God, acts of war, terrorist
acts, inability to obtain services, labor, or materials or reasonable substitutes therefor, governmental actions, civil commotions, fire or other
casualty, and other causes beyond the reasonable control of the party obligated to perform, except with respect to the obligations imposed with
regard to Rent and other charges to be paid by Tenant pursuant to this Lease (collectively, a " Force Majeure"), notwithstanding anything to
the contrary contained in this Lease, shall excuse the performance of such party for a period equal to any such prevention, delay or stoppage
and, therefore, if this Lease specifies a time period for performance of an obligation of either party, that time period shall be extended by the
period of any delay in such party's performance caused by a Force Majeure.
29.17 Waiver of Redemption by Tenant . Tenant hereby waives, for Tenant and for all those claiming under Tenant, any and all
rights now or hereafter existing to redeem by order or judgment of any court or by any legal process or writ, Tenant's right of occupancy of the
Premises after any termination of this Lease.
29.18 Notices. All notices, demands, statements, designations, approvals or other communications (collectively, " Notices") given or
required to be given by either party to the other hereunder or by law shall be in writing, shall be (A) sent by United States certified or
registered mail, postage prepaid, return receipt requested ("Mail"), (B) transmitted by telecopy, if such telecopy is promptly followed by a
Notice sent by Mail, (C) delivered by a nationally recognized overnight courier, or (D) delivered personally. Any Notice shall be sent,
transmitted, or delivered, as the case may be, to Tenant at the appropriate address set forth in Section 10 of the Summary, or to such other
place as Tenant may from time to time designate in a Notice to Landlord, or to Landlord at the addresses set forth below, or to such other
places as Landlord may from time to time designate in a Notice to Tenant. Any Notice will be deemed given (i) three (3) days after the date it
is posted if sent by Mail, (ii) the date the telecopy is transmitted, (iii) the date the overnight courier delivery is made, or (iv) the date personal
delivery is made. As of the date of this Lease, any Notices to Landlord must be sent, transmitted, or delivered, as the case may be, to the
following addresses:
Bayside Area Development, LLC
c/o HCP, Inc.
3760 Kilroy Airport Way, Suite 300
Long Beach, CA 90806
Attention: Legal Department
and:
HCP Life Science Estates
400 Oyster Point Boulevard, Suite 409
South San Francisco, CA 94080
Attention: Jon Bergschneider
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with a copy to:
Allen Matkins Leck Gamble Mallory & Natsis LLP
1901 Avenue of the Stars, Suite 1800
Los Angeles, California 90067
Attention: Anton N. Natsis, Esq.
29.19 Joint and Several. If there is more than one tenant, the obligations imposed upon Tenant under this Lease shall be joint and
several.
29.20 Authority. If Tenant is a corporation, trust or partnership, each individual executing this Lease on behalf of Tenant hereby
represents and warrants that Tenant is a duly formed and existing entity qualified to do business in the State of California and that Tenant has
full right and authority to execute and deliver this Lease and that each person signing on behalf of Tenant is authorized to do so. In such event,
Tenant shall, within ten (10) days after execution of this Lease, deliver to Landlord satisfactory evidence of such authority and, if a
corporation, upon demand by Landlord, also deliver to Landlord satisfactory evidence of (i) good standing in Tenant's state of incorporation
and (ii) qualification to do business in the State of California.
29.21 Attorneys' Fees. In the event that either Landlord or Tenant should bring suit for the possession of the Premises, for the
recovery of any sum due under this Lease, or because of the breach of any provision of this Lease or for any other relief against the other, then
all costs and expenses, including reasonable attorneys' fees, incurred by the prevailing party therein shall be paid by the other party, which
obligation on the part of the other party shall be deemed to have accrued on the date of the commencement of such action and shall be
enforceable whether or not the action is prosecuted to judgment.
29.22 Governing Law; WAIVER OF TRIAL BY JURY . This Lease shall be construed and enforced in accordance with the laws
of the State of California. IN ANY ACTION OR PROCEEDING ARISING HEREFROM, LANDLORD AND TENANT HEREBY
CONSENT TO (I) THE JURISDICTION OF ANY COMPETENT COURT WITHIN THE STATE OF CALIFORNIA, (II) SERVICE OF
PROCESS BY ANY MEANS AUTHORIZED BY CALIFORNIA LAW, AND (III) IN THE INTEREST OF SAVING TIME AND
EXPENSE, TRIAL WITHOUT A JURY IN ANY ACTION, PROCEEDING OR COUNTERCLAIM BROUGHT BY EITHER OF THE
PARTIES HERETO AGAINST THE OTHER OR THEIR SUCCESSORS IN RESPECT OF ANY MATTER ARISING OUT OF OR IN
CONNECTION WITH THIS LEASE, THE RELATIONSHIP OF LANDLORD AND TENANT, TENANT'S USE OR OCCUPANCY OF
THE PREMISES, AND/OR ANY CLAIM FOR INJURY OR DAMAGE, OR ANY EMERGENCY OR STATUTORY REMEDY. IN THE
EVENT LANDLORD COMMENCES ANY SUMMARY PROCEEDINGS OR ACTION FOR NONPAYMENT OF BASE RENT OR
ADDITIONAL RENT, TENANT SHALL NOT INTERPOSE ANY COUNTERCLAIM OF ANY NATURE OR DESCRIPTION (UNLESS
SUCH COUNTERCLAIM SHALL BE MANDATORY) IN ANY SUCH PROCEEDING OR ACTION, BUT SHALL BE RELEGATED TO
AN INDEPENDENT ACTION AT LAW.
29.23 Submission of Lease. Submission of this instrument for examination or signature by Tenant does not constitute a reservation
of, option for or option to lease, and it is not effective as a lease or otherwise until execution and delivery by both Landlord and Tenant.
29.24 Brokers. Landlord and Tenant hereby warrant to each other that they have had no dealings with any real estate broker or agent
in connection with the negotiation of this Lease, excepting only the real estate brokers or agents specified in Section 12 of the Summary (the
"Brokers"), and that they know of no other real estate broker or agent who is entitled to a commission in connection with this Lease. Each
party agrees to indemnify and defend the other party against and hold the other party harmless from any and all claims, demands, losses,
liabilities, lawsuits, judgments, costs and expenses (including without limitation reasonable attorneys' fees) with respect to any leasing
commission or equivalent compensation alleged to be owing on account of any dealings with any real estate broker or agent, other than the
Brokers, occurring by, through, or under the indemnifying party. The terms of this Section 29.24 shall survive the expiration or earlier
termination of the Lease Term.
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29.25 Independent Covenants. This Lease shall be construed as though the covenants herein between Landlord and Tenant are
independent and not dependent and Tenant hereby expressly waives the benefit of any statute to the contrary and agrees that if Landlord fails
to perform its obligations set forth herein, Tenant shall not be entitled to make any repairs or perform any acts hereunder at Landlord's expense
or to any setoff of the Rent or other amounts owing hereunder against Landlord.
29.26 Project or Building Name, Address and Signage. Landlord shall have the right at any time to change the name and/or
address of the Project or Building and to install, affix and maintain any and all signs on the exterior and on the interior of the Project or
Building as Landlord may, in Landlord's sole discretion, desire. Tenant shall not use the name of the Project or Building or use pictures or
illustrations of the Project or Building in advertising or other publicity or for any purpose other than as the address of the business to be
conducted by Tenant in the Premises, without the prior written consent of Landlord.
29.27 Counterparts. This Lease may be executed in counterparts with the same effect as if both parties hereto had executed the
same document. Both counterparts shall be construed together and shall constitute a single lease.
29.28 Confidentiality. Tenant acknowledges that the content of this Lease and any related documents are confidential
information. Tenant shall keep such confidential information strictly confidential and shall not disclose such confidential information to any
person or entity other than (a) Tenant's financial, legal, and space planning consultants or (b) as otherwise required of Tenant to comply with
federal securities law and the rules and regulations of the United States Securities and Exchange Commission.
29.29 Development of the Project.
29.29.1 Subdivision. Landlord reserves the right to subdivide all or a portion of the buildings and Common Areas. Tenant
agrees to execute and deliver, upon demand by Landlord and in the form requested by Landlord, any additional documents needed to conform
this Lease to the circumstances resulting from a subdivision and any all maps in connection therewith. Notwithstanding anything to the
contrary set forth in this Lease, the separate ownership of any buildings and/or Common Areas by an entity other than Landlord shall not
affect the calculation of Direct Expenses or Tenant's payment of Tenant's Share of Direct Expenses.
29.29.2 Construction of Property and Other Improvements. Tenant acknowledges that portions of the Project may be
under construction following Tenant's occupancy of the Premises, and that such construction may result in levels of noise, dust, obstruction of
access, etc. which are in excess of that present in a fully constructed project. Tenant hereby waives any and all rent offsets or claims of
constructive eviction which may arise in connection with such construction.
29.30 No Violation. Tenant hereby warrants and represents that neither its execution of nor performance under this Lease shall cause
Tenant to be in violation of any agreement, instrument, contract, law, rule or regulation by which Tenant is bound, and Tenant shall protect,
defend, indemnify and hold Landlord harmless against any claims, demands, losses, damages, liabilities, costs and expenses, including,
without limitation, reasonable attorneys' fees and costs, arising from Tenant's breach of this warranty and representation.
29.31 Transportation Management. Tenant shall fully comply with all present or future programs intended to manage parking,
transportation or traffic in and around the Project and/or the Building, and in connection therewith, Tenant shall take responsible action for the
transportation planning and management of all employees located at the Premises by working directly with Landlord, any governmental
transportation management organization or any other transportation-related committees or entities. Such programs may include, without
limitation: (i) restrictions on the number of peak-hour vehicle trips generated by Tenant; (ii) increased vehicle occupancy; (iii) implementation
of an in-house ridesharing program and an employee transportation coordinator; (iv) working with employees and any Project, Building or
area-wide ridesharing program manager; (v) instituting employer-sponsored incentives (financial or in-kind) to encourage employees to
rideshare; and (vi) utilizing flexible work shifts for employees.
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IN WITNESS WHEREOF, Landlord and Tenant have caused this Lease to be executed the day and date first above written.
LANDLORD:
TENANT:
BAYSIDE AREA DEVELOPMENT, LLC,
a Delaware limited liability company
By: /s/ Jon M. Bergschneider
Jon M. Bergschneider
Executive Vice President
VISTAGEN THERAPEUTICS, INC.,
a California corporation
By: /s/ Shawn K. Singh
Shawn K. Singh
Chief Executive Officer
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VISTAGEN THERAPEUTICS, INC.
INDEMNIFICATION AGREEMENT
Exhibit 10.84
THIS AGREEMENT is entered into, effective as of May 20, 2013 between VistaGen Therapeutics, Inc., a Nevada corporation (the
"Company"), and Jon S. Saxe (“Indemnitee”).
WHEREAS, it is essential to the Company to retain and attract as directors and officers the most capable persons available;
WHEREAS, Indemnitee is a director of the Company;
WHEREAS, both the Company and Indemnitee recognize the increased risk of litigation and other claims currently being asserted
against directors and officers of corporations; and
WHEREAS, in recognition of lndemnitee's need for substantial protection against personal liability in order to enhance Indemnitee's
continued and effective service to the Company, and in order to induce Indemnitee to provide services to the Company as a director , the
Company wishes to provide in this Agreement for the indemnification of and the advancing of expenses to Indemnitee to the fullest extent
(whether partial or complete) permitted by law and as set forth in this Agreement, and, to the extent insurance is maintained, for the coverage
of Indemnitee under the Company's directors' and officers' liability insurance policies.
NOW, THEREFORE, in consideration of the above premises and of lndemnitee's continuing to serve the Company directly or, at its
request, with another enterprise, and intending to be legally bound hereby, the parties agree as follows:
1. Certain Definitions:
(a) Board: the Board of Directors of the Company.
(b) Change in Control: shall be deemed to have occurred if (i) any "person" (as such term is used in Sections 13(d) and
14(d) of the Securities Exchange Act of 1934, as amended), other than a trustee or other fiduciary holding securities under an employee benefit
plan of the Company or a corporation owned directly or indirectly by the shareholders of the Company in substantially the same proportions
as their ownership of stock of the Company, is or becomes the "Beneficial Owner" (as defined in Rule 13d-3 under said Act), directly or
indirectly, of securities of the Company representing 20% or more of the total voting power represented by the Company's then outstanding
Voting Securities, or (ii) during any period of two consecutive years, individuals who at the beginning of such period constitute the Board and
any new director whose election by the Board or nomination for election by the Company's shareholders was approved by a vote of at least
two-thirds (2/3) of the directors then still in office who either were directors at the beginning of the period or whose election or nomination for
election was previously so approved, cease for any reason to constitute a majority thereof, or (iii) the shareholders of the Company approve a
merger or consolidation of the Company with any other corporation, other than a merger or consolidation that would result in the Voting
Securities of the Company outstanding immediately prior thereto continuing to represent (either by remaining outstanding or by being
converted into Voting Securities of the surviving entity) at least 80% of the total voting power represented by the Voting Securities of the
Company or such surviving entity outstanding immediately after such merger or consolidation, or the shareholders of the Company approve a
plan of complete liquidation of the Company or an agreement for the sale or disposition by the Company (in one transaction or a series of
transactions) of all or substantially all of the Company's assets.
(c) Expenses: any expense, liability, or loss, including attorneys' fees, judgments, fines, ERISA excise taxes and penalties,
amounts paid or to be paid in settlement, any interest, assessments, or other charges imposed thereon, and any federal, state, local, or foreign
taxes imposed as a result of the actual or deemed receipt of any payments under this Agreement, paid or incurred in connection with
investigating, defending, being a witness in, or participating in (including on appeal), or preparing for any of the foregoing in, any Proceeding
relating to any Indemnifiable Event.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jon S. Saxe
May 20, 2013
(d) Indemnifiable Event: any event or occurrence that takes place either prior to or after the execution of this Agreement,
related to the fact that Indemnitee is or was a director of the Company, or while a director is or was serving at the request of the Company as a
director, officer, employee, trustee, agent, or fiduciary of another foreign or domestic corporation, partnership, joint venture, employee benefit
plan, trust, or other enterprise, or was a director, officer, employee, or agent of a foreign or domestic corporation that was a predecessor
corporation of the Company or of another enterprise at the request of such predecessor corporation, or related to anything done or not done by
Indemnitee in any such capacity, whether or not the basis of the Proceeding is alleged action in an official capacity as a director, officer,
employee, or agent or in any other capacity while serving as a director, officer, employee, or agent of the Company, as described above.
(e) Independent Counsel: the person or body appointed in connection with Section 3.
(f) Proceeding: any threatened, pending, or completed action, suit, or proceeding (including an action by or in the right of
the Company), or any inquiry, hearing, or investigation, whether conducted by the Company or any other party, that Indemnitee in good faith
believes might lead to the institution of any such action, suit, or proceeding, whether civil, criminal, administrative, investigative, or other.
(g) Reviewing Party: the person or body appointed in accordance with Section 3.
(h) Voting Securities: any securities of the Company that vote generally in the election of directors.
2. Agreement to Indemnify.
(a) General Agreement. In the event Indemnitee was, is, or becomes a party to or witness or other participant in, or is
threatened to be made a party to or witness or other participant in, a Proceeding by reason of (or arising in part out of) an Indemnifiable Event,
the Company shall indemnify Indemnitee from and against any and all Expenses to the fullest extent permitted by law, as the same exists or
may hereafter be amended or interpreted (but in the case of any such amendment or interpretation, only to the extent that such amendment
or interpretation permits the Company to provide broader indemnification rights than were permitted prior thereto). The parties hereto intend
that this Agreement shall provide for indemnification in excess of that expressly permitted by statute, including, without limitation, any
indemnification provided by the Company's Articles of Incorporation, its Bylaws, vote of its shareholders or disinterested directors, or
applicable law.
(b) Initiation of Proceeding. Notwithstanding anything in this Agreement to the contrary, Indemnitee shall not be entitled to
indemnification pursuant to this Agreement in connection with any Proceeding initiated by Indemnitee against the Company or any director of
the Company unless (i) the Company has joined in or the Board has consented to the initiation of such Proceeding; (ii) the Proceeding is one
to enforce indemnification rights under Section 5; or (iii) the Proceeding is instituted after a Change in Control (other than a Change in
Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control) and
Independent Counsel has approved its initiation.
( c ) Expense Advances. If so requested by Indemnitee, the Company shall advance (within ten business days of such
request) any and all Expenses to Indemnitee (an "Expense Advance"); provided that, if and to the extent that the Reviewing Party determines
that Indemnitee would not be permitted to be so indemnified under applicable law, the Company shall be entitled to be reimbursed by
Indemnitee (who hereby agrees to reimburse the Company) for all such amounts theretofore paid. If Indemnitee has commenced or
commences legal proceedings in a court of competent jurisdiction to secure a determination that Indemnitee should be indemnified under
applicable law, as provided in Section 4, any determination made by the Reviewing Party that Indemnitee would not be permitted to be
indemnified under applicable law shall not be binding and Indemnitee shall not be required to reimburse the Company for any Expense
Advance until a final judicial determination is made with respect thereto (as to which all rights of appeal therefrom have been exhausted or
have lapsed). Indemnitee's obligation to reimburse the Company for Expense Advances shall be unsecured and no interest shall be charged
thereon.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jon S. Saxe
May 20, 2013
(d) Mandatory Indemnification. Notwithstanding any other provision of this Agreement, to the extent that Indemnitee has
been successful on the merits in defense of any Proceeding relating in whole or in part to an Indemnifiable Event or in defense of any issue or
matter therein, Indemnitee shall be indemnified against all Expenses incurred in connection therewith.
( e ) Partial Indemnification. If indemnitee is entitled under any provision of this Agreement to indemnification by the
Company for some or a portion of Expenses, but not, however, for the total amount thereof, the Company shall nevertheless indemnify
Indemnitee for the portion thereof to which Indemnitee is entitled.
(f) Prohibited Indemnification. No indemnification pursuant to this Agreement shall be paid by the Company on account of
any Proceeding in which final unappealed judgment beyond the right of appeal is rendered against Indemnitee for an accounting of profits
made from the purchase or sale by Indemnitee of securities of the Company pursuant to the provisions of Section 16(b) of the Securities
Exchange Act of 1934, as amended, or similar provisions of any federal, state, or local laws.
3. Reviewing Party. Prior to any Change in Control, the Reviewing Party shall be any appropriate person or body consisting of a
member or members of the Board or any other person or body appointed by the Board who is not a party to the particular Proceeding with
respect to which Indemnitee is seeking indemnification; after a Change in Control, the Reviewing Party shall be the Independent Counsel
referred to below. With respect to all matters arising after a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) concerning the rights of lndemnitee to indemnity
payments and Expense Advances under this Agreement or any other agreement or under applicable law or the Company's Articles of
Incorporation or Bylaws now or hereafter in effect relating to indemnification for Indemnifiable Events, the Company shall seek legal advice
only from Independent Counsel selected by Indemnitee and approved by the Company (which approval shall not be unreasonably withheld),
and who has not otherwise performed services for the Company or the Indemnitee (other than in connection with indemnification matters)
within the last five years. The Independent Counsel shall not include any person who, under the applicable standards of professional conduct
then prevailing, would have a conflict of interest in representing either the Company or Indemnitee in an action to determine Indemnitee's
rights under this Agreement. Such counsel, among other things, shall render its written opinion to the Company and Indemnitee as to whether
and to what extent the Indemnitee should be permitted to be indemnified under applicable law. The Company agrees to pay the reasonable fees
of the Independent Counsel and to indemnify fully such counsel against any and all expenses (including attorneys' fees), claims, liabilities,
loss, and damages arising out of or relating to this Agreement or the engagement of Independent Counsel pursuant hereto.
4. Indemnification Process and Appeal.
( a ) Indemnification Payment. Indemnitee shall be entitled to indemnification of Expenses, and shall receive payment
thereof, from the Company in accordance with this Agreement as soon as practicable after Indemnitee has made written demand on the
Company for indemnification, unless the Reviewing Party has given a written opinion to the Company that Indemnitee is not entitled to
indemnification under applicable law.
( b ) Suit to Enforce Rights. Regardless of any action by the Reviewing Party, if Indemnitee has not received full
indemnification within thirty days after making a demand in accordance with Section 4(a), Indemnitee shall have the right to enforce its
indemnification rights under this Agreement by commencing litigation in any court in the State of Nevada having subject matter jurisdiction
thereof and in which venue is proper seeking an initial determination by the court or challenging any determination by the Reviewing Party or
any aspect thereof. The Company hereby consents to service of process and to appear in any such proceeding. Any determination by the
Reviewing Party not challenged by the Indemnitee shall be binding on the Company and Indemnitee. The remedy provided for in this Section
4 shall be in addition to any other remedies available to Indemnitee in law or equity.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jon S. Saxe
May 20, 2013
( c ) Defense to Indemnification, Burden of Proof, and Presumptions. It shall be a defense to any action brought by
Indemnitee against the Company to enforce this Agreement (other than an action brought to enforce a claim for Expenses incurred in
defending a Proceeding in advance of its final disposition where the required undertaking has been tendered to the Company) that it is not
permissible under applicable law for the Company to indemnify Indemnitee for the amount claimed. In connection with any such action or any
determination by the Reviewing Party or otherwise as to whether Indemnitee is entitled to be indemnified hereunder, the burden of proving
such a defense or determination shall be on the Company. Neither the failure of the Reviewing Party or the Company (including its Board,
independent legal counsel, or its shareholders) to have made a determination prior to the commencement of such action by Indemnitee that
indemnification of the claimant is proper under the circumstances because he has met the standard of conduct set forth in applicable law, nor
an actual determination by the Reviewing Party or Company (including its Board, independent legal counsel, or its shareholders) that the
Indemnitee had not met such applicable standard of conduct, shall be a defense to the action or create a presumption that the Indemnitee has
not met the applicable standard of conduct. For purposes of this Agreement, the termination of any claim, action, suit, or proceeding, by
judgment, order, settlement (whether with or without court approval), conviction, or upon a plea of nolo contendere, or its equivalent, shall not
create a presumption that Indemnitee did not meet any particular standard of conduct or have any particular belief or that a court has
determined that indemnification is not permitted by applicable law.
5 . Indemnification for Expenses Incurred in Enforcing Rights. The Company shall indemnify Indemnitee against any and all
Expenses that are incurred by Indemnitee in connection with any action brought by Indemnitee for
(i) indemnification of Expenses by the Company under this Agreement or any other agreement or under applicable
law or the Company's Articles of Incorporation or Bylaws now or hereafter in effect relating to indemnification for
Indemnifiable Events; and/or
(ii) recovery under directors' and officers' liability insurance policies maintained by the Company, but only in the
event that Indemnitee ultimately is determined to be entitled to such indemnification or insurance recovery, as the case may
be. In addition, the Company shall, if so requested by Indemnitee, advance the foregoing Expenses to Indemnitee, subject to
and in accordance with Section 2(c).
6. Notification and Defense of Proceeding.
(a) Notice. Promptly after receipt by Indemnitee of notice of the commencement of any Proceeding, Indemnitee will, if a
claim in respect thereof is to be made against the Company under this Agreement, notify the Company of the commencement thereof; but the
omission so to notify the Company will not relieve it from any liability that it may have to Indemnitee, except as provided in Section 6(c).
(b) Defense. With respect to any Proceeding as to which Indemnitee notifies the Company of the commencement thereof,
the Company will be entitled to participate in the Proceeding at its own expense and except as otherwise provided below, to the extent the
Company so wishes, it may assume the defense thereof with counsel reasonably satisfactory to Indemnitee. After notice from the Company to
Indemnitee of its election to assume the defense of any Proceeding, the Company will not be liable to Indemnitee under this Agreement or
otherwise for any Expenses subsequently incurred by Indemnitee in connection with the defense of such Proceeding other than reasonable
costs of investigation or as otherwise provided below. Indemnitee shall have the right to employ his own counsel in such Proceeding, but all
Expenses related thereto incurred after notice from the Company of its assumption of the defense shall be at Indemnitee's expense unless: (i)
the employment of counsel by Indemnitee has been authorized by the Company; (ii) Indemnitee has reasonably determined that there may be
a conflict of interest between Indemnitee and the Company in the defense of the Proceeding, after a Change in Control (other than a Change in
Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control); (iii) the
employment of counsel by Indemnitee has been approved by the Independent Counsel; or (iv) the Company shall not in fact have employed
counsel to assume the defense of such Proceeding, in each of which case all Expenses of the Proceeding shall be borne by the Company. The
Company shall not be entitled to assume the defense of any Proceeding brought by or on behalf of the Company or as to which Indemnitee
shall have made the determination provided for in (ii) above.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jon S. Saxe
May 20, 2013
(c) Settlement of Claims. The Company shall not be liable to indemnify Indemnitee under this Agreement or otherwise for
any amounts paid in settlement of any Proceeding effected without the Company's written consent, provided, however, that if a Change in
Control has occured (other than a Change in Control approved by a majority of the directors on the Board who were directors immediately
prior to such Change in Control), the Company shall be liable for indemnification of Indemnitee for amounts paid in settlement if the
Independent Counsel has approved the settlement. The Company shall not settle any Proceeding in any manner that would impose any penalty
or limitation on Indemnitee without Indemnitee's written consent. Neither the Company nor the Indemnitee will unreasonably withhold their
consent to any proposed settlement. The Company shall not be liable to indemnify the Indemnitee under this Agreement with regard to any
judicial award if the Company was not given a reasonable and timely opportunity, at its expense, to participate in the defense of such action;
the Company's liability hereunder shall not be excused if participation in the Proceeding by the Company was barred by this Agreement.
7 . Establishment of Trust. In the event of a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) the Company shall, upon written request by
Indemnitee, create a Trust for the benefit of the Indemnitee and from time to time upon written request of Indemnitee shall fund the Trust in an
amount sufficient to satisfy any and all Expenses reasonably anticipated at the time of each such request to be incurred in connection with
investigating, preparing for, participating in, and/or defending any Proceeding relating to an Indemnifiable Event. The amount or amounts to
be deposited in the Trust pursuant to the foregoing funding obligation shall be determined by the Reviewing Party. The terms of the Trust
shall provide that: (i) the Trust shall not be revoked or the principal thereof invaded, without the written consent of the Indemnitee; (ii) the
Trustee shall advance, within ten business days of a request by the Indemnitee, any and all Expenses to the Indemnitee (and the Indemnitee
hereby agrees to reimburse the Trust under the same circumstances for which the Indemnitee would be required to reimburse the Company
under Section 2(c) of this Agreement); (iii) the Trust shall continue to be funded by the Company in accordance with the funding obligation set
forth above; (iv) the Trustee shall promptly pay to the Indemnitee all amounts for which the Indemnitee shall be entitled to indemnification
pursuant to this Agreement or otherwise; and (v) all unexpended funds in the Trust shall revert to the Company upon a final determination by
the Reviewing Party or a court of competent jurisdiction, as the case may be, that the Indemnitee has been fully indemnified under the terms
of this Agreement. The Trustee shall be chosen by the Indemnitee. Nothing in this Section 7 shall relieve the Company of any of its
obligations under this Agreement. All income earned on the assets held in the Trust shall be reported as income by the Company for federal,
state, local, and foreign tax purposes. The Company shall pay all costs of establishing and maintaining the Trust and shall indemnify the
Trustee against any and all expenses (including attorneys' fees), claims, liabilities, loss, and damages arising out of or relating to this
Agreement or the establishment and maintenance of the Trust.
8 . Non-Exclusivity. The rights of Indemnitee hereunder shall be in addition to any other rights Indemnitee may have under the
Company's Articles of Incorporation, Bylaws, applicable law, or otherwise. To the extent that a change in applicable law (whether by statute or
judicial decision) permits greater indemnification by agreement than would be afforded currently under the Company's Articles of
Incorporation, Bylaws, applicable law, or this Agreement, it is the intent of the parties that Indemnitee enjoy by this Agreement the greater
benefits so afforded by such change.
9 . Liability Insurance. To the extent the Company maintains an insurance policy or policies providing directors' and officers'
liability insurance, Indemnitee shall be covered by such policy or policies, in accordance with its or their terms, to the maximum extent of the
coverage available for any Company director or officer.
10. Period of Limitations. No legal action shall be brought and no cause of action shall be asserted by or on behalf of the Company
or any affiliate of the Company against Indemnitee, Indemnitee's spouse, heirs, executors, or personal or legal representatives after the
expiration of two (2) years from the date of accrual of such cause of action, or such longer period as may be required by state law under the
circumstances. Any claim or cause of action of the Company or its affiliate shall be extinguished and deemed released unless asserted by the
timely filing of a legal action within such period; provided, however, that if any shorter period of limitations is otherwise applicable to any
such cause of action the shorter period shall govern.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jon S. Saxe
May 20, 2013
11. Amendment of this Agreement. No supplement, modification, or amendment of this Agreement shall be binding unless executed
in writing by both of the parties hereto. No waiver of any of the provisions of this Agreement shall be binding unless in the form of a writing
signed by the party against whom enforcement of the waiver is sought, and no such waiver shall operate as a waiver of any other provisions
hereof (whether or not similar), nor shall such waiver constitute a continuing waiver. Except as specifically provided herein, no failure to
exercise or any delay in exercising any right or remedy hereunder shall constitute a waiver thereof.
12. Subrogation. In the event of payment under this Agreement, the Company shall be subrogated to the extent of such payment to
all of the rights of recovery of Indemnitee, who shall execute all papers required and shall do everything that may be necessary to secure such
rights, including the execution of such documents necessary to enable the Company effectively to bring suit to enforce such rights.
13. No Duplication of Payments. The Company shall not be liable under this Agreement to make any payment in connection with
any claim made against Indemnitee to the extent Indemnitee has otherwise received payment (under any insurance policy, Bylaw, or
otherwise) of the amounts otherwise Indemnifiable hereunder.
14. Binding Effect. This Agreement shall be binding upon and inure to the benefit of and be enforceable by the parties hereto and
their respective successors (including any direct or indirect successor by purchase, merger, consolidation, or otherwise to all or substantially
all of the business and/or assets of the Company), assigns, spouses, heirs, and personal and legal representatives. The Company shall require
and cause any successor (whether direct or indirect by purchase, merger, consolidation, or otherwise) to all, substantially all, or a substantial
part, of the business and/or assets of the Company, by written agreement in form and substance satisfactory to Indemnitee, expressly to
assume and agree to perform this Agreement in the same manner and to the same extent that the Company would be required to perform if no
such succession had taken place. The indemnification provided under this Agreement shall continue as to Indemnitee for any action taken or
not taken while serving in an indemnified capacity pertaining to an Indemnifiable Event even though he may have ceased to serve in such
capacity at the time of any Proceeding.
15. Severability. If any provision (or portion thereof) of this Agreement shall be held by a court of competent jurisdiction to be
invalid, void, or otherwise unenforceable, the remaining provisions shall remain enforceable to the fullest extent permitted by law.
Furthermore, to the fullest extent possible, the provisions of this Agreement (including, without limitation, each portion of this Agreement
containing any provision held to be invalid, void, or otherwise unenforceable, that is not itself invalid, void, or unenforceable) shall be
construed so as to give effect to the intent manifested by the provision held invalid, void, or unenforceable.
16. Governing Law. This Agreement shall be governed by and construed and enforced in accordance with the laws of the State of
California applicable to contracts made and to be performed in such State without giving effect to the principles of conflicts of laws.
17. Notices. All notices, demands, and other communications required or permitted hereunder shall be made in writing and shall be
deemed to have been duly given if delivered by hand, against receipt, or mailed, postage prepaid, certified or registered mail, return receipt
requested, and addressed to the Company at:
VistaGen Therapeutics, Inc.
384 Oyster Point Boulevard, No.8
South San Francisco, CA 94080
Attention: President
and to Indemnitee at:
Jon S. Saxe
435 Old Oak Court
Los Altos, CA 94022
Notice of change of address shall be effective only when done in accordance with this Section. All notices complying with this
Section shall be deemed to have been received on the date of delivery or on the third business day after mailing.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jon S. Saxe
May 20, 2013
IN WITNESS WHEREOF, the parties hereto have duly executed and delivered this Agreement as of the day specified above.
VISTAGEN THERAPEUTICS, INC.
By: /s/ Shawn Singh
Name: Shawn Singh
Title: Chief Executive Officer
JON S. SAXE
/s/ Jon S. Saxe
Indemnitee
VISTAGEN THERAPEUTICS, INC.
INDEMNIFICATION AGREEMENT
Exhibit 10.85
THIS AGREEMENT is entered into, effective as of May 20, 2013 between VistaGen Therapeutics, Inc., a Nevada corporation (the
"Company"), and Shawn K. Singh (“Indemnitee”).
WHEREAS, it is essential to the Company to retain and attract as directors and officers the most capable persons available;
WHEREAS, Indemnitee is a director of the Company;
WHEREAS, both the Company and Indemnitee recognize the increased risk of litigation and other claims currently being asserted
against directors and officers of corporations; and
WHEREAS, in recognition of lndemnitee's need for substantial protection against personal liability in order to enhance Indemnitee's
continued and effective service to the Company, and in order to induce Indemnitee to provide services to the Company as a director , the
Company wishes to provide in this Agreement for the indemnification of and the advancing of expenses to Indemnitee to the fullest extent
(whether partial or complete) permitted by law and as set forth in this Agreement, and, to the extent insurance is maintained, for the coverage
of Indemnitee under the Company's directors' and officers' liability insurance policies.
NOW, THEREFORE, in consideration of the above premises and of lndemnitee's continuing to serve the Company directly or, at its
request, with another enterprise, and intending to be legally bound hereby, the parties agree as follows:
1. Certain Definitions:
(a) Board: the Board of Directors of the Company.
(b) Change in Control: shall be deemed to have occurred if (i) any "person" (as such term is used in Sections 13(d) and
14(d) of the Securities Exchange Act of 1934, as amended), other than a trustee or other fiduciary holding securities under an employee
benefit plan of the Company or a corporation owned directly or indirectly by the shareholders of the Company in substantially the same
proportions as their ownership of stock of the Company, is or becomes the "Beneficial Owner" (as defined in Rule 13d-3 under said Act),
directly or indirectly, of securities of the Company representing 20% or more of the total voting power represented by the Company's then
outstanding Voting Securities, or (ii) during any period of two consecutive years, individuals who at the beginning of such period constitute
the Board and any new director whose election by the Board or nomination for election by the Company's shareholders was approved by a
vote of at least two-thirds (2/3) of the directors then still in office who either were directors at the beginning of the period or whose election
or nomination for election was previously so approved, cease for any reason to constitute a majority thereof, or (iii) the shareholders of the
Company approve a merger or consolidation of the Company with any other corporation, other than a merger or consolidation that would
result in the Voting Securities of the Company outstanding immediately prior thereto continuing to represent (either by remaining
outstanding or by being converted into Voting Securities of the surviving entity) at least 80% of the total voting power represented by the
Voting Securities of the Company or such surviving entity outstanding immediately after such merger or consolidation, or the shareholders
of the Company approve a plan of complete liquidation of the Company or an agreement for the sale or disposition by the Company (in one
transaction or a series of transactions) of all or substantially all of the Company's assets.
(c) Expenses: any expense, liability, or loss, including attorneys' fees, judgments, fines, ERISA excise taxes and penalties,
amounts paid or to be paid in settlement, any interest, assessments, or other charges imposed thereon, and any federal, state, local, or foreign
taxes imposed as a result of the actual or deemed receipt of any payments under this Agreement, paid or incurred in connection with
investigating, defending, being a witness in, or participating in (including on appeal), or preparing for any of the foregoing in, any
Proceeding relating to any Indemnifiable Event.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Shawn K. Singh
May 20, 2013
(d) Indemnifiable Event: any event or occurrence that takes place either prior to or after the execution of this Agreement,
related to the fact that Indemnitee is or was a director of the Company, or while a director is or was serving at the request of the Company as
a director, officer, employee, trustee, agent, or fiduciary of another foreign or domestic corporation, partnership, joint venture, employee
benefit plan, trust, or other enterprise, or was a director, officer, employee, or agent of a foreign or domestic corporation that was a
predecessor corporation of the Company or of another enterprise at the request of such predecessor corporation, or related to anything done
or not done by Indemnitee in any such capacity, whether or not the basis of the Proceeding is alleged action in an official capacity as a
director, officer, employee, or agent or in any other capacity while serving as a director, officer, employee, or agent of the Company, as
described above.
(e) Independent Counsel: the person or body appointed in connection with Section 3.
(f) Proceeding: any threatened, pending, or completed action, suit, or proceeding (including an action by or in the right of
the Company), or any inquiry, hearing, or investigation, whether conducted by the Company or any other party, that Indemnitee in good
faith believes might lead to the institution of any such action, suit, or proceeding, whether civil, criminal, administrative, investigative, or
other.
(g) Reviewing Party: the person or body appointed in accordance with Section 3.
(h) Voting Securities: any securities of the Company that vote generally in the election of directors.
2. Agreement to Indemnify.
(a) General Agreement. In the event Indemnitee was, is, or becomes a party to or witness or other participant in, or is
threatened to be made a party to or witness or other participant in, a Proceeding by reason of (or arising in part out of) an Indemnifiable
Event, the Company shall indemnify Indemnitee from and against any and all Expenses to the fullest extent permitted by law, as the same
exists or may hereafter be amended or interpreted (but in the case of any such amendment or interpretation, only to the extent that such
amendment or interpretation permits the Company to provide broader indemnification rights than were permitted prior thereto). The parties
hereto intend that this Agreement shall provide for indemnification in excess of that expressly permitted by statute, including, without
limitation, any indemnification provided by the Company's Articles of Incorporation, its Bylaws, vote of its shareholders or disinterested
directors, or applicable law.
(b) Initiation of Proceeding. Notwithstanding anything in this Agreement to the contrary, Indemnitee shall not be entitled
to indemnification pursuant to this Agreement in connection with any Proceeding initiated by Indemnitee against the Company or any
director of the Company unless (i) the Company has joined in or the Board has consented to the initiation of such Proceeding; (ii) the
Proceeding is one to enforce indemnification rights under Section 5; or (iii) the Proceeding is instituted after a Change in Control (other than
a Change in Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control)
and Independent Counsel has approved its initiation.
( c ) Expense Advances. If so requested by Indemnitee, the Company shall advance (within ten business days of such
request) any and all Expenses to Indemnitee (an "Expense Advance"); provided that, if and to the extent that the Reviewing Party determines
that Indemnitee would not be permitted to be so indemnified under applicable law, the Company shall be entitled to be reimbursed by
Indemnitee (who hereby agrees to reimburse the Company) for all such amounts theretofore paid. If Indemnitee has commenced or
commences legal proceedings in a court of competent jurisdiction to secure a determination that Indemnitee should be indemnified under
applicable law, as provided in Section 4, any determination made by the Reviewing Party that Indemnitee would not be permitted to be
indemnified under applicable law shall not be binding and Indemnitee shall not be required to reimburse the Company for any Expense
Advance until a final judicial determination is made with respect thereto (as to which all rights of appeal therefrom have been exhausted or
have lapsed). Indemnitee's obligation to reimburse the Company for Expense Advances shall be unsecured and no interest shall be charged
thereon.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Shawn K. Singh
May 20, 2013
(d) Mandatory Indemnification. Notwithstanding any other provision of this Agreement, to the extent that Indemnitee has
been successful on the merits in defense of any Proceeding relating in whole or in part to an Indemnifiable Event or in defense of any issue or
matter therein, Indemnitee shall be indemnified against all Expenses incurred in connection therewith.
( e ) Partial Indemnification. If indemnitee is entitled under any provision of this Agreement to indemnification by the
Company for some or a portion of Expenses, but not, however, for the total amount thereof, the Company shall nevertheless indemnify
Indemnitee for the portion thereof to which Indemnitee is entitled.
(f) Prohibited Indemnification. No indemnification pursuant to this Agreement shall be paid by the Company on account
of any Proceeding in which final unappealed judgment beyond the right of appeal is rendered against Indemnitee for an accounting of profits
made from the purchase or sale by Indemnitee of securities of the Company pursuant to the provisions of Section 16(b) of the Securities
Exchange Act of 1934, as amended, or similar provisions of any federal, state, or local laws.
3. Reviewing Party. Prior to any Change in Control, the Reviewing Party shall be any appropriate person or body consisting of a
member or members of the Board or any other person or body appointed by the Board who is not a party to the particular Proceeding with
respect to which Indemnitee is seeking indemnification; after a Change in Control, the Reviewing Party shall be the Independent Counsel
referred to below. With respect to all matters arising after a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) concerning the rights of lndemnitee to indemnity
payments and Expense Advances under this Agreement or any other agreement or under applicable law or the Company's Articles of
Incorporation or Bylaws now or hereafter in effect relating to indemnification for Indemnifiable Events, the Company shall seek legal advice
only from Independent Counsel selected by Indemnitee and approved by the Company (which approval shall not be unreasonably withheld),
and who has not otherwise performed services for the Company or the Indemnitee (other than in connection with indemnification matters)
within the last five years. The Independent Counsel shall not include any person who, under the applicable standards of professional conduct
then prevailing, would have a conflict of interest in representing either the Company or Indemnitee in an action to determine Indemnitee's
rights under this Agreement. Such counsel, among other things, shall render its written opinion to the Company and Indemnitee as to
whether and to what extent the Indemnitee should be permitted to be indemnified under applicable law. The Company agrees to pay the
reasonable fees of the Independent Counsel and to indemnify fully such counsel against any and all expenses (including attorneys' fees),
claims, liabilities, loss, and damages arising out of or relating to this Agreement or the engagement of Independent Counsel pursuant hereto.
4. Indemnification Process and Appeal.
( a ) Indemnification Payment. Indemnitee shall be entitled to indemnification of Expenses, and shall receive payment
thereof, from the Company in accordance with this Agreement as soon as practicable after Indemnitee has made written demand on the
Company for indemnification, unless the Reviewing Party has given a written opinion to the Company that Indemnitee is not entitled to
indemnification under applicable law.
( b ) Suit to Enforce Rights. Regardless of any action by the Reviewing Party, if Indemnitee has not received full
indemnification within thirty days after making a demand in accordance with Section 4(a), Indemnitee shall have the right to enforce its
indemnification rights under this Agreement by commencing litigation in any court in the State of Nevada having subject matter jurisdiction
thereof and in which venue is proper seeking an initial determination by the court or challenging any determination by the Reviewing Party
or any aspect thereof. The Company hereby consents to service of process and to appear in any such proceeding. Any determination by the
Reviewing Party not challenged by the Indemnitee shall be binding on the Company and Indemnitee. The remedy provided for in this
Section 4 shall be in addition to any other remedies available to Indemnitee in law or equity.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Shawn K. Singh
May 20, 2013
( c ) Defense to Indemnification, Burden of Proof, and Presumptions. It shall be a defense to any action brought by
Indemnitee against the Company to enforce this Agreement (other than an action brought to enforce a claim for Expenses incurred in
defending a Proceeding in advance of its final disposition where the required undertaking has been tendered to the Company) that it is not
permissible under applicable law for the Company to indemnify Indemnitee for the amount claimed. In connection with any such action or
any determination by the Reviewing Party or otherwise as to whether Indemnitee is entitled to be indemnified hereunder, the burden of
proving such a defense or determination shall be on the Company. Neither the failure of the Reviewing Party or the Company (including its
Board, independent legal counsel, or its shareholders) to have made a determination prior to the commencement of such action by
Indemnitee that indemnification of the claimant is proper under the circumstances because he has met the standard of conduct set forth in
applicable law, nor an actual determination by the Reviewing Party or Company (including its Board, independent legal counsel, or its
shareholders) that the Indemnitee had not met such applicable standard of conduct, shall be a defense to the action or create a presumption
that the Indemnitee has not met the applicable standard of conduct. For purposes of this Agreement, the termination of any claim, action,
suit, or proceeding, by judgment, order, settlement (whether with or without court approval), conviction, or upon a plea of nolo contendere,
or its equivalent, shall not create a presumption that Indemnitee did not meet any particular standard of conduct or have any particular belief
or that a court has determined that indemnification is not permitted by applicable law.
5 . Indemnification for Expenses Incurred in Enforcing Rights. The Company shall indemnify Indemnitee against any and all
Expenses that are incurred by Indemnitee in connection with any action brought by Indemnitee for
(i) indemnification of Expenses by the Company under this Agreement or any other agreement or under applicable
law or the Company's Articles of Incorporation or Bylaws now or hereafter in effect relating to indemnification for
Indemnifiable Events; and/or
(ii) recovery under directors' and officers' liability insurance policies maintained by the Company, but only in the
event that Indemnitee ultimately is determined to be entitled to such indemnification or insurance recovery, as the case may
be. In addition, the Company shall, if so requested by Indemnitee, advance the foregoing Expenses to Indemnitee, subject to
and in accordance with Section 2(c).
6. Notification and Defense of Proceeding.
(a) Notice. Promptly after receipt by Indemnitee of notice of the commencement of any Proceeding, Indemnitee will, if a
claim in respect thereof is to be made against the Company under this Agreement, notify the Company of the commencement thereof; but the
omission so to notify the Company will not relieve it from any liability that it may have to Indemnitee, except as provided in Section 6(c).
(b) Defense. With respect to any Proceeding as to which Indemnitee notifies the Company of the commencement thereof,
the Company will be entitled to participate in the Proceeding at its own expense and except as otherwise provided below, to the extent the
Company so wishes, it may assume the defense thereof with counsel reasonably satisfactory to Indemnitee. After notice from the Company
to Indemnitee of its election to assume the defense of any Proceeding, the Company will not be liable to Indemnitee under this Agreement or
otherwise for any Expenses subsequently incurred by Indemnitee in connection with the defense of such Proceeding other than reasonable
costs of investigation or as otherwise provided below. Indemnitee shall have the right to employ his own counsel in such Proceeding, but all
Expenses related thereto incurred after notice from the Company of its assumption of the defense shall be at Indemnitee's expense unless: (i)
the employment of counsel by Indemnitee has been authorized by the Company; (ii) Indemnitee has reasonably determined that there may
be a conflict of interest between Indemnitee and the Company in the defense of the Proceeding, after a Change in Control (other than a
Change in Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control);
(iii) the employment of counsel by Indemnitee has been approved by the Independent Counsel; or (iv) the Company shall not in fact have
employed counsel to assume the defense of such Proceeding, in each of which case all Expenses of the Proceeding shall be borne by the
Company. The Company shall not be entitled to assume the defense of any Proceeding brought by or on behalf of the Company or as to
which Indemnitee shall have made the determination provided for in (ii) above.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Shawn K. Singh
May 20, 2013
(c) Settlement of Claims. The Company shall not be liable to indemnify Indemnitee under this Agreement or otherwise for
any amounts paid in settlement of any Proceeding effected without the Company's written consent, provided, however, that if a Change in
Control has occured (other than a Change in Control approved by a majority of the directors on the Board who were directors immediately
prior to such Change in Control), the Company shall be liable for indemnification of Indemnitee for amounts paid in settlement if the
Independent Counsel has approved the settlement. The Company shall not settle any Proceeding in any manner that would impose any
penalty or limitation on Indemnitee without Indemnitee's written consent. Neither the Company nor the Indemnitee will unreasonably
withhold their consent to any proposed settlement. The Company shall not be liable to indemnify the Indemnitee under this Agreement with
regard to any judicial award if the Company was not given a reasonable and timely opportunity, at its expense, to participate in the defense
of such action; the Company's liability hereunder shall not be excused if participation in the Proceeding by the Company was barred by this
Agreement.
7 . Establishment of Trust. In the event of a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) the Company shall, upon written request by
Indemnitee, create a Trust for the benefit of the Indemnitee and from time to time upon written request of Indemnitee shall fund the Trust in
an amount sufficient to satisfy any and all Expenses reasonably anticipated at the time of each such request to be incurred in connection with
investigating, preparing for, participating in, and/or defending any Proceeding relating to an Indemnifiable Event. The amount or amounts to
be deposited in the Trust pursuant to the foregoing funding obligation shall be determined by the Reviewing Party. The terms of the Trust
shall provide that: (i) the Trust shall not be revoked or the principal thereof invaded, without the written consent of the Indemnitee; (ii) the
Trustee shall advance, within ten business days of a request by the Indemnitee, any and all Expenses to the Indemnitee (and the Indemnitee
hereby agrees to reimburse the Trust under the same circumstances for which the Indemnitee would be required to reimburse the Company
under Section 2(c) of this Agreement); (iii) the Trust shall continue to be funded by the Company in accordance with the funding obligation
set forth above; (iv) the Trustee shall promptly pay to the Indemnitee all amounts for which the Indemnitee shall be entitled to
indemnification pursuant to this Agreement or otherwise; and (v) all unexpended funds in the Trust shall revert to the Company upon a final
determination by the Reviewing Party or a court of competent jurisdiction, as the case may be, that the Indemnitee has been fully
indemnified under the terms of this Agreement. The Trustee shall be chosen by the Indemnitee. Nothing in this Section 7 shall relieve the
Company of any of its obligations under this Agreement. All income earned on the assets held in the Trust shall be reported as income by the
Company for federal, state, local, and foreign tax purposes. The Company shall pay all costs of establishing and maintaining the Trust and
shall indemnify the Trustee against any and all expenses (including attorneys' fees), claims, liabilities, loss, and damages arising out of or
relating to this Agreement or the establishment and maintenance of the Trust.
8 . Non-Exclusivity. The rights of Indemnitee hereunder shall be in addition to any other rights Indemnitee may have under the
Company's Articles of Incorporation, Bylaws, applicable law, or otherwise. To the extent that a change in applicable law (whether by statute
or judicial decision) permits greater indemnification by agreement than would be afforded currently under the Company's Articles of
Incorporation, Bylaws, applicable law, or this Agreement, it is the intent of the parties that Indemnitee enjoy by this Agreement the greater
benefits so afforded by such change.
9 . Liability Insurance. To the extent the Company maintains an insurance policy or policies providing directors' and officers'
liability insurance, Indemnitee shall be covered by such policy or policies, in accordance with its or their terms, to the maximum extent of the
coverage available for any Company director or officer.
10. Period of Limitations. No legal action shall be brought and no cause of action shall be asserted by or on behalf of the Company
or any affiliate of the Company against Indemnitee, Indemnitee's spouse, heirs, executors, or personal or legal representatives after the
expiration of two (2) years from the date of accrual of such cause of action, or such longer period as may be required by state law under the
circumstances. Any claim or cause of action of the Company or its affiliate shall be extinguished and deemed released unless asserted by the
timely filing of a legal action within such period; provided, however, that if any shorter period of limitations is otherwise applicable to any
such cause of action the shorter period shall govern.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Shawn K. Singh
May 20, 2013
1 1 . Amendment of this Agreement. No supplement, modification, or amendment of this Agreement shall be binding unless
executed in writing by both of the parties hereto. No waiver of any of the provisions of this Agreement shall be binding unless in the form of
a writing signed by the party against whom enforcement of the waiver is sought, and no such waiver shall operate as a waiver of any other
provisions hereof (whether or not similar), nor shall such waiver constitute a continuing waiver. Except as specifically provided herein, no
failure to exercise or any delay in exercising any right or remedy hereunder shall constitute a waiver thereof.
12. Subrogation. In the event of payment under this Agreement, the Company shall be subrogated to the extent of such payment to
all of the rights of recovery of Indemnitee, who shall execute all papers required and shall do everything that may be necessary to secure
such rights, including the execution of such documents necessary to enable the Company effectively to bring suit to enforce such rights.
13. No Duplication of Payments. The Company shall not be liable under this Agreement to make any payment in connection with
any claim made against Indemnitee to the extent Indemnitee has otherwise received payment (under any insurance policy, Bylaw, or
otherwise) of the amounts otherwise Indemnifiable hereunder.
14. Binding Effect. This Agreement shall be binding upon and inure to the benefit of and be enforceable by the parties hereto and
their respective successors (including any direct or indirect successor by purchase, merger, consolidation, or otherwise to all or substantially
all of the business and/or assets of the Company), assigns, spouses, heirs, and personal and legal representatives. The Company shall require
and cause any successor (whether direct or indirect by purchase, merger, consolidation, or otherwise) to all, substantially all, or a substantial
part, of the business and/or assets of the Company, by written agreement in form and substance satisfactory to Indemnitee, expressly to
assume and agree to perform this Agreement in the same manner and to the same extent that the Company would be required to perform if no
such succession had taken place. The indemnification provided under this Agreement shall continue as to Indemnitee for any action taken or
not taken while serving in an indemnified capacity pertaining to an Indemnifiable Event even though he may have ceased to serve in such
capacity at the time of any Proceeding.
15. Severability. If any provision (or portion thereof) of this Agreement shall be held by a court of competent jurisdiction to be
invalid, void, or otherwise unenforceable, the remaining provisions shall remain enforceable to the fullest extent permitted by law.
Furthermore, to the fullest extent possible, the provisions of this Agreement (including, without limitation, each portion of this Agreement
containing any provision held to be invalid, void, or otherwise unenforceable, that is not itself invalid, void, or unenforceable) shall be
construed so as to give effect to the intent manifested by the provision held invalid, void, or unenforceable.
16. Governing Law. This Agreement shall be governed by and construed and enforced in accordance with the laws of the State of
California applicable to contracts made and to be performed in such State without giving effect to the principles of conflicts of laws.
17. Notices. All notices, demands, and other communications required or permitted hereunder shall be made in writing and shall be
deemed to have been duly given if delivered by hand, against receipt, or mailed, postage prepaid, certified or registered mail, return receipt
requested, and addressed to the Company at:
VistaGen Therapeutics, Inc.
384 Oyster Point Boulevard, No.8
South San Francisco, CA 94080
Attention: President
and to Indemnitee at:
Shawn K. Singh
1737 Elizabeth Street
San Carlos, CA 94070
Notice of change of address shall be effective only when done in accordance with this Section. All notices complying with this
Section shall be deemed to have been received on the date of delivery or on the third business day after mailing.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Shawn K. Singh
May 20, 2013
IN WITNESS WHEREOF, the parties hereto have duly executed and delivered this Agreement as of the day specified above.
VISTAGEN THERAPEUTICS, INC.
By: /s/ H. Ralph Snodgrass
Name: H. Ralph Snodgrass
Title: President and Chief Scientific Officer
SHAWN K. SINGH
/s/ Shawn K. Singh
Indemnitee
VISTAGEN THERAPEUTICS, INC.
INDEMNIFICATION AGREEMENT
Exhibit 10.86
THIS AGREEMENT is entered into, effective as of May 20, 2013 between VistaGen Therapeutics, Inc., a Nevada corporation (the
"Company"), and H. Ralph Snodgrass, Ph. D. (“Indemnitee”).
WHEREAS, it is essential to the Company to retain and attract as directors and officers the most capable persons available;
WHEREAS, Indemnitee is a director of the Company;
WHEREAS, both the Company and Indemnitee recognize the increased risk of litigation and other claims currently being asserted
against directors and officers of corporations; and
WHEREAS, in recognition of lndemnitee's need for substantial protection against personal liability in order to enhance Indemnitee's
continued and effective service to the Company, and in order to induce Indemnitee to provide services to the Company as a director , the
Company wishes to provide in this Agreement for the indemnification of and the advancing of expenses to Indemnitee to the fullest extent
(whether partial or complete) permitted by law and as set forth in this Agreement, and, to the extent insurance is maintained, for the coverage
of Indemnitee under the Company's directors' and officers' liability insurance policies.
NOW, THEREFORE, in consideration of the above premises and of lndemnitee's continuing to serve the Company directly or, at its
request, with another enterprise, and intending to be legally bound hereby, the parties agree as follows:
1. Certain Definitions:
(a) Board: the Board of Directors of the Company.
(b) Change in Control: shall be deemed to have occurred if (i) any "person" (as such term is used in Sections 13(d) and
14(d) of the Securities Exchange Act of 1934, as amended), other than a trustee or other fiduciary holding securities under an employee benefit
plan of the Company or a corporation owned directly or indirectly by the shareholders of the Company in substantially the same proportions
as their ownership of stock of the Company, is or becomes the "Beneficial Owner" (as defined in Rule 13d-3 under said Act), directly or
indirectly, of securities of the Company representing 20% or more of the total voting power represented by the Company's then outstanding
Voting Securities, or (ii) during any period of two consecutive years, individuals who at the beginning of such period constitute the Board and
any new director whose election by the Board or nomination for election by the Company's shareholders was approved by a vote of at least
two-thirds (2/3) of the directors then still in office who either were directors at the beginning of the period or whose election or nomination for
election was previously so approved, cease for any reason to constitute a majority thereof, or (iii) the shareholders of the Company approve a
merger or consolidation of the Company with any other corporation, other than a merger or consolidation that would result in the Voting
Securities of the Company outstanding immediately prior thereto continuing to represent (either by remaining outstanding or by being
converted into Voting Securities of the surviving entity) at least 80% of the total voting power represented by the Voting Securities of the
Company or such surviving entity outstanding immediately after such merger or consolidation, or the shareholders of the Company approve a
plan of complete liquidation of the Company or an agreement for the sale or disposition by the Company (in one transaction or a series of
transactions) of all or substantially all of the Company's assets.
(c) Expenses: any expense, liability, or loss, including attorneys' fees, judgments, fines, ERISA excise taxes and penalties,
amounts paid or to be paid in settlement, any interest, assessments, or other charges imposed thereon, and any federal, state, local, or foreign
taxes imposed as a result of the actual or deemed receipt of any payments under this Agreement, paid or incurred in connection with
investigating, defending, being a witness in, or participating in (including on appeal), or preparing for any of the foregoing in, any Proceeding
relating to any Indemnifiable Event.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with H. Ralph Snodgrass, Ph. D.
May 20, 2013
(d) Indemnifiable Event: any event or occurrence that takes place either prior to or after the execution of this Agreement,
related to the fact that Indemnitee is or was a director of the Company, or while a director is or was serving at the request of the Company as a
director, officer, employee, trustee, agent, or fiduciary of another foreign or domestic corporation, partnership, joint venture, employee benefit
plan, trust, or other enterprise, or was a director, officer, employee, or agent of a foreign or domestic corporation that was a predecessor
corporation of the Company or of another enterprise at the request of such predecessor corporation, or related to anything done or not done by
Indemnitee in any such capacity, whether or not the basis of the Proceeding is alleged action in an official capacity as a director, officer,
employee, or agent or in any other capacity while serving as a director, officer, employee, or agent of the Company, as described above.
(e) Independent Counsel: the person or body appointed in connection with Section 3.
(f) Proceeding: any threatened, pending, or completed action, suit, or proceeding (including an action by or in the right of
the Company), or any inquiry, hearing, or investigation, whether conducted by the Company or any other party, that Indemnitee in good faith
believes might lead to the institution of any such action, suit, or proceeding, whether civil, criminal, administrative, investigative, or other.
(g) Reviewing Party: the person or body appointed in accordance with Section 3.
(h) Voting Securities: any securities of the Company that vote generally in the election of directors.
2. Agreement to Indemnify.
(a) General Agreement. In the event Indemnitee was, is, or becomes a party to or witness or other participant in, or is
threatened to be made a party to or witness or other participant in, a Proceeding by reason of (or arising in part out of) an Indemnifiable Event,
the Company shall indemnify Indemnitee from and against any and all Expenses to the fullest extent permitted by law, as the same exists or
may hereafter be amended or interpreted (but in the case of any such amendment or interpretation, only to the extent that such amendment
or interpretation permits the Company to provide broader indemnification rights than were permitted prior thereto). The parties hereto intend
that this Agreement shall provide for indemnification in excess of that expressly permitted by statute, including, without limitation, any
indemnification provided by the Company's Articles of Incorporation, its Bylaws, vote of its shareholders or disinterested directors, or
applicable law.
(b) Initiation of Proceeding. Notwithstanding anything in this Agreement to the contrary, Indemnitee shall not be entitled to
indemnification pursuant to this Agreement in connection with any Proceeding initiated by Indemnitee against the Company or any director of
the Company unless (i) the Company has joined in or the Board has consented to the initiation of such Proceeding; (ii) the Proceeding is one
to enforce indemnification rights under Section 5; or (iii) the Proceeding is instituted after a Change in Control (other than a Change in
Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control) and
Independent Counsel has approved its initiation.
( c ) Expense Advances. If so requested by Indemnitee, the Company shall advance (within ten business days of such
request) any and all Expenses to Indemnitee (an "Expense Advance"); provided that, if and to the extent that the Reviewing Party determines
that Indemnitee would not be permitted to be so indemnified under applicable law, the Company shall be entitled to be reimbursed by
Indemnitee (who hereby agrees to reimburse the Company) for all such amounts theretofore paid. If Indemnitee has commenced or
commences legal proceedings in a court of competent jurisdiction to secure a determination that Indemnitee should be indemnified under
applicable law, as provided in Section 4, any determination made by the Reviewing Party that Indemnitee would not be permitted to be
indemnified under applicable law shall not be binding and Indemnitee shall not be required to reimburse the Company for any Expense
Advance until a final judicial determination is made with respect thereto (as to which all rights of appeal therefrom have been exhausted or
have lapsed). Indemnitee's obligation to reimburse the Company for Expense Advances shall be unsecured and no interest shall be charged
thereon.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with H. Ralph Snodgrass, Ph. D.
May 20, 2013
(d) Mandatory Indemnification. Notwithstanding any other provision of this Agreement, to the extent that Indemnitee has
been successful on the merits in defense of any Proceeding relating in whole or in part to an Indemnifiable Event or in defense of any issue or
matter therein, Indemnitee shall be indemnified against all Expenses incurred in connection therewith.
( e ) Partial Indemnification. If indemnitee is entitled under any provision of this Agreement to indemnification by the
Company for some or a portion of Expenses, but not, however, for the total amount thereof, the Company shall nevertheless indemnify
Indemnitee for the portion thereof to which Indemnitee is entitled.
(f) Prohibited Indemnification. No indemnification pursuant to this Agreement shall be paid by the Company on account of
any Proceeding in which final unappealed judgment beyond the right of appeal is rendered against Indemnitee for an accounting of profits
made from the purchase or sale by Indemnitee of securities of the Company pursuant to the provisions of Section 16(b) of the Securities
Exchange Act of 1934, as amended, or similar provisions of any federal, state, or local laws.
3. Reviewing Party. Prior to any Change in Control, the Reviewing Party shall be any appropriate person or body consisting of a
member or members of the Board or any other person or body appointed by the Board who is not a party to the particular Proceeding with
respect to which Indemnitee is seeking indemnification; after a Change in Control, the Reviewing Party shall be the Independent Counsel
referred to below. With respect to all matters arising after a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) concerning the rights of lndemnitee to indemnity
payments and Expense Advances under this Agreement or any other agreement or under applicable law or the Company's Articles of
Incorporation or Bylaws now or hereafter in effect relating to indemnification for Indemnifiable Events, the Company shall seek legal advice
only from Independent Counsel selected by Indemnitee and approved by the Company (which approval shall not be unreasonably withheld),
and who has not otherwise performed services for the Company or the Indemnitee (other than in connection with indemnification matters)
within the last five years. The Independent Counsel shall not include any person who, under the applicable standards of professional conduct
then prevailing, would have a conflict of interest in representing either the Company or Indemnitee in an action to determine Indemnitee's
rights under this Agreement. Such counsel, among other things, shall render its written opinion to the Company and Indemnitee as to whether
and to what extent the Indemnitee should be permitted to be indemnified under applicable law. The Company agrees to pay the reasonable fees
of the Independent Counsel and to indemnify fully such counsel against any and all expenses (including attorneys' fees), claims, liabilities,
loss, and damages arising out of or relating to this Agreement or the engagement of Independent Counsel pursuant hereto.
4. Indemnification Process and Appeal.
( a ) Indemnification Payment. Indemnitee shall be entitled to indemnification of Expenses, and shall receive payment
thereof, from the Company in accordance with this Agreement as soon as practicable after Indemnitee has made written demand on the
Company for indemnification, unless the Reviewing Party has given a written opinion to the Company that Indemnitee is not entitled to
indemnification under applicable law.
( b ) Suit to Enforce Rights. Regardless of any action by the Reviewing Party, if Indemnitee has not received full
indemnification within thirty days after making a demand in accordance with Section 4(a), Indemnitee shall have the right to enforce its
indemnification rights under this Agreement by commencing litigation in any court in the State of Nevada having subject matter jurisdiction
thereof and in which venue is proper seeking an initial determination by the court or challenging any determination by the Reviewing Party or
any aspect thereof. The Company hereby consents to service of process and to appear in any such proceeding. Any determination by the
Reviewing Party not challenged by the Indemnitee shall be binding on the Company and Indemnitee. The remedy provided for in this Section
4 shall be in addition to any other remedies available to Indemnitee in law or equity.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with H. Ralph Snodgrass, Ph. D.
May 20, 2013
( c ) Defense to Indemnification, Burden of Proof, and Presumptions. It shall be a defense to any action brought by
Indemnitee against the Company to enforce this Agreement (other than an action brought to enforce a claim for Expenses incurred in
defending a Proceeding in advance of its final disposition where the required undertaking has been tendered to the Company) that it is not
permissible under applicable law for the Company to indemnify Indemnitee for the amount claimed. In connection with any such action or any
determination by the Reviewing Party or otherwise as to whether Indemnitee is entitled to be indemnified hereunder, the burden of proving
such a defense or determination shall be on the Company. Neither the failure of the Reviewing Party or the Company (including its Board,
independent legal counsel, or its shareholders) to have made a determination prior to the commencement of such action by Indemnitee that
indemnification of the claimant is proper under the circumstances because he has met the standard of conduct set forth in applicable law, nor
an actual determination by the Reviewing Party or Company (including its Board, independent legal counsel, or its shareholders) that the
Indemnitee had not met such applicable standard of conduct, shall be a defense to the action or create a presumption that the Indemnitee has
not met the applicable standard of conduct. For purposes of this Agreement, the termination of any claim, action, suit, or proceeding, by
judgment, order, settlement (whether with or without court approval), conviction, or upon a plea of nolo contendere, or its equivalent, shall not
create a presumption that Indemnitee did not meet any particular standard of conduct or have any particular belief or that a court has
determined that indemnification is not permitted by applicable law.
5 . Indemnification for Expenses Incurred in Enforcing Rights. The Company shall indemnify Indemnitee against any and all
Expenses that are incurred by Indemnitee in connection with any action brought by Indemnitee for
(i) indemnification of Expenses by the Company under this Agreement or any other agreement or under applicable
law or the Company's Articles of Incorporation or Bylaws now or hereafter in effect relating to indemnification for
Indemnifiable Events; and/or
(ii) recovery under directors' and officers' liability insurance policies maintained by the Company, but only in the
event that Indemnitee ultimately is determined to be entitled to such indemnification or insurance recovery, as the case may
be. In addition, the Company shall, if so requested by Indemnitee, advance the foregoing Expenses to Indemnitee, subject to
and in accordance with Section 2(c).
6. Notification and Defense of Proceeding.
(a) Notice. Promptly after receipt by Indemnitee of notice of the commencement of any Proceeding, Indemnitee will, if a
claim in respect thereof is to be made against the Company under this Agreement, notify the Company of the commencement thereof; but the
omission so to notify the Company will not relieve it from any liability that it may have to Indemnitee, except as provided in Section 6(c).
(b) Defense. With respect to any Proceeding as to which Indemnitee notifies the Company of the commencement thereof,
the Company will be entitled to participate in the Proceeding at its own expense and except as otherwise provided below, to the extent the
Company so wishes, it may assume the defense thereof with counsel reasonably satisfactory to Indemnitee. After notice from the Company to
Indemnitee of its election to assume the defense of any Proceeding, the Company will not be liable to Indemnitee under this Agreement or
otherwise for any Expenses subsequently incurred by Indemnitee in connection with the defense of such Proceeding other than reasonable
costs of investigation or as otherwise provided below. Indemnitee shall have the right to employ his own counsel in such Proceeding, but all
Expenses related thereto incurred after notice from the Company of its assumption of the defense shall be at Indemnitee's expense unless: (i)
the employment of counsel by Indemnitee has been authorized by the Company; (ii) Indemnitee has reasonably determined that there may be
a conflict of interest between Indemnitee and the Company in the defense of the Proceeding, after a Change in Control (other than a Change in
Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control); (iii) the
employment of counsel by Indemnitee has been approved by the Independent Counsel; or (iv) the Company shall not in fact have employed
counsel to assume the defense of such Proceeding, in each of which case all Expenses of the Proceeding shall be borne by the Company. The
Company shall not be entitled to assume the defense of any Proceeding brought by or on behalf of the Company or as to which Indemnitee
shall have made the determination provided for in (ii) above.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with H. Ralph Snodgrass, Ph. D.
May 20, 2013
(c) Settlement of Claims. The Company shall not be liable to indemnify Indemnitee under this Agreement or otherwise for
any amounts paid in settlement of any Proceeding effected without the Company's written consent, provided, however, that if a Change in
Control has occured (other than a Change in Control approved by a majority of the directors on the Board who were directors immediately
prior to such Change in Control), the Company shall be liable for indemnification of Indemnitee for amounts paid in settlement if the
Independent Counsel has approved the settlement. The Company shall not settle any Proceeding in any manner that would impose any penalty
or limitation on Indemnitee without Indemnitee's written consent. Neither the Company nor the Indemnitee will unreasonably withhold their
consent to any proposed settlement. The Company shall not be liable to indemnify the Indemnitee under this Agreement with regard to any
judicial award if the Company was not given a reasonable and timely opportunity, at its expense, to participate in the defense of such action;
the Company's liability hereunder shall not be excused if participation in the Proceeding by the Company was barred by this Agreement.
7 . Establishment of Trust. In the event of a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) the Company shall, upon written request by
Indemnitee, create a Trust for the benefit of the Indemnitee and from time to time upon written request of Indemnitee shall fund the Trust in an
amount sufficient to satisfy any and all Expenses reasonably anticipated at the time of each such request to be incurred in connection with
investigating, preparing for, participating in, and/or defending any Proceeding relating to an Indemnifiable Event. The amount or amounts to
be deposited in the Trust pursuant to the foregoing funding obligation shall be determined by the Reviewing Party. The terms of the Trust
shall provide that: (i) the Trust shall not be revoked or the principal thereof invaded, without the written consent of the Indemnitee; (ii) the
Trustee shall advance, within ten business days of a request by the Indemnitee, any and all Expenses to the Indemnitee (and the Indemnitee
hereby agrees to reimburse the Trust under the same circumstances for which the Indemnitee would be required to reimburse the Company
under Section 2(c) of this Agreement); (iii) the Trust shall continue to be funded by the Company in accordance with the funding obligation set
forth above; (iv) the Trustee shall promptly pay to the Indemnitee all amounts for which the Indemnitee shall be entitled to indemnification
pursuant to this Agreement or otherwise; and (v) all unexpended funds in the Trust shall revert to the Company upon a final determination by
the Reviewing Party or a court of competent jurisdiction, as the case may be, that the Indemnitee has been fully indemnified under the terms
of this Agreement. The Trustee shall be chosen by the Indemnitee. Nothing in this Section 7 shall relieve the Company of any of its
obligations under this Agreement. All income earned on the assets held in the Trust shall be reported as income by the Company for federal,
state, local, and foreign tax purposes. The Company shall pay all costs of establishing and maintaining the Trust and shall indemnify the
Trustee against any and all expenses (including attorneys' fees), claims, liabilities, loss, and damages arising out of or relating to this
Agreement or the establishment and maintenance of the Trust.
8 . Non-Exclusivity. The rights of Indemnitee hereunder shall be in addition to any other rights Indemnitee may have under the
Company's Articles of Incorporation, Bylaws, applicable law, or otherwise. To the extent that a change in applicable law (whether by statute or
judicial decision) permits greater indemnification by agreement than would be afforded currently under the Company's Articles of
Incorporation, Bylaws, applicable law, or this Agreement, it is the intent of the parties that Indemnitee enjoy by this Agreement the greater
benefits so afforded by such change.
9 . Liability Insurance. To the extent the Company maintains an insurance policy or policies providing directors' and officers'
liability insurance, Indemnitee shall be covered by such policy or policies, in accordance with its or their terms, to the maximum extent of the
coverage available for any Company director or officer.
10. Period of Limitations. No legal action shall be brought and no cause of action shall be asserted by or on behalf of the Company
or any affiliate of the Company against Indemnitee, Indemnitee's spouse, heirs, executors, or personal or legal representatives after the
expiration of two (2) years from the date of accrual of such cause of action, or such longer period as may be required by state law under the
circumstances. Any claim or cause of action of the Company or its affiliate shall be extinguished and deemed released unless asserted by the
timely filing of a legal action within such period; provided, however, that if any shorter period of limitations is otherwise applicable to any
such cause of action the shorter period shall govern.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with H. Ralph Snodgrass, Ph. D.
May 20, 2013
11. Amendment of this Agreement. No supplement, modification, or amendment of this Agreement shall be binding unless executed
in writing by both of the parties hereto. No waiver of any of the provisions of this Agreement shall be binding unless in the form of a writing
signed by the party against whom enforcement of the waiver is sought, and no such waiver shall operate as a waiver of any other provisions
hereof (whether or not similar), nor shall such waiver constitute a continuing waiver. Except as specifically provided herein, no failure to
exercise or any delay in exercising any right or remedy hereunder shall constitute a waiver thereof.
12. Subrogation. In the event of payment under this Agreement, the Company shall be subrogated to the extent of such payment to
all of the rights of recovery of Indemnitee, who shall execute all papers required and shall do everything that may be necessary to secure such
rights, including the execution of such documents necessary to enable the Company effectively to bring suit to enforce such rights.
13. No Duplication of Payments. The Company shall not be liable under this Agreement to make any payment in connection with
any claim made against Indemnitee to the extent Indemnitee has otherwise received payment (under any insurance policy, Bylaw, or
otherwise) of the amounts otherwise Indemnifiable hereunder.
14. Binding Effect. This Agreement shall be binding upon and inure to the benefit of and be enforceable by the parties hereto and
their respective successors (including any direct or indirect successor by purchase, merger, consolidation, or otherwise to all or substantially
all of the business and/or assets of the Company), assigns, spouses, heirs, and personal and legal representatives. The Company shall require
and cause any successor (whether direct or indirect by purchase, merger, consolidation, or otherwise) to all, substantially all, or a substantial
part, of the business and/or assets of the Company, by written agreement in form and substance satisfactory to Indemnitee, expressly to
assume and agree to perform this Agreement in the same manner and to the same extent that the Company would be required to perform if no
such succession had taken place. The indemnification provided under this Agreement shall continue as to Indemnitee for any action taken or
not taken while serving in an indemnified capacity pertaining to an Indemnifiable Event even though he may have ceased to serve in such
capacity at the time of any Proceeding.
15. Severability. If any provision (or portion thereof) of this Agreement shall be held by a court of competent jurisdiction to be
invalid, void, or otherwise unenforceable, the remaining provisions shall remain enforceable to the fullest extent permitted by law.
Furthermore, to the fullest extent possible, the provisions of this Agreement (including, without limitation, each portion of this Agreement
containing any provision held to be invalid, void, or otherwise unenforceable, that is not itself invalid, void, or unenforceable) shall be
construed so as to give effect to the intent manifested by the provision held invalid, void, or unenforceable.
16. Governing Law. This Agreement shall be governed by and construed and enforced in accordance with the laws of the State of
California applicable to contracts made and to be performed in such State without giving effect to the principles of conflicts of laws.
17. Notices. All notices, demands, and other communications required or permitted hereunder shall be made in writing and shall be
deemed to have been duly given if delivered by hand, against receipt, or mailed, postage prepaid, certified or registered mail, return receipt
requested, and addressed to the Company at:
VistaGen Therapeutics, Inc.
384 Oyster Point Boulevard, No.8
South San Francisco, CA 94080
Attention: President
and to Indemnitee at:
H. Ralph Snodgrass, Ph. D
20781 Via Corta
San Jose, CA 95120
Notice of change of address shall be effective only when done in accordance with this Section. All notices complying with this
Section shall be deemed to have been received on the date of delivery or on the third business day after mailing.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with H. Ralph Snodgrass, Ph. D.
May 20, 2013
IN WITNESS WHEREOF, the parties hereto have duly executed and delivered this Agreement as of the day specified above.
VISTAGEN THERAPEUTICS, INC.
By: /s/ Shawn Singh
Name: Shawn Singh
Title: Chief Executive Officer
H. RALPH SNODGRASS, Ph. D
/s/ H. Ralph Snodgrass, Ph. D
Indemnitee
VISTAGEN THERAPEUTICS, INC.
INDEMNIFICATION AGREEMENT
Exhibit 10.87
THIS AGREEMENT is entered into, effective as of May 20, 2013 between VistaGen Therapeutics, Inc., a Nevada corporation (the
"Company"), and Brian J. Underdown, Ph. D. (“Indemnitee”).
WHEREAS, it is essential to the Company to retain and attract as directors and officers the most capable persons available;
WHEREAS, Indemnitee is a director of the Company;
WHEREAS, both the Company and Indemnitee recognize the increased risk of litigation and other claims currently being asserted
against directors and officers of corporations; and
WHEREAS, in recognition of lndemnitee's need for substantial protection against personal liability in order to enhance Indemnitee's
continued and effective service to the Company, and in order to induce Indemnitee to provide services to the Company as a director , the
Company wishes to provide in this Agreement for the indemnification of and the advancing of expenses to Indemnitee to the fullest extent
(whether partial or complete) permitted by law and as set forth in this Agreement, and, to the extent insurance is maintained, for the coverage
of Indemnitee under the Company's directors' and officers' liability insurance policies.
NOW, THEREFORE, in consideration of the above premises and of lndemnitee's continuing to serve the Company directly or, at its
request, with another enterprise, and intending to be legally bound hereby, the parties agree as follows:
1. Certain Definitions:
(a) Board: the Board of Directors of the Company.
(b) Change in Control: shall be deemed to have occurred if (i) any "person" (as such term is used in Sections 13(d) and
14(d) of the Securities Exchange Act of 1934, as amended), other than a trustee or other fiduciary holding securities under an employee
benefit plan of the Company or a corporation owned directly or indirectly by the shareholders of the Company in substantially the same
proportions as their ownership of stock of the Company, is or becomes the "Beneficial Owner" (as defined in Rule 13d-3 under said Act),
directly or indirectly, of securities of the Company representing 20% or more of the total voting power represented by the Company's then
outstanding Voting Securities, or (ii) during any period of two consecutive years, individuals who at the beginning of such period constitute
the Board and any new director whose election by the Board or nomination for election by the Company's shareholders was approved by a
vote of at least two-thirds (2/3) of the directors then still in office who either were directors at the beginning of the period or whose election
or nomination for election was previously so approved, cease for any reason to constitute a majority thereof, or (iii) the shareholders of the
Company approve a merger or consolidation of the Company with any other corporation, other than a merger or consolidation that would
result in the Voting Securities of the Company outstanding immediately prior thereto continuing to represent (either by remaining
outstanding or by being converted into Voting Securities of the surviving entity) at least 80% of the total voting power represented by the
Voting Securities of the Company or such surviving entity outstanding immediately after such merger or consolidation, or the shareholders
of the Company approve a plan of complete liquidation of the Company or an agreement for the sale or disposition by the Company (in one
transaction or a series of transactions) of all or substantially all of the Company's assets.
(c) Expenses: any expense, liability, or loss, including attorneys' fees, judgments, fines, ERISA excise taxes and penalties,
amounts paid or to be paid in settlement, any interest, assessments, or other charges imposed thereon, and any federal, state, local, or foreign
taxes imposed as a result of the actual or deemed receipt of any payments under this Agreement, paid or incurred in connection with
investigating, defending, being a witness in, or participating in (including on appeal), or preparing for any of the foregoing in, any
Proceeding relating to any Indemnifiable Event.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Brian J. Underdown, Ph. D.
May 20, 2013
(d) Indemnifiable Event: any event or occurrence that takes place either prior to or after the execution of this Agreement,
related to the fact that Indemnitee is or was a director of the Company, or while a director is or was serving at the request of the Company as
a director, officer, employee, trustee, agent, or fiduciary of another foreign or domestic corporation, partnership, joint venture, employee
benefit plan, trust, or other enterprise, or was a director, officer, employee, or agent of a foreign or domestic corporation that was a
predecessor corporation of the Company or of another enterprise at the request of such predecessor corporation, or related to anything done
or not done by Indemnitee in any such capacity, whether or not the basis of the Proceeding is alleged action in an official capacity as a
director, officer, employee, or agent or in any other capacity while serving as a director, officer, employee, or agent of the Company, as
described above.
(e) Independent Counsel: the person or body appointed in connection with Section 3.
(f) Proceeding: any threatened, pending, or completed action, suit, or proceeding (including an action by or in the right of
the Company), or any inquiry, hearing, or investigation, whether conducted by the Company or any other party, that Indemnitee in good
faith believes might lead to the institution of any such action, suit, or proceeding, whether civil, criminal, administrative, investigative, or
other.
(g) Reviewing Party: the person or body appointed in accordance with Section 3.
(h) Voting Securities: any securities of the Company that vote generally in the election of directors.
2. Agreement to Indemnify.
(a) General Agreement. In the event Indemnitee was, is, or becomes a party to or witness or other participant in, or is
threatened to be made a party to or witness or other participant in, a Proceeding by reason of (or arising in part out of) an Indemnifiable
Event, the Company shall indemnify Indemnitee from and against any and all Expenses to the fullest extent permitted by law, as the same
exists or may hereafter be amended or interpreted (but in the case of any such amendment or interpretation, only to the extent that such
amendment or interpretation permits the Company to provide broader indemnification rights than were permitted prior thereto). The parties
hereto intend that this Agreement shall provide for indemnification in excess of that expressly permitted by statute, including, without
limitation, any indemnification provided by the Company's Articles of Incorporation, its Bylaws, vote of its shareholders or disinterested
directors, or applicable law.
(b) Initiation of Proceeding. Notwithstanding anything in this Agreement to the contrary, Indemnitee shall not be entitled
to indemnification pursuant to this Agreement in connection with any Proceeding initiated by Indemnitee against the Company or any
director of the Company unless (i) the Company has joined in or the Board has consented to the initiation of such Proceeding; (ii) the
Proceeding is one to enforce indemnification rights under Section 5; or (iii) the Proceeding is instituted after a Change in Control (other than
a Change in Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control)
and Independent Counsel has approved its initiation.
( c ) Expense Advances. If so requested by Indemnitee, the Company shall advance (within ten business days of such
request) any and all Expenses to Indemnitee (an "Expense Advance"); provided that, if and to the extent that the Reviewing Party determines
that Indemnitee would not be permitted to be so indemnified under applicable law, the Company shall be entitled to be reimbursed by
Indemnitee (who hereby agrees to reimburse the Company) for all such amounts theretofore paid. If Indemnitee has commenced or
commences legal proceedings in a court of competent jurisdiction to secure a determination that Indemnitee should be indemnified under
applicable law, as provided in Section 4, any determination made by the Reviewing Party that Indemnitee would not be permitted to be
indemnified under applicable law shall not be binding and Indemnitee shall not be required to reimburse the Company for any Expense
Advance until a final judicial determination is made with respect thereto (as to which all rights of appeal therefrom have been exhausted or
have lapsed). Indemnitee's obligation to reimburse the Company for Expense Advances shall be unsecured and no interest shall be charged
thereon.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Brian J. Underdown, Ph. D.
May 20, 2013
(d) Mandatory Indemnification. Notwithstanding any other provision of this Agreement, to the extent that Indemnitee has
been successful on the merits in defense of any Proceeding relating in whole or in part to an Indemnifiable Event or in defense of any issue or
matter therein, Indemnitee shall be indemnified against all Expenses incurred in connection therewith.
( e ) Partial Indemnification. If indemnitee is entitled under any provision of this Agreement to indemnification by the
Company for some or a portion of Expenses, but not, however, for the total amount thereof, the Company shall nevertheless indemnify
Indemnitee for the portion thereof to which Indemnitee is entitled.
(f) Prohibited Indemnification. No indemnification pursuant to this Agreement shall be paid by the Company on account
of any Proceeding in which final unappealed judgment beyond the right of appeal is rendered against Indemnitee for an accounting of profits
made from the purchase or sale by Indemnitee of securities of the Company pursuant to the provisions of Section 16(b) of the Securities
Exchange Act of 1934, as amended, or similar provisions of any federal, state, or local laws.
3. Reviewing Party. Prior to any Change in Control, the Reviewing Party shall be any appropriate person or body consisting of a
member or members of the Board or any other person or body appointed by the Board who is not a party to the particular Proceeding with
respect to which Indemnitee is seeking indemnification; after a Change in Control, the Reviewing Party shall be the Independent Counsel
referred to below. With respect to all matters arising after a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) concerning the rights of lndemnitee to indemnity
payments and Expense Advances under this Agreement or any other agreement or under applicable law or the Company's Articles of
Incorporation or Bylaws now or hereafter in effect relating to indemnification for Indemnifiable Events, the Company shall seek legal advice
only from Independent Counsel selected by Indemnitee and approved by the Company (which approval shall not be unreasonably withheld),
and who has not otherwise performed services for the Company or the Indemnitee (other than in connection with indemnification matters)
within the last five years. The Independent Counsel shall not include any person who, under the applicable standards of professional conduct
then prevailing, would have a conflict of interest in representing either the Company or Indemnitee in an action to determine Indemnitee's
rights under this Agreement. Such counsel, among other things, shall render its written opinion to the Company and Indemnitee as to
whether and to what extent the Indemnitee should be permitted to be indemnified under applicable law. The Company agrees to pay the
reasonable fees of the Independent Counsel and to indemnify fully such counsel against any and all expenses (including attorneys' fees),
claims, liabilities, loss, and damages arising out of or relating to this Agreement or the engagement of Independent Counsel pursuant hereto.
4. Indemnification Process and Appeal.
( a ) Indemnification Payment. Indemnitee shall be entitled to indemnification of Expenses, and shall receive payment
thereof, from the Company in accordance with this Agreement as soon as practicable after Indemnitee has made written demand on the
Company for indemnification, unless the Reviewing Party has given a written opinion to the Company that Indemnitee is not entitled to
indemnification under applicable law.
( b ) Suit to Enforce Rights. Regardless of any action by the Reviewing Party, if Indemnitee has not received full
indemnification within thirty days after making a demand in accordance with Section 4(a), Indemnitee shall have the right to enforce its
indemnification rights under this Agreement by commencing litigation in any court in the State of Nevada having subject matter jurisdiction
thereof and in which venue is proper seeking an initial determination by the court or challenging any determination by the Reviewing Party
or any aspect thereof. The Company hereby consents to service of process and to appear in any such proceeding. Any determination by the
Reviewing Party not challenged by the Indemnitee shall be binding on the Company and Indemnitee. The remedy provided for in this
Section 4 shall be in addition to any other remedies available to Indemnitee in law or equity.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Brian J. Underdown, Ph. D.
May 20, 2013
( c ) Defense to Indemnification, Burden of Proof, and Presumptions. It shall be a defense to any action brought by
Indemnitee against the Company to enforce this Agreement (other than an action brought to enforce a claim for Expenses incurred in
defending a Proceeding in advance of its final disposition where the required undertaking has been tendered to the Company) that it is not
permissible under applicable law for the Company to indemnify Indemnitee for the amount claimed. In connection with any such action or
any determination by the Reviewing Party or otherwise as to whether Indemnitee is entitled to be indemnified hereunder, the burden of
proving such a defense or determination shall be on the Company. Neither the failure of the Reviewing Party or the Company (including its
Board, independent legal counsel, or its shareholders) to have made a determination prior to the commencement of such action by
Indemnitee that indemnification of the claimant is proper under the circumstances because he has met the standard of conduct set forth in
applicable law, nor an actual determination by the Reviewing Party or Company (including its Board, independent legal counsel, or its
shareholders) that the Indemnitee had not met such applicable standard of conduct, shall be a defense to the action or create a presumption
that the Indemnitee has not met the applicable standard of conduct. For purposes of this Agreement, the termination of any claim, action,
suit, or proceeding, by judgment, order, settlement (whether with or without court approval), conviction, or upon a plea of nolo contendere,
or its equivalent, shall not create a presumption that Indemnitee did not meet any particular standard of conduct or have any particular belief
or that a court has determined that indemnification is not permitted by applicable law.
5 . Indemnification for Expenses Incurred in Enforcing Rights. The Company shall indemnify Indemnitee against any and all
Expenses that are incurred by Indemnitee in connection with any action brought by Indemnitee for
(i) indemnification of Expenses by the Company under this Agreement or any other agreement or under applicable
law or the Company's Articles of Incorporation or Bylaws now or hereafter in effect relating to indemnification for
Indemnifiable Events; and/or
(ii) recovery under directors' and officers' liability insurance policies maintained by the Company, but only in the
event that Indemnitee ultimately is determined to be entitled to such indemnification or insurance recovery, as the case may
be. In addition, the Company shall, if so requested by Indemnitee, advance the foregoing Expenses to Indemnitee, subject to
and in accordance with Section 2(c).
6. Notification and Defense of Proceeding.
(a) Notice. Promptly after receipt by Indemnitee of notice of the commencement of any Proceeding, Indemnitee will, if a
claim in respect thereof is to be made against the Company under this Agreement, notify the Company of the commencement thereof; but the
omission so to notify the Company will not relieve it from any liability that it may have to Indemnitee, except as provided in Section 6(c).
(b) Defense. With respect to any Proceeding as to which Indemnitee notifies the Company of the commencement thereof,
the Company will be entitled to participate in the Proceeding at its own expense and except as otherwise provided below, to the extent the
Company so wishes, it may assume the defense thereof with counsel reasonably satisfactory to Indemnitee. After notice from the Company
to Indemnitee of its election to assume the defense of any Proceeding, the Company will not be liable to Indemnitee under this Agreement or
otherwise for any Expenses subsequently incurred by Indemnitee in connection with the defense of such Proceeding other than reasonable
costs of investigation or as otherwise provided below. Indemnitee shall have the right to employ his own counsel in such Proceeding, but all
Expenses related thereto incurred after notice from the Company of its assumption of the defense shall be at Indemnitee's expense unless: (i)
the employment of counsel by Indemnitee has been authorized by the Company; (ii) Indemnitee has reasonably determined that there may
be a conflict of interest between Indemnitee and the Company in the defense of the Proceeding, after a Change in Control (other than a
Change in Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control);
(iii) the employment of counsel by Indemnitee has been approved by the Independent Counsel; or (iv) the Company shall not in fact have
employed counsel to assume the defense of such Proceeding, in each of which case all Expenses of the Proceeding shall be borne by the
Company. The Company shall not be entitled to assume the defense of any Proceeding brought by or on behalf of the Company or as to
which Indemnitee shall have made the determination provided for in (ii) above.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Brian J. Underdown, Ph. D.
May 20, 2013
(c) Settlement of Claims. The Company shall not be liable to indemnify Indemnitee under this Agreement or otherwise for
any amounts paid in settlement of any Proceeding effected without the Company's written consent, provided, however, that if a Change in
Control has occured (other than a Change in Control approved by a majority of the directors on the Board who were directors immediately
prior to such Change in Control), the Company shall be liable for indemnification of Indemnitee for amounts paid in settlement if the
Independent Counsel has approved the settlement. The Company shall not settle any Proceeding in any manner that would impose any
penalty or limitation on Indemnitee without Indemnitee's written consent. Neither the Company nor the Indemnitee will unreasonably
withhold their consent to any proposed settlement. The Company shall not be liable to indemnify the Indemnitee under this Agreement with
regard to any judicial award if the Company was not given a reasonable and timely opportunity, at its expense, to participate in the defense
of such action; the Company's liability hereunder shall not be excused if participation in the Proceeding by the Company was barred by this
Agreement.
7 . Establishment of Trust. In the event of a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) the Company shall, upon written request by
Indemnitee, create a Trust for the benefit of the Indemnitee and from time to time upon written request of Indemnitee shall fund the Trust in
an amount sufficient to satisfy any and all Expenses reasonably anticipated at the time of each such request to be incurred in connection with
investigating, preparing for, participating in, and/or defending any Proceeding relating to an Indemnifiable Event. The amount or amounts to
be deposited in the Trust pursuant to the foregoing funding obligation shall be determined by the Reviewing Party. The terms of the Trust
shall provide that: (i) the Trust shall not be revoked or the principal thereof invaded, without the written consent of the Indemnitee; (ii) the
Trustee shall advance, within ten business days of a request by the Indemnitee, any and all Expenses to the Indemnitee (and the Indemnitee
hereby agrees to reimburse the Trust under the same circumstances for which the Indemnitee would be required to reimburse the Company
under Section 2(c) of this Agreement); (iii) the Trust shall continue to be funded by the Company in accordance with the funding obligation
set forth above; (iv) the Trustee shall promptly pay to the Indemnitee all amounts for which the Indemnitee shall be entitled to
indemnification pursuant to this Agreement or otherwise; and (v) all unexpended funds in the Trust shall revert to the Company upon a final
determination by the Reviewing Party or a court of competent jurisdiction, as the case may be, that the Indemnitee has been fully
indemnified under the terms of this Agreement. The Trustee shall be chosen by the Indemnitee. Nothing in this Section 7 shall relieve the
Company of any of its obligations under this Agreement. All income earned on the assets held in the Trust shall be reported as income by the
Company for federal, state, local, and foreign tax purposes. The Company shall pay all costs of establishing and maintaining the Trust and
shall indemnify the Trustee against any and all expenses (including attorneys' fees), claims, liabilities, loss, and damages arising out of or
relating to this Agreement or the establishment and maintenance of the Trust.
8 . Non-Exclusivity. The rights of Indemnitee hereunder shall be in addition to any other rights Indemnitee may have under the
Company's Articles of Incorporation, Bylaws, applicable law, or otherwise. To the extent that a change in applicable law (whether by statute
or judicial decision) permits greater indemnification by agreement than would be afforded currently under the Company's Articles of
Incorporation, Bylaws, applicable law, or this Agreement, it is the intent of the parties that Indemnitee enjoy by this Agreement the greater
benefits so afforded by such change.
9 . Liability Insurance. To the extent the Company maintains an insurance policy or policies providing directors' and officers'
liability insurance, Indemnitee shall be covered by such policy or policies, in accordance with its or their terms, to the maximum extent of the
coverage available for any Company director or officer.
10. Period of Limitations. No legal action shall be brought and no cause of action shall be asserted by or on behalf of the Company
or any affiliate of the Company against Indemnitee, Indemnitee's spouse, heirs, executors, or personal or legal representatives after the
expiration of two (2) years from the date of accrual of such cause of action, or such longer period as may be required by state law under the
circumstances. Any claim or cause of action of the Company or its affiliate shall be extinguished and deemed released unless asserted by the
timely filing of a legal action within such period; provided, however, that if any shorter period of limitations is otherwise applicable to any
such cause of action the shorter period shall govern.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Brian J. Underdown, Ph. D.
May 20, 2013
1 1 . Amendment of this Agreement. No supplement, modification, or amendment of this Agreement shall be binding unless
executed in writing by both of the parties hereto. No waiver of any of the provisions of this Agreement shall be binding unless in the form of
a writing signed by the party against whom enforcement of the waiver is sought, and no such waiver shall operate as a waiver of any other
provisions hereof (whether or not similar), nor shall such waiver constitute a continuing waiver. Except as specifically provided herein, no
failure to exercise or any delay in exercising any right or remedy hereunder shall constitute a waiver thereof.
12. Subrogation. In the event of payment under this Agreement, the Company shall be subrogated to the extent of such payment to
all of the rights of recovery of Indemnitee, who shall execute all papers required and shall do everything that may be necessary to secure
such rights, including the execution of such documents necessary to enable the Company effectively to bring suit to enforce such rights.
13. No Duplication of Payments. The Company shall not be liable under this Agreement to make any payment in connection with
any claim made against Indemnitee to the extent Indemnitee has otherwise received payment (under any insurance policy, Bylaw, or
otherwise) of the amounts otherwise Indemnifiable hereunder.
14. Binding Effect. This Agreement shall be binding upon and inure to the benefit of and be enforceable by the parties hereto and
their respective successors (including any direct or indirect successor by purchase, merger, consolidation, or otherwise to all or substantially
all of the business and/or assets of the Company), assigns, spouses, heirs, and personal and legal representatives. The Company shall require
and cause any successor (whether direct or indirect by purchase, merger, consolidation, or otherwise) to all, substantially all, or a substantial
part, of the business and/or assets of the Company, by written agreement in form and substance satisfactory to Indemnitee, expressly to
assume and agree to perform this Agreement in the same manner and to the same extent that the Company would be required to perform if no
such succession had taken place. The indemnification provided under this Agreement shall continue as to Indemnitee for any action taken or
not taken while serving in an indemnified capacity pertaining to an Indemnifiable Event even though he may have ceased to serve in such
capacity at the time of any Proceeding.
15. Severability. If any provision (or portion thereof) of this Agreement shall be held by a court of competent jurisdiction to be
invalid, void, or otherwise unenforceable, the remaining provisions shall remain enforceable to the fullest extent permitted by law.
Furthermore, to the fullest extent possible, the provisions of this Agreement (including, without limitation, each portion of this Agreement
containing any provision held to be invalid, void, or otherwise unenforceable, that is not itself invalid, void, or unenforceable) shall be
construed so as to give effect to the intent manifested by the provision held invalid, void, or unenforceable.
16. Governing Law. This Agreement shall be governed by and construed and enforced in accordance with the laws of the State of
California applicable to contracts made and to be performed in such State without giving effect to the principles of conflicts of laws.
17. Notices. All notices, demands, and other communications required or permitted hereunder shall be made in writing and shall be
deemed to have been duly given if delivered by hand, against receipt, or mailed, postage prepaid, certified or registered mail, return receipt
requested, and addressed to the Company at:
VistaGen Therapeutics, Inc.
384 Oyster Point Boulevard, No.8
South San Francisco, CA 94080
Attention: President
and to Indemnitee at:
Brian J. Underdown, Ph. D
3-33 Duke Street
Hamilton, ON, Canada
L8P 1X2
Notice of change of address shall be effective only when done in accordance with this Section. All notices complying with this
Section shall be deemed to have been received on the date of delivery or on the third business day after mailing.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Brian J. Underdown, Ph. D.
May 20, 2013
IN WITNESS WHEREOF, the parties hereto have duly executed and delivered this Agreement as of the day specified above.
VISTAGEN THERAPEUTICS, INC.
By: /s/ Shawn Singh
Name: Shawn Singh
Title: Chief Executive Officer
BRIAN J. UNDERDOWN, Ph. D
_________________
Indemnitee
VISTAGEN THERAPEUTICS, INC.
INDEMNIFICATION AGREEMENT
Exhibit 10.88
THIS AGREEMENT is entered into, effective as of May 20, 2013 between VistaGen Therapeutics, Inc., a Nevada corporation (the
"Company"), and Jerrold D. Dotson (“Indemnitee”).
WHEREAS, it is essential to the Company to retain and attract as directors and officers the most capable persons available;
WHEREAS, Indemnitee is an officer of the Company;
WHEREAS, both the Company and Indemnitee recognize the increased risk of litigation and other claims currently being asserted
against directors and officers of corporations; and
WHEREAS, in recognition of lndemnitee's need for substantial protection against personal liability in order to enhance Indemnitee's
continued and effective service to the Company, and in order to induce Indemnitee to provide services to the Company as an officer, the
Company wishes to provide in this Agreement for the indemnification of and the advancing of expenses to Indemnitee to the fullest extent
(whether partial or complete) permitted by law and as set forth in this Agreement, and, to the extent insurance is maintained, for the coverage
of Indemnitee under the Company's directors' and officers' liability insurance policies.
NOW, THEREFORE, in consideration of the above premises and of lndemnitee's continuing to serve the Company directly or, at its
request, with another enterprise, and intending to be legally bound hereby, the parties agree as follows:
1. Certain Definitions:
(a) Board: the Board of Directors of the Company.
(b) Change in Control: shall be deemed to have occurred if (i) any "person" (as such term is used in Sections 13(d) and
14(d) of the Securities Exchange Act of 1934, as amended), other than a trustee or other fiduciary holding securities under an employee
benefit plan of the Company or a corporation owned directly or indirectly by the shareholders of the Company in substantially the same
proportions as their ownership of stock of the Company, is or becomes the "Beneficial Owner" (as defined in Rule 13d-3 under said Act),
directly or indirectly, of securities of the Company representing 20% or more of the total voting power represented by the Company's then
outstanding Voting Securities, or (ii) during any period of two consecutive years, individuals who at the beginning of such period constitute
the Board and any new director whose election by the Board or nomination for election by the Company's shareholders was approved by a
vote of at least two-thirds (2/3) of the directors then still in office who either were directors at the beginning of the period or whose election
or nomination for election was previously so approved, cease for any reason to constitute a majority thereof, or (iii) the shareholders of the
Company approve a merger or consolidation of the Company with any other corporation, other than a merger or consolidation that would
result in the Voting Securities of the Company outstanding immediately prior thereto continuing to represent (either by remaining
outstanding or by being converted into Voting Securities of the surviving entity) at least 80% of the total voting power represented by the
Voting Securities of the Company or such surviving entity outstanding immediately after such merger or consolidation, or the shareholders
of the Company approve a plan of complete liquidation of the Company or an agreement for the sale or disposition by the Company (in one
transaction or a series of transactions) of all or substantially all of the Company's assets.
(c) Expenses: any expense, liability, or loss, including attorneys' fees, judgments, fines, ERISA excise taxes and penalties,
amounts paid or to be paid in settlement, any interest, assessments, or other charges imposed thereon, and any federal, state, local, or foreign
taxes imposed as a result of the actual or deemed receipt of any payments under this Agreement, paid or incurred in connection with
investigating, defending, being a witness in, or participating in (including on appeal), or preparing for any of the foregoing in, any
Proceeding relating to any Indemnifiable Event.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jerrold D. Dotson
May 20, 2013
(d) Indemnifiable Event: any event or occurrence that takes place either prior to or after the execution of this Agreement,
related to the fact that Indemnitee is or was an officer of the Company, or while an officer is or was serving at the request of the Company as
a director, officer, employee, trustee, agent, or fiduciary of another foreign or domestic corporation, partnership, joint venture, employee
benefit plan, trust, or other enterprise, or was a director, officer, employee, or agent of a foreign or domestic corporation that was a
predecessor corporation of the Company or of another enterprise at the request of such predecessor corporation, or related to anything done
or not done by Indemnitee in any such capacity, whether or not the basis of the Proceeding is alleged action in an official capacity as a
director, officer, employee, or agent or in any other capacity while serving as a director, officer, employee, or agent of the Company, as
described above.
(e) Independent Counsel: the person or body appointed in connection with Section 3.
(f) Proceeding: any threatened, pending, or completed action, suit, or proceeding (including an action by or in the right of
the Company), or any inquiry, hearing, or investigation, whether conducted by the Company or any other party, that Indemnitee in good
faith believes might lead to the institution of any such action, suit, or proceeding, whether civil, criminal, administrative, investigative, or
other.
(g) Reviewing Party: the person or body appointed in accordance with Section 3.
(h) Voting Securities: any securities of the Company that vote generally in the election of directors.
2. Agreement to Indemnify.
(a) General Agreement. In the event Indemnitee was, is, or becomes a party to or witness or other participant in, or is
threatened to be made a party to or witness or other participant in, a Proceeding by reason of (or arising in part out of) an Indemnifiable
Event, the Company shall indemnify Indemnitee from and against any and all Expenses to the fullest extent permitted by law, as the same
exists or may hereafter be amended or interpreted (but in the case of any such amendment or interpretation, only to the extent that such
amendment or interpretation permits the Company to provide broader indemnification rights than were permitted prior thereto). The parties
hereto intend that this Agreement shall provide for indemnification in excess of that expressly permitted by statute, including, without
limitation, any indemnification provided by the Company's Articles of Incorporation, its Bylaws, vote of its shareholders or disinterested
directors, or applicable law.
(b) Initiation of Proceeding. Notwithstanding anything in this Agreement to the contrary, Indemnitee shall not be entitled
to indemnification pursuant to this Agreement in connection with any Proceeding initiated by Indemnitee against the Company or any
director of the Company unless (i) the Company has joined in or the Board has consented to the initiation of such Proceeding; (ii) the
Proceeding is one to enforce indemnification rights under Section 5; or (iii) the Proceeding is instituted after a Change in Control (other than
a Change in Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control)
and Independent Counsel has approved its initiation.
( c ) Expense Advances. If so requested by Indemnitee, the Company shall advance (within ten business days of such
request) any and all Expenses to Indemnitee (an "Expense Advance"); provided that, if and to the extent that the Reviewing Party determines
that Indemnitee would not be permitted to be so indemnified under applicable law, the Company shall be entitled to be reimbursed by
Indemnitee (who hereby agrees to reimburse the Company) for all such amounts theretofore paid. If Indemnitee has commenced or
commences legal proceedings in a court of competent jurisdiction to secure a determination that Indemnitee should be indemnified under
applicable law, as provided in Section 4, any determination made by the Reviewing Party that Indemnitee would not be permitted to be
indemnified under applicable law shall not be binding and Indemnitee shall not be required to reimburse the Company for any Expense
Advance until a final judicial determination is made with respect thereto (as to which all rights of appeal therefrom have been exhausted or
have lapsed). Indemnitee's obligation to reimburse the Company for Expense Advances shall be unsecured and no interest shall be charged
thereon.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jerrold D. Dotson
May 20, 2013
(d) Mandatory Indemnification. Notwithstanding any other provision of this Agreement, to the extent that Indemnitee has
been successful on the merits in defense of any Proceeding relating in whole or in part to an Indemnifiable Event or in defense of any issue or
matter therein, Indemnitee shall be indemnified against all Expenses incurred in connection therewith.
( e ) Partial Indemnification. If indemnitee is entitled under any provision of this Agreement to indemnification by the
Company for some or a portion of Expenses, but not, however, for the total amount thereof, the Company shall nevertheless indemnify
Indemnitee for the portion thereof to which Indemnitee is entitled.
(f) Prohibited Indemnification. No indemnification pursuant to this Agreement shall be paid by the Company on account
of any Proceeding in which final unappealed judgment beyond the right of appeal is rendered against Indemnitee for an accounting of profits
made from the purchase or sale by Indemnitee of securities of the Company pursuant to the provisions of Section 16(b) of the Securities
Exchange Act of 1934, as amended, or similar provisions of any federal, state, or local laws.
3. Reviewing Party. Prior to any Change in Control, the Reviewing Party shall be any appropriate person or body consisting of a
member or members of the Board or any other person or body appointed by the Board who is not a party to the particular Proceeding with
respect to which Indemnitee is seeking indemnification; after a Change in Control, the Reviewing Party shall be the Independent Counsel
referred to below. With respect to all matters arising after a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) concerning the rights of lndemnitee to indemnity
payments and Expense Advances under this Agreement or any other agreement or under applicable law or the Company's Articles of
Incorporation or Bylaws now or hereafter in effect relating to indemnification for Indemnifiable Events, the Company shall seek legal advice
only from Independent Counsel selected by Indemnitee and approved by the Company (which approval shall not be unreasonably withheld),
and who has not otherwise performed services for the Company or the Indemnitee (other than in connection with indemnification matters)
within the last five years. The Independent Counsel shall not include any person who, under the applicable standards of professional conduct
then prevailing, would have a conflict of interest in representing either the Company or Indemnitee in an action to determine Indemnitee's
rights under this Agreement. Such counsel, among other things, shall render its written opinion to the Company and Indemnitee as to
whether and to what extent the Indemnitee should be permitted to be indemnified under applicable law. The Company agrees to pay the
reasonable fees of the Independent Counsel and to indemnify fully such counsel against any and all expenses (including attorneys' fees),
claims, liabilities, loss, and damages arising out of or relating to this Agreement or the engagement of Independent Counsel pursuant hereto.
4. Indemnification Process and Appeal.
( a ) Indemnification Payment. Indemnitee shall be entitled to indemnification of Expenses, and shall receive payment
thereof, from the Company in accordance with this Agreement as soon as practicable after Indemnitee has made written demand on the
Company for indemnification, unless the Reviewing Party has given a written opinion to the Company that Indemnitee is not entitled to
indemnification under applicable law.
( b ) Suit to Enforce Rights. Regardless of any action by the Reviewing Party, if Indemnitee has not received full
indemnification within thirty days after making a demand in accordance with Section 4(a), Indemnitee shall have the right to enforce its
indemnification rights under this Agreement by commencing litigation in any court in the State of Nevada having subject matter jurisdiction
thereof and in which venue is proper seeking an initial determination by the court or challenging any determination by the Reviewing Party
or any aspect thereof. The Company hereby consents to service of process and to appear in any such proceeding. Any determination by the
Reviewing Party not challenged by the Indemnitee shall be binding on the Company and Indemnitee. The remedy provided for in this
Section 4 shall be in addition to any other remedies available to Indemnitee in law or equity.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jerrold D. Dotson
May 20, 2013
( c ) Defense to Indemnification, Burden of Proof, and Presumptions. It shall be a defense to any action brought by
Indemnitee against the Company to enforce this Agreement (other than an action brought to enforce a claim for Expenses incurred in
defending a Proceeding in advance of its final disposition where the required undertaking has been tendered to the Company) that it is not
permissible under applicable law for the Company to indemnify Indemnitee for the amount claimed. In connection with any such action or
any determination by the Reviewing Party or otherwise as to whether Indemnitee is entitled to be indemnified hereunder, the burden of
proving such a defense or determination shall be on the Company. Neither the failure of the Reviewing Party or the Company (including its
Board, independent legal counsel, or its shareholders) to have made a determination prior to the commencement of such action by
Indemnitee that indemnification of the claimant is proper under the circumstances because he has met the standard of conduct set forth in
applicable law, nor an actual determination by the Reviewing Party or Company (including its Board, independent legal counsel, or its
shareholders) that the Indemnitee had not met such applicable standard of conduct, shall be a defense to the action or create a presumption
that the Indemnitee has not met the applicable standard of conduct. For purposes of this Agreement, the termination of any claim, action,
suit, or proceeding, by judgment, order, settlement (whether with or without court approval), conviction, or upon a plea of nolo contendere,
or its equivalent, shall not create a presumption that Indemnitee did not meet any particular standard of conduct or have any particular belief
or that a court has determined that indemnification is not permitted by applicable law.
5 . Indemnification for Expenses Incurred in Enforcing Rights. The Company shall indemnify Indemnitee against any and all
Expenses that are incurred by Indemnitee in connection with any action brought by Indemnitee for
(i) indemnification of Expenses by the Company under this Agreement or any other agreement or under applicable
law or the Company's Articles of Incorporation or Bylaws now or hereafter in effect relating to indemnification for
Indemnifiable Events; and/or
(ii) recovery under directors' and officers' liability insurance policies maintained by the Company, but only in the
event that Indemnitee ultimately is determined to be entitled to such indemnification or insurance recovery, as the case may
be. In addition, the Company shall, if so requested by Indemnitee, advance the foregoing Expenses to Indemnitee, subject to
and in accordance with Section 2(c).
6. Notification and Defense of Proceeding.
(a) Notice. Promptly after receipt by Indemnitee of notice of the commencement of any Proceeding, Indemnitee will, if a
claim in respect thereof is to be made against the Company under this Agreement, notify the Company of the commencement thereof; but the
omission so to notify the Company will not relieve it from any liability that it may have to Indemnitee, except as provided in Section 6(c).
(b) Defense. With respect to any Proceeding as to which Indemnitee notifies the Company of the commencement thereof,
the Company will be entitled to participate in the Proceeding at its own expense and except as otherwise provided below, to the extent the
Company so wishes, it may assume the defense thereof with counsel reasonably satisfactory to Indemnitee. After notice from the Company
to Indemnitee of its election to assume the defense of any Proceeding, the Company will not be liable to Indemnitee under this Agreement or
otherwise for any Expenses subsequently incurred by Indemnitee in connection with the defense of such Proceeding other than reasonable
costs of investigation or as otherwise provided below. Indemnitee shall have the right to employ his own counsel in such Proceeding, but all
Expenses related thereto incurred after notice from the Company of its assumption of the defense shall be at Indemnitee's expense unless: (i)
the employment of counsel by Indemnitee has been authorized by the Company; (ii) Indemnitee has reasonably determined that there may
be a conflict of interest between Indemnitee and the Company in the defense of the Proceeding, after a Change in Control (other than a
Change in Control approved by a majority of the directors on the Board who were directors immediately prior to such Change in Control);
(iii) the employment of counsel by Indemnitee has been approved by the Independent Counsel; or (iv) the Company shall not in fact have
employed counsel to assume the defense of such Proceeding, in each of which case all Expenses of the Proceeding shall be borne by the
Company. The Company shall not be entitled to assume the defense of any Proceeding brought by or on behalf of the Company or as to
which Indemnitee shall have made the determination provided for in (ii) above.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jerrold D. Dotson
May 20, 2013
(c) Settlement of Claims. The Company shall not be liable to indemnify Indemnitee under this Agreement or otherwise for
any amounts paid in settlement of any Proceeding effected without the Company's written consent, provided, however, that if a Change in
Control has occured (other than a Change in Control approved by a majority of the directors on the Board who were directors immediately
prior to such Change in Control), the Company shall be liable for indemnification of Indemnitee for amounts paid in settlement if the
Independent Counsel has approved the settlement. The Company shall not settle any Proceeding in any manner that would impose any
penalty or limitation on Indemnitee without Indemnitee's written consent. Neither the Company nor the Indemnitee will unreasonably
withhold their consent to any proposed settlement. The Company shall not be liable to indemnify the Indemnitee under this Agreement with
regard to any judicial award if the Company was not given a reasonable and timely opportunity, at its expense, to participate in the defense
of such action; the Company's liability hereunder shall not be excused if participation in the Proceeding by the Company was barred by this
Agreement.
7 . Establishment of Trust. In the event of a Change in Control (other than a Change in Control approved by a majority of the
directors on the Board who were directors immediately prior to such Change in Control) the Company shall, upon written request by
Indemnitee, create a Trust for the benefit of the Indemnitee and from time to time upon written request of Indemnitee shall fund the Trust in
an amount sufficient to satisfy any and all Expenses reasonably anticipated at the time of each such request to be incurred in connection with
investigating, preparing for, participating in, and/or defending any Proceeding relating to an Indemnifiable Event. The amount or amounts to
be deposited in the Trust pursuant to the foregoing funding obligation shall be determined by the Reviewing Party. The terms of the Trust
shall provide that: (i) the Trust shall not be revoked or the principal thereof invaded, without the written consent of the Indemnitee; (ii) the
Trustee shall advance, within ten business days of a request by the Indemnitee, any and all Expenses to the Indemnitee (and the Indemnitee
hereby agrees to reimburse the Trust under the same circumstances for which the Indemnitee would be required to reimburse the Company
under Section 2(c) of this Agreement); (iii) the Trust shall continue to be funded by the Company in accordance with the funding obligation
set forth above; (iv) the Trustee shall promptly pay to the Indemnitee all amounts for which the Indemnitee shall be entitled to
indemnification pursuant to this Agreement or otherwise; and (v) all unexpended funds in the Trust shall revert to the Company upon a final
determination by the Reviewing Party or a court of competent jurisdiction, as the case may be, that the Indemnitee has been fully
indemnified under the terms of this Agreement. The Trustee shall be chosen by the Indemnitee. Nothing in this Section 7 shall relieve the
Company of any of its obligations under this Agreement. All income earned on the assets held in the Trust shall be reported as income by the
Company for federal, state, local, and foreign tax purposes. The Company shall pay all costs of establishing and maintaining the Trust and
shall indemnify the Trustee against any and all expenses (including attorneys' fees), claims, liabilities, loss, and damages arising out of or
relating to this Agreement or the establishment and maintenance of the Trust.
8 . Non-Exclusivity. The rights of Indemnitee hereunder shall be in addition to any other rights Indemnitee may have under the
Company's Articles of Incorporation, Bylaws, applicable law, or otherwise. To the extent that a change in applicable law (whether by statute
or judicial decision) permits greater indemnification by agreement than would be afforded currently under the Company's Articles of
Incorporation, Bylaws, applicable law, or this Agreement, it is the intent of the parties that Indemnitee enjoy by this Agreement the greater
benefits so afforded by such change.
9 . Liability Insurance. To the extent the Company maintains an insurance policy or policies providing directors' and officers'
liability insurance, Indemnitee shall be covered by such policy or policies, in accordance with its or their terms, to the maximum extent of the
coverage available for any Company director or officer.
10. Period of Limitations. No legal action shall be brought and no cause of action shall be asserted by or on behalf of the Company
or any affiliate of the Company against Indemnitee, Indemnitee's spouse, heirs, executors, or personal or legal representatives after the
expiration of two (2) years from the date of accrual of such cause of action, or such longer period as may be required by state law under the
circumstances. Any claim or cause of action of the Company or its affiliate shall be extinguished and deemed released unless asserted by the
timely filing of a legal action within such period; provided, however, that if any shorter period of limitations is otherwise applicable to any
such cause of action the shorter period shall govern.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jerrold D. Dotson
May 20, 2013
1 1 . Amendment of this Agreement. No supplement, modification, or amendment of this Agreement shall be binding unless
executed in writing by both of the parties hereto. No waiver of any of the provisions of this Agreement shall be binding unless in the form of
a writing signed by the party against whom enforcement of the waiver is sought, and no such waiver shall operate as a waiver of any other
provisions hereof (whether or not similar), nor shall such waiver constitute a continuing waiver. Except as specifically provided herein, no
failure to exercise or any delay in exercising any right or remedy hereunder shall constitute a waiver thereof.
12. Subrogation. In the event of payment under this Agreement, the Company shall be subrogated to the extent of such payment to
all of the rights of recovery of Indemnitee, who shall execute all papers required and shall do everything that may be necessary to secure
such rights, including the execution of such documents necessary to enable the Company effectively to bring suit to enforce such rights.
13. No Duplication of Payments. The Company shall not be liable under this Agreement to make any payment in connection with
any claim made against Indemnitee to the extent Indemnitee has otherwise received payment (under any insurance policy, Bylaw, or
otherwise) of the amounts otherwise Indemnifiable hereunder.
14. Binding Effect. This Agreement shall be binding upon and inure to the benefit of and be enforceable by the parties hereto and
their respective successors (including any direct or indirect successor by purchase, merger, consolidation, or otherwise to all or substantially
all of the business and/or assets of the Company), assigns, spouses, heirs, and personal and legal representatives. The Company shall require
and cause any successor (whether direct or indirect by purchase, merger, consolidation, or otherwise) to all, substantially all, or a substantial
part, of the business and/or assets of the Company, by written agreement in form and substance satisfactory to Indemnitee, expressly to
assume and agree to perform this Agreement in the same manner and to the same extent that the Company would be required to perform if no
such succession had taken place. The indemnification provided under this Agreement shall continue as to Indemnitee for any action taken or
not taken while serving in an indemnified capacity pertaining to an Indemnifiable Event even though he may have ceased to serve in such
capacity at the time of any Proceeding.
15. Severability. If any provision (or portion thereof) of this Agreement shall be held by a court of competent jurisdiction to be
invalid, void, or otherwise unenforceable, the remaining provisions shall remain enforceable to the fullest extent permitted by law.
Furthermore, to the fullest extent possible, the provisions of this Agreement (including, without limitation, each portion of this Agreement
containing any provision held to be invalid, void, or otherwise unenforceable, that is not itself invalid, void, or unenforceable) shall be
construed so as to give effect to the intent manifested by the provision held invalid, void, or unenforceable.
16. Governing Law. This Agreement shall be governed by and construed and enforced in accordance with the laws of the State of
California applicable to contracts made and to be performed in such State without giving effect to the principles of conflicts of laws.
17. Notices. All notices, demands, and other communications required or permitted hereunder shall be made in writing and shall be
deemed to have been duly given if delivered by hand, against receipt, or mailed, postage prepaid, certified or registered mail, return receipt
requested, and addressed to the Company at:
VistaGen Therapeutics, Inc.
384 Oyster Point Boulevard, No.8
South San Francisco, CA 94080
Attention: President
and to Indemnitee at:
Jerrold D. Dotson
3030 Oberon Drive
Walnut Creek, CA 94597
Notice of change of address shall be effective only when done in accordance with this Section. All notices complying with this
Section shall be deemed to have been received on the date of delivery or on the third business day after mailing.
VistaGen Therapeutics, Inc., a Nevada corporation
Indemnification Agreement with Jerrold D. Dotson
May 20, 2013
IN WITNESS WHEREOF, the parties hereto have duly executed and delivered this Agreement as of the day specified above.
VISTAGEN THERAPEUTICS, INC.
By: /s/ Shawn K. Singh
Name: Shawn K. Singh
Title: Chief Executive Officer
JERROLD D. DOTSON
/s/ Jerrold D. Dotson
Indemnitee
EXHIBIT 31.1
I, Shawn K. Singh, certify that;
CERTIFICATION
1. I have reviewed this Annual Report on Form 10-K of VistaGen Therapeutics, Inc., a Nevada corporation;
2. Based on my knowledge, this report, does not contain any untrue statement of a material fact or omit to state a material fact necessary
to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period
covered by the report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material
respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4. The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures
(as defined in Exchange Act Rules 13a-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and
15d-15(f)) for the registrant and have:
a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our
supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others
within those entities, particularly during the period in which this report is being prepared;
b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed
under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial
statements for external purposes in accordance with generally accepted accounting principles;
c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions
about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation;
and
d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the
registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is
reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial
reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent
functions):
a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which
are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s
internal control over financial reporting.
July 18, 2013
/s/ Shawn K. Singh
Shawn K. Singh, JD
Principal Executive Officer
EXHIBIT 31.2
I, Jerrold D. Dotson, certify that:
CERTIFICATION
1. I have reviewed this Annual Report on Form 10-K of VistaGen Therapeutics, Inc., a Nevada corporation;
2. Based on my knowledge, this report, does not contain any untrue statement of a material fact or omit to state a material fact necessary
to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period
covered by the report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material
respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4. The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures
(as defined in Exchange Act Rules 13a-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and
15d-15(f)) for the registrant and have:
a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our
supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others
within those entities, particularly during the period in which this report is being prepared;
b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed
under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial
statements for external purposes in accordance with generally accepted accounting principles;
c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions
about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation;
and
d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the
registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is
reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial
reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent
functions):
a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which
are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s
internal control over financial reporting.
July 18, 2013
/s/ Jerrold D. Dotson
Jerrold D. Dotson
Principal Financial Officer
CERTIFICATION PURSUANT TO 18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
EXHIBIT 32
Pursuant to 18 U.S.C. § 1350, as created by Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned officer of VistaGen
Therapeutics, Inc. (the “ Company ”) hereby certifies, to such officer’s knowledge, that:
(i) the accompanying Annual Report on Form 10-K of the Company for the annual period ended March 31, 2013 (the “ Report ”)
fully complies with the requirements of Section 13(a) or Section 15(d), as applicable, of the Securities Exchange Act of 1934, as amended; and
(ii) the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of
the Company.
July 18, 2013
/s/ Shawn K. Singh
Shawn K. Singh, JD
Principal Executive Officer
/s/ Jerrold D. Dotson
Jerrold D. Dotson
Principal Financial Officer