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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 10-K
(Mark One)
☒ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the Fiscal Year Ended December 31, 2020
OR
☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
Corvus Pharmaceuticals, Inc.
(Exact name of registrant as specified in its charter)
Delaware
(State or other jurisdiction
of incorporation)
001-37719
(Commission
File Number)
46-4670809
(IRS Employer
Identification Number)
863 Mitten Road, Suite 102, Burlingame, CA 94010
(Address of principal executive offices, including Zip Code)
Registrant’s telephone number, including area code: (650) 900-4520
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Common Stock, Par Value $0.0001 per share
Trading symbol(s)
CRVS
Name of each exchange on which registered
Nasdaq Global Market
Securities registered pursuant to Section 12(g) of the Act: None
Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes ☐ No ⌧
Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. Yes ☐ No ⌧
Indicate by check mark whether the issuer (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
⌧ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted 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 ⌧ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging
growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the
Exchange Act.
Large accelerated filer ☐
Non-accelerated filer ☒
Accelerated filer ☐
Smaller reporting company ☒
Emerging growth company ☒
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised
financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☒
Indicate by check mark whether the registrant has filed a report on and attestation to its management’s assessment of the effectiveness of its internal control over
financial reporting under Section 404(b) of the Sarbanes-Oxley Act (15 U.S.C. 7262(b)) by the registered public accounting firm that prepared or issued its audit report. ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒
As of June 30, 2020, the aggregate market value of Common Stock held by non-affiliates of the registrant was approximately $43.8 million, computed by reference to
the closing price as reported on The Nasdaq Stock Market. As of March 25, 2021, 38,309,551 shares of the registrant’s common stock were outstanding.
Portions of the registrant’s definitive proxy statement to be filed for its 2021 Annual Meeting of Stockholders are incorporated by reference into Part III hereof. Such
proxy statement will be filed with the Securities and Exchange Commission within 120 days of the end of the fiscal year covered by this Annual Report on Form 10-K.
DOCUMENTS INCORPORATED BY REFERENCE
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CORVUS PHARMACEUTICALS, INC.
ANNUAL REPORT ON FORM 10-K
TABLE OF CONTENTS
Business
PART I
ITEM 1.
ITEM 1A. Risk Factors
ITEM 1B. Unresolved Staff Comments
ITEM 2.
ITEM 3.
ITEM 4. Mine Safety Disclosures
PART II
ITEM 5. Market for Registrant’s Common Equity, Related Stockholder Matters, and Issuer Purchases of Equity
Properties
Legal Proceedings
Securities
Selected Financial Data
ITEM 6.
ITEM 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations
ITEM 7A. Quantitative and Qualitative Disclosures About Market Risk
Financial Statements and Supplementary Data
ITEM 8.
ITEM 9.
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
ITEM 9A. Controls and Procedures
ITEM 9B. Other Information
PART III
ITEM 10. Directors, Executive Officers of the Registrant and Corporate Governance Matters
ITEM 11. Executive Compensation
ITEM 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters
ITEM 13. Certain Relationships and Related Transactions, and Director Independence
ITEM 14. Principal Accounting Fees and Services
PART IV
ITEM 15. Exhibits and Financial Statement Schedules
ITEM 16. Form 10-K Summary
Signatures
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Forward-Looking Statements
This Annual Report on Form 10-K contains forward-looking statements that involve risks and uncertainties. All
statements other than statements of historical facts contained in this report are forward-looking statements. In some cases,
you can identify forward-looking statements by terminology such as “may,” “could,” “will,” “would,” “should,” “expect,”
“plan,” “anticipate,” “believe,” “estimate,” “intend,” “predict,” “seek,” “contemplate,” “potential” or “continue” or the
negative of these terms or other comparable terminology. These forward-looking statements include, but are not limited to,
statements about:
● The extent to which the COVID-19 coronavirus (“COVID-19”) and related governmental regulations and
restrictions may impact our business, including our research, clinical trials, manufacturing and financial
condition;
● our expectations and beliefs regarding the potential benefits of our product candidates;
● our expectations regarding the clinical effectiveness of our product candidates and utility of our biomarker
data;
● the anticipated timing, costs and conduct of our ongoing and planned clinical trials for CPI-006, CPI-818 and
ciforadenant (formerly CPI-444), and planned preclinical studies and clinical trials for other product
candidates in our development programs;
● our ability to develop, acquire and advance product candidates into, and successfully complete, clinical trials;
● the timing of the completion of our ongoing clinical trials of CPI-006, CPI-818 and ciforadenant and the
timing and availability of clinical data from such clinical trials;
● clinical and regulatory development plans with respect to CPI-006, CPI-818 and ciforadenant and our other
product candidates;
● our expectations regarding the potential market size and the size of the patient populations for CPI-006, CPI-
818 and ciforadenant and our other product candidates, if approved for commercial use;
● our ability to commercialize CPI-006 and our other product candidates, if approved;
● our commercialization, marketing and manufacturing capabilities and strategy;
● the pricing and reimbursement of our product candidates, if approved;
● the scope of protection we are able to establish and maintain for intellectual property rights covering our
product candidates, including the projected terms of patent protection;
● our or any existing or future collaborator’s ability to obtain and maintain intellectual property protection for
our technologies and product candidates and our ability to operate our business without infringing the
intellectual property rights of others;
● our ability to establish and maintain collaborations and retain commercial rights for our product candidates in
such collaborations;
● the potential benefits of strategic collaborations, including our collaboration with Angel Pharmaceuticals, and
our ability to enter into strategic arrangements;
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● developments and projections relating to our competitors and our industry, including competing therapies;
● our estimates regarding the effect of changes in the tax code as a result of recent federal tax legislation and
uncertainty as to how some of those changes may be applied;
● our estimates regarding expenses, future revenue, capital requirements and needs for additional financing;
and
● our financial performance.
Any forward-looking statements in this Annual Report on Form 10-K reflect our current views with respect to
future events or to our future financial performance and involve known and unknown risks, uncertainties and other factors
that may cause our actual results, performance or achievements to be materially different from any future results,
performance or achievements expressed or implied by these forward-looking statements. Factors that may cause actual
results to differ materially from current expectations include, among other things, those listed under Part I, Item 1A. Risk
Factors and discussed elsewhere in this Annual Report on Form 10-K. Given these uncertainties, you should not place
undue reliance on these forward-looking statements. Except as required by law, we assume no obligation to update or
revise these forward-looking statements for any reason, even if new information becomes available in the future.
This Annual Report on Form 10-K also contains estimates, projections and other information concerning our
industry, our business and the markets for certain drugs, including data regarding the estimated size of those markets, their
projected growth rates and the incidence of certain medical conditions. Information that is based on estimates, forecasts,
projections or similar methodologies is inherently subject to uncertainties, and actual events or circumstances may differ
materially from events and circumstances reflected in this information. Unless otherwise expressly stated, we obtained this
industry, business, market and other data from reports, research surveys, studies and similar data prepared by third parties,
industry, medical and general publications, government data and similar sources. In some cases, we do not expressly refer
to the sources from which this data is derived. In that regard, when we refer to one or more sources of this type of data in
any paragraph, you should assume that other data of this type appearing in the same paragraph is derived from the same
sources, unless otherwise expressly stated or the context otherwise requires.
Except where the context otherwise requires, in this Annual Report on Form 10-K, “we,” “us,” “our” and the
“Company” refer to Corvus Pharmaceuticals, Inc.
Trademarks
This Annual Report on Form 10-K includes trademarks, service marks and trade names owned by us or other
companies. All trademarks, service marks and trade names included in this Annual Report on Form 10-K are the property
of their respective owners.
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Risk Factor Summary
Below is a summary of the principal factors that make an investment in our common stock speculative or risky. This
summary does not address all of the risks that we face. Additional discussion of the risks summarized in this risk factor
summary, and other risks that we face, can be found below under the heading “Risk Factors” and should be carefully
considered, together with other information in this Annual Report on Form 10-K and our other filings with the Securities
and Exchange Commission (SEC) before making investment decisions regarding our common stock.
● We have a limited operating history, have incurred significant operating losses since our inception and expect to
incur significant losses for the foreseeable future. We may never generate any revenue or become profitable or, if
we achieve profitability, we may not be able to sustain it.
● We will require substantial additional financing to achieve our goals, and a failure to obtain this necessary capital
when needed on acceptable terms, or at all, could force us to delay, limit, reduce or terminate our product
development, other operations or commercialization efforts.
● The COVID-19 pandemic could adversely impact our business, including our clinical trials, and financial
condition.
● Our product candidates are in various stages of development and may fail or suffer delays that materially and
adversely affect their commercial viability. If we are unable to advance our product candidates through clinical
development, obtain regulatory approval and ultimately commercialize such product candidates, or experience
significant delays in doing so, our business will be materially harmed.
● Clinical drug development involves a lengthy and expensive process with an uncertain outcome, and the results of
preclinical studies and early clinical trials are not necessarily predictive of future results. Any product candidate
we or any of our existing or potential future collaborators advance into clinical trials, including CPI-006, CPI-818
and ciforadenant, may not have favorable results in later clinical trials, if any, or receive regulatory approval.
● Any termination or suspension of, or delays in the commencement or completion of, our planned clinical trials
could result in increased costs to us, delay or limit our ability to generate revenue and adversely affect our
commercial prospects.
● Our product candidates are subject to extensive regulation, compliance with which is costly and time consuming,
and such regulation may cause unanticipated delays or prevent the receipt of the required approvals to
commercialize our product candidates.
● We are conducting clinical trials for CPI-006, CPI-818 and ciforadenant, and we and Angel Pharmaceuticals may
in the future, conduct additional clinical trials of product candidates, at sites outside the United States, and the
FDA may not accept data from trials conducted in foreign locations.
● If we encounter difficulties enrolling subjects in our clinical trials, our clinical development activities could be
delayed or otherwise adversely affected.
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● The occurrence of serious complications or side effects in connection with use of our product candidates, either in
clinical trials or post-approval, could lead to discontinuation of our clinical development programs, refusal of
regulatory authorities to approve our product candidates or, post-approval, revocation of marketing authorizations
or refusal to approve new indications, which could severely harm our business, prospects, operating results and
financial condition.
● We may not be successful in our efforts to identify or discover additional product candidates.
● We rely, and expect to continue to rely, on third parties to conduct our clinical trials. If these third parties do not
meet our deadlines or otherwise conduct the trials as required, our clinical development programs could be
delayed or unsuccessful and we may not be able to obtain regulatory approval for or commercialize our product
candidates when expected, or at all.
● We rely on third parties to conduct some or all aspects of our manufacturing, research and preclinical and clinical
testing, and these third parties may not perform satisfactorily.
● We, or our third-party manufacturers, may be unable to successfully scale-up manufacturing of our product
candidates in sufficient quality and quantity, which would delay or prevent us from developing our product
candidates and commercializing approved products, if any.
● If we are unable to commercialize our product candidates or if we experience significant delays in obtaining
regulatory approval for, or commercializing, any or all of our product candidates, our business will be materially
and adversely affected.
● If we do not achieve our projected development goals in the time frames we announce and expect, the
commercialization of our products may be delayed and, as a result, our stock price may decline.
● We face competition from entities that have developed or may develop product candidates for cancer, including
companies developing novel treatments and technology platforms. If these companies develop technologies or
product candidates more rapidly than we do or their technologies are more effective, our ability to develop and
successfully commercialize product candidates may be adversely affected.
● An active, liquid and orderly market for our common stock may not be sustained.
● The trading price of the shares of our common stock could be highly volatile, and investors in our common stock
could incur substantial losses.
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Item 1. Business
Overview
Part I
We are a clinical stage, immunology focused biopharmaceutical company developing drugs and antibodies that
target the most critical cellular elements of the immune system. Our strategy is to focus our efforts on the development of
immune modulator product candidates to treat COVID-19, T-cell lymphomas, other cancers and autoimmune diseases. We
have built a pipeline of five programs, three of which are in clinical development.
Our lead product candidate is CPI-006, a potent humanized monoclonal antibody that is designed to react with a
specific site on CD73. In both preclinical and in vivo studies in cancer patients and patients with COVID-19, CPI-006 has
demonstrated binding to various immune cells and the inducement of a humoral adaptive immune response. We believe
CPI-006 has the potential to be an important new therapeutic agent with a novel mechanism of action for the treatment of a
broad range of infectious diseases and cancers.
We are evaluating CPI-006 in a global, randomized, double-blind, Phase 3 trial designed to evaluate the efficacy
and safety of CPI-006 compared to placebo in hospitalized patients with mild-to-moderate COVID-19. The primary
endpoint of the trial is the proportion of patients progressing to respiratory failure or death during the 28 days after dosing.
The trial was designed based on feedback received from the U.S. Food and Drug Administration, or FDA.
Our next product candidate, CPI-818, is a selective, covalent inhibitor of ITK and is in a multi-center Phase 1/1b
clinical trial in patients with various malignant T-cell lymphomas. CPI-818 is designed to inhibit the proliferation of certain
malignant T-cells, and we believe it also has the potential to regulate the growth of abnormal T cells involved in
autoimmunity.
Our third product candidate, ciforadenant (formerly CPI-444), is an oral, small molecule antagonist of the A2A
receptor for adenosine with which we completed a Phase 2 expansion protocol in combination with Genentech, Inc.’s
cancer immunotherapy, Tecentriq® (atezolizumab) for patients with either advanced or refractory renal cell cancer
(“RCC”). We have identified a novel biomarker that may enable us to select patients that we believe will be most likely to
benefit from ciforadenant. In studies presented at the American Society of Oncology (“ASCO”) meeting in June 2020,
patients expressing this marker in their tumor had a 17% response rate. Activity was seen with both CPI-444 as a
monotherapy and in combination with Tecentriq. We have refined our strategy with ciforadenant and plan to collaborate
with an academic consortium to evaluate ciforadenant in a front line RCC Phase 2 trial as a triplet combination with
pembrolizumab and a tyrosine kinase inhibitor (“TKI”).
Our product candidates are designed to exhibit a high degree of specificity, which we believe has the potential to
provide greater safety compared to other cancer therapies and may facilitate their development either as monotherapies or
in combination with other cancer therapies such as immune checkpoint inhibitors or chemotherapy.
We believe the breadth and status of our pipeline demonstrates our management team’s expertise in understanding
and developing immunology focused assets as well as in identifying product candidates that can be in-licensed and further
developed internally to treat many types of cancer. We hold worldwide rights to all of our product candidates (other than in
greater China).
In October 2020, we announced the formation and launch of Angel Pharmaceuticals Co., Ltd. (“Angel
Pharmaceuticals”), a new China based biopharmaceutical company with a mission to bring innovative quality medicines to
Chinese patients for treatment of serious diseases including cancer, autoimmune diseases and infectious diseases. We
formed Angel Pharmaceuticals as a wholly owned subsidiary and it launched with a post-money valuation of
approximately $106.0 million, based on an approximate $41.0 million cash investment from a Chinese investor group that
includes funds associated with Tigermed and Betta Pharmaceuticals, Hisun Pharmaceuticals and Zhejiang Puissance
Capital. Such cash is not available for our use. Contemporaneously with the financing, Angel Pharmaceuticals licensed the
rights to develop and commercialize our three clinical-stage candidates – CPI-006, CPI-818 and ciforadenant – in greater
China and obtained global rights to our BTK inhibitor preclinical programs. Under the collaboration, we
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currently have a 49.7% equity interest in Angel Pharmaceuticals, excluding 7% of Angel’s equity reserved for issuance
under the Employee Stock Ownership Plan (“ESOP”), and are entitled to designate three individuals on Angel’s five-
person Board of Directors.
Product Pipeline
Our product candidate pipeline includes the following:
CPI-006, B-Cell Activating anti-CD73 antibody. CPI-006 is an investigational, humanized, engineered anti
CD73 monoclonal antibody that is designed to activate various immune cells including B cells, which are the cells
responsible for antibody production. CPI-006 is also designed to inhibit the production of adenosine by blocking catalytic
conversion of adenosine monophosphate to adenosine. We in-licensed this antibody from Scripps in December 2014. We
have modified CPI-006 to potentially improve binding to CD73 and increase its inhibition of catalytic activity. CD73 is an
ectonucleotidase often found on lymphocytes, tumors and other tissues and is believed to play an important role in tumor
immune suppression by catalyzing the production of extracellular adenosine. CD73 is a cellular adhesion molecule
involved in lymphocyte activation and trafficking to lymphoid tissues. CD73 is expressed in lymph nodes where it plays a
role in immune response to antigens. These functions of CD73 are independent of adenosine production. CPI-006 is
designed to activate B cells and other immune cells resulting in the proliferation, migration and differentiation of B cells
into antibody producing plasma cells and memory B cells. In preclinical and clinical studies, both cancer patients and
patients with COVID-19 treated with CPI-006 experienced activation of B cells into antigen specific antibody producing
cells. Enhancement of antibody production and development of memory B cells are thought to improve immunity to
diseases such as viral infections and cancer, and also lead to immunologic memory preventing reinfection upon subsequent
exposure to pathogens.
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As depicted above, Phase 1 study results, along with preclinical research, shows that CPI-006 activates antigen
specific B cells, triggering the body’s inherent immune response to generate a robust and durable humoral response to the
SARS-CoV-2 virus. These results included the stimulation of the generation of high titers of durable, polyclonal IgG and
IgM antibody responses to SARS-CoV-2 and increased levels of memory B cells. This novel mechanism of action has
several advantages over passively administered monoclonal antibodies and could potentially be used to treat other
infectious diseases.
As compared to other anti-CD73 antibodies, in in vitro studies using human immune cells, CPI-006 led to
activation of B cells and differentiation into antibody producing plasmablasts. Changes on monocytes were also observed
and included increased expression of cell surface markers involved in enhanced antigen presentation. Together, we believe
these results suggest that CPI-006 has the potential to function as an immunostimulant. We are not aware of any other anti-
CD73 antibody that has been reported to possess these properties.
We believe that CPI-006 may have distinct advantages for the treatment of COVID-19, including:
● designed to enhance anti-SARS-CoV-2 antibodies to multiple viral variants;
● has the potential to improve long term immunity and protection from re-infection;
● could accelerate viral clearance and reduce the risk of spreading; and
● potential to increase cross-protection to mutants of SARS-COV-2 and other coronaviruses.
Based on all of these properties and early results, we believe that CPI-006 could, if successfully developed and approved,
become a foundational therapy for the treatment or prevention of COVID-19 and possibly, other infectious diseases.
CPI-006 COVID-19 Phase 1 Clinical Trial
In June 2020, we initiated a Phase 1 clinical trial to investigate CPI-006 as a novel immunotherapy approach for
the treatment of patients with COVID-19 based on CPI-006’s potential immunomodulatory effects.
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The open-label, Phase 1 clinical trial has enrolled 29 hospitalized COVID-19 high-risk patients with mild to
moderate symptoms as of March 4, 2021. Cohorts of patients received a single dose of CPI-006, with doses of 0.3, 1.0, 2.0,
3.0 and 5.0 mg/kg. Patients received medications, therapies, and interventions per standard treatment protocols for COVID-
19 for the duration of the study. The primary efficacy endpoint was the change in serum immunoglobulin (IgM and IgG)
anti-SARS-CoV-2 levels compared to baseline at day 28. Safety and clinical outcomes were also assessed. No drug related
toxicities were observed at any of the dosing levels. Of the 29 patients, no patients progressed to requiring mechanical
ventilation and the median time to discharge from the hospital was three days. These results are favorable, as published
reports suggest that approximately 20% of such patients will progress to requiring invasive mechanical ventilation. Patients
in the study generated high titers of polyclonal antibodies against a diverse range of targets on the SARS-CoV-2 virus that
were sustained over several months. They also had increased levels of circulating memory B cells, which could produce
long-term immunity. Our Phase 1 data showed that this response occurred quickly. We believe the polyclonal antibody
response and the potential mechanism of action of CPI-006 could reduce the potential for immune evasion due to viral
mutation and emergence of variants.
Magnitude and Duration of Anti-SARS-Cov2 Responses
The diagram below shows the anti-SARS-CoV-2 response generated in patients treated with CPI-006 in the Phase
1 study. The level and duration of antibody production has been shown in other third-party studies to be a good predictor of
clinical outcome.
In the four panels on the left of the slide, the serum titers over time from the pre-treatment to the day 28, day 66
and day 84 for IgG and IgM antibodies to trimeric spike protein and its receptor binding domain, or RBD, are shown.
Cohorts are color coded, with 0.3 mg/kg in green, 1 mg/kg in blue, 3 mg/kg in purple and 5 mg/kg in brown, with a
convalescent plasma control on the far right in gray. A dose response was observed from the lowest dose of 0.3mg/kg to
higher doses and titers are higher than those seen in convalescent plasma samples tested. Antibody responses were
increased out to day 28 to very high titers and these high titers were sustained for 84-plus days. Titers well above 100,000
were observed. For example, at 1 mg/kg, Day 56 IgG to spike was >200,000 and IgM to spike was >100,000.
We observed a dose response with 0.3mg/kg being least effective and a plateau being reached at 1-3mg/kg.
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We reported data from the Phase 1 clinical trial in November at the 2020 Society for Immunotherapy of Cancer
Annual Meeting (“SITC”). The data presented at SITC included results from 22 patients enrolled in the Phase 1 study
utilizing a cut-off date of November 4, 2020. This included enrollment in four dosing cohorts of the study (0.3, 1.0, 3.0 and
5.0 mg/kg). All patients received a single dose of CPI-006 administered via a 5-10 minute intravenous (“IV”) infusion. The
median age of the patients was 58 years (range 23-76 years). All of the patients had comorbidities that increased their
COVID-19 risk including diabetes, coronary disease, hypertension, obesity, chronic kidney disease, chronic lung disease
and/or cancer. 95% of patients were from minority populations that are at high risk of COVID-19 complications. The key
highlights of the data reported include:
Results Support the Further Evaluation of CPI-006 in COVID-19
● All patients had relatively low titers of anti-SARS-CoV-2 antibodies at the time of hospitalization despite having
varying durations of prior COVID-19 symptoms from 1-21 days (median 5 days); all patients had a confirmed
COVID-19 diagnosis by positive PCR nasal swab testing.
● All evaluable patients showed prompt anti-SARS-CoV-2 antibody responses within 7 days of administration of
CPI-006 at all dose levels.
● All patients recovered and were discharged from the hospital at a median of 3.5 (range 2-23) days.
● As of the November 4, 2020 cut-off date, there were no drug-related toxicity or safety issues reported.
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Antibody Response Results
● Four of four evaluable patients that received the 0.3 mg/kg dose had sustained high titers of IgG antibodies to
trimeric spike (“TS”) protein out to 84+ days (one patient 100+ days), without evidence of diminution of
response. In these patients, IgM antibody titers peaked at 28-56 days and remained elevated out to 84+ days.
Similar trends were seen in IgG and IgM antibody response to receptor binding domain (“RBD”).
● A dose response was observed comparing the 3.0 and 1.0 mg/kg dose to the 0.3 mg/kg dose. Higher and more
sustained titers of both IgG and IgM to both spike protein and RBD were seen out to 56 days when comparing
the 1.0 to 0.3 mg/kg doses. The IgM responses were noteworthy for the sustained prolonged elevation.
● Antibody responses from 3.0 and 5.0 mg/kg doses appeared similar to the 1.0 mg/kg dose, but the follow up
period for such doses was shorter as of the cut-off date.
● In viral neutralization assays, three of three patients developed anti-viral antibody responses out to day 56 that
blocked infectivity of receptor bearing cells in a pseudovirus neutralization assay.
● Memory B cells were elevated in 6 of 6 tested patients following treatment with CPI-006. Memory T effector
cells were also elevated following treatment and produced interferon-gamma and interleukin-2 in response to
SARS-CoV-2 antigen consistent with antigen specific Th1 biasing.
Polyclonal Antibody Response
The magnitude and diversity of the polyclonal responses were evaluated by mapping of antibody responses to the
subdomains of the TS protein including the N-terminal, RBD, S1 and S2 subdomains. Polyclonality and reactivity to
multiple antigenic determinants on the virus were found, which have the potential to lead to viral neutralization and
elimination and to reduce the potential for escape due to emergence of mutant forms of the virus. The mapping shows:
● IgG responses were polyclonal, polyspecific and directed to all subdomains.
● IgM responses were polyclonal and directed to all subdomains but are preferentially directed to the RBD.
We believe the totality of the data from the Phase 1 clinical trial supports the potential of CPI-006 as a treatment
for COVID-19. CPI-006, when administered at low doses, and has demonstrated a boost in antibody responses to the
SARS-CoV-2 virus. The responses were long-lived and the data reflect a dose response relationship with the 1.0 mg/kg
dose having produced higher and more prolonged titers than the 0.3 mg/kg dose.
CPI-006 COVID-19 Phase 3 Clinical Trial
In February 2021, we initiated a randomized double-blind Phase 3 clinical trial of CPI-006 for the treatment of
hospitalized patients with COVID-19. The Phase 3 study will evaluate the efficacy and safety of CPI-006 compared to
placebo in hospitalized patients with mild-to-moderate COVID-19 and is expected to enroll approximately 1,000 patients at
sites in North America, Europe, South Africa and Latin America. Patients will be randomized in a 1:1:1 ratio to receive a
single intravenous dose of either 2.0 mg/kg or 1.0 mg/kg dose of CPI-006 intravenously or placebo; all patients will receive
standard of care treatments for COVID-19. The primary endpoint is the proportion of patients progressing to respiratory
failure or death during the 28 days after dosing. Respiratory failure is defined as requiring non-invasive or invasive
mechanical ventilation. Additional secondary endpoints include time to recovery, time to resolution of COVID-19
symptoms, anti-viral antibody responses, etc. An interim futility and efficacy analysis will be conducted by an independent
data monitoring committee when approximately 60% of subjects complete the 28-day post-treatment visit. We expect to
complete enrollment in the study in the fourth quarter of 2021.
CPI-006 Oncology Phase 1/1b Clinical Trial
In February 2018, we initiated a Phase 1/1b clinical trial with CPI-006 administered alone and in combination
with ciforadenant and in combination with pembrolizumab and in a triplet combination of CPI-006, ciforadenant and
pembrolizumab. As of February 2021, we have enrolled over 95 patients on this trial at doses of up to 24 mg/kg every
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three weeks. Key findings from this trial as of March 4, 2021 include the observation that CPI-006 was well-tolerated and
evidence of B-cell activation and lymphocyte trafficking was observed in patients that received single doses as low as 1
mg/kg. Treatment with CPI-006 was also associated with increases in memory B-cells, the emergence of new B-cell clones
and, in some patients, the production of novel anti-tumor antibodies. Anti-tumor activity was observed in certain patients
receiving triplet combination therapy.
With our current focus on our Phase 3 trial with CPI-006 to treat COVID-19, we do not plan any further
enrollment in this trial at this time.
We hold a nonexclusive, worldwide license (except for greater China) for all fields of use under Scripps’ rights in
a hybridoma clone expressing an anti-CD73 antibody, and to progeny, mutants or unmodified derivatives of such
hybridoma and any antibodies expressed by such hybridoma. In 2016, we filed a patent application covering the
composition of matter of CPI 006. In 2019, we filed patent applications covering the use of CPI-006 for
immunomodulation and enhancement of anti-tumor immunity. In 2020, we filed a provisional U.S. patent application
directed to the use of CPI-006 in the treatment of COVID-19 and other infectious diseases.
CPI-818, ITK Inhibitor. CPI-818 is an investigational selective, orally bioavailable, covalent inhibitor of ITK
designed to have low nanomolar affinity. ITK, an enzyme that functions in T cell signaling and differentiation, is expressed
predominantly in T cells, which are lymphocytes that play a vital role in immune responses. One of the key survival
mechanisms of tumors is believed to be the reprogramming of T cells to create an inflammatory environment that inhibits
anti-tumor immune response and favors tumor growth. We believe highly selective inhibitors of this enzyme will facilitate
induction of T cell anti-tumor immunity and also may be useful in the treatment of T cell lymphomas.
ITK is an enzyme expressed predominantly in T cells where it plays a key role in T cell signaling. T cell signaling
involving ITK is required in the development of T cells within the thymus, where ITK regulates the production of various
T cell subsets and functions. The ITK cell signaling pathway is similar to the signaling that occurs in B cells, which is
mediated by a homologous enzyme known as BTK, the target of ibrutinib, an approved treatment for patients with B cell
lymphomas and leukemias. We believe that inhibiting ITK in malignant T cells may be of therapeutic benefit in patients
with T cell leukemias and lymphomas, analogous to the effects of ibrutinib on B cell lymphomas and leukemias. In
malignant T cells, ITK was found to be over expressed specifically in certain T cell lymphomas, including peripheral T cell
lymphoma (“PTCL”), angioimmunoblastic T cell lymphoma (“AITL”) and in a subgroup of T lymphoblastic leukemia and
lymphoma (“T ALL”).
In ITK genetic knockout mice, which completely lack expression of ITK, T cells exhibit defects in T helper cell
differentiation and cytokine secretion but retain the ability to differentiate into cytotoxic T cells that secrete IL 2 and IFNg,
which are the cells responsible for tumor rejection. We believe that skewing T helper cell differentiation to favor cytotoxic
T cells may be beneficial in treating many types of cancer.
We have developed CPI-818 by targeting the cysteine amino acid residue at position 442 in the ITK protein. We
believe covalent targeting of ITK has the potential to provide a selective and prolonged duration of activity without the
need for high systemic exposures and thereby improve the therapeutic window. This approach was previously used by our
cofounders to generate ibrutinib. We believe that the potential selectivity of CPI-818 could mimic the immune properties
seen in ITK knockout mice and skew the immune response toward a more favorable anti-tumor immune response. In
addition, ITK plays a role in the proliferation of some T-cell lymphomas and we believe its inhibition could lead to growth
arrest and/or tumor cell cytotoxicity. In our preclinical studies of CPI-818, objective tumor responses were observed in
dogs with spontaneous T-cell lymphomas.
CPI-818 is orally bioavailable and has achieved cellular occupancy of the target in vivo in various animal models.
Pre-clinical studies have demonstrated that CPI-818 was well-tolerated in vivo and resulted in inhibition of T-cell
activation. In March of 2019, we initiated a phase 1/1b study of CPI-818 in patients with advanced refractory T-cell
lymphomas.
CPI-818 is currently being studied in a Phase 1/1b clinical trial that was designed to select the recommended dose
of CPI-818 and evaluate its safety, pharmacokinetics (“PK”), target occupancy, biomarkers and efficacy. The study
employed an adaptive, expansion cohort design, with an initial phase that evaluated escalating doses (100, 200, 400, 600
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mg taken twice a day) in successive cohorts of patients, followed by a second phase that is designed to evaluate safety and
tumor response to the recommended dose of CPI-818 in disease-specific patient cohorts. By protocol design, treatment is
discontinued after one year or upon disease progression. The study enrolled 25 patients from the United States, Australia
and South Korea with several types of advanced, refractory T cell lymphomas, including nine patients with peripheral T-
cell lymphoma (“PTCL”), 12 patients with cutaneous T-cell lymphoma (“CTCL”), and four patients with other T-cell
lymphomas. All patients had failed multiple prior therapies.
In December 2020 at the American Society of Hematology Annual Meeting, we presented preliminary Phase 1/1b
clinical data with CPI-818in refractory T cell lymphomas in patients receiving adequate doses of the drug. The data
presented was as follows:
● Of the seven evaluable patients with PTCL, there were two objective tumor responses as of the cut-off date of
October 5, 2020:
o One patient, who previously failed chemotherapy and high dose chemotherapy with autologous bone
marrow transplantation, achieved a complete response (“CR”) with CPI-818 at month 8 that remained
ongoing after 12 months on study. The patient received CPI-818 for 12 months and the CR persisted
beyond discontinuation of therapy (per the study protocol, the patient stopped receiving therapy after
12 months on study). As of December 1, 2020, this patient was off all therapy for lymphoma and
remains disease free at 14+ months.
o One patient who failed multiple prior therapies achieved a partial response at four months on therapy
and remained on study as of October 5, 2020.
● Of the 11 evaluable patients with CTCL:
o One patient achieved a complete response in lymph node disease and continued to have stable
cutaneous disease at more than 12 months on therapy as of November 2, 2020.
o Three patients achieved stable disease on therapy for between 3 and 5 months.
● There was a dose dependent increase in receptor occupancy, with trough occupancy >75% observed at the 200,
400 and 600 mg doses.
● No dose limiting toxicities and no grade 3 or 4 treatment related adverse events were observed as of October 5,
2020.
Based on the interim results from our Phase 1/1b clinical trial, Angel Pharmaceuticals, together with us, plans to
initiate a global Phase 2 study of CPI-818 in peripheral T cell lymphomas. PTCL is more common in China than the United
States representing approximately 26% of non-Hodgkins lymphomas in China.
Presentation of Preclinical Data in ALPS at ASH meeting December 2020
Autoimmune lymphoproliferative syndrome (“ALPS”) is a rare genetic disease affecting children that manifests
with lymphadenopathy, splenomegaly, cytopenias (low blood counts) and autoimmunity. The disease is caused by a
mutation in the Fas gene, which provides instructions for making a signaling protein involved in the induction of apoptosis.
The mutation results in immune dysregulation due to abnormally high levels of “double negative” T cells (CD4 and CD8
double negative), which infiltrate the blood, spleen and lymphoid tissues. A similar mutation occurs in Fas-deficient
MRL/lpr mice, which are used as a model for this disease. These mice are frequently also used as a model for autoimmune
disease. CPI-818 has been studied in vivo in MRL/lpr mice and in vitro using abnormal cells from ALPS patients. These
data were presented in December 2020 at the American Society of Hematology Annual Meeting.
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Key highlights from the presentation include:
● ITK was expressed in double negative T cells from ALPS patients.
● In vitro, CPI-818 inhibited the activation of stimulated abnormal double negative T cells in ALPS
patients.
● In vivo studies in MRL/lpr mice demonstrated that treatment with CPI-818 reduced lymphadenopathy,
splenomegaly, and autoimmune skin and kidney disease.
The animal preclinical data and in vitro data with lymphocytes from ALPS patients support the use of CPI-818 in
autoimmunity and potentially as a treatment for ALPS.
We have filed patent applications covering composition of matter and uses of our ITK inhibitors and hold
exclusive worldwide rights (except for greater China) for all indications.
Ciforadenant Adenosine A2A Receptor Antagonist. Ciforadenant is an oral, small molecule antagonist of the
A2A receptor for adenosine that we in-licensed from Vernalis (R&D) Limited (“Vernalis”) in February 2015. Since
licensing ciforadenant, we have conducted extensive laboratory studies in vitro and in vivo in animal models to evaluate
ciforadenant’s immune enhancing and anti-tumor properties. In these studies, orally administered ciforadenant inhibited
tumor growth in multiple mouse models of cancer as a single agent, in combination with anti-PD-1, in combination with
anti-PD-L1, in combination with other immuno oncology agents and in combination with certain chemotherapy drugs. We
also have shown in vitro that ciforadenant bound potently and selectively to human activated T cells and blocked adenosine
mediated immunosuppression by restoring T cell function. In addition, we have shown anti-tumor activity in mice for a
significant time following oral administration, which appeared to be mediated through a long lasting memory immune
response.
Adenosine activates an immune checkpoint, the adenosine A2A receptor, that is used by the body to limit
inflammation and immune responses. It is produced during acute, inflammatory processes in two steps. Increased levels of
adenosine seen in tumors interact with the A2A and A2B receptors expressed on several cells of the immune system,
including T cells, NK cells, macrophages, dendritic cells and myeloid derived suppressor cells, as well as other cells, which
has the effect of dampening the immune response to the tumor.
A significant body of data indicates that targeting the adenosine cancer axis through the A2A receptor can
promote anti-tumor immune responses leading to tumor regression. Consistent with studies of the inhibition of the A2A
receptor, A2A receptor gene knockout mice, which completely lack expression of the A2A receptor, exhibit improved anti-
tumor immunity. In addition, several preclinical tumor model studies have shown that treatment with A2A receptor
inhibitors leads to tumor regression that is enhanced when administered in combination with various other checkpoint
inhibitors, such as anti-PD-1 therapies and anti-CTLA 4 therapies.
In January 2016, we began enrolling patients in a large expansion cohort trial for ciforadenant. This Phase 1/1b
clinical trial is designed to examine safety, tolerability, biomarkers and preliminary efficacy of ciforadenant in several solid
tumor types, both as a single agent and in combination with Genentech, Inc.’s cancer immunotherapy, Tecentriq, a fully
humanized monoclonal antibody targeting PD-(L)1. In 2018, we amended our Phase 1/1b protocol to enroll patients in a
Phase 1b/2 clinical trial with RCC who have failed therapies with both anti-PD-(L)1 antibodies and TKIs.
Interim Results Published in the Journal Cancer Discovery
Results in 68 patients with treatment-refractory RCC demonstrated an overall survival (“OS”) of 90% at more
than 25 months follow-up with ciforadenant administered in combination with atezolizumab. The OS for patients receiving
ciforadenant alone was over 69% at 16 months. At the time of enrollment, study participants had advanced refractory
disease and a poor prognosis. They had been treated with a median of three prior therapies (range: 1 to 5), and
approximately 72% had failed prior anti-PD-(L)1 therapy. The results from this study were published in January 2020 in
the journal Cancer Discovery.
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Key findings from the published results include:
● Disease control for more than 6 months was observed in 39% and 17% of patients receiving combination
therapy and monotherapy, respectively.
● For patients receiving combination therapy, 11% experienced a confirmed partial response (“PR”) (as
determined by RECIST criteria). Several additional patients experienced tumor regression not meeting
the criteria for a PR. For patients receiving monotherapy, one patient experienced a confirmed PR, one
experienced an unconfirmed PR, and several patients experienced tumor regression not meeting the PR
criteria.
● Responses were seen in both the combination therapy and monotherapy arms, and in patients who failed
prior anti-PD-(L)1 therapy.
● Progression-free survival (as assessed by RECIST criteria) was 5.8 months with combination therapy
and 4.1 months with monotherapy.
● OS was 90% at 25 months follow-up with combination therapy and 69% at 16 months follow-up with
monotherapy.
● Combination therapy was superior to monotherapy with respect to OS, response rate, disease control rate
and progression-free survival.
● The recently described adenosine gene signature showed a statistically significant correlation with tumor
response and disease control rates (p<0.008). We evaluated adenosine gene signatures in pretreatment
biopsies from 30 patients. Of the patients showing a low adenosine gene signature, none exhibited signs
of tumor regression. In contrast, patients with a high adenosine gene signature had a 17% (N=18) overall
response rate by RECIST criteria.
● Ciforadenant was well tolerated with grade 3 adverse events that were infrequent (less than 5%) and
reversible.
This study supports the tumor immune enhancing potential of adenosine pathway blockade. The unique
mechanism of action and safety results suggest that this treatment, if successfully developed and approved, may be
valuable, particularly in patients who have failed anti-PD-(L)1 therapy or as a combination to prevent the development of
resistance. The studies also demonstrate that RCC exhibited high levels of adenosine pathway related genes. We expect to
be able to utilize this biomarker in future studies to target patients most likely to benefit from therapy with ciforadenant.
Updated Data at the ASCO20 Virtual Scientific Program
Updated data on 51 RCC patients that were treated with ciforadenant monotherapy or in combination with
Genentech’s Tecentriq® (atezolizumab), an anti-PD-L1 antibody, and whose tumors were biopsied to test with the
adenosine gene signature was reported at ASCO 2020. The key updates from the presentation include:
● 31 patients (30 evaluable) were positive for the and 20 patients were negative. Patients had a median of three
prior therapies, including 86% that failed a prior anti-PD-(L)1 therapy.
● In the AdenoSig positive group, there were five PRs, (as assessed by RECIST criteria) for an ORR of 17%
and six additional patients that had tumor regression not meeting the criteria for a PR.
● In the AdenoSig negative group, there were no PRs and no patients with tumor regression.
● In the AdenoSig positive group, the progression free survival curve plateaued at 23% at 40 weeks, compared
to declining to 0% in the AdenoSig negative group.
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Refractory, late-line RCC has become a crowded space, with several recently approved drugs resulting in
extensive patient heterogeneity and complexities, making development of combinations with new agents difficult. Given
these considerations, our prioritization of CPI-006 in COVID-19, and the potential mechanism of action and safety results
for ciforadenant, we have decided to pursue a strategy in front line RCC. In front line RCC, the field is most interested in
strategies that increase response rate; especially complete response rate or deep responses.
We are now planning a Phase 2 study of ciforadenant in a triplet combination with pembrolizumab and lenvatinib.
We plan to do this study with the Kidney Cancer Consortium. The trial is planned to enroll approximately 60 patients. The
endpoint goal will be to show that 35% or more of the patients achieve deep tumor responses, defined as greater than 80%
reduction of tumor volume. This compares to historical levels of 20% of patients achieving a deep response with pembro
plus TKIs. The adenosine signature biomarker will also be evaluated.
Ciforadenant is also being evaluated in combination with the anti-CD38 antibody, daratumumab (Darzalex) in
patients with advanced refractory multiple myeloma. The objective of this Phase 1 clinical trial is to evaluate whether
ciforadenant can overcome resistance in patients who have failed daratumumab treatment.
The issued U.S. patents that we in licensed from Vernalis for ciforadenant are directed to the composition of
matter of ciforadenant and its method-of-use for treating disorders treatable by purine receptor blocking. The composition
of matter patent covering ciforadenant is expected to expire in the United States in July 2029, excluding any patent term
extension that may be available. We hold an exclusive, worldwide license (except for greater China) under these patent
rights and related know how, including a limited right to grant sublicenses, for all fields of use, to develop, manufacture
and commercialize products containing certain adenosine receptor antagonists, including ciforadenant. We have also filed
patent applications covering the use of ciforadenant in combination with other checkpoint inhibitors, and the use of various
biomarkers to select and monitor patients receiving therapy.
CPI-182, Anti-CXCR2 Antibody designed to block inflammation and Myeloid Suppression. In 2017, we in-
licensed this monoclonal antibody designed to block CXCR2, a novel target expressed on neutrophils and various
inflammatory cells including myeloid derived suppressor cells (“MDSC”). Preclinical studies have demonstrated that this
antibody blocked neutrophil function and migration, and MDSCs. MDSCs are involved in tumor immunosuppression and
blockade of these cells may improve anti-tumor immunity. A publication describing this antibody was published in the
journal MABS in January 2021. Preclinical data in vivo in mice demonstrated that CPI-182 was active in models of
rheumatoid arthritis and in models of atopic dermatitis. We believe these data support the role of CXCR in inflammatory
diseases and demonstrate that CPI-182 may have the potential to treat these conditions. This product candidate is now in
Investigational New Drug application (“IND”)-enabling studies and scale-up manufacturing.
CPI-935, Adenosine A2B Receptor Antagonist. Adenosine A2B receptors have been found to play an important
role in the immune response to tumors as well as in inflammation and fibrosis. Similar to adenosine A2A receptors,
adenosine binds to adenosine A2B receptors, which leads to immunosuppression. Preclinical models have shown that
inhibition of A2B receptors prevented fibrosis. In 2018, we selected a development candidate for this program, a small
molecule antagonist of the A2B receptor.
Manufacturing
We do not own or operate, and currently have no plans to establish any manufacturing facilities. We currently rely,
and expect to continue to rely, on third parties for the manufacture of our product candidates for clinical testing, as well as
for manufacture of any products that we may commercialize. We are able to internally produce small quantities of our
product candidates required for relatively short preclinical animal studies. We believe that this allows us to accelerate the
drug development process by not having to rely on third parties for all of our research and development needs. However,
we currently rely, and expect to continue to rely, on a number of contract manufacturers to produce sufficient quantities of
our product candidates for use in more lengthy preclinical development and clinical trials and in relation to any future
commercialization of our product candidates. Additional contract manufacturers are used to fill, label, package and
distribute investigational drug products. This strategy allows us to maintain a more efficient infrastructure, avoid depending
on our own manufacturing facility and equipment while simultaneously enabling us to focus our expertise on developing
our products. Although we believe we have multiple potential sources for the
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manufacturing of our product candidates, we currently rely on several different manufacturers who supply different
components of the ciforadenant and CPI-818 molecules, on one manufacturer for CPI-006 drug substance and other third-
party manufacturers to produce our other product candidates.
Competition
The pharmaceutical and biotechnology industries are characterized by intense competition and rely heavily on the
ability to move quickly, adapt to changing medical and market needs, and develop and maintain strong intellectual property
positions. We believe that the development experience of our scientific and management teams, as well as the strength and
promise of our product candidates, provides us with a competitive advantage; nevertheless, we face potential competition
from myriad sources, including pharmaceutical and biotechnology companies, academic institutions, governmental
agencies and public and private research institutions.
Kyowa Hakko Kirin has approval in Japan and the United States for istradefylline, an A2A antagonist, in
Parkinson’s disease. Within oncology, Novartis has announced an exclusive licensing agreement with Palobiofarma SL and
is conducting a Phase 1 trial with an A2A antagonist. AstraZeneca plc is conducting clinical trials with an A2A antagonist
for use in cancer therapy. Merck KgaA has entered into a pre-clinical collaboration with Domain Therapeutics Inc. to
develop programs targeting the adenosine pathway. In addition, Redoxtherapies, which was acquired by Juno Therapeutics
and subsequently by Celgene, and Arcus Biosciences are developing A2A receptor antagonists for cancer. Astra Zeneca,
Bristol-Myers Squib, and Novartis, in partnership with Surface Oncology, have initiated clinical trials with anti-CD73
antibodies in cancer patients. More generally, in the field of immuno-oncology, there are large pharmaceutical companies
with approved products or products in late-stage development that target other immune checkpoints, including PD-1, PD-
L1 or CTLA-4. These companies include Bristol-Myers Squibb (nivolumab, ipilimumab), Merck (pembrolizumab),
Genentech (atezolizumab) and AstraZeneca (durvalumab, tremelimumab). Janssen Pharmaceuticals and AbbVie are co-
marketing Imbruvica (ibrutinib), which is a small molecule inhibitor of the kinase BTK that has also been reported to
inhibit ITK.
Intellectual Property
We strive to protect and enhance the proprietary technology, inventions, and improvements that are commercially
important to our business, including seeking, maintaining and defending patent rights, whether developed internally or
licensed from our collaborators or other third parties. We do not yet own any issued patents relating to our product
candidates. Our policy is to seek to protect our proprietary position by, among other methods, filing patent applications in
the United States and in jurisdictions outside of the United States covering our proprietary technology, inventions,
improvements and product candidates that are important to the development and implementation of our business. We also
rely on trade secrets and know-how relating to our proprietary technology and product candidates, continuing innovation,
and in-licensing opportunities to develop, strengthen and maintain our proprietary position in the field of immuno-
oncology. We also plan to rely on data exclusivity, market exclusivity, and patent term extensions when available. Our
commercial success will depend in part on our ability to obtain and maintain patent and other proprietary protection for our
technology, inventions, and improvements; to preserve the confidentiality of our trade secrets; to obtain and maintain
licenses to use intellectual property owned by third parties; to defend and enforce our proprietary rights, including any
patents that we may own in the future; and to operate without infringing on the valid and enforceable patents and other
proprietary rights of third parties.
We have in-licensed patents and patent applications directed to certain of our product candidates and related uses
thereof. We also possess and in-license substantial know-how and trade secrets relating to the development and
commercialization of our product candidates, including related manufacturing processes and technology. As of March 2,
2020, our owned and licensed patent portfolio consisted of fourteen licensed U.S. issued patents, four licensed U.S.
pending patent applications, twelve owned U.S. pending patent applications, four owned U.S. provisional patent
applications, and seven owned PCT International patent applications directed to ciforadenant, CPI-006, and CPI-818, and
certain of our other proprietary technology, inventions, improvements or other potential product candidates. In addition, our
owned and licensed patent portfolio included forty-four licensed patents, nine licensed patent applications, and sixty-three
owned patent applications pending in jurisdictions outside of the United States that are foreign
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counterparts to one or more of the foregoing U.S. patents and patent applications. The patents and patent applications
outside of the United States in our portfolio are held primarily in Europe, Canada, Japan, Australia and China.
With respect to the immuno-oncology product candidates and processes we intend to develop and commercialize
in the normal course of business, we intend to pursue patent protection covering, when possible, compositions, methods of
use, dosing and formulations. We may also pursue patent protection with respect to manufacturing and drug development
processes and technologies.
Issued patents can provide protection for varying periods of time, depending upon the date of filing of the patent
application, the date of patent issuance, and the legal term of patents in the countries in which they are obtained. In general,
patents issued for applications filed in the United States can provide exclusionary rights for 20 years from the earliest
effective filing date. In addition, in certain instances, the term of an issued United States patent that covers or claims an
FDA approved product can be extended to recapture a portion of the term effectively lost as a result of the FDA regulatory
review period, which is called patent term extension. The restoration period cannot be longer than five years and the total
patent term, including the restoration period, must not exceed 14 years following FDA approval. The term of patents
outside of the United States varies in accordance with the laws of the foreign jurisdiction, but typically is also 20 years
from the earliest effective filing date. The issued United States patents we license from Vernalis directed to the composition
of matter of ciforadenant and its method of use for treating disorders treatable by purine receptor blocking are expected to
expire between January 2022 and July 2029, excluding any patent term extension that may be available. The pending U.S.
patent application and PCT International patent applications, if granted as patents, that we own directed to the composition
of matter and methods of treatment for CPI-006 are expected to expire between December 2036 and June 2037, excluding
any patent term extension that may be available. The pending U.S. and foreign patent applications, if granted as patents,
that we own directed to the composition of matter and methods of treatment for CPI 818 are expected to expire November
2037, excluding any patent term extension that may be available. However, the actual protection afforded by a patent varies
on a product-by-product basis, from country-to-country, and depends upon many factors, including the type of patent, the
scope of its coverage, the availability of regulatory-related extensions, the availability of legal remedies in a particular
country, and the validity and enforceability of the patent.
The patent positions of companies like ours are generally uncertain and involve complex legal and factual
questions. No consistent policy regarding the scope of claims allowable in patents in the field of immuno-oncology has
emerged in the United States. The relevant patent laws and their interpretation outside of the United States is also
uncertain. Changes in either the patent laws or their interpretation in the United States and other countries may diminish
our ability to protect our technology or product candidates and enforce the patent rights that we license, and could affect
the value of such intellectual property. In particular, our ability to stop third parties from making, using, selling, offering to
sell, or importing products that infringe our intellectual property will depend in part on our success in obtaining and
enforcing patent claims that cover our technology, inventions, and improvements. With respect to both licensed and
company-owned intellectual property, we cannot guarantee that patents will be granted with respect to any of our pending
patent applications or with respect to any patent applications we may file in the future, nor can we be sure that any patents
that may be granted to us in the future will be commercially useful in protecting our products, the methods of use or
manufacture of those products. Moreover, even the issued patents that we license do not guarantee us the right to practice
our technology in relation to the commercialization of our products. Patent and other intellectual property rights in the
pharmaceutical and biotechnology space are evolving and involve many risks and uncertainties. For example, third parties
may have blocking patents that could be used to prevent us from commercializing our product candidates and practicing
our proprietary technology, and the issued patents that we in-license and those that may issue in the future may be
challenged, invalidated, or circumvented, which could limit our ability to stop competitors from marketing related products
or could limit the term of patent protection that otherwise may exist for our product candidates. In addition, the scope of
the rights granted under any issued patents may not provide us with protection or competitive advantages against
competitors with similar technology. Furthermore, our competitors may independently develop similar technologies that
are outside the scope of the rights granted under any issued patents that we own or exclusively in-license. For these
reasons, we may face competition with respect to our product candidates. Moreover, because of the extensive time required
for development, testing and regulatory review of a potential product, it is possible that, before any particular product
candidate can be commercialized, any patent protection for such product may expire or remain in
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force for only a short period following commercialization, thereby reducing the commercial advantage the patent provides.
Licenses and Collaborations
Vernalis Licensing Agreement
In February 2015, we entered into a license agreement with Vernalis, pursuant to which we were granted an
exclusive, worldwide license under certain patent rights and know-how, including a limited right to grant sublicenses, for
all fields of use to develop, manufacture and commercialize products containing certain adenosine receptor antagonists,
including ciforadenant. The issued U.S. patents that we in-licensed from Vernalis pursuant to this agreement are directed to
the composition of matter of ciforadenant and its method of use for treating disorders treatable by purine receptor blocking.
These patents are expected to expire in the United States between January 2022 and July 2029, excluding any patent term
extension that may be available. Vernalis has the first right to prosecute and maintain the licensed patent rights worldwide,
subject to our right with respect to certain of the licensed patents to continue prosecution and maintenance if Vernalis elects
not to do so. We also have the right to prosecute and maintain any patent rights that we may own that cover the licensed
compounds that do not fall within the licensed patent rights. Pursuant to this agreement, we are required to use
commercially reasonable efforts to conduct certain activities to obtain marketing authorizations for licensed products and to
conduct certain preclinical and clinical studies for ciforadenant. We also must use commercially reasonable efforts to
conduct certain preclinical and clinical studies to support the use of ciforadenant as an immunotherapeutic agent for cancer
studies, and to meet certain specified development, regulatory and commercial milestones within specified time periods.
Pursuant to this agreement, we made a one-time cash payment to Vernalis in the amount of $1.0 million upon
entering into the agreement. We are also required to make cash milestone payments to Vernalis upon the successful
completion of clinical and regulatory milestones for licensed products depending on the indications for which such licensed
products are developed and upon achievement of certain sales milestones. In February 2017, we made a milestone payment
of $3 million to Vernalis following the expansion of a cohort of patients with renal cell cancer treated with single-agent
ciforadenant in our Phase 1/1b clinical trial. The aggregate potential milestone payments are approximately $220 million
for all indications.
We have also agreed to pay Vernalis tiered incremental royalties based on the annual net sales of licensed products
containing ciforadenant on a product-by-product and country-by-country basis, subject to certain offsets and reductions.
The tiered royalty rates for products containing ciforadenant range from the mid-single digits up to the low-double digits
on a country-by-country net sales basis. The royalties on other licensed products that do not include ciforadenant also
increase with the amount of net sales on a product-by-product and country-by-country basis and range from the low-single
digits up to the mid-single digits on a country-by-country net sales basis.
The agreement will expire on a product-by-product and country-by-country basis upon the expiration of our
payment obligations to Vernalis in respect of a particular product and country. Both parties have the right to terminate the
agreement in the event of an uncured material breach by the other party. We may also terminate the agreement at our
convenience by providing 90 days written notice, provided that we have not received notice of our own default under the
agreement at the time we exercise such termination right. Vernalis may also terminate the agreement if we challenge a
licensed patent or undergo a bankruptcy event.
Scripps Licensing Agreement
In December 2014, we entered into a license agreement with Scripps, pursuant to which we were granted a non-
exclusive, world-wide license for all fields of use under Scripps’ rights in certain know-how and technology related to a
mouse hybridoma clone expressing an anti-human CD73 antibody, and to progeny, mutants or unmodified derivatives of
such hybridoma and any antibodies expressed by such hybridoma, from which we developed CPI-006. Scripps also granted
us the right to grant sublicenses in conjunction with other proprietary rights we hold, or to others collaborating with or
performing services for us. Under this license agreement, Scripps has agreed not to grant any additional commercial
licenses with respect to such materials, other than march-in rights granted to the U.S. government.
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Upon execution of the agreement, we made a one-time cash payment to Scripps of $10,000 and are also obligated
to pay a minimum annual fee to Scripps of $25,000. The first minimum annual fee payment is due on the first anniversary
of the effective date of the agreement and will be due on each subsequent anniversary of the effective date for the term of
the agreement. We are also required to make performance-based cash payments upon successful completion of clinical and
sales milestones. The aggregate potential milestone payments are $2.6 million. We are also required to pay royalties on net
sales of licensed products (including CPI-006) sold by us, our affiliates and our sublicensees at a rate in the low-single
digits. In addition, should we sublicense the rights licensed under the agreement, we have agreed to pay a percentage of
sublicense revenue received at single digit percentages based on the achievement of development milestones.
Our license agreement with Scripps will terminate upon expiration of our obligation to pay royalties to Scripps
under the license agreement. The license agreement is terminable by the consent of the parties, at will by us or upon
providing 90 days written notice to Scripps, or by Scripps for certain material breaches by us, or if we undergo a
bankruptcy event. In addition, Scripps may terminate our license on a product-by-product basis, or the entire agreement, if
we fail to meet specified diligence obligations related to the development and commercialization of licensed products.
Scripps may also terminate the agreement after the third anniversary of the effective date of the agreement if it reasonably
believes, based on reports we provide to Scripps, that we have not used commercially reasonable efforts as required under
the agreement, subject to a specified notice and cure period.
Genentech Collaboration Agreements
In October 2015, we entered into a clinical trial collaboration agreement with Genentech to evaluate the safety,
tolerability and preliminary efficacy of ciforadenant combined with Genentech’s investigational cancer immunotherapy,
Tecentriq, a fully humanized monoclonal antibody targeting PD-L1, in a variety of solid tumors in our Phase 1/1b clinical
trial. Pursuant to this agreement, we will be responsible for the conduct and cost of the relevant studies, under the
supervision of a joint development committee made up of our representatives and representatives of Genentech. Genentech
will supply Tecentriq. As part of the agreement, we granted Genentech certain rights of first negotiation to participate in
future clinical trials that we may conduct evaluating the administration of ciforadenant in combination with an anti-PD-1 or
anti-PD-L1 antibody. If we do not reach agreement on the terms of any such participation by Genentech within a specified
time period, we retain the right to collaborate with third parties in such activities. We also granted Genentech certain rights
of first negotiation should we decide to license development and commercialization rights to ciforadenant. Should we not
reach agreement on the terms of such a license within a specified time period, we retain the right to enter into a license with
another third party.
We and Genentech each have the right to terminate the agreement for material breach by the other party. In
addition, the agreement may be terminated by either party due to safety considerations, if directed by a regulatory authority
or if development of ciforadenant or Tecentriq is discontinued. Further, the agreement will expire after a set period of time
following the provision by us of the final clinical study report to Genentech.
In May 2017, we entered into a second clinical trial collaboration agreement with Genentech. Under the new
agreement, ciforadenant administered in combination with Tecentriq will be evaluated in a Phase 1b/2 randomized,
controlled clinical study as second-line therapy in patients with NSCLC who are resistant and/or refractory to prior therapy
with an anti-PD-(L)1 antibody. It is anticipated that the study will enroll up to 65 patients in the treatment arm. Genentech
will be responsible for the conduct of the study and we will share the cost of the Phase 1b/2 trial, which began enrolling
patients in the fourth quarter of 2017. We are responsible for supplying ciforadenant and retain global development and
commercialization rights to ciforadenant. We and Genentech each have the right to terminate the agreement for material
breach by the other party. In addition, the agreement may be terminated by either party due to safety considerations, if
directed by a regulatory authority or if development of ciforadenant or Tecentriq is discontinued. Further, the agreement
will expire after a set period of time following the provision by us of the final clinical study report to Genentech.
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Monash License Agreement
In April 2017, we entered into a license agreement with Monash University (“Monash”), pursuant to which we
were granted an exclusive, sublicensable worldwide license under certain know-how, patent rights and other intellectual
property rights controlled by Monash to research, develop, and commercialize certain antibodies directed to CXCR2 for the
treatment of human diseases.
Upon execution of the agreement, we made a one-time cash payment to Monash of $275,000 and reimbursed
Monash for certain patent prosecution costs incurred prior to execution of the agreement. We are also obligated to pay an
annual license maintenance fee to Monash of $25,000 until a certain development milestone is met with respect to the
licensed product, after which no further maintenance fee will be due. We are also required to make development and sales
milestone payments to Monash with respect to the licensed products in the aggregate of up to $45.1 million. We are also
required to pay to Monash tiered royalties on net sales of licensed products sold by us, our affiliates and our sublicensees at
a rate ranging in the low-single digits. In addition, should we sublicense our rights under the agreement, we have agreed to
pay a percentage of sublicense revenue received at specified rates that are currently at low double digit percentages and
decrease to single digit percentages based on the achievement of development milestones.
The term of our agreement with Monash continues until the expiration of our obligation to pay royalties to
Monash thereunder. The license agreement is terminable at will by us upon providing 30 days written notice to Monash, or
by either party for material breaches by the other party. In addition, Monash may terminate the entire agreement or convert
the license to a non-exclusive license if we have materially breached our obligation to use commercially reasonable efforts
to develop and commercialize a licensed product, subject to a specified notice and cure mechanism.
Regulation
Government authorities in the United States, at the federal, state and local level, and other countries extensively
regulate, among other things, the research, development, testing, manufacture, quality control, approval, labeling,
packaging, storage, record-keeping, promotion, advertising, distribution, marketing and export and import of products such
as those we are developing. A new drug must be approved by the FDA through the New Drug Application (“NDA”)
process and a new biologic must be approved by the FDA through the Biologics License Application (“BLA”) process
before it may be legally marketed in the United States.
United States Drug Development Process
In the United States, the FDA regulates drugs under the federal Food, Drug, and Cosmetic Act (“FDCA”), and in
the case of biologics, also under the Public Health Service Act (“PHSA”), and their implementing regulations. The process
of obtaining regulatory approvals and the subsequent compliance with appropriate federal, state, local and foreign statutes
and regulations require the expenditure of substantial time and financial resources. Failure to comply with the applicable
U.S. requirements at any time during the product development process, approval process or after approval may subject an
applicant to administrative or judicial sanctions. These sanctions could include the FDA’s refusal to approve pending
applications, withdrawal of an approval, a clinical hold, warning letters, product recalls, product seizures, total or partial
suspension of production or distribution, injunctions, fines, refusals of government contracts, restitution, disgorgement or
civil or criminal penalties. Any agency or judicial enforcement action could have a material adverse effect on us.
The process required by the FDA before a drug or biologic may be marketed in the United States generally
involves the following:
● completion of preclinical laboratory tests, animal studies and formulation studies in accordance with Good
Laboratory Practice (“GLP”) regulations and other applicable regulations;
● submission to the FDA of an IND, which must become effective before human clinical trials may begin;
● approval by an institutional review board (“IRB”) or ethics committee at each clinical site before the trial is
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commenced;
● performance of adequate and well-controlled human clinical trials in accordance with Good Clinical Practice
(“GCP”) regulations to establish the safety and efficacy of the proposed drug, or safety, purity and potency of
the proposed biologic for its intended use;
● submission to the FDA of an NDA or BLA after completion of all clinical trials;
● satisfactory completion of an FDA Advisory Committee review, if applicable;
● a determination by the FDA within 60 days of its receipt of an NDA or BLA to file the application for
review;
● satisfactory completion of an FDA inspection of the manufacturing facility or facilities at which the drug is
produced to assess compliance with current Good Manufacturing Practice (“cGMP”) requirements to assure
that the facilities, methods and controls are adequate to preserve the drug’s identity, strength, quality and
purity, and of selected clinical investigation sites to assess compliance with GCP; and
● FDA review and approval of the NDA or BLA to permit commercial marketing of the product for particular
indications for use in the United States.
Once a pharmaceutical candidate is identified for development, it enters the preclinical testing stage. Preclinical
tests include laboratory evaluations of product chemistry, toxicity and formulation, as well as animal studies. An IND
sponsor must submit the results of the preclinical tests, together with manufacturing information and analytical data, to the
FDA as part of the IND. The sponsor will also include a protocol detailing, among other things, the objectives of the first
phase of the clinical trial, the parameters to be used in monitoring safety, and the effectiveness criteria to be evaluated, if
the first phase lends itself to an efficacy evaluation. Some preclinical testing may continue even after the IND is submitted.
The IND automatically becomes effective 30 days after receipt by the FDA, unless the FDA, within the 30-day time period,
places the clinical trial on a clinical hold. In such a case, the IND sponsor and the FDA must resolve any outstanding
concerns before the clinical trial can begin. Clinical holds also may be imposed by the FDA at any time before or during
clinical trials due to safety concerns about on-going or proposed clinical trials or non-compliance with specific FDA
requirements, and the trials may not begin or continue until the FDA notifies the sponsor that the hold has been lifted. All
clinical trials must be conducted under the supervision of one or more qualified investigators in accordance with GCP
regulations. They must be conducted under protocols detailing the objectives of the trial, dosing procedures, subject
selection and exclusion criteria and the safety and effectiveness criteria to be evaluated. Each protocol must be submitted to
the FDA as part of the IND, and timely safety reports must be submitted to the FDA and the investigators for serious and
unexpected adverse events. An IRB at each institution participating in the clinical trial must review and approve each
protocol before a clinical trial commences at that institution and must also approve the information regarding the trial and
the consent form that must be provided to each trial subject or his or her legal representative, monitor the study until
completed and otherwise comply with IRB regulations.
Human clinical trials are typically conducted in three sequential phases that may overlap or be combined:
● Phase 1: The product candidate is initially introduced into healthy human subjects and tested for safety,
dosage tolerance, absorption, metabolism, distribution and excretion. In the case of some products for severe
or life-threatening diseases, such as cancer, especially when the product may be too inherently toxic to
ethically administer to healthy volunteers, the initial human testing is often conducted in patients. Sponsors
sometimes designate their Phase 1 trials as Phase 1a or Phase 1b. Phase 1b trials are typically aimed at
confirming dosing, pharmacokinetics and safety in larger number of patients. Some Phase 1b studies evaluate
biomarkers or surrogate markers that may be associated with efficacy in patients with specific types of
diseases.
● Phase 2: The product candidate is evaluated in a limited patient population to identify possible adverse
effects and safety risks, to preliminarily evaluate the efficacy of the product for specific targeted diseases and
to determine dosage tolerance and appropriate dosage.
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● Phase 3: The product candidate is administered to an expanded patient population to provide statistically
significant evidence of clinical efficacy and further test for safety, generally at geographically dispersed
clinical study sites. These clinical trials are intended to establish the overall risk-benefit ratio of the product
candidate and provide, if appropriate, an adequate basis for product labeling.
Post-approval trials, sometimes referred to as Phase 4 studies, may be conducted after initial marketing approval.
These trials are used to gain additional experience from the treatment of patients in the intended therapeutic indication. In
certain instances, the FDA may mandate the performance of Phase 4 clinical trials as a condition of approval of an NDA or
BLA.
The FDA or the sponsor may suspend a clinical trial at any time on various grounds, including a finding that the
research subjects or patients are being exposed to an unacceptable health risk. Similarly, an IRB can suspend or terminate
approval of a clinical trial at its institution if the clinical trial is not being conducted in accordance with the IRB’s
requirements or if the drug has been associated with unexpected serious harm to patients. In addition, some clinical trials
are overseen by an independent group of qualified experts organized by the sponsor, known as a data safety monitoring
board or committee. Depending on its charter, this group may determine whether a trial may move forward at designated
check points based on access to certain data from the trial.
During the development of a new drug or biologic, sponsors are given opportunities to meet with the FDA at
certain points. These points may be prior to submission of an IND, at the end of Phase 2, and before an NDA or BLA is
submitted. Meetings at other times may be requested. These meetings can provide an opportunity for the sponsor to share
information about the data gathered to date, for the FDA to provide advice, and for the sponsor and the FDA to reach
agreement on the next phase of development. Sponsors typically use the meetings at the end of the Phase 2 trial to discuss
Phase 2 clinical results and present plans for the pivotal Phase 3 clinical trial that they believe will support approval of the
new drug or biologic.
Concurrent with clinical trials, companies usually complete additional animal studies and must also develop
additional information about the chemistry and physical characteristics of the drug and finalize a process for manufacturing
the product in commercial quantities in accordance with cGMP requirements. The manufacturing process must be capable
of consistently producing quality batches of the product candidate and, among other things, the manufacturer must develop
methods for testing the identity, strength, quality and purity of the final drug. In addition, appropriate packaging must be
selected and tested and stability studies must be conducted to demonstrate that the product candidate does not undergo
unacceptable deterioration over its shelf life. While the IND is active and before approval, progress reports summarizing
the results of the clinical trials and nonclinical studies performed since the last progress report must be submitted at least
annually to the FDA, and written IND safety reports must be submitted to the FDA and investigators for serious and
unexpected suspected adverse events, findings from other studies suggesting a significant risk to humans exposed to the
same or similar drugs, findings from animal or in vitro testing suggesting a significant risk to humans, and any clinically
important increased incidence of a serious suspected adverse reaction compared to that listed in the protocol or investigator
brochure.
There are also requirements governing the reporting of ongoing clinical trials and completed trial results to public
registries. Sponsors of certain clinical trials of FDA-regulated products are required to register and disclose specified
clinical trial information, which is publicly available at www.clinicaltrials.gov.
United States Review and Approval Process
Assuming successful completion of all required testing in accordance with all applicable regulatory requirements,
the results of product development, preclinical and other non-clinical studies and clinical trials, along with descriptions of
the manufacturing process, analytical tests conducted on the chemistry of the drug, proposed labeling and other relevant
information are submitted to the FDA as part of an NDA or BLA requesting approval to market the product. The
submission of an NDA or BLA is subject to the payment of user fees; a waiver of such fees may be obtained under certain
limited circumstances.
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Within 60 days following submission of the application, the FDA reviews all NDAs and BLAs submitted to
ensure that they are sufficiently complete for substantive review before it accepts them for filing. The FDA may request
additional information rather than accept an NDA or BLA for filing. In this event, the NDA or BLA must be resubmitted
with the additional information. The resubmitted application also is subject to review before the FDA accepts it for filing.
Once the submission is accepted for filing, the FDA begins an in depth substantive review. The FDA reviews an
NDA to determine, among other things, whether a product is safe and effective for its intended use and whether its
manufacturing is cGMP compliant to assure and preserve the product’s identity, strength, quality and purity. The FDA
reviews a BLA to determine, among other things whether the product is safe, pure and potent and the facility in which it is
manufactured, processed, packed or held meets standards designed to assure the product’s continued safety, purity and
potency. Before approving an NDA or BLA, the FDA will inspect the facility or facilities where the product is
manufactured. The FDA may refer the NDA or BLA to an advisory committee for review, evaluation and recommendation
as to whether the application should be approved and under what conditions. The FDA is not bound by the
recommendation of an advisory committee, but it generally follows such recommendations. The approval process is
lengthy and often difficult, and the FDA may refuse to approve an NDA or BLA if the applicable regulatory criteria are not
satisfied or may require additional clinical or other data and information. Even if such data and information are submitted,
the FDA may ultimately decide that the NDA or BLA does not satisfy the criteria for approval.
After the FDA evaluates an NDA or BLA, it will issue an approval letter or a Complete Response Letter. An
approval letter authorizes commercial marketing of the drug with prescribing information for specific indications. A
Complete Response Letter indicates that the review cycle of the application is complete and the application will not be
approved in its present form. A Complete Response Letter usually describes the specific deficiencies in the NDA or BLA
identified by the FDA and may require additional clinical data, such as an additional pivotal Phase 3 trial or other
significant and time-consuming requirements related to clinical trials, nonclinical studies or manufacturing. If a Complete
Response Letter is issued, the sponsor must resubmit the NDA or BLA, addressing all of the deficiencies identified in the
letter, or withdraw the application. Even if such data and information are submitted, the FDA may decide that the NDA or
BLA does not satisfy the criteria for approval. If a product receives regulatory approval, the approval may be significantly
limited to specific diseases and dosages or the indications for use may otherwise be limited, which could restrict the
commercial value of the product. In addition, the FDA may require a sponsor to conduct Phase 4 testing, which involves
clinical trials designed to further assess a drug’s safety and effectiveness after NDA or BLA approval, and may require
testing and surveillance programs to monitor the safety of approved products which have been commercialized. The FDA
may also place other conditions on approval including the requirement for a risk evaluation and mitigation strategy
(“REMS”) to assure the safe use of the drug. If the FDA concludes a REMS is needed, the sponsor of the NDA must
submit a proposed REMS. The FDA will not approve the NDA without an approved REMS, if required. A REMS could
include medication guides, physician communication plans or elements to assure safe use, such as restricted distribution
methods, patient registries and other risk minimization tools. Any of these limitations on approval or marketing could
restrict the commercial promotion, distribution, prescription or dispensing of products. Marketing approval may be
withdrawn for non-compliance with regulatory requirements or if problems occur following initial marketing.
The Food and Drug Administration Safety and Innovation Act (“FDASIA”) made permanent the Pediatric
Research Equity Act (“PREA”), which requires a sponsor to conduct pediatric clinical trials for most drugs and biologics,
for a new active ingredient, new indication, new dosage form, new dosing regimen or new route of administration. Under
PREA, original NDAs, BLAs and supplements thereto must contain a pediatric assessment unless the sponsor has received
a deferral or waiver. The required assessment must evaluate the safety and effectiveness of the product for the claimed
indications in all relevant pediatric subpopulations and support dosing and administration for each pediatric subpopulation
for which the product is safe and effective. The sponsor or FDA may request a deferral of pediatric clinical trials for some
or all of the pediatric subpopulations. A deferral may be granted for several reasons, including a finding that the drug or
biologic is ready for approval for use in adults before pediatric clinical trials are complete or that additional safety or
effectiveness data needs to be collected before the pediatric clinical trials begin. The FDA must send a non-compliance
letter to any sponsor that fails to submit the required assessment, keep a deferral current or fails to submit a request for
approval of a pediatric formulation.
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Orphan Drug Designation
Under the Orphan Drug Act, the FDA may grant orphan designation to a drug or biologic intended to treat a rare
disease or condition, which is a disease or condition that affects fewer than 200,000 individuals in the United States or, if it
affects more than 200,000 individuals in the United States, there is no reasonable expectation that the cost of developing
and making a drug or biologic product available in the United States for this type of disease or condition will be recovered
from sales of the product. Orphan designation must be requested before submitting an NDA or BLA. After the FDA grants
orphan designation, the identity of the therapeutic agent and its potential orphan use are disclosed publicly by the FDA.
Orphan designation does not convey any advantage in or shorten the duration of the regulatory review and approval
process.
If a product that has orphan designation subsequently receives the first FDA approval for the disease or condition
for which it has such designation, the product is entitled to orphan product exclusivity, which means that the FDA may not
approve any other applications to market the same drug or biological product for the same indication for seven years,
except in limited circumstances, such as a showing of clinical superiority to the product with orphan exclusivity or inability
to manufacture the product in sufficient quantities. The designation of such drug or biologic also entitles a party to
financial incentives such as opportunities for grant funding towards clinical trial costs, tax advantages and user-fee waivers.
However, competitors may receive approval of different products for the indication for which the orphan product has
exclusivity or obtain approval for the same product but for a different indication for which the orphan product has
exclusivity. Orphan exclusivity also could block the approval of a product candidate for seven years if a competitor obtains
approval of the same drug or biologic as defined by the FDA or if such product candidate is determined to be contained
within the competitor’s product for the same indication or disease. If an orphan designated product receives marketing
approval for an indication broader than what is designated, it may not be entitled to orphan exclusivity. Orphan drug status
in the European Union has similar but not identical benefits in that jurisdiction.
Expedited Development and Review Programs
The FDA has a Fast Track program that is intended to expedite or facilitate the process for reviewing product
candidates that meet certain criteria. Specifically, new drugs and biologics are eligible for Fast Track designation if they are
intended to treat a serious or life-threatening disease or condition and nonclinical or clinical data demonstrate the potential
to address unmet medical needs for the disease or condition. Fast Track designation applies to the combination of the
product candidate and the specific indication for which it is being studied. The FDA may consider for review sections of
the NDA or BLA for a Fast Track review designation on a rolling basis before the complete application is submitted, if the
sponsor provides a schedule for the submission of the sections of the NDA or BLA, the FDA agrees to accept sections of
the NDA or BLA and determines that the schedule is acceptable, and the sponsor pays any required user fees upon
submission of the first section of the NDA or BLA.
Any product candidate submitted to the FDA for approval, including a product candidate with a Fast Track
designation, may also be eligible for other types of FDA programs intended to expedite development and review, such as
priority review and accelerated approval. A product candidate is eligible for priority review if it is designed to treat a
serious condition, and if approved, would provide a significant improvement in safety or effectiveness compared to
marketed products. The FDA will attempt to direct additional resources to the evaluation of an application designated for
priority review in an effort to facilitate the review. The FDA endeavors to review applications with priority review
designations within six months of the filing date as compared to ten months for review of original BLAs and new
molecular entity NDAs under its standard review goals.
In addition, a product candidate may be eligible for accelerated approval. Drug and biologic product candidates
intended to treat serious or life-threatening diseases or conditions may be eligible for accelerated approval upon a
determination that the product candidate has an effect on a surrogate endpoint that is reasonably likely to predict clinical
benefit, or on a clinical endpoint that can be measured earlier than irreversible morbidity or mortality, that is reasonably
likely to predict an effect on irreversible morbidity or mortality or other clinical benefit, taking into account the severity,
rarity, or prevalence of the condition and the availability or lack of alternative treatments. As a condition of approval, the
FDA may require that a sponsor of a drug or biologic receiving accelerated approval perform adequate and well-controlled
post-marketing clinical trials. A product receiving accelerated approval may be subjected to expedited
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withdrawal procedures if the sponsor fails to conduct any required post-marketing trials in a timely manner, or if such trials
fail to verify the predicted clinical benefit. In addition, the FDA currently requires as a condition for accelerated approval
pre-approval of promotional materials, which could adversely impact the timing of the commercial launch of the product.
FDASIA established a category of drugs and biologics referred to as “breakthrough therapies” that may be eligible
to receive Breakthrough Therapy designation. A sponsor may seek FDA designation of a drug or biologic candidate as a
“breakthrough therapy” if the product is intended, alone or in combination with one or more other products, to treat a
serious or life-threatening disease or condition and preliminary clinical evidence indicates that the product may
demonstrate substantial improvement over existing therapies on one or more clinically significant endpoints, such as
substantial treatment effects observed early in clinical development. The designation includes all of the Fast Track program
features, as well as more intensive FDA interaction and guidance. The Breakthrough Therapy designation is a distinct
status from both accelerated approval and priority review, which can also be granted to the same drug if relevant criteria are
met. If a product is designated as breakthrough therapy, the FDA will expedite the development and review of such drug.
All requests for breakthrough therapy designation will be reviewed within 60 days of receipt, and the FDA will either grant
or deny the request.
Fast Track designation, Breakthrough Therapy designation, priority review and accelerated approval do not
change the standards for approval but may expedite the development or approval process.
Post-approval requirements
Once an approval is granted, the FDA may withdraw the approval if compliance with regulatory standards is not
maintained or if problems occur after the product reaches the market. Later discovery of previously unknown problems
with a product may result in restrictions on the product or even complete withdrawal of the product from the market. After
approval, some types of changes to the approved product, such as adding new indications, certain manufacturing changes
and additional labeling claims, are subject to further FDA review and approval. Drug and biologics manufacturers and
other entities involved in the manufacture and distribution of approved drugs and biologics are required to register their
establishments with the FDA and certain state agencies, and are subject to periodic unannounced inspections by the FDA
and certain state agencies for compliance with cGMP regulations and other laws and regulations.
Any drug products manufactured or distributed by us or our partners pursuant to FDA approvals will be subject to
continuing regulation by the FDA, including, among other things, record-keeping requirements, reporting of adverse
experiences with the drug, providing the FDA with updated safety and efficacy information, drug sampling and distribution
requirements, complying with certain electronic records and signature requirements, and complying with FDA promotion
and advertising requirements. The FDA strictly regulates labeling, advertising, promotion and other types of information
on products that are placed on the market and imposes requirements and restrictions on drug and biologics manufacturers,
such as those related to direct-to-consumer advertising, the prohibition on promoting products for uses or in patient
populations that are not described in the product’s approved labeling (known as “off-label use”), industry-sponsored
scientific and educational activities, and promotional activities involving the internet. Discovery of previously unknown
problems or the failure to comply with the applicable regulatory requirements may result in restrictions on the marketing of
a product or withdrawal of the product from the market as well as possible civil or criminal sanctions. Failure to comply
with the applicable U.S. requirements at any time during the product development process, approval process or after
approval, may subject an applicant or manufacturer to administrative or judicial civil or criminal sanctions and adverse
publicity. FDA sanctions could include refusal to approve pending applications, withdrawal of an approval, clinical hold,
warning or untitled letters, product recalls, product seizures, total or partial suspension of production or distribution,
injunctions, fines, refusals of government contracts, mandated corrective advertising or communications with doctors,
debarment, restitution, disgorgement of profits, or civil or criminal penalties.
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Patent Term Restoration and Marketing Exclusivity
Depending upon the timing, duration and specifics of FDA approval of our product candidates, some of the U.S.
patents that we may be granted in the future may be eligible for limited patent term extension under the Drug Price
Competition and Patent Term Restoration Act of 1984, referred to as the Hatch-Waxman Amendments. The Hatch-
Waxman Amendments permit a patent restoration term of up to five years as compensation for patent term lost during
product development and the FDA regulatory review process. However, patent term restoration cannot extend the
remaining term of a patent beyond a total of 14 years from the product’s approval date. The patent term restoration period
is generally one-half the time between the effective date of an IND and the submission date of an NDA or BLA, plus the
time between the submission date of an NDA or BLA and the approval of that application, less any time the applicant did
not act with due diligence. Only one patent applicable to an approved drug is eligible for the extension, and the extension
must be applied for prior to expiration of the patent. The United States Patent and Trademark Office, in consultation with
the FDA, reviews and approves the application for any patent term extension or restoration. In the future, we intend to
apply for restorations of patent term for patents that may be issued to us, depending on the expected length of clinical trials
and other factors involved in the filing of the relevant marketing application.
Market exclusivity provisions under the FDCA can also delay the submission or the approval of certain marketing
applications. The FDCA provides a five-year period of non-patent marketing exclusivity within the United States to the
first applicant to obtain approval of an NDA for a new chemical entity. A drug is a new chemical entity if the FDA has not
previously approved any other new drug containing the same active moiety, which is the molecule or ion responsible for
the action of the drug substance. During the exclusivity period, the FDA may not approve or even accept for review an
abbreviated new drug application (“ANDA”) or a NDA submitted under Section 505(b)(2), or 505(b)(2) NDA, submitted
by another company for another drug based on the same active moiety, regardless of whether the drug is intended for the
same indication as the original innovative drug or for another indication, where the applicant does not own or have a legal
right of reference to all the data required for approval. However, an application may be submitted after four years if it
contains a certification of patent invalidity or non-infringement to one of the patents listed with the FDA by the innovator
NDA holder. The FDCA alternatively provides three years of marketing exclusivity for an NDA, or supplement to an
existing NDA if new clinical investigations, other than bioavailability studies, that were conducted or sponsored by the
applicant are deemed by the FDA to be essential to the approval of the application, for example new indications, dosages or
strengths of an existing drug. This three-year exclusivity covers only the modification for which the drug received approval
on the basis of the new clinical investigations and does not prohibit the FDA from approving ANDAs or 505(b)(2) NDAs
for drugs containing the active agent for the original indication or condition of use. Five-year and three-year exclusivity
will not delay the submission or approval of a full NDA. However, an applicant submitting a full NDA would be required
to conduct or obtain a right of reference to all of the preclinical studies and adequate and well-controlled clinical trials
necessary to demonstrate safety and effectiveness.
Pediatric exclusivity is a type of marketing exclusivity available in the United States. Pediatric exclusivity under
the Best Pharmaceuticals for Children Act provides for an additional six months of marketing exclusivity if a sponsor
conducts clinical trials in children in response to a written request from the FDA. If such written request does not include
clinical trials in neonates, the FDA is required to include its rationale for not requesting those clinical trials. The FDA may
request studies on approved or unapproved indications in separate written requests. The issuance of a written request does
not require the sponsor to undertake the described clinical trials. In addition, orphan drug exclusivity, as described above,
may offer a seven-year period of marketing exclusivity, except in certain circumstances.
Biosimilars and Exclusivity
The Affordable Care Act includes a subtitle called the Biologics Price Competition and Innovation Act of 2009
(“BPCIA”), which created an abbreviated approval pathway for biological products that are biosimilar to or
interchangeable with an FDA-licensed reference biological product. The FDA has issued several guidance documents
outlining an approach to review and approval of biosimilars.
Biosimilarity, which requires that there be no clinically meaningful differences between the biological product and
the reference product in terms of safety, purity, and potency, can be shown through analytical studies, animal studies, and a
clinical study or studies. Interchangeability requires that a product is biosimilar to the reference product
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and the product must demonstrate that it can be expected to produce the same clinical results as the reference product in
any given patient and, for products that are administered multiple times to an individual, the biologic and the reference
biologic may be alternated or switched after one has been previously administered without increasing safety risks or risks
of diminished efficacy relative to exclusive use of the reference biologic. However, complexities associated with the larger,
and often more complex, structures of biological products, as well as the processes by which such products are
manufactured, pose significant hurdles to implementation of the abbreviated approval pathway that are still being
addressed by the FDA.
Under the BPCIA, an application for a biosimilar product may not be submitted to the FDA until four years
following the date that the reference product was first licensed by the FDA. In addition, the approval of a biosimilar
product may not be made effective by the FDA until twelve years from the date on which the reference product was first
licensed. During this twelve-year period of exclusivity, another company may still market a competing version of the
reference product if the FDA approves a full BLA for the competing product containing the sponsor’s own preclinical data
and data from adequate and well-controlled clinical trials to demonstrate the safety, purity and potency of their product.
The BPCIA also created certain exclusivity periods for biosimilars approved as interchangeable products. At this juncture,
it is unclear whether products deemed “interchangeable” by the FDA will, in fact, be readily substituted by pharmacies,
which are governed by state pharmacy law.
The BPCIA is complex and continues to be interpreted and implemented by the FDA. In addition, recent
government proposals have sought to reduce the twelve-year reference product exclusivity period. Other aspects of the
BPCIA, some of which may impact the BPCIA exclusivity provisions, have also been the subject of recent litigation. As a
result, the ultimate impact, implementation and meaning of the BPCIA is subject to significant uncertainty.
FDA Regulation of Companion Diagnostics
We expect that certain of our product candidates may require an in vitro diagnostic to identify appropriate patient
populations for our product candidates. These diagnostics, often referred to as companion diagnostics, are regulated as
medical devices. In the United States, the FDCA and its implementing regulations, and other federal and state statutes and
regulations govern, among other things, medical device design and development, preclinical and clinical testing, premarket
clearance or approval, registration and listing, manufacturing, labeling, storage, advertising and promotion, sales and
distribution, export and import, and post-market surveillance. Unless an exemption applies, diagnostic tests require
marketing clearance or approval from the FDA prior to commercial distribution. The two primary types of FDA marketing
authorization applicable to a medical device are premarket notification, also called 510(k) clearance, and premarket
approval (“PMA”). We expect that any companion diagnostic developed for our product candidates will utilize the PMA
pathway.
If use of companion diagnostic is essential to safe and effective use of a drug or biologic product, then the FDA
generally will require approval or clearance of the diagnostic contemporaneously with the approval of the therapeutic
product. On August 6, 2014, the FDA issued a final guidance document addressing the development and approval process
for “In Vitro Companion Diagnostic Devices.” According to the guidance, for novel product candidates, a companion
diagnostic device and its corresponding drug candidate should be approved or cleared contemporaneously by FDA for the
use indicated in the therapeutic product labeling. The guidance also explains that a companion diagnostic device used to
make treatment decisions in clinical trials of a drug generally will be considered an investigational device, unless it is
employed for an intended use for which the device is already approved or cleared. If used to make critical treatment
decisions, such as patient selection, the diagnostic device generally will be considered a significant risk device under the
FDA’s Investigational Device Exemption (“IDE”) regulations. Thus, the sponsor of the diagnostic device will be required
to comply with the IDE regulations. According to the guidance, if a diagnostic device and a drug are to be studied together
to support their respective approvals, both products can be studied in the same investigational study, if the study meets both
the requirements of the IDE regulations and the IND regulations. The guidance provides that depending on the details of
the study plan and subjects, a sponsor may seek to submit an IND alone, or both an IND and an IDE.
The FDA has generally required companion diagnostics intended to select the patients who will respond to cancer
treatment to obtain approval of a PMA for that diagnostic simultaneously with approval of the therapeutic. The
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PMA process, including the gathering of clinical and preclinical data and the submission to and review by the FDA, can
take several years or longer. It involves a rigorous premarket review during which the applicant must prepare and provide
the FDA with reasonable assurance of the device’s safety and effectiveness and information about the device and its
components regarding, among other things, device design, manufacturing and labeling. In addition, PMAs for certain
devices must generally include the results from extensive preclinical and adequate and well-controlled clinical trials to
establish the safety and effectiveness of the device for each indication for which FDA approval is sought. In particular, for
a diagnostic, the applicant must demonstrate that the diagnostic produces reproducible results when the same sample is
tested multiple times by multiple users at multiple laboratories. As part of the PMA review, the FDA will typically inspect
the manufacturer’s facilities for compliance with the Quality System Regulation (“QSR”),which imposes elaborate testing,
control, documentation and other quality assurance requirements.
If the FDA evaluations of both the PMA application and the manufacturing facilities are favorable, the FDA will
either issue an approval letter or an approvable letter, which usually contains a number of conditions that must be met in
order to secure the final approval of the PMA, such as changes in labeling, or specific additional information, such as
submission of final labeling, in order to secure final approval of the PMA. If the FDA concludes that the applicable criteria
have been met, the FDA will issue a PMA for the approved indications, which can be more limited than those originally
sought by the applicant. The PMA can include post-approval conditions that the FDA believes necessary to ensure the
safety and effectiveness of the device, including, among other things, restrictions on labeling, promotion, sale and
distribution.
If the FDA’s evaluation of the PMA or manufacturing facilities is not favorable, the FDA will deny approval of
the PMA or issue a not approvable letter. A not approvable letter will outline the deficiencies in the application and, where
practical, will identify what is necessary to make the PMA approvable. The FDA may also determine that additional
clinical trials are necessary, in which case the PMA approval may be delayed for several months or years while the trials
are conducted and then the data submitted in an amendment to the PMA. Once granted, PMA approval may be withdrawn
by the FDA if compliance with post approval requirements, conditions of approval or other regulatory standards is not
maintained or problems are identified following initial marketing. PMA approval is not guaranteed, and the FDA may
ultimately respond to a PMA submission with a not approvable determination based on deficiencies in the application and
require additional clinical trial or other data that may be expensive and time-consuming to generate and that can
substantially delay approval.
After a device is placed on the market, it remains subject to significant regulatory requirements. Medical devices
may be marketed only for the uses and indications for which they are cleared or approved. Device manufacturers must also
establish registration and device listings with the FDA. A medical device manufacturer’s manufacturing processes and
those of its suppliers are required to comply with the applicable portions of the QSR, which cover the methods and
documentation of the design, testing, production, processes, controls, quality assurance, labeling, packaging and shipping
of medical devices. Domestic facility records and manufacturing processes are subject to periodic unscheduled inspections
by the FDA. The FDA also may inspect foreign facilities that export products to the United States.
Government Regulation Outside of the United States
In addition to regulations in the United States, we will be subject to a variety of regulations in other jurisdictions
governing, among other things, clinical studies and any commercial sales and distribution of our product candidates.
Whether or not we obtain FDA approval for a product candidate, we must obtain the requisite approvals from
regulatory authorities in foreign countries prior to the commencement of clinical studies or marketing of the product
candidates in those countries. The requirements and process governing the conduct of clinical studies, product licensing,
pricing and reimbursement vary from country to country. Failure to comply with applicable foreign regulatory
requirements, may be subject to, among other things, fines, suspension or withdrawal of regulatory approvals, product
recalls, seizure of products, operating restrictions and criminal prosecution.
Clinical Trials
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Certain countries outside of the United States have a similar process that requires the submission of a clinical
study application much like the IND prior to the commencement of human clinical studies. In the European Union (“EU”),
for example, a clinical trial authorization (“CTA”) must be submitted to each country’s national health authority and an
independent ethics committee, much like the FDA and the IRB, respectively. Once the CTA is approved by the national
health authority and the ethics committee has granted a positive opinion in relation to the conduct of the trial in the relevant
member state(s),in accordance with a country’s requirements, clinical study development may proceed.
The CTA must include, among other things, a copy of the trial protocol and an investigational medicinal product
dossier containing information about the manufacture and quality of the medicinal product under investigation. Currently,
CTAs must be submitted to the competent authority in each EU member state in which the trial will be conducted. Under
the new Regulation on Clinical Trials, which is currently expected to take effect by early 2022, there will be a centralized
application procedure where one national authority takes the lead in reviewing the application and the other national
authorities have only limited involvement. Any substantial changes to the trial protocol or other information submitted with
the CTA must be notified to or approved by the relevant competent authorities and ethics committees. Medicines used in
clinical trials must be manufactured in accordance with GMP. Other national and European Union-wide regulatory
requirements may also apply.
Clinical studies of medicinal products in the European Union must be conducted in accordance with EU and
national regulations and the International Conference on Harmonization (“ICH”) guidelines on GCP as well as the
applicable regulatory requirements and the ethical principles that have their origin in the Declaration of Helsinki. If the
sponsor of the clinical trial is not established within the EU, it must appoint an EU entity to act as its legal representative.
The sponsor must take out a clinical trial insurance policy, and in most EU countries, the sponsor is liable to provide ‘no
fault’ compensation to any study subject injured in the clinical trial.
Marketing Authorizations
To obtain regulatory approval of an investigational medicinal product under European Union regulatory systems,
we must submit a marketing authorization application. The application used to file the NDA or BLA in the United States is
similar to that required in the European Union, with the exception of, among other things, country-specific document
requirements. The process for doing this depends, among other things, on the nature of the medicinal product.
The centralized procedure results in a single marketing authorization, issued by the European Commission, based
on the opinion of the EMA’s Committee for Human Medicinal Products (“CHMP”), which is valid across the entire
territory of the EU. The centralized procedure is compulsory for human medicines that are: (i) derived from biotechnology
processes, such as genetic engineering, (ii) contain a new active substance indicated for the treatment of certain diseases,
such as HIV/AIDS, cancer, diabetes, neurodegenerative diseases, autoimmune and other immune dysfunctions and viral
diseases, (iii) designated orphan medicines and (iv) advanced therapy medicinal products, or ATMPs, such as gene therapy,
somatic cell therapy or tissue-engineered medicines. The centralized procedure may at the request of the applicant also be
used in certain other cases. It is likely that the centralized procedure would apply to the products we are developing.
Under the centralized procedure, the maximum timeframe for the evaluation of a MAA by the EMA is 210 days.
In exceptional cases, the CHMP might perform an accelerated review of a marketing authorization in no more than 150
days (not including clock stops). Innovative products that target an unmet medical need and are expected to be of major
public health interest may be eligible for a number of expedited development and review programs, such as the PRIME
scheme, which provides incentives similar to the breakthrough therapy designation in the U.S. PRIME is a voluntary
scheme aimed at enhancing the EMA’s support for the development of medicines that target unmet medical needs. It is
based on increased interaction and early dialogue with companies developing promising medicines, to optimize their
product development plans and speed up their evaluation to help them reach patients earlier. Product developers that
benefit from PRIME designation can expect to be eligible for accelerated assessment but this is not guaranteed. The
benefits of a PRIME designation include the appointment of a CHMP rapporteur before submission of a marketing
authorization application, early dialogue and scientific advice at key development milestones, and the potential to qualify
products for accelerated review earlier in the application process.
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MAs have an initial duration of five years. After these five years, the authorization may be renewed for an
unlimited period on the basis of a reevaluation of the risk-benefit balance.
Data and Marketing Exclusivity
The European Union also provides opportunities for market exclusivity. Upon receiving marketing authorization,
new chemical entities generally receive eight years of data exclusivity and an additional two years of market exclusivity. If
granted, data exclusivity prevents regulatory authorities in the European Union from referencing the innovator’s data to
assess a generic or biosimilar application. During the additional two-year period of market exclusivity, a generic or
biosimilar marketing authorization application can be submitted, and the innovator’s data may be referenced, but no
generic or biosimilar product can be marketed until the expiration of the market exclusivity. . The overall ten-year market
exclusivity period may be extended to a maximum of eleven years if, during the first eight years a new therapeutic
indication with significant clinical benefit over existing therapies is approved. However, there is no guarantee that a
product will be considered by the European Union’s regulatory authorities to be a new chemical entity, and products may
not qualify for data exclusivity.
Orphan Medicinal Products
The criteria for designating an “orphan medicinal product” in the European Union are similar in principle to those
in the United States. A medicinal product may be designated as orphan if (1) it is intended for the diagnosis, prevention or
treatment of a life-threatening or chronically debilitating condition; (2) either (a) such condition affects no more than five
in 10,000 persons in the European Union when the application is made, or (b) the product, without the benefits derived
from orphan status, would not generate sufficient return in the European Union to justify investment; and (3) there exists
no satisfactory method of diagnosis, prevention or treatment of such condition authorized for marketing in the European
Union, or if such a method exists, the product will be of significant benefit to those affected by the condition. The
application for orphan drug designation must be submitted before the application for marketing authorization. Orphan
medicinal products are eligible for financial incentives such as reduction of fees or fee waivers and are, upon grant of a
marketing authorization, entitled to ten years of market exclusivity for the approved therapeutic indication. During the ten-
year market exclusivity period, the EMA cannot accept a marketing authorization application for the same indication, in
respect of a similar medicinal product. An orphan product can also obtain an additional two years of market exclusivity in
the European Union for pediatric studies. No extension to any supplementary protection certificate can be granted on the
basis of pediatric studies for orphan indications. Orphan drug designation does not convey any advantage in, or shorten the
duration of, the regulatory review and approval process.
The 10-year market exclusivity may be reduced to six years if, at the end of the fifth year, it is established that the
product no longer meets the criteria for orphan designation, for example, if the product is sufficiently profitable not to
justify maintenance of market exclusivity. In addition, marketing authorization may be granted to a similar product for the
same indication at any time if (1) the second applicant can establish that its product, although similar, is safer, more
effective or otherwise clinically superior; (2) the applicant consents to a second orphan medicinal product application; or
(3) the applicant cannot supply enough orphan medicinal product.
Post-Approval Requirements
Similar to the United States, both marketing authorization holders and manufacturers of medicinal products are
subject to comprehensive regulatory oversight by the EMA, the European Commission and/or the competent regulatory
authorities of the member states. The holder of a marketing authorization must establish and maintain a pharmacovigilance
system and appoint an individual qualified person for pharmacovigilance who is responsible for oversight of that system.
Key obligations include expedited reporting of suspected serious adverse reactions and submission of periodic safety
update reports, or PSURs.
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All new marketing authorization applications must include a risk management plan, or RMP, describing the
risk management system that the company will put in place and documenting measures to prevent or minimize the risks
associated with the product. The regulatory authorities may also impose specific obligations as a condition of the marketing
authorization. Such risk-minimization measures or post-authorization obligations may include additional safety monitoring,
more frequent submission of PSURs, or the conduct of additional clinical trials or post-authorization safety studies.
The advertising and promotion of medicinal products is also subject to laws concerning promotion of
medicinal products, interactions with physicians, misleading and comparative advertising and unfair commercial practices.
All advertising and promotional activities for the product must be consistent with the approved summary of product
characteristics, and therefore all off-label promotion is prohibited. Direct-to-consumer advertising of prescription
medicines is also prohibited in the EU. Although general requirements for advertising and promotion of medicinal products
are established under EU directives, the details are governed by regulations in each member state and can differ from one
country to another.
Failure to comply with EU and member state laws that apply to the conduct of clinical trials, manufacturing
approval, marketing authorization of medicinal products and marketing of such products, both before and after grant of the
MA, manufacturing of pharmaceutical products, statutory health insurance, bribery and anti-corruption or with other
applicable regulatory requirements may result in administrative, civil or criminal penalties. These penalties could include
delays or refusal to authorize the conduct of clinical trials, or to grant marketing authorizations, product withdrawals and
recalls, product seizures, suspension, withdrawal or variation of the marketing authorization, total or partial suspension of
production, distribution, manufacturing or clinical trials, operating restrictions, injunctions, suspension of licenses, fines
and criminal penalties.
Approval and Regulation of Companion Diagnostics
In the EU, in vitro diagnostic medical devices are regulated by Directive 98/79/EC which regulates the placing on
the market, the CE-marking, the essential requirements, the conformity assessment procedures, the registration obligations
for manufactures and devices as well as the vigilance procedure. In vitro diagnostic medical devices must comply with the
requirements provided for in the Directive, and with further requirements implemented at national level (as the case may
be).
The regulation of companion diagnostics will be subject to further requirements as of the entry into force of the in-
vitro diagnostic devices Regulation (No 2017/746) which introduces a new classification system for companion diagnostics
which are now specifically defined as diagnostic tests that support the safe and effective use of a specific medicinal
product, by identifying patients that are suitable or unsuitable for treatment. Companion diagnostics will have to undergo a
conformity assessment by a notified body. Before it can issue a CE certificate, the notified body must seek a scientific
opinion from the EMA on the suitability of the companion diagnostic to the medicinal product concerned if the medicinal
product falls exclusively within the scope of the centralized procedure for the authorization of medicines, or the medicinal
product is already authorized through the centralized procedure, or a marketing authorization application for the medicinal
product has been submitted through the centralized procedure. For other substances, the notified body can seek the opinion
from a national competent authorities or the EMA.
The aforementioned EU rules are generally applicable in the European Economic Area (“EEA”), which consists
of the 27 EU member states plus Norway, Liechtenstein and Iceland.
For other countries outside of the European Union, such as countries in Eastern Europe, Latin America or Asia,
the requirements governing the conduct of clinical studies, product licensing, pricing and reimbursement vary from country
to country. In all cases, again, the clinical studies are conducted in accordance with GCP and the applicable regulatory
requirements and the ethical principles that have their origin in the Declaration of Helsinki.
If we fail to comply with applicable foreign regulatory requirements, we may be subject to, among other things,
fines, suspension or withdrawal of regulatory approvals, product recalls, seizure of products, operating restrictions and
criminal prosecution.
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Other Healthcare Laws
In addition to FDA restrictions on marketing of pharmaceutical and biological products, other U.S. federal and
state healthcare regulatory laws restrict business practices in the pharmaceutical industry, which include, but are not limited
to, state and federal anti-kickback, fraud & abuse, false claims, price reporting, consumer fraud and physician payment
transparency laws. These laws may affect our sales, marketing and other promotional activities by limiting the kinds of
financial arrangements we may have with physicians, customers and third-party payors including discount practices,
customer support, education and training programs, physician consulting and other service arrangements. In addition,
manufacturers can be held liable under the False Claims Act even when they do not submit claims directly to government
payors if they are deemed to “cause” the submission of false or fraudulent claims by, for example, providing inaccurate
billing or coding information to customers or promoting a product off-label. These laws are broadly written, and it is often
difficult to determine precisely how these laws will be applied to specific circumstances. Such laws include:
● The federal Anti-Kickback Statute, which prohibits, among other things, any person or entity from
knowingly and willfully offering, paying, soliciting, receiving or providing any remuneration, directly or
indirectly, overtly or covertly, to induce or in return for purchasing, leasing, ordering or arranging for or
recommending the purchase, lease or order of any item or service reimbursable, in whole or in part, under
Medicare, Medicaid or other federal healthcare programs. A person or entity does not need to have actual
knowledge of the federal Anti-Kickback Statute or specific intent to violate it to have committed a violation;
● The federal false claims laws, including the False Claims Act, which prohibit any person or entity from,
among other things, knowingly presenting, or causing to be presented, a false, fictitious or fraudulent claim
for payment to, or approval by, the federal government or knowingly making, using or causing to be made or
used a false record or statement material to a false or fraudulent claim to the federal government. In addition,
the government may assert that a claim including items or services resulting from a violation of the federal
Anti-Kickback Statute constitutes a false or fraudulent claim for purposes of the False Claims Act;
● The federal Health Insurance Portability and Accountability Act of 1996 (“HIPAA”), which prohibits, among
other actions, knowingly and willfully executing, or attempting to execute, a scheme to defraud any
healthcare benefit program, including private third-party payors, knowingly and willfully embezzling or
stealing from a healthcare benefit program, willfully obstructing a criminal investigation of a healthcare
offense, and knowingly and willfully falsifying, concealing or covering up a material fact or making any
materially false, fictitious or fraudulent statement in connection with the delivery of or payment for
healthcare benefits, items or services. Similar to the federal Anti-Kickback Statute, a person or entity does
not need to have actual knowledge of the statute or specific intent to violate it to have committed a violation;
● The Physician Payments Sunshine Act, which imposed, among other things, new annual reporting
requirements for covered manufacturers for certain payments and “transfers of value” provided to physicians
(as defined by statute) and teaching hospitals, as well as ownership and investment interests held by
physicians and their immediate family members and will be expanded to include certain other healthcare
professionals in 2022 for payments made in 2021; and
● Analogous state laws and regulations, such as state anti-kickback and false claims laws, may apply to sales or
marketing arrangements and claims involving healthcare items or services reimbursed by non-governmental
third-party payors, including private insurers.
If our operations are found to be in violation of any of such laws or any other governmental regulations that apply
to us, we may be subject to penalties, including, without limitation, administrative, civil and criminal penalties, damages,
fines, disgorgement, contractual damages, reputational harm, diminished profits and future earnings, the curtailment or
restructuring of our operations, exclusion from participation in federal and state healthcare programs and
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individual imprisonment, any of which could adversely affect our ability to operate our business and our financial results.
To the extent that any of our product candidates, once approved, are sold in a foreign country, we may be subject
to similar foreign laws and regulations, which may include, for instance, applicable post-marketing requirements, including
safety surveillance, anti-fraud and abuse laws, and implementation of corporate compliance programs and reporting of
payments or other transfers of value to healthcare professionals.
Coverage and Reimbursement
Significant uncertainty exists as to the coverage and reimbursement status of any pharmaceutical or biological
product for which we obtain regulatory approval. In the United States and markets in other countries, patients who are
prescribed treatments for their conditions and providers performing the prescribed services generally rely on third-party
payors to reimburse all or part of the associated healthcare costs. Patients are unlikely to use our products unless coverage
is provided and reimbursement is adequate to cover a significant portion of the cost of our products. Sales of any product
candidates for which we receive regulatory approval for commercial sale will therefore depend, in part, on the availability
of coverage and adequate reimbursement from third-party payors. Third- party payors include government authorities,
managed care plans, private health insurers and other organizations.
The process for determining whether a third-party payor will provide coverage for a pharmaceutical or biological
product typically is separate from the process for setting the price of such product or for establishing the reimbursement
rate that the payor will pay for the product once coverage is approved. Third-party payors may limit coverage to specific
products on an approved list, also known as a formulary, which might not include all of the FDA-approved products for a
particular indication. A decision by a third-party payor not to cover our product candidates could reduce physician
utilization of our products once approved and have a material adverse effect on our sales, results of operations and financial
condition. Moreover, a third-party payor’s decision to provide coverage for a pharmaceutical or biological product does not
imply that an adequate reimbursement rate will be approved. Adequate third-party reimbursement may not be available to
enable us to maintain price levels sufficient to realize an appropriate return on our investment in product development. In
addition, coverage and reimbursement for new products can differ significantly from payor to payor. One third-party
payor’s decision to cover a particular medical product or service does not ensure that other payors will also provide
coverage for the medical product or service, or will provide coverage at an adequate reimbursement rate. As a result, the
coverage determination process will require us to provide scientific and clinical support for the use of our products to each
payor separately and will be a time consuming process.
The containment of healthcare costs has become a priority of federal, state and foreign governments, and the
prices of pharmaceutical or biological products have been a focus in this effort. Third-party payors are increasingly
challenging the prices charged for medical products and services, examining the medical necessity and reviewing the cost-
effectiveness of pharmaceutical products, biological products, medical devices and medical services, in addition to
questioning safety and efficacy. If these third-party payors do not consider our product candidates to be cost-effective
compared to other available therapies, they may not cover our products after FDA approval or, if they do, the level of
payment may not be sufficient to allow us to sell our products at a profit.
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Healthcare Reform
A primary trend in the U.S. healthcare industry and elsewhere is cost containment. Government authorities and
other third-party payors have attempted to control costs by limiting coverage and the amount of reimbursement for
particular medical products. For example, in March 2010, the Affordable Care Act, or ACA, was enacted, which, among
other things, increased the minimum Medicaid rebates owed by most manufacturers under the Medicaid Drug Rebate
Program; introduced a new methodology by which rebates owed by manufacturers under the Medicaid Drug Rebate
Program are calculated for drugs that are inhaled, infused, instilled, implanted or injected; extended the Medicaid Drug
Rebate Program to utilization of prescriptions of individuals enrolled in Medicaid managed care plans; imposed mandatory
discounts for certain Medicare Part D beneficiaries as a condition for manufacturers’ outpatient drugs coverage under
Medicare Part D; subjected drug manufacturers to new annual fees based on pharmaceutical companies’ share of sales to
federal healthcare programs, and created a new Patient Centered Outcomes Research Institute to oversee, identify priorities
in and conduct comparative clinical effectiveness research, along with funding for such research.
Since its enactment, there have been judicial, executive and Congressional legislative challenges to certain aspects
of the ACA.
For example, the Tax Cuts and Jobs Act was enacted, which, among other things, removed penalties for not
complying with the ACA’s individual mandate to carry health insurance. On December 14, 2018, a U.S. District Court
Judge in the Northern District of Texas, ruled that the individual mandate is a critical and inseverable feature of the ACA,
and therefore, because it was repealed as part of the Tax Act, the remaining provisions of the ACA are invalid as well. On
December 18, 2019, the U.S. Court of Appeals for the 5th Circuit upheld the District Court's decision that the individual
mandate was unconstitutional but remanded the case back to the District Court to determine whether the remaining
provisions of the ACA are invalid as well. The U.S. Supreme Court is currently reviewing the case, although it is unclear
how the Supreme Court will rule. It is also unclear how other efforts, if any, to challenge, replace, modify, repeal or
otherwise invalidate the ACA will impact the law or our business.
In addition, the Budget Control Act of 2011 and the Bipartisan Budget Act of 2015 led to aggregate reductions of
Medicare payments to providers of up to 2% per fiscal year that will remain in effect through 2030, with the exception of a
temporary suspension from May 1, 2020 through March 31, 2021, unless additional Congressional action is taken. On
January 2, 2013, the American Taxpayer Relief Act was signed into law, which, among other things, further reduced
Medicare payments to several types of providers, including hospitals, imaging centers and cancer treatment centers and
increased the statute of limitations period for the government to recover overpayments to providers from three to
five years.
Moreover, there has recently been heightened governmental scrutiny over the manner in which manufacturers set
prices for their marketed products, which has resulted in several Congressional inquiries and proposed and enacted
legislation designed, among other things, to bring more transparency to product pricing, review the relationship between
pricing and manufacturer patient programs and reform government program reimbursement methodologies for
pharmaceutical products. In addition, individual states in the United States have also become increasingly active in
implementing regulations designed to control pharmaceutical product pricing, including price or patient reimbursement
constraints, discounts, restrictions on certain product access and marketing cost disclosure and transparency measures and,
in some cases, mechanisms to encourage importation from other countries and bulk purchasing. Furthermore, there has
been increased interest by third party payors and governmental authorities in reference pricing systems and publication of
discounts and list prices.
Similar political, economic and regulatory developments are occurring in the EU and may affect the ability of
pharmaceutical companies to profitably commercialize their products. In addition to continuing pressure on prices and cost
containment measures, legislative developments at the EU or member state level may result in significant additional
requirements or obstacles. The delivery of healthcare in the EU, including the establishment and operation of health
services and the pricing and reimbursement of medicines, is almost exclusively a matter for national, rather than EU, law
and policy. National governments and health service providers have different priorities and approaches to the delivery of
health care and the pricing and reimbursement of products in that context. In general, however, the healthcare budgetary
constraints in most EU member states have resulted in restrictions on the pricing and reimbursement of medicines by
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relevant health service providers. Coupled with ever-increasing EU and national regulatory burdens on those wishing to
develop and market products, this could restrict or regulate post-approval activities and affect the ability of pharmaceutical
companies to commercialize their products. In international markets, reimbursement and healthcare payment systems vary
significantly by country, and many countries have instituted price ceilings on specific products and therapies
In the future, there may continue to be additional proposals relating to the reform of the U.S. healthcare system
and international healthcare systems. We expect that additional state and federal healthcare reform measures will be
adopted in the future, any of which could limit the amounts that federal and state governments will pay for healthcare
products and services, which could result in limited coverage and reimbursement and reduced demand for our products,
once approved, or additional pricing pressures. Any reduction in reimbursement from Medicare or other government-
funded programs may result in a similar reduction in payments from private payors. The implementation of cost
containment measures or other healthcare reforms may prevent us from being able to generate revenue, attain profitability
or commercialize our product candidates.
Data Privacy and Security
Numerous state, federal and foreign laws, including consumer protection laws and regulations, govern the
collection, dissemination, use, access to, confidentiality and security of personal information, including health-related
information. In the United States, numerous federal and state laws and regulations, including data breach notification laws,
health information privacy and security laws, including HIPAA, and federal and state consumer protection laws and
regulations (e.g., Section 5 of the FTC Act), that govern the collection, use, disclosure, and protection of health-related and
other personal information could apply to our operations or the operations of our partners. In addition, certain state and
non-U.S. laws, such as the California Consumer Privacy Act, or the CCPA, the California Privacy Rights Act, or the
CPRA, and the EU General Data Protection Regulation, or the GDPR, govern the privacy and security of personal
information, including health-related information in certain circumstances, some of which are more stringent than HIPAA
and many of which differ from each other in significant ways and may not have the same effect, thus complicating
compliance efforts. Failure to comply with these laws, where applicable, can result in the imposition of significant civil
and/or criminal penalties and private litigation. Privacy and security laws, regulations, and other obligations are constantly
evolving, may conflict with each other to complicate compliance efforts, and can result in investigations, proceedings, or
actions that lead to significant civil and/or criminal penalties and restrictions on data processing.
Research and Development Expenses
Our research and development expenses were $31.8 million, $38.0 million and $38.6 million for the years ended
December 31, 2020, 2019, and 2018, respectively. Please see “Management’s Discussion and Analysis of Financial
Condition and Results of Operations-Research and Development Expenses” for additional detail regarding our research and
development activities.
Environment
Our third-party manufacturers are subject to inspections by the FDA for compliance with cGMP and other U.S.
regulatory requirements, including U.S. federal, state and local regulations regarding environmental protection and
hazardous and controlled substance controls, among others. Environmental laws and regulations are complex, change
frequently and have tended to become more stringent over time. We have incurred, and may continue to incur, significant
expenditures to ensure we are in compliance with these laws and regulations. We would be subject to significant penalties
for failure to comply with these laws and regulations.
Human Capital Resources
As of December 31, 2020, we had 42 total employees, all of whom were full-time and 31 of whom were primarily
engaged in research and development activities.
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Facilities
We currently lease a total of approximately 27,280 square feet of office and research and development facilities in
Burlingame, California. Our lease expires in 2023. We regularly explore alternatives which would provide us with
additional space to accommodate our anticipated growth.
Legal Proceedings
We are not currently a party to any material legal proceedings.
Corporate Information
We were incorporated in Delaware on January 27, 2014 and began operations in November 2014. Our principal
executive offices are located at 863 Mitten Road, Suite 102, Burlingame, California 94010, and our telephone number is
(650) 900-4520. Our website address is http://www.corvuspharma.com. The information on our website is not incorporated
by reference in this Annual Report on Form 10-K or in any other filings we make with the SEC.
We are an emerging growth company as defined in the Jumpstart Our Business Startups Act of 2012 (JOBS Act).
We will remain an emerging growth company until the earlier of (1) December 31, 2021, (2) the last day of the fiscal year
in which we have total annual gross revenue of at least $1.07 billion, (3) the last day of the fiscal year in which we are
deemed to be a “large accelerated filer” as defined in Rule 12b-2 under the Exchange Act, which would occur if the market
value of our common stock held by non-affiliates exceeded $700.0 million as of the last business day of the second fiscal
quarter of such fiscal year, or (4) the date on which we have issued more than $1.0 billion in non-convertible debt securities
during the prior three-year period. An emerging growth company may take advantage of specified reduced reporting
requirements and is relieved of certain other significant requirements that are otherwise generally applicable to public
companies. As an emerging growth company,
● We may present only two years of audited consolidated financial statements, plus unaudited condensed
consolidated financial statements for any interim period, and related management’s discussion and analysis
of financial condition and results of operations;
● We may avail ourselves of the exemption from the requirement to obtain an attestation and report from our
auditors on the assessment of our internal control over financial reporting pursuant to the Sarbanes-Oxley
Act of 2002 (“Sarbanes-Oxley”);
● We may provide less extensive disclosure about our executive compensation arrangements; and
● We may not require stockholder non-binding advisory votes on executive compensation or golden parachute
arrangements.
We have chosen to opt out of the extended transition periods available to emerging growth companies under the
JOBS Act for complying with new or revised accounting standards. Section 107 of the JOBS Act provides that our decision
to opt out of the extended transition periods for complying with new or revised accounting standards is irrevocable.
Financial Information about Segments
We view our operations and manage our business as one reportable segment. See Note 2 to our audited
consolidated financial statements included in this Annual Report on Form 10-K. Additional information required by this
item is incorporated herein by reference to Part II, Item 6, “Selected Financial Data.”
Available Information
We file electronically with the SEC our annual reports on Form 10-K, quarterly reports on Form 10-Q and
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current reports on Form 8-K pursuant to Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended. We
make available on our website at http://www.corvuspharma.com, free of charge, copies of these reports, as soon as
reasonably practicable after we electronically file such material with, or furnish it to, the SEC. The public may read or copy
any materials we file with the SEC. The SEC maintains a website that contains reports, proxy and information statements,
and other information regarding issuers that file electronically with the SEC. The address of that website is www.sec.gov.
The information on or accessible through the SEC and our website is not incorporated into, and is not considered part of,
this filing. Further, our references to the URLs for these websites are intended to be inactive textual references only.
Item 1A.
Risk Factors
Our business involves significant risks, some of which are described below. You should consider carefully the risks
and uncertainties described below, together with all of the other information in this Annual Report on Form 10-K,
including our audited consolidated financial statements and related notes included elsewhere in this Annual Report on
Form 10-K and “Management’s Discussion and Analysis of Financial Condition and Results of Operations.” If any of the
following risks are realized, our business, financial condition, results of operations and prospects could be materially and
adversely affected. Many of the following risks and uncertainties are, and will be, exacerbated by the COVID-19 pandemic
and any worsening of the global business and economic environment as a result. Additional risks and uncertainties not
presently known to us or that we currently deem immaterial may also impair our business operations.
Risks Related to Our Limited Operating History, Financial Condition and Capital Requirements
We have a limited operating history, have incurred significant operating losses since our inception and expect to incur
significant losses for the foreseeable future. We may never generate any revenue or become profitable or, if we achieve
profitability, we may not be able to sustain it.
We are a clinical-stage biopharmaceutical company with a limited operating history. Biopharmaceutical product
development is a highly speculative undertaking and involves a substantial degree of risk. To date, we have focused
primarily on developing our lead product candidates, CPI-006, CPI-818 and ciforadenant, and researching additional
product candidates. We have incurred significant operating losses since we were founded in January 2014 and have not yet
generated any revenue from sales. If our product candidates are not approved, we may never generate any revenue. We
incurred a net loss of $6.0 million, $46.7 million and $46.9 million for the years ended December 31, 2020, 2019 and 2018,
respectively. We had an accumulated deficit of $223.1 million as of December 31, 2020. We expect to continue to incur
losses for the foreseeable future, and we anticipate these losses will increase as we continue our development of, seek
regulatory approval for and, if approved, begin to commercialize CPI-006, CPI-818 and ciforadenant, and as we develop
other product candidates. Even if we achieve profitability in the future, we may not be able to sustain it in subsequent
periods. Our prior losses, combined with expected future losses, have had and will continue to have an adverse effect on
our stockholders’ equity and results of operations.
We will require substantial additional financing to achieve our goals, and a failure to obtain this necessary capital when
needed on acceptable terms, or at all, could force us to delay, limit, reduce or terminate our product development, other
operations or commercialization efforts.
Since commencing our operations in 2014, the majority of our efforts have been focused on the research and
development of CPI-006, CPI-818 and ciforadenant. We believe that we will continue to expend substantial resources for
the foreseeable future as we continue clinical development of, seek regulatory approval for and, if approved, prepare for
the commercialization of ciforadenant, CPI-006, and CPI-818, as well as product candidates under our other development
programs. These expenditures will include costs associated with research and development, conducting preclinical studies
and clinical trials, obtaining regulatory approvals, manufacturing and supply, sales and marketing and general operations.
In addition, other unanticipated costs may arise. Because the outcome of any clinical trial and/or
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regulatory approval process is highly uncertain, we may not be able to accurately estimate the actual amounts necessary to
successfully complete the development, regulatory approval process and commercialization of CPI-006, CPI-818 and
ciforadenant or any other product candidates.
As of December 31, 2020, we had capital resources consisting of cash, cash equivalents and marketable securities
of $44.3 million. We do not expect our existing capital resources to be sufficient to enable us to fund the completion of all
of our ongoing and planned clinical trials and remaining development program of any of ciforadenant, CPI-006 or CPI-818
through commercialization. In addition, while Angel Pharmaceuticals has received outside investment of approximately
$41.0 million in connection with its formation and licensing of certain of our intellectual property, such cash is not
available for our use. Our operating plan may change as a result of many factors, including those described below as well
as others currently unknown to us, and we may need to seek additional funds sooner than planned, through public or
private equity, including pursuant to the Sales Agreement with Jefferies, debt financings or other sources, such as strategic
collaborations. Such financing would result in dilution to stockholders, imposition of debt covenants and repayment
obligations or other restrictions that may affect our business. If we raise additional capital through strategic collaboration
agreements, we may have to relinquish valuable rights to our product candidates, including possible future revenue
streams. For example, in October 2020 we formed Angel Pharmaceuticals with a group of investors in China to create a
new China-based biopharmaceutical company with a mission to bring innovative quality medicines to Chinese patients for
treatment of serious diseases including cancer, autoimmune diseases and infectious diseases. We granted Angel
Pharmaceuticals a license to rights to develop and commercialize our three clinical-stage candidates – CPI-006, CPI-818
and ciforadenant – in greater China and Angel obtained global rights to our BTK inhibitor preclinical programs. In
addition, additional funding may not be available to us on acceptable terms, or at all, and any additional fundraising efforts
may divert our management from their day-to-day activities, which may adversely affect our ability to develop and
commercialize our product candidates. Furthermore, even if we believe we have sufficient funds for our current or future
operating plans, we may seek additional capital due to favorable market conditions or strategic considerations.
The amount and timing of any expenditures needed to implement our development and commercialization
programs will depend on numerous factors, including, but not limited to:
● the type, number, scope, progress, expansions, results of and timing of our ongoing and planned clinical trials
of CPI-006, CPI-818 and ciforadenant and any of our planned preclinical studies and clinical trials of other
product candidates which we are pursuing or may choose to pursue in the future;
● whether our current Phase 3 clinical trial of CPI-006 is successful;
● the impact of changes in the COVID-19 pandemic, including the impact of vaccines and therapeutic
treatments;
● the need for, and the progress, costs and results of, any additional clinical trials of CPI-006, CPI-818 and
ciforadenant or any of our other product candidates we may initiate based on the results of our planned
clinical trials or discussions with the FDA, including any additional trials the FDA or other regulatory
agencies may require;
● the costs of obtaining, maintaining and enforcing our patents and other intellectual property rights;
● the costs and timing of obtaining or maintaining manufacturing for CPI-006, CPI-818 and ciforadenant and
our other product candidates, including commercial manufacturing if any product candidate is approved;
● the costs and timing of establishing sales and marketing capabilities;
● our ability to achieve sufficient market acceptance, coverage and reimbursement from third-party payors and
adequate market share for our product candidates;
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● the terms and timing of establishing collaborations, license agreements and other partnerships;
● whether the FDA accepts data from any clinical trials of our product candidates conducted by Angel
Pharmaceuticals in China;
● costs associated with any new product candidates that we may develop, in-license or acquire;
● Angel Pharmaceuticals’ ability to develop and commercialize product candidates in China;
● the effect of competing technological and market developments;
● our ability to attract, hire and retain qualified personnel;
● our ability to establish and maintain partnering arrangements for development; and
● the costs associated with being a public company.
Several of these factors are outside of our control and if we are unable to obtain funding on a timely basis, we will
be unable to complete the clinical trials for CPI-006, CPI-818 and ciforadenant and our other product candidates, and we
may be required to significantly curtail some or all of our activities.
The COVID-19 pandemic could adversely impact our business, including our clinical trials, and financial condition.
In December 2019, a novel strain of coronavirus, COVID-19, was reported to have surfaced in Wuhan, China. Since
then, the COVID-19 pandemic has spread to most countries, including the United States and European and Asia-Pacific
countries, including countries in which we have planned or active clinical trial sites. As the COVID-19 pandemic continues
to spread around the globe, we will likely experience disruptions that could severely impact our business and clinical trials,
including:
● delays or difficulties in enrolling patients in our clinical trials;
● delays or difficulties in clinical site initiation, including difficulties in recruiting clinical site investigators and
clinical site staff;
● diversion of healthcare resources away from the conduct of clinical trials, including the diversion of hospitals
serving as our clinical trial sites and hospital staff supporting the conduct of our clinical trials;
● interruption of key clinical trial activities, such as clinical trial site monitoring, due to limitations on travel
imposed or recommended by federal or state governments, employers and others or interruption of clinical
trial subject visits and study procedures, the occurrence of which could affect the integrity of clinical trial
data;
● risk that participants enrolled in our clinical trials will contract the COVID-19 pandemic while the clinical
trial is ongoing, which could impact the results of the clinical trial, including by increasing the number of
observed adverse events;
● limitations in employee resources that would otherwise be focused on the conduct of our clinical trials,
including because of sickness of employees or their families or the desire of employees to avoid contact with
large groups of people;
● delays in receiving authorization from local regulatory authorities to initiate our planned clinical trials;
● delays in clinical sites receiving the supplies and materials needed to conduct our clinical trials;
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● interruption in global shipping that may affect the transport of clinical trial materials, such as investigational
drug product used in our clinical trials;
● changes in local regulations as part of a response to the COVID-19 pandemic which may require us to change
the ways in which our clinical trials are conducted, which may result in unexpected costs, or to discontinue
such clinical trials altogether;
● interruptions or delays in preclinical studies due to restricted or limited operations at our research and
development laboratory facilities;
● delays in necessary interactions with local regulators, ethics committees and other important agencies and
contractors due to limitations in employee resources or forced furlough of government employees; and
● refusal of the FDA to accept data from clinical trials in affected geographies outside the United States.
In addition, the spread of the COVID-19 pandemic has had an impact and may continue to severely impact the
trading price of shares of our common stock and could further severely impact our ability to raise additional capital on a
timely basis or at all.
The COVID-19 pandemic continues to rapidly evolve. The extent to which the COVID-19 pandemic may impact
our business, including our clinical trials, and financial condition will depend on future developments, which are highly
uncertain and cannot be predicted with confidence, such as the ultimate geographic spread of the disease, the duration of
the pandemic, travel restrictions and social distancing in the United States and other countries, business closures or
business disruptions and the effectiveness of actions taken in the United States and other countries to contain and treat the
disease.
Risks Related to the Discovery and Development of Our Product Candidates
Our product candidates are in various stages of development and may fail or suffer delays that materially and adversely
affect their commercial viability. If we are unable to advance our product candidates through clinical development,
obtain regulatory approval and ultimately commercialize such product candidates, or experience significant delays in
doing so, our business will be materially harmed.
We have invested a significant portion of our efforts and financial resources in the development of our most
advanced product candidates, CPI-006, ciforadenant and CPI-818, which are being evaluated in Phase 3, Phase 1b/2 and
Phase 1/1b clinical trials, respectively. Although we believe our Phase 3 trial of CPI-006 for the treatment of hospitalized
patients with COVID-19, if it meets its primary endpoint, may be sufficient to support submission of a Biologics License
Application (”BLA”) by the FDA, the FDA may disagree and we may be required to conduct additional trials to support
the submission of a BLA CPI-006. We have no products on the market and our ability to achieve and sustain profitability
depends on obtaining regulatory approvals for and successfully commercializing our product candidates, either alone or
with third parties. Before obtaining regulatory approval for the commercial distribution of our product candidates, we or
our collaborator must conduct extensive preclinical tests and clinical trials to demonstrate sufficient safety and efficacy of
our product candidates in patients.
As a result, we may not have the financial resources to continue development of, or to modify existing or enter
into new collaborations for, a product candidate if we experience any issues that delay or prevent regulatory approval of, or
our ability to commercialize, product candidates, including:
● negative or inconclusive results from our clinical trials, the clinical trials of our collaborators, including Angel
Pharmaceuticals, or the clinical trials of others for product candidates similar to ours, leading to a decision or
requirement to conduct additional preclinical testing or clinical trials or abandon a program;
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● changes in the COVID-19 pandemic, including the impact of vaccines and therapeutic treatments;
● product-related side effects experienced by participants in our clinical trials, the clinical trials of our collaborators
or by individuals using drugs or therapeutic biologics similar to our product candidates;
● the extent to which the COVID-19 pandemic may impact our clinical trials;
● delays in submitting INDs or comparable foreign applications or delays or failure in obtaining the necessary
approvals from regulators to commence a clinical trial, or a suspension or termination of a clinical trial once
commenced;
● conditions imposed by the United States Food and Drug Administration (“FDA”) or comparable foreign
authorities regarding the scope or design of our clinical trials;
● delays in enrolling research subjects in clinical trials;
● high drop-out rates of research subjects;
● inadequate supply or quality of product candidate components or materials or other supplies necessary for the
conduct of our clinical trials or the clinical trials of our collaborators;
● greater than anticipated clinical trial costs;
● delay in the development or approval of companion diagnostic tests for our product candidates;
● unfavorable FDA or other regulatory agency inspection and review of a clinical trial site;
● failure of our third-party contractors or investigators to comply with regulatory requirements or otherwise meet
their contractual obligations in a timely manner, or at all;
● delays and changes in regulatory requirements, policy and guidelines, including the imposition of additional
regulatory oversight around clinical testing generally or with respect to our technology in particular; or
● varying interpretations of data by the FDA and similar foreign regulatory agencies.
In addition, disruptions at the FDA and other regulatory agencies that are unrelated to our company or our
products could also cause delays to the regulatory approval process for our products. For example, over the last several
years, including from December 2018 into January 2019, the U.S. government has shut down several times and certain
regulatory agencies, including the FDA, have had to furlough critical employees and stop critical activities. If a prolonged
government shutdown occurs, it could significantly impact the ability of the FDA to timely review and process our
regulatory submissions.
We could find that the product candidates we or our collaborators pursue are not safe or effective. Furthermore, if
one or more of our product candidates, particularly in relation to the adenosine pathway, generally prove to be ineffective,
unsafe or commercially unviable, the development of our entire platform and pipeline could be delayed, potentially
permanently. Any of these occurrences may materially and adversely affect our business, financial condition, results of
operations and prospects.
Of the large number of drugs in development in the pharmaceutical industry, only a small percentage result in the
submission of a New Drug Application (“NDA”) or BLA to the FDA or comparable marketing applications to foreign
regulatory authorities, and even fewer are approved for commercialization. Furthermore, even if we do receive regulatory
approval to market ciforadenant, CPI-006 or CPI-818, any such approval may be subject to limitations on the indicated
uses for which we may market the product. Accordingly, even if we are able to obtain the requisite financing to
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continue to fund our development programs, we cannot assure our stockholders that ciforadenant, CPI-006 or CPI-818 will
be successfully developed or commercialized. If we or any of our existing or potential future collaborators are unable to
develop, or obtain regulatory approval for, or, if approved, successfully commercialize ciforadenant, CPI-006 or CPI-818,
we may not be able to generate sufficient revenue to continue our business.
Clinical drug development involves a lengthy and expensive process with an uncertain outcome, and the results of
preclinical studies and early clinical trials are not necessarily predictive of future results. Any product candidate we or
any of our existing or potential future collaborators advance into clinical trials, including CPI-006, CPI-818 and
ciforadenant, may not have favorable results in later clinical trials, if any, or receive regulatory approval.
Clinical testing is expensive and can take many years to complete, and its outcome is inherently uncertain. Failure
can occur at any time during the clinical trial process. The results of preclinical studies and early clinical trials of our
product candidates may not be predictive of the results of later-stage clinical trials. Product candidates in later stages of
clinical trials may fail to show the desired safety and efficacy traits despite having progressed through preclinical studies
and initial clinical trials. A number of companies in the biopharmaceutical industry have suffered significant setbacks in
advanced clinical trials due to lack of efficacy or adverse safety profiles, notwithstanding promising results in earlier trials.
Furthermore, our ongoing and planned clinical trials will need to demonstrate sufficient safety and efficacy for
approval by regulatory authorities in larger patient populations. Since the initiation of our Phase 1/1b clinical trial in
January 2016, ciforadenant has been administered to more than 300 cancer patients and, while it has generally been well
tolerated, there have been possibly drug-related or drug-related serious adverse events observed during the trial, and limited
information is available concerning long-term safety and efficacy. It remains possible that patients enrolled in our Phase
1/1b clinical trial or our amended Phase 1b/2 clinical trial for ciforadenant could respond in unexpected ways. Our Phase
1/1b and our amended Phase 1b/2 clinical trials are conducted in patients with advanced cancers who have failed other
approved therapies for their disease, and as such, it may be difficult to establish safety and efficacy in this type of patient
population. Furthermore, a portion of our Phase 1/1b clinical trial, our amended Phase 1b/2 clinical trial and Genentech’s
Phase 1b/2 clinical trial under our collaboration agreement, includes the administration of ciforadenant in combination with
Genentech’s cancer immunotherapy, Tecentriq, which could exacerbate immune system related adverse events, cause
increased toxicity or otherwise lead to unexpected adverse events. As a result, there can be no assurance that the results of
historical clinical studies of ciforadenant conducted by third parties or the results of our clinical studies to-date will be
indicative of the ongoing results of our Phase 1/1b clinical trial or amended Phase 1b/2 clinical trial, Genentech’s Phase
1b/2 clinical trial or any future clinical trial of ciforadenant.
In March 2018, we began enrolling patients in our Phase 1/1b trial evaluating CPI-006 in cancer patients. The
protocol is designed to enroll successive cohorts of patients with advanced cancers who will receive increasing doses of
CPI-006 both alone, or in combination with ciforadenant or an anti-PD-1. CPI-006 has been well tolerated in the clinical
trial at doses up to 24 mg/kg, although a limited number of patients have been enrolled and the follow-up period has
necessarily been short, and we have observed one patient with Grade 3 anemia. We have seen 1 patient develop Grade 3
hyponatremia at a dose of 24 mg/kg. However, CD73 is involved in several physiological systems and the administration
of anti-CD73 antibodies such as CPI-006 could result in unforeseen safety issues. Similar to our Phase 1/1b clinical trial of
ciforadenant, it is possible that patients enrolled in our Phase 1/1b clinical trial for CPI-006 could respond in unexpected
ways and that the administration of CPI-006 in combination with ciforadenant and pembrolizumab could exacerbate
immune system related adverse events. As a result, there can be no assurance that we will be able to establish the safety
and efficacy of CPI-006 or that we will be able to successfully complete our Phase 1/1b clinical trial.
In July 2020, we initiated a Phase 1 clinical trial with CPI-006 in hospitalized COVID-19 patients. As of March 4,
2021, we have enrolled 29 patients in our Phase 1 trial and have not observed any safety issues. In February 2021, we
initiated a Phase 3 trial with CPI-006 in hospitalized COVID-19 patients. The Phase 3 trial is planned to enroll
approximately 1,000 patients and in such a larger patient population there may be unforeseen safety issues and there can be
no assurance that we will be able to successfully complete our Phase 3 clinical trial.
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In March 2019, we initiated a multi-center Phase 1/1b clinical trial evaluating CPI-818 in patients with various
malignant T-cell lymphomas. Similar to our clinical trials of ciforadenant and CPI-006, it is possible that patients enrolled
in our Phase 1/1b clinical trial for CPI-818 could respond in unexpected ways.
Under our collaboration with Angel Pharmaceuticals, it will be responsible for the clinical development and
commercialization, including all related expenses, of the licensed pipeline programs in greater China, and for the pre-
clinical BTK program globally. It plans to initiate clinical trials in greater China for CPI-006, CPI-818 and ciforadenant in
the next 12 to 18 months and such trials will be subject to many of the same risks as our ongoing clinical programs.
For the foregoing reasons, we cannot be certain that our ongoing or planned clinical trials or any other future
clinical trials will be successful. Any safety concerns observed in any one of our clinical trials in our targeted indications
could limit the prospects for regulatory approval of our product candidates in those and other indications, which could have
a material adverse effect on our business, financial condition and results of operations.
Any termination or suspension of, or delays in the commencement or completion of, our planned clinical trials could
result in increased costs to us, delay or limit our ability to generate revenue and adversely affect our commercial
prospects.
Before we can initiate clinical trials in the United States for any of our product and development candidates, we
must submit the results of preclinical testing to the FDA along with other information, including information about product
candidate chemistry, manufacturing and controls and our proposed clinical trial protocol, as part of an IND application. In
addition, we may rely in part on preclinical, clinical and quality data generated by clinical research organizations (“CROs”)
and other third parties for regulatory submissions for our product candidates. If these third parties do not make timely
regulatory submissions for our product candidates, it will delay our plans for our clinical trials. If those third parties do not
make this data available to us, we will likely have to develop all necessary preclinical and clinical data on our own, which
will lead to significant delays and increase development costs of the product candidate. In addition, the FDA may require
us to conduct additional preclinical testing for any product candidate before it allows us to initiate clinical testing under any
IND, which may lead to additional delays and increase the costs of our preclinical development. Delays in the completion
of our planned clinical trials for product candidates could significantly affect our product development costs.
While we initiated our Phase 1/1b clinical trial for ciforadenant in January 2016, our Phase 1/1b clinical trial for
CPI-006 in cancer in March 2018, our Phase 1/1b clinical trial for CPI-818 in March 2019 and our Phase 3 clinical trial for
CPI-006 for COVID-19 patients in February 2021, we do not know whether any of our other planned trials, including a
planned front-line Phase 2 trial of ciforadenant in RCC patients, will begin on time in the future or whether any of our trials
will be completed on schedule, if at all. The commencement and completion of clinical trials can be delayed for a number
of reasons, including delays related to:
● the FDA failing to grant permission to proceed or placing the clinical trial on hold;
● subjects failing to enroll or remain in our trial at the rate we expect;
● subjects choosing an alternative treatment or vaccine for the indication for which we are developing CPI-006,
CPI-818 and ciforadenant or other product candidates, or participating in competing clinical trials;
● lack of adequate funding to continue the clinical trial;
● subjects experiencing severe or unexpected drug-related adverse effects;
● a facility manufacturing CPI-006, CPI-818 and ciforadenant, any of our other product candidates or any of their
components being ordered by the FDA or other regulatory authorities to temporarily or permanently shut down
due to violations of good manufacturing practice (“cGMP”) regulations or other applicable requirements, or
infections or cross-contaminations of product candidates in the manufacturing process;
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● any changes to our manufacturing process that may be necessary or desired;
● any failure or delay in reaching an agreement with CROs and clinical trial sites;
● third-party clinical investigators losing the licenses or permits necessary to perform our clinical trials, not
performing our clinical trials on our anticipated schedule or consistent with the clinical trial protocol, good
clinical practices (“GCP”) or regulatory requirements or other third parties not performing data collection or
analysis in a timely or accurate manner;
● third-party contractors becoming debarred or suspended or otherwise penalized by the FDA or other government
or regulatory authorities for violations of regulatory requirements, in which case we may need to find a substitute
contractor, and we may not be able to use some or all of the data produced by such contractors in support of our
marketing applications;
● one or more Institutional Review Boards (“IRBs”) refusing to approve, suspending or terminating the trial at an
investigational site, precluding enrollment of additional subjects, or withdrawing its approval of the trial; or
● patients failing to complete a trial or return for post-treatment follow-up.
In addition, disruptions caused by the COVID-19 pandemic may increase the likelihood that we encounter such
difficulties or delays in initiating, enrolling, conducting or completing our planned and ongoing clinical trials. We could
also encounter delays if a clinical trial is suspended or terminated by us, by the IRBs of the institutions in which such trials
are being conducted, by the Data Safety Monitoring Board for such trial or by the FDA or other regulatory authorities.
Such authorities may impose such a suspension or termination due to a number of factors, including failure to conduct the
clinical trial in accordance with regulatory requirements or our clinical protocols, inspection of the clinical trial operations
or trial site by the FDA or other regulatory authorities resulting in the imposition of a clinical hold, unforeseen safety issues
or adverse side effects, failure to demonstrate a benefit from using a drug, changes in governmental regulations or
administrative actions or lack of adequate funding to continue the clinical trial. In addition, changes in regulatory
requirements and policies may occur, and we may need to amend clinical trial protocols to comply with these changes.
Amendments may require us to resubmit our clinical trial protocols to IRBs for reexamination, which may impact the costs,
timing or successful completion of a clinical trial.
If we experience delays in the completion of, or termination of, any clinical trial of our product candidates, the
commercial prospects of our product candidates will be harmed, and our ability to generate product revenues from any of
these product candidates will be delayed. In addition, any delays in completing our clinical trials will increase our costs,
slow down our product candidate development and approval process and jeopardize our ability to commence product sales
and generate revenues. See also the risk factor below titled “If we encounter difficulties enrolling subjects in our clinical
trials, our clinical development activities could be delayed or otherwise adversely affected.”
In addition, many of the factors that cause, or lead to, termination or suspension of, or a delay in the
commencement or completion of, clinical trials may also ultimately lead to the denial of regulatory approval of a product
candidate. For example, if we make manufacturing or formulation changes to our product candidates, we may need to
conduct additional studies to bridge our modified product candidates to earlier versions. Further, if one or more clinical
trials are delayed, our competitors may be able to bring products to market before we do, and the commercial viability of
CPI-006, CPI-818 and ciforadenant or other product candidates could be significantly reduced. Any of these occurrences
may harm our business, financial condition and prospects significantly.
Interim “top-line” and preliminary data from our clinical trials that we announce or publish from time to time may
change as more patient data become available and are subject to audit and verification procedures that could result in
material changes in the final data.
From time to time, we may publicly disclose interim, top-line or preliminary data from our clinical trials, which is
based on a preliminary analysis of then-available data, and the results and related findings and conclusions are subject
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to change following a more comprehensive review of the data related to the particular study or trial. We also make
assumptions, estimations, calculations and conclusions as part of our analyses of data, and we may not have received or
had the opportunity to fully and carefully evaluate all data. As a result, the top-line or preliminary results that we report
may differ from future results of the same studies, or different conclusions or considerations may qualify such results, once
additional data have been received and fully evaluated. Top-line or preliminary data also remain subject to audit and
verification procedures that may result in the final data being materially different from the top-line or preliminary data we
previously published. As a result, top-line and preliminary data should be viewed with caution until the final data are
available.
From time to time, we may also disclose interim data from our preclinical studies and clinical trials. For instance,
in September and October 2020, we reported interim data from our Phase 1 clinical trial of CPI-006 for the treatment of
COVID-19 and in December 2020 we reported interim data from our Phase 1/1b clinical trial of CPI-818 for the treatment
of T-cell lymphoma. Interim data from clinical trials that we may complete are subject to the risk that one or more of the
clinical outcomes may materially change as patient enrollment continues and more patient data become available. Adverse
differences between interim data and final data could significantly harm our business prospects. Further, disclosure of
interim data by us or by our competitors could result in volatility in the price of our common stock.
Further, others, including regulatory agencies, may not accept or agree with our assumptions, estimates,
calculations, conclusions or analyses or may interpret or weigh the importance of data differently, which could impact the
value of the particular program, the approvability or commercialization of the particular product candidate or product and
our company in general. In addition, the information we choose to publicly disclose regarding a particular study or clinical
trial is based on what is typically extensive information, and you or others may not agree with what we determine is
material or otherwise appropriate information to include in our disclosure.
If the interim, top-line or preliminary data that we report differ from actual results, or if others, including
regulatory authorities, disagree with the conclusions reached, our ability to obtain approval for, and commercialize, our
product candidates may be harmed, which could harm our business, operating results, prospects or financial condition.
Our product candidates are subject to extensive regulation, compliance with which is costly and time consuming, and
such regulation may cause unanticipated delays or prevent the receipt of the required approvals to commercialize our
product candidates.
The clinical development, manufacturing, labeling, storage, record-keeping, advertising, promotion, import,
export, marketing and distribution of our product candidates are subject to extensive regulation by the FDA in the United
States and by comparable authorities in foreign markets. In the United States, we are not permitted to market our product
candidates until we receive regulatory approval from the FDA. The process of obtaining regulatory approval is expensive,
often takes many years and can vary substantially based upon the type, complexity and novelty of the product candidates
involved, as well as the target indications and patient population. Approval policies or regulations may change, and the
FDA has substantial discretion in the drug approval process, including the ability to delay, limit or deny approval of a
product candidate for many reasons. Despite the time and expense invested in clinical development of product candidates,
regulatory approval is never guaranteed.
The FDA or comparable foreign regulatory authorities, including in China, can delay, limit or deny approval of a
product candidate for many reasons, including:
● such authorities may disagree with the design or implementation of our or any of our existing or potential
future collaborators’ clinical trials;
● we or any of our existing or potential future collaborators may be unable to demonstrate to the satisfaction of
the FDA or other regulatory authorities that a product candidate is safe and effective for any indication;
● such authorities may not accept clinical data from trials which are conducted at clinical facilities or in
countries where the standard of care is potentially different from that of the United States;
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● we or any of our existing or potential future collaborators may be unable to demonstrate that a product
candidate’s clinical and other benefits outweigh its safety risks;
● such authorities may disagree with our interpretation of data from preclinical studies or clinical trials;
● approval may be granted only for indications that are significantly more limited than what we apply for
and/or with other significant restrictions on distribution and use;
● such authorities may find deficiencies in the manufacturing processes or facilities of third-party
manufacturers with which we or any of our existing or potential future collaborators contract for clinical and
commercial supplies; or
● the approval policies or regulations of such authorities may significantly change in a manner rendering our or
any of our existing or potential future collaborators’ clinical data insufficient for approval.
With respect to foreign markets, approval procedures vary among countries and, in addition to the foregoing risks,
may involve additional product testing, administrative review periods and agreements with pricing authorities. In addition,
events raising questions about the safety of certain marketed pharmaceuticals may result in increased cautiousness by the
FDA and comparable foreign regulatory authorities, including in China, in reviewing new drugs based on safety, efficacy
or other regulatory considerations and may result in significant delays in obtaining regulatory approvals. Any delay in
obtaining, or inability to obtain, applicable regulatory approvals would prevent us or any of our existing or potential future
collaborators from commercializing our product candidates.
We are conducting clinical trials for CPI-006, CPI-818 and ciforadenant, and we and Angel Pharmaceuticals may in
the future, conduct additional clinical trials of product candidates, at sites outside the United States, and the FDA may
not accept data from trials conducted in foreign locations.
We are currently conducting our Phase 3 trial with CPI -006 in hospitalized patients with COVID-19 at sites in
North America, Europe, South Africa and South America. We are also conducting oncology clinical trials with CPI-818,
ciforadenant and CPI-006 in North America, Australia and South Korea. In addition, Angel Pharmaceuticals currently
intends to initiate clinical trials in China for CPI-006, CPI-818 and ciforadenant in the next 12 to 18 months, and we expect
its clinical trial activity in China to be part of our planned global pivotal study for ciforadenant. While the FDA may accept
data from clinical trials conducted outside the United States, acceptance of this data is subject to certain conditions
imposed by the FDA. For example, the clinical trial must be well designed and conducted in accordance with GCP
requirements, and the FDA must be able to validate the clinical trial data through an on-site inspection, if necessary. If a
marketing application is based solely on foreign clinical data, the FDA also requires such data to be applicable to the U.S.
population and U.S. medical practice, and for the clinical trials to have been performed by clinical investigators of
recognized competence. There can be no assurance the FDA will accept data from trials conducted outside of the United
States, including any trials conducted by us or Angel Pharmaceuticals. If the FDA does not accept the data from our or
Angel Pharmaceuticals’ clinical trials for ciforadenant, CPI-006 or CPI-818, or any other product candidates, it would
likely result in the need for additional trials, which would be costly and time-consuming and delay or permanently halt our
development of CPI-006, CPI-818 and ciforadenant or any other product candidates.
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If we are required by the FDA or similar regulatory authorities to obtain approval, clearance or certification of a
companion diagnostic device in connection with approval of one of our product candidates, and we do not obtain or
face delays in obtaining approval, clearance or certification of a companion diagnostic device, we will not be able to
commercialize the product candidate and our ability to generate revenue will be materially impaired.
According to FDA guidance, if the FDA determines that a companion diagnostic device is essential to the safe and
effective use of a novel therapeutic product or indication, the FDA generally will not approve the therapeutic product or
new therapeutic product indication if the companion diagnostic is not also approved or cleared for that indication. We plan
to collaborate with patient diagnostic companies during our clinical trial enrollment process to help identify patients with
tumor gene alterations that we believe are most likely to respond to our product candidates. If a satisfactory companion
diagnostic is not commercially available, we may be required to create or obtain one that would be subject to regulatory
approval requirements. The process of obtaining or creating such diagnostic is time consuming and costly.
Companion diagnostics are developed in conjunction with clinical programs for the associated product and are
subject to regulation as medical devices by the FDA and comparable foreign regulatory authorities, and, to date, the FDA
has required premarket approval of all companion diagnostics for cancer therapies. Generally, when a companion
diagnostic is essential to the safe and effective use of a therapeutic product, the FDA requires that the companion
diagnostic be approved before or concurrent with approval of the therapeutic product and before a product can be
commercialized. The approval of a companion diagnostic as part of the therapeutic product’s labeling limits the use of the
therapeutic product to only those patients who express the specific genetic alteration that the companion diagnostic was
developed to detect.
If the FDA or a comparable foreign regulatory authority requires approval, certification or clearance of a
companion diagnostic for any of our product candidates, whether before or after the product candidate obtains marketing
approval, we and/ or third-party collaborators may encounter difficulties in developing and obtaining approval, clearance of
certification for these companion diagnostics. Any delay or failure by us or third-party collaborators to develop or obtain
regulatory approval, clearance of certification of a companion diagnostic could delay or prevent approval or continued
marketing of our related product candidates. We may also experience delays in developing a sustainable, reproducible and
scalable manufacturing process for the companion diagnostic or in transferring that process to commercial partners or
negotiating insurance reimbursement plans, all of which may prevent us from completing our clinical trials or
commercializing our product candidates, if approved, on a timely or profitable basis, if at all.
Approval, clearance or certification of companion diagnostics may be subject to further legislative or regulatory
reforms notably in the EU. On May 25, 2017, the new In Vitro Medical Devices Regulation (“IVDR”) entered into force.
The IVDR repeals and replaces the EU In Vitro Diagnostic Medical Devices Directive. Unlike directives, which must be
implemented into the national laws of the EU member states, regulations are directly applicable, i.e., without the need for
adoption of EU member states laws implementing them, in all EU member states and are intended to eliminate current
differences in the regulation of medical devices among EU member states. The IVDR, among other things, is intended to
establish a uniform, transparent, predictable and sustainable regulatory framework across the EU for medical devices and
ensure a high level of safety and health while supporting innovation. The IVDR will, however, only become applicable in
May 2022.
The regulation of companion diagnostics will be subject to further requirements as of the entry into force of the
IVDR which introduces a new classification system for companion diagnostics which are now specifically defined as
diagnostic tests that support the safe and effective use of a specific medicinal product, by identifying patients that are
suitable or unsuitable for treatment. Companion diagnostics will have to undergo a conformity assessment by a notified
body. Before it can issue a CE certificate, the notified body must seek a scientific opinion from the EMA on the suitability
of the companion diagnostic to the medicinal product concerned if the medicinal product falls exclusively within the scope
of the centralized procedure for the authorization of medicines, or the medicinal product is already authorized through the
centralized procedure, or a marketing authorization application for the medicinal product has been submitted through the
centralized procedure. For other substances, the notified body can seek the opinion from a national competent authorities or
the EMA.
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These modifications may make it more difficult and costly for us to obtain regulatory clearances or approvals for
our companion diagnostics or to manufacture, market or distribute our products after clearance or approval is obtained.
If we encounter difficulties enrolling subjects in our clinical trials, our clinical development activities could be delayed
or otherwise adversely affected.
Subject enrollment, a significant factor in the timing of clinical trials, is affected by many factors including the
size and nature of the patient population, the proximity of patients to clinical sites, the eligibility criteria for the trial, the
design of the clinical trial, the risk that enrolled patients will not complete a clinical trial, our ability to recruit clinical trial
investigators with the appropriate competencies and experience, competing clinical trials and clinicians’ and patients’
perceptions as to the potential advantages of the product candidate being studied in relation to other available therapies,
including any new drugs that may be approved for the indications we are investigating. We will be required to identify and
enroll a sufficient number of subjects for each of our clinical trials. Potential subjects for any planned clinical trials may not
be adequately diagnosed or identified with the diseases which we are targeting or may not meet the entry criteria for our
studies. We also may encounter difficulties in identifying and enrolling subjects with a stage of disease appropriate for our
planned clinical trials. We may not be able to initiate or continue clinical trials if we are unable to locate a sufficient
number of eligible subjects to participate in the clinical trials required by the FDA or other foreign regulatory agencies. In
addition, the process of finding and diagnosing subjects may prove costly.
In February 2020, we initiated a Phase 3 trial with CPI-006 in hospitalized patients with COVID-19. This trial is
planned to enroll 1,000 patients at multiple sites in North America, Europe, South Africa and South America. The
completion of enrollment of this trial will be affected by many factors including whether vaccines reduce the population of
hospitalized COVID-19 patients, the impact of a number of clinical trials that are recruiting from the same patient
population as our trial the potential unwillingness of clinical trial sites to put patients on our trial due to a lack of hospital
resources. We are also enrolling patients with T-cell lymphomas in our Phase 1/1b clinical trial of CPI-818. If patients are
unwilling to participate in our studies for any reason, including the existence of competitive clinical trials for similar
patient populations, the availability of approved therapies or negative perceptions of the safety or efficacy of our product
candidates, the timeline for recruiting subjects, conducting studies and obtaining regulatory approval of our product
candidates may be delayed. Our inability to enroll a sufficient number of subjects for any of our future clinical trials would
result in significant delays or may require us to abandon one or more clinical trials altogether.
We believe we have appropriately considered the above factors in our trials when determining expected clinical
trial timelines, but we cannot assure our stockholders that our assumptions are correct or that we will not experience delays
in enrollment, which would result in the delay of completion of such trials beyond our expected timelines. Furthermore, the
COVID-19 pandemic could significantly affect enrollment in our future and planned clinical trials to an extent that we have
not considered within our expected timelines.
The occurrence of serious complications or side effects in connection with use of our product candidates, either in
clinical trials or post-approval, could lead to discontinuation of our clinical development programs, refusal of
regulatory authorities to approve our product candidates or, post-approval, revocation of marketing authorizations or
refusal to approve new indications, which could severely harm our business, prospects, operating results and financial
condition.
During the conduct of clinical trials, patients report changes in their health, including illnesses, injuries and
discomforts, to their study doctor. Often, it is not possible to determine whether or not the product candidate being studied
caused these conditions. It is possible that as we test our product candidates in larger, longer and more extensive clinical
programs with different dosing regimens and in combination with other immunotherapies, or as use of these product
candidates becomes more widespread if they receive regulatory approval, illnesses, injuries, discomforts and other adverse
events that were observed in earlier trials, as well as conditions that did not occur or went undetected in previous trials, will
be reported by subjects. For example, possibly drug-related or drug-related serious adverse events have been observed
during our Phase 1/1b clinical trial and our amended Phase 1b/2 clinical trial in patients receiving combination therapy
with ciforadenant and Tecentriq include hemolytic anemia, encephalitis, hepatitis, pneumonitis, mucositis, myocarditis and
dermatitis. Other toxicities observed during our Phase 1/1b clinical trial and our amended
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Phase 1b/2 clinical trial were mild and are commonly seen in patients with advanced cancers, such as nausea, vomiting,
fatigue, rash, diarrhea, fever, abdominal pain, cough, constipation and decreased appetite. Other immune-oncology drugs
also have been found occasionally to induce immune related toxicities such as colitis, hepatitis, pneumonitis, meningitis,
myocarditis and various endocrine diseases. Such side effects could also be exacerbated when ciforadenant is administered
in combination with Tecentriq which is provided for in a portion of our Phase 1/1b clinical trial and amended Phase 1b/2
clinical trial as well as in Genentech’s Phase 1b/2 clinical trial under our collaboration agreement, or when ciforadenant is
administered in higher doses, which we added as part of a protocol amendment.
In March 2018, we began enrolling patients in our Phase 1/1b clinical trial evaluating CPI-006. We have
completed the dose escalation stage where patients receive CPI-006 alone and in combination with ciforadenant and we
selected the recommended dose of 18 mg/kg and initiated the disease expansion phase in both the monotherapy and the
combination arm with ciforadenant of our CPI-006 clinical trial. We are also enrolled patients in the dose escalation phase
in the pembrolizumab combination arm of the trial. To date, only a limited number of patients have been enrolled and the
follow-up period has been short. No dose-limiting toxicities have been observed at doses up to and including 18 mg/kg. In
July 2020, we began enrolling COVID-19 patients in a Phase 1 clinical trial, and in February 2021, a Phase 3 clinical trial
of CPI-006. As of March 4, 2021,no serious adverse events have been observed, however, the follow-up period has
necessarily been short. COVID-19 is a poorly understood disease with multiple organ dysfunction and potential adverse
effects of CPI-006 in these patients may be difficult to predict.
In March 2019, we initiated a multi-center Phase 1/1b clinical trial evaluating CPI-818 in patients with various
malignant T-cell lymphomas and have completed enrollment in the dose escalation portion of the trial. As of March 4,
2021, a limited number of patients have been enrolled and, although no serious adverse events have been observed, the
follow-up period has necessarily been short.
Many times side effects are only detectable after investigational products are tested in large-scale, Phase 3 clinical
trials or, in some cases, after they are made available to patients on a commercial scale after approval. Results of our
current clinical trials and any future clinical trials we undertake could reveal a high and unacceptable severity and
prevalence of these or other side effects. In such an event, our trials could be suspended or terminated, and the FDA or
comparable foreign regulatory authorities could order us to cease further development of or deny approval of our product
candidates for any or all targeted indications. Drug-related side effects could affect patient recruitment or the ability of
enrolled patients to complete the trial or result in potential product liability claims. Any of these occurrences may harm our
business, financial condition and prospects significantly.
In addition, if one or more of our product candidates receives marketing approval, and we or others later identify
undesirable side effects caused by such products, a number of potentially significant negative consequences could result,
including:
● regulatory authorities may withdraw approvals of such product;
● regulatory authorities may require additional warnings on the label;
● we may be required to create a medication guide outlining the risks of such side effects for distribution to
patients;
● we could be sued and held liable for harm caused to patients; and
● our reputation may suffer.
Any of these events could prevent us from achieving or maintaining market acceptance of the particular product
candidate, if approved, and could significantly harm our business, results of operations and prospects.
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We may not be successful in our efforts to identify or discover additional product candidates.
The success of our business depends primarily upon our ability to develop and commercialize CPI-006, CPI-818
and ciforadenant. Although CPI-006, CPI-818 and ciforadenant are currently in clinical development, our research
programs may fail to identify other potential product candidates, or advance them into and through clinical development
for a number of reasons. Our research methodology may be unsuccessful in identifying other potential product candidates
or our other potential product candidates may be shown to have harmful side effects or may have other characteristics that
may make the products unmarketable or unlikely to receive marketing approval. It may also take greater human and
financial resources to identify additional therapeutic opportunities for our product candidates or to develop suitable
potential product candidates through our research programs than we will possess, thereby limiting our ability to diversify
and expand our product candidate portfolio.
Risks Related to Our Reliance on Third Parties
We rely, and expect to continue to rely, on third parties to conduct our clinical trials. If these third parties do not meet
our deadlines or otherwise conduct the trials as required, our clinical development programs could be delayed or
unsuccessful and we may not be able to obtain regulatory approval for or commercialize our product candidates when
expected, or at all.
We do not have the ability to conduct all aspects of our preclinical testing or clinical trials ourselves. As a result,
we are dependent on third parties to conduct our Phase 3 clinical trial for CPI-006, our Phase 1/1b clinical trial and our
amended Phase 1b/2 clinical trial for ciforadenant, our Phase 1/1b and Phase 1 clinical trials for CPI-006, and our Phase
1/1b clinical trial for CPI-818, and expect to continue to be dependent on third parties to conduct any future clinical studies
of CPI-006, CPI-818 and ciforadenant and preclinical and clinical trials for our other product candidates. The timing of the
initiation and completion of these trials will therefore be controlled by such third parties and may occur at times
substantially different from our estimates. Specifically, we use and rely on medical institutions, clinical investigators,
CROs and consultants to conduct our trials in accordance with our clinical protocols and regulatory requirements. Such
CROs, investigators and other third parties play a significant role in the conduct of these trials and subsequent collection
and analysis of data, and we will control only certain aspects of their activities. Nevertheless, we are responsible for
ensuring that each of our studies is conducted in accordance with the applicable protocol and legal, regulatory and
scientific standards, and our reliance on the CROs and other third parties does not relieve us of our regulatory
responsibilities. We and our CROs are required to comply with GCP requirements, which are regulations and guidelines
enforced by the FDA, the Competent Authorities of the member states of the European Union and comparable foreign
regulatory authorities for all of our product candidates in clinical development.
Regulatory authorities enforce these GCPs through periodic inspections of trial sponsors, principal investigators
and trial sites. If we or any of our CROs or trial sites fail to comply with applicable GCPs, the clinical data generated in our
clinical trials may be deemed unreliable, and the FDA, EMA or comparable foreign regulatory authorities may require us
to perform additional clinical trials before approving our marketing applications. In addition, our clinical trials must be
conducted with product produced under cGMP regulations. Our failure to comply with these regulations may require us to
repeat clinical trials, which would delay the regulatory approval process.
There is no guarantee that any such CROs, investigators or other third parties will devote adequate time and
resources to such trials or perform as contractually required. If any of these third parties fail to meet expected deadlines,
adhere to our clinical protocols or meet regulatory requirements, or otherwise performs in a substandard manner, our
clinical trials may be extended, delayed or terminated. These difficulties may be exacerbated as a result of the ongoing
COVID-19 pandemic.
If any of our clinical trial sites terminates for any reason, including as a result of the COVID-19 pandemic, we
may experience the loss of follow-up information on subjects enrolled in such clinical trials unless we are able to transfer
those subjects to another qualified clinical trial site, which may be difficult or impossible.
In addition, principal investigators for our clinical trials may serve as scientific advisors or consultants to us from
time to time and may receive cash or equity compensation in connection with such services. If these relationships
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and any related compensation result in perceived or actual conflicts of interest, or the FDA concludes that the financial
relationship may have affected the interpretation of the study, the integrity of the data generated at the applicable clinical
trial site may be questioned and the utility of the clinical trial itself may be jeopardized, which could result in the delay or
rejection of any NDA or BLA we submit by the FDA. Any such delay or rejection could prevent us from commercializing
CPI-006, CPI-818 and ciforadenant or our other product candidates.
We rely on third parties to conduct some or all aspects of our manufacturing, research and preclinical and clinical
testing, and these third parties may not perform satisfactorily.
We do not expect to independently conduct all aspects of our manufacturing, research and preclinical and clinical
testing. We currently rely, and expect to continue to rely, on third parties with respect to these items. If these third parties
do not successfully carry out their contractual duties, meet expected deadlines or conduct our studies in accordance with
regulatory requirements or our stated study plans and protocols, we may not be able to complete, or may be delayed in
completing, the preclinical and clinical studies required to support future IND submissions and approval of our product
candidates. These difficulties may be exacerbated as a result of the ongoing COVID-19 pandemic. Furthermore, any of
these third parties may terminate its engagement with us at any time. If we need to enter into alternative arrangements, it
could delay our product development activities, and we may not be able to negotiate alternative arrangements on
commercially reasonable terms, or at all.
We and our contract manufacturers are subject to significant regulation with respect to manufacturing our products
and the contract manufacturers on which we rely may not continue to meet regulatory requirements.
We do not currently have nor do we plan to acquire the infrastructure or internal capability to manufacture our
clinical drug supplies for use in the conduct of our trials, and we lack the resources and the capability to manufacture any
of our product candidates on a clinical or commercial scale. We currently rely on several different manufacturers who
supply different parts of the ciforadenant and CPI-818 molecules, on one manufacturer for CPI-006 drug substance and on
other third-party manufacturers to produce our other product candidates.
All entities involved in the preparation of therapeutics for clinical studies or commercial sale, including our
existing contract manufacturers for our product candidates, are subject to extensive regulation. Components of a finished
therapeutic product approved for commercial sale or used in late-stage clinical studies must be manufactured in accordance
with cGMP requirements. These regulations govern manufacturing processes and procedures, including record keeping,
and the implementation and operation of quality systems to control and assure the quality of investigational products and
products approved for sale. Poor control of production processes can lead to the introduction of adventitious agents or other
contaminants, or to inadvertent changes in the properties or stability of our product candidates that may not be detectable in
final product testing. We or our contract manufacturers must supply all necessary documentation in support of an NDA or
BLA on a timely basis and must adhere to the FDA’s Good Laboratory Practice regulations and cGMP regulations enforced
by the FDA through its facilities inspection program. Our facilities and quality systems and the facilities and quality
systems of some or all of our third-party contractors must pass a pre-approval inspection for compliance with the
applicable regulations as a condition of regulatory approval of our product candidates or any of our other potential
products. In addition, the regulatory authorities may, at any time, audit or inspect our manufacturing facilities or those of
our third-party contractors involved with the preparation of our product candidates or the associated quality systems for
compliance with the regulations applicable to the activities being conducted. We do not control the manufacturing process
of, and are completely dependent on, our contract manufacturing partners for compliance with cGMPs.
The regulatory authorities also may, at any time following approval of a product for sale, audit the manufacturing
facilities of our third-party contractors. If any such inspection or audit identifies a failure to comply with applicable
regulations or if a violation of our product specifications or applicable regulations occurs independent of such an inspection
or audit, we or the relevant regulatory authority may require remedial measures that may be costly and/or time-consuming
for us or a third party to implement and that may include the temporary or permanent suspension of a clinical study or
commercial sales or the temporary or permanent closure of a facility. Such violations could also result in civil and/or
criminal penalties, and the FDA may impose regulatory sanctions including, among other things, refusal
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to approve a pending application for a new drug product or biologic product, revocation of a pre-existing approval or
closing one or more manufacturing facilities.
In addition, if supply from an approved manufacturer is interrupted, there could be a significant disruption in
commercial supply. An alternative manufacturer would need to be qualified through an NDA or BLA supplement which
could result in further delay. The regulatory agencies may also require additional studies if a new manufacturer is relied
upon for commercial production. Changing manufacturers may involve substantial costs and is likely to result in a delay in
our desired clinical and commercial timelines.
We, or our third-party manufacturers, may be unable to successfully scale-up manufacturing of our product candidates
in sufficient quality and quantity, which would delay or prevent us from developing our product candidates and
commercializing approved products, if any.
In order to conduct clinical trials of our product candidates, we will need to manufacture them in large quantities.
We, or any manufacturing partners, may be unable to successfully increase the manufacturing capacity for any of our
product candidates in a timely or cost-effective manner, or at all. In addition, quality issues may arise during scale-up
activities. If we or any manufacturing partners are unable to successfully scale up the manufacture of our product
candidates in sufficient quality and quantity, the development, testing and clinical trials of that product candidate may be
delayed or become infeasible, and regulatory approval or commercial launch of any resulting product may be delayed or
not obtained, which could significantly harm our business.
In addition, the supply chain for the manufacturing of our product candidates is complicated and can involve
several parties. If we were to experience any supply chain issues, including as a result of the COVID-19 pandemic, our
product supply could be seriously disrupted. We expect that the logistical challenges associated with our supply chain will
grow more complex as we expand enrollment in our clinical trials for CPI-006 and CPI-818 and as we commence any
clinical trials for additional product candidates.
Our reliance on third parties requires us to share our trade secrets, which increases the possibility that a competitor will
discover them or that our trade secrets will be misappropriated or disclosed.
Because we rely on third parties to research and develop and to manufacture our product candidates, we must
share trade secrets with them. We seek to protect our proprietary technology in part by entering into confidentiality
agreements and, if applicable, material transfer agreements, consulting agreements or other similar agreements with our
advisors, employees, third-party contractors and consultants prior to beginning research or disclosing proprietary
information. These agreements typically limit the rights of the third parties to use or disclose our confidential information,
including our trade secrets. Despite the contractual provisions employed when working with third parties, the need to share
trade secrets and other confidential information increases the risk that such trade secrets become known by our
competitors, are inadvertently incorporated into the technology of others, or are disclosed or used in violation of these
agreements. Given that our proprietary position is based, in part, on our know-how and trade secrets, a competitor’s
independent discovery of our trade secrets or other unauthorized use or disclosure would impair our competitive position
and may have a material adverse effect on our business.
In addition, these agreements typically restrict the ability of our advisors, employees, third-party contractors and
consultants to publish data potentially relating to our trade secrets, although our agreements may contain certain limited
publication rights. For example, any academic institution that we may collaborate with in the future will likely expect to be
granted rights to publish data arising out of such collaboration. In the future we may also conduct joint research and
development programs that may require us to share trade secrets under the terms of our research and development or
similar agreements. Despite our efforts to protect our trade secrets, our competitors may discover our trade secrets, either
through breach of our agreements with third parties, independent development or publication of information by any of our
third-party collaborators. A competitor’s discovery of our trade secrets would impair our competitive position and have an
adverse impact on our business.
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Risks Related to Commercialization of Our Product Candidates
If we are unable to commercialize our product candidates or if we experience significant delays in obtaining regulatory
approval for, or commercializing, any or all of our product candidates, our business will be materially and adversely
affected.
Our ability to generate product revenue will depend heavily on our ability to successfully develop and
commercialize our product candidates. We do not expect that such commercialization of any of our product candidates will
occur for at least the next several years, if ever. Our ability to commercialize our product candidates effectively will depend
on several factors, including the following:
● successful completion of preclinical studies and clinical trials, including the ability to demonstrate safety and
efficacy of our product candidates;
● managing the complexity of our clinical trial designs;
● receipt of marketing approvals from the FDA and similar foreign regulatory authorities;
● establishing commercial manufacturing capabilities by making arrangements with third-party manufacturers;
● successfully launching commercial sales of any approved products, whether alone or in collaboration with
others;
● acceptance of any approved products by patients, the medical community and third-party payors;
● establishing market share while competing with other therapies;
● a continued acceptable safety profile of any approved products;
● maintaining compliance with post-approval regulation and other requirements; and
● qualifying for, identifying, registering, maintaining, enforcing and defending intellectual property rights and
claims covering our product candidates.
If we experience significant delays or an inability to commercialize our product candidates, our business, financial
condition and results of operations will be materially adversely affected.
If we do not achieve our projected development goals in the time frames we announce and expect, the
commercialization of our products may be delayed and, as a result, our stock price may decline.
We estimate the timing of the accomplishment of various scientific, clinical, regulatory and other product
development goals, which we sometimes refer to as milestones. These milestones may include the commencement or
completion of scientific studies and clinical trials and the submission of regulatory filings. From time to time, we may
publicly announce the expected timing of some of these milestones. All of these milestones will be based on a variety of
assumptions, and the actual timing of these milestones can vary dramatically compared to our estimates, in some cases for
reasons beyond our control. For example, the COVID-19 pandemic has had a significant impact on the ability of
biopharmaceutical companies to conduct clinical trials and, while we have not yet experienced delays resulting from the
pandemic, there can be no assurance that we will be able to avoid such delays in the future. If we do not meet these
milestones as publicly announced, the commercialization of our products may be delayed and, as a result, our stock price
may decline.
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Any approved products could be subject to restrictions or withdrawal from the market, and we may be subject to
penalties if we fail to comply with regulatory requirements or if we experience unanticipated problems with our product
candidates, when and if any of them are approved.
Following potential approval of any of our product candidates, the FDA may impose significant restrictions on a
product’s indicated uses or marketing or impose ongoing requirements for potentially costly and time consuming post-
approval studies, post-market surveillance or clinical trials. Following approval, if any, of CPI-006, CPI-818 and
ciforadenant or any other product candidate, such candidate will also be subject to ongoing FDA requirements governing
the labeling, packaging, storage, distribution, safety surveillance, advertising, promotion, recordkeeping and reporting of
safety and other post-market information. If we or a regulatory agency discovers previously unknown problems with a
product, such as adverse events of unanticipated severity or frequency, or problems with the facility where the product is
manufactured, a regulatory agency may impose restrictions on that product, the manufacturing facility or us, including
requesting recall or withdrawal of the product from the market or suspension of manufacturing.
If we or the manufacturing facilities for CPI-006, CPI-818 and ciforadenant or any other product candidate that
may receive regulatory approval, if any, fail to comply with applicable regulatory requirements, a regulatory agency may:
● issue warning letters or untitled letters;
● seek an injunction or impose civil or criminal penalties or monetary fines;
● suspend or withdraw regulatory approval;
● suspend any ongoing clinical trials;
● refuse to approve pending applications or supplements or applications filed by us;
● suspend or impose restrictions on operations, including costly new manufacturing requirements; or
● seize or detain products, refuse to permit the import or export of product or request that we initiate a product
recall.
The occurrence of any event or penalty described above may inhibit our ability to commercialize our product
candidates and generate revenue.
The FDA has the authority to require a risk evaluation and mitigation strategy (“REMS”) as part of an NDA or
BLA or after approval, which may impose further requirements or restrictions on the distribution or use of an approved
drug, such as limiting prescribing to certain physicians or medical centers that have undergone specialized training,
limiting treatment to patients who meet certain safe-use criteria and requiring treated patients to enroll in a registry.
In addition, if CPI-006, CPI-818 and ciforadenant or any of our other product candidates is approved, our product
labeling, advertising and promotion will be subject to regulatory requirements and continuing regulatory review. The FDA
strictly regulates the promotional claims that may be made about prescription products. In particular, a product may not be
promoted for uses that are not approved by the FDA as reflected in the product’s approved labeling. If we receive
marketing approval for a product candidate, physicians may nevertheless prescribe it to their patients in a manner that is
inconsistent with the approved label. If we are found to have promoted such off-label uses, we may become subject to
significant liability. The FDA and other agencies actively enforce the laws and regulations prohibiting the promotion of
off-label uses, and a company that is found to have improperly promoted off-label uses may be subject to significant
sanctions. The federal government has levied large civil and criminal fines against companies for alleged improper
promotion and has enjoined several companies from engaging in off-label promotion. The FDA has also requested that
companies enter into consent decrees or permanent injunctions under which specified promotional conduct is changed or
curtailed.
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Any government investigation of alleged violations of law could require us to expend significant time and
resources in response, and could generate negative publicity. Any failure to comply with ongoing regulatory requirements
may significantly and adversely affect our ability to commercialize our product candidates.
Further, the FDA’s and other regulatory authorities’ policies may change and additional government regulations
may be enacted that could prevent, limit or delay regulatory approval of our product candidates. For instance, the EU has
adopted the Clinical Trials Regulation (“CTR”) in April 2014, which is expected to come into application in 2022. The
CTR will be directly applicable in all EU member states, repealing the current Clinical Trials Directive. Conduct of all
clinical trials performed in the European Union will continue to be bound by currently applicable provisions until the new
CTR becomes applicable. The extent to which ongoing clinical trials will be governed by the CTR will depend on when the
CTR becomes applicable and on the duration of the individual clinical trial. If a clinical trial continues for more than three
years from the day on which the CTR becomes applicable the CTR will at that time begin to apply to the clinical trial. The
CTR harmonizes the assessment and supervision processes for clinical trials throughout the EU via a Clinical Trials
Information System, which will notably contain a centralized EU portal and database.
We also cannot predict the likelihood, nature or extent of government regulation that may arise from future
legislation or administrative action, either in the United States or abroad. For example, the results of the 2020 U.S.
Presidential Election may impact our business and industry. Namely, the Trump administration took several executive
actions, including the issuance of a number of Executive Orders, that could impose significant burdens on, or otherwise
materially delay, the FDA’s ability to engage in routine oversight activities such as implementing statutes through
rulemaking, issuance of guidance, and review and approval of marketing applications. It is difficult to predict whether or
how these orders will be implemented, or whether they will be rescinded and replaced under the Biden administration. The
policies and priorities of the new administration are unknown and could materially impact the regulations governing our
product candidates. If we are slow or unable to adapt to changes in existing requirements or the adoption of new
requirements or policies, or if we are not able to maintain regulatory compliance, we may be subject to enforcement action
and we may not achieve or sustain profitability.
Disruptions at the FDA and other government agencies caused by funding shortages or global health concerns could
hinder their ability to hire, retain or deploy key leadership and other personnel, or otherwise prevent new or modified
products from being developed, approved or commercialized in a timely manner or at all, which could negatively impact
our business.
The ability of the FDA to review and/or approve new products can be affected by a variety of factors, including
government budget and funding levels, statutory, regulatory, and policy changes, the FDA’s ability to hire and retain key
personnel and accept the payment of user fees, and other events that may otherwise affect the FDA’s ability to perform
routine functions. Average review times at the FDA have fluctuated in recent years as a result. In addition, government
funding of other government agencies that fund research and development activities is subject to the political process,
which is inherently fluid and unpredictable.
Disruptions at the FDA and other agencies such as the EMA, following its relocation to Amsterdam and resulting
staff changes, may also slow the time necessary for new drugs and biologics or modifications to approved drugs or
biologics to be reviewed and/or approved by necessary government agencies, which would adversely affect our business.
For example, over the last several years, including for 35 days beginning on December 22, 2018, the U.S. government has
shut down several times and certain regulatory agencies, such as the FDA, have had to furlough critical FDA employees
and stop critical activities.
Separately, in response to the global COVID-19 pandemic, on March 10, 2020 the FDA announced its intention to
postpone most inspections of foreign manufacturing facilities, and subsequently, on March 18, 2020, the FDA announced
its intention to temporarily postpone routine surveillance inspections of domestic manufacturing facilities. Subsequently,
on July 10, 2020 the FDA announced its intention to resume certain on-site inspections of domestic manufacturing
facilities subject to a risk-based prioritization system. The FDA intends to use this risk-based assessment system to identify
the categories of regulatory activity that can occur within a given geographic area, ranging from mission critical
inspections to resumption of all regulatory activities. Regulatory authorities outside the United States may adopt similar
restrictions or other policy measures in response to the COVID-19 pandemic. If a prolonged
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government shutdown occurs, or if global health concerns continue to prevent the FDA or other regulatory authorities from
conducting their regular inspections, reviews, or other regulatory activities, it could significantly impact the ability of the
FDA or other regulatory authorities to timely review and process our regulatory submissions, which could have a material
adverse effect on our business.
Even if we receive regulatory approval we still may not be able to successfully commercialize CPI-006, CPI-818 and
ciforadenant or any other product candidate, and the revenue that we generate from sales, if any, could be limited.
Even if CPI-006, CPI-818 and ciforadenant or any of our other product candidates receive regulatory approval,
they may not gain market acceptance among physicians, patients, healthcare payors or the medical community. The degree
of market acceptance of our product candidates will depend on a number of factors, including:
● demonstration of clinical efficacy and safety compared to other more-established products;
● the indications for which our product candidates are approved;
● the limitation of our targeted patient population and other limitations or warnings contained in any FDA-
approved labeling;
● acceptance of a new formulation by healthcare providers and their patients;
● our ability to obtain and maintain sufficient third-party coverage and reimbursement from government
healthcare programs, including Medicare and Medicaid, private health insurers and other third-party payors;
● the willingness of patients to pay out-of-pocket in the absence of third-party coverage and reimbursement;
● the prevalence and severity of any adverse effects;
● pricing and cost-effectiveness;
● the timing of market introduction of our product candidates as well as competitive drugs;
● the effectiveness of our or any of our existing or potential future collaborators’ sales and marketing
strategies; and
● unfavorable publicity relating to the product candidate.
If any product candidate is approved but does not achieve an adequate level of acceptance by physicians,
hospitals, healthcare payors or patients, we may not generate sufficient revenue from that product candidate and may not
become or remain profitable. Our efforts to educate the medical community and third-party payors regarding the benefits of
CPI-006, CPI-818 and ciforadenant or any of our other product candidates may require significant resources and may never
be successful.
Failure to obtain or maintain adequate coverage and reimbursement for our product candidates, if approved, could
limit our ability to market those products and decrease our ability to generate revenue.
Successful commercial sales of any approved products will depend on the availability of adequate coverage and
reimbursement from government health administration authorities, private health insurers and other third-party payors.
Each third-party payor separately decides which products it will cover and establishes the reimbursement level, and there is
no guarantee that any of our product candidates that may be approved for marketing by regulatory authorities will receive
adequate coverage or reimbursement levels. Obtaining and maintaining coverage approval for a product candidate is time-
consuming, costly and may be difficult. We may be required to conduct expensive pharmacoeconomic
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studies to justify coverage and reimbursement or the level of coverage and reimbursement relative to other therapies. If
coverage and adequate reimbursement are not available or limited, we may not be able to successfully commercialize any
product candidate for which we obtain marketing approval. Government authorities and third-party payors have attempted
to control costs by limiting coverage and the amount of reimbursement for particular medications. Increasingly, third-party
payors are requiring that drug companies provide them with predetermined discounts from list prices and are challenging
the prices charged for drugs and biologics. Even if we obtain coverage for a given product, the resulting reimbursement
rates may be inadequate and may affect the demand for, or the price of, any product candidate for which we obtain
marketing approval.
Recently enacted legislation, future legislation and healthcare reform measures may increase the difficulty and cost for
us to obtain marketing approval for and commercialize our product candidates and affect the prices we may obtain.
In the United States and some foreign jurisdictions, there have been, and we expect there will continue to be, a
number of legislative and regulatory changes to the healthcare system, including cost-containment measures that may
reduce or limit coverage and reimbursement for newly approved drugs and biologics and affect our ability to profitably sell
any product candidates for which we obtain marketing approval.
For example, in March 2010, the Patient Protection and Affordable Care Act, as amended by the Health Care and
Education Reconciliation Act, collectively referred to as the ACA, was enacted with a goal of reducing the cost of
healthcare and substantially changing the way healthcare is financed by both governmental and private insurers. TheACA,
among other things, subjected biological products to potential competition by lower-cost biosimilars; addressed a new
methodology by which rebates owed by manufacturers under the Medicaid Drug Rebate Program are calculated for drugs
that are inhaled, infused, instilled, implanted or injected; increased the minimum Medicaid rebates owed by manufacturers
under the Medicaid Drug Rebate Program; extended the rebate program to individuals enrolled in Medicaid managed care
organizations; established annual fees and taxes on manufacturers of certain prescription drugs; created a new Medicare
Part D coverage gap discount program, in which manufacturers must agree to offer point-of-sale discounts off negotiated
prices of applicable brand drugs to eligible beneficiaries during their coverage gap period, as a condition for the
manufacturer’s outpatient drugs to be covered under Medicare Part D; and established a new Patient-Centered Outcomes
Research Institute to oversee, identify priorities and conduct comparative clinical effectiveness research, along with
funding for such research.
Since its enactment, there have been judicial, executive and Congressional challenges to certain aspects of the
ACA. For example, the Tax Cuts and Jobs Act was enacted, which, among other things, removes penalties for not
complying with the ACA’s individual mandate to carry health insurance. On December 14, 2018, a U.S. District Court
Judge in the Northern District of Texas, ruled that the individual mandate is a critical and inseverable feature of the ACA,
and therefore, because it was repealed as part of the Tax Act, the remaining provisions of the ACA are invalid as well. On
December 18, 2019, the U.S. Court of Appeals for the 5th Circuit upheld the District Court's decision that the individual
mandate was unconstitutional but remanded the case back to the District Court to determine whether the remaining
provisions of the ACA are invalid as well. The U.S. Supreme Court is currently reviewing the case, although it is unclear
when a decision will be made or how the Supreme Court will rule. In addition, there may be other efforts to challenge,
replace, modify, repeal, or otherwise invalidate the ACA. We are continuing to monitor any changes to the ACA that, in
turn, may potentially impact our business in the future.
In addition, other legislative changes have been proposed and adopted in the United States since the Affordable
Care Act was enacted. These new laws, among other things, included aggregate reductions of Medicare payments to
providers of 2% per fiscal year that will remain in effect through 2030, with the exception of a temporary suspension from
May 1, 2020 through March 31, 2021, unless additional Congressional action is taken. In addition, in January 2013, the
American Taxpayer Relief Act of 2012 was signed into law, which, among other things, further reduced Medicare
payments to several types of providers, including hospitals, imaging centers and cancer treatment centers. Recently there
has been heightened governmental scrutiny over the manner in which manufacturers set prices for their marketed products,
which has resulted in several Congressional inquiries and proposed bills designed to, among other things, reform
government program reimbursement methodologies. Additionally, individual states in the United States have also become
increasingly active in passing legislation and implementing regulations designed to control pharmaceutical
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product pricing, including price or patient reimbursement constraints, discounts, restrictions on certain product access and
marketing cost disclosure and transparency measures, and, in some cases, designed to encourage importation from other
countries and bulk purchasing.
We expect that the ACA, these new laws and other healthcare reform measures that may be adopted in the future
may result in additional reductions in Medicare and other healthcare funding, more rigorous coverage criteria, new
payment methodologies and additional downward pressure on the price that we receive for any approved product. Any
reduction in reimbursement from Medicare or other government programs may result in a similar reduction in payments
from private payors. The implementation of cost containment measures or other healthcare reforms may prevent us from
being able to generate revenue, attain profitability or commercialize our product candidates, if approved.
In the European Union, similar political, economic and regulatory developments may affect our ability to
profitably commercialize our product candidates, if approved. In addition to continuing pressure on prices and cost
containment measures, legislative developments at the European Union or member state level may result in significant
additional requirements or obstacles that may increase our operating costs. The delivery of healthcare in the European
Union, including the establishment and operation of health services and the pricing and reimbursement of medicines, is
almost exclusively a matter for national, rather than European Union, law and policy. National governments and health
service providers have different priorities and approaches to the delivery of health care and the pricing and reimbursement
of products in that context. In general, however, the healthcare budgetary constraints in most European Union member
states have resulted in restrictions on the pricing and reimbursement of medicines by relevant health service providers.
Coupled with ever-increasing European Union and national regulatory burdens on those wishing to develop and market
products, this could prevent or delay marketing approval of our product candidates, restrict or regulate post-approval
activities and affect our ability to commercialize our product candidates, if approved. In markets outside of the United
States and European Union, reimbursement and healthcare payment systems vary significantly by country, and many
countries have instituted price ceilings on specific products and therapies.
We cannot predict the likelihood, nature or extent of government regulation that may arise from future legislation
or administrative action in the United States, the European Union or any other jurisdiction. If we or any third parties we
may engage are slow or unable to adapt to changes in existing requirements or the adoption of new requirements or
policies, or if we or such third parties are not able to maintain regulatory compliance, our product candidates may lose any
regulatory approval that may have been obtained and we may not achieve or sustain profitability.
Any product candidates for which we intend to seek approval as biologic products may face competition sooner than
anticipated.
The ACA includes a subtitle called the Biologics Price Competition and Innovation Act of 2009 (“BPCIA”),
which created an abbreviated approval pathway for biological products that are biosimilar to or interchangeable with an
FDA-licensed reference biological product. Under the BPCIA, an application for a biosimilar product may not be
submitted to the FDA until four years following the date that the reference product was first licensed by the FDA. In
addition, the approval of a biosimilar product may not be made effective by the FDA until twelve years from the date on
which the reference product was first licensed. During this twelve-year period of exclusivity, another company may still
market a competing version of the reference product if the FDA approves a full BLA for the competing product containing
the sponsor’s own preclinical data and data from adequate and well-controlled clinical trials to demonstrate the safety,
purity and potency of its product. The law is complex and is still being interpreted and implemented by the FDA. Any
processes adopted by the FDA to implement the BPCIA could have a material adverse effect on the future commercial
prospects for our biological products.
Though ciforadenant and CPI-818 are small molecules and will not be regulated as biological products, CPI-006,
which we are evaluating in a Phase 1/1b oncology clinical trial and a Phase 1 COVID-19 clinical trial, is a biological
product. We believe that any of our future product candidates approved as a biological product under a BLA should qualify
for the twelve-year period of exclusivity. However, there is a risk that this exclusivity could be shortened due to
Congressional action or otherwise, or that the FDA will not consider our product candidates to be reference products for
competing products, potentially creating the opportunity for generic competition sooner than anticipated.
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Other aspects of the BPCIA, some of which may impact the BPCIA exclusivity provisions, have also been the subject of
recent litigation. Moreover, the extent to which a biosimilar, once approved, could be substituted for any one of our
reference products in a way that is similar to traditional generic substitution for non-biological products will depend on a
number of marketplace and regulatory factors that are still developing.
We may fail to obtain orphan drug designations from the FDA for our product candidates, and even if we obtain such
designations, we may be unable to maintain the benefits associated with orphan drug designation, including the
potential for market exclusivity.
Under the Orphan Drug Act, the FDA may grant orphan drug designation to a drug or biologic intended to treat a
rare disease or condition, which is defined as one occurring in a patient population of fewer than 200,000 in the United
States, or a patient population greater than 200,000 in the United States where there is no reasonable expectation that the
cost of developing the drug or biologic will be recovered from sales in the United States. In the United States, orphan drug
designation entitles a party to financial incentives such as opportunities for grant funding towards clinical trial costs, tax
advantages and user-fee waivers. In addition, if a product that has orphan drug designation subsequently receives the first
FDA approval for the disease for which it has such designation, the product is entitled to orphan drug exclusivity, which
means that the FDA may not approve any other applications, including a full NDA or BLA, to market the same drug or
biologic for the same indication for seven years, except in limited circumstances, such as a showing of clinical superiority
to the product with orphan drug exclusivity or where the manufacturer is unable to assure sufficient product quantity.
While we have not obtained nor have we sought to obtain orphan designation for any product candidate, we
believe many of the potential indications of our product candidates, if approved, could qualify for orphan drug designation.
For instance, if ciforadenant, CPI-006 or CPI-818 is approved for the treatment of certain solid tumors with small patient
populations, such as melanoma, renal or triple-negative breast cancer, it is possible that it could qualify for orphan drug
designation with respect to such indications. As a result, we may seek to obtain orphan drug designation for our product
candidates for any qualifying indications they may be approved for in the future. Even if we obtain such designations, we
may not be the first to obtain marketing approval of our product candidate for the orphan-designated indication due to the
uncertainties associated with developing pharmaceutical products. In addition, exclusive marketing rights in the United
States may be limited if we seek approval for an indication broader than the orphan-designated indication or may be lost if
the FDA later determines that the request for designation was materially defective or if the manufacturer is unable to assure
sufficient quantities of the product to meet the needs of patients with the rare disease or condition. Further, even if we
obtain orphan drug exclusivity for a product, that exclusivity may not effectively protect the product from competition
because different drugs with different active moieties can be approved for the same condition. Even after an orphan product
is approved, the FDA can subsequently approve the same drug with the same active moiety for the same condition if the
FDA concludes that the later drug is safer, more effective or makes a major contribution to patient care. Orphan drug
designation neither shortens the development time or regulatory review time of a drug, nor gives the drug any advantage in
the regulatory review or approval process. In addition, while we may seek orphan drug designation for our product
candidates, we may never receive such designations.
We may expend our limited resources to pursue a particular product candidate and fail to capitalize on product
candidates that may be more profitable or for which there is a greater likelihood of success.
Because we have limited financial and managerial resources, we focus on specific product candidates, including
CPI-006, CPI-818 and ciforadenant. As a result, we may forgo or delay pursuit of opportunities with other product
candidates that later prove to have greater commercial potential. Our resource allocation decisions may cause us to fail to
capitalize on viable commercial products or profitable market opportunities. Our spending on current and future research
and development programs and product candidates for specific indications may not yield any commercially viable product
candidates. If we do not accurately evaluate the commercial potential or target market for a particular product candidate,
we may relinquish valuable rights to that product candidate through collaboration, licensing or other royalty arrangements
in cases in which it would have been more advantageous for us to retain sole development and commercialization rights to
such product candidate.
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We may not be successful in establishing and maintaining development or other strategic collaborations, which could
adversely affect our ability to develop and commercialize product candidates.
In connection with our Phase 1/1b clinical trial for ciforadenant, we entered into a clinical trial collaboration
agreement with Genentech in October 2015. Pursuant to the agreement, Genentech provides access to, and supplies of, its
cancer immunotherapy, Tecentriq, to be used in combination with ciforadenant during the clinical trial. The collaboration
operates under a joint development committee with equal representation from both companies. In May 2017, we signed a
second clinical trial collaboration agreement with Genentech. Under this second agreement, ciforadenant administered in
combination with Tecentriq is being evaluated in a Phase 1b/2 randomized, controlled clinical study as second-line therapy
in patients with non-small cell lung cancer who are resistant and/or refractory to prior therapy with an anti-PD-(L)1
antibody. However, we and Genentech each have the right to terminate the respective collaboration agreements due to
material breach by either party, for safety considerations, if directed by a regulatory authority or if development of
ciforadenant or Tecentriq is discontinued. If we fail to maintain these strategic collaborations with Genentech (1) the
development of ciforadenant in combination with Tecentriq may be terminated or delayed; (2) our cash expenditures
related to development of ciforadenant could increase significantly, and we may need to seek additional financing; (3) we
may be required to hire additional employees or otherwise develop expertise for which we have not budgeted; (4) we will
bear all of the risk related to the development of ciforadenant as a combination therapy; and (5) we will need to seek
collaborations with other companies that have anti-PD-1 or anti-PD-L1 antibodies, which will significantly delay our
development program and could have a material adverse effect on our business, financial condition and results of
operations.
We may form strategic alliances and collaborative partnerships in the future, and we may not realize the benefits of
such alliances.
In addition to our collaboration agreements with Genentech, we may form additional strategic alliances, create
joint ventures or collaborations or enter into licensing arrangements with third parties that we believe will complement or
augment our existing business, including for the continued development or commercialization of our product candidates.
These relationships may result in or include non-recurring and other charges, increased near- and long-term expenditures,
the issuance of securities that dilute our existing stockholders or disruptions to our management and business. In addition,
we face significant competition in seeking appropriate strategic partners, and the negotiation process is time-consuming
and complex. Moreover, we may not be successful in our efforts to establish a strategic partnership or other alternative
arrangements for our product candidates because third parties may view the risk of failure in future clinical trials as too
significant or the commercial opportunity for our product candidates as too limited. We cannot be certain that, following a
strategic transaction or license, we will achieve the revenue or specific net income that justifies such transaction.
Even if we are successful in our efforts to establish strategic alliances or collaborative partnerships, the terms that
we agree upon may not be favorable to us, and we may not be able to maintain such strategic alliances or collaborative
partnerships if, for example, development or approval of a product candidate is delayed, the safety of a product candidate is
questioned or sales of an approved product candidate are unsatisfactory. In addition, any existing or potential future
strategic alliances or collaborative partnerships may be terminable by our strategic partners, and we may not be able to
adequately protect our rights under these agreements. Furthermore, strategic partners may negotiate for certain rights to
control decisions regarding the development and commercialization of our product candidates, if approved, and may not
conduct those activities in the same manner as we do. Any termination of strategic alliances or collaborative partnerships
we enter into in the future, or any delay in entering into collaborative partnership agreements related to our product
candidates, could delay the development and commercialization of our product candidates and reduce their competitiveness
if they reach the market, which could have a material adverse effect on our business, financial condition and results of
operations.
In October 2020, we formed Angel Pharmaceuticals with a group of investors in China to create a new China-
based biopharmaceutical company with a mission to bring innovative quality medicines to Chinese patients for treatment of
serious diseases including cancer, autoimmune diseases and infectious diseases. We granted Angel Pharmaceuticals a
license to rights to develop and commercialize our three clinical-stage candidates – CPI-006, CPI-818 and ciforadenant – in
greater China and obtained global rights to our BTK inhibitor preclinical programs. While certain of our executive
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officers and directors will initially be on the board of directors of Angel Pharmaceuticals, we have limited control over it
and so we will be subject to many of the same risks set forth above with respect to all collaborations. Angel
Pharmaceuticals will also be subject to many of the same risks that are set forth in this “Risk Factors” section pertaining to
operations, government regulation, and intellectual property, which may adversely affect Angel Pharmaceuticals’ ability to
develop and commercialize products.
We face competition from entities that have developed or may develop product candidates for cancer, including
companies developing novel treatments and technology platforms. If these companies develop technologies or product
candidates more rapidly than we do or their technologies are more effective, our ability to develop and successfully
commercialize product candidates may be adversely affected.
Our competitors have developed, are developing or will develop product candidates and processes competitive
with our product candidates. Competitive therapeutic treatments include those that have already been approved and
accepted by the medical community and any new treatments that enter the market. We believe that a significant number of
products are currently under development, and may become commercially available in the future, for the treatment of
conditions for which we may attempt to develop product candidates. In particular, there is intense and rapidly evolving
competition in the immunoregulatory therapeutics field. Our competitors include larger and better funded pharmaceutical,
biopharmaceutical, biotechnological and therapeutics companies. Moreover, we also compete with universities and other
research institutions that may be active in oncology research and could be in direct competition with us. We also compete
with these organizations to recruit management, scientists and clinical development personnel, which could negatively
affect our level of expertise and our ability to execute our business plan. We will also face competition in establishing
clinical trial sites, registering subjects for clinical trials and in identifying and in-licensing new product candidates. Smaller
or early-stage companies may also prove to be significant competitors, particularly through collaborative arrangements
with large and established companies.
Kyowa Hakko Kirin has approval in Japan and the US for istradefylline, an A2A antagonist, in Parkinson’s
disease. Within oncology, Novartis has announced an exclusive licensing agreement with Palobiofarma SL and is
conducting a Phase 1 trial with an A2A antagonist. AstraZeneca plc is conducting clinical trials with an A2A antagonist for
use in cancer therapy. Merck KgaA has entered into a pre-clinical collaboration with Domain Therapeutics Inc. to develop
programs targeting the adenosine pathway. In addition, Redoxtherapies, Inc., which was acquired by Juno Therapeutics and
subsequently by Celgene, and Arcus Biosciences, Inc. are developing A2A receptor antagonists for cancer. Astra Zeneca,
Bristol-Myers Squib, and Novartis in partnership with Surface Oncology, Inc. have initiated clinical trials with anti-CD73
antibodies in cancer patients. More generally, in the field of immuno-oncology, there are large pharmaceutical companies
with approved products or products in late-stage development that target other immune checkpoints, including PD-1, PD-
L1 or CTLA-4. These companies include Bristol-Myers Squibb (nivolumab, ipilimumab), Merck (pembrolizumab),
Genentech (atezolizumab) and AstraZeneca (durvalumab, tremelimumab). There is also intense competition to develop
COVID-19 therapeutic drugs and vaccines, many of which are further along in clinical development than CPI-006. If any
such therapeutic drugs or vaccines were to gain approval, the utility of CPI-006 as a therapeutic for the treatment of
COVID-19 could be negated.
Many of our competitors have significantly greater financial, technical, manufacturing, marketing, sales and
supply resources or experience than we do. If we successfully obtain approval for any product candidate, we will face
competition based on many different factors, including the safety and effectiveness of our products, the ease with which
our products can be administered and the extent to which patients accept relatively new routes of administration, the timing
and scope of regulatory approvals for these products, the availability and cost of manufacturing, marketing and sales
capabilities, price, reimbursement coverage and patent position. Competing products could present superior treatment
alternatives, including by being more effective, safer, less expensive or marketed and sold more effectively than any
products we may develop. Competitive products may make any products we develop obsolete or noncompetitive before we
recover the expense of developing and commercializing our product candidates.
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The market opportunities for our product candidates may be limited to those patients who are ineligible for or have
failed prior treatments and may be small.
Cancer therapies are sometimes characterized as first-line, second-line or third-line, and the FDA often approves
new therapies initially only for third-line use. When cancer is detected early enough, first line therapy is sometimes
adequate to cure the cancer or prolong life without a cure. Whenever first-line therapy, usually chemotherapy, hormone
therapy, surgery or a combination of these, proves unsuccessful, second-line therapy may be administered. Second-line
therapies often consist of more chemotherapy, radiation, antibody drugs, tumor targeted small molecules or a combination
of these. Third-line therapies can include bone marrow transplantation, antibody and small molecule targeted therapies,
more invasive forms of surgery and new technologies. In markets with approved therapies, we expect to initially seek
approval of our product candidates as a later stage therapy for patients who have failed other approved treatments.
Subsequently, for those drugs that prove to be sufficiently beneficial, if any, we would expect to seek approval as a second-
line therapy and potentially as a first-line therapy, but there is no guarantee that our product candidates, even if approved,
would be approved for second-line or first-line therapy. In addition, we may have to conduct additional clinical trials prior
to gaining approval for second-line or first-line therapy.
Our projections of both the number of people who have the cancers we are targeting, as well as the subset of
people with these cancers in a position to receive later stage therapy and who have the potential to benefit from treatment
with our product candidates, are based on our beliefs and estimates. These estimates have been derived from a variety of
sources, including scientific literature, surveys of clinics, patient foundations or market research and may prove to be
incorrect. Further, new studies may change the estimated incidence or prevalence of these cancers. The number of patients
may turn out to be lower than expected. In addition, the potentially addressable patient population for our product
candidates may be limited or may not be amenable to treatment with our product candidates. Even if we obtain significant
market share for our product candidates, we may never achieve profitability without obtaining regulatory approval for
additional indications, including use as a first or second-line therapy.
We have no sales, marketing or distribution capabilities, and we may have to invest significant resources to develop
these capabilities.
We have no internal sales, marketing or distribution capabilities. If CPI-006, CPI-818 and ciforadenant or any of
our other product candidates ultimately receives regulatory approval, we may not be able to effectively market and
distribute the product candidate. We may have to seek collaborators or invest significant amounts of financial and
management resources to develop internal sales, distribution and marketing capabilities, some of which will be committed
prior to any confirmation that CPI-006, CPI-818 and ciforadenant or any of our other product candidates will be approved,
if at all. We may not be able to enter into collaborations or hire consultants or external service providers to assist us in
sales, marketing and distribution functions on acceptable financial terms or at all. Even if we determine to perform sales,
marketing and distribution functions ourselves, we could face a number of additional related risks, including:
● we may not be able to attract and build an effective marketing department or sales force;
● the cost of establishing a marketing department or sales force may exceed our available financial resources
and the revenue generated by CPI-006, CPI-818 and ciforadenant or any other product candidates that we
may develop, in-license or acquire; and
● our direct sales and marketing efforts may not be successful.
Governments may impose price controls, which may adversely affect our future profitability.
We intend to seek approval to market our product candidates in both the United States and in foreign jurisdictions.
In some foreign countries, particularly in the European Union, the pricing of prescription pharmaceuticals is subject to
governmental control. In these countries, pricing negotiations with governmental authorities can take considerable time
after the receipt of marketing approval for a product candidate. To obtain reimbursement or pricing approval in some
countries, we may be required to conduct clinical trials to compare the cost-effectiveness of our
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product candidates to other available therapies, which is time-consuming and costly. If reimbursement of our future
products is unavailable or limited in scope or amount, or if pricing is set at unsatisfactory levels, we may be unable to
achieve or sustain profitability.
Risks Related to Our Business Operations
Our operating results may fluctuate significantly, which makes our future operating results difficult to predict and
could cause our operating results to fall below expectations or any guidance we may provide.
Our quarterly and annual operating results may fluctuate significantly, which makes it difficult for us to predict
our future operating results. These fluctuations may occur due to a variety of factors, many of which are outside of our
control, including, but not limited to:
● the timing and cost of, and level of investment in, research, development and commercialization activities
relating to our product candidates, which may change from time to time;
● coverage and reimbursement policies with respect to our product candidates, if approved, and potential future
drugs that compete with our product candidates;
● the cost of manufacturing our product candidates, which may vary depending on the quantity of production
and the terms of our agreements with manufacturers;
● expenditures that we may incur to acquire, develop or commercialize additional product candidates and
technologies;
● the level of demand for any approved products, which may vary significantly;
● future accounting pronouncements or changes in our accounting policies; and
● the timing and success or failure of clinical trials for our product candidates or competing product candidates,
or any other change in the competitive landscape of our industry, including consolidation among our
competitors or partners.
The cumulative effects of these factors could result in large fluctuations and unpredictability in our quarterly and
annual operating results. As a result, comparing our operating results on a period-to-period basis may not be meaningful.
Investors should not rely on our past results as an indication of our future performance.
This variability and unpredictability could also result in our failing to meet the expectations of industry or
financial analysts or investors for any period. If our revenue or operating results fall below the expectations of analysts or
investors or below any forecasts we may provide to the market, or if the forecasts we provide to the market are below the
expectations of analysts or investors, the price of our common stock could decline substantially. Such a stock price decline
could occur even when we have met any previously publicly stated revenue or earnings guidance we may provide.
We are dependent on the services of our President and Chief Executive Officer, Richard A. Miller, M.D., and other key
executives, and if we are not able to retain these members of our management or recruit additional management,
clinical and scientific personnel, our business will suffer.
We are dependent on the principal members of our management and scientific staff. The loss of service of any of
our management could harm our business. In addition, we are dependent on our continued ability to attract, retain and
motivate highly qualified management, clinical and scientific personnel. If we are not able to retain our management,
particularly our President and Chief Executive Officer, Dr. Miller, and to attract, on acceptable terms, additional qualified
personnel necessary for the continued development of our business, we may not be able to sustain our
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operations or grow. Although we have executed employment agreements with each member of our current executive
management team, including Dr. Miller, these agreements are terminable at will with or without notice and, therefore, we
may not be able to retain their services as expected.
We will need to expand and effectively manage our managerial, operational, financial and other resources in order
to successfully pursue our clinical development and commercialization efforts. We may not be able to attract or retain
qualified management and scientific and clinical personnel in the future due to the intense competition for qualified
personnel among pharmaceutical, biotechnology and other businesses, particularly in the San Francisco Bay Area. Our
industry has experienced a high rate of turnover of management personnel in recent years. If we are not able to attract,
integrate, retain and motivate necessary personnel to accomplish our business objectives, we may experience constraints
that will significantly impede the achievement of our development objectives, our ability to raise additional capital and our
ability to implement our business strategy.
In addition, we do not currently maintain “key person” life insurance on the lives of our executives or any of our
employees. This lack of insurance means that we may not have adequate compensation for the loss of the services of these
individuals.
We may encounter difficulties in managing our growth and expanding our operations successfully.
We will need to grow our organization substantially to continue development and pursue the potential
commercialization of CPI-006, CPI-818 and ciforadenant and our other product candidates. As we seek to advance CPI-
006, CPI-818 and ciforadenant and other product candidates, we will need to expand our financial, development,
regulatory, manufacturing, marketing and sales capabilities or contract with third parties to provide these capabilities for us.
As our operations expand, we expect that we will need to manage additional relationships with various strategic partners,
suppliers and other third parties. Our future financial performance and our ability to commercialize our product candidates
and to compete effectively will depend, in part, on our ability to manage any future growth effectively.
We are subject to various federal and state healthcare laws and regulations, and our failure to comply with these laws
and regulations could harm our results of operations and financial condition.
Although we do not currently have any products on the market, if we obtain FDA approval for any of our product
candidates and begin commercializing those products in the United States, our operations may be directly, or indirectly
through our customers and third-party payors, subject to various U.S. federal and state healthcare laws and regulations.
These laws will affect our operations, sales and marketing practices, and our relationships with physicians and other
customers and third-party payors. Such laws include:
● the federal Anti-Kickback Statute, which prohibits, among other things, persons or entities from knowingly
and willfully soliciting, offering, receiving or providing remuneration, directly or indirectly, in cash or in
kind, to induce or reward, or in return for, either the referral of an individual for, or the purchase, order or
recommendation of, any good or service, for which payment may be made under a federal healthcare
program such as Medicare and Medicaid. A person or entity does not need to have actual knowledge of the
federal Anti-Kickback Statute or specific intent to violate it to have committed a violation;
● the federal False Claims Act, which imposes criminal and civil penalties, including through civil
whistleblower or qui tam actions, against individuals or entities for knowingly presenting, or causing to be
presented, to the federal government, claims for payment that are false or fraudulent or making a false
statement to avoid, decrease or conceal an obligation to pay money to the federal government; in addition,
the government may assert that a claim including items or services resulting from a violation of the federal
Anti-Kickback Statute constitutes a false or fraudulent claim for purposes of the federal False Claims Act;
● the federal Health Insurance Portability and Accountability Act of 1996 (“HIPAA”), which imposes criminal
and civil liability for executing a scheme to defraud any healthcare benefit program or making false
statements relating to healthcare matters. Similar to the federal Anti-Kickback Statute, a person or
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entity does not need to have actual knowledge of the statute or specific intent to violate it to have committed
a violation;
● the federal Physician Payment Sunshine Act, which requires manufacturers of drugs, devices, biologics and
medical supplies for which payment is available under Medicare, Medicaid or the Children’s Health
Insurance Program (with certain exceptions) to report annually to the government information related to
payments or other “transfers of value” made to physicians (defined to include doctors, dentists, optometrists,
podiatrists and chiropractors) and teaching hospitals, and requires applicable manufacturers and group
purchasing organizations to report annually to the government ownership and investment interests held by
the physicians described above and their immediate family members and payments or other “transfers of
value” to such physician owners (manufacturers are required to submit reports to the government by the
90th day of each calendar year). Additional reporting and transparency requirements for payments to
physician assistants, nurse practitioners, clinical nurse specialists, certified registered nurse anesthetists,
anesthesiology assistants and certified nurse midwives go into effect in 2022 for payments made in 2021; and
● analogous state and foreign laws and regulations, such as state anti-kickback and false claims laws, which
may apply to sales or marketing arrangements and claims involving healthcare items or services reimbursed
by non-governmental third-party payors, including private insurers; state laws that require pharmaceutical
companies to comply with the pharmaceutical industry’s voluntary compliance guidelines and the relevant
compliance guidance promulgated by the federal government; and state laws that require drug manufacturers
to report information related to payments and other transfers of value to physicians and other healthcare
providers or marketing expenditures and pricing information.
Ensuring that our internal operations and business arrangements with third-parties comply with applicable
healthcare laws and regulations could involve substantial costs. If our operations are found to be in violation of such laws
or any other governmental laws and regulations that may apply to us, we may be subject to significant penalties, including
civil, criminal and administrative penalties, damages, fines, exclusion from U.S. government funded healthcare programs,
such as Medicare and Medicaid, disgorgement, individual imprisonment, contractual damages, reputational harm,
diminished profits and the curtailment or restructuring of our operations.
We and our current and any existing or future collaborators, third-party manufacturers and suppliers will or may use
biological materials and may use hazardous materials, and any claims relating to improper handling, storage or
disposal of these materials could be time consuming or costly.
We and our current and any existing or future collaborators, third-party manufacturers or suppliers will or may use
biological materials and may use hazardous materials, including chemicals and biological agents and compounds that could
be dangerous to human health and safety of the environment. Our operations and the operations of our third-party
manufacturers and suppliers also produce hazardous waste products. Federal, state and local laws and regulations govern
the use, generation, manufacture, storage, handling and disposal of these materials and wastes. Compliance with applicable
environmental laws and regulations may be expensive, and current or future environmental laws and regulations may
impair our product development efforts. In addition, we cannot eliminate the risk of accidental injury or contamination
from these materials or wastes. We do not carry specific biological or hazardous waste insurance coverage, and our
property, casualty and general liability insurance policies specifically exclude coverage for damages and fines arising from
biological or hazardous waste exposure or contamination. In the event of contamination or injury, we could be held liable
for damages or be penalized with fines in an amount exceeding our resources, and our clinical trials or regulatory approvals
could be suspended.
If product liability lawsuits are brought against us, we may incur substantial liabilities and may be required to limit
commercialization of CPI-006, CPI-818 and ciforadenant or our other product candidates.
We face an inherent risk of product liability as a result of the clinical testing of CPI-006, CPI-818 and
ciforadenant, and the planned clinical testing of our other product candidates and will face an even greater risk if we
commercialize our product candidates. For example, we may be sued if CPI-006, CPI-818 and ciforadenant or our other
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product candidates allegedly cause injury or are found to be otherwise unsuitable during product testing, manufacturing,
marketing or sale. Any such product liability claims may include allegations of defects in manufacturing, defects in design,
a failure to warn of dangers inherent in the product candidate, negligence, strict liability and a breach of warranties. Claims
could also be asserted under state consumer protection acts.
If we cannot successfully defend ourselves against product liability claims, we may incur substantial liabilities or
be required to limit or cease the commercialization of our product candidates. Even a successful defense would require
significant financial and management resources. Regardless of the merits or eventual outcome, liability claims may result
in:
● decreased demand for CPI-006, CPI-818 and ciforadenant or our other product candidates;
● injury to our reputation;
● withdrawal of clinical trial participants;
● costs to defend the related litigation;
● a diversion of management’s time and our resources;
● substantial monetary awards to trial participants or patients;
● product recalls, withdrawals or labeling, marketing or promotional restrictions;
● loss of revenue;
● the inability to commercialize CPI-006, CPI-818 and ciforadenant or our other product candidates; and
● a decline in our stock price.
We have product liability insurance coverage in an amount and on terms and conditions that are customary for
similarly situated companies and that are satisfactory to our board of directors. Our inability to retain sufficient product
liability insurance at an acceptable cost to protect against potential product liability claims could prevent or inhibit the
commercialization of CPI-006, CPI-818 and ciforadenant or our other product candidates. Although we plan to maintain
such insurance, any claim that may be brought against us could result in a court judgment or settlement in an amount that is
not covered, in whole or in part, by our insurance or that is in excess of the limits of our insurance coverage. Our insurance
policies will also have various exclusions, and we may be subject to a product liability claim for which we have no
coverage. We may have to pay any amounts awarded by a court or negotiated in a settlement that exceed our coverage
limitations or that are not covered by our insurance, and we may not have, or be able to obtain, sufficient capital to pay
such amounts.
We and any of our existing or potential future collaborators will be required to report to regulatory authorities if any
products that may be approved in the future cause or contribute to adverse medical events, and any failure to do so
would result in sanctions that would materially harm our business.
If we and any of our existing or potential future collaborators are successful in commercializing our products, the
FDA and foreign regulatory authorities would require that we and any of our existing or potential future collaborators
report certain information about adverse medical events if those products may have caused or contributed to those adverse
events. The timing of our obligation to report would be triggered by the date we become aware of the adverse event as well
as the nature of the event. We and any of our existing or potential future collaborators or CROs may fail to report adverse
events within the prescribed timeframe. If we or any of our existing or potential future collaborators or CROs fail to
comply with such reporting obligations, the FDA or a foreign regulatory authority could
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take action, including criminal prosecution, the imposition of civil monetary penalties, seizure of our products or delay in
approval or clearance of future products.
Our employees, independent contractors, principal investigators, CROs, consultants and vendors may engage in
misconduct or other improper activities, including noncompliance with regulatory standards and requirements.
We are exposed to the risk that our employees, independent contractors, principal investigators, CROs, consultants
and vendors may engage in misconduct or other illegal activity. Misconduct by these parties could include intentional,
reckless and/or negligent conduct involving the improper use or misrepresentation of information obtained in the course of
clinical trials, the creation of fraudulent data in our preclinical studies or clinical trials or illegal misappropriation of drug
product, which could result in regulatory sanctions and cause serious harm to our reputation. It is not always possible to
identify and deter misconduct by employees and other third parties, and the precautions we take to detect and prevent this
activity may not be effective in controlling unknown or unmanaged risks or losses or in protecting us from governmental
investigations or other actions or lawsuits stemming from a failure to be in compliance with such laws or regulations. In
addition, we are subject to the risk that a person or government could allege such fraud or other misconduct, even if none
occurred. If any such actions are instituted against us, and we are not successful in defending ourselves or asserting our
rights, those actions could have a significant impact on our business, including the imposition of fines and other sanctions.
Risks Related to Our Intellectual Property
Our rights to develop and commercialize our product candidates are subject in part to the terms and conditions of
licenses granted to us by other companies. The patent protection, prosecution and enforcement for some of our product
candidates may be dependent on third parties.
We currently are heavily reliant upon licenses of certain patent rights and proprietary technology from third parties
that is important or necessary to the development of our technology and products, including technology related to our
product candidates. For example, we rely on our license agreement with Vernalis for rights with respect to the intellectual
property covering ciforadenant and certain development candidates under our A2B receptor antagonist program. Further,
we rely on our license agreement with The Scripps Research Institute for rights related to our lead development candidate
for our anti-CD73 program, CPI-006. These and other licenses we may enter into in the future may not provide adequate
rights to use such intellectual property and technology in all relevant fields of use or in all territories in which we may wish
to develop or commercialize our technology and products in the future. As a result, we may not be able to develop and
commercialize our technology and products in fields of use and territories for which we are not granted rights pursuant to
such licenses.
Licenses to additional third-party technology that may be required for our development programs may not be
available in the future or may not be available on commercially reasonable terms, which could have a material adverse
effect on our business and financial condition.
In some circumstances, we may not have the right to control the preparation, filing, prosecution and enforcement
of patent applications, or to maintain the patents, covering technology that we license from third parties. In addition, some
of our agreements with our licensors require us to obtain consent from the licensor before we can enforce patent rights, and
our licensor may withhold such consent or may not provide it on a timely basis. Therefore, we cannot be certain that our
licensors or collaborators will prosecute, maintain, enforce and defend such intellectual property rights in a manner
consistent with the best interests of our business, including by taking reasonable measures to protect the confidentiality of
know-how and trade secrets, or by paying all applicable prosecution and maintenance fees related to intellectual property
registrations for any of our product candidates. We also cannot be certain that our licensors have drafted or prosecuted the
patents and patent applications licensed to us in compliance with applicable laws and regulations, which may affect the
validity and enforceability of such patents or any patents that may issue from such applications. If they fail to do so, this
could cause us to lose rights in any applicable intellectual property that we in-license, and as a result our ability to develop
and commercialize products or product candidates may be adversely affected and we may be unable to prevent competitors
from making, using and selling competing products.
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Our success depends on our ability to protect our intellectual property and our proprietary technologies.
Our commercial success depends in part on our ability to obtain and maintain patent protection and trade secret
protection for our product candidates, proprietary technologies and their uses as well as our ability to operate without
infringing upon the proprietary rights of others. We generally seek to protect our proprietary position by filing patent
applications in the United States and abroad related to our product candidates, proprietary technologies and their uses that
are important to our business. There can be no assurance that our patent applications or those of our licensors will result in
additional patents being issued or that issued patents will afford sufficient protection against competitors with similar
technology, nor can there be any assurance that the patents issued will not be infringed, designed around or invalidated by
third parties. Even issued patents may later be found invalid or unenforceable or may be modified or revoked in
proceedings instituted by third parties before various patent offices or in courts. The degree of future protection for our
proprietary rights is uncertain. Only limited protection may be available and may not adequately protect our rights or
permit us to gain or keep any competitive advantage. This failure to properly protect the intellectual property rights relating
to our product candidates could have a material adverse effect on our financial condition and results of operations.
While we have rights to an issued composition-of-matter patent in the United States and corresponding issued
patents in certain foreign territories covering ciforadenant, we cannot be certain that the claims in any of our patent
applications covering composition-of-matter of our other product candidates will be considered patentable by the United
States Patent and Trademark Office (“USPTO”), courts in the United States or by the patent offices and courts in foreign
countries, nor can we be certain that the claims in our issued composition-of-matter patents will not be found invalid or
unenforceable if challenged.
The patent application process is subject to numerous risks and uncertainties, and there can be no assurance that
we or any of our existing or potential future collaborators will be successful in protecting our product candidates by
obtaining and defending patents. These risks and uncertainties include the following:
● the USPTO and various foreign governmental patent agencies require compliance with a number of
procedural, documentary, fee payment and other provisions during the patent process, the noncompliance
with which can result in abandonment or lapse of a patent or patent application, and partial or complete loss
of patent rights in the relevant jurisdiction;
● patent applications may not result in any patents being issued;
● patents that may be issued or in-licensed may be challenged, invalidated, modified, revoked, circumvented,
found to be unenforceable or otherwise may not provide any competitive advantage;
● our competitors, many of whom have substantially greater resources than we do and many of whom have
made significant investments in competing technologies, may seek or may have already obtained patents that
will limit, interfere with or eliminate our ability to make, use and sell our potential product candidates;
● there may be significant pressure on the U.S. government and international governmental bodies to limit the
scope of patent protection both inside and outside the United States for disease treatments that prove
successful, as a matter of public policy regarding worldwide health concerns; and
● countries other than the United States may have patent laws less favorable to patentees than those upheld by
U.S. courts, allowing foreign competitors a better opportunity to create, develop and market competing
product candidates.
The patent prosecution process is also expensive and time-consuming, and we may not be able to file and
prosecute all necessary or desirable patent applications at a reasonable cost or in a timely manner. It is also possible that we
will fail to identify patentable aspects of our research and development output before it is too late to obtain patent
protection. Although we enter into non-disclosure and confidentiality agreements with parties who have access to
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patentable aspects of our research and development output, such as our employees, corporate collaborators, outside
scientific collaborators, CROs, contract manufacturers, consultants, advisors and other third parties, any of these parties
may breach such agreements and disclose such output before a patent application is filed, thereby jeopardizing our ability
to seek patent protection.
The issuance of a patent is not conclusive as to its inventorship, scope, validity or enforceability, and our patents,
if issued, or the patent rights that we license from others, may be challenged in the courts or patent offices in the United
States and abroad. Such challenges may result in loss of exclusivity or in patent claims being narrowed, invalidated or held
unenforceable, which could limit our ability to stop others from using or commercializing similar or identical products, or
limit the duration of the patent protection of our products and product candidates. Given the amount of time required for
the development, testing and regulatory review of new product candidates, patents protecting such candidates might expire
before or shortly after such candidates are commercialized. As a result, our intellectual property may not provide us with
sufficient rights to exclude others from commercializing products similar or identical to ours.
If we are unable to protect the confidentiality of our trade secrets, our business and competitive position would be
harmed.
In addition, we rely on the protection of our trade secrets, including unpatented know-how, technology and other
proprietary information to maintain our competitive position. Although we have taken steps to protect our trade secrets and
unpatented know-how, including entering into confidentiality agreements with third parties, and confidential information
and inventions agreements with employees, consultants and advisors. Despite these efforts, we cannot provide any
assurances that all such agreements have been duly executed, and any of these parties may breach the agreements and
disclose our proprietary information, including our trade secrets, and we may not be able to obtain adequate remedies for
such breaches. Enforcing a claim that a party illegally disclosed or misappropriated a trade secret is difficult, expensive and
time-consuming, and the outcome is unpredictable. In addition, some courts inside and outside the United States are less
willing or unwilling to protect trade secrets. Moreover, third parties may still obtain this information or may come upon
this or similar information independently, and we would have no right to prevent them from using that technology or
information to compete with us. If any of these events occurs or if we otherwise lose protection for our trade secrets, the
value of this information may be greatly reduced and our competitive position would be harmed. If we do not apply for
patent protection prior to such publication or if we cannot otherwise maintain the confidentiality of our proprietary
technology and other confidential information, then our ability to obtain patent protection or to protect our trade secret
information may be jeopardized.
Our commercial success depends significantly on our ability to operate without infringing the patents and other
proprietary rights of third parties. Claims by third parties that we infringe their proprietary rights may result in liability
for damages or prevent or delay our developmental and commercialization efforts.
Our commercial success depends in part on our avoiding infringement of the patents and proprietary rights of third
parties. Other entities may have or obtain patents or proprietary rights that could limit our ability to make, use, sell, offer
for sale or import our product candidates and future approved products or impair our competitive position. There is a
substantial amount of litigation, both within and outside the United States, involving patent and other intellectual property
rights in the biotechnology and pharmaceutical industries, including patent infringement lawsuits, interferences,
oppositions, reexaminations, inter partes review (“IPR”) proceedings and post-grant review (“PGR”) proceedings before
the USPTO and/or corresponding foreign patent offices. Numerous third-party U.S. and foreign issued patents and pending
patent applications exist in the fields in which we are developing product candidates. There may be third-party patents or
patent applications with claims to materials, formulations, methods of manufacture or methods for treatment related to the
use or manufacture of our product candidates. For example, we are aware of an issued patent in Australia that may be
relevant to commercialization of ciforadenant in that country. That Australian patent is expected to expire in 2022. Our
ability to commercialize ciforadenant in Australia prior to 2022 could be adversely affected if we do not obtain a license
under such patent. We are also aware of a corresponding patent application that has been issued in the United States and
which is expected to expire in 2023. However, to the extent that any claims of this patent may be interpreted to cover our
potential uses of ciforadenant, we do not believe that such claims would be valid and enforceable if asserted. We have filed
a PGR petition challenging the patentability of certain claims of the patent and the
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patentee subsequently disclaimed every challenged claim. As the biotechnology industry expands and more patents are
issued, the risk increases that our product candidates may be subject to claims of infringement of the patent rights of third
parties. Because patent applications are maintained as confidential for a certain period of time, until the relevant
application is published we may be unaware of third-party patent applications that, if issued as patents, may be infringed by
commercialization of CPI-006, CPI-818 and ciforadenant or our other product candidates, and cannot be certain that we
were the first to file a patent application related to a product candidate or technology. Moreover, because patent
applications can take many years to issue, there may be currently-pending patent applications that may later result in issued
patents that our product candidates may infringe. In addition, identification of third-party patent rights that may be relevant
to our technology is difficult because patent searching is imperfect due to differences in terminology among patents,
incomplete databases and the difficulty in assessing the meaning of patent claims. Any claims of patent infringement
asserted by third parties would be time consuming and could:
● result in costly litigation;
● divert the time and attention of our technical personnel and management;
● cause development delays;
● prevent us from commercializing CPI-006, CPI-818 and ciforadenant or our other product candidates until
the asserted patent expires or is held finally invalid or not infringed in a court of law;
● require us to develop non-infringing technology, which may not be possible on a cost-effective basis; or
● require us to enter into royalty or licensing agreements, which may not be available on commercially
reasonable terms, or at all.
Although no third party has asserted a claim of patent infringement against us as of the date of this report, others
may hold proprietary rights that could prevent CPI-006, CPI-818 and ciforadenant or our other product candidates from
being marketed. Any patent-related legal action against us claiming damages and seeking to enjoin commercial activities
relating to our product candidates or processes could subject us to potential liability for damages, including treble damages
if we were determined to willfully infringe, and require us to obtain a license to manufacture or market CPI-006, CPI-818
and ciforadenant or our other product candidates.
Defense of these claims, regardless of their merit, would involve substantial litigation expense and would be a
substantial diversion of employee resources from our business. We cannot predict whether we would prevail in any such
actions or that any license required under any of these patents would be made available on commercially acceptable terms,
if at all. Moreover, even if we or our future strategic partners were able to obtain a license, the rights may be nonexclusive,
which could result in our competitors gaining access to the same intellectual property. In addition, we cannot be certain that
we could redesign our product candidates or processes to avoid infringement, if necessary. Accordingly, an adverse
determination in a judicial or administrative proceeding, or the failure to obtain necessary licenses, could prevent us from
developing and commercializing CPI-006, CPI-818 and ciforadenant or our other product candidates, which could harm
our business, financial condition and operating results. In addition, intellectual property litigation, regardless of its
outcome, may cause negative publicity and could prohibit us from marketing or otherwise commercializing our product
candidates and technology.
We may be involved in lawsuits to protect or enforce our patents or the patents of our licensors, which could be
expensive, time consuming, and unsuccessful. Further, our issued patents could be found invalid or unenforceable if
challenged in court.
Competitors may infringe our intellectual property rights or those of our licensors. To prevent infringement or
unauthorized use, we may be required to file infringement claims, which can be expensive and time-consuming. In
addition, in a patent infringement proceeding, a court may decide that a patent we own or in-license is not valid, is
unenforceable and/or is not infringed. If we or any of our existing or potential future collaborators were to initiate legal
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proceedings against a third party to enforce a patent directed at one of our product candidates, the defendant could
counterclaim that our patent is invalid and/or unenforceable in whole or in part. In patent litigation in the United States,
defendant counterclaims alleging invalidity and/or unenforceability are commonplace. Grounds for a validity challenge
include an alleged failure to meet any of several statutory requirements, including lack of novelty, obviousness or non-
enablement. Grounds for an unenforceability assertion could include an allegation that someone connected with
prosecution of the patent withheld relevant information from the USPTO or made a misleading statement during
prosecution. Third parties may also raise similar claims before the USPTO, even outside the context of litigation. The
outcome following legal assertions of invalidity and unenforceability is unpredictable, and prior art could render our
patents or those of our licensors invalid. If a defendant were to prevail on a legal assertion of invalidity and/or
unenforceability, we would lose at least part, and perhaps all, of the patent protection on such product candidate. Such a
loss of patent protection would have a material adverse impact on our business.
Interference proceedings provoked by third parties or brought by us or declared by the USPTO may be necessary
to determine the priority of inventions with respect to our patents or patent applications or those of our licensors. An
unfavorable outcome could require us to cease using the related technology or to attempt to license rights to it from the
prevailing party. Our business could be harmed if the prevailing party does not offer us a license on commercially
reasonable terms. Our defense of litigation or interference proceedings may fail and, even if successful, may result in
substantial costs and distract our management and other employees. In addition, the uncertainties associated with litigation
could have a material adverse effect on our ability to raise the funds necessary to continue our clinical trials, continue our
research programs, license necessary technology from third parties or enter into development or manufacturing
partnerships that would help us bring our product candidates to market.
Even if resolved in our favor, litigation or other legal proceedings relating to our intellectual property rights may
cause us to incur significant expenses, and could distract our technical and management personnel from their normal
responsibilities. In addition, there could be public announcements of the results of hearings, motions or other interim
proceedings or developments and if securities analysts or investors perceive these results to be negative, it could have a
substantial adverse effect on the price of our common stock. Such litigation or proceedings could substantially increase our
operating losses and reduce the resources available for development activities or any future sales, marketing or distribution
activities. We may not have sufficient financial or other resources to conduct such litigation or proceedings adequately.
Some of our competitors may be able to sustain the costs of such litigation or proceedings more effectively than we can
because of their greater financial resources. Uncertainties resulting from the initiation and continuation of patent litigation
or other proceedings could compromise our ability to compete in the marketplace.
Furthermore, because of the substantial amount of discovery required in connection with intellectual property
litigation, there is a risk that some of our confidential information could be compromised by disclosure during this type of
litigation. There could also be public announcements of the results of hearings, motions or other interim proceedings or
developments. If securities analysts or investors perceive these results to be negative, it could have a material adverse
effect on the price of our common stock.
Recent patent reform legislation could increase the uncertainties and costs surrounding the prosecution of our patent
applications and the enforcement or defense of our issued patents.
On September 16, 2011, the Leahy-Smith America Invents Act (“Leahy-Smith Act”) was signed into law. The
Leahy-Smith Act includes a number of significant changes to U.S. patent law. These include provisions that affect the way
patent applications will be prosecuted and may also affect patent litigation. In particular, under the Leahy-Smith Act, the
United States transitioned in March 2013 to a “first to file” system in which the first inventor to file a patent application
will be entitled to the patent. Third parties are allowed to submit prior art before the issuance of a patent by the USPTO,
and may become involved in post-grant proceedings including opposition, derivation, reexamination, inter-partes review or
interference proceedings challenging our patent rights or the patent rights of others. An adverse determination in any such
submission, proceeding or litigation could reduce the scope or enforceability of, or invalidate, our patent rights, which
could adversely affect our competitive position.
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We may not be successful in obtaining or maintaining necessary rights to our product candidates through acquisitions
and in-licenses.
We currently have rights to the intellectual property, through licenses from third parties and under patents that we
own, to develop our product candidates. Because our programs may require the use of proprietary rights held by third
parties, the growth of our business will depend in part on our ability to acquire, in-license or use these proprietary rights.
For example, our product candidates may require specific formulations to work effectively and efficiently and the rights to
these formulations may be held by others. We may be unable to acquire or in-license any compositions, methods of use,
processes or other third-party intellectual property rights from third parties that we identify as necessary for our product
candidates. The licensing and acquisition of third-party intellectual property rights is a competitive area, and a number of
more established companies are also pursuing strategies to license or acquire third-party intellectual property rights that we
may consider attractive. These established companies may 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 assign or license rights to us. We also may be unable to license or acquire third-party
intellectual property rights on terms that would allow us to make an appropriate return on our investment.
We have collaborated with U.S. academic institutions and may in the future collaborate with U.S. and foreign
academic institutions to accelerate our preclinical research or development under written agreements with these
institutions. These institutions may provide us with an option to negotiate a license to any of the institution’s rights in
technology resulting from the collaboration. Regardless of such option, we may be unable to negotiate a license within the
specified timeframe or under terms that are acceptable to us. If we are unable to do so, the institution may offer the
intellectual property rights to other parties, potentially blocking our ability to pursue our program.
If we are unable to successfully obtain rights to required third-party intellectual property rights or maintain the
existing intellectual property rights we have, we may have to abandon development of that program and our business and
financial condition could suffer.
We may fail to comply with any of our obligations under existing agreements pursuant to which we license or have
otherwise acquired intellectual property rights or technology, which could result in the loss of rights or technology that
are material to our business.
Licensing of intellectual property is of critical importance to our business and involves complex legal, business
and scientific issues. We are party to various agreements that we depend on for rights to use various technologies that are
material to our business, including intellectual property rights covering ciforadenant and methods relating to its use and
manufacture. In each of these cases, our rights to use the licensed intellectual property are subject to the continuation of
and our compliance with the terms of these agreements. Disputes may arise regarding our rights to intellectual property
licensed to us from a third party, including but not limited to:
● the scope of rights granted under the license agreement and other interpretation-related issues;
● the extent to which our technology and processes infringe on intellectual property of the licensor that is not
subject to the licensing agreement;
● the sublicensing of patent and other rights;
● our diligence obligations under the license agreement and what activities satisfy those diligence obligations;
● the ownership of inventions and know-how resulting from the creation or use of intellectual property by us,
alone or with our licensors and collaborators;
● the scope and duration of our payment obligations;
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● our rights upon termination of such agreement; and
● the scope and duration of exclusivity obligations of each party to the agreement.
If disputes over intellectual property and other rights that we have licensed or acquired from third parties prevent
or impair our ability to maintain our current licensing arrangements on acceptable terms, we may be unable to successfully
develop and commercialize the affected product candidates. If we fail to comply with our obligations under current or
future licensing agreements, these agreements may be terminated or the scope of our rights under them may be reduced and
we might be unable to develop, manufacture or market any product that is licensed under these agreements.
We may be subject to claims that we have wrongfully hired an employee from a competitor or that we or our employees
have wrongfully used or disclosed alleged confidential information or trade secrets of their former employers.
As is common in the pharmaceutical industry, in addition to our employees, we engage the services of consultants
to assist us in the development of our product candidates. Many of these consultants, and many of our employees, were
previously employed at, or may have previously provided or may be currently providing consulting services to, other
pharmaceutical companies including our competitors or potential competitors. We may become subject to claims that we,
our employees or a consultant inadvertently or otherwise used or disclosed trade secrets or other information proprietary to
their former employers or their former or current clients. Litigation may be necessary to defend against these claims. If we
fail in defending any such claims, in addition to paying monetary damages, we may lose valuable intellectual property
rights, which could adversely affect our business. Even if we are successful in defending against these claims, litigation
could result in substantial costs and be a distraction to our management team.
We may be subject to claims challenging the inventorship or ownership of our patents and other intellectual property.
We may also be subject to claims that former employees, collaborators or other third parties have an ownership
interest in our patents or other intellectual property. Litigation may be necessary to defend against these and other claims
challenging inventorship or ownership. If we fail in defending any such claims, in addition to paying monetary damages,
we may lose valuable intellectual property rights. Such an outcome could have a material adverse effect on our business.
Even if we are successful in defending against such claims, litigation could result in substantial costs and distraction to
management and other employees.
If we do not obtain patent term extension for our product candidates, our business may be materially harmed.
Depending upon the timing, duration and specifics of potential FDA marketing approval of ciforadenant, CPI-006
, CPI-818 or other product candidates, one or more of our U.S. patents may be eligible for limited patent term restoration
under the Drug Price Competition and Patent Term Restoration Act of 1984 (“Hatch-Waxman Amendments”). The Hatch-
Waxman Amendments permit a patent restoration term of up to five years as compensation for patent term lost during
product development and the FDA regulatory review process. However, we may not be granted an extension because of,
for example, failing to apply within applicable deadlines, failing to apply prior to expiration of relevant patents or
otherwise failing to satisfy applicable requirements. Moreover, the applicable time period or the scope of patent protection
afforded could be less than we request. If we are unable to obtain patent term extension or restoration or the term of any
such extension is less than we request, our competitors may obtain approval of competing products following our patent
expiration, and our revenue could be reduced, possibly materially.
If our trademarks and trade names are not adequately protected, then we may not be able to build name recognition in
our markets of interest and our business may be adversely affected.
Our registered or unregistered trademarks or trade names may be challenged, infringed, circumvented or declared
generic or determined to be infringing on other marks. We may not be able to protect our rights to these trademarks and
trade names, which we need to build name recognition among potential partners or customers in our markets of interest. At
times, competitors may adopt trade names or trademarks similar to ours, thereby impeding our ability to build brand
identity and possibly leading to market confusion. In addition, there could be potential trade name
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or trademark infringement claims brought by owners of other registered trademarks or trademarks that incorporate
variations of our registered or unregistered trademarks or trade names. Over the long term, if we are unable to establish
name recognition based on our trademarks and trade names, then we may not be able to compete effectively and our
business may be adversely affected. Our efforts to enforce or protect our proprietary rights related to trademarks, trade
secrets, domain names, copyrights or other intellectual property may be ineffective and could result in substantial costs and
diversion of resources and could adversely affect our financial condition or results of operations.
Changes in U.S. patent law could diminish the value of patents in general, thereby impairing our ability to protect our
product candidates.
As is the case with other biopharmaceutical companies, our success is heavily dependent on intellectual property,
particularly patents. Obtaining and enforcing patents in the biopharmaceutical industry involve a high degree of
technological and legal complexity. Therefore, obtaining and enforcing biopharmaceutical patents is costly, time
consuming and inherently uncertain. In addition, Congress may pass patent reform legislation that is unfavorable to us. The
Supreme Court has ruled on several patent cases in recent years, either narrowing the scope of patent protection available
in certain circumstances or weakening the rights of patent owners in certain situations. In addition to increasing uncertainty
with regard to our ability to obtain patents in the future, this combination of events has created uncertainty with respect to
the value of patents, once obtained. Depending on decisions by Congress, the federal courts and the USPTO, the laws and
regulations governing patents could change in unpredictable ways that would weaken our ability to obtain new patents or to
enforce our existing patents and patents we might obtain in the future.
We may not be able to protect our intellectual property rights throughout the world.
While we have issued patents directed at ciforadenant in the United States and certain foreign territories, and
pending patent applications directed at CPI-006, CPI-818, ciforadenant and other product candidates in the United States
and other countries, filing, prosecuting and defending patents on CPI-006, CPI-818, ciforadenant and our other product
candidates in all countries throughout the world would be prohibitively expensive, and our intellectual property rights in
some countries outside the United States can be less extensive than those in the United States. In addition, the laws of some
foreign countries do not protect intellectual property rights to the same extent as federal and state laws in the United States.
Consequently, we may not be able to prevent third parties from practicing our inventions in all countries outside the United
States, or from selling or importing products made using our inventions in and into the United States or other jurisdictions.
Competitors may use our technologies in jurisdictions where we have not obtained patent protection to develop their own
products and, further, may export otherwise infringing products to territories where we have patent protection but
enforcement is not as strong as that in the United States. These products may compete with our product candidates, and our
patents or other intellectual property rights may not be effective or sufficient to prevent them from competing.
The legal systems of many foreign countries do not favor the enforcement of patents and other intellectual
property protection, which could make it difficult for us to stop the infringement of our patents or marketing of competing
products in violation of our proprietary rights. Proceedings to enforce our patent rights in foreign jurisdictions could result
in substantial costs and divert our efforts and attention from other aspects of our business, could put our patents at risk of
being invalidated or interpreted narrowly and our patent applications at risk of not issuing and could provoke third parties
to assert claims against us. We may not prevail in any lawsuits that we initiate, and the damages or other remedies awarded,
if any, may not be commercially meaningful. Accordingly, our efforts to enforce our intellectual property rights around the
world may be inadequate to obtain a significant commercial advantage from the intellectual property that we develop or
license.
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Intellectual property rights do not necessarily address all potential threats to our competitive advantage.
The degree of future protection afforded by our intellectual property rights is uncertain because intellectual
property rights have limitations, and may not adequately protect our business or permit us to maintain our competitive
advantage. For example:
● others may be able to make adenosine antagonists that are similar to our product candidates but that are not
covered by the claims of the patents that we own or have exclusively licensed;
● we or our licensors or future collaborators might not have been the first to make the inventions covered by
the issued patent or pending patent application that we own or have exclusively licensed;
● we or our licensors or future collaborators might not have been the first to file patent applications covering
certain of our inventions;
● others may independently develop similar or alternative technologies or duplicate any of our technologies
without infringing our intellectual property rights;
● it is possible that our pending patent applications will not lead to issued patents;
● issued patents that we own or have exclusively licensed may be held invalid or unenforceable, as a result of
legal challenges by our competitors;
● our competitors might conduct research and development activities in countries where we do not have patent
rights and then use the information learned from such activities to develop competitive products for sale in
our major commercial markets;
● we may not develop additional proprietary technologies that are patentable; and
● the patents of others may have an adverse effect on our business.
Should any of these events occur, they could significantly harm our business, results of operations and prospects.
Risks Related to Our Common Stock
An active, liquid and orderly market for our common stock may not be sustained.
Although our common stock is listed on The Nasdaq Global Market (“Nasdaq”), an active trading market for our
common stock may not be sustained on Nasdaq or any other exchange in the future. The lack of an active market may
impair our stockholders’ ability to sell their shares at the time they wish to sell them or at a price that they consider
reasonable. If an active market for our common stock is not sustained, it may also be difficult for our stockholders to sell
shares without depressing the market price for the shares or at all. An inactive market may also impair our ability to raise
capital by selling shares and may impair our ability to acquire other businesses, applications or technologies using our
shares as consideration, which, in turn, could materially adversely affect our business. In any event, we have a limited
public float and, as a result, our common stock has been and will likely continue to be less liquid than many other listed
companies and trading may be adversely affected.
The trading price of the shares of our common stock could be highly volatile, and investors in our common stock could
incur substantial losses.
Our stock price has been volatile. The stock market in general and the market for stock of pharmaceutical
companies in particular have experienced extreme volatility that has often been unrelated to the operating performance
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of particular companies. The market price for our common stock may be influenced by those factors discussed in this “Risk
Factors” section and many others, including:
● our ability to enroll subjects in our planned clinical trials;
● results of the clinical trials, and the results of trials of our competitors or those of other companies in our
market sector;
● results for our Phase 1 clinical trial of CPI-006 for COVID-19 expected in the fourth quarter of 2020;
● regulatory approval of CPI-006, CPI-818, ciforadenant and our other product candidates, or limitations to
specific label indications or patient populations for its use, or changes or delays in the regulatory review
process;
● Angel Pharmaceuticals’ ability to develop and commercialize product candidates in China;
● regulatory developments in the United States and foreign countries;
● changes in the structure of healthcare payment systems, especially in light of current reforms to the U.S.
healthcare system;
● the success or failure of our efforts to acquire, license or develop additional product candidates;
● innovations or new products developed by us or our competitors;
● announcements by us or our competitors of significant acquisitions, strategic partnerships, joint ventures or
capital commitments;
● manufacturing, supply or distribution delays or shortages;
● any changes to our relationship with any manufacturers, suppliers, collaborators or other strategic partners;
● achievement of product sales and profitability;
● variations in our financial results or those of companies that are perceived to be similar to us;
● market conditions in the pharmaceutical sector and issuance of securities analysts’ reports or
recommendations;
● trading volume of our common stock;
● an inability to obtain additional funding;
● sales of our stock by insiders and stockholders;
● general economic, industry and market conditions other events or factors, many of which are beyond our
control, including recession or depression resulting from the current COVID-19 pandemic;
● additions or departures of key personnel; and
● intellectual property, product liability or other litigation against us.
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As a result of this volatility, investors may experience losses on their investment in our common stock.
In addition, in the past, stockholders have initiated class action lawsuits against pharmaceutical companies
following periods of volatility in the market prices of these companies’ stock. Such litigation, if instituted against us, could
cause us to incur substantial costs and divert management’s attention and resources, which could have a material adverse
effect on our business, financial condition and results of operations.
Our failure to meet the continued listing requirements of Nasdaq could result in a delisting of our common stock.
If we fail to satisfy the continued listing requirements of Nasdaq, such as the corporate governance requirements
or the minimum closing bid price requirement, Nasdaq may take steps to delist our common stock. Such a delisting would
likely have a negative effect on the price of our common stock and would impair our stockholders’ ability to sell or
purchase our common stock when they wish to do so. In the event of a delisting, we can provide no assurance that any
action taken by us to restore compliance with listing requirements would allow our common stock to become listed again,
stabilize the market price or improve the liquidity of our common stock, prevent our common stock from dropping below
the Nasdaq minimum bid price requirement or prevent future non-compliance with Nasdaq’s listing requirements.
Because a small number of our existing stockholders own a majority of our voting stock, a stockholder’s ability to
influence corporate matters will be limited.
As of December 31, 2020, our executive officers, directors and greater than 5% stockholders, in the aggregate,
owned approximately 50% of our outstanding common stock, including 1,458,000 shares of our common stock subject to
prefunded warrants as described in Note 1 in Item 8, Financial Statements and Supplementary Data. As a result, such
persons, acting together, have the ability to control our management and affairs and substantially all matters submitted to
our stockholders for approval, including the election and removal of directors and approval of any significant transaction.
This concentration of ownership may have the effect of delaying, deferring or preventing a change in control, impeding a
merger, consolidation, takeover or other business combination involving us, or discouraging a potential acquiror from
making a tender offer or otherwise attempting to obtain control of our business, even if such a transaction would benefit
other stockholders.
We do not currently intend to pay dividends on our common stock, and, consequently, our stockholders’ ability to
achieve a return on their investment will depend on appreciation, if any, in the price of our common stock.
We have never declared or paid any cash dividend on our common stock. We currently anticipate that we will
retain future earnings for the development, operation and expansion of our business and do not anticipate declaring or
paying any cash dividends for the foreseeable future. Any return to stockholders will therefore be limited to the
appreciation of their stock. There is no guarantee that shares of our common stock will appreciate in value or even maintain
the price at which stockholders have purchased their shares.
To the extent that we raise additional capital by issuing equity securities, the share ownership of existing
stockholders will be diluted. For example, on April 3, 2017, we filed a Registration Statement on Form S-3 (File No. 333-
217102), covering the offering of up to $250 million of shares of common stock, preferred stock, warrants and units. In
March 2018, we sold 8,117,647 shares of our common stock for net proceeds of $64.9 million in an underwritten public
offering pursuant to our Registration Statement on Form S-3 (File No. 333-217102). On March 9, 2020 we filed a
Registration Statement on Form S-3 (File No. 333-237040), covering the offering of up to $200 million of shares of
common stock, preferred stock, warrants and units and entered into the Sales Agreement with Jefferies to sell shares of our
common stock, from time to time, with aggregate gross sales proceeds of up to $50,000,000, through an at-the-market
equity offering program under which Jefferies will act as our sales agent. As of December 31, 2020, we had sold 310,734
shares of common stock pursuant to the Sales Agreement. As of December 31, 2020, $48.7 million remained for sale under
the Sales Agreement.
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Sales of a substantial number of shares of our common stock by our existing stockholders in the public market could
cause our stock price to fall.
Sales of a substantial number of shares of our common stock in the public market could occur at any time. These
sales, or the perception in the market that the holders of a large number of shares intend to sell shares, could reduce the
market price of our common stock. Moreover, certain holders of shares of our common stock have rights, subject to certain
conditions, to require us to file registration statements covering their shares or to include their shares in registration
statements that we may file for ourselves or other stockholders. We have registered and intend to continue to register all
shares of common stock that we may issue under our equity compensation plans. Once we register these shares, they can be
freely sold in the public market upon issuance, subject to volume limitations applicable to affiliates.
We are an emerging growth company, and the reduced reporting requirements applicable to emerging growth
companies may make our common stock less attractive to investors.
We are an “emerging growth company,” as defined in the JOBS Act. For as long as we continue to be an emerging
growth company, we may take advantage of exemptions from various reporting requirements that are applicable to other
public companies that are not emerging growth companies, including, but not limited to, not being required to comply with
the auditor attestation requirements of Section 404 of Sarbanes-Oxley, reduced disclosure obligations regarding executive
compensation in our Annual Report on Form 10-K and our periodic reports and proxy statements and exemptions from the
requirements of holding nonbinding advisory votes on executive compensation and stockholder approval of any golden
parachute payments not previously approved. We will remain an emerging growth company until the earlier of
(1) December 31, 2021, (2) the last day of the fiscal year in which we have total annual gross revenue of at least
$1.07 billion, (3) the last day of the fiscal year in which we are deemed to be a “large accelerated filer” as defined in
Rule 12b-2 under the Exchange Act, which would occur if the market value of our common stock held by non-affiliates
exceeded $700.0 million as of the last business day of the second fiscal quarter of such fiscal year, or (4) the date on which
we have issued more than $1.0 billion in non-convertible debt securities during the prior three-year period. Even after we
no longer qualify as an emerging growth company, we may still qualify as a “smaller reporting company” which may allow
us to take advantage of many of the same exemptions from disclosure requirements including not being required to comply
with the auditor attestation requirements of Section 404(b) of the Sarbanes-Oxley Act. If investors find our common stock
less attractive as a result, there may be a less active trading market for our common stock and our stock price may be more
volatile.
If we fail to maintain proper and effective internal control over financial reporting, our ability to produce accurate and
timely consolidated financial statements could be impaired, investors may lose confidence in our financial reporting and
the trading price of our common stock may decline.
Pursuant to Section 404 of Sarbanes-Oxley, if we are an accelerated filer when we lose our status as an “emerging
growth company”, our independent registered public accounting firm will be required to attest to the effectiveness of our
internal control over financial reporting. The rules governing the standards that must be met for management to assess our
internal control over financial reporting are complex and require significant documentation, testing and possible
remediation. To continue to comply with the requirements of being a reporting company under the Exchange Act, as we
continue to grow, we will need to upgrade our systems including information technology; implement additional financial
and management controls, reporting systems and procedures; and hire additional accounting and finance staff. If we or, if
required, our auditors are unable to conclude that our internal control over financial reporting is effective, investors may
lose confidence in our financial reporting and the trading price of our common stock may decline.
We cannot assure our stockholders that there will not be material weaknesses or significant deficiencies in our
internal control over financial reporting in the future. Any failure to maintain internal control over financial reporting could
severely inhibit our ability to accurately report our financial condition, results of operations or cash flows. If we are unable
to conclude that our internal control over financial reporting is effective, or if our independent registered public accounting
firm determines we have a material weakness or significant deficiency in our internal control over financial reporting once
that firm begin its Section 404 reviews, investors may lose confidence in the accuracy and completeness of our financial
reports, the market price of our common stock could decline, and we could be subject to
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sanctions or investigations by Nasdaq, the SEC or other regulatory authorities. Failure to remedy any material weakness in
our internal control over financial reporting, or to implement or maintain other effective control systems required of public
companies, could also restrict our future access to the capital markets.
Provisions in our charter documents and under Delaware law could discourage a takeover that stockholders may
consider favorable and may lead to entrenchment of management.
Our amended and restated certificate of incorporation and amended and restated bylaws contain provisions that
could significantly reduce the value of our shares to a potential acquiror or delay or prevent changes in control or changes
in our management without the consent of our board of directors. The provisions in our charter documents include the
following:
● a classified board of directors with three-year staggered terms, which may delay the ability of stockholders to
change the membership of a majority of our board of directors;
● no cumulative voting in the election of directors, which limits the ability of minority stockholders to elect
director candidates;
● the exclusive right of our board of directors, unless the board of directors grants such right to the
stockholders, to elect a director to fill a vacancy created by the expansion of the board of directors or the
resignation, death or removal of a director, which prevents stockholders from being able to fill vacancies on
our board of directors;
● the required approval of at least 66 2/3% of the shares entitled to vote to remove a director for cause, and the
prohibition on removal of directors without cause;
● the ability of our board of directors to authorize the issuance of shares of preferred stock and to determine the
price and other terms of those shares, including preferences and voting rights, without stockholder approval,
which could be used to significantly dilute the ownership of a hostile acquiror;
● the ability of our board of directors to alter our amended and restated bylaws without obtaining stockholder
approval;
● the required approval of at least 66 2/3% of the shares entitled to vote to adopt, amend or repeal our amended
and restated bylaws or repeal the provisions of our amended and restated certificate of incorporation
regarding the election and removal of directors;
● a prohibition on stockholder action by written consent, which forces stockholder action to be taken at an
annual or special meeting of our stockholders;
● an exclusive forum provision providing that the Court of Chancery of the State of Delaware will be the
exclusive forum for certain actions and proceedings;
● the requirement that a special meeting of stockholders may be called only by the board of directors, which
may delay the ability of our stockholders to force consideration of a proposal or to take action, including the
removal of directors; and
● advance notice procedures that stockholders must comply with in order to nominate candidates to our board
of directors or to propose matters to be acted upon at a stockholders’ meeting, which may discourage or deter
a potential acquiror from conducting a solicitation of proxies to elect the acquiror’s own slate of directors or
otherwise attempting to obtain control of us.
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We are also subject to the anti-takeover provisions contained in Section 203 of the Delaware General Corporation
Law. Under Section 203, a corporation may not, in general, engage in a business combination with any holder of 15% or
more of its capital stock unless the holder has held the stock for three years or, among other exceptions, the board of
directors has approved the transaction.
Our amended and restated certificate of incorporation and amended and restated bylaws provide that the Court of
Chancery of the State of Delaware is the exclusive forum for substantially all disputes between us and our stockholders,
which could limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us or our directors,
officers or employees.
Our amended and restated certificate of incorporation and amended and restated bylaws provide that the Court of
Chancery of the State of Delaware is the exclusive forum for any derivative action or proceeding brought on our behalf,
any action asserting a breach of fiduciary duty, any action asserting a claim against us arising pursuant to the Delaware
General Corporation Law, our amended and restated certificate of incorporation or our amended and restated bylaws, or
any action asserting a claim against us that is governed by the internal affairs doctrine. This provision may limit a
stockholder’s ability to bring a claim in a judicial forum that it finds favorable for disputes with us or our directors, officers
or other employees, which may discourage such lawsuits against us and our directors, officers and other employees.
Alternatively, if a court were to find this provision in our amended and restated certificate of incorporation and amended
and restated bylaws to be inapplicable or unenforceable in an action, we may incur additional costs associated with
resolving such action in other jurisdictions, which could adversely affect our business and financial condition. This
provision would not apply to suits brought to enforce a duty or liability created by the Exchange Act or any other claim for
which the U.S. federal courts have exclusive jurisdiction.
General Risks
Our future growth may depend, in part, on our ability to operate in foreign markets, where we would be subject to
additional regulatory burdens and other risks and uncertainties.
Our future growth may depend, in part, on our ability to develop and commercialize our product candidates in
foreign markets. We are not permitted to market or promote any of our product candidates before we receive regulatory
approval from applicable regulatory authorities in foreign markets, and we may never receive such regulatory approvals for
any of our product candidates. To obtain separate regulatory approval in many other countries we must comply with
numerous and varying regulatory requirements regarding safety and efficacy and governing, among other things, clinical
trials, commercial sales, pricing and distribution of our product candidates. If we obtain regulatory approval of our product
candidates and ultimately commercialize our product candidates in foreign markets, we would be subject to additional risks
and uncertainties, including the burden of complying with complex and changing foreign regulatory, tax, accounting and
legal requirements and the reduced protection of intellectual property rights in some foreign countries.
Recent U.S. tax legislation and future changes to applicable U.S. or foreign tax laws and regulations may have a
material adverse effect on our business, financial condition and results of operations.
We are subject to income and other taxes in the U.S. and foreign jurisdictions. Changes in laws and policy relating
to taxes or trade may have an adverse effect on our business, financial condition and results of operations. For example, the
U.S. government recently enacted significant tax reform, and certain provisions of the new law may adversely affect us.
Changes include, but are not limited to, a federal corporate tax rate decrease from 35% to 21% for tax years beginning after
December 31, 2017, the transition of U.S. international taxation from a worldwide tax system to a more generally territorial
system, and a one-time transition tax on the mandatory deemed repatriation of foreign earnings. The legislation is unclear
in many respects and could be subject to potential amendments and technical corrections, and will be subject to
interpretations and implementing regulations by the Treasury and Internal Revenue Service, any of which could mitigate or
increase certain adverse effects of the legislation. In addition, it is unclear how these U.S. federal income tax changes will
affect state and local taxation. Generally, future changes in applicable U.S. or foreign tax laws and regulations, or their
interpretation and application could have an adverse effect on our business, financial conditions and results of operations.
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Our internal computer systems, or those of any of our existing or potential future collaborators, CROs or other
contractors or consultants, may fail or suffer security breaches, which could result in a material disruption of our
product development programs.
We maintain sensitive company data on our computer networks, including our intellectual property and
proprietary business information. We face a number of threats to our networks from unauthorized access, security breaches
and other system disruptions. Despite the implementation of security measures, our information technology and other
internal computer systems and those of our current and any future CROs and other contractors, consultants and
collaborators are vulnerable to damage from cyberattacks, “phishing” attacks, computer viruses, unauthorized access,
natural disasters, terrorism, war and telecommunication and electrical failures. Attacks upon information technology
systems are increasing in their frequency, levels of persistence, sophistication and intensity, and are being conducted by
sophisticated and organized groups and individuals with a wide range of motives and expertise. As a result of the COVID-
19 pandemic, we may also face increased cybersecurity risks due to our reliance on internet technology and the number of
our employees who are working remotely, which may create additional opportunities for cybercriminals to exploit
vulnerabilities. Furthermore, because the techniques used to obtain unauthorized access to, or to sabotage, systems change
frequently and often are not recognized until launched against a target, we may be unable to anticipate these techniques or
implement adequate preventative measures. We may also experience security breaches that may remain undetected for an
extended period. Any such security breach may compromise information stored on our networks, or those of our vendors,
and may result in significant data losses or theft of our intellectual property or proprietary business information. Further, if
such an event were to occur and cause interruptions in our operations, it could result in a material disruption of our
development programs and our business operations, whether due to a loss of our trade secrets or other similar disruptions.
For example, the loss of clinical trial data from completed or future clinical trials could result in delays in our regulatory
approval efforts and significantly increase our costs to recover or reproduce the data. In addition, such a breach may require
notification to governmental agencies, the media or individuals pursuant to various federal and state privacy and security
laws, if applicable, including HIPAA, as amended by the Health Information Technology for Economic and Clinical Health
Act, and regulations implemented thereunder, as well as regulations promulgated by the Federal Trade Commission and
state breach notification laws. We would also be exposed to a risk of loss, including financial assets or litigation and
potential liability, which could materially adversely affect our business, reputation, financial condition, results of
operations and prospects. We also rely on third parties to manufacture our product candidates, and similar events relating to
their computer systems could also have a material adverse effect on our business. To the extent that any disruption or
security breach were to result in a loss of, or damage to, our data or applications, or inappropriate disclosure of confidential
or proprietary information, we could incur liability and the further development and commercialization of our product
candidates could be delayed.
Changes in and failures to comply with U.S. and foreign privacy and data protection laws, regulations and standards
may adversely affect our business, operations and financial performance.
We are subject to or affected by numerous federal, state and foreign laws and regulations, as well as regulatory
guidance, governing the collection, use, disclosure, retention, and security of personal data, such as information that we
collect about patients and healthcare providers in connection with clinical trials in the United States and abroad. The global
data protection landscape is rapidly evolving, and implementation standards and enforcement practices are likely to remain
uncertain for the foreseeable future. This evolution may create uncertainty in our business, affect our or our collaborators’,
service providers’ and contractors’ ability to operate in certain jurisdictions or to collect, store, transfer use and share
personal information, necessitate the acceptance of more onerous obligations in our contracts, result in liability or impose
additional costs on us. In the United States, numerous federal and state laws and regulations could apply to our operations
or the operations of our partners, including state data breach notification laws, state health information privacy laws, and
federal and state consumer protection laws and regulations (e.g. Section 5 of the FTC Act), that govern the collection, use,
disclosure, and protection of health-related and other personal information. In addition, we may obtain health information
from third parties (including research institutions from which we obtain clinical trial data) that are subject to privacy and
security requirements under HIPAA. Depending on the facts and circumstances, we could be subject to criminal penalties if
we knowingly obtain, use, or disclose individually identifiable health information that was provided to us by a HIPAA-
covered entity in a manner that is not authorized or permitted by HIPAA.
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Further, California enacted the CCPA, on June 28, 2018, which went into effect on January 1, 2020. The CCPA
gives California residents expanded rights to access and delete their personal information, opt out of certain personal
information sharing, and receive detailed information about how their personal information is used. The CCPA provides for
civil penalties for violations, as well as a private right of action for data breaches that is expected to increase data breach
litigation. Although there are limited exemptions for health-related information, including clinical trial data, the CCPA may
increase our compliance costs and potential liability. Further, the CPRA, recently passed in California, which will impose
additional data protection obligations on covered businesses, including additional consumer rights processes, limitations on
data uses, new audit requirements for higher risk data, and opt outs for certain uses of sensitive data. It will also create a
new California data protection agency authorized to issue substantive regulations and could result in increased privacy and
information security enforcement. The majority of the provisions will go into effect on January 1, 2023, and additional
compliance investment and potential business process changes may be required. Similar laws have been proposed in other
states and at the federal level, and if passed, such laws may have potentially conflicting requirements that would make
compliance challenging.
Our operations abroad may also be subject to increased scrutiny or attention from data protection authorities.
Many countries in these regions have established or are in the process of establishing privacy and data security legal
frameworks with which we, our collaborators, service providers, including our CRO, and contractors must comply. For
example, the GDPR, which went into effect in May 2018, imposes strict requirements for processing the personal data of
individuals within the EEA, including clinical trial data. The GDPR has and will continue to increase compliance burdens
on us, including by mandating potentially burdensome documentation requirements and granting certain rights to
individuals to control how we collect, use, disclose, retain and process information about them. The processing of sensitive
personal data, such as physical health condition, may impose heightened compliance burdens under the GDPR and is a
topic of active interest among foreign regulators. Further, recent legal developments in Europe have created complexity and
uncertainty regarding transfers of personal data from the EEA to the United States, e.g. on July 16, 2020, the Court of
Justice of the European Union, or the CJEU invalidated the EU-US Privacy Shield Framework, or the Privacy Shield under
which personal data could be transferred from the EEA to US entities who had self-certified under the Privacy Shield
scheme. While the CJEU upheld the adequacy of the standard contractual clauses (a standard form of contract approved by
the European Commission as an adequate personal data transfer mechanism, and potential alternative to the Privacy
Shield), it made clear that reliance on them alone may not necessarily be sufficient in all circumstances. Use of the standard
contractual clauses must now be assessed on a case-by-case basis taking into account the legal regime applicable in the
destination country, in particular applicable surveillance laws and rights of individuals and additional measures and/or
contractual provisions may need to be put in place, however, the nature of these additional measures is currently uncertain.
As supervisory authorities issue further guidance on personal data export mechanisms, including circumstances where the
standard contractual clauses cannot be used, and/or start taking enforcement action, we could suffer additional costs,
complaints and/or regulatory investigations or fines, and/or if we are otherwise unable to transfer personal data between
and among countries and regions in which we operate, it could affect the manner in which we provide our services, the
geographical location or segregation of our relevant systems and operations, and could adversely affect our financial
results. In addition, the GDPR provides for robust regulatory enforcement and fines of up to €20 million or 4% of the
annual global revenue of the noncompliant company, whichever is greater. Further, from January 1, 2021, we will have to
comply with the GDPR and the UK GDPR, which, together with the amended UK Data Protection Act 2018, retains the
GDPR in United Kingdom national law, the latter regime having the ability to separately fine up to the greater of £17.5
million or 4% of global turnover. The relationship between the United Kingdom and the EU in relation to certain aspects of
data protection law remains unclear, and it is unclear how United Kingdom data protection laws and regulations will
develop in the medium to longer term, and how data transfers to and from the United Kingdom will be regulated in the
long term. Currently there is a four to six-month grace period agreed in the EU and United Kingdom Trade and
Cooperation Agreement, ending June 30, 2021 at the latest, whilst the parties discuss an adequacy decision. However, it is
not clear whether (and when) an adequacy decision may be granted by the European Commission enabling data transfers
from EU member states to the United Kingdom long term without additional measures. These changes may lead to
additional costs and increase our overall risk exposure.
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As we expand into other foreign countries and jurisdictions, we may be subject to additional laws and regulations
that may affect how we conduct business. The cost of compliance with these laws, regulations and standards is high and is
likely to increase in the future. Any failure or perceived failure by us or our collaborators, service providers and contractors
to comply with federal, state or foreign laws or regulation, our internal policies and procedures or our contracts governing
processing of personal information could result in negative publicity, diversion of management time and effort and
proceedings against us by governmental entities or others. In many jurisdictions, enforcement actions and consequences for
noncompliance are rising.
Our operations could be subject to earthquakes, power shortages, telecommunications failures, water shortages,
floods, hurricanes, typhoons, fires, extreme weather conditions, medical epidemics and pandemics, such as the COVID-19
pandemic, and other natural or manmade disasters or business interruptions, for which we are predominantly self-insured.
We currently rely on several different manufacturers who supply different parts of the ciforadenant molecule and CPI-818
molecule, on one manufacturer for CPI-006 drug substance and on other third-party manufacturers to produce our other
product candidates. Our ability to obtain clinical supplies of CPI-006, CPI-818 and ciforadenant or our other product
candidates could be disrupted if the operations of these suppliers were affected by a man-made or natural disaster or other
business interruption. The occurrence of any of these business disruptions could seriously harm our operations and
financial condition and increase our costs and expenses.
In response to the COVID-19 pandemic, we have limited the use of our physical facilities and many of our employees
work remotely. We intend to make full use of our physical facilities after national, state and local authorities have indicated
that it is safe to do so. In the event of a continuation of shelter-in-place orders or mandated local travel restrictions, our
employees conducting research and development activities may not be able to access our facilities and our activities may
be significantly limited or curtailed, possibly for an extended period of time. Furthermore, it is possible that over the long
term our operational efficiency may be decreased if our employees and third-party collaborators are unable to meet and
work in the same physical location.
Our ability to use net operating loss carryforwards and other tax attributes may be limited.
We have incurred substantial losses during our history and do not expect to become profitable in the near future,
and we may never achieve profitability. To the extent that we continue to generate taxable losses, unused losses will carry
forward to offset future taxable income, if any, until such unused losses expire. As of December 31, 2020, we had federal
net operating loss (“NOL”) carryforwards of approximately $177.2 million and state NOL carryforwards of approximately
$206.7 million available to offset future taxable income. If not utilized, the federal and state NOL carryforwards will begin
to expire in various years beginning in 2034. As of December 31, 2020, we also had $6.8 million of federal and
$3.9 million of state research and development tax credit carryforwards available to reduce future income taxes. The
federal research and development tax credits will begin to expire in 2035, if not utilized. The state research and
development tax credits have no expiration date. Utilization of NOL carryforwards and credits may be subject to an annual
limitation due to the “ownership change” provisions under Sections 382 and 383 of the Internal Revenue Code of 1986, as
amended. An “ownership change” is generally defined as a cumulative change in the ownership interest of significant
stockholders over a rolling three-year period in excess of 50 percentage points. Similar provisions under state tax law may
also apply. If finalized, Treasury Regulations currently proposed under Section 382 of the Code may further limit our
ability to utilize our pre-change NOLs or credits if we undergo a future ownership change. We may experience an
ownership change in the future as a result of subsequent shifts in our stock ownership, some of which changes are outside
our control. Such ownership changes could result in the expiration of our NOL carryforwards and other tax attributes
before they can be utilized and, if we are profitable, our future cash flows could be adversely affected due to our increased
tax liability.
Additionally, under the Tax Cut and Jobs Act (the “Tax Act”), as modified by the Coronavirus Aid, Relief, and
Economic Security Act (the “CARES Act”), NOL carryforwards arising in tax years beginning after December 31, 2020
are limited to 80% of taxable income. Under the Tax Act, federal NOL carryforwards arising in tax years beginning after
December 31, 2017 may be carried forward indefinitely. Under the CARES Act, federal NOL carryforwards arising in tax
years beginning after December 31, 2017 and before January 1, 2021 may be carried back to each of the five tax years
preceding the tax year of such loss. The changes in the carryforward and carryback periods as well as the limitation on use
of NOL carryforwards may significantly impact our ability to use NOL carryforwards, particularly for tax years
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beginning after December 31, 2020, as well as the timing of any such use, and could adversely affect our results of
operations.
If securities or industry analysts do not publish research or reports or publish unfavorable research or reports about
our business, our stock price and trading volume could decline.
The trading market for our common stock is influenced by the research and reports that industry or securities analysts
publish about us or our business. If any of the analysts who cover us issue an adverse or misleading opinion regarding us,
our business model, our intellectual property or our stock performance, or if our target studies and operating results fail to
meet the expectations of analysts, our stock price would likely decline. If one or more of these analysts cease coverage of
us or fail to publish reports on us regularly, we could lose visibility in the financial markets, which in turn could cause our
stock price or trading volume to decline.
Item 1B. Unresolved Staff Comments
None
Item 2. Properties
We currently lease approximately 27,280 square feet of office and research and development facilities in
Burlingame, California. Our lease expires in 2023. We frequently explore alternatives that would provide us with additional
space to accommodate our anticipated growth.
Item 3. Legal Proceedings
We are not currently a party to any material litigation or legal proceedings; however, we may from time to time be
involved in various legal proceedings incident to the ordinary course of our business.
Item 4. Mine Safety Disclosures
Not applicable.
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Part II
Item 5. Market for Registrant’s Common Equity, Related Stockholder Matters, and Issuer Purchases of Equity
Securities
Market Information for Common Stock
Our common stock has been listed on The Nasdaq Global Market under the symbol “CRVS” since March 23,
2016. Prior to that there was no public trading market for our common stock. The following table sets forth for the
indicated periods the high and low sales prices per share for our common stock on the Nasdaq stock market.
2020
First Quarter
Second Quarter
Third Quarter
Fourth Quarter
2019
First Quarter
Second Quarter
Third Quarter
Fourth Quarter
Holders of Record
Price Range
High
Low
$
$
$
$
$
$
$
$
6.35
4.24
6.88
5.74
5.44
4.75
8.10
5.10
$
$
$
$
$
$
$
$
1.01
1.91
2.51
3.64
3.55
3.23
2.91
2.53
As of March 25, 2021, there were approximately 23 stockholders of record of our common stock. The actual
number of stockholders is greater than this number of record holders, and includes stockholders who are beneficial owners,
but whose shares are held in street name by brokers and other nominees. This number of holders of record also does not
include stockholders whose shares may be held in trust by other entities.
Dividend Policy
We currently intend to retain future earnings, if any, for use in operation of our business and to fund future growth.
We have never declared or paid any cash dividends on our capital stock and do not anticipate paying any cash dividends in
the foreseeable future. Payment of cash dividends, if any, in the future will be at the discretion of our board of directors and
will depend on then-existing conditions, including our financial condition, operating results, contractual restrictions, capital
requirements, business prospects and other factors our board of directors may deem relevant.
Stock Performance Graph
The following graph shows the total stockholder’s return on an investment of $100 in cash at market close on
March 23, 2016 (the first day of trading of our common stock), through December 31, 2020 for (i) our common stock,
(ii) the Nasdaq Composite Index and (iii) the Nasdaq Biotechnology Index.
Pursuant to applicable Securities and Exchange Commission rules, all values assume reinvestment of the full
amount of all dividends, however, no dividends have been declared on our common stock to date. The stockholder return
shown on the graph below is not necessarily indicative of future performance, and we do not make or endorse any
predictions as to future stockholder return. This graph and the table below it shall not be deemed “soliciting material” or be
deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 as amended (the “Exchange Act”), or
otherwise subject to the liabilities under that Section, and shall not be deemed to be incorporated by reference into any
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of our filings under the Securities Act of 1933, as amended (the “Securities Act”), whether made before or after the date
hereof and irrespective of any general incorporation language in any such filing.
$100 investment in stock or index
Corvus (CRVS)
NASDAQ Composite Index (IXIC)
NASDAQ Biotech Index (˄NBI)
March 23, December 31, December 31, December 31, December 31, December 31,
2016
$ 100.00
$ 100.00
$ 100.00
$
$
$
2016
2017
2018
2019
100.35
112.88
104.36
$
$
$
72.70
144.76
126.33
$
$
$
25.75
139.14
114.55
$
$
$
38.18
188.15
142.51
$
$
$
2020
26.46
269.88
180.33
Securities Authorized for Issuance Under Equity Compensation Plans
The information required by this Item regarding equity compensation plans is incorporated by reference to the
information set forth in PART III Item 12 of this Annual Report on Form 10-K.
Use of Proceeds from Registered Securities
None.
Recent Sales of Unregistered Equity Securities
In November 2019, we entered into an exchange agreement (the “Exchange Agreement”) with entities affiliated
with Biotechnology Value Fund, L.P. (the “Exchanging Stockholders”), pursuant to which we exchanged an aggregate of
1,458,000 shares of our common stock owned by the Exchanging Stockholders for warrants (the “Exchange Warrants”) to
purchase an aggregate of 1,458,000 shares of common stock (subject to adjustment in the event of stock splits,
recapitalizations and other similar events affecting common stock), with an exercise price of $0.0001 per share. The
Exchange Warrants were issued without registration under the Securities Act of 1933, as amended (the “Securities Act”), in
reliance on the exemption from registration contained in Section 3(a)(9) of the Securities Act.
Issuer Purchases of Equity Securities by the Issuer and Affiliated Purchasers
None.
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Item 6. Selected Financial Data
You should read the following selected financial data together with the information under “Item 7. Management’s
Discussion and Analysis of Financial Condition and Results of Operations” and our consolidated financial statements and
related notes included in Part II, Item 8 of this Annual Report on Form 10 K. The selected consolidated statement of
operations data for each of the years ended December 31, 2020, 2019 and 2018 and the consolidated balance sheet data as
of December 31, 2020 and 2019 are derived from our audited consolidated financial statements included elsewhere in this
Annual Report on Form 10-K. The consolidated statement of operations data for the years ended December 31, 2017 and
2016 and the consolidated balance sheet data as of December 31, 2018, 2017 and 2016 are derived from our audited
consolidated financial statements which are not included in this Annual Report on Form 10-K. Our historical results of any
prior periods are not necessary indicative of results to be expected in any future period.
Consolidated Statements of Operations and Comprehensive Loss Data:
2020
Operating expenses:
Research and development
General and administrative
Total operating expenses
Loss from operations
Interest income and other expense, net.
Gain on deconsolidation of Angel Pharmaceuticals
Loss from equity method investment
Net loss
Net loss per share, basic and diluted
Shares used to compute net loss per share, basic and diluted
Other comprehensive income (loss):
Unrealized gain (loss) on marketable securities
Comprehensive loss
Consolidated Balance Sheet Data:
Cash, cash equivalents and marketable securities
Working capital
Total assets
Convertible preferred stock
Total stockholders’ equity (deficit)
Year Ended December 31,
2018
(In thousands, except share and per share amounts)
2019
2017
$
37,975
10,879
48,854
(48,854)
2,182
—
—
(46,672) $
(1.59) $
$
38,586
10,636
49,222
(49,222)
2,283
—
—
(46,939) $
(1.71) $
$
46,305
10,219
56,524
(56,524)
861
—
—
(55,663) $
(2.72) $
29,349,810
27,509,960
20,488,506
2016
29,356
7,620
36,976
(36,976)
601
—
—
(36,375)
(2.36)
15,422,041
$
$
31,830
11,930
43,760
(43,760)
540
37,459
(234)
(5,995) $
(0.20) $
$
$
29,478,878
(25)
(6,020) $
63
(46,609) $
7
(46,932) $
(2)
(55,665) $
6
(36,369)
$
2020
Year Ended December 31,
2018
2017
2019
2016
(In thousands)
$ 44,259
33,187
85,529
$ 77,982
69,119
83,646
$ 114,597
108,562
118,232
$ 90,055
82,265
94,775
—
—
—
—
$ 72,148
$ 71,111
$ 110,336
$ 84,835
83
$ 134,896
130,089
140,150
—
$ 132,801
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Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations
The following discussion should be read in conjunction with the consolidated financial statements and notes
thereto included elsewhere in this Annual report on Form 10-K. This Annual Report on Form 10-K, including the following
sections, contains forward-looking statements within the meaning of the federal securities laws. These statements are
subject to risks and uncertainties that could cause actual results and events to differ materially from those expressed or
implied by such forward-looking statements. For a detailed discussion of these risks and uncertainties, see the “Risk
Factors” section in Item 1A of this Annual Report on Form 10-K. We caution the reader not to place undue reliance on
these forward-looking statements, which reflect management’s analysis only as of the date of this Form 10-K. We undertake
no obligation to update forward-looking statements, which reflect events or circumstances occurring after the date of this
Form 10-K.
Overview
We are a clinical stage, immunology focused biopharmaceutical company developing drugs and antibodies that
target the most critical cellular elements of the immune system. Our strategy is to focus our efforts on the development of
immune modulator product candidates to treat COVID-19, T-cell lymphomas, other cancers and autoimmune diseases. We
have built a pipeline of five programs, three of which are in clinical development.
Our lead product candidate is CPI-006, a potent humanized monoclonal antibody that is designed to react with a
specific site on CD73. In both preclinical and in vivo studies in cancer patients and patients with COVID-19, CPI-006 has
demonstrated binding to various immune cells and the inducement of a humoral adaptive immune response. We believe
CPI-006 has the potential to be an important new therapeutic agent with a novel mechanism of action for the treatment of a
broad range of infectious diseases and cancers.
We are evaluating CPI-006 in a global, randomized, double-blind, Phase 3 trial designed to evaluate the efficacy
and safety of CPI-006 compared to placebo in hospitalized patients with mild-to-moderate COVID-19. The primary
endpoint of the trial is the proportion of patients progressing to respiratory failure or death during the 28 days after dosing.
The trial was designed with input from the U.S. Food and Drug Administration, or FDA.
Our next product candidate, CPI-818, is a selective, covalent inhibitor of ITK and is in a multi-center Phase 1/1b
clinical trial in patients with various malignant T-cell lymphomas. CPI-818 is designed to inhibit the proliferation of certain
malignant T-cells, and we believe it also has the potential to regulate the growth of abnormal T cells involved in
autoimmunity.
Our third product candidate, ciforadenant (formerly CPI-444), is an oral, small molecule antagonist of the A2A
receptor for adenosine with which we completed a Phase 2 expansion protocol in combination with Genentech, Inc.’s
cancer immunotherapy, Tecentriq® (atezolizumab) for patients with either advanced or refractory renal cell cancer
(“RCC”). We have identified a novel biomarker that may enable us to select patients most likely to benefit from
ciforadenant. In studies presented at the American Society of Oncology (“ASCO”) meeting in 2020, patients expressing
this marker in their tumor had a 17% response rate. Activity was seen with both CPI-444 as a monotherapy and in
combination with Tecentriq. We have refined our strategy with ciforadenant and plan to collaborate with an academic
consortium to evaluate ciforadenant in a first line RCC Phase 2 trial as a triplet combination with pembrolizumab and a
tyrosine kinase inhibitor (“TKI”).
To date, the majority of our efforts have been focused on the research, development and advancement of CPI-006,
CPI-818 and ciforadenant, and we have not generated any revenue from product sales and, as a result, we have incurred
significant losses. We expect to continue to incur significant research and development and general and administrative
expenses related to our operations. Our net loss for the years ended December 31, 2020 and 2019 was $6.0 million and
$46.7 million, respectively. As of December 31, 2020, we had an accumulated deficit of $223.1 million. We expect to
continue to incur losses for the foreseeable future, and we anticipate these losses will increase as we continue our
development of, seek regulatory approval for and begin to commercialize CPI-006, CPI-818 and ciforadenant, and as we
develop other product candidates. Even if we achieve profitability in the future, we may not be able to sustain profitability
in subsequent periods.
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Since our inception and through December 31, 2019, we have funded our operations primarily through the sale
and issuance of stock. On March 22, 2016, our registration statement on Form S-1 (File No. 333-208850) relating to our
initial public offering (“IPO”) of our common stock was declared effective by the SEC. Shares of our common stock began
trading on the Nasdaq Global Market on March 23, 2016. The IPO closed on March 29, 2016, pursuant to which we sold
4,700,000 shares of our common stock at a public offering price of $15.00 per share. In April 2016, we sold an additional
502,618 shares of our common stock to the underwriters upon partial exercise of their over-allotment option, at the initial
offering price of $15.00 per share. We received aggregate net proceeds of approximately $70.6 million, after underwriting
discounts, commissions and offering expenses. Immediately prior to the consummation of the IPO, all of our outstanding
shares of convertible preferred stock were converted into 14.3 million shares of our common stock. In March 2018, in a
follow-on offering, we sold 8,117,647 shares of our common stock at a price of $8.50 per share, which included 1,058,823
shares issued pursuant to the underwriters’ exercise of their option to purchase additional shares of common stock. We
received aggregate net proceeds of approximately $64.9 million, after underwriting discounts, commissions and offering
expenses.
In March 2020, we entered into a open market sales agreement (the “Sales Agreement”) with Jefferies LLC
(“Jeffries”) to sell shares of the Company’s common stock, from time to time, with aggregate gross sales proceeds of up to
$50,000,000, through an at-the-market equity offering program under which Jeffries acts as our sales agent. Jeffries is
entitled to compensation for its services equal to 3.0% of the gross proceeds of any shares of common stock sold through
Jeffries under the Sales Agreement. As of December 31, 2020, we had sold 310,734 shares of our common stock for net
proceeds of approximately $1.2 million pursuant to the Sales Agreement. As of December 31, 2020, $48.7 million
remained for sale under the Sales Agreement.
In October 2020, we announced the formation and launch of Angel Pharmaceuticals Co., Ltd. (“Angel
Pharmaceuticals”), a new China based biopharmaceutical company with a mission to bring innovative quality medicines to
Chinese patients for treatment of serious diseases including cancer, autoimmune diseases and infectious diseases. We
formed Angel Pharmaceuticals as a wholly owned subsidiary and it launched with a post-money valuation of
approximately $106.0 million, based on an approximate $41.0 million cash investment from a Chinese investor group that
includes funds associated with Tigermed and Betta Pharmaceuticals, Hisun Pharmaceuticals and Zhejiang Puissance
Capital. Such cash is not available for our use. Contemporaneously with the financing, Angel Pharmaceuticals licensed the
rights to develop and commercialize our three clinical-stage candidates – CPI-006, CPI-818 and ciforadenant – in greater
China and obtained global rights to our BTK inhibitor preclinical programs. Under the collaboration, we currently have a
49.7% equity interest in Angel Pharmaceuticals, excluding 7% of Angel’s equity reserved for issuance under the Angel
ESOP, and are entitled to designate three individuals on Angel’s five-person Board of Directors.
As of December 31, 2020, we had capital resources consisting of cash, cash equivalents and marketable securities
of approximately $44.3 million. We do not expect our existing capital resources to be sufficient to enable us to fund the
completion of all of our ongoing or planned clinical trials and remaining development program of any of ciforadenant,
CPI-006 or CPI-818 through commercialization. In addition, our operating plan may change as a result of many factors,
including those described in the section of this report entitled “Risk Factors” and others currently unknown to us, and we
may need to seek additional funds sooner than planned, through public or private equity, debt financings or other sources,
such as strategic collaborations. Such financing would result in dilution to stockholders, imposition of debt covenants and
repayment obligations or other restrictions that may affect our business. If we raise additional capital through strategic
collaboration agreements, we may have to relinquish valuable rights to our product candidates, including possible future
revenue streams. In addition, additional funding may not be available to us on acceptable terms or at all and any additional
fundraising efforts may divert our management from its day-to-day activities, which may adversely affect our ability to
develop and commercialize our product candidates. Furthermore, even if we believe we have sufficient funds for our
current or future operating plans, we may seek additional capital due to favorable market conditions or strategic
considerations.
We currently have no manufacturing capabilities and do not intend to establish any such capabilities. We have no
commercial manufacturing facilities for our product candidates. As such, we are dependent on third parties to supply our
product candidates according to our specifications, in sufficient quantities, on time, in compliance with appropriate
regulatory standards and at competitive prices.
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Impact of COVID-19
COVID-19 was first identified in Wuhan, China in December 2019, and subsequently declared a pandemic by the
World Health Organization. COVID-19 has placed strains on the providers of healthcare services, including the healthcare
institutions where we conduct our clinical trials. These strains have resulted in institutions prohibiting the initiation of new
clinical trials, enrollment in existing clinical trials and restricting the on-site monitoring of clinical trials. As our oncology
clinical trial enrollment goals for 2020 were largely completed in our first quarter, we have not been significantly affected
by any clinical trial enrollment restrictions. Patients in our ongoing oncology clinical trials have generally completed their
scheduled visits and we have been able to collect the essential data from those visits. We also follow FDA guidance on
clinical trial conduct during the COVID-19 pandemic, including the remote monitoring of clinical data.
In alignment with public health guidance designed to slow the spread of COVID-19, as of mid-March 2020, we
implemented a reduced onsite staffing model and transitioned to a remote work plan for all employees other than those
providing essential services, such as our laboratory staff. For our onsite employees, we have implemented heightened
health and safety measures designed to comply with applicable federal, state and local guidelines in response to the
COVID-19 pandemic. We are further supporting all of our employees by leveraging virtual meeting technology and
encouraging employees to follow local health authority guidance. We may need to undertake additional actions that could
impact our operations if required by applicable laws or regulations or if we determine such actions to be in the best
interests of our employees.
Components of Results of Operations
Revenue
To date, we have not generated any revenues. We do not expect to receive any revenues from any product
candidates that we develop unless and until we obtain regulatory approval and commercialize our products or enter into
revenue-generating collaboration agreements with third parties.
Research and Development Expenses
Our research and development expenses consist primarily of costs incurred to conduct research and development
of our product candidates. We record research and development expenses as incurred. Research and development expenses
include:
● employee-related expenses, including salaries, benefits, travel and non-cash stock-based compensation
expense;
● external research and development expenses incurred under arrangements with third parties, such as contract
research organizations, preclinical testing organizations, contract manufacturing organizations, academic and
non-profit institutions and consultants;
● costs to acquire technologies to be used in research and development that have not reached technological
feasibility and have no alternative future use;
● license fees; and
● other expenses, which include direct and allocated expenses for laboratory, facilities and other costs.
We plan to increase our research and development expenses substantially as we continue the development and
potential commercialization of our product candidates. Our current planned research and development activities include the
following:
● enrollment and completion of our Phase 3 clinical trial of CPI-006 in hospitalized COVID-19 patients;
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● completion of our Phase 1/1b clinical trial and amended Phase 1b/2 clinical trial of ciforadenant;
● completion of our ongoing Phase 1/1b clinical trial of CPI-006 in cancer patients;
● enrollment and completion of our ongoing Phase 1/1b clinical trial of CPI-818;
● process development and manufacturing of drug supply of CPI-006, CPI-818 and ciforadenant; and
● preclinical studies under our other programs in order to select development product candidates.
In addition to our product candidates that are in clinical development, we believe it is important to continue
substantial investment in potential new product candidates to build the value of our product candidate pipeline and our
business.
Our expenditures on current and future preclinical and clinical development programs are subject to numerous
uncertainties related to timing and cost to completion. The duration, costs and timing of clinical trials and development of
product candidates will depend on a variety of factors, including many of which are beyond our control. The process of
conducting the necessary clinical research to obtain regulatory approval is costly and time consuming, and the successful
development of our product candidates is uncertain. The risks and uncertainties associated with our research and
development projects are discussed more fully in “Part I, Item 1A—Risk Factors.” As a result of these risks and
uncertainties, we are unable to determine with any degree of certainty the duration and completion costs of our research
and development projects or if, when or to what extent we will generate revenues from the commercialization and sale of
any of our product candidates that obtain regulatory approval. We may never succeed in achieving regulatory approval for
any of our product candidates.
General and Administrative Expenses
General and administrative expenses include personnel costs, expenses for outside professional services and
allocated expenses. Personnel costs consist of salaries, benefits and stock-based compensation. Outside professional
services consist of legal, accounting and audit services and other consulting fees. Allocated expenses consist of rent
expense related to our office and research and development facility.
We expect that our general and administrative expenses will increase in the future as we increase our headcount to
support our continued research and development and potential commercialization of one or more of our product candidates.
Results of Operations
Comparison of the periods below as indicated (in thousands):
Year ended December 31,
2019
2018
2020
Change
Change
2019 to 2020
2018 to 2019
Operating expenses:
Research and development
General and administrative
Total operating expenses
Loss from operations
Interest income and other expense, net
Gain on deconsolidation of Angel Pharmaceuticals
Loss from equity method investment
Net loss
10,879
48,854
11,930
43,760
$ 31,830 $ 37,975 $ 38,586
10,636
49,222
(43,760) (48,854) (49,222)
2,283
—
—
$ (6,145) $
1,051
(5,094)
5,094
(1,642)
37,459
(234)
$ (5,995) $ (46,672) $ (46,939) $ 40,677
2,182
—
—
37,459
(234)
540
$
(611)
243
(368)
368
(101)
—
—
267
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Research and Development Expenses
Research and development expenses for the years ended December 31, 2020 and 2019, consisted of the following
costs by program (specific program costs consist solely of external costs):
Ciforadenant (formerly CPI-444)
CPI‑006
CPI-818
Other programs
Unallocated employee and overhead costs
Change
Change
Year ended December 31,
2019
2020
2018
2019 to 2020
2018 to 2019
$ 3,784 $ 5,750 $ 10,378 $ (1,966) $ (4,628)
666
6,108
6,774
1,870
4,707
6,577
104
877
981
1,377
15,711 17,893
16,516
(611)
$ 31,830 $ 37,975 $ 38,586
2,182
(3,843)
(336)
(2,182)
$ (6,145) $
8,956
2,734
645
For the year ended December 31, 2020, the decrease in ciforadenant costs of $2.0 million as compared to the year
ended December 31, 2019, primarily consisted of a decrease of $1.5 million in clinical trial expenses, a decrease of $0.2
million in drug manufacturing costs and a decrease of $0.3 million in other outside services.
For the year ended December 31, 2020, the increase in CPI-006 costs of $2.2 million as compared to the year
ended December 31, 2019, primarily consisted of an increase of $3.5 million in clinical trial expenses as well as an
increase of $0.4 million in other outside services, partially offset by a decrease of $1.7 million in drug manufacturing costs.
For the year ended December 31, 2020, the decrease in CPI-818 costs of $3.8 million as compared to the year
ended December 31, 2019, primarily consisted of a decrease of $2.7 million in drug manufacturing costs, a decrease of
$0.4 million in clinical trial expenses and a decrease of $0.7 million in other outside services.
For the year ended December 31, 2020, the decrease in costs related to other programs of $0.3 million as
compared to the year ended December 31, 2019, primarily consisted of a decrease of $0.6 million in outside services,
partially offset by an increase of $0.3 million in drug manufacturing costs.
For the year ended December 31, 2020, the decrease in unallocated costs of $2.2 million as compared to the year
ended December 31, 2019, primarily consisted of a decrease of $1.5 million in outside services and a decrease of $0.7
million in personnel and related costs.
For the year ended December 31, 2019, the decrease in ciforadenant costs of $4.6 million as compared to the year
ended December 31, 2018, primarily consisted of a decrease of $2.8 million in drug manufacturing costs, a decrease of
$1.3 million in clinical trial expenses associated with lower enrollment in accordance with our protocol amendment
focusing on RCC and mCRPC patients and a decrease of $0.5 million in other outside services.
For the year ended December 31, 2019, the increase in CPI-006 costs of $0.7 million as compared to the year
ended December 31, 2018, primarily consisted of an increase of $1.2 million in clinical trial expenses, partially offset by a
decrease of $0.3 million in drug manufacturing costs and a decrease of $0.2 million in other outside services.
For the year ended December 31, 2019, the increase in CPI-818 costs of $1.9 million as compared to the year
ended December 31, 2018, primarily consisted of an increase of $2.2 million in clinical trial expenses, an increase of $0.6
million in drug manufacturing costs, and an increase of $0.2 million in other outside services, partially offset by a decrease
of $1.1 million in IND-enabling study costs.
For the year ended December 31, 2019, the increase in costs related to other programs of $0.1 million as
compared to the year ended December 31, 2018, primarily consisted of outside chemical synthesis and testing of research
compounds.
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For the year ended December 31, 2019, the increase in unallocated costs of $1.4 million as compared to the year
ended December 31, 2018, primarily consisted of an increase in personnel and related costs.
General and Administrative Expenses
For the year ended December 31, 2020, the increase in general and administrative expenses of $1.1 million as
compared to the year ended December 31, 2019, primarily consisted of an increase of $1.9 million in outside professional
services, partially offset by a decrease of $0.8 million in personnel and related costs.
For the year ended December 31, 2019, the increase in general and administrative expenses of $0.2 million as
compared to the year ended December 31, 2018, primarily consisted of an increase in personnel and related costs.
Interest Income and Other Expense, net
For the year ended December 31, 2020, the decrease in interest income and other expense, net of $1.6 million as
compared to the year ended December 31, 2019, primarily consisted of a decrease in interest income earned due to a
decrease in cash equivalents and marketable securities and a decrease in interest rates.
For the year ended December 31, 2019, the decrease in interest income and other expense, net of $0.1 million as
compared to the year ended December 31, 2018, primarily consisted of a decrease in interest income earned due to a
decrease in cash equivalents and marketable securities.
Gain on deconsolidation of Angel Pharmaceuticals
For the year ended December 31, 2020, the gain on deconsolidation of Angel Pharmaceuticals of $37.5 million
represents the fair value of our investment in Angel Pharmaceuticals at the date Angel Pharmaceuticals was deconsolidated
from our financial statements.
Loss from equity method investment
For the year ended December 31, 2020, the loss from equity method investment of $0.2 million represents our
share of the Angel Pharmaceutical’s loss for the period from deconsolidation of our investment in Angel Pharmaceuticals
through December 31, 2020.
Liquidity and Capital Resources
Sources of Liquidity
As of December 31, 2020, we had cash, cash equivalents and marketable securities of $44.3 million and an
accumulated deficit of $223.1 million, compared to cash, cash equivalents and marketable securities of $78.0 million and
an accumulated deficit of $217.1 million as of December 31, 2019. We have financed our operations primarily through
sales of our common stock and convertible preferred stock.
In March 2016, we consummated our IPO and sold 4,700,000 shares of our common stock at a price of $15.00 per
share, and in April 2016, sold 502,618 shares at a price of $15.00 per share pursuant to the partial exercise of the
underwriters’ option to purchase additional shares of common stock. We received net proceeds of approximately
$70.6 million, after deducting underwriting discounts, commissions and offering expenses. Immediately prior to the
consummation of our IPO, all outstanding shares of the convertible preferred stock were converted into common stock on a
one-for-one basis.
In March 2018, in a follow-on offering, we sold 8,117,647 shares of our common stock at a price of $8.50 per
share, which included 1,058,823 shares issued pursuant to the underwriters’ exercise of their option to purchase additional
shares of common stock. We received aggregate net proceeds of approximately $64.9 million, after underwriting discounts,
commissions and offering expenses.
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On February 17, 2021, we completed a follow-on public offering in which we sold 9,783,660 shares of common
stock at a price of $3.50 per share, which included 1,212,231 shares issued pursuant to the underwriters’ exercise of their
option to purchase additional shares of common stock. We received aggregate net proceeds of approximately $31.8 million,
net of underwriting discounts and commissions and offering expenses.
In March 2020, we entered into a Sales Agreement Jefferies LLC to sell shares of the Company’s common stock,
from time to time, with aggregate gross sales proceeds of up to $50,000,000, through an at-the-market equity offering
program under which Jeffries acts as our sales agent. Jeffries is entitled to compensation for its services equal to up to 3.0%
of the gross proceeds of any shares of common stock sold through Jeffries under the Sales Agreement. During the year
ended December 31, 2020, we received net proceeds of approximately $1.2 million from the sale of 310,734 shares of our
common stock pursuant to the Sales Agreement. As of December 31, 2020, $48.7 million remained for sale under the Sales
Agreement.
We believe our current cash, cash equivalents and marketable securities, including the net proceeds from our
February 2021 follow-on offering, will be sufficient to fund our planned expenditures and meet our obligations through at
least the next twelve months from the issuance of our consolidated financial statements as of and for year ended December
31, 2020. The amounts and timing of our actual expenditures depend on numerous factors, including:
● the progress, timing, costs and results of clinical trials for CPI-006, CPI-818 and ciforadenant;
● the extent to which the COVID-19 pandemic may impact our business, including our clinical trials and
financial condition;
● the timing, progress, costs and results of preclinical and clinical development activities for our other product
candidates;
● the number and scope of preclinical and clinical programs we decide to pursue;
● the costs involved in prosecuting, maintaining and enforcing patent and other intellectual property rights;
● the cost and timing of regulatory approvals;
● our efforts to enhance operational systems and hire additional personnel, including personnel to support
development of our product candidates and satisfy our obligations as a public company; and
● other factors described in the section of this report entitled “Risk Factors.”
We expect to increase our spending in connection with the development and commercialization of our product
candidates. Until such time, if ever, as we can generate substantial revenue from product sales, we expect to fund our
operations and capital funding needs through equity and/or debt financings. We may also enter into additional collaboration
arrangements or selectively partner for clinical development and commercialization. The sale of additional equity would
result in dilution to our stockholders. The incurrence of debt financing would result in debt service obligations and the
governing documents would likely include operating and financing covenants that would restrict our operations. In
addition, sufficient additional funding may not be available on acceptable terms, or at all. If we are not able to secure
adequate additional funding, we may be forced to make reductions in spending, extend payment terms with suppliers,
liquidate assets where possible and/or suspend or curtail planned programs. Any of these actions could have a material
effect on our business, financial condition and results of operations.
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Summary of Statement of Cash Flows
The following table summarizes our cash flows for the periods indicated (in thousands):
Year ended December 31,
2019
2018
2020
Change
Change
2019 to 2020
2018 to 2019
Net cash provided by (used in):
Operating activities
Investing activities
Financing activities
Net increase (decrease) in cash and cash equivalents
Cash Flows from Operating Activities
$ (34,778) $ (37,321) $ (40,988) $ 2,543
41,514
1,286
$ 11,301 $ (34,042) $ (5,910) $ 45,343
3,255 (30,192)
65,270
44,769
1,310
24
$
3,667
33,447
(65,246)
$ (28,132)
Cash used in operating activities during the year ended December 31, 2020 was $34.8 million, which primarily
consisted of a net loss of $6.0 million, adjusted by non-cash charges of $6.8 million, primarily consisting of $5.7 million of
stock compensation expense, a non-cash gain on deconsolidation of Angel Pharmaceuticals of $37.5 million, an increase of
$1.7 million in accounts payable and accrued and other liabilities and a decrease of $0.4 million in prepaid and other
current and non-current assets, partially offset by a decrease of $0.2 million in operating lease liability, net of operating
lease right-of-use asset amortization.
Cash used in operating activities during the year ended December 31, 2019 was $37.3 million, which primarily
consisted of a net loss of $46.7 million, adjusted by non-cash charges of $7.4 million, primarily consisting of $7.3 million
of stock compensation expense, an increase of $2.5 million in accounts payable and accrued and other liabilities and an
increase of $0.4 million in prepaid and other current assets, primarily associated with the timing of payments to vendors.
Cash used in operating activities during the year ended December 31, 2018 was $41.0 million, which primarily
consisted of a net loss of $46.9 million, adjusted by non-cash charges of $7.4 million, primarily consisting of $7.1 million
of stock compensation expense, a decrease of $2.0 million in accounts payable and accrued and other liabilities and a
decrease of $0.6 million in current and other assets, primarily associated with the timing of payments to vendors.
Cash Flows from Investing Activities
Cash provided by investing activities during the year ended December 31, 2020 was $44.8 million, which
consisted of proceeds from maturities of marketable securities of $86.4 million and proceeds from sales of marketable
securities of $1.0 million, partially offset by purchases of marketable securities of $42.5 million and purchases of property
and equipment of $0.1 million.
Cash provided by investing activities during the year ended December 31, 2019 was $3.3 million, which consisted
of proceeds from maturities of marketable securities of $141.9 million, which were partially offset by purchases of
marketable securities of $138.6 million.
Cash used in investing activities during the year ended December 31, 2018 was $30.2 million, which consisted of
purchases of marketable securities of $161.9 million and purchases of property and equipment of $0.4 million, which were
partially offset by proceeds from maturities of marketable securities of $132.0 million.
Cash Flows from Financing Activities
Cash provided by financing activities during the year ended December 31, 2020 was $1.3 million, which consisted
of $1.2 million in net proceeds from the issuance of common stock through our at-the-market offering program and $0.1
million of proceeds from the exercise of stock options.
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Cash provided by financing activities during the year ended December 31, 2019 was negligible.
Cash provided by financing activities during the year ended December 31, 2018 was $65.3 million, consisting of
$64.9 million of net proceeds from our follow-on offering and $0.4 million of proceeds from the exercise of stock options.
Off-Balance Sheet Arrangements
We have not entered into any off-balance sheet arrangements and do not have any holdings in variable interest
entities.
Contractual Obligations
We lease our facilities under a non-cancelable operating lease that expires in 2023. As of December 31, 2020,
contractual obligations were as follows (in thousands):
Contractual obligations:
Operating lease obligations
Total contractual obligations
Payment Due by Period
Total
Less than
1 year
2 - 3 years
4 - 5 years
5 years
More than
$ 2,559
$ 2,559
$ 1,260
$ 1,260
$ 1,299
$ 1,299
$
$
— $
— $
—
—
In August 2015 we entered into an agreement for a line of credit of $0.1 million for the purpose of issuing our
landlord a letter of credit of $0.1 million as a security deposit under our facility lease. We pledged money market funds and
marketable securities as collateral for the line of credit. Pursuant to our license agreements with each of Vernalis and
Scripps, we have obligations to make future milestone and royalty payments to these parties. However, because these
amounts are contingent, they have not been included on our balance sheet.
Critical Accounting Policies
Our management’s discussion and analysis of our financial condition and results of operations is based on our
consolidated financial statements, which have been prepared in accordance with United States generally accepted
accounting principles (“U.S. GAAP”). The preparation of these consolidated financial statements requires our management
to make judgments and estimates that affect the reported amounts of assets and liabilities and the disclosure of contingent
assets and liabilities at the date of the consolidated financial statements, as well as the reported revenue generated and
expenses incurred during the reporting periods. Our estimates are based on our historical experience and on various other
factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments
about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ
from these judgments and estimates under different assumptions or conditions and any such differences may be material.
We believe that the accounting policies discussed below are critical to understanding our historical and future performance,
as these policies relate to the more significant areas involving management’s judgments and estimates. Our significant
accounting policies are more fully described in Note 2 of Notes to Consolidated Financial Statements in Part II, Item 8 of
this Annual Report on Form 10-K.
Cash, Cash Equivalents and Marketable Securities
We consider all highly liquid investment securities with remaining maturities at the date of purchase of
three months or less to be cash equivalents.
Investments with remaining maturities, at the date of purchase, greater than three months, but less than one year
are considered short-term. We determined the appropriate classification of marketable securities at the time of purchase and
evaluates such designation as of each balance sheet date. To date, all marketable securities have been classified as
available-for-sale and are carried at fair value with unrealized gains and losses, if any, included as a component of
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accumulated other comprehensive income (loss) in stockholders’ equity (deficit). Interest and realized gains and losses are
included in interest income. Realized gains and losses are recognized based on the specific identification method.
Research and Development Expenses
We record research and development expenses as incurred. We account for nonrefundable advance payments for
goods and services that will be used in future research and development activities as expenses when the goods have been
received or when the service has been performed rather than when the payment is made. Research and development
expenses consist of costs incurred by us for the discovery and development of our product candidates and include:
● employee-related expenses, including salaries, benefits, travel and non-cash stock-based compensation
expense;
● external research and development expenses incurred under arrangements with third parties, such as contract
research organizations, contract manufacturing organizations, academic and non-profit institutions and
consultants;
● costs to acquire technologies to be used in research and development that have not reached technological
feasibility and have no alternative future use;
● license fees; and
● other expenses, which include direct and allocated expenses for laboratory, facilities and other costs.
Clinical Trial Accruals
Costs for preclinical studies and clinical trial activities are recognized based on an evaluation of the vendors’
progress towards completion of specific tasks, using data such as clinical site activations, patient enrollment or information
provided to us by our vendors regarding their actual costs incurred. Payments for these activities are based on the terms of
individual contracts and payment timing may differ significantly from the period in which the services are performed. We
determine accrual estimates through reports from and discussions with applicable personnel and outside service providers
as to the progress or state of completion, or the services completed. Our estimates of accrued expenses as of each balance
sheet date are based on the facts and circumstances known at the time
Recent Accounting Pronouncements
See Note 2 in Item 8 “Financial Statements and Supplementary Data.”
Segment Information
We have one primary business activity and operate as one reportable segment.
JOBS Act Accounting Election
We are an emerging growth company, as defined in the JOBS Act. Under the JOBS Act, emerging growth
companies can delay adopting new or revised accounting standards issued subsequent to the enactment of the JOBS Act
until such time as those standards apply to private companies. We have irrevocably elected not to avail ourselves of this
exemption from new or revised accounting standards and, therefore, will be subject to the same new or revised accounting
standards as other public companies that are not emerging growth companies. We also rely on other exemptions provided
by the JOBS Act, including, without limitation, providing an auditor’s attestation report on our system of internal controls
over financial reporting pursuant to Section 404(b) of the Sarbanes-Oxley Act. We will remain an emerging growth
company until the earlier of (1) December 31, 2021, (2) the last day of the fiscal year in which we have total annual gross
revenue of at least $1.07 billion, (3) the last day of the fiscal year in which we are
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deemed to be a “large accelerated filer” as defined in Rule 12b-2 under the Exchange Act, which would occur if the market
value of our common stock that is held by non-affiliates exceeded $700.0 million as of the last business day of the second
fiscal quarter of such fiscal year, or (4) the date on which we have issued more than $1.0 billion in non-convertible debt
during the prior three-year period. Even after we no longer qualify as an emerging growth company, we may still qualify as
a “smaller reporting company” which may allow us to take advantage of many of the same exemptions from disclosure
requirements including not being required to comply with the auditor attestation requirements of Section 404(b) of the
Sarbanes-Oxley Act.
Item 7A. Quantitative and Qualitative Disclosures about Market Risk
We are exposed to market risk related to changes in interest rates. We had cash, cash equivalents and marketable
securities of $44.3 million as of December 31, 2020, which consisted of U.S. Treasury securities, U.S. government agency
securities and corporate debt obligations. Such interest-earning instruments carry a degree of interest rate risk; however,
historical fluctuations of interest income have not been significant. Due to the short-term duration of our investment
portfolio and the low risk profile of our investments, an immediate 10% increase in interest rates would not have a material
effect on the fair market value of our portfolio.
We do not have any foreign currency or other derivative financial instruments.
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Item 8. Financial Statements and Supplementary Data
CORVUS PHARMACEUTICALS, INC.
ANNUAL REPORT ON FORM 10-K
INDEX TO CONSOLIDATED FINANCIAL STATEMENTS
Report of Independent Registered Public Accounting Firm
Consolidated Financial Statements
Consolidated Balance Sheets
Consolidated Statements of Operations and Comprehensive Loss
Consolidated Statements of Stockholders’ Equity
Consolidated Statements of Cash Flows
Notes to Consolidated Financial Statements
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96
97
98
99
100
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Report of Independent Registered Public Accounting Firm
To the Board of Directors and Stockholders of Corvus Pharmaceuticals, Inc.
Opinion on the Financial Statements
We have audited the accompanying consolidated balance sheets of Corvus Pharmaceuticals, Inc. (the “Company”) as of
December 31, 2020 and 2019, and the related consolidated statements of operations and comprehensive loss, of changes in
stockholders’ equity and of cash flows for each of the three years in the period ended December 31, 2020, including the
related notes (collectively referred to as the “consolidated financial statements”). In our opinion, the consolidated financial
statements present fairly, in all material respects, the financial position of the Company as of December 31, 2020, and the
results of its operations and its cash flows for each of the three years in the period ended December 31, 2020 in conformity
with accounting principles generally accepted in the United States of America.
Basis for Opinion
These consolidated financial statements are the responsibility of the Company’s management. Our responsibility is to
express an opinion on the Company’s consolidated financial statements based on our audits. We are a public accounting
firm registered with the Public Company Accounting Oversight Board (United States) (PCAOB) and are required to be
independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and
regulations of the Securities and Exchange Commission and the PCAOB.
We conducted our audits of these consolidated financial statements in accordance with the standards of the PCAOB. Those
standards require that we plan and perform the audit to obtain reasonable assurance about whether the consolidated
financial statements are free of material misstatement, whether due to error or fraud. The Company is not required to have,
nor were we engaged to perform, an audit of its internal control over financial reporting. As part of our audits, we are
required to obtain an understanding of internal control over financial reporting 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.
Our audits included performing procedures to assess the risks of material misstatement of the consolidated financial
statements, whether due to error or fraud, and performing procedures that respond to those risks. Such procedures included
examining, on a test basis, evidence regarding the amounts and disclosures in the consolidated financial statements. Our
audits also included evaluating the accounting principles used and significant estimates made by management, as well as
evaluating the overall presentation of the consolidated financial statements. We believe that our audits provide a reasonable
basis for our opinion.
Emphasis of Matter
As discussed in Note 1 to the consolidated financial statements, the Company will require additional financing to fund
future operations. Management’s plans in regard to this matter are described in Note 1.
/s/ PricewaterhouseCoopers LLP
San Jose, California
March 25, 2021
We have served as the Company’s auditor since 2015
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CORVUS PHARMACEUTICALS, INC.
CONSOLIDATED BALANCE SHEETS
(in thousands, except share data)
Assets
Current assets:
Cash and cash equivalents
Marketable securities
Prepaid and other current assets
Total current assets
Property and equipment, net
Operating lease right-of-use asset
Investment in Angel Pharmaceuticals
Other assets
Total assets
Liabilities and Stockholders’ Equity
Current liabilities:
Accounts payable
Operating lease liability
Accrued and other liabilities
Total current liabilities
Operating lease liability
Total liabilities
Commitments and contingencies (Note 13)
Stockholders’ equity:
December 31,
2020
December 31,
2019
$
$
$
$
$
$
16,455
27,804
1,077
45,336
906
1,648
37,225
414
85,529
3,467
1,078
7,604
12,149
1,232
13,381
5,154
72,828
1,362
79,344
1,462
2,327
—
513
83,646
2,448
878
6,899
10,225
2,310
12,535
Preferred stock: $0.0001 par value; 10,000,000 shares authorized at December 31, 2020
and December 31, 2019; 0 shares issued and outstanding at December 31, 2020 and
December 31, 2019
Common stock: $0.0001 par value; 290,000,000 shares authorized at December 31, 2020
and December 31, 2019; 28,372,634 and 27,953,233 shares issued and outstanding at
December 31, 2020 and December 31, 2019, respectively
Additional paid-in capital
Accumulated other comprehensive income
Accumulated deficit
Total stockholders’ equity
Total liabilities and stockholders’ equity
—
—
3
295,281
4
(223,140)
72,148
85,529
$
3
288,224
29
(217,145)
71,111
83,646
$
The accompanying notes are an integral part of these consolidated financial statements.
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CORVUS PHARMACEUTICALS, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(in thousands, except share and per share data)
Year Ended December 31,
2019
2018
2020
Operating expenses:
Research and development
General and administrative
Total operating expenses
Loss from operations
Interest income and other expense, net
Gain on deconsolidation of Angel Pharmaceuticals
Loss from equity method investment
Net loss
Net loss per share, basic and diluted
Shares used to compute net loss per share, basic and diluted
Other comprehensive loss:
Unrealized gain (loss) on marketable securities
Comprehensive loss
$
$
31,830
11,930
43,760
(43,760)
540
37,459
(234)
(5,995) $
(0.20) $
$
$
29,478,878
$
37,975
10,879
48,854
(48,854)
2,182
–
–
(46,672) $
(1.59) $
38,586
10,636
49,222
(49,222)
2,283
–
–
(46,939)
(1.71)
27,509,960
29,349,810
(25)
(6,020) $
63
(46,609) $
7
(46,932)
$
The accompanying notes are an integral part of these consolidated financial statements.
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CORVUS PHARMACEUTICALS, INC.
CONSOLIDATED STATEMENTS OF CHANGES IN STOCKHOLDERS’ EQUITY
(in thousands, except share and per share data)
Common Stock
Balance at December 31, 2017
Issuance of common stock upon follow-on public offering, net
Common stock issued on exercise of stock options
Vesting of restricted stock issued upon early exercise of stock
options
Stock-based compensation expense
Unrealized gain on marketable securities
Net loss
Balance at December 31, 2018
Retirement of common stock in exchange for common stock
warrant
Issuance of common stock warrant in exchange for retirement
of common stock
Common stock issued on exercise of stock options
Vesting of restricted stock issued upon early exercise of stock
options
Stock-based compensation expense
Unrealized gain on marketable securities
Net loss
Balance at December 31, 2019
Issuance of common stock in connection with at-the-market
offering, net
Common stock issued on exercise of stock options
Stock-based compensation expense
Unrealized loss on marketable securities
Net loss
Balance at December 31, 2020
Shares
21,041,250
8,117,647
165,033
—
—
—
—
29,323,930
(1,458,000)
—
87,303
—
—
—
—
27,953,233
310,734
108,667
—
—
—
28,372,634
$
$
$
$
Amount
2
1
—
—
—
—
—
3
—
—
—
—
—
—
—
3
—
—
—
—
—
3
$
$
$
$
Additional
Paid-in
Capital
208,408
64,876
393
28
7,135
—
—
280,840
(5,030)
5,030
24
12
7,348
—
—
288,224
1,222
88
5,747
—
—
295,281
Accumulated
Other
Comprehensive
Income (Loss)
$
(41)
—
—
$
Accumulated
Deficit
(123,534)
—
—
—
—
7
—
(34)
—
—
—
—
—
63
—
29
—
—
—
(25)
—
4
—
—
—
(46,939)
(170,473)
—
—
—
—
—
—
(46,672)
(217,145)
—
—
—
—
(5,995)
(223,140)
$
$
$
$
$
$
Total
Stockholders’
Equity
$
$
$
$
84,835
64,877
393
28
7,135
7
(46,939)
110,336
(5,030)
5,030
24
12
7,348
63
(46,672)
71,111
1,222
88
5,747
(25)
(5,995)
72,148
The accompanying notes are an integral part of these consolidated financial statements.
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CORVUS PHARMACEUTICALS, INC.
CONSOLIDATED STATEMENTS OF CASH FLOWS
(in thousands)
Cash flows from operating activities
Net loss
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
Accretion related to marketable securities
Stock-based compensation
Gain on deconsolidation of Angel Pharmaceuticals
Loss from equity method investment
Changes in operating assets and liabilities:
Prepaid and other current assets
Operating lease right-of-use asset
Other assets
Accounts payable
Accrued and other liabilities
Operating lease liability
Net cash used in operating activities
Cash flows from investing activities
Purchases of marketable securities
Sales of marketable securities
Maturities of marketable securities
Purchases of property and equipment
Net cash provided by (used in) investing activities
Cash flows from financing activities
Proceeds from issuance of common stock, net (includes $30,850 in aggregate
gross proceeds from related parties for the year ended December 31, 2018)
Proceeds from issuance of common stock in connection with at-the-
market offering, net
Proceeds from exercise of common stock options
Net cash provided by financing activities
Net increase (decrease) in cash and cash equivalents
Cash and cash equivalents at beginning of the period
Cash and cash equivalents at end of the period
Supplemental disclosures of cash flow information
Purchases of property and equipment incurred but not paid
Year Ended December 31,
2019
2018
2020
$ (5,995) $ (46,672) $
(46,939)
632
154
5,747
(37,459)
234
285
679
99
1,019
705
(878)
(34,778)
(42,540)
1,009
86,376
(76)
44,769
743
(644)
7,348
—
—
(370)
599
(50)
450
2,042
(767)
(37,321)
(138,586)
–
141,866
(25)
3,255
847
(608)
7,135
—
—
187
—
406
(1,456)
(560)
—
(40,988)
(161,861)
—
132,024
(355)
(30,192)
—
—
64,877
1,222
88
1,310
11,301
5,154
$ 16,455
—
24
24
(34,042)
39,196
5,154
$
$
—
393
65,270
(5,910)
45,106
39,196
$
— $
— $
84
The accompanying notes are an integral part of these consolidated financial statements.
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1. Organization
CORVUS PHARMACEUTICALS, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
Corvus Pharmaceuticals, Inc. (“Corvus” or the “Company”) was incorporated in Delaware on January 27, 2014
and commenced operations in November 2014. Corvus is a clinical-stage biopharmaceutical company. The Company’s
operations are located in Burlingame, California.
Presentation
The consolidated financial statements include the accounts of the Company and its wholly-owned subsidiaries,
Corvus Biopharmaceuticals, Ltd. and Corvus Hong Kong Limited. All significant intercompany accounts and transactions
have been eliminated from the consolidated financial statements.
Initial Public Offering
On March 22, 2016, the Company’s registration statement on Form S-1 (File No. 333-208850) relating to its
initial public offering (“IPO”) of its common stock was declared effective by the Securities and Exchange Commission
(“SEC”) and the shares of its common stock began trading on the Nasdaq Global Market on March 23, 2016. The public
offering price of the shares sold in the IPO was $15.00 per share. The IPO closed on March 29, 2016, pursuant to which the
Company sold 4,700,000 shares of its common stock. On April 26, 2016, the Company sold an additional 502,618 shares
of its common stock to the underwriters upon partial exercise of their over-allotment option, at the initial offering price of
$15.00 per share. The Company received aggregate net proceeds of approximately $70.6 million, after underwriting
discounts, commissions and offering expenses. Immediately prior to the consummation of the IPO, all outstanding shares
of convertible preferred stock were converted into common stock.
Follow-on Public Offering
In March 2018, the Company completed a follow-on public offering in which the Company sold 8,117,647 shares
of common stock at a price of $8.50 per share, which included 1,058,823 shares issued pursuant to the underwriters’
exercise of their option to purchase additional shares of common stock. The aggregate net proceeds received by the
Company from the offering were approximately $64.9 million, net of underwriting discounts and commissions and offering
expenses payable by the Company.
Liquidity
The Company is subject to risks and uncertainties common to early-stage companies in the biotechnology
industry, including, but not limited to, development by competitors of new technological innovations, protection of
proprietary technology, dependence on key personnel, contract manufacturer and contract research organizations,
compliance with government regulations and the need to obtain additional financing to fund operations. Since commencing
operations in 2014, the majority of the Company’s efforts have been focused on the research and development of CPI-006,
CPI-818 and ciforadenant. The Company believes that it will continue to expend substantial resources for the foreseeable
future as it continues clinical development of, seek regulatory approval for and, if approved, prepare for the
commercialization of ciforadenant, CPI-006, and CPI-818, as well as product candidates under the Company’s other
development programs. These expenditures will include costs associated with research and development, conducting
preclinical studies and clinical trials, obtaining regulatory approvals, manufacturing and supply, sales and marketing and
general operations. In addition, other unanticipated costs may arise. Because the outcome of any clinical trial and/or
regulatory approval process is highly uncertain, the Company may not be able to accurately estimate the actual amounts
necessary to successfully complete the development, regulatory approval process and commercialization of CPI-006, CPI-
818, and ciforadenant or any other product candidates. The Company does not expect its existing capital resources to be
sufficient to enable it to fund the completion of its clinical trials and remaining
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development program of CPI-006, CPI-818 and ciforadenant through commercialization. In addition, its operating plan
may change as a result of many factors.
The Company has incurred significant losses and negative cash flows from operations in all periods since
inception and had an accumulated deficit of $223.1 million as of December 31, 2020. The Company has historically
financed its operations primarily through the sale of redeemable convertible preferred stock and common stock. While the
Company has been able to raise multiple rounds of financing, there can be no assurance that in the event the Company
requires additional financing, such financing will be available on terms which are favorable or at all. Failure to generate
sufficient cash flows from operations, raise additional capital or reduce certain discretionary spending would have a
material adverse effect on the Company’s ability to achieve its intended business objectives.
As of December 31, 2020, the Company had cash, cash equivalents and short-term marketable securities of $44.3
million. Management believes that the Company’s current cash, cash equivalents and short-term marketable securities will
be sufficient to fund its planned operations for at least 12 months from the date of the issuance of these financial
statements.
The current COVID-19 (coronavirus) pandemic, which is impacting worldwide economic activity, poses risks that
the Company or its employees, contractors, suppliers, and other partners may be prevented from conducting business
activities for an indefinite period of time, including due to shutdowns that may be requested or mandated by governmental
authorities. The extent to which COVID-19 impacts the Company’s business, including its clinical trials and financial
condition, will depend on future developments, which are highly uncertain and cannot be predicted with confidence, such
as the ultimate geographic spread of the disease, the duration of the pandemic, travel restrictions and social distancing in
the United States and other countries, business closures or business disruptions and the effectiveness of actions taken in the
United States and other countries to contain and treat the disease. As COVID-19 continues to spread around the globe, we
will likely experience disruptions, including delays or difficulties in enrolling patients in our clinical trials, delays or
difficulties in clinical site initiation, interruption of key clinical trial activities, delays in clinical sites receiving the supplies
and materials needed to conduct our clinical trials and delays in necessary interactions with local regulatory authorities.
COVID-19 may also impact the Company’s ability to raise additional capital on a timely basis or at all, which could
negatively impact short-term and long-term liquidity.
Exchange Warrants
On November 8, 2019, the Company entered into an exchange agreement (the “Exchange Agreement”) with an
investor and its affiliates (the “Exchanging Stockholders”), pursuant to which the Company exchanged an aggregate of
1,458,000 shares of the Company’s common stock, par value $0.0001 per share, owned by the Exchanging Stockholders
for pre-funded warrants (the “Exchange Warrants”) to purchase an aggregate of 1,458,000 shares of common stock (subject
to adjustment in the event of any stock dividends and splits, reverse stock split, recapitalization, reorganization or similar
transaction, as described in the Exchange Warrants), with an exercise price of $0.0001 per share. The Exchange Warrants
will expire ten years from the date of issuance. The Exchange Warrants are exercisable at any time prior to expiration
except that the Exchange Warrants cannot be exercised by the Exchanging Stockholders if, after giving effect thereto, the
Exchanging Stockholders would beneficially own more than 9.99% of the Company’s common stock, subject to certain
exceptions. In accordance with Accounting Standards Codification Topic 505, Equity, and Accounting Research Bulletin
43, the Company recorded the retirement of the common stock exchanged as a reduction of common shares outstanding
and elected to record the excess over par value as a debit to additional paid-in-capital at the fair value of the Exchange
Warrants on the issuance date. The Exchange Warrants are classified as equity in accordance with Accounting Standards
Codification Topic 480, Distinguishing Liabilities from Equity, and Accounting Standards Codification Topic 815,
Derivatives and Hedging, and the fair value of the Exchange Warrants was recorded as a credit to additional paid-in capital
and is not subject to remeasurement. The Company determined that the fair value of the Exchange Warrants is substantially
similar to the fair value of the retired shares on the issuance date due to the negligible exercise price for the Exchange
Warrants. As of December 31, 2020, none of the Exchange Warrants have been exercised.
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2. Summary of Significant Accounting Policies
Basis of Presentation
The accompanying consolidated financial statements have been prepared in conformity with accounting principles
generally accepted in the United States of America (“U.S. GAAP”). The Company’s functional and reporting currency is
the U.S. dollar, except for its investment in its equity method investee which is the Chinese yuan. The accompanying
consolidated financial statements have been prepared on a going-concern basis, which contemplates the realization of
assets and discharge of liabilities in the normal course of business. Since its inception, the Company has incurred
significant losses and negative cash flows from operations. As of December 31, 2020, the Company had an accumulated
deficit of $223.1 million and cash, cash equivalents and marketable securities of $44.3 million. The Company has financed
its operations primarily with the proceeds from the sale of stock. The Company will need to raise additional capital to meet
its business objectives. The Company believes that its current cash, cash equivalents and marketable securities will be
sufficient to fund its planned expenditures and meet its obligations through at least the next twelve months from the
issuance of these financial statements.
Use of Estimates
The preparation of the Company’s consolidated financial statements in conformity with U.S. GAAP requires
management to make estimates and assumptions that affect the amounts reported in the consolidated financial statements
and accompanying notes. Actual results could differ from such estimates.
Concentrations of Credit Risk and Other Risks and Uncertainties
Substantially all of the Company’s cash and cash equivalents are deposited in accounts with two financial
institutions that management believes are of high credit quality. Such deposits may, at times, exceed federally insured
limits. The Company maintains its cash with an accredited financial institution and accordingly, such funds are subject to
minimal credit risk. The Company’s marketable securities consist of investments in U.S. Treasury securities, U.S.
government agency securities and corporate debt obligations, which can be subject to certain credit risks. However, the
Company mitigates the risks by investing in high-grade instruments, limiting its exposure to any one issuer, and monitoring
the ongoing creditworthiness of the financial institutions and issuers. The Company has not experienced any losses on its
deposits of cash, cash equivalents or marketable securities.
The Company is subject to a number of risks similar to other early stage biopharmaceutical companies, including,
but not limited to, the need to obtain adequate additional funding, possible failure of preclinical testing or clinical trials, its
reliance on third parties to conduct its clinical trials, the need to obtain marketing approval for its product candidates,
competitors developing new technological innovations, the need to successfully commercialize and gain market acceptance
of the Company’s product candidates, its right to develop and commercialize its product candidates pursuant to the terms
and conditions of the licenses granted to the Company, and protection of proprietary technology. If the Company does not
successfully commercialize or partner any of its product candidates, it will be unable to generate product revenue or
achieve profitability.
Segments
Operating segments are identified as components of an enterprise about which separate discrete financial
information is available for evaluation by the chief operating decision-maker in making decisions regarding resource
allocation and assessing performance. The Company views its operations and manages its business in one operating
segment, that of the development of and commercialization of precisely targeted oncology therapies.
Cash, Cash Equivalents and Marketable Securities
The Company considers all highly liquid investment securities with remaining maturities at the date of purchase
of three months or less to be cash equivalents.
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Investments with remaining maturities, at the date of purchase, greater than three months are classified as
“available-for-sale” and are carried at fair value with unrealized gains and losses, if any, included as a component of
accumulated other comprehensive income (loss) in stockholders’ equity. Interest and realized gains and losses are included
in interest income. Realized gains and losses are recognized based on the specific identification model.
Fair Value Measurements
Fair value accounting is applied for all financial assets and liabilities and non-financial assets and liabilities that
are recognized or disclosed at fair value in the consolidated financial statements on a recurring basis (at least annually).
The carrying amount of the Company’s financial instruments, including cash equivalents, accounts payable and accrued
liabilities, approximate fair value due to their short-term maturities.
Variable Interest Entities
The Company determines at the inception of each arrangement whether an entity in which the Company holds an
investment or in which the Company has other variable interests is considered a variable interest entity ("VIE"). The
Company consolidates VIEs when it is the primary beneficiary. The primary beneficiary of a VIE is the party that meets
both of the following criteria: (1) has the power to make decisions that most significantly affect the economic performance
of the VIE and (2) has the obligation to absorb losses or the right to receive benefits that in either case could potentially be
significant to the VIE. Periodically, the Company assesses whether any changes in the interest or relationship with the
entity affect the determination of whether the entity is still a VIE and, if so, whether the Company is the primary
beneficiary. If the Company is not the primary beneficiary in a VIE, the Company accounts for the investment or other
variable interest in accordance with applicable GAAP.
Investments in Equity Securities
Investments in equity securities over which the Company is able to exercise significant influence over the
investee, but does not control the investee, and is not the primary beneficiary of the investee’s activities that are considered
VIEs are accounted for using the equity method. Adjustments are made to investments accounted for using the equity
method for any earnings or losses incurred and are recorded in loss from operations. Investments in equity securities which
do not have readily determinable fair values and for which the Company is not able to exercise significant influence over
the investee are accounted for under the measurement alternative which is the cost minus impairment, if any, plus or minus
changes resulting from observable price changes in orderly transactions for the identical or similar securities of the same
investee and adjustments related to the basis differences, if any.
Property and Equipment, Net
Property and equipment are stated at cost and depreciated using the straight-line method over the estimated useful
lives of the respective assets:
Laboratory equipment
Computer equipment and purchased software
Leasehold improvements
5 years
3 years
Shorter of asset's useful life or remaining term of lease
Maintenance and repairs that do not extend the life or improve the asset are expensed when incurred. When assets
are retired or otherwise disposed of, the cost and accumulated depreciation or amortization are removed from the balance
sheet and any resulting gain or loss is reflected in operations.
Impairment of Long-Lived Assets
The Company regularly reviews the carrying value and estimated lives of all of its long-lived assets, including
property and equipment, to determine whether indicators of impairment may exist which warrant adjustments to carrying
values or estimated useful lives. The determinants used for this evaluation include management’s estimate of the asset’s
ability to generate positive income from operations and positive cash flow in future periods as well as the strategic
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significance of the assets to the Company’s business objectives. Should impairment exist, the impairment loss to be
recognized is measured by the amount by which the carrying amount of the asset exceeds the projected discounted future
net cash flows arising from the asset. All long-lived assets are maintained in the United States of America.
Research and Development Expenses
The Company records research and development expenses as incurred. The Company accounts for nonrefundable
advance payments for goods and services that will be used in future research and development activities as expenses when
the goods have been received or when the service has been performed rather than when the payment is made. Research and
development expenses consist of costs incurred by the Company for the discovery and development of the Company’s
product candidates and include:
● employee-related expenses, including salaries, benefits, travel and non-cash stock-based compensation
expense;
● external research and development expenses incurred under arrangements with third parties, such as contract
research organizations, contract manufacturing organizations, academic and non-profit institutions and
consultants;
● costs to acquire technologies to be used in research and development that have not reached technological
feasibility and have no alternative future use;
● license fees; and
● other expenses, which include direct and allocated expenses for laboratory, facilities and other costs.
Clinical Trial Accruals
Costs for preclinical studies and clinical trial activities are recognized based on an evaluation of the vendors’
progress towards completion of specific tasks, using data such as clinical site activations, patient enrollment or information
provided to the Company by its vendors regarding their actual costs incurred. Payments for these activities are based on the
terms of individual contracts and payment timing may differ significantly from the period in which the services are
performed. The Company determines accrual estimates through reports from and discussions with applicable personnel and
outside service providers as to the progress or state of completion, or the services completed. The Company’s estimates of
accrued expenses as of each balance sheet date are based on the facts and circumstances known at the time.
Stock-Based Compensation
The Company maintains incentive plans under which incentive stock options and nonqualified stock options may
be granted to employees and non-employee service providers.
The Company accounts for stock-based employee compensation arrangements in accordance with the provisions
of ASC 718, “Compensation—Stock Compensation.” For stock options granted to employees, the Company recognizes
compensation expense for all stock-based awards based on the grant-date estimated fair values. The value of the award is
recognized as an expense ratably over the requisite service period. The fair value of stock options is determined using the
Black-Scholes option pricing model. Forfeitures are accounted for when they occur.
Stock-based compensation expense related to stock options granted to non-employees is recognized based on the
fair value of the stock options, determined using the Black-Scholes option pricing model. The awards generally vest over
the time period the Company expects to receive service from the non-employee.
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Income Taxes
The Company accounts for income taxes under the asset and liability method. The Company estimates actual
current tax exposure together with assessing temporary differences resulting from differences in accounting for reporting
purposes and tax purposes for certain items, such as accruals and allowances not currently deductible for tax purposes.
These temporary differences result in deferred tax assets and liabilities, which are included in the Company’s balance
sheets. In general, deferred tax assets represent future tax benefits to be received when certain expenses previously
recognized in the Company’s statements of operations and comprehensive loss become deductible expenses, under
applicable income tax laws or when net operating loss or credit carryforwards are utilized. Accordingly, realization of the
Company’s deferred tax assets is dependent on future taxable income against which these deductions, losses and credits can
be utilized.
The Company must assess the likelihood that the Company’s deferred tax assets will be recovered from future
taxable income and a valuation allowance is recorded when it is more likely than not that the deferred tax asset will not be
recovered. The Company applies judgment in the determination of the financial statement recognition and measurement of
a tax position taken or expected to be taken in a tax return. Based on the available evidence, the Company is unable, at this
time, to support the determination that it is more likely than not that its deferred tax assets will be utilized in the future.
Accordingly, the Company recorded a full valuation allowance for all periods presented. The Company intends to maintain
a valuation allowance until sufficient evidence exists to support its reversal.
The Company recognizes benefits of uncertain tax positions if it is more likely than not such positions will be
sustained upon examination based solely on their technical merits as the largest amount of benefit that is more likely than
not to be realized upon the ultimate settlement. The Company recognizes any material interest and penalties related to
unrecognized tax benefits in income tax expense. The Company is required to file income tax returns in the U.S. federal
jurisdiction. The Company currently is not under examination by the Internal Revenue Service or other jurisdictions for
any tax years.
Comprehensive Loss
Comprehensive loss includes net loss as well as other changes in stockholders’ equity that result from transactions
and economic events other than those with stockholders. The Company’s only element of other comprehensive loss in any
period presented was unrealized gains and losses on available-for-sale marketable securities.
Net Loss per Share
Basic net loss per share is calculated by dividing the net loss by the weighted average number of common shares
outstanding and Exchange Warrants outstanding during the period, without consideration of potentially dilutive securities.
In accordance with Accounting Standards Codification Topic 260, Earnings Per Share, the Exchange Warrants are
included in the computation of basic net loss per share because the exercise price is negligible and they are fully vested and
exercisable at any time after the original issuance date. Diluted net loss per share is computed by dividing the net loss by
the weighted average number of common shares, Exchange Warrants, and potentially dilutive securities outstanding for the
period. Diluted net loss per share is the same as basic net loss per share for all periods presented since the effect of
potentially dilutive securities is anti-dilutive given the net loss of the Company.
Recent Accounting Pronouncements
In February 2016, the FASB issued ASU No. 2016-02, Leases (Topic 842), which requires lessees to recognize
leases on-balance sheet and disclose key information about leasing arrangements. Topic 842 was subsequently amended by
ASU No. 2018-01, Land Easement Practical Expedient for Transition to Topic 842; ASU No. 2018-10, Codification
Improvements to Topic 842, Leases; and ASU No. 2018-11, Targeted Improvements. The new standard establishes a right-
of-use (ROU) model that requires a lessee to recognize an ROU asset and lease liability on the balance sheet. Leases will
be classified as finance or operating, with classification affecting the pattern and classification of expense recognition in
the statement of operations. The Company adopted the new standard on January 1, 2019 and chose to apply the provisions
of ASC 842 as of the effective date with no restatement of prior periods. Additionally, the Company
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has elected the ‘package of practical expedients’, which permit it not to reassess under the new standard its prior
conclusions about lease identification, lease classification and initial direct costs. The Company did not elect the use-of-
hindsight or the practical expedient pertaining to land easements; the latter is not applicable to the Company. The Company
determines if an arrangement is a lease at inception and accounts for lease and non-lease components separately. The
Company has elected not to apply the recognition requirements of Topic 842 for leases with a term of 12 months or less.
Upon adoption of ASU 2016-02, the Company recognized an operating lease, right-of-use asset of $2.8 million and a
corresponding liability of $3.8 million and eliminated $1.0 million of deferred rent in the Company’s consolidated balance
sheet. The adoption of ASU 2016-02 did not have any impact on the Company’s consolidated statements of operations and
comprehensive loss. See also Note 12.
In December 2019, the FASB issued ASU No. 2019-12, "Income Taxes (Topic 740): Simplifying the Accounting
for Income Taxes", which is intended to improve consistency and simplify several areas of existing guidance. ASU 2019-
12 removes certain exceptions to the general principles related to the approach for intraperiod tax allocation, the
methodology for calculating income taxes in an interim period and the recognition of deferred tax liabilities for outside
basis differences. This new standard will be effective for the Company for fiscal years beginning after December 15, 2020,
including interim periods within those fiscal years. Early adoption is permitted. The Company will adopt this standard
effective January 1, 2021.
3. Net Loss per Share
The following table shows the calculation of net loss per share (in thousands, except share and per share data):
Numerator:
Net loss - basic and diluted
Denominator:
Weighted average common shares outstanding
Less: weighted average common shares subject to repurchase
Weighted average common shares outstanding used to compute basic
and diluted net loss per share
Net loss per share, basic and diluted
Year Ended December 31,
2019
2018
2020
$
(5,995) $
(46,672) $
(46,939)
29,478,878
29,364,535
(14,725)
27,686,909
(176,949)
—
29,478,878
$
(0.20) $
29,349,810
27,509,960
(1.71)
(1.59) $
The amounts in the table below were excluded from the calculation of diluted net loss per share, due to their anti-
dilutive effect:
Common stock subject to repurchase
Outstanding options
Total shares of common stock equivalents
—
6,664,173
6,664,173
—
5,643,410
5,643,410
4. Fair Value Measurements
Year Ended December 31,
2019
2020
2018
43,076
3,778,259
3,821,335
Financial assets and liabilities are measured and recorded at fair value. The Company is required to disclose
information on all assets and liabilities reported at fair value that enables an assessment of the inputs used in determining
the reported fair values. The fair value hierarchy prioritizes valuation inputs based on the observable nature of those inputs.
The fair value hierarchy applies only to the valuation inputs used in determining the reported fair value of the investments
and is not a measure of the investment credit quality. The hierarchy defines three levels of valuation inputs:
● Level 1—Quoted prices in active markets for identical assets or liabilities
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● Level 2—Inputs other than quoted prices included within Level 1 that are observable for the asset or liability,
either directly or indirectly
● Level 3—Unobservable inputs that reflect the Company’s own assumptions about the assumptions market
participants would use in pricing the asset or liability
There have been no transfers of assets and liabilities between levels of hierarchy.
The Company’s Level 2 investments are valued using third-party pricing sources. The pricing services utilize
industry standard valuation models, including both income and market-based approaches, for which all significant inputs
are observable, either directly or indirectly, to estimate fair value. These inputs include reported trades of and broker/dealer
quotes on the same or similar investments, issuer credit spreads, benchmark investments, prepayment/default projections
based on historical data and other observable inputs.
The following tables present information as of December 31, 2020 and 2019 about the Company’s assets that are
measured at fair value on a recurring basis and indicate the level of the fair value hierarchy the Company utilized to
determine such fair values (in thousands):
Assets
Cash equivalents
Marketable securities
Assets
Cash equivalents
Marketable securities
December 31, 2020
(Level 1)
Fair Value Measured Using
(Level 2)
(Level 3)
Total
Balance
15,974
6,074
22,048
$
$
— $
21,730
21,730
$
— $
—
— $
15,974
27,804
43,778
December 31, 2019
(Level 1)
Fair Value Measured Using
(Level 2)
(Level 3)
Total
Balance
4,252
7,023
11,275
$
$
— $
65,805
65,805
$
— $
—
— $
4,252
72,828
77,080
$
$
$
$
As of December 31, 2020, marketable securities had a maximum remaining maturity of eleven months.
As of December 31, 2020 and 2019, the fair value of available for sale marketable securities by type of security
were as follows (in thousands):
December 31, 2020
Gross
Gross
U.S. Treasury securities
U.S. Government agency securities
108
Amortized Unrealized Unrealized
Gains
Losses
$ — $ — $
Cost
$ 6,074
21,726
$ 27,800
5
5
$
$
Fair
Value
6,074
(1)
21,730
(1) $ 27,804
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U.S. Treasury securities
U.S. Government agency securities
Corporate debt obligations
5. Equity Method Investment
December 31, 2019
Gross
Gross
Amortized Unrealized Unrealized
Gains
Losses
Cost
$ 7,019
17,701
48,079
$ 72,799
$
$
4
16
17
37
$
$
Fair
Value
— $
7,023
— 17,717
48,088
(8)
(8) $ 72,828
In August 2020, the Company established Angel Pharmaceuticals Co. Ltd. (“Angel”), a wholly-owned corporate
venture in the People’s Republic of China (“China”) designed to develop, manufacture, and commercialize CPI-006, CPI-
444, and CPI-818 compounds for distribution within the countries of China, Taiwan, Macao, and Hong Kong (collectively,
the “Territories”) based on intellectual property licenses to be contributed to Angel by the Company.
In October 2020, Angel raised financing from third-party investors, the licenses were entered into and the
Company’s ownership interest was reduced to 53.2%. Under the license agreements, the Company is required to provide
manufacturing supply services for future supply of drug products for use in clinical trials, research and development,
operational support, and participate in the joint steering committee which oversees the development and commercialization
of the compounds. Angel is not required to make any payments to the Company regarding the licensed compounds or the
additional services outlined in the agreement. After a 7 year Exclusive Grant Back Period, Angel license grants to the
company for sole or jointly owned IP will be non-exclusive, fully paid and sublicensable. During the Exclusive Grant
Back Period, Angel license grants to the company for sole and joint IP are exclusive, fully paid and sublicensable.
As a result of the financing, the Company reassessed its interest in Angel and determined that while Angel is a
VIE, the Company is not considered the primary beneficiary of such VIE since Corvus does not have the power, through
voting or similar rights and the license agreements, to direct the activities of Angel that most significantly impact Angel’s
economic performance. Further, the Company determined that as it has a significant influence over Angel, and, therefore, it
shall account for its investment in Angel using the equity method starting in October 2020, the date it lost control over
Angel. At the date of loss of control, the Company derecognized all of Angel’s assets and liabilities from its balance sheet,
recognized the retained equity interest at its fair value of $37.5 million, and recognized a gain of $37.5 million, which is
included in gain on deconsolidation of Angel Pharmaceuticals on the consolidated statement of operations for the year
ended December 31, 2020.
As of December 31, 2020, the Company’s ownership interest in Angel was approximately 49.7%, excluding 7%
of Angel’s equity reserved for issuance under the Angel ESOP. The Company recognized its share of losses in Angel for
the total amount of $0.2 million as loss from equity method investment on the consolidated statement of operations for the
year ended December 31, 2020.
The Company’s maximum exposure to losses from its investment in Angel is to the extent of the carrying value of
its investment since the Company is not obligated to provide additional financial support. At December 31, 2020 the
Company reviewed its investment in Angel for impairment by determining whether events or changes in circumstances
indicate that the carrying amount of the investment may not be recoverable. In making this judgment, the Company
considered available quantitative and qualitative evidence in evaluating potential impairment of these investments. The
Company determined that the carrying value of the investment did not exceed its fair value and, therefore, there are no
indicators that its investment in Angel is impaired.
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Summary Financial Information
Summary financial information for Angel Pharmaceuticals is as follows:
Balance Sheet Data (unaudited)
Current assets
Current liabilities
Stockholders' equity
Statement of Operations Data (unaudited)
Net loss
Share of loss from investments accounted for using the equity method (1)
As of
December 31, 2020
(In thousands)
$
38,883
97
38,786
Year Ended
December 31, 2020
(In thousands)
$
(274)
(234)
(1) The Company’s share of loss is based on pro-rated net loss beginning October 2020 upon the deconsolidation of Angel
Pharmaceuticals.
6. License and Collaboration Agreements
Scripps Licensing Agreement
In December 2014, the Company entered into a license agreement with The Scripps Research Institute
(“Scripps”), pursuant to which it was granted a non-exclusive, world-wide license for all fields of use under Scripps’ rights
in certain know-how and technology related to a mouse hybridoma clone expressing an anti-human CD73 antibody, and to
progeny, mutants or unmodified derivatives of such hybridoma and any antibodies expressed by such hybridoma, from
which we developed CPI-006. Scripps also granted the Company the right to grant sublicenses in conjunction with other
proprietary rights the Company holds, or to others collaborating with or performing services for the Company. Under this
license agreement, Scripps has agreed not to grant any additional commercial licenses with respect to such materials, other
than march-in rights granted to the U.S. government.
Upon execution of the agreement, the Company made a one-time cash payment to Scripps of $10,000 in 2015 and
is also obligated to pay a minimum annual fee to Scripps of $25,000. The one-time cash payment was recorded as research
and development expense as technological feasibility of the asset had not been established and there was no alternative
future use. A minimum annual fee payment is due on each anniversary of the effective date of the agreement for the term of
the agreement. The Company is also required to make performance-based cash payments upon successful completion of
clinical and sales milestones. The aggregate potential milestone payments are $2.6 million. The Company is also required
to pay royalties on net sales of licensed products (including CPI-006) sold by it, its affiliates and its sublicensees at a rate in
the low-single digits. In addition, should the Company sublicense the rights licensed under the agreement, it has agreed to
pay a percentage of sublicense revenue received at specified rates that start at double digit percentages and decrease to
single digit percentages based on the elapsed time from the effective date of the agreement and the time of entry into such
sublicense. To date, no milestone payments have been made.
The Company’s license agreement with Scripps will terminate upon expiration of its obligation to pay royalties to
Scripps under the license agreement. The Company’s license agreement with Scripps is terminable by the consent of the
parties, at will by the Company upon providing 90 days written notice to Scripps, or by Scripps for certain material
breaches, or if the Company undergoes a bankruptcy event. In addition, Scripps may terminate the license on a product-by-
product basis, or the entire agreement, if the Company fails to meet specified diligence obligations related to
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the development and commercialization of licensed products. Scripps may also terminate the agreement after the third
anniversary of the effective date of the agreement if it reasonably believes, based on reports the Company provides to
Scripps, that the Company has not used commercially reasonable efforts as required under the agreement, subject to a
specified notice and cure period.
Vernalis Licensing Agreement
In February 2015, the Company entered into a license agreement with Vernalis (R&D) Limited (“Vernalis”),
which was subsequently amended as of November 5, 2015, and, pursuant to which the Company was granted an exclusive,
worldwide license under certain patent rights and know-how, including a limited right to grant sublicenses, for all fields of
use to develop, manufacture and commercialize products containing certain adenosine receptor antagonists, including
ciforadenant. Pursuant to this agreement, the Company made a one-time cash payment to Vernalis in the amount of
$1.0 million, which was recorded as research and development expense as technological feasibility of the asset had not
been established and there was no alternative future use. The Company is also required to make cash milestone payments
to Vernalis upon the successful completion of clinical and regulatory milestones for licensed products depending on the
indications for which such licensed products are developed and upon achievement of certain sales milestones. In February
2017, the Company made a milestone payment of $3.0 million to Vernalis following the expansion of a cohort of patients
with renal cell cancer treated with single agent ciforadenant in the Company’s Phase 1/1b clinical trial. The aggregate
potential milestone payments are approximately $220 million for all The Company has also agreed to pay Vernalis tiered
incremental royalties based on the annual net sales of licensed products containing ciforadenant on a product-by-product
and country-by-country basis, subject to certain offsets and reductions. The tiered royalty rates for products containing
ciforadenant range from the mid-single digits up to the low-double digits on a country-by-country net sales basis. The
royalties on other licensed products that do not include ciforadenant also increase with the amount of net sales on a
product-by-product and country-by-country basis and range from the low-single digits up to the mid-single digits on a
country-by-country net sales basis. The Company is also obligated to pay to Vernalis certain sales milestones as indicated
above when worldwide net sales reach specified levels over an agreed upon time period.
The agreement will expire on a product-by-product and country-by-country basis upon the expiration of the
Company’s payment obligations to Vernalis in respect of a particular product and country. Both parties have the right to
terminate the agreement for an uncured material breach by the other party. The Company may also terminate the agreement
at its convenience by providing 90 days written notice, provided that the Company has not received notice of its own
default under the agreement at the time the Company exercises such termination right. Vernalis may also terminate the
agreement if the Company challenges a licensed patent or undergoes a bankruptcy event.
Genentech Collaboration Agreement
In October 2015, the Company entered into a clinical trial collaboration agreement with Genentech to evaluate the
safety, tolerability and preliminary efficacy of ciforadenant combined with Genentech’s investigational cancer
immunotherapy, Tecentriq (atezolizumab), a fully humanized monoclonal antibody targeting protein programmed cell
death ligand 1(“PD-(L)1”), in a variety of solid tumors in a Phase 1/1b clinical trial. Pursuant to this agreement, the
Company will be responsible for the conduct and cost of the relevant studies, under the supervision of a joint development
committee made up of representatives of the Company and representatives of Genentech. Genentech will supply Tecentriq.
As part of the agreement, the Company granted Genentech certain rights of first negotiation to participate in future clinical
trials that the Company may conduct evaluating the administration of ciforadenant in combination with an anti-PD-1 or
anti-PD-L1 antibody. If the Company and Genentech do not reach agreement on the terms of any such participation by
Genentech within a specified time period, the Company retains the right to collaborate with third parties in such activities.
The Company also granted Genentech certain rights of first negotiation should it decide to license development and
commercialization rights to ciforadenant. Should the Company and Genentech not reach agreement on the terms of such a
license within a specified time period, it retains the right to enter into a license with another third party.
The Company and Genentech each have the right to terminate the agreement for material breach by the other
party. In addition, the agreement may be terminated by either party due to safety considerations, if directed by a
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regulatory authority or if development of ciforadenant or Tecentriq is discontinued. Further, the agreement will expire after
a set period of time following the provision by the Company of the final clinical study report to Genentech.
In May 2017, the Company signed a second clinical trial collaboration agreement with Genentech. Under the
second agreement, ciforadenant administered in combination with Tecentriq is being evaluated in a Phase 1b/2 randomized,
controlled clinical study, known as Morpheus, as second-line therapy in patients with non-small cell lung cancer who are
resistant and/or refractory to prior therapy with an anti-PD-(L)1 antibody. The patients in the Morpheus trial are currently
in the follow-up phase of the trial. Genentech is responsible for the conduct of the study and the parties share the cost of the
Morpheus trial, which began enrolling patients in the fourth quarter of 2017. The Company is responsible for supplying
ciforadenant and retains global development and commercialization rights to ciforadenant. The Company and Genentech
each have the right to terminate the agreement for material breach by the other party. In addition, the agreement may be
terminated by either party due to safety considerations, if directed by a regulatory authority or if development of
ciforadenant or Tecentriq is discontinued.
Monash License Agreement
In April 2017, the Company entered into a license agreement with Monash University (“Monash”), pursuant to
which the Company was granted an exclusive, sublicensable worldwide license under certain know-how, patent rights and
other intellectual property rights controlled by Monash to research, develop, and commercialize certain antibodies directed
to CXCR2 for the treatment of human diseases.
Upon execution of the agreement, the Company made a one-time cash payment to Monash of $275,000 and
reimbursed Monash for certain patent prosecution costs incurred prior to execution of the agreement. The Company is also
obligated to pay an annual license maintenance fee to Monash of $25,000 until a certain development milestone is met with
respect to the licensed product, after which no further maintenance fee will be due. The Company is also required to make
development and sales milestone payments to Monash with respect to the licensed products in the aggregate of up to
$45.1 million. The Company is also required to pay to Monash tiered royalties on net sales of licensed products sold by it,
its affiliates and its sublicensees at a rate ranging in the low-single digits. In addition, should the Company sublicense its
rights under the agreement, the Company has agreed to pay a percentage of sublicense revenue received at specified rates
that are currently at low double digit percentages and decrease to single digit percentages based on the achievement of
development milestones.
The term of the Company’s agreement with Monash continues until the expiration of its obligation to pay royalties
to Monash thereunder. The license agreement is terminable at will by the Company upon providing 30 days written notice
to Monash, or by either party for material breaches by the other party. In addition, Monash may terminate the entire
agreement or convert the license to a non-exclusive license if the Company has materially breached our obligation to use
commercially reasonable efforts to develop and commercialize a licensed product, subject to a specified notice and cure
mechanism.
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7. Balance Sheet Components (in thousands):
Prepaid and Other Current Assets
Interest receivable
Prepaid research and development manufacturing expenses
Prepaid facility expenses
Prepaid insurance
Other
Property and Equipment
Laboratory equipment
Computer equipment and purchased software
Leasehold improvements
Less: accumulated depreciation and amortization
Accrued and Other Liabilities
Accrued clinical trial related
Accrued manufacturing expense
Personnel related
Other
8. Common Stock
December 31, December 31,
2020
2019
$
$
$
$
$
$
86
181
160
244
406
1,077
2,472
142
2,084
4,698
(3,792)
906
4,681
321
2,225
377
7,604
$
$
$
$
$
$
329
240
157
150
486
1,362
2,396
142
2,084
4,622
(3,160)
1,462
4,300
696
1,624
279
6,899
As of December 31, 2020, the amended and restated certificate of incorporation authorizes the Company to issue
290 million shares of common stock and 10 million shares of preferred stock.
Each share of common stock is entitled to one vote. Common stockholders are entitled to dividends if and when
declared by the board of directors. As of December 31, 2020, no dividends on common stock had been declared.
In March 2020, the Company entered into an open market sale agreement (the “Sales Agreement”) with Jefferies
LLC (“Jefferies”) to sell shares of the Company’s common stock, from time to time, with aggregate gross sales proceeds of
up to $50,000,000, through an at-the-market equity offering program under which Jefferies will act as its sales agent. The
issuance and sale of shares of common stock by the Company pursuant to the Sales Agreement are deemed an “at-the-
market” offering under the Securities Act of 1933, as amended. Jefferies is entitled to compensation for its services equal to
up to 3.0% of the gross proceeds of any shares of common stock sold through Jefferies under the Sales Agreement.
During the year ended December 31, 2020, the Company sold an aggregate of 310,734 shares under its at-the-
market offering program at an average price of approximately $4.06 per share resulting in net proceeds of $1.2 million. As
of December 31, 2020, $48.7 million remained for sale under the Sales Agreement.
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The Company has reserved shares of common stock, for issuance as follows:
Exchange warrants
Shares available for future option grants
Outstanding options
Unvested restricted common stock (founders and early
exercise of stock options)
Shares reserved for employee stock purchase plan
Total
2020
1,458,000
1,692,753
6,664,173
December 31,
2019
1,458,000
1,704,183
5,643,410
—
400,000
10,214,926
—
400,000
9,205,593
2018
—
2,486,637
3,778,259
43,076
400,000
6,707,972
9. Stock Option Plans
In February 2014, the Company adopted the 2014 Equity Incentive Plan (the “2014 Plan”), which was
subsequently amended in November 2014, July 2015 and September 2015, under which it granted incentive stock options
(“ISOs”) or non-qualified stock options (“NSOs”). Terms of stock agreements, including vesting requirements, are
determined by the board of directors or a committee authorized by the board of directors, subject to the provisions of the
2014 Plan. In general, awards granted by the Company vest over four years and have maximum exercise term of 10 years.
The 2014 Plan provides that grants must be at an exercise price of 100% of fair market value of the Company’s common
stock as determined by the board of directors on the date of the grant.
In connection with the consummation of the IPO in March 2016, the 2016 Equity Incentive Award Plan (the
“2016 Plan”), became effective. Under the 2016 Plan, incentive stock options, non-statutory stock options, stock purchase
rights and other stock-based awards may be granted. Terms of stock agreements, including vesting requirements, are
determined by the board of directors or a committee authorized by the board of directors, subject to the provisions of the
2016 Plan. In general, awards granted by the Company vest over four years and have a maximum exercise term of 10
years. The 2016 Plan provides that grants must be at an exercise price of 100% of fair market value of the Company’s
common stock as determined by the board of directors on the date of the grant. In conjunction with adopting the 2016 Plan,
the 2014 Plan was terminated and no further awards will be granted under the 2014 Plan. Options outstanding under the
2014 Plan as of the effective date of the 2016 Plan that are forfeited or lapse unexercised may be re-issued under the 2016
Plan, up to a maximum of 1,136,229 shares.
Activity under the Company’s stock option plans is set forth below:
Options Outstanding
Shares
Available
for Grant
1,704,183
1,118,000
(1,620,000)
—
490,570
1,692,753
Number of
Options
Weighted ‑
Average
Exercise
Price
5,643,410
$
—
1,620,000
(108,667)
(490,570)
6,664,173
$
8.05
—
3.85
0.81
6.54
7.26
Balance at December 31, 2019
Additional shares authorized
Options granted
Options exercised
Options forfeited
Balance at December 31, 2020
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The following tables summarize information about stock options outstanding at December 31, 2020 and 2019:
Options Outstanding
at December 31, 2020
Weighted
Average
Remaining
Contractual
Life (in Years)
5.56
8.85
9.65
7.42
6.47
5.17
7.72
Number
190,500
1,628,459
1,707,500
899,959
955,947
1,281,808
6,664,173
$
$
$
$
$
$
$
Options Outstanding
at December 31, 2019
Weighted
Average
Remaining
Contractual
Life (in Years)
5.66
9.75
8.94
7.98
6.51
8.38
Number
191,000
2,027,500
1,061,522
1,051,738
1,311,650
5,643,410
$
$
$
$
$
$
Weighted
Average
Exercise Price
1.09
3.53
4.00
5.98
10.77
15.44
7.26
Weighted
Average
Exercise Price
0.36
3.61
5.95
10.83
15.49
8.05
Exercise Price
$0.28 - $2.00
$2.56 - $3.84
$5.82
$3.88
$5.94 - $8.91
$9.52 - $14.28
$14.43 - $21.64
Exercise Price
$0.28 - $2.56
$3.01 - $4.65
$4.84
$7.59
$9.52 - $14.43
$15.00 - $16.70
Options Vested
at December 31, 2020
Weighted
Average
Remaining
Contractual
Life (in Years)
2.28
8.53
8.08
6.97
6.31
5.15
6.22
Number
100,500
468,939
130,106
482,065
762,488
1,265,434
3,209,532
$
$
$
$
$
$
$
Options Vested
at December 31, 2019
Weighted
Average
Exercise
Price
0.28
3.56
3.99
5.98
10.76
15.42
10.23
Weighted
Average
Remaining
Contractual
Life (in Years)
5.52
6.01
8.90
7.93
6.44
7.05
Number
184,730
32,375
261,504
593,596
1,138,764
2,210,969
Weighted
Average
Exercise
Price
0.29
4.64
5.98
10.90
15.40
11.66
$
$
$
$
$
$
The weighted average grant date fair value of options granted for the years ended December 31, 2020, 2019 and
2018, was $2.66, $2.53 and $5.23, respectively.
Options outstanding and exercisable that had vested or were expected to vest at December 31, 2020 were as
follows:
Vested
Expected to vest
Number
of shares
3,209,532
3,454,641
$
$
Weighted
Average
Exercise Price
10.23
4.50
Weighted
Average
Remaining
Contractual
Life (years)
6.22
9.11
Aggregate
Intrinsic
Value
(in thousands)
339
193
$
$
In the table above, aggregate intrinsic value represents the difference between the exercise price of the options to
purchase common stock and the fair value of the Company’s common stock of $3.56 per share as of December 31, 2020.
The aggregate intrinsic value of stock options exercised in the years ended December 31, 2020, 2019 and 2018,
was $0.3 million, $0.4 million and $1.1 million, respectively.
The total fair value of options that vested in the year ended December 31, 2020, 2019 and 2018, was $6.0 million,
$7.8 million, and $7.1 million, respectively.
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10. Stock-Based Compensation
The Company’s results of operations include expenses relating to stock-based awards as follows (in thousands):
Research and development
General and administrative
Total
Valuation Assumptions
Year Ended December 31,
2019
$ 3,103
4,245
$ 7,348
2018
$ 2,919
4,216
$ 7,135
2020
$ 2,791
2,956
$ 5,747
The Company estimated the fair value of employee stock options using the Black-Scholes valuation model. The
fair value of employee stock options is being amortized on a straight-line basis over the requisite service period of the
awards. The fair value of employee stock options were estimated using the following assumptions for the years ended
December 31, 2020, 2019 and 2018:
Risk-free interest rate
Expected volatility
Expected term (in years)
Expected dividend yield
Year Ended December 31,
2019
2018
2020
0.5 %
82.7 %
6.0
0 %
1.9 %
82.1 %
6.0
0 %
2.8 %
82.7 %
6.0
0 %
Risk-free Interest Rate: The Company based the risk-free interest rate over the expected term of the options
based on the constant maturity rate of U.S. Treasury securities with similar maturities as of the date of the grant.
Volatility: The Company uses an average historical stock price volatility of a peer group of publicly traded
companies to be representative of its expected future stock price volatility, as the Company does not have sufficient trading
history for its common stock. For purposes of identifying these peer companies, the Company considers the industry, stage
of development, size and financial leverage of potential comparable companies. For each grant, the Company measures
historical volatility over a period equivalent to the expected term. The Company will continue to apply this process until a
sufficient amount of historical information regarding the volatility of its own stock price becomes available.
Expected Term: The Company uses the simplified method prescribed in the ASC 718, Compensation—Stock
Compensation, to calculate the expected term of options granted to employees and directors.
Expected Dividends: The Company has not paid and does not anticipate paying any dividends in the near future.
At December 31, 2020, 2019 and 2018, the unrecognized compensation expense associated with respect to options
granted to employees was $10.4 million, $13.4 million and $15.8 million, respectively, and is expected to be recognized on
a straight-line basis over 2.78, 2.71, and 2.72 years, respectively.
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11. Income Taxes
The components of loss before income tax is as follows (in thousands):
Domestic
Foreign
2020
December 31,
2019
$ (5,995) $ (46,672) $ (47,096)
157
$ (5,995) $ (46,672) $ (46,939)
—
—
2018
During the years ended December 31, 2020, 2019 and 2018, the Company recorded no income tax benefits for the
net operating losses (NOLs) incurred due to the uncertainty of realizing a benefit from those items.
A reconciliation of the Company’s effective tax rate to the U.S. Federal statutory rate is as follows:
December 31,
2020
2019
2018
Federal tax benefit at statutory rate
State tax, net of Federal benefit
Change in valuation allowance
Research and development tax credits
Share based Compensation
162(m) covered employees compensation limitation
FIN48 Reserve
Deconsolidation gain
Prior year federal true-up
Other
Effective income tax rate
21 %
6 %
(28)%
4 %
(1)%
21 %
32 %
(83)%
65 %
(34)%
(20)% —
(552)%
597 % —
(25)% —
(1)%
21 %
9 %
(41)%
3 %
(1)%
—
(1)%
—
10 %
(1)%
0 %
(1)% —
0 %
0 %
The effective tax rate is different from the federal statutory tax rate primarily due to the deconsolidation gain,
uncertain tax positions, share based compensation and a valuation allowance against deferred tax assets as a result of the
Company’s history of losses.
The principal components of the Company’s net deferred tax assets are as follows (in thousands)
Deferred tax assets
Net operating loss carryforwards
Tax credit carryforwards
Capitalized tax assets
Accruals
Stock compensation
Operating lease liability
Other
Total deferred tax assets
Deferred tax liabilities
Operating lease right-of-use asset
Valuation allowance
Net deferred tax assets
2020
December 31,
2019
2018
$ 42,344
7,894
63
207
4,942
646
47
$ 56,143
$ 42,486
6,990
(3)
152
4,317
892
40
$ 54,874
$ 31,533
6,441
138
188
2,879
—
58
$ 41,237
$
$
(461) $
(651) $
(55,682)
(54,223)
— $
— $
—
(41,237)
—
The Company recorded a valuation allowance against its deferred tax assets at December 31, 2020 and 2019
because Company management believed that it was more likely than not that these assets would not be fully realized in the
future. The valuation allowance increased by approximately $1.5 million and $13.0 million for the years ended
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December 31, 2020 and 2019, respectively. Changes in the valuation allowance for deferred tax assets relate primarily to
the increase in the Company’s net operating loss carryforward.
As of December 31, 2020, the Company had federal NOL carryforwards of approximately $177.2 million and
state NOL carryforwards of approximately $206.7 million which are available to reduce future taxable income. The NOLs
will begin to expire in 2034, if not utilized. Utilization of the net operating loss carryforwards are subject to various
limitations due to the ownership change limitations provided by Internal Revenue Code (IRC) Section 382 and similar state
provisions.
On March 27, 2020, the Coronavirus Aid, Relief, and Economic Security ("CARES") Act was enacted and signed
into law. The tax relief measures for businesses include suspension of annual deduction limitation of 80% of taxable
income from net operating losses generated in a tax year beginning after December 31, 2017, changes in the deductibility
of interest, acceleration of alternative minimum tax credit refunds, and a technical correction to allow accelerated
deductions for qualified improvement property. The CARES Act did not have a material impact on the Company’s
financial statements.
On December 21, 2020, the Consolidated Appropriations Act, 2021 was enacted and signed into law for further
COVID-19 economic relief and extension of certain expiring tax provisions. The act provides for a temporary full
deduction for business expenses for food and beverages provided by a restaurant for 2021 and 2022. The Consolidated
Appropriations Act did not have a material impact on the Company’s financial statements
On June 29, 2020, Assembly Bill 85 (“A.B. 85”) was signed into California law. A.B. 85 provides for a three-year
suspension of the use of net operating losses for medium and large businesses and a three-year cap on the use of business
incentive tax credits to offset no more than $5.0 million of tax per year. A.B. 85 suspends the use of net operating losses for
taxable years 2020, 2021 and 2022 for certain taxpayers with taxable income of $1.0 million or more. The carryover period
for any net operating losses that are suspended under this provision will be extended. A.B. 85 also requires that business
incentive tax credits including carryovers may not reduce the applicable tax by more than $5.0 million for taxable years
2020, 2021 and 2022. The Company does not expect the impact of this standard on its consolidated financial statements to
be material.
As of December 31, 2020, the Company also had $6.8 million of federal and $3.9 million of state research and
development tax credit carryforwards available to reduce future income taxes. The federal research and development tax
credits will begin to expire 2035, if not utilized. The state research and development tax credits have no expiration date.
U.S. income and foreign withholding taxes have not been recognized on the excess of the amount for financial
reporting over the tax basis of investments in foreign subsidiaries that are essentially permanent in duration. This excess
totaled approximately $37.2 million as of December 31, 2020, which will be indefinitely reinvested; deferred income taxes
have not been provided on such foreign earnings.
As of December 31, 2020, the Company had unrecognized tax benefits (“UTBs”) of approximately $12.2 million.
All of the deferred tax assets associated with these UTBs are fully offset by a valuation allowance. The following table
summarizes the activity related to UTBs:
Unrecognized tax benefits beginning of the period
Decrease related to the prior year
Increased related to the current year
Unrecognized tax benefits, end of the period
2020
$ 1,885
10,272
$ 12,157
December 31,
2019
$ 1,804
(365)
446
$ 1,885
—
2018
$ 1,219
—
585
$ 1,804
The Company follows the provisions of ASC 740, Accounting for Income Taxes, and the accounting guidance
related to accounting for uncertainty in income taxes. The Company determines its uncertain tax positions based on a
determination of whether and how much of a tax benefit taken by the Company in its tax filings or positions is more likely
than not to be sustained upon examination by the relevant income tax authorities. None of the Company’s
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unrecognized tax benefits that, if recognized, would affect its effective tax rate. The Company does not anticipate the total
amounts of unrecognized tax benefits will significantly increase or decrease in the next 12 months. The Company will
recognize both accrued interest and penalties related to unrecognized benefits in income tax expense. Management
determined that no accrual for interest or penalties was required as of December 31, 2020, 2019 and 2018.
The Company currently has no federal or state tax examinations in progress nor has it had any federal or state
examinations since inception. As a result of the Company’s net operating loss carryforwards, all of its tax years are subject
to federal, state and foreign tax examinations.
12. Facility Lease
In January 2015, the Company signed an initial operating lease, effective February 1, 2015 for 8,138 square feet
of office and laboratory space with a one year term. Between January 2015 and October 2018, the Company entered into a
series of lease amendments to increase the amount of leased space to 27,280 square feet and extend the expiration of the
lease to February 2023. The lease agreement includes annual rent escalations. Under the lease and subsequent amendments,
the landlord provided approximately $1.9 million in free rent and lease incentives. The Company records rent expense on a
straight-line basis over the effective term of the lease, including any free rent periods and incentives. As the interest rate
implicit in lease arrangements is typically not readily available, in calculating the present value of the lease payments, the
Company has utilized its incremental borrowing rate, which is determined based on the prevailing market rates for
collateralized debt with maturity dates commensurate with the term of its lease. The Company’s facility lease is a net lease,
as the non-lease components (i.e. common area maintenance) are paid separately from rent based on actual costs incurred.
Therefore, the non-lease components were not included in the right-of-use asset and liability and are reflected as an
expense in the period incurred.
As of December 31, 2020 and 2019, the right-of-use asset under operating lease was $1.6 million and $2.3
million, respectively. The elements of lease expense were as follows (in thousands):
Costs of operating lease
Operating lease costs
Costs of non-lease components (previously
common area maintenance)
Total operating lease cost
Other Information
Operating cash flows used for operating lease
Remaining lease term
Discount rate
Statements of operations and
comprehensive loss location
Research and development,
General and administrative
Research and development,
General and administrative
Year Ended
December 31,
2019
2018
2020
$
$
957
$
960
$
748
351
1,308
$
324
1,284
$
296
1,044
$
1,506
2.1 years
$
1,449
3.1 years
10.0%
10.0%
$
1,389
4.1 years
—
As of December 31, 2020, minimum rental commitments under this lease were as follows (in thousands)
Year Ended December 31 (in thousands)
2021
2022
Total lease payments
Less: imputed interest
Total
119
$
$
1,260
1,299
2,559
(249)
2,310
Table of Contents
As of December 31, 2019, minimum rental commitments under this lease were as follows (in thousands)
Year Ended December 31 (in thousands)
2020
2021
2022
Total lease payments
Less: imputed interest
Total
13. Commitments and Contingencies
$
$
1,159
1,260
1,299
3,718
(530)
3,188
In August 2015, the Company entered into an agreement for a line of credit of $0.1 million for the purpose of
issuing its landlord a letter of credit of $0.1 million as a security deposit under its facility lease. The Company pledged
money market funds and marketable securities as collateral for the line of credit. For further discussion of the Company’s
facility lease agreement, see Note 12.
Pursuant to the Company’s license agreements with each of Vernalis and Scripps, it has obligations to make future
milestone and royalty payments to these parties, respectively. However, because these amounts are contingent, they have
not been included on the Company’s balance sheet. For further discussion of the Vernalis and Scripps licensing agreements,
see Note 6.
Indemnifications
In the ordinary course of business, the Company enters into agreements that may include indemnification
provisions. Pursuant to such agreements, the Company may indemnify, hold harmless and defend an indemnified party for
losses suffered or incurred by the indemnified party. Some of the provisions will limit losses to those arising from third-
party actions. In some cases, the indemnification will continue after the termination of the agreement. The maximum
potential amount of future payments the Company could be required to make under these provisions is not determinable.
The Company has never incurred material costs to defend lawsuits or settle claims related to these indemnification
provisions. The Company has also entered into indemnification agreements with its directors and officers that may require
the Company to indemnify its directors and officers against liabilities that may arise by reason of their status or service as
directors or officers to the fullest extent permitted by Delaware corporate law. There have been no claims to date and the
Company has a directors and officers insurance policy that may enable it to recover a portion of any amounts paid for
future claims.
Legal Proceedings
The Company is not a party to any material legal proceedings.
14. Related Party Transactions
In March 2018, the Company completed a follow-on public offering in which the Company sold 8,117,647 shares
of common stock at a price of $8.50 per share, which included 1,058,823 shares issued pursuant to the underwriters’
exercise of their option to purchase additional shares of common stock. The aggregate net proceeds received by the
Company from the offering were approximately $64.9 million, net of underwriting discounts and commissions and offering
expenses payable by the Company.
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The following aggregate number of shares of common stock were sold to our owners of more than 5% of our
common stock, directors, or executive officers during the March 2018 underwritten public offering:
Owners of More Than 5% of Our Common Stock
FMR LLC
OrbiMed Advisors LLC (1)
Novo Holdings A/S (2)
Adams Street Partners (3)
Board of Directors
Richard A. Miller, M.D.
Number of
Shares of
Common Stock
Aggregate
Purchase
Price
$
1,176,470
588,235
1,176,470
588,235
9,999,995
4,999,998
9,999,995
4,999,998
100,000
850,000
(2) Peter Thompson, M.D., a member of our Board of Directors since November 2014, is a Private Equity Partner at
OrbiMed Advisors, LLC.
(3) Peter Moldt, Ph.D., a Partner at Novo Ventures (US) Inc., which provide certain consultancy services to Novo
Holdings A/S, served as a member of our Board of Directors from January 2015 to January 2019.
(4) Elisha P. (Terry) Gould III, a member of our Board of Directors since November 2014, is a Partner at Adams Street
Partners, LLC.
15. Quarterly Selected Financial Data (unaudited)
Quarter Ended
(in thousands, except per share amounts)
Operating expenses
Net loss
Net loss per share, basic and diluted
(in thousands, except per share amounts)
Operating expenses
Net loss
Net loss per share, basic and diluted
16. Subsequent Event
December 31, September 30,
2020
9,879
27,347
0.92
$
$
$
$
2020
9,845
(9,796)
June 30,
2020
$ 10,767
(10,611)
(0.36) $
(0.33) $
Quarter Ended
March 31,
2020
$ 13,269
(12,935)
(0.44)
December 31, September 30,
2019
11,440
(11,047)
$
2019
11,513
(11,004)
June 30,
2019
$ 13,596
(12,978)
(0.38) $
(0.37) $
(0.44) $
March 31,
2019
$ 12,305
(11,643)
(0.40)
$
$
On February 17, 2021, the Company completed a follow-on public offering in which the Company sold 9,783,660
shares of common stock at a price of $3.50 per share, which included 1,212,231 shares issued pursuant to the underwriters’
exercise of their option to purchase additional shares of common stock. The aggregate net proceeds received by the
Company from the offering were approximately $31.8 million, net of underwriting discounts and commissions and offering
expenses.
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The following aggregate number of shares of common stock were sold to our owners of more than 5% of our
common stock, directors, or executive officers during the February 17, 2021 underwritten public offering:
Owners of More Than 5% of Our Common Stock
OrbiMed Advisors LLC (1)
Board of Directors
Richard A. Miller, M.D.
Number of
Shares of
Common Stock
Aggregate
Purchase
Price
1,285,714
$
4,499,999
100,000
350,000
(1) Peter Thompson, M.D., a member of our Board of Directors since November 2014, is a Private Equity Partner at
OrbiMed Advisors, LLC.
Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
None
Item 9A. Controls and Procedures
Evaluation of Disclosure Controls and Procedures.
The term “disclosure controls and procedures,” as defined in Rules 13a-15(e) and 15d-15(e) under the Securities
Exchange Act of 1934, as amended (the “Exchange Act”) refers to controls and procedures that are designed to ensure that
information required to be disclosed by a company in the reports that it files or submits under the Exchange Act is
recorded, processed, summarized and reported, within the time periods specified in the SEC’s rules and forms. Disclosure
controls and procedures include, without limitation, controls and procedures designed to ensure that information required
to be disclosed by a company in the reports that it files or submits under the Exchange Act is accumulated and
communicated to the company’s management, including its principal executive and principal financial officers, or persons
performing similar functions, as appropriate to allow timely decisions regarding required disclosure. Our management
recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable
assurance of achieving their objectives and our management necessarily applies its judgment in evaluating the cost-benefit
relationship of possible controls and procedures. Due to the inherent limitations of control systems, not all misstatements
may be detected. These inherent limitations include the realities that judgments in decision-making can be faulty and that
breakdowns can occur because of a simple error or mistake. Our disclosure controls and procedures are designed to provide
reasonable assurance of achieving their control objectives.
Our management, with the participation of our Chief Executive Officer and Chief Financial Officer, has evaluated
the effectiveness of our disclosure controls and procedures as of December 31, 2020, the end of the period covered by this
Annual Report on Form 10-K. Based upon such evaluation, our Chief Executive Officer and Chief Financial Officer have
concluded that our disclosure controls and procedures were effective at the reasonable assurance level as of such date.
Management’s Annual Report on Internal Control Over Financial Reporting
Our management is responsible for establishing and maintaining adequate internal control over financial reporting
(as defined in Rule 13a-15(f) and 15d-15(f) of the Exchange Act). Internal control over financial reporting is a process
designed by, or under the supervision of, our Chief Executive Officer and Chief Financial Officer, and effected by our
Board of Directors, management and other personnel, 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 and includes those policies and procedures that:
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● Pertain to the maintenance of records that accurately and fairly reflect in reasonable detail the transactions
and dispositions of the assets of our company;
● Provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial
statements in accordance with generally accepted accounting principles, and that our receipts and
expenditures are being made only in accordance with authorizations of our management and directors; and
● Provide reasonable assurances regarding prevention or timely detection of unauthorized acquisition, use or
disposition of our assets that could have a material adverse effect on our financial statements.
Under the supervision and with the participation of our management, including our Chief Executive Officer and
Chief Financial Officer, we conducted an evaluation of the effectiveness of our internal control over financial reporting as
of December 31, 2020 based on the criteria established in Internal Control - Integrated Framework issued by the
Committee of Sponsoring Organizations of the Treadway Commission, or COSO 2013. Based on our evaluation under the
criteria set forth in Internal Control - Integrated Framework issued by the COSO, our management concluded our internal
control over financial reporting was effective as of December 31, 2020.
Internal control over financial reporting has inherent limitations. Internal control over financial reporting is a
process that involves human diligence and compliance and is subject to lapses in judgment and breakdowns resulting from
human failures. Internal control over financial reporting also can be circumvented by collusion or improper management
override. Because of such limitations, there is a risk that material misstatements will not be prevented or detected on a
timely basis by internal control over financial reporting. However, these inherent limitations are known features of the
financial reporting process. Therefore, it is possible to design into the process safeguards to reduce, though not eliminate,
this risk.
Attestation Report of the Registered Public Accounting Firm
This Annual Report on Form 10-K does not include an attestation report of our registered public accounting firm
on our internal controls due to an exemption established by the JOBS Act for “emerging growth companies.”
Changes in Internal Control Over Financial Reporting
There were no changes in our internal control over financial reporting that occurred during the fiscal year ended
December 31, 2020 that has materially affected, or is reasonably likely to materially affect, our internal control over
financial reporting.
Item 9B. Other Information
Not applicable.
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Item 10. Directors, Executive Officers and Corporate Governance
PART III
The information required by this Item will be set forth in the Company’s proxy statement to be filed with the SEC
within 120 days after the Company’s fiscal year end and is incorporated herein by reference.
We have adopted a code of business conduct and ethics that applies to all employees, including our principal
executive officer, principal financial officer, principal accounting officer or controller, or persons performing similar
functions. The code of business conduct and ethics is available on our website at http://corvuspharma.com. Amendments
to, and waivers from, the code of business conduct and ethics that apply to any director, executive officer or persons
performing similar functions will be disclosed at the website address provided above and, to the extent required by
applicable regulations, on a Current Report on Form 8-K filed with the SEC.
Item 11. Executive Compensation
The information required by this Item will be set forth in the Company’s proxy statement to be filed with the SEC
within 120 days after the Company’s fiscal year end and is incorporated herein by reference.
Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters
The information required by this Item will be set forth in the Company’s proxy statement to be filed with the SEC
within 120 days after the Company’s fiscal year end and is incorporated herein by reference.
Item 13. Certain Relationships and Related Transactions and Director Independence
The information required by this Item will be set forth in the Company’s proxy statement to be filed with the SEC
within 120 days after the Company’s fiscal year end and is incorporated herein by reference.
Item 14. Principal Accountant Fees and Services
The information required by this Item will be set forth in the Company’s proxy statement to be filed with the SEC
within 120 days after the Company’s fiscal year end and is incorporated herein by reference.
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Item 15. Exhibits and Financial Statement Schedules
(1)
Financial Statements:
PART IV
The consolidated financial statements required by Item 15(a) are filed as part of this Annual Report on Form 10-K
under Item 8 “Consolidated Financial Statements and Supplementary Data.”
(2)
Financial Statement Schedules:
All schedules are omitted because they are not applicable or the required information is shown in the consolidated
financial statements or notes thereto.
(3)
Exhibits.
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EXHIBIT INDEX
Exhibit
Number
Exhibit Description
Form
Date
Number Herewith
Incorporated by Reference
Filed
3.1 Amended and Restated Certificate of Incorporation.
3.2 Amended and Restated Bylaws.
4.1 Reference is made to Exhibits 3.1 through 3.2.
4.2 Form of Common Stock Certificate.
4.3 Amended and Restated Investors’ Rights Agreement, dated
September 16, 2015, by and among Corvus
Pharmaceuticals, Inc. and the investors listed therein.
4.4 Form of Warrant
4.5 Description of Registrant’s Securities Registered Pursuant to
Section 12 of the Securities Exchange Act of 1934
10.1(a) Office Lease, dated as of January 27, 2015, by and between
Corvus Pharmaceuticals, Inc. and ARE-819/863 Mitten
Road, LLC.
8-K 3/29/2016
8-K 3/29/2016
S-1
S-1/A
1/4/2016
2/8/2016
8-K 11/12/2019
3.1
3.2
4.2
4.3
4.1
S-1
1/4/2016
10.2(a)
X
10.1(b) First Amendment to Office Lease, dated as of March 19, 2015,
S-1
1/4/2016
10.2(b)
by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC.
10.1(c) Second Amendment to Office Lease, dated as of August 20,
S-1
1/4/2016
10.2(c)
2015, by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC
10.1(d) Third Amendment to Office Lease, dated as of June 27, 2016,
10-Q
8/4/2016
10.1(d)
by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC.
10.1(e) Fourth Amendment to Office Lease, dated as of August 15,
10-Q 11/3/2016
10.1(e)
2016, by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC.
10.1(f) Fifth Amendment to Office Lease, dated as of March 2, 2018,
10-Q
5/3/2018
10.3
by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC.
10.1(g) Sixth Amendment to Office Lease, dated as of April 5, 2018,
10-Q
8/2/2018
10.2
by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC.
10.1(h) Seventh Amendment to Office Lease, dated as of October 11,
2018, by and between Corvus Pharmaceuticals, Inc. and ARE-
819/863 Mitten Road, LLC.
10.2(a)# 2014 Equity Incentive Plan.
10.2(b)# Amendment to the 2014 Equity Incentive Plan, dated
November 26, 2014.
10.2(c)# Amendment to the 2014 Equity Incentive Plan, dated July 24,
2015.
10.2(d)# Amendment to the 2014 Equity Incentive Plan, dated
September 14, 2015.
10.2(e)# Form of Stock Option Grant Notice and Stock Option
Agreement under the 2014 Equity Incentive Award Plan.
10.2(f)# Form of Restricted Stock Purchase Right Grant Notice and
Restricted Stock Purchase Agreement under the 2014 Equity
Incentive Plan.
10.3(a)# 2016 Equity Incentive Award Plan.
10.3(b)# Form of Stock Option Grant Notice and Stock Option
Agreement under the 2016 Equity Incentive Award Plan.
10-K
3/7/2019
10.1(h)
S-1
S-1
S-1
S-1
S-1
S-1
1/4/2016
1/4/2016
10.4(a)
10.4(b)
1/4/2016
10.4(c)
1/4/2016
10.4(d)
1/4/2016
10.4(e)
1/4/2016
10.4(f)
S-8
S-1
3/29/2016
1/4/2016
99.2(a)
10.5(b)
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Table of Contents
Exhibit
Number
10.3(c)# Form of Restricted Stock Award Agreement and Restricted
Stock Award Grant Notice under the 2016 Equity Incentive
Award Plan.
Exhibit Description
10.3(d)# Form of Restricted Stock Unit Award Agreement and
Restricted Stock Unit Award Grant Notice under the 2016
Equity Incentive Award Plan.
Incorporated by Reference
Filed
Form
S-1
Date
1/4/2016
Number Herewith
10.5(c)
S-1
1/4/2016
10.5(d)
10.4# Form of Indemnification Agreement for directors and officers.
10.5# Amended and Restated Employment Agreement, dated as of
S-1
S-1
1/4/2016
1/4/2016
10.6
10.7
December 22, 2015, by and between Corvus
Pharmaceuticals, Inc. and Richard A. Miller.
10.6# Amended and Restated Employment Agreement, dated as of
S-1
1/4/2016
10.8
December 22, 2015, by and between Corvus
Pharmaceuticals, Inc. and Leiv Lea.
10.7(a)# Offer Letter, dated as of November 27, 2014, by and between
Corvus Pharmaceuticals, Inc. and William B. Jones.
10.7(b)# Change in Control and Severance Agreement, dated
S-1
S-1
1/4/2016
10.9(a)
1/4/2016
10.9(b)
December 23, 2015, by and between Corvus
Pharmaceuticals, Inc. and William B. Jones.
10.8(a)# Employment Agreement, dated as of November 26, 2014 by
10-Q
5/3/2018
10.2
and between Corvus Pharmaceuticals, Inc. and Joseph J.
Buggy.
10.8(b)# Transition and Consulting Agreement, dated as of June 30,
10-Q 7/30/2020
10.2
2020 by and between Corvus Pharmaceuticals, Inc. and
Joseph J. Buggy.
10.9(a)# Offer Letter, dated as of January 7, 2019 by and between
10-K
3/7/2019 10.11(a)
Corvus Pharmaceuticals, Inc. and Mehrdad Mobasher.
10.9(b)# Change in Control and Severance Agreement, dated January
28, 2019, by and between Corvus Pharmaceuticals, Inc. and
Mehrdad Mobasher.
10-K
3/7/2019 10.11(b)
10.10# Corvus Pharmaceuticals, Inc. 2016 Employee Stock Purchase
S-8
3/29/2016
99.3
Plan.
10.11# Non-Employee Director Compensation Program.
10.12(a)† License Agreement, dated February 25, 2015, by and between
Corvus Pharmaceuticals, Inc. and Vernalis (R&D) Limited.
S-1
10.12
1/4/2016
S-1/A 3/10/2016 10.13(a)
10.12(b)† Amendment to License Agreement dated November 5, 2015,
S-1
1/4/2016 10.13(b)
by and between Corvus Pharmaceuticals, Inc. and Vernalis
(R&D) Limited.
10.13† License Agreement, dated December 20, 2014, by and
between Corvus Pharmaceuticals, Inc. and The Scripps
Research Institute
S-1
1/4/2016
10.14
10.14(a)† Phase I/IB Combination Study Agreement, dated October 5,
S-1/A
2/8/2016
10.15
2015, by and between Corvus Pharmaceuticals, Inc. and
Genentech, Inc.
10.14(b) Amendment No. 1 to the Phase I/IB Combination Study
10-K
3/9/2020 10.16(b)
Agreement, dated December 20, 2017, by and between Corvus
Pharmaceuticals, Inc. and Genentech, Inc.
10.14(c) †† Amendment No. 2 to the Phase I/IB Combination Study
Agreement, dated August 1, 2019, by and between Corvus
Pharmaceuticals, Inc. and Genentech, Inc.
10.15(a) Phase 1b/II Combination Study Agreement dated May 1,
2017, by and between Corvus Pharmaceuticals, Inc. and
Genentech, Inc.
10-K
3/9/2020 10.16(c)
10-Q
8/3/2017
10.1
127
Table of Contents
Exhibit
Incorporated by Reference
Filed
Number
10.15(b) Amendment No. 1 to the Phase 1b/II Combination Study
Exhibit Description
Form
10-K
Number Herewith
Date
3/9/2020 10.17(b)
Agreement dated December 20, 2017, by and between Corvus
Pharmaceuticals, Inc. and Genentech, Inc.
10.16†† Exclusive License Agreement dated April 21, 2017, by and
10-K
3/9/2020
10.18
between Corvus Pharmaceuticals, Inc. and Monash University.
10.17 Exchange Agreement, dated November 8, 2019, by and
8-K 11/12/2019
10.1
among Corvus Pharmaceuticals, Inc., Biotechnology Value
Fund II, L.P. and Biotechnology Value Trading Fund OS, L.P.
10.18 Framework Agreement, dated as of October 5, 2020, by and
8-K 10/5/2020
2.1
between Corvus Hong Kong Limited, Jiaxing Puissance Angel
Equity Investment Partnership (Limited Partnership) and AP
BIOTECH DEVELOPMENT CORP.
10.19 Open Market Sale Agreement, dated March 9, 2020, by and
S-3
3/9/2020
1.2
between Corvus Pharmaceuticals, Inc. and Jefferies LLC.
21.1 List of subsidiaries
23.1 Consent of Independent Registered Public Accounting Firm.
24.1 Power of Attorney (included on signature page)
31.1 Certification by Chief Executive Officer pursuant to
Section 302 of the Sarbanes-Oxley Act of 2002.
31.2 Certification by Chief Financial Officer pursuant to
Section 302 of the Sarbanes-Oxley Act of 2002.
32.1** Certification of Chief Executive Officer and Chief Financial
Officer pursuant to 18 USC Section 1350 as adopted pursuant
to Section 906 of the Sarbanes-Oxley Act of 2002.
101.INS Inline XBRL Instance Document.
101.SCH Inline XBRL Taxonomy Extension Schema Document.
101.CAL Inline XBRL Taxonomy Extension Calculation Linkbase
Document.
101.DEF Inline XBRL Taxonomy Extension Definition Linkbase
Document.
101.LAB Inline XBRL Taxonomy Extension Label Linkbase Document.
101.PRE Inline XBRL Taxonomy Extension Presentation Linkbase
Document.
104 The cover page of Corvus Pharmaceuticals, Inc.’s Annual
Report on Form 10-K for the year ended December 31, 2020,
formatted in Inline XBRL (contained in Exhibit 101)
X
X
X
X
X
X
X
X
X
X
X
X
X
† Confidential treatment has been granted for a portion of this exhibit.
†† Portions of this exhibit have been omitted in accordance with Item 601(b)(10) of Regulation S-K.
# Indicates management contract or compensatory plan.
** The certification attached as Exhibit 32.1 that accompanies this Annual Report on Form 10-K is not deemed filed with
the Securities and Exchange Commission and is not to be incorporated by reference into any filing of Corvus
Pharmaceuticals, Inc. under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, as
amended, whether made before or after the date of this Annual Report on Form 10-K, irrespective of any general
incorporation language contained in such filing.
128
Table of Contents
Item 16. Form 10-K Summary
Registrants may voluntarily include a summary of information required by Form 10-K under this Item 16. We
have elected not to include such summary.
129
Table of Contents
Pursuant to the requirements 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.
SIGNATURES
Date: March 25, 2021
Date: March 25, 2021
CORVUS PHARMACEUTICALS, INC.
By:
By:
/s/ RICHARD. A. MILLER
Richard A. Miller, M.D.
President, Chief Executive Officer and Director
(Principal Executive Officer)
/s/ LEIV LEA
Leiv Lea
Chief Financial Officer
(Principal Financial and Accounting Officer)
POWER OF ATTORNEY
Each person whose individual signature appears below hereby authorizes and appoints Richard A. Miller, M.D.
and Leiv Lea and each of them, with full power of substitution and resubstitution, as his or her true and lawful attorney-in-
fact and agent to act in his or her name, place and stead and to execute in the name and on behalf of each person,
individually and in each capacity stated below, and to file 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 agents full power and authority to do and perform each and every act
and thing, ratifying and confirming all that said attorney-in-fact and agents or his substitute or substitutes may lawfully do
or cause to be done by virtue thereof. Pursuant to the requirements of the Securities Exchange Act of 1934, this report has
been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated.
/s/ RICHARD A. MILLER, M.D.
Richard A. Miller, M.D.
President, Chief Executive Officer and Director
(Principal Executive Officer)
/s/ LEIV LEA
Leiv Lea
/s/ IAN T. CLARK
Ian T. Clark
/s/ TERRY GOULD
Elisha P. (Terry) Gould III
/s/ LINDA S. GRAIS, M.D., J.D.
Linda S. Grais, M.D., J.D.
/s/ STEVE E. KROGNES
Steve E. Krognes
/s/ EDITH P. MITCHELL, M.D.
Edith P. Mitchell, M.D.
/s/ SCOTT W. MORRISON
Scott W. Morrison
/s/ PETER THOMPSON, M.D.
Peter Thompson, M.D.
Chief Financial Officer
(Principal Financial and Accounting Officer)
Director
Director
Director
Director
Director
Director
Director
130
March 25, 2021
March 25, 2021
March 25, 2021
March 25, 2021
March 25, 2021
March 25, 2021
March 25, 2021
March 25, 2021
March 25, 2021
DESCRIPTION OF REGISTRANT’S SECURITIES
REGISTERED PURSUANT TO SECTION 12 OF THE
SECURITIES EXCHANGE ACT OF 1934
Exhibit 4.5
As of December 31, 2020, Corvus Pharmaceuticals, Inc. had common stock, $0.0001 par value per share, registered under
Section 12 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and listed on The Nasdaq Global Market under
the trading symbol “CRVS.”
1
DESCRIPTION OF CAPITAL STOCK
The following summary describes our capital stock and the material provisions of our amended and restated certificate of
incorporation, our amended and restated bylaws, the amended and restated investors’ rights agreement to which we and certain of our
stockholders are parties and of the Delaware General Corporation Law. Because the following is only a summary, it does not contain all
of the information that may be important to you. For a complete description, you should refer to our amended and restated certificate of
incorporation, amended and restated bylaws and amended and restated investor rights agreement, copies of which are incorporated by
reference as Exhibits 3.1, 3.2 and 4.3, respectively, to our Annual Report on Form 10-K.
General
Our authorized capital stock consists of 300,000,000 shares of common stock, $0.0001 par value per share, and 10,000,000 shares
of preferred stock, $0.0001 par value per share.
Common Stock
Voting Rights
Each holder of our common stock is entitled to one vote for each share on all matters submitted to a vote of the stockholders,
including the election of directors. Our stockholders do not have cumulative voting rights in the election of directors. Accordingly,
holders of a majority of the voting shares are able to elect all of the directors. In addition, the affirmative vote of holders of 66 2/3% of
the voting power of all of the then outstanding voting stock is required to take certain actions, including amending certain provisions of
our amended and restated certificate of incorporation, such as the provisions relating to amending our amended and restated bylaws, the
classified board of directors and director liability.
Dividends
Subject to preferences that may be applicable to any then outstanding preferred stock, holders of our common stock are entitled to
receive dividends, if any, as may be declared from time to time by our board of directors out of legally available funds.
Liquidation
In the event of our liquidation, dissolution or winding up, holders of our common stock will be entitled to share ratably in the net
assets legally available for distribution to stockholders after the payment of all of our debts and other liabilities and the satisfaction of
any liquidation preference granted to the holders of any then outstanding shares of preferred stock.
Rights and Preferences
Holders of our common stock have no preemptive, conversion, subscription or other rights, and there are no redemption or
sinking fund provisions applicable to our common stock. The rights, preferences and privileges of the holders of our common stock are
subject to and may be adversely affected by the rights of the holders of shares of any series of our preferred stock that we may designate
in the future.
Fully Paid and Nonassessable
All of our outstanding shares of common stock are fully paid and nonassessable.
Preferred Stock
Our board of directors has the authority, without further action by our stockholders, to issue up to 10,000,000 shares of preferred
stock in one or more series and to fix the rights, preferences, privileges and restrictions thereof. These rights, preferences and privileges
could include dividend rights, conversion rights, voting rights, terms of redemption, liquidation preferences, sinking fund terms and the
number of shares constituting, or the designation of, such series, any or all of which may be greater than the rights of our common stock.
The issuance of our preferred stock could adversely affect the voting power of holders of common stock and the likelihood that such
holders will receive dividend payments and payments upon our liquidation. In addition, the issuance of preferred stock could have the
effect of delaying, deferring or preventing a change in control of our company or other corporate action. As of January 31, 2020, no
shares of preferred stock were outstanding.
Registration Rights
Under our amended and restated investors’ rights agreement, as of December 31, 2019, the holders of approximately 10 million
shares of common stock, or their transferees, have the right to require us to register their shares under the Securities Act so that those
shares may be publicly resold, and the holders of approximately 10 million shares of common stock, or their transferees, have the right to
include their shares in any registration statement we file, in each case as described below.
Demand Registration Rights
Based on the number of shares outstanding as of December 31, 2019, the holders of approximately 10 million shares of our
common stock, or their transferees, are entitled to certain demand registration rights. The holders of at least 30% of these shares can, on
not more than two occasions, request that we register all or a portion of their shares if the aggregate price to the public of the shares
offered is at least $5.0 million (after deductions of underwriters’ discounts and expenses related to the issuance).
Piggyback Registration Rights
Based on the number of shares outstanding as of December 31, 2019, in the event that we determine to register any of our
securities under the Securities Act of 1933, as amended (the “Securities Act”) (subject to certain exceptions), either for our own account
or for the account of other security holders, the holders of approximately 10 million shares of our common stock, or their transferees, are
entitled to certain “piggyback” registration rights allowing the holders to include their shares in such registration, subject to certain
marketing and other limitations. As a result, whenever we propose to file a registration statement under the Securities Act, other than
with respect to a registration related to employee benefit plans, the offer and sale of debt securities, or corporate reorganizations or
certain other transactions, the holders of these shares are entitled to notice of the registration and have the right, subject to limitations that
the underwriters may impose on the number of shares included in the registration, to include their shares in the registration. In an
underwritten offering, the managing underwriter, if any, has the right, subject to specified conditions, to exclude or limit the number of
shares such holders may include.
Form S-3 Registration Rights
Based on the number of shares outstanding as of December 31, 2019, the holders of approximately 10 million shares of our
common stock, or their transferees, are entitled to certain Form S-3 registration rights. The holders of any of these shares can make a
written request that we register their shares on Form S-3 if we are eligible to file a registration statement on Form S-3 and if the
aggregate price to the public of the shares offered is at least $2.0 million (after deductions of underwriters’ discounts and expenses
related to the issuance). These stockholders may make an unlimited number of requests for registration on Form S-3, but in no event
shall we be required to file more than two registrations on Form S-3 in any given twelve-month period.
Expenses of Registration
We will pay the registration expenses of the holders of the shares registered pursuant to the demand, piggyback and Form S-3
registration rights described above, including the expenses in an amount not to exceed $35,000 of one special counsel for the selling
holders.
Expiration of Registration Rights
The demand, piggyback and Form S-3 registration rights described above will expire, with respect to any particular stockholder,
upon the earlier of four years after the consummation of our initial public offering in March 2016 or when that stockholder can sell all of
its shares under Rule 144 of the Securities Act during any 90-day period (and without the requirement for the Company to be in
compliance with the current public information required under Section c(1) of Rule 144 of the Securities Act).
Anti-Takeover Effects of Provisions of our Amended and Restated Certificate of Incorporation, our Amended and Restated
Bylaws and Delaware Law
Certain provisions of Delaware law and our amended and restated certificate of incorporation and our amended and restated
bylaws contain provisions that could make the following transactions more difficult: acquisition of us by means of a tender offer;
acquisition of us by means of a proxy contest or otherwise; or removal of our incumbent officers and directors. It is possible that these
provisions could make it more difficult to accomplish or could deter transactions that stockholders may otherwise consider to be in their
best interest or in our best interests, including transactions that might result in a premium over the market price for our shares.
These provisions, summarized below, are expected to discourage coercive takeover practices and inadequate takeover bids. These
provisions are also designed to encourage persons seeking to acquire control of us to first negotiate with our board of directors. We
believe that the benefits of increased protection of our potential ability to negotiate with the proponent of an unfriendly or unsolicited
proposal to acquire or restructure us outweigh the disadvantages of discouraging these proposals because negotiation of these proposals
could result in an improvement of their terms.
Delaware Anti-Takeover Statute
We are subject to Section 203 of the Delaware General Corporation Law, which prohibits persons deemed “interested
stockholders” from engaging in a “business combination” with a publicly-held Delaware corporation for three years following the date
these persons become interested stockholders unless the business combination is, or the transaction in which the person became an
interested stockholder was, approved in a prescribed manner or another prescribed exception applies. Generally, an “interested
stockholder” is a person who, together with affiliates and associates, owns, or within three years prior to the determination of interested
stockholder status did own, 15% or more of a corporation’s voting stock. Generally, a “business combination” includes a merger, asset or
stock sale, or other transaction resulting in a financial benefit to the interested stockholder. The existence of this provision may have an
anti-takeover effect with respect to transactions not approved in advance by the board of directors, such as discouraging takeover
attempts that might result in a premium over the market price of our common stock.
Undesignated Preferred Stock
The ability to authorize undesignated preferred stock makes it possible for our board of directors to issue preferred stock with
voting or other rights or preferences that could impede the success of any attempt to change control of us. These and other provisions
may have the effect of deterring hostile takeovers or delaying changes in control or management of our company.
Special Stockholder Meetings
Our amended and restated bylaws provide that a special meeting of stockholders may be called at any time by our board of
directors, but such special meetings may not be called by the stockholders or any other person or persons.
Requirements for Advance Notification of Stockholder Nominations and Proposals
Our amended and restated bylaws establish advance notice procedures with respect to stockholder proposals and the nomination
of candidates for election as directors, other than nominations made by or at the direction of the board of directors or a committee of the
board of directors.
Stockholder Action by Written Consent
Our amended and restated certificate of incorporation and our amended and restated bylaws preclude stockholder action by
written consent without a meeting.
Classified Board; Election and Removal of Directors; Filling Vacancies
Our board of directors is divided into three classes. The directors in each class serve for a three-year term, with one class being
elected each year by our stockholders, with staggered three-year terms. Only one class of directors will be elected at each annual meeting
of our stockholders, with the other classes continuing for the remainder of their respective three-year terms. Because our stockholders do
not have cumulative voting rights, our stockholders holding a majority of the shares of common stock outstanding will be able to elect all
of our directors. Our amended and restated certificate of incorporation provides for the removal of any of our directors only for cause and
requires a stockholder vote by the holders of at least a 66 2/3% of the voting power of the then outstanding voting stock. Furthermore,
any vacancy on our board of directors, however occurring, including a vacancy resulting from an increase in the size of the board, may
only be filled by the affirmative vote of a majority of the directors then in office unless the board of directors determines that such
vacancies shall be filled by the stockholders. This system of electing and removing directors and filling vacancies may tend to discourage
a third party from making a tender offer or otherwise attempting to obtain control of us, because it generally makes it more difficult for
stockholders to replace a majority of the directors.
Choice of Forum
Our amended and restated certificate of incorporation and our amended and restated bylaws provide that, unless we consent in
writing to the selection of an alternative forum, the Court of Chancery of the State of Delaware will be the exclusive forum for: any
derivative action or proceeding brought on our behalf; any action asserting a claim of breach of fiduciary duty; any action asserting a
claim against us arising pursuant to the Delaware General Corporation Law, our amended and restated certificate of incorporation or our
amended and restated bylaws; or any action asserting a claim against us that is governed by the internal affairs doctrine. Although our
amended and restated certificate of incorporation and amended and restated bylaws contain the choice of forum provision described
above, it is possible that a court could find that such a provision is inapplicable for a particular claim or action or that such provision is
unenforceable.
Amendment of Charter Provisions
The amendment of any of the above provisions in our amended and restated certificate of incorporation, except for the provision
making it possible for our board of directors to issue undesignated preferred stock, or the amendment of any provision in our bylaws
(other than by action of the board of directors), requires approval by a stockholder vote by the holders of at least a 66 2/3% of the voting
power of the then outstanding voting stock.
The provisions of the Delaware General Corporation Law, our amended and restated certificate of incorporation and our amended
and restated bylaws could have the effect of discouraging others from attempting hostile takeovers and, as a consequence, they may also
inhibit temporary fluctuations in the market price of our common stock that often result from actual or rumored hostile takeover attempts.
These provisions may also have the effect of preventing changes in our management. It is possible that these provisions could make it
more difficult to accomplish transactions that stockholders may otherwise deem to be in their best interests.
Limitations of Liability and Indemnification Matters
Our amended and restated certificate of incorporation contains provisions that limit the liability of our directors for monetary
damages to the fullest extent permitted by Delaware law. Consequently, our directors will not be personally liable to us or our
stockholders for monetary damages for any breach of fiduciary duties as directors, except liability for:
● any breach of the director’s duty of loyalty to us or our stockholders;
● any act or omission not in good faith or that involves intentional misconduct or a knowing violation of law;
● unlawful payments of dividends or unlawful stock repurchases or redemptions as provided in Section 174 of the Delaware
General Corporation Law; or
● any transaction from which the director derived an improper personal benefit.
Each of our amended and restated certificate of incorporation and amended and restated bylaws provide that we are required to
indemnify our directors and officers, in each case to the fullest extent permitted by Delaware law. Our amended and restated bylaws also
obligate us to advance expenses incurred by a director or officer in advance of the final disposition of any action or proceeding, and
permit us to secure insurance on behalf of any officer, director, employee or other agent for any liability arising out of his or her actions
in that capacity regardless of whether we would otherwise be permitted to indemnify him or her under Delaware law. We have entered
and expect to continue to enter into agreements to indemnify our directors, executive officers and other employees as determined by our
board of directors. With specified exceptions, these agreements provide for indemnification for related expenses including, among other
things, attorneys’ fees, judgments, fines and settlement amounts incurred by any of these individuals in any action or proceeding. We
believe that these bylaw provisions and indemnification agreements are necessary to attract and retain qualified persons as directors and
officers. We also maintain directors’ and officers’ liability insurance.
The limitation of liability and indemnification provisions in our amended and restated certificate of incorporation and amended
and restated bylaws may discourage stockholders from bringing a lawsuit against our directors and officers for breach of their fiduciary
duty. They may also reduce the likelihood of derivative litigation against our directors and officers, even though an action, if successful,
might benefit us and our stockholders. Further, a stockholder’s investment may be adversely affected to the extent that we pay the costs
of settlement and damages.
Transfer Agent and Registrar
The transfer agent and registrar for our common stock is Computershare, Inc. The transfer agent and registrar’s address is 480
Washington Boulevard, 29th Floor, Jersey City, New Jersey 07130.
The following is a list of subsidiaries of the Company as of December 31, 2020:
List of Subsidiaries
Subsidiary Legal Name
Corvus Biopharmaceuticals, Ltd.
Corvus Hong Kong Limited
Exhibit 21.1
State or other Jurisdiction of
Incorporation
Cayman Islands
Hong Kong
CONSENT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
We hereby consent to the incorporation by reference in the Registration Statements on Form S-3 (No. 333-
237040), and Form S-8 (No. 333-223622, No. 333-216590, No. 333-210456, No. 333-231331 and No. 333-237933) of
Corvus Pharmaceuticals. Inc. of our report dated March 25, 2021 relating to the financial statements, which appear in this
Form 10-K.
Exhibit 23.1
/s/ PricewaterhouseCoopers LLP
San Jose, California
March 25, 2021
Exhibit 31.1
I, Richard A. Miller, certify that:
CERTIFICATIONS
1.
2.
3.
4.
I have reviewed this Annual Report on Form 10-K of Corvus Pharmaceuticals, Inc. for the year ended
December 31, 2020;
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 this report;
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;
The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls
and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-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)
b)
c)
d)
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;
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;
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
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 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)
b)
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
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.
7
Date: March 25, 2021
/s/ RICHARD A. MILLER
Richard A. Miller, M.D.
President and Chief Executive Officer
(Principal Executive Officer)
Exhibit 31.2
I, Leiv Lea, certify that:
CERTIFICATIONS
1.
2.
3.
4.
I have reviewed this Annual Report on Form 10-K of Corvus Pharmaceuticals, Inc. for the year ended
December 31, 2020;
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 this report;
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;
The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls
and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-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)
b)
c)
d)
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;
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;
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
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 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)
b)
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
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.
7
Date: March 25, 2021
/s/ LEIV LEA
Leiv Lea
Chief Financial Officer
(Principal Financial and Accounting Officer)
SECTION 1350 CERTIFICATIONS*
Exhibit 32.1
In connection with the Annual Report of Corvus Pharmaceuticals, Inc. (the “Company”) on Form 10-K for the
fiscal year ended December 31, 2020, as filed with the Securities and Exchange Commission (the “Report”), Richard A.
Miller, President and Chief Executive Officer (Principal Executive Officer) of the Company, and Leiv Lea, Chief Financial
Officer (Principal Financial and Accounting Officer) of the Company, each hereby certifies, pursuant to the requirement
set forth in Rule 13a-14(b) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and Section 1350 of
Chapter 63 of Title 18 of the United States Code (18 U.S.C. § 1350), that, to the best of his knowledge:
1.
2.
The Report, to which this Certification is attached as Exhibit 32.1, fully complies with the requirements
of Section 13(a) or 15(d) of the Exchange Act; and
The information contained in the Report fairly presents, in all material respects, the financial condition
and results of operations of the Company for the period covered by the Report.
Dated: March 25, 2021
/s/ RICHARD A. MILLER
Richard A. Miller, M.D.
President and Chief Executive Officer
(Principal Executive Officer)
/s/ LEIV LEA
Leiv Lea
Chief Financial Officer
(Principal Financial and Accounting Officer)
*
This certification accompanies the Annual Report on Form 10-K, to which it relates, is not deemed filed with the
Securities and Exchange Commission and is not to be incorporated by reference into any filing of the Company
under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, as amended (whether made
before or after the date of the Form 10-K), irrespective of any general incorporation language contained in such
filing.