UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
FORM 10-K
☒
☐
ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(D) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE FISCAL
YEAR ENDED DECEMBER 31, 2021.
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(D) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE
TRANSITION PERIOD FROM TO
COMMISSION FILE NUMBER: 001-36790
PREDICTIVE ONCOLOGY INC.
(Exact name of registrant as specified in its charter)
Delaware
(State or other jurisdiction
of incorporation or organization)
33-1007393
(IRS Employer
Identification No.)
2915 Commers Drive, Suite 900
Eagan, Minnesota 55121
(Address and Zip Code of principal executive offices)
(Registrant’s telephone number, including area code): (651) 389-4800
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Common stock, $0.01 par value
Trading symbol(s)
POAI
Name of each exchange on which registered
NASDAQ Capital Market
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 checkmark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934
during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing
requirements for the past 90 days. Yes ☒ 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 such files).
☒Yes ☐ No
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, 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 Act). Yes ☐ No ☒
State the aggregate market value of the voting and non-voting common equity held by non-affiliates computed by reference to the price at which the
common equity was last sold, or the average bid and asked price of such common equity, as of the last business day of the registrant’s most recently
completed second fiscal quarter: $85,590,000 as of June 30, 2021, based upon 65,339,695 shares at $1.31 per share as reported on the NASDAQ Capital
Market.
Indicate the number of shares outstanding of each of the registrant’s classes of common stock, as of the last practicable date: As of March 24, 2022, the
registrant had 65,911,001 shares of common stock, par value $.01 per share outstanding.
DOCUMENTS INCORPORATED BY REFERENCE
TABLE OF CONTENTS
PART I
ITEM 1. BUSINESS
ITEM 1A. RISK FACTORS
ITEM 1B. UNRESOLVED STAFF COMMENTS
ITEM 2. PROPERTIES
ITEM 3. LEGAL PROCEEDINGS
ITEM 4. MINE SAFETY DISCLOSURES
PART II
ITEM 5. MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER
PURCHASES OF EQUITY SECURITIES
ITEM 6. SELECTED FINANCIAL DATA
ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
ITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA
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 AND CORPORATE GOVERNANCE
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, FINANCIAL STATEMENT SCHEDULES
SIGNATURES
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ITEM 1. BUSINESS
General
PART I
References in this annual report on Form 10-K to “Predictive”, “Company”, “we”, “us”, and “our” refer to the business of Predictive Oncology Inc.
(NASDAQ: POAI) and its wholly-owned subsidiaries.
Cautionary Statement Concerning Forward-Looking Statements
This Annual Report on Form 10-K contains various "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as
amended (the "Securities Act"), and Section 21E of the Securities Exchange Act of 1934, as amended (the "Exchange Act"). Forward-looking statements
represent our expectations and beliefs concerning future results or events, based on information available to us on the date of the filing of this Form 10-K,
and are subject to various risks and uncertainties. Factors that could cause actual results or events to differ materially from those referenced in the
forward-looking statements are listed in Part I, Item 1A. Risk Factors and in Part II, Item 7. Management's Discussion and Analysis of Financial Condition
and Results of Operations. We disclaim any intent or obligation to update or revise any of the forward-looking statements, whether in response to new
information, unforeseen events, changed circumstances or otherwise, except as required by applicable law.
Overview
We operate in four primary business areas: first, the application of artificial intelligence (“AI”) in our precision medicine business, to provide AI-driven
predictive models of tumor drug response to improve clinical outcomes for patients and to assist pharmaceutical, diagnostic, and biotech industries in the
development of new personalized drugs and diagnostics; second, creation and development of tumor-specific 3D cell culture models driving accurate
prediction of clinical outcomes; third, contract services and research focused on solubility improvements, stability studies, and protein production, and;
fourth, production of the United States Food and Drug Administration (“FDA”)-cleared STREAMWAY® System for automated, direct-to-drain medical
fluid disposal and associated products.
We have four reportable segments: Helomics®, zPREDICTA®, SolubleTM and Skyline®. The Helomics segment includes clinical testing and contract
research services that include the application of AI. Our zPREDICTA, Inc. (“zPREDICTA”) segment, which was effective upon the closing of the
acquisition of zPREDICTA on November 24, 2021, specializes in organ-specific disease models that provide 3D reconstruction of human tissues accurately
representing each disease state and mimicking drug response enabling accurate testing of anticancer agents. Our Soluble segment provides services using a
self-contained, automated system that conducts high-throughput, self-interaction chromatography screens, using additives and excipients commonly
included in protein formulations resulting in soluble and physically stable formulations for biologics. Our Skyline segment consists of the STREAMWAY
System product sales, and our TumorGenesis® subsidiary (Research and Development) is included within corporate. Going forward, we have determined
that we will focus our resources on the Helomics and zPREDICTA segments and our primary mission statements to accelerate patient-centric drug
discovery to improve patient outcomes in cancer treatment, harnessing the power of AI, and to develop tumor-specific 3D cell culture models that provide
accurate 3D reconstruction of human tissues representing each cancer disease state.
On November 24, 2021, we acquired zPREDICTA in a merger transaction, and at that time we identified zPREDICTA as a reportable segment.
zPREDICTA’s business, which involves integration of organ-specific cellular and extracellular elements into 3D cell culture models for in vitro cancer drug
testing, represents a unique segment in the Predictive offerings.
HELOMICS
Our precision medicine business, conducted in our Helomics division, is committed to improving the effectiveness of cancer therapy using our proprietary,
multi-omic tumor profiling platform, a one-of-a-kind database of historical tumor data, and the power of AI to build predictive models of tumor drug
response.
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Helomics’ mission is to improve clinical outcomes for patients by partnering with pharmaceutical, diagnostic, and academic organizations to bring
innovative clinical products and technologies to the marketplace. Our Patient-centric Drug Discovery using Active Learning asset (“PeDAL”™) is a unique
technology that combines our proprietary, clinically validated patient tumor cell line assay (“TruTumor”™), a vast knowledgebase of proprietary and public
data together (“TumorSpace”™) with active learning - the active learning allowing the efficient exploration of compound drug responses against a large
diverse patient “space”. PeDAL offers researchers the opportunity to efficiently and cost-effectively bring patient diversity much earlier in the drug
discovery process. PeDAL works by iterative cycles of active-learning powered Learn-Predict-Test to guide the testing of patient-specific compound
responses using the TruTumor assay and patient cell lines to build a comprehensive predictive model of patient responses to compounds. This predictive
model can then be used to rank compounds by the fraction of patients of certain profiles that respond as well as the set of compounds that provide the best
coverage across patients. PeDAL will be used in fee-for-service projects with pharmaceutical companies.
Contract Research Organization (“CRO”) and AI-Driven Business
We believe leveraging our unique, historical database of the drug responses of over 150,000 patient tumors to build AI and data-driven multi-omic
predictive models of tumor drug response and outcome will provide actionable insights critical to both new drug development and individualizing patient
treatment. Through the course of over 15 years of clinical testing of the responses of patient tumors to drugs, Helomics has amassed a huge proprietary
knowledgebase of 150,000 patient cases. This data has been rigorously de-identified and aggregated to build a unique, proprietary model of tumor drug
response that we call TumorSpace. The TumorSpace model and its data provide a priori knowledge for the machine learning approaches we employ as part
of the PeDAL approach.
TumorSpace model provides a significant competitive advantage to our business offerings. PeDAL's unique patient and tumor-centric AI-driven approach
can rapidly and cost-effectively screen hundreds of compounds in thousands of tumor cell lines, and gain valuable information about off-target effects and
deliver:
● A ranked list of drug candidates by responsiveness
● Sets of drug candidates that provide maximum patient coverage
● Biomarker profiles of patients that respond to specific drug candidates
PeDAL also can deliver drug candidates targeted at a specific patient profile as early as the hit-to-lead stage of discovery, significantly increasing the
chance of clinical success, leading to a dramatic improvement in both the success, time, and cost of your oncology discovery programs. The AI-driven
models will also provide clinical decision support to help oncologists individualize treatment.
Our CRO/AI business leverages our core competence in profiling the drug response of patient tumors. Our large knowledgebase of tumor drug response
and other data, together with proven AI, has created a unique capability for oncology drug discovery that allows for the highly efficient screening of drug
responses from thousands of diverse, well-characterized patient primary tumor cell lines. This novel disruptive patient-centric approach is ideally suited to
the early part of drug discovery (especially hit-to-lead, lead optimization, and pre-clinical), resulting in better prioritization of compounds and better
coverage of patient diversity. This will dramatically improve the chances of successfully translating discoveries, resulting in lowered costs, shortened
timelines, and most importantly enhanced “speed-to-patient” for new therapies.
Our CRO services business applies PeDAL to address a range of needs from discovery through clinical and translational research, to clinical trials and
diagnostic development and validation as noted below:
Research
Development
● Biomarker discovery
● Drug discovery
● Drug-repurposing
● Patient enrichment & selection for trials
● Clinical trial optimization
● Adaptive trials
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Clinical Decision Support
● Patient stratification
● Treatment selection
We believe this market segment has significant growth potential and we believe we are differentiated from traditional CRO’s and other precision medicine
and AI companies through these unique assets:
● Clinically validated TruTumor platform;
● TumorSpace model of over 150,000 tumor cases;
● Experienced AI team and AI/Core® platform;
● Ability to access outcome data going back over ten years for over 120,000 of the tumor cases in our database.
Industry and Market Background and Analysis – Precision Medicine Business
Precision medicine is an emerging approach for disease treatment and prevention that considers individual variability in genes, disease, environment, and
lifestyle for each case to develop effective therapies. This approach allows doctors and researchers to predict more accurately which treatment, dose, and
therapeutic regimen could provide the best possible outcome.
Precision medicine, precisely targeting drugs based on the genomic profile of the patient, has become the aspiration for cancer therapy. Over the past
several decades, researchers have identified molecular patterns that are useful in defining the prognosis of a given cancer, determining the appropriate
treatments, and designing targeted treatments to address specific molecular alterations. The objective of this precision oncology is to develop treatments
tailored to the genetic changes in each person’s cancer, intended to improve the effectiveness of the therapeutic regimen, and minimize the treatment’s
effects on healthy cells. However, for a majority of patients the reality is that while many mutations in the patient’s tumor can be identified most are not
actionable with current protocols, due to a lack of research regarding which mutations in a tumor confer a sensitivity to a particular drug. As a result, the
impact of targeted therapies is low, and uptake in clinical practice is inconsistent.
There is now a growing realization that genomics alone will not be enough to achieve the promise of personalized therapeutics, especially for cancer. A
multi-omic approach (e.g., assessing the genome, transcriptome, epigenome, proteome, responseome, and microbiome) provides researchers and clinicians
the comprehensive information necessary for new drug development and individualized therapy. Comparatively, the multi-omic approach provides a three-
dimensional, 360-degree view of the cancer, while genomics alone is just a flat, one-dimensional view. However, multi-omic data is difficult to access
quickly as it is both costly and time consuming to initiate prospective data collection, and few comprehensive, multi-omic datasets exist, especially specific
to cancer. Our Helomics TumorSpace database addresses this need.
Clinical Testing
Via our Helomics subsidiary, we offer a group of clinically relevant, cancer-related tumor profiling and biomarker tests for gynecological cancers that
determine how likely the patient is to respond to various types of chemotherapy and which therapies might be indicated by relevant tumor biomarkers.
Clinic diagnostic testing is comprised of our Tumor Drug Response Testing (ChemoFx) and Genomic Profiling (BioSpeciFx) tests. The Tumor Drug
Response Testing test determines how a patient’s tumor specimen reacts to a panel of various chemotherapy drugs, while the Genomic Profiling test
evaluates the expression and/or status of a particular gene related to a patient’s tumor specimen. Our proprietary TruTumor platform provides us with the
ability to work with actual live tumor cells to study the unique biology of the patient’s tumor in order to understand how the patient responds to treatment.
Testing involves obtaining tumor tissue during biopsy or surgery which is then sent to our Clinical Laboratory Improvement Amendments (“CLIA”)
certified laboratory using a special collection kit. Tumor Drug Response Testing is a fresh tissue platform that uses the patient’s own live tumor cells to
help physicians identify effective treatment options for each gynecologic cancer patient.
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Genomic Profiling offers a select group of clinically relevant protein expression and genetic mutation tests associated with drug response and disease
prognosis. Physicians can select biomarkers for testing from carefully chosen panels of relevant tests, intuitively organized by cancer pathway and tumor
type. Results for these tests are presented in a clear, easy to understand format, including summaries of the clinical relevance of each marker.
Business Strategy for Precision Medicine Business
We are a data and AI-driven discovery services company that provides AI-driven predictive models of tumor drug response to improve clinical outcomes
for patients by leveraging our two primary unique assets:
● TruTumor - a clinically validated tumor-profiling platform that can generate drug response profiles and other multi-omic data. Over $200 million
has been invested in this platform by us and previous owners and was clinically validated in ovarian cancer.
● TumorSpace model contains data on the drug response profiles across 131 cancer types over 10+ years of clinical testing.
Over 38,000 of the more than 150,000 clinically validated cases in our TumorSpace database are specific to ovarian cancer. The data in TumorSpace is
highly differentiated, having both drug response data, biomarkers, and access to historical outcome data from those patient samples. We intend to generate
additional data (genomics and transcriptomics) from these tumor samples to deliver a multi-omic approach to the pharmaceutical industry.
Through our Helomics subsidiary, we will utilize both this historical data and the TumorSpace platform to build AI-driven predictive models of tumor drug
response and outcome. During 2022, we will commercialize these AI-driven predictive models in revenue generating service projects with pharmaceutical,
biotech, and diagnostic companies.
A key part of our commercialization strategy is the understanding that our AI-driven models of tumor drug response serve a key unmet need of
pharmaceutical, diagnostic, and biotech industries for actionable multi-omic insights on cancer. In collaboration with these companies, using the predictive
models, we will accelerate the search for more individualized and effective cancer treatments, through revenue generating projects in biomarker discovery,
drug screening, drug repurposing, and clinical trials.
Our commercial strategy has identified a portfolio of revenue generating project types that leverage the predictive models, our AI expertise, PeDAL tumor
profiling, and CLIA laboratory to provide custom solutions utilizing our full array of assets and expertise.
The Cancer Quest 2020 initiative focused initially on ovarian cancer, which is where we have the most expertise, samples, data, and access to outcomes.
We are expanding the initiative to include cancers of the lung, breast, colon, and prostate, and will actively seek partners to assist in that effort.
We recently completed our product validation for Discovery 21in January 2022, the proof of concept for PeDAL, which incorporates CoRE™, our active
machine learning program, with tumor profile data and human tumor samples, to efficiently determine the most effective drug treatment for a specific
cancer type. With each iteration of PeDAL, the program learns, predicts, and then directs the most informative wet lab experimentation, while building the
predictive model.
Discovery 21 is a predictive model, built in an efficient manner using PeDAL. The model revealed drug response patterns that provide insight into the
treatment of ovarian cancer. The validation results demonstrated the accuracy of the model that predicted drug response. Within the clinical sector, we will
also be able to utilize similar predictive models (once validated) for new clinical decision support tools for individualizing therapy for patients with cancer.
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These clinical decision support tools are on a longer revenue horizon than the fee-for-service research projects with pharmaceutical companies but,
importantly, will provide a steady stream of additional data generation to refine the predictive models for both clinical and research applications.
zPREDICTA
zPREDICTA develops tumor-specific in vitro models for oncology drug discovery and research by biopharmaceutical companies and other clients and
partners. zPREDICTA’s 3D product models accelerate the drug development process for its clients and partners by leveraging the expertise in
carcinogenesis, metastasis and the tumor microenvironment. It develops complex in vitro models that recapitulate the physiological environment of human
tissue.
From target discovery and lead optimization to preclinical evaluation of efficacy and toxicity, the objective is to develop the tools necessary to accurately
identify compounds that will have the highest probability of improving human health. Product offerings include preclinical testing services based on our
proprietary models directly to clients in the biopharmaceutical industry.
zPREDICTA has expertise in creating human, disease-specific tissue microenvironments for testing drug efficacy and safety. Unlike other platforms, the
patented 3D models utilize proprietary organ-specific extracellular matrix formulations that match the in vivo milieu of the organ of interest. These models
reconstruct both cellular and extracellular compartments of each tissue, which is especially essential for testing of immuno-oncology agents.
zPREDICTA technology demonstrates high clinical relevance, enabling its pharma clients to manage pipeline attrition more efficiently by identifying drugs
that are effective in patients, from the hundreds, and often thousands, of compounds in development. The tumor-specific models are used a number of
biopharmaceutical companies to evaluate the efficacy and toxicity of their therapeutic pipelines. Our models replicate the extracellular matrix (“ECM”) of
individual organs and disease-specific soluble microenvironment mimicking the biology of human disease, and as such, demonstrate high correlation with
clinical response.
The zPREDICTA 3D tumor-specific models incorporate tissue-specific extracellular matrices and tumor-specific medium supplements allowing for a true
reconstruction of tumor microenvironment. Our approach is compatible with multiple classes of immuno-oncology agents from naked antibodies and
antibody-drug conjugates, to bi- and tri-specific compounds, and CAR-T cells. The organ-specific disease models provide 3D reconstruction of human
tissues accurately representing each disease state and mimicking drug response.
Our platform incorporates both cellular and extracellular elements of tissue microenvironment in an organ- and disease-specific manner.
Extracellular components
● extracellular matrix
Cell-cell interactions
● tumor-tumor interactions
● soluble factors (cytokines, etc.)
● tumor-stroma interactions
Our platform is designed to evaluate drug candidates and drug combinations within the native microenvironment of human tissues. Our technology is a
patient-derived 3D culture platform that recreates the complex human organ microenvironment thereby preserving the critical interactions between a tumor
and its surroundings. Our platform supports long-term survival and proliferation of malignant and non-malignant cellular components of tissues. This
includes tumor cells, stroma, and immune components. Anticancer compounds tested in our models exhibit high correlation with clinical response when
comparing treatment outcomes in the clinic with cellular behavior in response to the therapeutic regimen. Our organ-specific technology is compatible with
multiple drug classes, including small molecules, antibodies, antibody-drug conjugates, immunomodulatory agents, CAR-T cells, etc. Our platform is fully
customizable to the tumor and tissue of interest. It is compatible with multiple cell types, drug classes, and downstream analysis methods.
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Applications include providing efficacy screening of anticancer compounds, evaluation of mechanisms of drug resistance, identification of new drug
combinations, rescue of failed drug candidates, assessment of off-target toxicity, target discovery and biomarker discovery.
SOLUBLE BIOTECH
Our subsidiary, Soluble Biotech Inc. (“Soluble”), focuses on contract services and research for biopharmaceutical company clients and academic
collaborators, focused on solubility improvements, stability studies, and protein production. Specifically, Soluble provides optimized FDA-approved
formulations for vaccines, antibodies, and other protein therapeutics in a faster and lower cost basis to its customers. In addition, Soluble enables protein
degradation studies, which based on current projections, potentially substantial line of business for the Company.
The primary assets of Soluble are our automated High Throughput Self-Interaction Chromatography (HSC™). HSC is a self-contained, automated system
that conducts high-throughput, self-interaction chromatography screens on excipients previously approved by the FDA for protein formulations. Our
technology measures second virial coefficient (B22 value) of protein-protein interactions to identify excipients that promote protein solubility in solutions.
The data generated from HSC screens are analyzed by a proprietary predictive algorithm to identify the optimal combination(s) of buffers, pH, and
excipients, resulting in increased solubility and physical stability of proteins. Several of our clients have seen ten-fold and hundred-fold increases in their
protein’s solubility while maintaining physical stability. For biopharmaceutical clients this means faster development times and quicker progression of
molecules into the clinic. For academic collaborators, this means further progression of biochemical & biology studies necessary to advance fundamental
research in areas of unmet medical need.
In addition, Soluble provides comprehensive protein stability analysis. Analysis via time-dependent shelf-life studies and forced degradation studies
designed to quickly determine which of the previously FDA approved additives that will improve the solubility and stability of proteins in solutions.
Services include pre-formulation development, stability assessment, and biophysical characterization which evaluate variables including pH, temperature,
humidity, light, oxidizing agents, and mechanical stress to determine the most promising additives, formulation of B22 values and confirmation on
conformation stability. We provide clients with a list of the most promising additives from a set of over 40 different additives that can increase the
solubility and stability of protein formulations.
Soluble also offers protein solubility kits that allow rapid identification of soluble formulations. We provide four different kits to fulfill customer solubility
requirements. The kits are in 96-well format and provide the tools and methods to compare relative solubility across 88 common formulations (with 8
controls). Soluble kits utilize a simple mix and spin protocol that quickly evaluates aggregation behavior as a function of pH, salt, and additives costing
significantly less than if manually determined. In addition, we provide innovative technologies for bacterial detection and removal in therapeutic proteins
that continue to be a significant issue in the pharmaceutical field.
In addition, Soluble supplies proprietary technologies for bacterial endotoxin detection and removal. Endotoxin is an inherent byproduct of bacterial
expression of therapeutic proteins. However, therapeutic proteins are required to have extremely low endotoxin levels. Soluble provides a product to
remove endotoxin that works through multiple molecular interactions for efficient removal over a wide range of buffer conditions with minimal product
loss. The detection of endotoxin can also be adversely affected by the protein therapeutic itself. To address this, Soluble provides sample treatment kits to
minimize detection interference while using standard detection assays.
SKYLINE MEDICAL – The STREAMWAY System
Sold through our subsidiary, Skyline Medical Inc. (“Skyline Medical”), the STREAMWAY System virtually eliminates staff exposure to blood, irrigation
fluid, and other potentially infectious fluids found in the healthcare environment. Antiquated manual fluid handling methods that require hand carrying and
emptying filled fluid canisters present both an exposure risk and potential liability. Skyline Medical’s STREAMWAY System fully automates the
collection, measurement, and disposal of waste fluids and is designed to: 1) reduce overhead costs to hospitals and surgical centers; 2) improve compliance
with the Occupational Safety and Health Administration (“OSHA”) and other regulatory agency safety guidelines; 3) improve efficiency in the operating
room and radiology and endoscopy departments, thereby leading to greater profitability; and 4) provide greater environmental stewardship by helping to
eliminate the approximately 50 million potentially disease-infected canisters that go into landfills each year in the United States. We continue to operate the
Skyline Medical business by continually improving our strategic opportunities, while focusing our resources on our precision medicine business.
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Industry and Market Background and Analysis - Infectious and Biohazardous Waste Management
There has long been recognition of the collective potential for ill effects to healthcare workers from exposure to infectious/biohazardous materials. Federal
and state regulatory agencies have issued mandatory guidelines for the control of such materials, and in particular, bloodborne pathogens. OSHA’s
Bloodborne Pathogens Standard (29 CFR 1910.1030) requires employers to adopt engineering and work practice controls that would eliminate or minimize
employee exposure from hazards associated with bloodborne pathogens. In 2001, in response to the Needlestick Safety and Prevention Act, OSHA revised
the Bloodborne Pathogens Standard. The revised standard clarifies and emphasizes the need for employers to select safer needle devices and to involve
employees in identifying and choosing these devices. The revised standard also calls for the use of “automated controls” as it pertains to the minimization
of healthcare exposure to bloodborne pathogens.
Most surgical procedures produce potentially infectious materials that must be disposed with the lowest possible risk of cross-contamination to healthcare
workers. Current standards of care allow for these fluids to be retained in canisters and located in the operating room where they can be monitored
throughout the surgical procedure. Once the procedure is complete these canisters and their contents are disposed using a variety of methods, all of which
include manual handling and result in a heightened risk to healthcare workers for exposure to their contents. Canisters are the most prevalent means of
collecting and disposing of infectious fluids in hospitals today. Traditional, non-powered canisters and related suction and fluid disposable products are
exempt and do not require FDA clearance.
We believe that our virtually hands free direct-to-drain technology (1) significantly reduces the risk of healthcare worker exposure to these infectious fluids
by replacing canisters, (2) further reduces the risk of worker exposure when compared to powered canister technology that requires transport to and from
the operating room, (3) reduces the cost per procedure for handling these fluids, and (4) enhances the surgical team’s ability to collect data to accurately
assess the patient’s status during and after procedures. In addition to the traditional canister method of waste fluid disposal, several other powered medical
devices have been developed that address some of the deficiencies described above. Most of these competing products continue to utilize some variation on
the existing canister technology, and while not directly addressing the canister, most have been successful in eliminating the need for an expensive gel and
its associated handling and disposal costs. Our existing competitors with products already on the market have a clear competitive advantage over us in
terms of brand recognition and market exposure. In addition, many of our competitors have extensive marketing and development budgets that could
overpower an emerging growth company like ours.
We expect the hospital surgery market to continue to increase due to population growth, the aging of the population, and expansion of surgical procedures
to new areas (for example, use of the endoscope) which requires more fluid management and new medical technology.
STREAMWAY System Product Sales
Our Skyline Medical division consists primarily of sales of the STREAMWAY System, as well as sales of the proprietary cleaning fluid and filters for use
with the STREAMWAY System. We manufacture an environmentally conscious system for the collection and disposal of infectious fluids resulting from
surgical and other medical procedures. We have been granted patents for the STREAMWAY System in the United States, Canada, and Europe. We
distribute our products to medical facilities where bodily and irrigation fluids produced during medical procedures must be contained, measured,
documented, and disposed. Our products minimize the exposure potential to the healthcare workers who handle such fluids.
The STREAMWAY System is a wall-mounted fully automated system that disposes of an unlimited amount of suction fluid providing uninterrupted
performance for physicians while virtually eliminating healthcare workers’ exposure to potentially infectious fluids collected during surgical and other
patient procedures. We also manufacture and sell two disposable products required for the operation of the STREAMWAY System: a bifurcated dual port
procedure filter with tissue trap and a single use bottle of cleaning solution. Both items are utilized on a single procedure basis and must be discarded after
use. The STREAMWAY disposables are a critical component of our business model. Recurring revenues from the sale of the disposables are expected to be
significantly higher over time than the revenues from the initial sale of the unit. We have exclusive distribution rights to the disposable solution.
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TUMORGENESIS
Our subsidiary TumorGenesis is our research and development arm for Helomics and zPREDICTA. TumorGenesis also specializes in media that help
cancer cells grow outside the patient’s body and retain their DNA/RNA and proteomic signatures. With this tool, researchers are able to expand and study
cancer cell types inherent in blood tumors and organ systems of all mammals, including humans.
Competition and Competitive Advantages
Precision Medicine Business. We presently have clinical information, including tumor drug response data and an in-house bioinformatics AI platform.
Cancer treatments require at least 5 years of testing to see progression-free survival rates. While competitors must wait for this data, we can leverage that
data today. Other companies within our market segment are spending significant investment dollars to generate this data which they cannot leverage until
the future. We can leverage the data today by sequencing the tumors and gathering the outcome data which is measured in months instead of years. In
addition, the following points detail the key differentiators in our model building approach.
● AI Models are built with real world data on how patient tumors responded to drugs, together with clinical outcome (progression-free survival/overall
survival).
● We believe this patient-centric, highly standardized, and curated, multi-omic tumor model offers a better chance of generating serviceable predictive
models of drug-response and outcomes than competitive approaches in the market today. The information embodied in the AI-driven predictive model
provides insights into each tumor’s response to different therapeutic options, resulting in the ability to provide actionable insights critical to both new
drug development and individualizing patient treatment.
zPREDICTA. Our next-generation technology based on extensive research of the human tumor microenvironment creating accurate reconstruction of the
organ-specific 3D tissue microenvironment enabling evaluation of therapeutic agents under conditions mimicking human physiology. The main
competitive advantage of zPREDICTA’s technology is the tumor-specific nature of its systems. 3D models replicate tissue heterogeneity and provides long-
term maintenance of primary human cells, organoids, and cell lines under the native conditions of human disease. The 3D models are formulated to mimic
the tissue and disease of interest instead of pursuing a one-size-fits-all approach taken by other companies. Services provide reliable prediction of clinical
outcomes based on accurate reconstruction of cellular and extracellular compartments of human tissues.
Soluble Biotech. HSC Technology is a self-contained, automated system that conducts high-throughput, self-interaction chromatography screens on FDA
approved excipients for protein formulations. The HSC Instrument and its technology has been validated over the past twelve years via industry and
academic collaborations. The data generated from HSC screens are analyzed by a proprietary predictive algorithm to identify the optimal combination(s) of
buffers, pH, and excipients, resulting in increased solubility and physical stability of proteins. Several of our clients have seen ten-fold and hundred-fold
increases in their protein’s solubility while maintaining physical stability. For biopharmaceutical clients this means faster development times and quicker
progression of molecules into the clinic.
Skyline Medical. We believe that the STREAMWAY System is unique to the industry in that it not only allows continuous suction but also provides for
unlimited capacity, eliminating the need to interrupt a procedure to change canisters. To our knowledge, the STREAMWAY System is the only known fully
automated direct‐to‐drain system that is wall‐mounted and able to collect, measure, and dispose of an unlimited amount of waste fluid without interruption.
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Suppliers
We buy our raw materials from several suppliers and, except as set forth below, the loss of any one supplier would not materially adversely affect our
business. We rely on sole suppliers for certain materials used to perform our molecular diagnostic tests. We also purchase reagents used in our molecular
diagnostic tests from sole-source suppliers. While we have developed alternate sourcing strategies for these materials and vendors, we cannot be certain
that these strategies will be effective or that the alternative sources will be available in a timely manner. If our current suppliers can no longer provide us
with the materials, we need to perform molecular diagnostic tests, if the materials do not meet our quality specifications, or if we cannot obtain acceptable
substitute materials, there could be an interruption in molecular diagnostic test processing. In the event of the loss of these suppliers, we could experience
delays and interruptions that might adversely affect the financial performance of our business.
We also have single suppliers for the manufacturing of certain of our Skyline Medical products. Alternative suppliers are available in the market; however,
we could experience delays and interruptions that might adversely affect the financial performance of our business including time for machine tooling
specific to our products.
We have existing and good relationships with our service vendors.
Research and Development (“R&D”)
We spent $315,850 and $372,710 in 2021 and 2020, respectively, on R&D.
Intellectual Property
We believe that to maintain a competitive advantage in the marketplace, we must develop and maintain protection of the proprietary aspects of our
technology. We rely on a combination of patent, trade secret intellectual property rights, and other measures to protect our intellectual property to develop
and maintain our competitive position. We seek to protect our trade secrets and proprietary know-how, in part, with confidentiality agreements with
employees, although we cannot be certain that the agreements will not be breached, or that we will have adequate remedies if a breach were to occur.
zPREDICTA. Our technology is a patient-derived 3D culture platform that recreates the complex human organ microenvironment thereby preserving the
critical interactions between a tumor and its surroundings. Our models replicate the extracellular matrix of individual organs and disease-specific soluble
microenvironment mimicking the biology of human disease, and as such, demonstrate high correlation with clinical response. Patents include
US10,501,717, US11,124,756 and pending application US16/321,277.
Skyline Medical. In general, our patents are directed to a system and method for collecting waste fluid from a surgical procedure while ensuring there is no
interruption of suction during the surgical procedure and no limit on the volume of waste fluid that can be collected. We hold the following granted patents
in the United States, and a pending application in the United States on our earlier STREAMWAY System models: US7469727, US8123731, and US
Publication No. US20090216205 (collectively, the “Patents”). The Patents will begin to expire on August 8, 2023.
On January 25, 2014, we filed a non-provisional Patent Cooperation Treaty (“PCT”) Application No. PCT/US2014/013081 claiming priority from the U.S.
Provisional Patent Application, number 61756763 which was filed on January 25, 2013. The PCT allows an applicant to file a single patent application to
seek patent protection for an invention simultaneously in each of the 148-member countries of the PCT, including the United States.
The United States Patent Office has assigned application #14/763,459 to our previously filed PCT application.
As of November 22, 2017, we were informed that the European Patent Office allowed all our claims for application #14743665.3-1651 and on as of July
11, 2018, we were informed that the European Patent #EP2948200 was granted and published validating in the following countries: Belgium, Germany,
Spain, France, United Kingdom, Ireland, Italy, Netherlands, Norway, Poland, and Sweden. Our PCT patent application is for an enhanced model of the
surgical fluid waste management system. We utilize this enhanced technology in the updated version of the STREAMWAY System unit we began selling in
2014.
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Government Regulation
Our businesses are subject to or impacted by extensive and frequently changing laws and regulations in the United States (at both the federal and state
levels) and the other jurisdictions in which we conduct business, including some specific to our business, some specific to our industry, and others relating
to conducting business generally (e.g., U.S. Foreign Corrupt Practices Act). We also are subject to inspections and audits by governmental agencies. The
table below highlights key regulatory schemes applicable to our businesses:
CLIA and State Clinical Laboratory
Licensing
CLIA regulates the operations of virtually all clinical laboratories, requiring that they be certified by the federal
government and that they comply with various technical, operational, personnel, and quality requirements intended to
ensure that the services provided are accurate, reliable, and timely.
State laws may require additional personnel qualifications or licenses, quality control, record maintenance,
proficiency testing, or detailed review of our scientific method validations and technical procedures for certain tests.
Medicare and Medicaid; Fraud and
Abuse
Violations of these laws and regulations may result in monetary fines, criminal and civil penalties and/or suspension
or exclusion from participation in Medicare, Medicaid, and other federal or state healthcare programs.
Diagnostic testing services provided under Medicare and Medicaid programs are subject to complex, evolving,
stringent, and frequently ambiguous federal and state laws, and regulations, including those relating to billing,
coverage, and reimbursement.
Anti-kickback laws and regulations prohibit making payments or furnishing other benefits to influence the referral of
tests billed to Medicare, Medicaid, or certain other federal or state healthcare programs.
In addition, federal and state anti-self-referral laws generally prohibit Medicare and Medicaid payments for clinical
tests referred by physicians who have an ownership or investment interest in, or a compensation arrangement with, the
testing laboratory, unless specific exceptions are met.
Federal substance abuse legislation enacted in 2018 contains anti-kickback provisions that are, by their terms,
applicable to laboratory testing paid for by all payers. Upon full review of the legislation, we were in compliance at
that time and continue to maintain compliance. We monitor regularly and reflect this in our annual compliance report.
Some states have similar laws that are not limited in applicability to only Medicare and Medicaid referrals and could
also affect tests that are paid for by health plans and other non-governmental payers.
Violations of these laws and regulations may result in monetary fines, criminal and civil penalties and/or suspension
or exclusion from participation in Medicare, Medicaid, and other federal or state healthcare programs.
The FDA has potential regulatory responsibility over, among other areas, instruments, software, test kits, reagents and
other devices used by clinical laboratories to perform diagnostic testing in the United States. The FDA may assert
regulatory oversight over these areas, and legislative proposals addressing FDA oversight of laboratory developed
tests have been introduced in the past and may be enacted in the future. See “Item 1A. Risk Factors” for a discussion
of the possible impact of such regulatory or legislative developments.
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FDA
Environmental, Health and Safety We are subject to laws and regulations related to the protection of the environment, the health and safety of
employees, and the handling, transportation, and disposal of medical specimens, infectious and hazardous waste,
radioactive materials, various aspects of pertinent technologies and methods of protection.
Several organizations maintain oversight function including:
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OSHA (Occupational Safety and Health Administration)
EPA (Environmental Protection Agency)
DOT (Department of Transportation)
USPS (US Postal Service)
US Public Health Service
JCAHO (Joint Commission on Accreditation of Healthcare Organizations)
NFPA (National Fire Protection Association)
AIA (American Institute of Architects)
AORN (Association of Operating Room Nurses)
Privacy and Security of Health and
Personal Information
We are subject to laws and regulations regarding protecting the security and privacy of certain healthcare and personal
information, including: (1) the federal Health Insurance Portability and Accountability Act and the regulations
thereunder, which establish (a) a complex regulatory framework including requirements for safeguarding protected
health information and (b) comprehensive federal standards regarding the uses and disclosures of protected health
information; (2) state laws; and (3) the European Union's General Data Protection Regulation.
A healthcare provider may be subject to penalties for non-compliance and may be required to notify individuals or
state, federal, or county governments if the provider discovers certain breaches of personal information or protected
health information.
To date, no regulatory agency has established exclusive jurisdiction over the area of biohazardous and infectious waste in healthcare facilities.
FDA Clearance of STREAMWAY System under Section 510(k)
The FDA Center for Devices and Radiological Health requires 510(k) submitters to provide information that compares its new device to a marketed device
of a similar type, in order to determine whether the device is substantially equivalent.
We filed the 510(k) submission for clearance of the STREAMWAY System device on March 14, 2009 and received written confirmation on April 1, 2009
that our 510(k) has been cleared by the FDA.
Following this 510(k) clearance by the FDA, we continue to be subject to the normal ongoing audits and reviews by the FDA and other governing
agencies. These audits and reviews are standard and typical in the medical device industry, and we do not anticipate being affected by any extraordinary
guidelines or regulations.
Our subsidiary, Skyline Medical has successfully passed FDA audits in the past, with no observations or 483 warning letters issued.
Application for Electrical Safety Testing and Certification for STREAMWAY System
We sought and achieved testing and certification to the IEC 60606-1 and IEC 60606-1-2, two internationally recognized standards.
The 60601-1 3rd edition certification for our STREAMWAY System is valid and enables us to continue to market and sell our product domestically and
internationally.
We have contracted with TUV, a nationally recognized testing laboratory-NRTL, to certify our STREAMWAY System to the new 60601-1 3rd Edition in
late 2016. We attained certification to the new standard, and then submitted it to our Notified Body (BSI) for recommendation for our CE Mark, which we
received in June 2017, allowing us to sell products outside of the United States.
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Effective November 21, 2016, we received a Medical Device Establishment License to sell the STREAMWAY System and related disposables in Canada.
ISO Certification
Our subsidiary, Skyline Medical, hired BSI (British Standards Institute) to be its Notified Body and to perform audits to ISO 13485:2003 Standards. On
June 1, 2016, we successfully passed the audit of our Quality Management System and received our Certificate of Registration for ISO 13485:2016. Our
certificate number is FM 649810.
Employees
We have 30 full-time employees and 2 part-time employees as of December 31, 2021.
Executive Offices
Our principal executive offices are located at 2915 Commers Drive; Suite 900; Eagan, Minnesota 55121 and our telephone number is (651) 389-4800.
Corporate History
We were originally incorporated on April 23, 2002 and reincorporated in Delaware in 2013. We changed our name from Skyline Medical Inc. to Precision
Therapeutics Inc. on February 1, 2018 and to Predictive Oncology Inc. on June 13, 2019.
Available Information
Our website address is http://www.predictive-oncology.com. Information contained on our website is not incorporated by reference into this Annual Report
on Form 10-K unless expressly noted.
We file reports with the Securities and Exchange Commission (“SEC”), which we make available on our website free of charge at
http://investors.predictive-oncology.com/financial-information These reports include Annual Reports on Form 10-K, Quarterly Reports on Form 10-Q and
Current Reports on Form 8-K, each of which is provided on our website as soon as reasonably practicable after we electronically file such materials with,
or furnish them to, the SEC. We also make, or will make, available through our website other reports filed with or furnished to the SEC under the Securities
Exchange Act of 1934, as amended, including our proxy statements and reports filed by officers and directors under Section 16(a) of that Act. You can also
read and copy any materials we file with the SEC at the SEC’s Public Reference Room at 100 F Street, N.E., Washington, DC 20549. You can obtain
additional information about the operation of the Public Reference Room by calling the SEC at 1-800-SEC-0330. In addition, the SEC maintains a website
(http://www.sec.gov) that contains reports, proxy and information statements, and other information regarding issuers that file electronically with the SEC,
including us.
You can obtain copies of exhibits to our filings electronically at the SEC’s website at www.sec.gov or by mail from the Public Reference Section of the
SEC at 100 F Street, N.E., Washington, D.C. 20549 at prescribed rates. The exhibits are also available as part of the Annual Report on Form 10-K for the
year ended December 31, 2021, which is available on our corporate website.
ITEM 1A. RISK FACTORS.
You should carefully consider the risks described below before making an investment decision. Our business could be harmed by any of these risks. The
trading price of our common stock could decline due to any of these risks, and you may lose all or part of your investment. The risks described below are
not the only ones that we may face. Additional risks that are not currently known to us or that we currently consider immaterial may also impair our
business, financial condition or results of operations. In assessing these risks, you should also refer to the other information contained in this Form 10-K,
including our financial statements and related notes.
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Risk Factors Relating to Our Business
Our limited operating history with respect to our precision medicine services makes evaluation of our business difficult.
Our precision medicine services were launched with the initial investment in Helomics during the first quarter of 2018 and have not generated significant
revenue to date. Our ability to implement a successful business plan with respect to precision medicine remains unproven and no assurance can be given
that we will ever generate sufficient revenues to sustain our business. We have a limited operating history which makes it difficult to evaluate our
performance. Our prospects should be considered in light of these risks, and the expenses, technical obstacles, difficulties, market penetration rate, and
delays frequently encountered in connection with the development of new businesses. These factors include uncertainty as to whether we will be able to:
● Succeed in uncertain markets;
● Respond effectively to competitive pressures;
● Successfully address intellectual property issues of others;
● Protect and expand our intellectual property rights; and
● Continue to develop and upgrade our products.
In connection with developing our CRO business, we have committed and will continue to commit significant capital to investments in early-stage
companies, all of which may be lost, and which may require us to raise significant additional capital, and our entering into new lines of business will
result in significant diversion of management resources, all of which may result in failure of our business.
We have committed significant capital and management resources to developing our CRO business and other new business areas, and we intend to continue
to devote significant capital and management resources to new businesses. Therefore, we could invest significant capital in business enterprises with no
certainty when or whether we will realize a return on these investments. Investments using cash will deplete our capital resources, meaning we will be
required to raise significant amounts of new capital. There is no assurance that we will be successful in raising sufficient capital, and the terms of any such
financing will be dilutive to our stockholders. We may also acquire technologies or companies by issuing stock or other equity securities rather than, or in
addition to, payment of cash, which may have the result of diluting our stockholders’ investments. Further, the energy and resources of our officers and
personnel may be substantially diverted to new lines of business, which are unproven. If these businesses are unsuccessful or require too great of a financial
investment to be profitable, our business may fail.
We rely on sole suppliers for some of the materials used in our molecular diagnostic tests, and we may not be able to find replacements or transition to
alternative suppliers in a timely manner.
We rely on sole suppliers for certain materials used to perform our molecular diagnostic tests. We also purchase reagents used in our molecular diagnostic
tests from sole-source suppliers. While we have developed alternate sourcing strategies for these materials and vendors, we cannot be certain whether these
strategies will be effective, or the alternative sources will be available in a timely manner. If these suppliers can no longer provide us with the materials
needed to perform our molecular diagnostic tests, if the materials do not meet required quality specifications, or if we cannot obtain acceptable substitute
materials, an interruption in molecular diagnostic test processing could occur. Any such interruption may directly impact our revenue and cause us to incur
higher costs.
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If we are sued for product liability or errors and omissions liability, we could face substantial liabilities that exceed our resources.
The marketing, sale, and use of our molecular diagnostic tests could lead to product liability claims if someone were to allege that the molecular diagnostic
test failed to perform as it was designed. We may also be subject to liability for errors in the results we provide to physicians or for a misunderstanding of,
or inappropriate reliance upon, the information we provide. A product liability or errors and omissions liability claim could result in substantial damages
and be costly and time consuming for us to defend. Although we maintain product liability and errors and omissions insurance, we cannot be certain that
our insurance would fully protect us from the financial impact of defending against these types of claims or any judgments, fines, or settlement costs
arising out of such claims. Any product liability or errors and omissions liability claim brought against us, with or without merit, could increase our
insurance rates or prevent us from securing insurance coverage in the future. Additionally, any product liability lawsuit could cause injury to our reputation
or cause us to suspend sales of our products and solutions. The occurrence of any of these events could have a material adverse effect on our business,
financial condition, and results of operations.
If our R&D and commercialization efforts for our TruTumor and PeDAL platforms take longer than expected, the commercial revenues from the
service offerings that use these platforms could also be delayed.
Our CRO business offers various services to pharma, diagnostics, and biotech companies. These services use our TruTumor tumor platform and our
PeDAL platform. These platforms are the subject of active R&D to further improve them for commercial use in order to help our clients in their drug
discovery, biomarker, and clinical trial activities. We could face delays in this R&D, for example:
● we may not be able to secure access to and approval to use clinical data from academic hospital partners in a timely manner;
● clinical testing volume (number of specimens coming to us for testing) may not grow sufficiently to drive additional data generation as well as
further development of the TruTumor platform;
● patient consent to use the patient’s data and tumor material for R&D may not be sufficient to support R&D; and
● we may not be able to attract and retain the appropriately qualified staff to perform the necessary R&D.
We have a limited operating history with the CRO business particularly services using our PeDAL, platform as these are new to the market, which makes it
difficult to forecast our future revenues. While we are committed to the buildout of the CRO services for the long term, we cannot predict at this time, with
any certainty, the future viability of either business unit.
We face significant competition in the surgical fluid waste management industry, including competition from companies with considerably greater
resources than ours, and if we are unable to compete effectively with these companies, our market share may decline, and our business could be
harmed.
The surgical fluid waste management industry is highly competitive with numerous competitors ranging from well-established manufacturers to innovative
start-ups. Several of our competitors have significantly greater financial, technological, engineering, manufacturing, marketing, and distribution resources
than we do. Their greater capabilities in these areas may enable them to compete more effectively on the basis of price and production and more quickly
develop new products and technologies.
Companies with significantly greater resources than ours may be able to reverse engineer our products and/or circumvent our intellectual property position.
Such action, if successful, would greatly reduce our competitive advantage in the marketplace.
We believe our ability to compete successfully with our STREAMWAY System depends on a number of factors, including, without limitation, our technical
innovations of unlimited suction and unlimited capacity capabilities, our innovative and advanced research and development capabilities, strength of our
intellectual property rights, sales and distribution channels, and advanced manufacturing capabilities. We plan to employ these and other elements as we
develop our products and technologies, but there are many other factors beyond our control. We may not be able to compete successfully in the future, and
increased competition may result in price reductions, reduced profit margins, loss of market share, and an inability to generate cash flows that are sufficient
to maintain or expand our development and marketing of new products, which could adversely impact the trading price of the shares of our common stock.
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If demand for our STREAMWAY System or molecular diagnostic tests is unexpectedly high or if we experience problems in scaling our operations,
there is no assurance that there will not be supply interruptions or delays that could limit the growth of our revenue.
We have contracted with a manufacturing company that follows ISO compliance regulations of the FDA and that can manufacture products at high
volumes. However, if demand for our product is higher than anticipated, there is no assurance that we or our manufacturing partners will be able to produce
the product in sufficiently higher quantity to satisfy demands.
Likewise, as demand for our molecular diagnostic tests grow, we will need to continue to scale our testing capacity and processing technology to expand
our customer service, billing, and systems processes and to enhance our internal quality assurance program. We will also need additional certified
laboratory scientists and other scientific and technical personnel to process higher volumes of our molecular diagnostic tests. We cannot guarantee that
increases in scale, related improvements, and quality assurance will be implemented successfully or that appropriate personnel will be available. Failure to
implement necessary procedures, transition to new processes, or hire the necessary personnel could result in higher costs of processing tests or an inability
to meet demand. There can be no assurance that we will be able to perform our testing on a timely basis at a level consistent with demand, or that our
efforts to scale our operations will not negatively affect the quality of test results.
If we encounter difficulties in scaling our operations as a result of, among other things, quality control and quality assurance issues and availability of
reagents and raw material supplies, we will likely experience reduced sales, increased repair or re-engineering costs, defects, and increased expenses due to
switching to alternate suppliers. Any of these results would reduce our revenues and gross margins. Although we attempt to match our capabilities to
estimates of marketplace demand, to the extent demand materially varies from our estimates, we may experience constraints in our operations and delivery
capacity, which could adversely impact revenue in a given fiscal period. Any supply interruptions or inadequate supply would have a material adverse
effect on our results of operations.
If we encounter difficulty meeting market demand or quality standards our reputation could be harmed, and our future prospects and business could suffer,
causing a material adverse effect on our business, financial condition, and results of operations.
We may require additional financing to finance operating expenses and fulfill our business plan. Such financing, if available, will be dilutive.
We have not achieved profitability and anticipate that we will continue to incur net losses at least through the remainder of 2022. We may need to raise
additional capital to finance operating expenses, invest in our sales organization and new product development, compete in the international marketplace,
and develop the strategic assets of our Helomics businesses, especially over the longer term. We would attempt to raise these funds through equity or debt
financing that may include public offerings, private placements, alternative offerings, further draws on our equity line with Oasis Capital, LLC, or other
means. Such additional financing would be dilutive to existing stockholders, and there is no assurance that such financing would be available upon
acceptable terms. If such financing or adequate funds from operations are not available, we would be forced to limit our business activities, which would
have a material adverse effect on our results of operations and financial condition. These possibilities, to the extent available, may be on terms that result in
significant dilution to our existing shareholders or that result in our existing shareholders losing part or all of their investment.
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Our business and operations have been and will likely continue to be materially and adversely affected by the COVID-19 pandemic.
The current COVID-19 worldwide pandemic has presented substantial public health challenges. In response to the crisis, emergency measures have been
imposed by governments worldwide, including mandatory social distancing and the shutdown of non-essential businesses. These measures have adversely
impacted the global economy, disrupted global supply chains and created significant volatility and disruption of financial markets, and our business and
operations have been and will likely continue to be materially and adversely affected. For example, our contract manufacturer for the STREAMWAY®
System has been forced to change locations, thereby delaying our order fulfillment for parts. We have also reduced on-site staff at several of our facilities,
resulting in delayed production, less efficiency, and our sales staff is unable to visit with hospital administrators who are our customers and potential
customers. In addition, COVID-19 has impacted the Company’s capital and financial resources, including our overall liquidity position and outlook. For
instance, our accounts receivable has slowed while our suppliers continue to ask for pre-delivery deposits. Ultimately, the extent of the impact of the
COVID-19 pandemic on our future operational and financial performance will depend on, among other matters, the duration and intensity of the pandemic;
the level of success of global vaccination efforts; governmental and private sector responses to the pandemic and the impact of such responses on us; and
the impact of the pandemic on our employees, customers, suppliers, operations and sales, all of which are uncertain and cannot be predicted. These factors
may remain prevalent for a significant period of time even after the pandemic subsides, including due to a continued or prolonged recession in the U.S. or
other major economies. Even in areas where "stay-at-home" restrictions, masking and social distancing measures have been lifted and the number of
COVID-19 cases have declined, some jurisdictions may re-impose these measures as and if variant strains emerge or cases rise. The impacts of the
COVID-19 pandemic, as with any adverse public health developments, could have a material adverse effect on our business, results of operations, liquidity
or financial condition and heighten or exacerbate risks described in this Annual Report on Form 10-K.
We are dependent on a few key executive officers for our success. Our inability to retain those officers would impede our business plan and growth
strategies, which would have a negative impact on our business and the value of an investment.
Our success depends on the skills, experience, and performance of key members of our management team. We heavily depend on our management team: J.
Melville Engle, our Chief Executive Officer (“CEO”), and Bob Myers, our Chief Financial Officer (“CFO”). We have entered into employment agreements
with the CEO and the CFO and may expand the relatively small number of executives. Were we to lose one or more of these key individuals, we would be
forced to expend significant time and money in the pursuit of a replacement, which could result in both a delay in the implementation of our business plan
and the diversion of our limited working capital. We can give no assurance that we would be able to find satisfactory replacements for these key individuals
at all, or on terms that are not unduly expensive or burdensome to us.
If we are required to write down goodwill and other intangible assets, our financial condition and operating results would be negatively affected.
When we acquire a business, a substantial portion of the purchase price of the acquisition is allocated to goodwill and other identifiable intangible assets.
The amount of the purchase price which is allocated to goodwill and other intangible assets is determined by the excess of the purchase price over the net
identifiable assets acquired. For example, when we acquired Helomics, we acquired $3,725,000 in intangible assets and $23,790,290 in goodwill, which
represented the excess of the consideration transferred over the fair values of assets acquired and liabilities assumed and represents the future economic
benefits arising from other assets acquired that could not be individually identified and separately recognized. We test intangible assets and goodwill for
impairment at least annually. During the year ended December 31, 2021, we recorded an impairment of goodwill completing the full impairment of the
goodwill acquired at the acquisition of Helomics in 2019. We also recorded a full impairment of the net book value of our intangible assets acquired at the
acquisition of Helomics in 2019. On November 24, 2021, we acquired $6,857,790 in goodwill and $3,780,000 of intangible assets as a part of our
acquisition of zPREDICTA. Under current accounting standards, if we determine that intangible assets or goodwill are impaired in the future, we will be
required to write down these assets. Any write-downs that may be required to be recorded would adversely affect our financial condition and operating
results.
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We may fail to realize the anticipated benefits of the zPREDICTA acquisition.
The success of the zPREDICTA acquisition will depend, in part, on our ability to realize the anticipated growth opportunities and synergies from
combining our companies, Predictive and zPREDICTA. The integration will be a time consuming and expensive process and may disrupt our operations if
it is not completed in a timely and efficient manner. In addition, we may not achieve anticipated synergies or other benefits of the merger. Following the
merger, we operate as a combined organization utilizing common information and communication systems, operating procedures, financial controls, and
human resources practices. We may encounter the following integration difficulties, resulting in costs and delays:
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failure to successfully manage relationships with customers and other important relationships;
failure of customers to continue using our services;
difficulties in successfully integrating our management teams and employees;
challenges encountered in managing larger operations;
losses of key employees;
failure to manage our growth and growth strategies;
diversion of the attention of management from other ongoing business concerns;
incompatibility of technologies and systems;
impairment charges incurred to write down the carrying amount of intangible assets generated as a result of the merger; and
incompatibility of business cultures.
If our operations after the merger do not meet the expectations of our existing or prospective customers, then these customers and prospective customers
may cease doing business with us altogether, which would harm our results of operations, financial condition, and business prospects. If the management
team is not able to develop strategies and implement a business plan that successfully addresses these difficulties, we may not realize the anticipated
benefits of the merger.
Risks Related to Our Intellectual Property
Our business is dependent upon proprietary intellectual property rights, which if we were unable to protect, could have a material adverse effect on our
business.
We rely on a combination of patent, trade secret and other intellectual property rights, contractual restrictions, and other measures to protect our intellectual
property. We currently own and may in the future own or license additional patent rights or trade secrets in the U.S., with non-provisional patents elsewhere
in the world that cover certain of our products. We rely on patent laws and other intellectual property laws, nondisclosure and other contractual provisions,
and technical measures to protect our products and intangible assets.
If we fail to protect our intellectual property, third parties may be able to compete more effectively against us and we may incur substantial litigation costs
in our attempts to recover or restrict use of our intellectual property. While we apply for patents covering our products and technologies and uses thereof,
we may fail to apply for patents on important products and technologies in a timely fashion, or at all, or we may fail to apply for patents in relevant
jurisdictions. Others could seek to design around our current or future patented technologies. These intellectual property rights are important to our ongoing
operations and no assurance can be given that any measure we implement will be sufficient to protect our intellectual property rights.
Further, competitors could willfully infringe upon our intellectual property rights, design around our protected technology, or develop their own
competitive technologies that arguably fall outside of our intellectual property rights. Others may independently develop similar or alternative products and
technologies or replicate any of our products and technologies. Also, with respect to our trade secrets and proprietary know-how, we cannot be certain that
the confidentiality agreements we have entered into with employees will not be breached, or that we will have adequate remedies for any breach. In
addition, we may lose the protection afforded by these rights through patent expirations, legal challenges, or governmental action. If our intellectual
property does not adequately protect us against competitors’ products and methods, our competitive position could be adversely affected, as could our
business and the results of our operations. To the extent our intellectual property offers inadequate protection, or is found to be invalid or unenforceable, we
would be exposed to a greater risk of competition. If our intellectual property does not provide adequate coverage of our competitors’ products, our
competitive position could be adversely affected, as could our overall business.
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If we become subject to intellectual property actions, it could hinder our ability to deliver our products and services and our business could be
negatively impacted.
We could be subject to legal or regulatory actions alleging intellectual property infringement or similar claims against us. Companies may apply for or be
awarded patents or have other intellectual property rights covering aspects of our technologies or businesses. Litigation may be necessary for us to enforce
our patents and proprietary rights or to determine the scope, coverage, and validity of the proprietary rights of others. The outcome of any litigation or other
proceeding is inherently uncertain and might not be favorable to us, and we might not be able to obtain licenses to technology that we require on acceptable
terms, or at all. Moreover, if it is determined that our products infringe on the intellectual property rights of third parties, we could be prevented from
marketing our products. While we are currently not subject to any material intellectual property litigation, any future litigation alleging intellectual property
infringement could be costly, particularly in light of our limited resources. Similarly, if we determine that third parties are infringing on our patents or other
intellectual property rights, our limited resources may prevent us from litigating or otherwise taking actions to enforce our rights. Any such litigation or
inability to enforce our rights could require us to change our business practices, hinder or prevent our ability to deliver our products and services, and result
in a negative impact to our business. Expansion of our business via product line enhancements or new product lines to drive increased growth in current or
new markets may be inhibited by the intellectual property rights of our competitors and/or suppliers. Our inability to successfully mitigate those factors
may significantly reduce our market opportunity and subsequent growth. Any litigation that may be necessary in the future could result in substantial costs
and diversion of resources and could have a material adverse effect on our business, financial condition, and operating results.
Risk Factors Relating to Regulation
Our business is subject to intense governmental regulation and scrutiny, both in the U.S. and abroad.
The production, marketing, and R&D of our products is subject to extensive regulation and review by the FDA and other governmental authorities both in
the United States and abroad. In addition to testing and approval procedures, extensive regulations also govern marketing, manufacturing, distribution,
labeling, and record keeping. If we do not comply with applicable regulatory requirements, violations could result in warning letters, non-approvals,
suspensions of regulatory approvals, civil penalties and criminal fines, product seizures and recalls, operating restrictions, injunctions, and criminal
prosecution.
Periodically, legislative or regulatory proposals are introduced that could alter the review and approval process relating to medical products. It is possible
that the FDA will issue additional regulations further restricting the sale of our present or proposed products. Any change in legislation or regulations that
governs the review and approval process relating to our current and future products could make it more difficult and costlier to obtain approval for new
products, or to produce, market, and distribute existing products.
If the FDA begins to enforce regulation of our molecular diagnostic tests, we could incur substantial costs and delays associated with trying to obtain
pre-market clearance or approval and costs associated with complying with post-market requirements.
Clinical laboratory tests like our molecular diagnostic tests are regulated under CLIA as well as by applicable state laws. Most Laboratory Developed Tests
(“LDTs”) are currently not subject to the FDA’s regulation (although reagents, instruments, software, or components provided by third parties and used to
perform LDTs may be subject to regulation). In October 2014, the FDA issued two draft guidance documents: “Framework for Regulatory Oversight of
Laboratory Developed Tests”, which provides an overview of how the FDA would regulate LDTs through a risk-based approach, and “FDA Notification
and Medical Device Reporting for Laboratory Developed Tests”, which provides guidance on how the FDA intends to collect information on existing
LDTs, including adverse event reports. On January 13, 2017, the FDA also issued a discussion paper on LDTs. Pursuant to the Framework for Regulatory
Oversight draft guidance, LDT manufacturers would be subject to medical device registration, listing, and adverse event reporting requirements. The risk-
based classification considers the LDT’s intended use, technological characteristics, and the risk to patients if the LDT were to fail.
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Pursuant to the Framework for Regulatory Oversight draft guidance, LDT manufacturers would be required to either submit a pre-market application and
receive the FDA’s approval before an LDT may be marketed or submit a pre-market notification in advance of marketing. These requirements would be
phased in, starting with higher risk LDTs, following the issuance of the FDA’s final guidance on this topic, which the FDA has identified as a priority. The
draft guidance provides that LDTs that are already marketed at the time the final guidance is issued would not be withdrawn from the market during the
FDA’s review process.
There is no timeframe within which the FDA must issue its final guidance, but issuance of this final guidance has been identified among a list of the FDA’s
priorities. As of the date of this filing, the FDA has not issued its final guidance. In August 2020, however, the U.S. Department of Health and Human
Services – the parent agency for FDA – announced that the FDA “will not require premarket review of LDTs absent notice-and-comment rulemaking, as
opposed to through guidance documents, compliance manuals, website statements, or other informal issuances.” It is unclear at this time whether the Biden
Administration will rescind or reverse this policy. It is also unclear at this time when, or if, the FDA will finalize its plans to end enforcement discretion
(e.g., via notice and comment rulemaking or otherwise), and even then, the new regulatory requirements are expected to be phased‑in over time.
Nevertheless, the FDA may attempt to regulate certain LDTs on a case‑by‑case basis at any time.
Legislative proposals addressing the FDA’s oversight of LDTs have been introduced in previous Congresses, and we expect that new legislative proposals
will be introduced from time‑to‑time. The likelihood that Congress will pass such legislation and the extent to which such legislation may affect the FDA’s
plans to regulate certain LDTs as medical devices is difficult to predict at this time. If the FDA ultimately regulates certain LDTs, whether via final
guidance, final regulation, or as instructed by Congress, our molecular diagnostic tests may be subject to certain additional regulatory requirements. The
cost of conducting clinical trials and otherwise developing data and information to support pre-market applications may be significant. If we are required to
submit applications for our currently marketed tests, we may be required to conduct additional studies, which may be time-consuming and costly and could
result in our currently marketed tests being withdrawn from the market. If our tests are allowed to remain on the market, but there is uncertainty in the
marketplace about our tests, and if we are required by the FDA to label them investigational, or if labeling claims the FDA allows us to make are limited,
orders may decline, and reimbursement may be adversely affected. Continued compliance with the FDA’s regulations would increase the cost of conducting
our business, and subject us to heightened regulation by the FDA and penalties for failure to comply with these requirements.
In sum, we cannot predict the timing or form of any such guidance or regulation, or the potential effect on our existing molecular diagnostic tests or our
tests in development, or the potential impact of such guidance or regulation on our business, financial condition, and results of operations.
If we fail to comply with Federal, State, and foreign laboratory licensing requirements, we could lose the ability to perform our tests or experience
disruptions to our business.
We are subject to CLIA, a federal law that regulates clinical laboratories that perform testing on specimens derived from humans for the purpose of
providing information for the diagnosis, prevention, or treatment of disease. CLIA regulations mandate specific standards in the areas of personnel
qualifications, administration, and participation in proficiency testing, patient test management, and quality assurance. CLIA certification is also required in
order for our business to be eligible to bill Federal and State healthcare programs, as well as many private third-party payors, for our molecular diagnostic
tests. To renew these certifications, we are subject to survey and inspection every two years. Moreover, CLIA inspectors may make random inspections of
our clinical reference laboratories. Pennsylvania laws also require that we maintain a license and establish standards for the day-to-day operation of our
clinical reference laboratory in Pittsburgh, Pennsylvania. In addition, our Pittsburgh laboratory is required to be licensed on a test-specific basis by certain
other states. If we were unable to obtain or lose our CLIA certificate or State licenses for our laboratories, whether as a result of revocation, suspension, or
limitation, we would no longer be able to perform our molecular diagnostic tests, which could have a material adverse effect on our business, financial
condition, and results of operations. If we were to lose our licenses issued by the States in which we are required to hold licenses, we would not be able to
test specimens from those States. New molecular diagnostic tests we may develop may be subject to new approvals by governmental bodies, and we may
not be able to offer our new molecular diagnostic tests to patients in such jurisdictions until such approvals are received.
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Complying with numerous statutes and regulations pertaining to our molecular diagnostics business is an expensive and time-consuming process, and
any failure to comply could result in substantial penalties.
We are subject to regulation by both the Federal government and the States in which we conduct our molecular diagnostics business, including:
● The Food, Drug, and Cosmetic Act, as supplemented by various other statutes;
● The Prescription Drug Marketing Act of 1987, the amendments thereto, and the regulations promulgated thereunder and contained in 21 C.F.R. Parts
203 and 205;
● CLIA and State licensing requirements;
● Manufacturing and promotion laws;
● Medicare and Medicaid billing and payment regulations applicable to clinical laboratories;
● The Federal Anti-Kickback Statute, which prohibits knowingly and willfully offering, paying, soliciting, or receiving remuneration, directly or
indirectly, in exchange for or to induce either the referral of an individual, or the furnishing, arranging for, or recommending of an item or service
that is reimbursable, in whole or in part, by a federal healthcare program;
● The Federal Stark physician self-referral law (and state equivalents), which prohibits a physician from making a referral for certain designated health
services covered by the Medicare program, including laboratory and pathology services, if the physician or an immediate family member has a
financial relationship with the entity providing the designated health services, unless the financial relationship falls within an applicable exception to
the prohibition;
● The Federal Health Insurance Portability and Accountability Act of 1996 (“HIPAA”), which established comprehensive federal standards with
respect to the privacy and security of protected health information and requirements for the use of certain standardized electronic transactions, and
amendments made in 2013 to HIPAA under the Health Information Technology for Economic and Clinical Health Act, which strengthen and expand
HIPAA privacy and security compliance requirements, increase penalties for violators, extend enforcement authority to state attorneys general, and
impose requirements for breach notification;
● The Federal Civil Monetary Penalties Law, which prohibits, among other things, the offering or transfer of remuneration to a Medicare or state
healthcare program beneficiary if the person knows or should know it is likely to influence the beneficiary’s selection of a particular provider,
practitioner, or supplier of services reimbursable by Medicare or a state healthcare program, unless an exception applies;
● The Federal False Claims Act, which imposes liability on any person or entity that, among other things, knowingly presents, or causes to be
presented, a false or fraudulent claim for payment to the federal government;
● Other Federal and State fraud and abuse laws, prohibitions on self-referral, fee-splitting restrictions, prohibitions on the provision of products at no or
discounted cost to induce physician or patient adoption, and false claims acts, which may extend to services reimbursable by any third-party payor,
including private insurers;
● The prohibition on reassignment of Medicare claims, which, subject to certain exceptions, precludes the reassignment of Medicare claims to any
other party;
● The rules regarding billing for diagnostic tests reimbursable by the Medicare program, which prohibit a physician or other supplier from marking up
the price of the technical component or professional component of a diagnostic test ordered by the physician or other supplier and supervised or
performed by a physician who does not “share a practice” with the billing physician or supplier; and
● State laws that prohibit other specified practices related to billing such as billing physicians for testing that they order, waiving coinsurance, co-
payments, deductibles, and other amounts owed by patients, and billing a State Medicaid program at a price that is higher than what is charged to
other payors.
We have implemented policies and procedures designed to comply with these laws and regulations. We periodically conduct internal reviews of our
compliance with these laws. Our compliance is also subject to governmental review. The growth of our business may increase the potential of violating
these laws, regulations, or our internal policies and procedures. The risk that we are found in violation of these, or other laws and regulations is further
increased by the fact that many have not been fully interpreted by the regulatory authorities or the courts, and their provisions are open to a variety of
interpretations. Violations of Federal or State regulations may incur investigation or enforcement action by the FDA, Department of Justice, State agencies,
or other legal authorities, and may result in substantial civil, criminal, or other sanctions. Any action brought against us for violation of these or other laws
or regulations, even if we successfully defend against it, could cause us to incur significant legal expenses and divert managements’ attention from the
operation of our business. If our operations are found to be in violation of any of these laws and regulations, we may be subject to civil and criminal
penalties, damages, and fines, we could be required to refund payments received by it, we could face possible exclusion from Medicare, Medicaid and other
Federal or State healthcare programs, and we could even be required to cease operations. Any of the foregoing consequences could have a material adverse
effect on our business, financial condition, and results of operations.
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If we use hazardous materials in a manner that causes contamination or injury, we could be liable for resulting damages.
We are subject to Federal, State, and local laws, rules and regulations governing the use, discharge, storage, handling, and disposal of biological material,
chemicals, and waste. We cannot eliminate the risk of accidental contamination or injury to employees or third parties from the use, storage, handling, or
disposal of these materials. In the event of contamination or injury, we could be held liable for any resulting damages, remediation costs, and any related
penalties or fines. This liability could exceed our resources or any applicable insurance coverage we may have. The cost of compliance with these laws and
regulations may become significant, and our failure to comply may result in substantial fines or other consequences, and either could have a significant
impact on our operating results.
The healthcare regulatory and political framework is uncertain and evolving.
Healthcare laws and regulations are rapidly evolving and may change significantly in the future, which could adversely affect our financial condition and
results of operations. For example, in March 2010, the Patient Protection and Affordable Care Act, (“ACA”), was adopted, which is a healthcare reform
measure that provided healthcare insurance for approximately 30 million additional Americans. The ACA includes a variety of healthcare reform
provisions and requirements that became effective at varying times through 2018 and substantially changed the way healthcare is financed by both
governmental and private insurers, which may significantly impact our industry and our business. For instance, the ACA requires “Applicable
Manufacturers” to disclose to the Secretary of the Department of Health & Human Services drug sample distributions and certain payments or transfers of
value to covered recipients (physicians and teaching hospitals) on an annual basis. “Applicable Manufacturers” and “Applicable Group Purchasing
Organizations” must also disclose certain physician ownership or investment interests. The data submitted will ultimately be made available on a public
website. Based upon the structure of our relationship with our clients, we may be included in the definition of “Applicable Manufacturer” for purposes of
the disclosure requirements or may provide services that include the transfer of drug samples and/or other items of value to covered recipients. As such, we
may be required to disclose or provide information that is subject to disclosure. There may be certain risks and penalties associated with the failure to
properly make such disclosures, including but not limited to the specific civil liabilities set forth in the ACA, which allows for a maximum civil monetary
penalty per “Applicable Manufacturer” of $1,150,000 per year. There may be additional risks and claims made by third parties derived from an improper
disclosure that are difficult to ascertain at this time.
We cannot predict whether future healthcare initiatives will be implemented at the federal or state level, or how any future legislation or regulation may
affect us. The U.S. Supreme Court is currently reviewing the constitutionality of the ACA, although it is unclear when a decision will be made. Further, it is
possible that additional governmental action will be taken in response to the COVID-19 pandemic.
Risks Related to the Securities Markets and Ownership of Our Common Stock
Our certificate of incorporation, as amended, provides that, to the fullest extent permitted by law, the Court of Chancery of the State of Delaware will
be the exclusive forum for certain legal actions between us and our stockholders, which could limit our stockholders’ ability to obtain a judicial forum
viewed by the stockholders as more favorable for disputes with us or our directors, officers, or employees.
Our certificate of incorporation, as amended, provides that, to the fullest extent permitted by law, the Court of Chancery of the State of Delaware shall be
the sole and exclusive forum for (1) any derivative action or proceeding brought on behalf of the corporation, (2) any action asserting a claim of breach of a
fiduciary duty owed by any director or officer of the corporation to the corporation or the corporation’s stockholders, (3) any action asserting a claim
against the corporation arising pursuant to any provision of the General Corporation Law or the corporation’s Certificate of Incorporation or Bylaws, or (4)
any action asserting a claim against the corporation governed by the internal affairs doctrine. This exclusive forum provision does not apply to suits brought
to enforce a duty or liability created by the Securities Exchange Act of 1934. It could apply, however, to a suit that falls within one or more of the
categories enumerated in the exclusive forum provision and asserts claims under the Securities Act, as amended, inasmuch as Section 22 of the Securities
Act creates concurrent jurisdiction for federal and state courts over all suits brought to enforce any duty or liability created by the Securities Act or the rule
and regulations thereunder. There is uncertainty as to whether a court would enforce such provision with respect to claims under the Securities Act, and our
stockholders will not be deemed to have waived our compliance with the federal securities laws and the rules and regulations thereunder.
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Any person or entity purchasing or otherwise acquiring any interest in any of our securities shall be deemed to have notice of and consented to these
provisions. These exclusive-forum provisions may limit a stockholder’s ability to bring a claim in a judicial forum of their choosing for disputes with us or
our directors, officers, or other employees, which may discourage lawsuits against us and our directors, officers, and other employees.
If a court were to find the choice of forum provision contained in our certificate of incorporation, as amended, to be inapplicable or unenforceable in an
action, we may incur additional costs associated with resolving such action in other jurisdictions, which could harm our business, results of operations, and
financial condition. Even if we are successful in defending against these claims, litigation could result in substantial costs and be a distraction to
management.
Our common stock could be delisted from The NASDAQ Capital Market, which delisting could hinder your ability to obtain accurate quotations on the
price of our common stock or dispose of our common stock in the secondary market.
On February 17, 2022, we received a letter from the Listing Qualifications Department (the “Staff”) of The NASDAQ Stock Market LLC (“NASDAQ”)
informing the Company that because the closing bid price for the Company’s common stock listed on NASDAQ was below $1.00 for 30 consecutive
trading days, the Company does not comply with the minimum closing bid price requirement for continued listing on The NASDAQ Capital Market under
NASDAQ Marketplace Rule 5550(a)(2), requiring a minimum bid price of $1.00 per share (the “Minimum Bid Price Requirement”). The notification has
no immediate effect on the listing of the Company’s common stock.
In accordance with NASDAQ’s Marketplace Rule 5810(c)(3)(A), the Company has a period of 180 calendar days, or until August 16, 2022, to regain
compliance with the Minimum Bid Price Requirement. If at any time before August 16, 2022 the bid price of the Company’s common stock closes at or
above $1.00 per share for a minimum of 10 consecutive business days, NASDAQ will provide written notification that the Company has achieved
compliance with the Minimum Bid Price Requirement.
The letter also disclosed that in the event the Company does not regain compliance with the Minimum Bid Price Requirement by August 16, 2022, the
Company may be eligible for additional time. To qualify for additional time, the Company would be required to meet the continued listing requirement for
market value of publicly held shares and all other initial listing standards for The NASDAQ Capital Market, with the exception of the bid price
requirement, and would need to provide written notice of its intention to cure the deficiency during the second compliance period, by effecting a reverse
stock split, if necessary. However, if it appears to the Staff that the Company will not be able to cure the deficiency, or if the Company is otherwise not
eligible, the Staff would notify the Company that its securities would be subject to delisting. In the event of such notification, the Company may appeal the
Staff’s determination to delist its securities, but there can be no assurance the Staff would grant the Company’s request for continued listing.
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The Company intends to continue actively monitoring the bid price for its common stock between now and August 16, 2022 and will consider available
options to resolve the deficiency and regain compliance with the Minimum Bid Price Requirement.
In the event our common stock is delisted from The NASDAQ Capital Market and we are also unable to maintain listing on another alternate exchange,
trading in our common stock could thereafter be conducted in FINRA’s OTC Bulletin Board or in the over-the-counter markets in the so-called pink sheets.
In such event, the liquidity of our common stock would likely be impaired, not only in the number of shares which could be bought and sold, but also
through delays in the timing of the transactions, and there would likely be a reduction in our coverage by security analysts and the news media, thereby
resulting in lower prices for our common stock than might otherwise prevail.
Limitations on director and officer liability and indemnification of our officers and directors by us may discourage stockholders from bringing a suit
against a director.
Our Certificate of Incorporation and Bylaws provide, with certain exceptions as permitted by governing state law, that a director or officer shall not be
personally liable to us or our stockholders for breach of fiduciary duty as a Director, except for acts or omissions which involve intentional misconduct,
fraud, knowing violation of law, or unlawful payments of dividends. These provisions may discourage stockholders from bringing a suit against a director
for breach of fiduciary duty and may reduce the likelihood of derivative litigation brought by stockholders on our behalf against a director. In addition, our
certificate of incorporation and bylaws may provide for mandatory indemnification of directors and officers to the fullest extent permitted by governing
state law.
We do not expect to pay dividends for the foreseeable future, and we may never pay dividends; investors must rely on stock appreciation, if any, for any
return on investment in our common stock.
We currently intend to retain any future earnings to support the development and expansion of our business and do not anticipate paying cash dividends in
the foreseeable future. Our payment of any future dividends will be at the discretion of our Board of Directors after taking into account various factors,
including but not limited to, our financial condition, operating results, cash needs, growth plans, and the terms of any credit agreements that we may be a
party to at the time. In addition, our ability to pay dividends on our common stock may be limited by state law. Accordingly, investors must rely on sales of
their common stock after price appreciation, which may never occur, as the only way to realize certain returns on their investment. As a result, investors
must rely on stock appreciation and a liquid trading market for any return on investment in our common stock.
Our Board of Directors’ ability to issue undesignated preferred stock and the existence of anti-takeover provisions may depress the value of our
common stock.
Our authorized capital includes 20 million shares of preferred stock. Of this amount and 79,246 shares have been designated as series B convertible
preferred stock and the remaining authorized shares are undesignated preferred stock. Our Board of Directors has the power to issue any or all of the shares
of undesignated preferred stock, including the authority to establish one or more series and to fix the powers, preferences, rights, and limitations of such
class or series, without seeking stockholder approval. Further, as a Delaware corporation, we are subject to provisions of the Delaware General Corporation
Law regarding business combinations. We may, in the future, consider adopting additional anti-takeover measures. The authority of our Board of Directors
to issue undesignated stock and the anti-takeover provisions of Delaware law, as well as any future anti-takeover measures adopted by us, may, in certain
circumstances, delay, deter, or prevent takeover attempts and other changes in control not approved by our Board of Directors. As a result, our stockholders
may lose opportunities to dispose of their shares at favorable prices generally available in takeover attempts or that may be available under a merger
proposal and the market price, voting, and other rights of the holders of common stock may also be affected.
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General Risk Factors
Our success is dependent on our ability to attract and retain technical personnel, sales and marketing personnel, and other skilled management.
Our success depends to a significant degree on our ability to attract, retain, and motivate highly skilled and qualified personnel. Failure to attract and retain
necessary technical, sales and marketing personnel, and skilled management could adversely affect our business. If we fail to attract, train, and retain
sufficient numbers of these highly qualified people, our business, financial condition, and results of operations could be materially and adversely affected.
Our ability to use net operating loss and tax credit carryforwards and certain built-in losses to reduce future tax payments is limited by provisions of the
Internal Revenue Code and may be subject to further limitation because of prior or future offerings of our stock or other transactions.
Sections 382 and 383 of the United States Internal Revenue Code of 1986, as amended (the “Code”) contain rules that limit the ability of a company that
undergoes an ownership change, which is generally an increase in the ownership percentage of certain stockholders in the stock of a company by more than
50% over a three-year period, to utilize its net operating loss and tax credit carryforwards and certain built-in losses recognized in years after the ownership
change. These rules generally operate by focusing on ownership changes involving stockholders owning directly or indirectly 5% or more of the stock of a
company and any change in ownership arising from a new issuance of stock by that company. Generally, if an ownership change, as defined by Section 382
of the Code, occurs, the yearly taxable income limitation on the use of net operating loss and tax credit carryforwards and certain built-in losses is equal to
the product of the applicable long-term tax-exempt rate and the value of stock immediately before the ownership change. We have not assessed the
potential impact of Sections 382 and 383.
Costs incurred because we are a public company may affect our profitability.
As a public company, we incur significant legal, accounting, and other expenses and are subject to the SEC’s rules and regulations relating to public
disclosure that generally involve a substantial expenditure of financial resources. In addition, the Sarbanes-Oxley Act of 2002, as well as rules
subsequently implemented by the SEC, require changes in corporate governance practices of public companies. Full compliance with such rules and
regulations requires significant legal and financial compliance costs and makes some activities more time-consuming and costlier, which may negatively
impact our financial results. To the extent our earnings suffer as a result of the financial impact of our SEC reporting or compliance costs, our ability to
develop an active trading market for our securities could be harmed.
Shares eligible for future sale may adversely affect the market.
From time to time, certain stockholders may be eligible to sell some or all of their shares of common stock pursuant to Rule 144, promulgated under the
Securities Act subject to certain limitations. In general, pursuant to Rule 144 as in effect as of the date of this filing, a stockholder (or stockholders whose
shares are aggregated) who has satisfied the applicable holding period and is not deemed to have been one of our affiliates at the time of sale, or at any time
during the three months preceding a sale, may sell their shares of common stock. Any substantial sale, or cumulative sales, of our common stock pursuant
to Rule 144 or pursuant to any resale prospectus may have a material adverse effect on the market price of our securities.
We expect volatility in the price of our common stock, which may subject us to securities litigation.
The market for our common stock may be characterized by significant price volatility when compared to seasoned issuers, and we expect that our share
price will be more volatile than a seasoned issuer for the indefinite future. In the past, plaintiffs have often initiated securities class action litigation against
companies following periods of volatility in the market price of their securities. We may in the future be the target of similar litigation. Securities litigation
could result in substantial costs and liabilities and could divert management’s attention and resources.
Acquisitions involve risks that could result in adverse changes to operating results, cash flows, and liquidity.
We may desire to make strategic acquisitions in the future. However, we may not be able to identify suitable acquisition opportunities, or we may be unable
to obtain the consent of our stockholders and therefore, may not be able to complete such acquisitions. We may pay for acquisitions with our common stock
or with convertible securities, which may dilute shareholders’ investment in our common stock, or we may decide to pursue acquisitions that our investors
may not agree with. In connection with potential acquisitions, we may agree to substantial earn-out arrangements. To the extent we defer the payment of
the purchase price for any acquisition through a cash earn-out arrangement, cash flows will be reduced in subsequent periods.
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In addition, acquisitions, including our recent acquisition of zPREDICTA, Inc. may expose us to operational challenges and risks, including:
● the ability to profitably manage acquired businesses or successfully integrate the operations of acquired businesses, as well as the acquired business’s
financial reporting and accounting control systems into our existing platforms;
● increased indebtedness and contingent purchase price obligations associated with an acquisition;
● the ability to fund cash flow shortages that may occur if anticipated revenue is not realized or is delayed, whether by general economic or market
conditions, or unforeseen internal difficulties;
● the availability of funding sufficient to meet increased capital needs;
● diversion of management’s time and attention from existing operations; and
● the ability to retain or hire qualified personnel required for expanded operations.
Completing acquisitions may require significant management time and financial resources because we may need to assimilate widely dispersed operations
with different corporate cultures. In addition, acquired companies may have liabilities that we failed to or were unable to discover in the course of
performing due diligence investigations. We cannot assure the shareholders’ that the indemnification granted by sellers of acquired companies will be
sufficient in amount, scope, or duration to fully offset the possible liabilities associated with businesses or properties we assume upon consummation of an
acquisition. We may learn additional information about our acquired businesses that could have a material adverse effect on us, such as unknown or
contingent liabilities and liabilities related to compliance with applicable laws. Any such liabilities, individually or in the aggregate, could have a material
adverse effect on our business. Failure to successfully manage the operational challenges and risks associated with, or resulting from, acquisitions could
adversely affect our results of operations, cash flows, and liquidity. Borrowings or issuances of convertible securities associated with these acquisitions
may also result in higher levels of indebtedness, which could adversely impact our ability to service our debt within the scheduled repayment terms.
Security breaches, loss of data and other disruptions to our business or the business of our third-party service providers could compromise sensitive
information related to our business or prevent us from accessing critical information and expose us to liability, which could adversely affect our
business and reputation.
Our business requires that we collect and store sensitive data, including protected health and credit card information and proprietary business and financial
information. We face a number of risks relative to the protection of, and the service providers’ protection of, this critical information, including loss of
access, inappropriate disclosure, and inappropriate access, as well as risks associated with our ability to identify and audit such events. The secure
processing, storage, maintenance, and transmission of this critical information are vital to our operations and business strategy, and we devote significant
resources to protecting such information. Although we take measures to protect sensitive information from unauthorized access or disclosure, our
information technology and infrastructure may be vulnerable to attacks by hackers or viruses or otherwise breached due to employee error, malfeasance, or
other activities. While we have not experienced any such attack or breach, if such event would occur and cause interruptions in our operations, our
networks could be compromised and the information we store on those networks could be accessed by unauthorized parties, publicly disclosed, lost, or
stolen. Unauthorized access, loss, or dissemination could disrupt our operations, including collecting, processing, and preparing company financial
information, managing the administrative aspects of our business, and damaging our reputation, any of which could adversely affect our business. In
addition, the interpretation and application of consumer, health-related, and data protection laws in the United States are often uncertain, contradictory, and
in flux. It is possible that these laws may be interpreted and applied in a manner that is inconsistent with our practices. If so, this could result in
government-imposed fines or orders requiring that we change our practices, which could adversely affect our business. Complying with these various laws
could cause us to incur substantial costs or require us to change our business practices, systems, and compliance procedures in a manner adverse to our
business. Additionally, in connection with the ongoing COVID-19 pandemic, many of our employees have the ability to work remotely, which may
increase the risk of security breaches, loss of data, and other disruptions as a consequence of more employees accessing sensitive and critical information
from remote locations.
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If we are unable to prevent such security breaches or privacy violations or implement satisfactory remedial measures in connection with security incidents,
we may suffer loss of reputation, financial loss, and civil or criminal fines or other penalties. In addition, these breaches and other forms of inappropriate
access can be difficult to detect, and any delay in identifying them may lead to increased harm of the type described above.
If our information technology and communications systems fail or we experience a significant interruption in our operation, our reputation, business,
and results of operations could be materially and adversely affected.
The efficient operation of our business is dependent on information technology and communications systems. The failure of these systems to operate as
anticipated could disrupt our business and result in decreased revenue and increased overhead costs. In addition, we do not have complete redundancy for
all of our systems and our disaster recovery planning cannot account for all eventualities. Our information technology and communications systems,
including the information technology systems and services that are maintained by third-party vendors, are vulnerable to damage or interruption from
natural disasters, fire, terrorist attacks, malicious attacks by computer viruses or hackers, and power loss or failure of computer systems, Internet,
telecommunications or data networks. If these systems or services become unavailable or suffer a security breach, we may expend significant resources to
address these problems, and our reputation, business, and results of operations could be materially and adversely affected.
ITEM 1B. UNRESOLVED STAFF COMMENTS.
Not applicable.
ITEM 2. PROPERTIES.
Our corporate offices are located in Eagan, Minnesota. We lease 5,773 square feet at this location, of which 2,945 square feet is used for office space and
2,828 is used for manufacturing. The lease as amended has a one-year term that ended January 31, 2022, and as of December 10, 2021 has a second
amended six-month term until July 31, 2022. Management and the landlord have orally agreed to further extensions as needed.
The offices of our Helomics subsidiary are located in Pittsburgh, Pennsylvania. We lease 17,417 square feet at this location, of which approximately 1,000
square feet are used for office space and 16,417 square feet is used for laboratory operations. The lease, as amended, has a two-year term ending February
28, 2023.
zPREDICTA’s offices are located in San Jose, California. We lease approximately 1,236 square feet at this location. The lease is month-to-month tenancy.
Soluble Biotech’s offices are located in Birmingham, Alabama. We lease approximately 5,274 square feet at this location. The lease is effective through
August 25, 2025.
TumorGenesis’s offices are located in Salem, Massachusetts. We lease approximately 1,450 square feet at this location. The lease is effective through May
31, 2023.
We expect that the current space will be adequate for our current office and laboratory needs.
ITEM 3. LEGAL PROCEEDINGS.
Not applicable.
ITEM 4. MINE SAFETY DISCLOSURES.
Not applicable.
29
PART II
ITEM 5. MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF
EQUITY SECURITIES.
Market Information
Effective June 13, 2019, our common stock was listed on the NASDAQ Capital Market under the symbol “POAI”. Prior to this, effective February 2, 2018,
our common stock was listed on the NASDAQ Capital Market under the symbol “AIPT”. Prior to February 2, 2018, our common stock was listed on The
NASDAQ Capital Market under the symbol “SKLN”.
Holders
As of March [22], 2022, there were approximately [157] stockholders of record of our common stock.
Dividend Policy
We follow a policy of retaining earnings, if any, to finance the expansion of our business. We have not paid, and do not expect to declare or pay, cash
dividends on common stock in the foreseeable future.
Securities Authorized for Issuance under Equity Compensation Plans
The information required by Item 5 is incorporated herein by reference to Item 12 below.
Recent Sales of Unregistered Securities
Information regarding sales of unregistered securities during the periods covered hereby has been included in previous reports on Form 8-K or 10-Q. For
additional information on such sales, see “Management’s Discussion and Analysis of Financial Condition and Results of Operations – Liquidity and Capital
Resources – Financing Transactions.”
ITEM 6. SELECTED FINANCIAL DATA.
Not Required.
ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS.
Information Regarding Forward-Looking Statements
This Annual Report on Form 10-K contains “forward-looking statements” that indicate certain risks and uncertainties, many of which are beyond our
control. Actual results could differ materially and adversely from those anticipated in such forward-looking statements as a result of certain factors,
including those set forth below and elsewhere in this report. Important factors that may cause actual results to differ from projections include:
● We may not be able to continue operating without additional financing;
● Current negative operating cash flows;
● Our capital needs to accomplish our goals, including any further financing, which may be highly dilutive and may include onerous terms;
● Risks related to recent and future acquisitions, including the possibility of impairment of goodwill and risks related to the benefits and costs
of acquisition;
● Risks related to our partnerships with other companies, including the need to negotiate the definitive agreements; possible failure to realize
anticipated benefits of these partnerships; and costs of providing funding to our partner companies, which may never be repaid or provide
anticipated returns;
● Risk that we will be unable to protect our intellectual property or claims that we are infringing on others’ intellectual property;
30
● The impact of competition;
● Acquisition and maintenance of any necessary regulatory clearances applicable to applications of our technology;
● Risk we may not be able to attract or retain qualified senior management personnel, including sales and marketing personnel;
● Risk that we never become profitable if our products and services are not accepted by potential customers;
● Possible impact of government regulation and scrutiny;
● Unexpected costs and operating deficits, and lower than expected sales and revenues, if any;
● Adverse results of any legal proceedings;
● The volatility of our operating results and financial condition,
● Management of growth; and
● Risk that our business and operations will continue to be materially and adversely affected by the COVID-19 pandemic, which has impacted
on a significant supplier; has resulted in delayed production and less efficiency; and has impacted on our sales efforts, accounts receivable,
and terms demanded by suppliers; and may impact financing transactions; and
● Other specific risks that may be alluded to in this report.
All statements, other than statements of historical facts, included in this report regarding our growth strategy, future operations, financial position,
estimated revenue or losses, projected costs, prospects and plans, and objectives of management are forward-looking statements. When used in this report,
the words “will,” “may,” “believe,” “anticipate,” “intend,” “estimate,” “expect,” “project,” “plan,” and similar expressions are intended to identify forward-
looking statements, although not all forward-looking statements contain such identifying words. All forward-looking statements speak only as of the date of
this report. We do not undertake any obligation to update any forward-looking statements or other information contained herein. Potential investors should
not place undue reliance on these forward-looking statements. Although we believe that our plans, intentions, and expectations reflected in or suggested by
the forward-looking statements in this report are reasonable, we cannot assure potential investors that these plans, intentions or expectations will be
achieved. We disclose important factors that could cause actual results to differ materially from expectations in the “Risk Factors” section and elsewhere in
this report. These cautionary statements qualify all forward-looking statements attributable to us or persons acting on our behalf.
Information regarding market and industry statistics contained in this report is included based on information available to us that we believe is accurate. It
is generally based on academic and other publications that are not produced for purposes of securities offerings or economic analysis. We have not
reviewed or included data from all sources, and we cannot assure potential investors of the accuracy or completeness of the data included in this
report. Forecasts and other forward-looking information obtained from these sources are subject to the same qualifications and the additional uncertainties
accompanying any estimates of future market size, revenue, and market acceptance of products and services. We have no obligation to update forward-
looking information to reflect actual results or changes in assumptions or other factors that could affect those statements.
Overview
We operate in four primary business areas: first, the application of artificial intelligence (“AI”) in our precision medicine business, to provide AI-driven
predictive models of tumor drug response to improve clinical outcomes for patients and to assist pharmaceutical, diagnostic, and biotech industries in the
development of new personalized drugs and diagnostics; second, creation of tumor-specific 3D cell culture models driving accurate prediction of clinical
outcomes; third, contract services and research focused on solubility improvements, stability studies, and protein production and; fourth, production of the
United States Food and Drug Administration (“FDA”)-cleared STREAMWAY System for automated, direct-to-drain medical fluid disposal and associated
products
We have four reportable segments: Helomics®, zPREDICTA®, SolubleTM and Skyline®. The Helomics segment includes clinical testing and contract
research services that include the application of AI. Our zPREDICTA segment specializes in organ-specific disease models that provide 3D reconstruction
of human tissues accurately representing each disease state and mimicking drug response enabling accurate testing of anticancer agents. Our Soluble
segment provides services using a self-contained, automated system that conducts high-throughput, self-interaction chromatography screens, using
additives and excipients commonly included in protein formulations resulting in soluble and physically stable formulations for biologics. Our Skyline
segment consists of the STREAMWAY System product sales, and our TumorGenesis subsidiary is included within corporate. Going forward, we have
determined that we will focus our resources on the Helomics and zPREDICTA segments and our primary mission statements to accelerate patient-centric
drug discovery to improve patient outcomes in cancer treatment, harnessing the power of AI, and to develop tumor-specific 3D cell culture models that
provide accurate 3D reconstruction of human tissues representing each cancer disease state.
31
Capital Requirements
Since inception, we have been unprofitable. We incurred net losses of $19,657,174 and $25,884,397 for the years ended December 31, 2021, and December
31, 2020, respectively. As of December 31, 2021, and December 31, 2020, we had an accumulated deficit of $128,040,282 and $108,383,108, respectively.
We have never generated sufficient revenues to fund our capital requirements. Since 2017, we have diversified our business by investing in ventures,
including making significant loans and investments in early-stage companies. These activities led to the acquisition of Helomics in April 2019, the
purchase of the assets of two businesses in 2020 and the acquisition of zPREDICTA in November 2021, each of which have accelerated our capital needs.
We have funded our operations through a variety of debt and equity instruments. See “Liquidity and Capital Resources – Liquidity and Plan of Financing”
and “Liquidity and Capital Resources – Financing Transactions” below.
Our future cash requirements and the adequacy of available funds depend on our ability to generate revenues from our Helomics and zPREDICTA
segments; our ability to continue to sell our Skyline Medical products and to reach profitability in the Skyline Medical business, our ability to generate
revenue from our Soluble reportable segment and the availability of future financing to fulfill our business plans. See “Liquidity and Capital Resources –
Liquidity and Plan of Financing” below.
Our limited history of operations, especially in our precision medicine business, and our change in the emphasis of our business, starting in 2017, makes
prediction of future operating results difficult. We believe that period-to-period comparisons of our operating results should not be relied on as predictive of
our future results.
Results of Operations
Comparison of Year Ended December 31, 2021 with Year Ended December 31, 2020
Revenue
Cost of goods sold
General and administrative expense
Operations expense
Sales and marketing expense
$
2021
1,420,680 $
487,024
10,932,125
2,698,565
774,530
Difference
2020
1,252,272 $
447,192
10,351,973
2,351,709
584,937
168,408
(39,832)
(580,152)
(346,856)
(189,593)
Revenue. We recorded revenue of $1,420,680 in 2021, compared to $1,252,272 in 2020. Our Skyline division was responsible for the majority of the
revenue, with Soluble generating $233,293 and $2,870 and Helomics generating $13,367 and $64,188 in revenue in the years ended December 31, 2021
and 2020, respectively. We sold 15 STREAMWAY System units in 2021 and 25 STREAMWAY System units in 2020.
Cost of sales. Cost of sales was $487,024 and $447,192 in 2021 and 2020, respectively. The increase in cost of sales is primarily due to increased cost of
disposables and costs associated with our repair and maintenance contracts The gross profit margin was 66% in 2021 compared to 64% in 2020. Our
margins increased in 2021 due to higher margins associated with our Soluble operating segment and from our Skyline Medical operating segment
disposable product margins.
32
General and Administrative expense. General and administrative (“G&A”) expense primarily consists of management salaries, professional fees, consulting
fees, travel expense, administrative fees and general office expenses.
G&A expense increased by $580,152 to $10,932,125 in 2021 from $10,351,973 in 2020. The increase was primarily due to increases in staff related
expenses including additional headcount, as well as certain one-time expenses related to severance incurred as part of the departure of our former CEO.
Additional increases included higher costs for consulting expenses and fees to our Board of Directors. Also, increased depreciation was driven by newly
added assets supporting our Helomics division. These increases were offset by lower share-based compensation and lower costs for investor relations.
Operations expense. Operations expense in our current stage primarily consists of expenses related to product development, prototyping and testing
including staff related expenses for individuals performing this work.
Operations expense increased by $346,856 to $2,698,565 in 2021 compared to $2,351,709 in 2020. The increase in operations expense in 2021 was
primarily due to higher payroll costs and higher costs associated with cloud computing, offset by decreased costs associated with consulting.
Sales and marketing expense. Sales and marketing expense consists of expenses required to sell products through independent reps, attendance at trade
shows, product literature and other sales and marketing activities.
Sales and marketing expenses increased by $189,593 to $774,530 in 2021 compared to $584,937 in 2020. The increase in 2021 was due to increased
expenses in web development, public relations, and market research.
Loss on goodwill impairment. We incurred a loss on impairment of goodwill of $2,813,792 and $12,876,498 during 2021 and 2020, respectively, all
relating to the goodwill acquired in the Helomics acquisition in 2019. Our goodwill, for our Helomics operating segment, following the impairment was $0
and $2,813,792 at December 31, 2021 and December 31, 2020, respectively. The cumulative losses on goodwill are $23,790,290 as of December 31, 2021.
See Note 10 to our audited consolidated financial statements included in this annual report.
Loss on intangible asset impairment. We incurred a loss on impairment of intangibles of $2,893,548 during the year ended December 31, 2021. The
impairment recorded relates to the intangible assets of our Helomics operating segment and none of the Company’s other operating segments. The value of
the intangible assets of the Helomics operating segment following the impairment was $0 at December 31, 2021. See Note 10 to our audited consolidated
financial statements included in this annual report.
Loss on impairment of acquired software. We incurred a loss on impairment on acquired software of $1,249,727 during the year ended December 31, 2021.
The impairment recorded relates to the acquired software asset of our Helomics operating segment and none of the Company’s other operating segments.
The value of the acquired software asset of the Helomics operating segment following the impairment was $0 at December 31, 2021. Please see Note 10 to
our audited consolidated financial statements included in this annual report for further information.
Other income. We earned other income of $184,528 in 2021 compared to $843,440 in 2020. Other income included interest income and gains on settlement
of outstanding payables during 2021. Other income was comprised of gain on the forgiveness of the Paycheck Protection Program loan of $541,867 and
gains on settlement of outstanding payables during 2020.
Other expense. We incurred other expenses of $239,631 in 2021 compared to $2,427,026 in 2020. Other expenses consisted primarily of interest expense,
payment penalties and amortization of original issue discounts.
Gain on derivative instruments. We incurred a gain of $164,902 in 2021 compared to a gain of $1,765,907 in 2020, primarily related to the changes in fair
market value on derivatives.
Gain on notes receivable associated with asset purchase. We recorded a gain of $1,290,000 in 2020 related to the gain on notes receivable in connection
with our acquisition of certain assets in 2020.
33
Income Taxes. We recognized $661,658 income tax benefit in our consolidated statement of net loss in the year ended December 31, 2021 related to the
release of the valuation allowance following the zPREDICTA acquisition and zero related to our U.S. operating losses, as all tax benefits are fully reserved.
Liquidity and Capital Resources
Cash Flows
Net cash used in operating activities was $12,208,929 in 2021, compared with net cash used of $12,257,732 in 2020. Cash used in operating activities
increased in 2021 primarily due to operating losses as well as outflows related to payments on accounts payables and payments for accrued expenses,
inventories and prepaid expenses.
Cash flows used in investing activities were $10,607,536 in 2021, and $167,456 in 2020. Cash flows used in investing activities in 2021 were primarily
related to the acquisition of our zPREDICTA subsidiary in the amount of $9,590,214 and $910,429 of cash outflows related to purchases of fixed assets.
Cash flows used in investing activities in 2020 were primarily for purchases of fixed assets, offset by disposals of fixed assets.
Net cash provided by financing activities was $50,340,748 in 2021 compared to net cash provided of $12,952,689 in 2020. Cash flows provided by
financing activities in 2021 were primarily due from proceeds from the issuance of common stock and warrants of $50,523,527 in several equity offerings
and proceeds from the exercise of warrants into common stock of $4,513,871, offset by repayment of debt and payment penalties of $5,236,214.
Liquidity and Plan of Financing
Since our inception, we have incurred significant losses, and our accumulated deficit was $128,040,282 as of December 31, 2021. We have committed
significant capital and management resources to develop our CRO business and other new business areas and intend to continue to devote significant
resources to the Helomics and zPREDICTA business and other new business in this market. Our business will need to generate significantly more revenue
to sufficiently fund our operations without external financing. Our operations from inception have been funded with private placements of convertible debt
securities and equity securities, public offerings, and loan agreements. We have not achieved profitability and anticipate that we will continue to incur net
losses at least through the remainder of 2022. We had revenues of $1,420,680 and $1,252,272 in 2021 and 2020, respectively, but we had negative
operating cash flows of $12,208,929 and $12,257,732 in 2021 and 2020, respectively. Our cash balance was $28,202,615 as of December 31, 2021, and our
accounts payable and accrued expenses were an aggregate $2,284,415. See “Financing Transactions” below.
We believe that our existing capital resources will be sufficient to support our operating plan for the next twelve months and beyond. However, we may
also seek to raise additional capital to support our growth through additional debt, equity or other alternatives or a combination thereof. We would raise
such capital through equity or debt financing to fund our capital and equipment investments and our operations.
Financing Transactions
We have funded our operations through a combination of debt and equity instruments including an early bank loan (since repaid), and a variety of debt and
equity offerings. Since late 2018, these financing transactions have consisted of (1) secured convertible notes to private investors starting in late 2018, the
remaining amount of which was repaid on March 1, 2021; (2) a series of loans from Dr. Carl Schwartz, our former CEO, starting in late 2018, which were
exchanged for common stock in 2020; and (3) a number of public offerings, registered direct offerings and private placements, including an equity line
arrangement (offerings), since 2019.
34
2021 Offerings
In January and February 2021, the Company completed a series of five offerings, all of which were priced at-the-market under applicable NASDAQ rules.
The first four offerings were registered direct offerings of common stock under its shelf registration statement, and in each such case, in a concurrent
private placement, the Company also issued such investors one warrant to purchase common stock for each two shares purchased in the transaction.
Following those four offerings, the Company completed a private placement of common stock, with each investor receiving one warrant to purchase
common stock for each two shares purchased in the transaction. In June 2021, the Company completed a registered direct offering of common stock and
warrants. The warrants became exercisable on the effective date of an increase in the number of shares of the Company’s authorized common stock, which
occurred on August 17, 2021, and expire three years after the initial exercise date. In each case, each such investor warrant is exercisable immediately upon
issuance and will expire five and one-half years from the issue date. In each case, the Company paid to the placement agent an aggregate fee equal to 7.5%
of the aggregate gross proceeds received by the Company in the offering and a management fee equal to 1% of the aggregate gross proceeds received by
the Company in the offering and reimbursed the placement agent for certain non-accountable and out-of-pocket expenses. In addition, the Company
granted to the placement agent, or its assigns warrants to purchase 7.5% of the shares sold to investors in the offering at an exercise price equal to 125% of
the price of the shares in the transaction, with a term of five years for the registered direct offerings (three years for the June 2021 offering) or five and one-
half years for the private placement.
These 2021 offerings were as follows:
Exercise Price
per Share –
investor
Warrants
Exercise Price
per Share –
Placement
Agent
Warrants
$1.0525
Placement
Agent
Warrants
273,813
Gross Proceeds of
Offering
$3,074,007
$0.80
$1.00
$1.00
1,100,000
3,414,970
2,200,000
Shares
3,650,840
Investor
Warrants
1,825,420
Sale Price
per Share*
$0.842
Offering Closing
Date
January 12, 2021
(registered direct)
January 21, 2021
(registered direct)
January 26, 2021
(registered direct)
February 16, 2021
(registered direct)
February 23, 2021
(private
placement)
June 16, 2021
(registered direct)
Total
* Sale price includes one share and a warrant to purchase one-half share (or one whole share in the case of the June 16, 2021 offering).
$17,635,344
$55,737,571
$21,341,252
$7,389,004
$2,200,000
$4,097,964
38,057,775
26,786,843
15,520,911
15,520,911
1,164,068
4,222,288
2,853,958
9,043,766
4,521,883
1,707,485
2,111,144
$1.71875
$2.1875
$2.4375
256,123
316,672
678,282
165,000
$1.375
$1.25
$1.50
$1.20
$1.95
$1.75
$2.00
$2.00
$1.25
$1.20
Net Proceeds of
Offering
$2,731,767
$1,932,050
$3,668,687
$6,679,989
$16,064,739
$19,446,296
$50,523,528
35
Secured Notes and Repayment in Full
On March 1, 2021, the Company used $5,906,802 of the proceeds of the private placement on February 23, 2021, described above under “2021 Offerings”,
to repay in full the outstanding principal and interest and applicable premium amounts under the convertible secured promissory notes to two private
investors in the original principal amount of an aggregate $2,297,727 issued in September 2018, the secured promissory note with a principal amount of
$847,500 issued during September 2019 and the secured promissory note with a principal amount of $1,450,000 issued on February 5, 2020.
2021 Warrant Exercises
During the year ended December 31, 2021, the holders of outstanding investor warrants have exercised such warrants for the total purchase of 5,269,059
shares at a weighted average exercise price of $0.86 per share, for total proceeds of $4,513,871.
Equity Line
On October 24, 2019, the Company entered into an equity purchase agreement with an investor, providing for an equity financing facility. Upon the terms
and subject to the conditions in the purchase agreement, the investor is committed to purchase shares having an aggregate value of up to $15,000,000 of the
Company’s common stock for a period of up to three years. The Company issued to the investor 104,651 commitment shares at a fair market value of
$450,000 for entering into the agreement. From time to time during the three-year commitment period, provided that the closing conditions are satisfied,
the Company may provide the investor with put notices to purchase a specified number of shares subject to certain limitations and conditions and at
specified prices, which generally represent discounts to the market price of the common stock. As of December 31, 2021, there was $9,113,829 of
remaining available balance under the equity line, subject to shareholder approval required for additional purchases, as well as requirements for market
conditions including trading volume and stock price, and subject to other limitations. During the year ended December 31, 2021, the Company issued
647,504, shares of its common stock valued at $675,590 pursuant to the equity line.
Dr. Schwartz Notes
In November 2018, Dr. Schwartz made a loan to the Company with a principal balance of $370,000. As of December 31, 2018, one promissory note was
held with a principal balance of $370,000 and an unamortized discount of $63,028. From November 30, 2018 through July 15, 2019, Dr. Schwartz made
numerous loans to the Company in the total amount of $1,920,000 under two promissory notes. As consideration for these amounts, Dr. Schwartz received
promissory notes and warrants to purchase 22,129 shares of the Company’s common stock at $8.36 per share. Further, beginning on February 1, 2019 and
the first day of each calendar month thereafter while the note remained outstanding, a number of additional warrants were issued. Beginning in October
2019, the Company and Dr Schwartz began to renegotiate the note. Due to the negotiations, the Company did not issue any additional warrants because
they would be cancelled under the new deal.
During January 2020, the Company entered into an exchange agreement with Dr. Schwartz. Under the exchange agreement, the two outstanding notes were
cancelled and in exchange a new combined promissory note in the amount of $2,115,000 (the “2020 Schwartz Note”) bearing 12% interest per annum and
maturing on September 30, 2020 was issued. In addition to the 2020 Schwartz Note, Dr. Schwartz received 50,000 shares of the Company’s common stock.
All warrants issued under the prior promissory notes were cancelled under the exchange agreement; no rights and obligations remain under the cancelled
notes. The Company determined that the exchange agreement had, in substance, occurred at December 31, 2019.
Effective as of April 21, 2020, the Company and Dr. Schwartz, entered into an exchange agreement relating to the 2020 Schwartz Note. The 2020 Schwartz
Note bore twelve percent (12%) interest per annum and had a maturity date of September 30, 2020. The accrued interest on the note through April 21, 2020
was $77,878, resulting in a total balance of $2,192,878 in principal and accrued interest on the 2020 Schwartz Note as of such date. Dr. Schwartz and the
Company agreed to exchange the 2020 Schwartz Note for newly issued shares of common stock of the Company at market value. Pursuant to the exchange
agreement, Dr. Schwartz was issued 1,533,481 shares of newly issued common stock at an exchange rate of $1.43 per share, equal to the closing price of
the common stock on April 21, 2020. In 2021, the Company determined that due to a calculation error, the balance of the 2020 Schwartz Note should have
been higher by $143,573 at the time of the exchange agreement, and on February 24, 2021, the Company issued an additional 100,401 shares to Dr.
Schwartz.
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2020 Offerings
On March 19, 2020, in a private placement we sold and issued (1) 260,000 shares of common stock, at a sale price of $2.121 per share; (2) prefunded
warrants to acquire 1,390,166 shares of common stock, sold at $2.12 per share and exercisable at an exercise price of $0.001 per share; (3) warrants to
acquire 1,650,166 shares of common stock at $1.88 per share, exercisable immediately and terminating five and one-half years after the date of issuance;
and (4) warrants to acquire 1,650,166 shares of common stock at $1.88 per share, exercisable immediately and terminating two years after the date of
issuance. The sale resulted in gross proceeds of $3,498,612 and net proceeds of $3,127,112. The Company paid the Placement Agent an aggregate fee equal
to 7.5% of the aggregate gross proceeds received by the Company in the offering. The Company also paid the Placement Agent a management fee equal to
1% of the aggregate gross aggregate gross proceeds received by the Company in the offering and reimbursed the Placement Agent for $25,000 in non-
accountable expenses and up to $40,000 in legal and other out-of-pocket expenses. In addition, the Company granted to the Placement Agent, or its assigns
warrants to purchase up to an aggregate of 123,762 shares of its common stock (which represents 7.5% of the Shares sold to investors in the private
placement) at an exercise price equal to 125% of the price of the Shares in the private placement, or $2.65125. These placement agent warrants will expire
on March 18, 2025.
During May 2020, the Company sold 1,396,826 shares of common stock in a registered direct offering under its shelf registration statement. In a concurrent
private placement, the Company also issued such investors warrants to purchase up to an aggregate of 1,396,826 shares of our common stock. The Shares
and the Warrants were sold at a combined offering price of $1.575 per Share and associated Warrant. Each Warrant is exercisable immediately upon
issuance at an exercise price of $1.45 per share and will expire five and one-half years from the issue date. The sale of the offering shares and associated
warrants resulted in gross proceeds of $2,200,001 and net proceeds of $1,930,100 after deducting the placement agent fees and estimated offering expenses
payable by the Company. The Company granted to the placement agent, or its assigns warrants to purchase up to an aggregate of 104,762 shares of its
common stock at an exercise price of $1.9688.
On June 25, 2020, the Company entered into agreements with the holders of an aggregate of 1,396,826 of the warrants issued in connection with the May
2020 registered direct offering, under which the investors exercised the warrants and received the same number new warrants. The investors paid an
exercise price of $1.45 per share plus an additional $0.125 for each new warrant. The Company issued 1,396,826 shares and issued new warrants which are
exercisable immediately and have a term of five and one-half years and an exercise price per share equal to $1.80. The Company received $2,130,701 in
gross proceeds and net proceeds of $1,865,800 after deducting the placement agent fees and estimated offering expenses payable by the Company. Before
deducting placement agent fees and expenses, the Company received approximately $2,200,000 from the transactions. Pursuant to an engagement letter,
the Company agreed to pay the Placement Agent a cash fee equal to 7.5% of the gross proceeds received from the exercise and the sale of the New
Warrants. The Company also paid the Placement Agent a management fee equal to 1% of the aggregate gross aggregate gross proceeds received by the
Company in the offering and reimbursed the Placement Agent for $25,000 in non-accountable expenses and up to $40,000 in legal and other out-of-pocket
expenses. In addition, the Company granted to the Placement Agent, or its assigns warrants to purchase up to an aggregate of 104,763 shares of its common
stock (which represents 7.5% of the shares sold to investors in the exercise transaction) at an exercise price equal to 125% of the exercise price of the New
Warrants, or $2.25.
In connection with the equity line arrangement entered into with Oasis Capital, LLC (“Oasis”) in October 2019, during the year ended December 31, 2020,
we issued an aggregate 4,231,073 shares of common stock to Oasis for net proceeds of $4,891,348.
2020 Conversions
In June through September 2019, the Company entered into a private placement securities purchase agreement with investors for shares of Series E
convertible preferred stock. The Company issued 258 preferred shares. In May 2020, we notified the holders of our Series E Convertible Preferred Stock of
our election to convert the outstanding shares of Series E Stock into common stock effective on June 13, 2020 pursuant to the terms of the Series E Stock.
Prior to the conversion, there were 207.7 shares of Series E Stock outstanding. Each share of Series E Stock converted into 0.056857% of the issued and
outstanding shares of common stock immediately prior to conversion; therefore, the 207.7 outstanding shares of Series E Stock on June 13, 2020 converted
into 1,257,416 shares of common stock equal to 11.8% of the outstanding shares of common stock as of June 12, 2020.
37
2020 Paycheck Protection Program Loan and Forgiveness
On April 20, 2020, the Company entered into a promissory note with Park State Bank, which provides for an unsecured loan of $541,867 pursuant to the
Paycheck Protection Program (the “PPP”) under the Coronavirus Aid, Relief, and Economic Security Act and applicable regulations (the “CARES Act”).
The promissory note has a term of 2 years with a 1% per annum interest rate. Payments are deferred for 6 months from the date of the promissory note and
the Company can apply for forgiveness of all or a portion of the promissory note after 60 days for covered use of funds.
Pursuant to the terms of the PPP, the promissory note, or a portion thereof, may be forgiven if proceeds are used for qualifying expenses as described in the
CARES Act, such as payroll costs, costs used to continue group health care benefits, mortgage interest payments, rent and utilities. The Company has used
all proceeds for qualifying expenses. The Company received forgiveness for the loan under the Paycheck Protection Program and recognized a gain in other
income for the full amount of the loan during the fourth quarter of 2020.
Issuances of Securities in Acquisitions
On April 4, 2019, the Company completed a forward triangular merger with Helomics Acquisition Inc., a wholly-owned subsidiary of the Company and
Helomics, acquiring the remaining 75% of the capital stock of Helomics not already held by the Company. Upon the acquisition, all outstanding shares of
Helomics stock not already held by the Company were converted into the right to receive a proportionate share of 400,000 shares of common stock and
3,500,000 shares of Series D convertible preferred stock of the Company. On April 4, 2020, the 3,500,000 shares of Series D convertible preferred stock
were converted into 350,004 shares of common stock. Also, on April 4, 2019, the Company completed an exchange offer with the holders of certain notes
and warrants of Helomics, in which the Company issued 863,732 shares of common stock to the noteholders in exchange for their notes and issued
warrants to purchase up to 1,425,506 shares of common stock of the Company at an exercise price of $10.00 per share in exchange for the Helomics
warrants held by the noteholders. An additional 59,700 Company warrants at an exercise price of $0.10 per share were exchanged for Helomics warrants
held by other parties. On September 14, 2020, the Company agreed to amend the 1,425,506 Company warrants that were originally exercisable at $10.00
per share to allow the holders to exercise the warrants at an exercise price of $0.845 per share, equal to the then-current market value of the common stock.
On May 27, 2020, the Company entered into an Asset Purchase Agreement with InventaBioTech, Inc. (“InventaBioTech”) and two of its subsidiaries,
Soluble Therapeutics, Inc. (“Soluble”), and BioDtech, Inc. (“BioDtech”), and simultaneously completed the acquisition of substantially all of Soluble’s and
BioDtech’s assets. In exchange, the Company issued 125,000 shares of common stock and waived all existing claims that the Company has or may have
against InventaBioTech (f/k/a CytoBioscience, Inc.), including the nonpayment of $1,290,000 owed by InventaBioTech to the Company. See Note 5 to the
Consolidated Financial Statements.
On July 1, 2020, the Company entered into an Asset Purchase Agreement with Quantitative Medicine LLC (“Seller”), a Delaware limited liability company
and its owners and simultaneously completed the acquisition of substantially all of the assets owned by Seller. Quantitative Medicine is a biomedical
analytics and computational biology company that developed a novel, computational drug discovery platform called CoRE. CoRE is designed to
dramatically reduce the time, cost, and financial risk of discovering new therapeutic drugs by predicting the main effects of drugs on target molecules that
mediate disease. In exchange for Seller’s assets, including CoRE, the Company provided consideration in the form of 954,719 shares of common stock,
which, when issued, had a fair value of $1,470,267. One half of the shares issued, or 477,359 shares were deposited and held in escrow upon issuance,
while 207,144 of the remaining shares were issued to Carnegie Mellon University (“CMU”) in satisfaction of all pre-closing amounts owed to CMU under
a technology licensing agreement that was assumed by the Company on the closing date. Half of the shares held in escrow will be released on the six-
month anniversary of the closing date, and the other half will be released on the one-year anniversary of the closing date; provided, however, that all or
some of the escrow shares may be released and returned to the Company for reimbursement in the event that the Company suffers a loss against which the
Selling Parties have indemnified the Company pursuant to the Agreement. See Note 5 to the Consolidated Financial Statements.
38
Critical Accounting Policies and Estimates
The discussion and analysis of our financial condition and results of operations are based upon our audited consolidated Financial Statements, which have
been prepared in accordance with U.S. Generally Accepted Accounting Principles (“U.S. GAAP”). The preparation of these financial statements requires
management to make estimates and assumptions that affect the reported amounts of assets and liabilities as of the date of our financial statements, the
reported amounts of revenues and expenses during the reporting periods presented, as well as our disclosures of contingent assets and liabilities. On an on-
going basis, we evaluate our estimates and assumptions, including, but not limited to, fair value of stock-based compensation, fair value of acquired
intangible assets and goodwill, useful lives of intangible assets and fixed assets and income taxes.
We base our estimates and assumptions on our historical experience and on various other information available to us at the time that these estimates and
assumptions are made. We believe that these estimates and assumptions are reasonable under the circumstances and form the basis for our making
judgments about the carrying values of our assets and liabilities that are not readily apparent from other sources. Actual results and outcomes could differ
from our estimates primarily due to incorrect sales forecasting. We utilize a pipeline generated by our sales team and speak directly with all departments
regarding estimates and assumptions. If, for any reason, those estimates, and assumptions vary substantially it would also impact our cost of goods and
associated operating expenses. The other volatile area for estimates and assumptions is determining financing needs. Depending on how we choose to fund
will affect numerous expense categories so the potential for underestimating those expenses is a viable concern.
Our significant accounting policies are described in “Note 1 – Summary of Significant Accounting Policies,” in Notes to audited consolidated Financial
Statements of this Annual Report on Form 10-K. We believe that the following discussion addresses our critical accounting policies and reflects those areas
that require more significant judgments and use of estimates and assumptions in the preparation of our audited consolidated Financial Statements.
Revenue Recognition. We recognize revenue in accordance with ASC 606, Revenue Recognition.
Effective January 1, 2018, we adopted Accounting Standards Update (“ASU”) No. 2014-09, Revenue from Contracts with Customers (Topic 606), which
outlines a single comprehensive model for entities to use in accounting for revenue arising from contracts with customers. The standard’s core principle is
that an entity will recognize revenue when it transfers promised goods or services to customers in an amount that reflects the consideration to which the
entity expects to be entitled in exchange for those goods or services.
Revenue from Product Sales. We have medical device revenue consisting primarily of sales of the STREAMWAY System, as well as sales of the
proprietary cleaning fluid and filters for use with the STREAMWAY System. This revenue stream is reported within both the domestic and international
revenue segments. We sell our medical device products directly to hospitals and other medical facilities using employed sales representatives and
independent contractors. Purchase orders, which are governed by sales agreements in all cases, state the final terms for unit price, quantity, shipping and
payment terms. The unit price is considered the observable stand-alone selling price for the arrangements. Our sales agreement, Terms and Conditions, is a
dually executed contract providing explicit criteria supporting the sale of the STREAMWAY System. We consider the combination of a purchase order and
acceptance of our Terms and Conditions to be a customer’s contract in all cases.
Product sales for medical devices consist of a single performance obligation that we satisfy at a point in time. We recognize product revenue when the
following events have occurred: (1) we have transferred physical possession of the products, (2) we have a present right to payment, (3) the customer has
legal title to the products, and (d) the customer bears significant risks and rewards of ownership of the products. Based on the shipping terms specified in
the sales agreements and purchase orders, these criteria are generally met when the products are shipped from our facilities (“FOB origin,” which is our
standard shipping terms). As a result, we determined that the customer is able to direct the use of, and obtain substantially all of the benefits from, the
products at the time the products are shipped. We may, at our discretion, negotiate different shipping terms with customers which may affect the timing of
revenue recognition. Our standard payment terms for customers are generally 30 to 60 days after we transfer control of the product to the customer. We
allow returns of defective disposable merchandise if the customer requests a return merchandise authorization from us.
39
Customers may also purchase a maintenance plan for the medical devices from us, which requires us to service the STREAMWAY System for a period of
one year subsequent to the one-year anniversary date of the original STREAMWAY System invoice. The maintenance plan is considered a separate
performance obligation from the product sale, is charged separately from the product sale, and is recognized over time (ratably over the one-year period) as
maintenance services are earned and provided. A time-elapsed output method is used to measure progress because we transfer control evenly by providing
a stand-ready service. We have determined that this method provides a faithful depiction of the transfer of services to our customers.
All amounts billed to a customer in a sales transaction for medical devices related to shipping and handling, if any, represent revenues earned for the goods
provided, and these amounts have been included in revenue. Costs related to such shipping and handling billing are classified as cost of goods sold.
Revenue from Clinical Testing. Clinic diagnostic testing is comprised of our Tumor Drug Response Testing (ChemoFx) and Genomic Profiling
(BioSpeciFx) tests. The Tumor Drug Response Testing test determines how a patient’s tumor specimen reacts to a panel of various chemotherapy drugs,
while the Genomic Profiling test evaluates the expression and/or status of a particular gene related to a patient’s tumor specimen. Revenues are recognized
when control of the promised goods or services is transferred to customers, in an amount that reflects the consideration we expect to be entitled to in
exchange for those goods or services. The estimated uncollectible amounts are generally considered implicit price concessions that are a reduction in
revenue. Payments terms vary for contracts and services sold by our Helomics subsidiary. Our performance obligations are satisfied at one point in time
when test reports are delivered, and studies are completed.
For service revenues, we estimate the transaction price which is the amount of consideration we expect to be entitled to receive in exchange for providing
services based on our historical collection experience using a portfolio approach as a practical expedient to account for patient contracts as collective
groups rather than individually. We monitor our estimates of transaction price to depict conditions that exist at each reporting date. If we subsequently
determine that we will collect more consideration than we originally estimated for a contract with a patient, we will account for the change as an increase to
the estimate of the transaction price, provided that such downward adjustment does not result in a significant reversal of cumulative revenue recognized.
We recognize revenue from these patients when contracts as defined in ASC 606, Revenue from Contracts with Customers are established at the amount of
consideration to which we expect to be entitled or when we receive substantially all of the consideration subsequent to the performance obligations being
satisfied.
CRO Revenue. Contract revenues are generally derived from studies conducted with biopharmaceutical and pharmaceutical companies. The specific
methodology for revenue recognition is determined on a case-by-case basis according to the facts and circumstances applicable to a given contract. We
typically use an input method that recognizes revenue based on our efforts to satisfy the performance obligation relative to the total expected inputs to the
satisfaction of that performance obligation. For contracts with multiple performance obligations, we allocate the contract’s transaction price to each
performance obligation on the basis of the standalone-selling price of each distinct good or service in the contract. Advance payments received in excess of
revenues recognized are classified as deferred revenue until such time as the revenue recognition criteria have been met. Payment terms are net 30 from the
invoice date, which is sent to the customer as we satisfy the performance obligation relative to the total expected inputs to the satisfaction of that
performance obligation.
Variable Consideration. We record revenue from distributors and direct end customers in an amount that reflects the transaction price we expect to be
entitled to after transferring control of those goods or services. Our current contracts do not contain any features that create variability in the amount or
timing of revenue to be earned.
Warranty. We generally provide one-year warranties against defects in materials and workmanship on product sales and will either repair the products or
provide replacements at no charge to customers. As they are considered assurance-type warranties, we do not account for them as separate performance
obligations. Warranty reserve requirements are based on a specific assessment of the products sold with warranties where a customer asserts a claim for
warranty or a product defect.
40
Contract Balances. We record a receivable when we have an unconditional right to receive consideration after the performance obligations are satisfied.
Our deferred revenues relate primarily to maintenance plans and CRO revenue.
Practical Expedients. We have elected the practical expedient not to determine whether contracts with customers contain significant financing components
as well as the practical expedient to recognize shipping and handling costs at point of sale.
Stock-Based Compensation. We account for share-based compensation expense in accordance with ASC 718, Compensation—Stock Compensation,
which requires us to measure and recognize compensation expense in our financial statements based on the fair value at the date of grant for our share-
based awards. We recognize compensation expense for these equity-classified awards over their requisite service period and adjust for forfeitures as they
occur.
ASC 718 requires companies to estimate the fair value of stock-based payment awards on the date of grant using an option-pricing model. We use the
Black-Scholes option-pricing model which requires the input of significant assumptions including an estimate of the average period of time employees and
directors will retain vested stock options before exercising them, the estimated volatility of our common stock price over the expected term, the number of
options that will ultimately be forfeited before completing vesting requirements and the risk-free interest rate.
When an option or warrant is granted in place of cash compensation for services, we deem the value of the service rendered to be the value of the option or
warrant. In most cases, however, an option or warrant is granted in addition to other forms of compensation and its separate value is difficult to determine
without utilizing an option pricing model. For that reason we also use the Black-Scholes option-pricing model to value options and warrants granted to
non-employees, which requires the input of significant assumptions including an estimate of the average period that investors or consultants will retain
vested stock options and warrants before exercising them, the estimated volatility of our common stock price over the expected term, the number of options
and warrants that will ultimately be forfeited before completing vesting requirements and the risk-free interest rate. Changes in the assumptions can
materially affect the estimate of fair value of stock-based compensation and, consequently, the related expense recognizes that. We have been on the
NASDAQ Capital Market since 2015 and have had a volatile stock including reverse stock splits. The assumptions we use in calculating the fair value of
stock-based payment awards represent our best estimates, which involve inherent uncertainties and the application of management's judgment. As a result,
if factors change and we use different assumptions, our equity-based consulting and interest expense could be materially different in the future.
In the case of standard options to employees we determined the expected life to be the midpoint between the vesting term and the legal term. In the case of
options or warrants granted to non-employees, we estimated the life to be the legal term unless there was a compelling reason to make it shorter.
Business Combination. We accounted for the zPREDICTA merger as a business combination, using the acquisition method of accounting. This method
requires, among other things, that assets acquired, and liabilities assumed be recognized at fair value as of the acquisition date. The fair value for the assets
acquired and the liabilities assumed are based on information knowable and determined by management as of the acquisition date. We allocate the purchase
price to tangible and intangible assets acquired and liabilities assumed, based on their estimated fair values. The excess of the purchase price, if any, over
the aggregate fair value of assets acquired and liabilities assumed is allocated to goodwill.
Fixed Assets. We account for assets acquired at fair value as of the acquisition date. The fair value for assets acquired are based on their estimated fair
values. Fixed assets are stated at cost less accumulated depreciation. Depreciation of fixed assets is computed using the straight-line method over the
estimated useful lives of the respective assets.
41
Goodwill and Other Intangible Impairment. In accordance with ASC 350, Intangibles – Goodwill and Other, goodwill is calculated as the difference
between the acquisition date fair value of the consideration transferred and the fair value of net assets acquired. Goodwill is an asset representing the future
economic benefits arising from other assets acquired in a business combination. Goodwill is an indefinite-lived intangible asset and is not amortized.
Goodwill is not amortized but is tested on an annual basis for impairment at the reporting unit level as of December 31, or whenever events or changes in
circumstances indicate that the carrying amount may not be fully recoverable.
To determine whether goodwill is impaired, annually or more frequently if needed, the Company performs a multi-step impairment test. The Company first
has the option to assess qualitative factors to determine if it is more likely than not that the carrying value of a reporting unit exceeds its estimated fair
value. The Company may also elect to skip the qualitative testing and proceed directly to the quantitative testing. When performing quantitative testing, the
Company first estimates the fair values of its reporting units using discounted cash flows. To determine fair values, the Company is required to make
assumptions about a wide variety of internal and external factors. Significant assumptions used in the impairment analysis include financial projections of
free cash flow (including significant assumptions about operations including the rate of future revenue growth, capital requirements, and income taxes),
long-term growth rates for determining terminal value and discount rates. Comparative market multiples are used to corroborate the results of the
discounted cash flow test. These assumptions require significant judgement. Pursuant to ASU 2017-04, Simplifying the Test for Goodwill Impairment, the
single step is to determine the estimated fair value of the reporting unit and compare it to the carrying value of the reporting unit, including goodwill. To the
extent the carrying amount of goodwill exceeds the implied goodwill, the difference is the amount of the goodwill impairment. The Company also
completes a reconciliation between the implied equity valuation prepared and the Company’s market capitalization. The majority of the inputs used in the
discounted cash flow model are unobservable and thus are considered to be Level 3 inputs. The inputs for the market capitalization calculation are
considered Level 1 inputs. See Note 10 – Intangible Assets and Goodwill.
In the Helomics acquisition, the Company recorded goodwill of $23,790,290. The goodwill was recorded to the Helomics segment which represents a
single reporting unit. The cumulative losses on goodwill are $23,790,290 as of December 31, 2021. See Note 10 to our audited consolidated financial
statements included in this annual report.
On November 24, 2021, the Company acquired goodwill of $6,857,790 in connection with the acquisition of zPREDICTA. The Company determined the
value of the goodwill associated with the zPREDICTA reporting unit was fully recoverable at December 31, 2021.
Long-lived Assets
The Company reviews finite-lived identifiable intangible assets for impairment in accordance with ASC 360, Property, Plant and Equipment, whenever
events or changes in circumstances indicate the carrying amount may not be recoverable. Events or changes in circumstances that indicate the carrying
amount may not be recoverable include, but are not limited to, a significant change in the medical device marketplace and a significant adverse change in
the business climate in which the Company operates.
The Company prepared an undiscounted cash flow as of December 31, 2021 to evaluate long-lived assets based on a triggering event per ASC 360. The
Company concluded that the undiscounted cash flows did not support the carrying values of its the long-lived assets within the Helomics asset group at
December 31, 2021. The Company determined the value of the intangibles and the software license acquired were fully impaired as of December 31, 2021
and recognized an impairment loss on its long-lived intangible assets of $2,893,548 and $1,249,727 impairment loss related to the acquired software. See
Note 10 – Intangible Assets and Goodwill.
Based on a triggering event as of December 31, 2020, the Company prepared an undiscounted cash flows per ASC 360 to evaluate its other long-lived
assets. The Company concluded that the undiscounted cash flows of the long-lived assets exceeded the carrying values. The Company concluded there was
no impairment of its finite lived assets as of December 31, 2020.
42
Income Taxes. Deferred income taxes are provided on a liability method, whereby deferred tax assets are recognized for deductible temporary differences
and operating loss and tax credit carryforwards. Deferred tax liabilities are recognized for taxable temporary differences, which are the differences between
the reported amounts of assets and liabilities and their tax bases. Deferred tax assets are reduced by a valuation allowance when, in the opinion of
management, it is more likely than not that some portion or all the deferred tax assets will not be realized. Deferred tax assets and liabilities are adjusted for
the effects of changes in tax laws and rates on the date of enactment. The Company recognizes the financial statement benefit of a tax position only after
determining that the relevant tax authority would more likely than not sustain the position following an audit. For tax positions meeting the more-likely-
than-not threshold, the amount recognized in the consolidated financial statements is the largest benefit that has a greater than 50 percent likelihood of
being realized upon ultimate settlement with the relevant tax authority.
Recent Accounting Developments
See “Note 1 - Summary of Significant Accounting Policies - Recently Adopted Accounting Standards” in Notes to Consolidated Financial Statements of
this Annual Report on Form 10-K.
Off-Balance Sheet Transactions
We have no off-balance sheet transactions.
ITEM 7A. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.
Not required.
ITEM 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA.
Our financial statements and supplementary data are included beginning on pages F-1 of this report.
ITEM 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE.
None.
ITEM 9A. CONTROLS AND PROCEDURES.
Disclosure Controls and Procedures
Rule 13a-15(e) under the Securities Exchange Act of 1934, as amended (the Exchange Act), defines the term “disclosure controls and procedures” as those
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 recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms and that such information is
accumulated and communicated to our management, including our principal executive and principal financial officers, or persons performing similar
functions, as appropriate to allow timely decisions regarding required disclosure.
Management, with the participation of our Chief Executive Officer and Chief Financial Officer, has evaluated the effectiveness of our disclosure controls
and procedures, as defined in Rules 13a-15(e) and 15d-15(e) of the Securities Exchange Act of 1934, as of December 31, 2021. Based on that evaluation,
our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-
15(e) under the Exchange Act) were effective as of December 31, 2021.
43
Management’s Report on Internal Control Over Financial Reporting
We are responsible for establishing and maintaining adequate internal control over financial reporting. As defined in the securities laws, internal control
over financial reporting is a process designed by, or under the supervision of, our principal executive and principal 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 (i)
pertain to the maintenance of records that in reasonable detail accurately and fairly reflect the acquisitions and dispositions of our assets; (ii) 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 management and directors; and (iii)
provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of our assets that could have a
material effect on the financial statements. Because of its inherent limitations, internal control over financial reporting may not prevent or detect
misstatements.
Under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, we carried out an
evaluation of the effectiveness of our internal control over financial reporting (as defined in Rule 13a-15(f) under the Securities Exchange Act of 1934) as
of December 31, 2021 based on the criteria in “Internal Control - Integrated Framework (2013)” issued by the Committee of Sponsoring Organizations of
the Treadway Commission (“COSO”) in 2013. Based upon this evaluation, we concluded that our internal control over financial reporting were effective as
of December 31, 2021.
Changes in Internal Control Over Financial Reporting
There were no changes in our internal control over financial reporting (as defined in Rule 13a-15(f) under the Securities Exchange Act of 1934) during the
three months ended December 31, 2021 that has materially affected, or are reasonably likely to materially affect, our internal control over financial
reporting.
ITEM 9B. OTHER INFORMATION.
None.
ITEM 10. DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE.
PART III
The Board may be increased or decreased from time to time by resolution of the stockholders or the Board. Our Board presently consists of seven directors.
Directors are elected at each annual meeting, and each director shall serve until his or her term expires, his or her earlier death, or a successor is elected and
qualified or until the director resigns or is removed. Directors are elected by the highest number of votes cast at a meeting at which a quorum is present.
Any vacancies may be filled by the vote of a majority of the Board of Directors, although less than a quorum, and any such person elected to fill a vacancy
shall serve as a director until the next annual meeting of stockholders.
The Board does not intend to alter the manner in which it evaluates candidates for the Board based on whether or not the candidate was recommended by a
stockholder. To submit a candidate for consideration for nomination, stockholders must submit such nomination in writing to our Secretary at 2915
Commers Drive, Suite 900, Eagan, MN 55121.
Executive Officers and Directors of the Registrant
The following table identifies our executive officers and directors for the year ended December 31, 2021:
Name
J. Melville Engle
Age
Position Held
71
Chief Executive Officer and Chairman of the Board of Directors
44
Bob Myers
Chuck Nuzum
Daniel E. Handley, Ph.D.
Gregory S. St. Clair
(1) (2) (3) (5)
(3)
(1)
Nancy Chung-Welch, Ph.D.
(1) (2) (4) (5)
Christina Jenkins, M.D.
Raymond F. Vennare
(4)
(3)
(1) Member of the Audit Committee
(2) Member of the Compensation Committee
(3) Member of the Nominating and Governance Committee
(4) Member of the Merger & Acquisition Committee
(5) Member of the Finance Committee
67
73
62
56
61
50
69
Chief Financial Officer
Director
Director
Director
Director
Director
Director
J. Melville Engle was appointed Chief Executive Officer on March 19, 2021. Mr. Engle resigned from the Compensation and Governance Committees
concurrently with his appointment as CEO.
Each director will serve until their successors are elected and have duly qualified.
There are no family relationships among our directors and executive officers. Our executive officers are appointed by our Board of Directors and serve at
the Board’s discretion.
Classified Board of Directors
On March 22, 2019, our stockholders approved amendments to the Certificate of Incorporation and Bylaws to establish a classified Board of Directors, and
we filed the Amended and Restated Certificate of Incorporation. The amendments to our Certificate of Incorporation and Bylaws provide for the division of
the members of our shareholders into three classes, with the term of each class expiring in different years. As a result of this stockholder approval, three
classes of directors were created: Class I continuing for a term expiring in 2022, Class II for a term expiring in 2023, and Class III for a term, expiring in
2024. Beginning with the 2019 annual meeting of stockholders, the class of directors up for election or reelection will be elected to three-year terms. The
current directors are divided into classes as follows:
CLASS I
(term expiring in 2022)
Chuck Nuzum
Daniel E. Handley
Business Experience
CLASS II
(term expiring in 2023)
J. Melville Engle
Nancy Chung-Welch
Gregory S. St. Clair
CLASS III
(term expiring in 2024)
Christina Jenkins
Raymond Vennare
J. Melville Engle, Chief Executive Officer, and Chairman of the Board of Directors. Effective March 19, 2021, J. Melville Engle was appointed our
Chief Executive Officer. Mr. Engle had served as a director since 2016. He became the Chairman of the Board in January 2020. Mr. Engle has worked in
the healthcare industry for the past three decades. Since 2012, he had served as President and Chief Executive Officer of Engle Strategic Solutions, a
consulting company focused on CEO development and coaching, senior management consulting, corporate problem solving and strategic and operational
planning. He was a director of Windgap Medical, Inc., and has held executive positions at prominent companies including Chairman and Chief Executive
Officer at ThermoGenesis Corp., Regional Head/Director, North America at Merck Generics, President and Chief Executive Officer of Dey, L.P. and CFO,
at Allergan, Inc. In addition to ThermoGenesis, he has served on the Board of Directors of several public companies, including Oxygen Biotherapeutics and
Anika Therapeutics. Mr. Engle holds a BS in Accounting from the University of Colorado and an MBA in Finance from the University of Southern
California. He has served as a Trustee of the Queen of the Valley Medical Center Foundation, was a Board Member of the Napa Valley Community
Foundation, and at the Napa College Foundation. He was also Vice Chair of the Thunderbird Global Council at the Thunderbird School of Global
Management in Glendale, Arizona.
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Bob Myers, Chief Financial Officer. Effective July 1, 2012, Mr. Myers was appointed as our Chief Financial Officer. Mr. Myers was our Acting Chief
Financial Officer and Corporate Secretary since December 2011. He has over 40 years’ experience in multiple industries focusing on medical device,
service and manufacturing and prior to joining the Company was a financial contractor represented by various contracting firms in the Minneapolis area.
He has spent much of his career as a Chief Financial Officer and/or Controller. Mr. Myers was a contract CFO at Disetronic Medical, contract Corporate
Controller for Diametric Medical Devices and contract CFO for Cannon Equipment. Previously he held executive positions with American Express,
Capitol Distributors, and International Creative Management and was a public accountant with the international firm of Laventhol & Horwath. Mr. Myers
has an MBA in Finance from Adelphi University and a BBA in Public Accounting from Hofstra University.
Daniel E. Handley M.S., Ph.D., Director. Dr. Handley was appointed to the Board on February 19, 2020. He serves as a Professor and the Director of the
Clinical and Translational Genome Research Institute of Southern California University of Health Sciences. Previously, he was the Chief Scientific Officer
of the Clinical and Translational Genome Research Institute, a Florida 501(c)3 non-profit corporation. During that time, he also held a courtesy faculty
appointment in the Department of Biological Sciences at Florida Gulf Coast University. He previously served as the Chief Scientific Officer for Advanced
Healthcare Technology Solutions, Inc., Life-Seq, LLC, as a senior researcher at the Procter & Gamble Co., a senior administrator, researcher, and
laboratory manager at the David Geffen UCLA School of Medicine, and as a founding biotechnology inventor for the National Genetics Institute. He holds
a B.A. in Biophysics from Johns Hopkins University, an M.S. in Logic and Computation from Carnegie Mellon University, a Ph.D. in Human Genetics
from the University of Pittsburgh. He completed his post-doctoral training at Magee-Women’s Research Institute researching advanced genomic
technologies applied to fetal and maternal health. He is a veteran of the U.S. Navy, having served as a nuclear propulsion instructor and a submarine
nuclear reactor operator.
Chuck Nuzum. Mr. Nuzum was appointed to the Board on July 9, 2020. Mr. Nuzum has extensive experience as a CFO that ranges from private start-ups
to large publicly-traded companies. Mr. Nuzum presently provides financial consulting services on a project basis to companies such as McKesson,
BioMarin, AutoDesk and Squire Patton Boggs, mentors start-up companies and serves on the Board of Directors of several companies. Previously he was
co-founder and CFO of the Tyburn Group, a financial services company that creates and delivers prepaid payroll and general purpose card programs for
customers. For the four years prior, Mr. Nuzum served as the Controller of Dey, L.P., a large pharmaceutical manufacturing subsidiary of Merck KGaA.
Prior to that he was co-founder, Executive Vice President and CFO of SVC Financials Services, one of the first companies in the field to integrate a mobile
money solution for global distribution, Vice President of Finance and Administration at Tiburon, Inc., a leader in public safety and justice information
systems, and CFO of Winebid.com the world’s leading e-commerce wine auction company. For more than two decades, Mr. Nuzum was CFO of Loomis
Fargo & Co., the well-known international provider of ATM systems, armored cars and other security services. Mr. Nuzum, a Certified Public Accountant,
earned his BA at the University of Washington at Seattle.
Gregory S. St. Clair. Mr. St. Clair was appointed to the Board on July 9, 2020. Mr. St. Clair is the Founder and Managing Member of SunStone
Consulting, LLC, a healthcare consulting firm that serves healthcare providers throughout the United States since 2002. As frequently sought experts on
issues related to compliance, reimbursement and revenue integrity, Mr. St. Clair and his team are constantly on-call to assist clients as they address
financial challenges through creative solutions to the nation’s health systems. Previously, Mr. St. Clair worked as a national vice president for CGI,
ImrGlobal, and Orion Consulting and as national director for Coopers & Lybrand. He holds a B.S. in both Accounting and Finance from Juniata College in
Huntington, Pennsylvania.
46
Nancy Chung-Welch, Ph.D. Dr. Chung-Welch was appointed to the Board on July 9, 2020. Dr. Chung-Welch is currently an independent consultant
advising life science companies and their institutional investors on life science companies, technologies and industries with an emphasis on the research
product/tools market. Previously she was a Director, Business Development at Cell Signaling Technology and was Director, Business Development at
Thermo Fisher Scientific and Technical Marketing Manager for Fisher Scientific. She has over 25 years of marketing and business development experience
in the life sciences market. Dr. Chung-Welch has a balanced blend of business and technical/analytical strengths to provide sound foundation for
technology/IP assessments and external partnerships. She has a strong record of domestic and international experience in business and customer needs
analysis, technology assessment, licensing, distribution deals, partnerships, strategic alliances, strategic customer relationships, mergers/acquisitions. She
previously served as Instructor in Surgery and Assistant in Physiology at Harvard Medical School and the Massachusetts General Hospital with expertise in
basic science research, including cell biology, tissue culture, vascular physiology, genomics, proteomics, and lab automation applications. She is also a
hands-on marketing executive and has conceptualized, launched, and managed products and services in the laboratory, medical, biotech/pharma, academic
and government markets. She received her Ph.D. in Vascular Physiology and Cell Biology from Boston University.
Christina Jenkins, M.D. was appointed to the Board on April 21, 2021. Dr. Jenkins is a strategic advisor and venture investor whose expertise spans
clinical medicine, venture capital, health systems and health plans. She applies her unique perspective of providers, payers and consumers to help leaders
optimize growth and health outcomes. Currently, Dr. Jenkins is a Venture Partner at Phoenix Venture Partners (PVP), where she co-leads the firm’s seed-
stage investment strategy in the healthcare/life sciences vertical. She is focused on hardware-enabled platform companies that are transforming the way we
diagnose, monitor and treat health conditions. Dr. Jenkins also leads investments for Portfolia, Inc.’s FemTech and Active Aging and Longevity funds,
focusing on evidence-backed digital health and device companies targeting the health of women. She also is a director of Independence Health Group (the
parent company of Independence Blue Cross and AmeriHealth Caritas), a board of directors observer at Madorra Inc., and an advisory board member of
multiple value-generating healthcare companies. Dr. Jenkins is also a member of the Kauffman Fellows, a global leadership program in venture capital,
completing her fellowship at New Enterprise Associates. Previously, she was the founding CEO of OneCity Health Services, a subsidiary of NYC Health +
Hospitals, building a team from two to 130 and leading a successful $1.2 billion effort to design and implement technology-enabled care models and
accelerate value-based payment (financial risk) readiness for one million lives. She was also a Clinical Instructor in Internal Medicine at Mount Sinai
Medical Center in New York City, and began her career as a financial analyst (FMP) with GE Healthcare. She earned her M.D. from Northwestern
University Medical School, where she was Class President, and her B.S. in Industrial Management at Purdue University.
Raymond F. Vennare was appointed to the Board on September 13, 2021. Mr. Vennare brings more than thirty years of experience to his work as an
accomplished senior executive, board director and biotechnology entrepreneur. As a professional who has built and managed companies on behalf of
institutional investors, private foundations and research institutions, he is recognized as an expert in the practice of company creation, technology
commercialization, business development and corporate governance. Mr. Vennare is currently (and has been since 2015), Chairman of the Board and CEO
of Cvergenx, Inc., a genomic informatics company developing decision-support tools for radiation oncology, and since 2019 has been on the Board of
Directors of Cvergenx Technologies India Private, Ltd. He also serves as a trusted and confidential advisor to clients as diverse as nationally ranked
universities and philanthropic foundations to multi-national publicly traded companies and early-stage start-ups. Previously Mr. Vennare was Co-founder,
President and CEO of ThermalTherapeutic Systems, Inc. (Medical Device); President and Chief Executive Officer of ImmunoSite, Inc. (Diagnostics);
Senior Vice President and Chief Information Officer, TissueInformatics, Inc. (Bioinformatics); Founder, President and Partner in VSInteractive
(Information Technology) and, Founder and President of the Fine Art Inventory Network (On-line Commerce). From June 2018 to December 2020, he was
Vice Chairman of Guangzhou INDA Biotechnology Company, Ltd. Mr. Vennare has a Master’s Degree in Business and Ethics from Duquesne University,
a Master’s Degree in Art History and Museum Studies from Case Western Reserve University and a Bachelor’s Degree from the University of Pittsburgh.
Richard L. Gabriel resigned as a member of the Board of Directors effective May 1, 2021. Mr. Gabriel’s resignation is in connection with his assuming a
management position with the Company.
47
Board Committee Structures
The Board of Directors has determined that each current member of the Audit Committee, the Compensation Committee and the Nominating and
Governance Committee meets the applicable SEC and NASDAQ rules and regulations regarding “independence” and that each member is free of any
relationship that would impair their individual exercise of independent judgment with regard to us.
Below is a description of each committee of the Board of Directors as such committees are presently constituted.
Audit Committee
The Audit Committee was established by the Board in accordance with Section 3(a)(58)(A) of the Exchange Act to oversee our corporate accounting and
financial reporting processes and audits of our financial statements.
All members of the Audit Committee are independent directors. Pursuant to its charter and the authority delegated to it by the Board of Directors, the Audit
Committee has sole authority for oversight of our independent registered public accounting firm. In addition, the Audit Committee reviews the results and
scope of the audit and other services provided by our independent registered public accounting firm, and also reviews our accounting and control
procedures and policies. The Audit Committee meets as often as it determines necessary but not less frequently than once every fiscal quarter.
Our Audit Committee currently consists of Mr. Nuzum, as the chairperson, Mr. St. Clair and Dr. Chung-Welch. During 2020, the Audit Committee
chairperson was Ms. Prior, who was replaced on the committee and as chairperson by Mr. Nuzum in July 2020. Each Audit Committee member is a non-
employee director of the Board. The Board of Directors has determined that all current members of our Audit Committee are independent. The Audit
Committee met eight times in fiscal 2021.
Audit Committee Financial Expert
The Board has determined that Mr. Nuzum meets the criteria as an “audit committee financial expert,” as defined in Item 407(d)(5)(ii) of Regulation S-K
under the Securities Act of 1933, as amended. As noted above, Mr. Nuzum, Mr. St. Clair, and Dr. Chung-Welch are independent within the meaning of
NASDAQ’s listing standards.
Compensation Committee
The Compensation Committee of the Board of Directors currently consists of three directors, Mr. Nuzum, as the chairperson, Dr. Chung-Welch and Mr. St.
Clair. The members of the Compensation Committee were appointed by the Board of Directors and consist entirely of directors who are “outside directors”
for purposes of Section 162(m) of the Internal Revenue Code of 1986, as amended, “non-employee directors” for purposes of Rule 16b-3 under the
Exchange Act and “independent” as independence is currently defined in Rule 4200(a) (15) of the NASDAQ listing standards. In fiscal 2021, the
Compensation Committee met eight times. The functions of the Compensation Committee include, among other things:
●
●
●
●
●
●
approving the annual compensation packages, including base salaries, incentive compensation, deferred compensation and stock-based
compensation, for our executive officers;
administering our stock incentive plans, and subject to Board approval in the case of executive officers, approving grants of stock, stock options
and other equity awards under such plans;
approving the terms of employment agreements for our executive officers;
developing, recommending, reviewing and administering compensation plans for members of the Board of Directors;
reviewing and discussing the compensation discussion and analysis with management; and
preparing any compensation committee report required to be included in the annual proxy statement.
48
All Compensation Committee approvals regarding compensation to be paid or awarded to our executive officers are rendered with the full power of the
Board, though not necessarily reviewed by the full Board.
Our Chief Executive Officer may not be present during any Board or Compensation Committee voting or deliberations with respect to his compensation.
Our Chief Executive Officer may, however, be present during any other voting or deliberations regarding compensation of our other executive officers but
may not vote on such items of business.
Compensation Committee Interlocks and Insider Participation
As indicated above, the Compensation Committee consists of Mr. Nuzum, Dr. Chung-Welch and Mr. St. Clair. No member of the Compensation Committee
has ever been an executive officer or employee of ours. None of our officers currently serves, or has served during the last completed year, on the
compensation committee or the Board of Directors of any other entity that has one or more officers serving as a member of the Board of Directors or the
Compensation Committee.
Nominating and Governance Committee
The Nominating and Governance Committee of the Board of Directors currently consists of Dr. Handley, as the chairperson Mr. Nuzum and Mr. Vennare.
All members of the Nominating and Governance Committee are “independent directors,” as such term is defined by The NASDAQ Market Listing Rule
5605(a)(2), and free from any relationship that, in the opinion of the Board, would interfere with the exercise of his or her independent judgment as a
member of the Committee.
The members of the Committee shall be elected annually by the Board. Committee members may be removed for any reason or no reason at the discretion
of the Board, and the Board may fill any Committee vacancy that is created by such removal or otherwise. The Committee’s chairperson shall be
designated by the full Board or, if it does not do so, the Committee members shall elect a chairperson upon the affirmative vote of a majority of the
directors serving on the Committee. In fiscal 2021, the Nominating and Governance Committee met four times
The Committee may form and delegate authority to subcommittees as it may deem appropriate in its sole discretion.
In furtherance of its purposes, the Committee:
●
Evaluates the composition, organization and governance of the Board, determines future requirements and make recommendations to the Board
for approval;
● Determines desired Board and committee skills and attributes and criteria for selecting new directors;
● Reviews candidates for Board membership consistent with the Committee’s criteria for selecting new directors or as recommended by our
stockholders. Annually, the Committee recommends a slate of nominees to the Board for consideration at our annual stockholders’ meeting;
● Develops a plan for, and consults with the Board regarding, management succession; and
● Advises the Board generally on corporate governance matters.
In addition, the Committee, if and when deemed appropriate by the Board or the Committee, develops and recommends to the Board a set of corporate
governance principles applicable to the Company, and reviews and reassesses the adequacy of such guidelines annually and recommends to the Board any
changes deemed appropriate. The Committee also advises the Board on (1) committee member qualifications, (2) appointments, removals and rotation of
committee members, (3) committee structure and operations (including authority to delegate to subcommittees), and (4) committee reporting to the Board.
Finally, the Committee performs any other activities consistent with its charter, our Certification of Incorporation, Bylaws and governing law as the
Committee or the Board deems appropriate.
49
The Committee has the authority to obtain advice and seek assistance from internal or external legal, accounting or other advisors. The Committee has the
sole authority to retain and terminate any search firm to be used to identify director candidates, including sole authority to approve such search firm’s fees
and other retention terms.
Merger & Acquisition Committee
The Merger & Acquisition Committee of the Board of Directors currently consists of, Dr. Jenkins, as the chairperson, and Dr. Chung-Welch and Mr. Engle.
The Merger & Acquisition Committee advises the Company with respect to any considered mergers, acquisitions, joint ventures and/or consolidations of
any type.
Diversity
The Board of Directors currently has no formal policy regarding attaining diversity on the Board.
Section 16(a) Beneficial Ownership Reporting Compliance
Section 16(a) of the Securities Exchange Act of 1934, as amended, requires our officers and directors, and persons who own more than ten percent of a
registered class of our equity securities, to file reports of ownership and changes in ownership of such securities with the Securities and Exchange
Commission. Officers, directors and greater than ten percent stockholders are required by Securities and Exchange Commission regulations to furnish us
with copies of all Section 16(a) forms they file. Based solely on review of the copies of Forms 3 and 4 and amendments thereto furnished to us during the
fiscal year ended December 31, 2021 and Forms 5 and amendments thereto furnished to us with respect to such fiscal year, or written representations that
no Forms 5 were required, we believe that the following is the list of our officers, directors and greater than ten percent beneficial owners who have failed
to file on a timely basis all Section 16(a) filing requirements during the fiscal year ended December 31, 2021: Carl Schwartz 1 late reporting and 1 late
amendment covering 1 transaction; Charles Lee Nuzum Sr 2 late reporting covering 2 transactions; Christina Lee Jenkins MD 2 late reporting covering 2
transactions; and Raymond Vennare 1 late reporting covering 1 transaction.
Code of Ethics
We have adopted a Code of Ethics that applies to all of our employees, officers (including our principal executive officer, principal financial officer,
principal accounting officer or controller, and persons performing similar functions) and directors. Our Code of Ethics satisfies the requirements of Item
406(b) of Regulation S-K and is included as an exhibit to this Form 10-K.
ITEM 11. EXECUTIVE COMPENSATION.
Overview
This section describes the material elements of the compensation awarded to, earned by or paid to our Chief Executive Officer and our Chief Financial
Officer, collectively referred to as the “Named Executive Officers.” We did not have any other executive officers, as determined in accordance with SEC
rules, during 2020.
Summary Compensation Table for Fiscal 2021 and 2020
The following table provides information regarding the compensation earned during the fiscal years ended December 31, 2021 and December 31, 2020 by
each of the Named Executive Officers:
50
Name and
Principal
Position
Year
Salary
Bonus
J. Melville Engle (2)
2021
$
391,342 $
Carl Schwartz, CEO (3)
Bob Myers, CFO (4)
2021
2020
2021
2020
$
$
$
$
541,827 $
430,000 $
371,965 $
327,838 $
20,000 $
- $
37,667 $
15,334 $
(1)
Stock
Awards
(1)
Option
Awards
- $
- $
- $
- $
582,280 $
46,002 $
All Other
Compensation
Total
Compensation
- $
- $
- $
- $
- $
- $
391,342
163,493 $
- $
1,287,600
476,002
- $
- $
429,632
343,172
(1) Represents the actual compensation cost granted during 2021 and 2020 as determined pursuant to FASB ASC 718, Stock Compensation.
(2) On March 19, 2021 Mr. Engle was named Chief Executive Officer. Mr. Engle received an annual salary of $475,000. Mr. Engle is eligible for a
Long-Term Incentive Program (“LTIP”) structured to reward performance. The LTIP awards will each vest after three years (rolling) subject to
continued employment, with the amount that vests to be based on two or more measures of employment performance, including shareholder
return (increase in common stock price and accomplishment of profit budgets). The LTIP awards consist of 300,000 Restricted Stock Unit’s
(“RSU’s”). Each RSU awards consists of three equal tranches, corresponding to the three years in the performance period. The level of vesting for
each tranche will vary based on (1) the level of achievement of performance goals for the corresponding fiscal year and (2) continued employment
of Mr. Engle through January 1, 2024. On February 28, 2022, Mr. Engle received an annual salary increase to $524,400. Mr. Engle received a
2021 bonus of $191,760, paid in 2022.
(3) Effective as of March 19, 2021, Dr. Schwartz resigned as Chief Executive Officer. Dr. Schwartz received a retirement package for $460,000 in
base salary, unused accrued vacation for $81,827 and the vesting of all RSU’s equaling 400,000 shares of POAI common stock, par value $0.01.
Additionally, Dr. Schwartz received interest payments completing his original loan debt from prior years. Dr. Schwartz received a salary increase
to $460,000 annually on September 23, 2020 retroactively effective to July 1, 2020. Dr. Schwartz received 300,000 restricted stock units on
September 23, 2020, payable in shares of common stock and vesting in equal annual installments over three years.
(4) Mr. Myers received a cash bonus of $20,000 in 2021 awarded by the Board of Directors. Mr. Myers received 23,134 shares of common stock in
2021, due to vesting of his September 23, 2020 RSU’s. Mr. Myers is eligible for a Long-Term Incentive Program (“LTIP”) structured to reward
performance. The LTIP awards will each vest after three years (rolling) subject to continued employment, with the amount that vests to be based
on two or more measures of employment performance, including shareholder return (increase in common stock price and accomplishment of
profit budgets). The LTIP awards consist of 150,000 Restricted Stock Unit’s (“RSU’s”). Each RSU awards consists of three equal tranches,
corresponding to the three years in the performance period. The level of vesting for each tranche will vary based on (1) the level of achievement
of performance goals for the corresponding fiscal year and (2) continued employment of Mr. Myers through January 1, 2024. On February 28,
2022, Mr. Myers received an annual increase to $380,880. Mr. Myers received a 2021 bonus of $106,950, paid in 2022. Mr. Myers received a
salary increase to $345,000 annually on September 23, 2020 retroactively effective to July 1, 2020. Mr. Myers received 100,000 restricted stock
units on September 23, 2020, payable in shares of common stock and vesting in equal annual installments over three years.
Outstanding Equity Awards at Fiscal Year-end for Fiscal 2021
The following table sets forth certain information regarding outstanding equity awards held by the named executive officers as of December 31, 2021:
51
J. Melville Engle
Carl Schwartz
Bob Myers
Grant Date
12/31/2016
3/31/2017
6/22/2017
6/30/2017
9/30/2017
12/31/2017
3/31/2018
6/30/2018
9/30/2018
12/31/2018
3/31/2019
4/4/2019
6/30/2019
9/30/2019
12/31/2019
3/31/2020
4/3/2020
6/30/2020
9/30/2020
12/31/2020
5/17/2021
7/19/2013
6/30/2015
6/30/2015
3/31/2016
6/30/2016
9/30/2016
12/31/2016
12/31/2016
3/31/2017
6/22/2017
11/10/2017
1/2/2018
6/30/2018
8/1/2018
1/2/2019
4/4/2019
7/1/2019
8/1/2019
9/1/2019
3/31/2020
6/30/2020
9/30/2020
12/31/2020
8/13/2012
3/18/2013
3/6/2014
9/16/2016
6/22/2017
4/4/2019
9/23/2020
5/17/2021
Options
Number of
Securities
Underlying
Options
Exercisable
Number of
Securities
Underlying
Options
Unexercisable
Option
Exercise
Price
Option
Expiration
Date
Restricted Stock Units
Number of
Units of
Stock That
Have Not
Vested
Market Value
Of Units of
Stock
That Have
Not Vested
179
238
12,500
340
344
2,475
455
443
472
4,038
667
12,500
669
990
13,410
3,174
15,267
3,049
6,142
47,788
-
7
26
26
59
133
121
179
714
238
37,689
2,834
14,175
12,168
4,490
32,305
20,000
4,219
5,128
6,050
3,174
3,049
6,142
20,481
53
42
14
357
30,411
16,600
—
—
28.00
21.00
14.70
14.70
14.54
10.10
11.00
11.30
10.60
6.19
7.50
7.48
7.48
5.05
2.61
1.58
1.31
1.64
0.81
0.73
-
1.54
1.54
775.00
42.50
37.50
41.25
1.54
28.00
21.00
1.54
1.54
1.54
1.54
1.54
1.54
1.54
7.90
6.50
5.51
1.58
1.64
0.81
0.73
12/31/2026
3/31/2027
6/22/2027
6/30/2027
9/30/2027
12/31/2027
3/31/2028
6/30/2028
9/30/2028
12/31/2028
3/31/2029
4/4/2029
6/30/2029
9/30/2029
12/31/2029
3/31/2030
4/3/2030
6/30/2030
9/30/2030
12/31/2030
-
7/19/2023
6/30/2025
6/30/2025
3/31/2026
6/30/2026
9/30/2026
12/31/2026
12/31/2026
3/31/2027
6/22/2027
11/10/2027
1/2/2028
6/30/2028
8/1/2028
1/2/2029
4/4/2029
7/1/2029
8/1/2029
9/1/2029
3/31/2030
6/30/2030
9/30/2030
12/31/2030
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
300,000 $
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
285,570
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
8/13/2022
3/18/2023
3/6/2024
9/16/2026
6/22/2027
4/4/2029
1.54
1.54
1.54
1.54
1.54
1.54
—
—
—
—
—
—
—
—
—
—
66,666 $
150,000 $
—
—
—
—
—
—
63,459
142,785
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
$
52
Executive Compensation Components for Fiscal 2021
Base Salary. Base salary is an important element of our executive compensation program as it provides executives with a fixed, regular, non-contingent
earnings stream to support annual living and other expenses. As a component of total compensation, we generally set base salaries at levels believed to
attract and retain an experienced management team that will successfully grow our business and create stockholder value. We also utilize base salaries to
reward individual performance and contributions to our overall business objectives but seek to do so in a manner that does not detract from the executives’
incentive to realize additional compensation through our stock options.
The Compensation Committee reviews the Chief Executive Officer’s salary at least annually. The Compensation Committee may recommend adjustments
to the Chief Executive Officer’s base salary based upon the Compensation Committee’s review of his current base salary, incentive cash compensation and
equity-based compensation, as well as his performance and comparative market data. The Compensation Committee also reviews other executives’ salaries
throughout the year, with input from the Chief Executive Officer. The Compensation Committee may recommend adjustments to other executives’ base
salary based upon the Chief Executive Officer’s recommendation and the reviewed executives’ responsibilities, experience, and performance, as well as
comparative market data.
In utilizing comparative data, the Compensation Committee seeks to recommend salaries for each executive at a level that is appropriate after giving
consideration to experience for the relevant position and the executive’s performance. The Compensation Committee reviews performance for both our
Company (based upon achievement of strategic initiatives) and each individual executive. Based upon these factors, the Compensation Committee may
recommend adjustments to base salaries to better align individual compensation with comparative market compensation, to provide merit-based increases
based upon individual or company achievement, or to account for changes in roles and responsibilities.
Bonuses. Until 2018, the Chief Financial Officer received 20% contractual cash bonuses. Any other bonus for the CFO, as well as for the CEO, if offered,
were determined by the Compensation Committee. The bonuses in past years were a combination of cash and employee stock options. The CFO signed an
amended contract whereby the contractual bonuses were removed subsequent to August 1, 2018. All bonuses subsequent to 2018 are part of a structured
program established by the Compensation Committee and approved by the Board of Directors.
Stock Options and Other Equity Grants. Consistent with our compensation philosophies related to performance-based compensation, long-term stockholder
value creation and alignment of executive interests with those of stockholders, we make periodic grants of long-term compensation in the form of stock
options to our executive officers, directors and others in the organization.
Stock options provide executive officers with the opportunity to purchase common stock at a price fixed on the grant date regardless of future market price.
A stock option becomes valuable only if the common stock price increases above the option exercise price and the holder of the option remains employed
during the period required for the option shares to vest. This provides an incentive for an option holder to remain employed by us. In addition, stock options
link a significant portion of an employee’s compensation to stockholders’ interests by providing an incentive to achieve corporate goals and increase
stockholder value. Under our Amended and Restated 2012 Stock Incentive Plan (the “2012 Plan”), we may also make grants of restricted stock awards,
restricted stock units, performance share awards, performance unit awards and stock appreciation rights to officers and other employees. We adopted the
2012 Plan to give us flexibility in the types of awards that we could grant to our executive officers and other employees.
53
Amendment to Stock Option Plan. On September 3, 2020, our stockholders approved amendments to the 2012 Plan to increase the share reserve under the
2012 Plan by an aggregate 750,000 shares from the most recent reserve of 1,000,000 shares to an aggregate 1,750,000 shares. On August 17, 2021, our
stockholders approved amendments to the 2012 Plan to increase the share reserve under the 2012 Plan by an aggregate 1,500,000 shares from the most
recent reserve of 1,750,000 shares to an aggregate 3,250,000 shares. As of December 31, 2021, options to purchase 1,062,871 shares of common stock are
subject to outstanding stock options under the 2012 Plan. In determining the amount of the increase in the 2012 Plan, the Board took into account its
intention to grant further equity awards to current and future executive officers and key employees and directors.
Restricted Stock Units. Consistent with our compensation philosophies related to performance-based compensation, long-term stockholder value creation
and alignment of executive interests with those of stockholders, we make periodic grants of long-term compensation in the form of restricted stock units to
our executive officers.
Restricted stock units provide executive officers with stock that is not fully transferable until certain conditions are met. Upon satisfaction of the conditions,
the stock is no longer restricted, and becomes transferable to the officer.
Limited Perquisites; Other Benefits. We provide our employees with a full complement of employee benefits, including health and dental insurance, short
term and long-term disability insurance, life insurance, a 401(k) plan, FSA flex plan and Section 125 plan.
Long Term Incentive Plan for Executive Officers
On May 17, 2021, the Committee adopted and approved a 2021 Long Term Incentive Plan (the “LTIP”) to provide appropriate incentives to the
Company’s executive officers over the critical three-year performance period consisting of fiscal years 2021, 2022 and 2023. Under the LTIP, the Company
granted restricted stock units (“RSUs”) to the Company’s current CEO, J. Melville Engle, and its CFO, Bob Myers, pursuant to the Company’s Amended
and Restated 2012 Stock Incentive Plan (as amended, the “Stock Incentive Plan”).
The LTIP awards consist of 300,000 RSUs for the CEO and 150,000 RSUs for the CFO granted as of May 17, 2021. Each RSU award consists of
three equal tranches, corresponding to the three years in the performance period. These RSUs will vest on January 1, 2024, with the level of vesting of each
tranche based on (1) the level of achievement of performance goals for the corresponding fiscal year (see below) and (2) continued employment of the
executive through January 1, 2024. For each tranche, the RSUs will vest at the 100% level for performance at the target level; 50% for performance at the
threshold level (with no vesting below the threshold level); and 150% for maximum performance (in other words, for maximum performance on both
performance components in a fiscal year, the payout for that year would be 150% of the number of RSUs in the corresponding tranche). The level of
vesting for each component is prorated between the threshold level and the target level, and between the target level and the maximum level. To the extent
vested, the awards will vest on or before March 15, 2024, following the determination of the Company’s earnings per share in 2023.
Performance-based vesting of the RSUs in the tranche for each fiscal year (100,000 RSUs per year for the CEO and 50,000 RSUs per year for the
CFO) will be based equally on two components of performance:
(1) Stock Price. A stock price component is based on the average closing share price of the Company’s common stock over the last 20 trading days
of the fiscal year, as set forth in the LTIP.
(2) Earnings (Loss) Per Share. An earnings component is based on the Company’s earnings (loss) per common share for that fiscal year, as set forth
in the LTIP.
If the Committee determines that circumstances have changed and modification is required to reflect the original intent of the performance goals,
the Committee may in its discretion increase (but not decrease) the number of RSUs that vest for any of the covered years.
On August 10, 2021, the stockholders approved an amendment to the Amended and Restated 2012 Stock Incentive Plan to increase the reserve of
shares of common stock authorized for issuance thereunder by 1,500,000, to 3,250,000 shares. Therefore, all RSUs awarded under the LTIP will be paid in
shares of common stock, rather than cash payments that might have been required had such plan amendment not been approved.
54
Employment Contracts
Employment Agreement with Former Chief Executive Officer.
On November 10, 2017, we entered into an employment agreement with Dr. Carl Schwartz, who has served as Chief Executive Officer from December 1,
2016 through March 19,2021. Under the agreement, the employment of Dr. Schwartz is at will.
On July 1, 2019, we entered into an amended employment agreement with Dr. Schwartz. The annualized base salary for Dr. Schwartz was $400,000 for
both 2019 and 2018. Such base salary may be adjusted by us but may not be reduced except in connection with a reduction imposed on substantially all
employees as part of a general reduction.
On September 23, 2020, the Compensation Committee of the Board of Directors of the Company approved the elements of a compensation program for the
executive officers of the Company. The base salaries of the executive officers were increased by 15%, effective as of July 1, 2020, resulting in annualized
base salaries of $460,000 for Dr. Schwartz. In addition, Dr. Schwartz was awarded a one-time, special interim grant of retention equity awards for 2020 on
September 23, 2020 of 300,000 restricted stock units payable in shares of common stock and vesting in equal annual installments over three years, subject
to continued employment, with accelerated vesting upon certain events, including involuntary termination without cause, voluntary termination for good
reason or retirement after at least eighteen months upon at least six months’ notice.
Retirement of Former Chief Executive Officer
On March 19, 2021, Dr. Schwartz retired through his resignation as the Chief Executive Officer of the Company. In connection with the
resignation, Dr. Schwartz and the Company simultaneously entered into a Transition and Separation Agreement pursuant to which, among other things, Dr.
Schwartz agreed to retire from his employment and resign as a member of the Board and to provide certain transition services to the Company in exchange
for the issuance to Dr. Schwartz of 100,000 shares of common stock. The Company and Dr. Schwartz also entered into an Agreement and Release pursuant
to which, among other things, Dr. Schwartz and the Company released each other from any and all claims each may have against the other, and the
Company agreed to provide Dr. Schwartz with certain separation benefits, including $460,000 (gross) in severance pay, equal to one year of his base salary,
and the vesting of the 300,000 restricted stock units previously granted to Dr. Schwartz.
Employment Agreement with Current Chief Executive Officer
On April 5, 2021, the Company and J. Melville Engle, the Company’s current Chief Executive Officer, entered into an Employment Agreement
(the “Agreement”) effective as of March 19, 2021, the first date of Mr. Engle’s employment. Pursuant to the Agreement, Mr. Engle is entitled to an annual
base salary of $475,000. He will also be eligible (i) to receive an annual cash bonus equal to up to 50% of his salary, or at the discretion of the
Compensation Committee (the “Committee”) of the Company’s Board of Directors, a higher percentage based on his performance and (ii) to participate in
a long-term incentive plan to be adopted and maintained by the Committee. Under the LTIP, Mr. Engle will receive 100,000 restricted shares of Company
common stock or restricted stock units for each of the next three calendar years of his employment, vesting over three years and subject to continued
employment, with the amount that vests to be based on his performance. Mr. Engle will also be eligible to participate in the standard employee benefit
plans generally available to executive employees of the Company, and, at the discretion of the Committee, to receive grants of stock options or other equity
awards. Any grants of equity awards, including those above, will be made from the Company’s Amended and Restated 2012 Stock Incentive Plan or
successor plans.
Under the Agreement, Mr. Engle’s employment by the Company is at-will. If his employment is terminated by the Company without “cause” or if
he voluntarily resigns with “good reason” (in each case as defined in the Agreement), then Mr. Engle will be entitled to receive from the Company payment
of his base salary then in effect through his last date of employment, plus accrued, unused vacation pay. In addition, Mr. Engle will be entitled to (a)
severance pay in an amount equal to 12 months of his base salary then in effect, less applicable taxes and withholdings; and (b) a bonus payment on a pro-
rata basis through the date of his termination.
55
The Agreement also contains customary provisions with respect to confidentiality and intellectual property, in addition to ones prohibiting Mr.
Engle from soliciting the Company’s employees and from engaging in certain activities that are competitive with the Company for a period of 12 months
after termination of his employment.
Employment Agreement with Chief Financial Officer.
On August 13, 2012, we entered into an employment agreement with Bob Myers, who has served as Chief Financial Officer since July 1, 2012. Under the
agreement the employment of Mr. Myers is at will.
On August 20, 2018, we entered into an amendment to employment agreement with Mr. Myers. Effective August 1, 2018, Mr. Myers received an
annualized base salary of $250,000. Effective August 1, 2019, Mr. Myers received an annualized base salary of $300,000.
On September 23, 2020, the Compensation Committee of the Board of Directors of the Company approved the elements of a compensation program for the
executive officers of the Company. The base salaries of the executive officers were increased by 15%, effective as of July 1, 2020, resulting in annualized
base salaries of $345,000 for Mr. Myers. In addition, Mr. Myers was awarded a one-time, special interim grant of retention equity awards for 2020 on
September 23, 2020 of 100,000 restricted stock units payable in shares of common stock and vesting in equal annual installments over three years, subject
to continued employment, with accelerated vesting upon certain events, including involuntary termination without cause, voluntary termination for good
reason or retirement after at least eighteen months upon at least six months’ notice.
Base salaries for Mr. Myers may be adjusted by us but may not be reduced except in connection with a reduction imposed on substantially all employees as
part of a general reduction. He will also each be eligible to receive an annual incentive bonus for each calendar year at the end of which he remains
employed by us, subject to the attainment of certain objectives.
In addition, as a part of the compensation program approved in September 2020, Mr. Myers will be eligible for an annual bonus and a long-term incentive
program effective January 1, 2021. Based on Company and personal performance vs. annual objectives to be established by the officers and the Committee
and to be evaluated by the Committee, the officers will be granted an annual bonus opportunity ranging from 0% to 50% of base salary, or at the Board’s
discretion, a higher percentage based on performance. Also, under the long-term incentive program, the officer will receive annual grants of restricted stock
units on January 1 of each calendar year starting in 2021. Each grant will consist of 50,000 restricted stock units with vesting of each grant over three years
based on performance and continued employment.
Mr. Myers is entitled to five (5) weeks of paid vacation per each calendar year earned ratably over each calendar year, to be taken at such times as
employee and Company shall determine and provided that no vacation time shall unreasonably interfere with the duties required to be rendered by
employee.
If we terminate his employment without cause or if he terminates his employment for “good reason,” he shall be entitled to receive us severance pay in an
amount equal to:(1) before the first anniversary of the date of the agreement, three months of base salary, or (2) on or after the first anniversary of the date
of the agreement, twelve months of base salary, in either case less applicable taxes and withholdings. In that event, he will receive a bonus payment on a
pro-rata basis through the date of termination and any accrued, unused vacation pay. The severance pay, bonus payment, and other consideration are
conditioned upon executive’s execution of a full and final release of liability. “Cause” is defined to mean: 1) that he engages in willful misconduct or fails
to follow the reasonable and lawful instructions of the Board, if such conduct is not cured within 30 days after notice; 2) he embezzles or misappropriates
assets from us or any of our subsidiaries; 3) his violation of his obligations in the agreement, if such conduct is not cured within 30 days after notice; 4)
breach of any agreement between him and us or to which we and Mr. Myers are parties, or a breach of his fiduciary responsibility to us; 5) commission by
Mr. Myers of fraud or other willful conduct that adversely affects our business or reputation; or, 6) we have a reasonable belief he engaged in some form of
harassment or other improper conduct prohibited by Company policy or the law. “Good reason” is defined as (1) a material diminution in his position,
duties, base salary, and responsibilities; or (2) our notice to Mr. Myers that his position will be relocated to an office which is greater than 100 miles from
his prior office location. In all cases of Good Reason, he must have given notice to us that an alleged Good Reason event has occurred, and the
circumstances must remain uncorrected by us after the expiration of 30 days after receipt by us of such notice.
56
During Mr. Myers employment and for twelve months thereafter, regardless of the reason for the termination, he may not engage in a competing business,
as defined in the agreement and will not solicit any person to leave employment with us or solicit our clients or prospective clients with whom he worked,
solicited, marketed, or obtained confidential information about during his employment with us, regarding services or products that are competitive with any
of our services or products.
Potential Payments Upon Termination or Change of Control
Most of our stock option agreements provide for an acceleration of vesting in the event of a change in control as defined in the agreements and in the 2012
Stock Incentive Plan. However, the stock option agreements awarded to Bob Myers provide that upon the termination of such employee’s employment
without cause or for good reason, such employee’s options shall become fully vested, and the vested shares may be purchased for up to five years after such
termination (or such lesser period for the option if the remaining period of the option is less than five years after such termination). In addition, in the event
of such employee’s retirement, death or disability, such employee’s options shall become fully vested, and the vested shares may be purchased for the entire
remaining period of the option. Also, see “Employment Contracts” above for a description of certain severance compensation arrangements.
Director Compensation
Effective June 17, 2021 the Board adopted a Director Compensation Program under which the members of the Board of Directors receive quarterly awards
of common stock and cash as compensation for their services as directors and annual awards of common stock and cash for services as committee
members. These awards were implemented to replace the previous program of quarterly stock option grants to directors. The June 2020 annual common
stock award remains in place as described below.
The compensation program pays all of the compensation in the form of stock and cash awards (with the cash component payable in additional shares at the
election of the director. The cash component is equal to 28% of the total value of the award (or 38.9% of the share component of the award), intended to
pay the tax on the full award.
Each director receives a quarterly award of $8,333 on the last day of the quarter, consisting of (i) shares with a value of $6,000 and (ii) $2,333 in cash (or
additional shares).
For each board committee, each director receives an additional annual award of $11,112, consisting of (i) shares with a value of $8,000 and (ii) $3,112 in
cash (or additional shares), payable on December 31.
Director compensation will continue to be paid to all members of the Board of Directors through December 31, 2021. Starting in 2022, director
compensation will be limited to Non-Employee Directors (directors who are not employees of POAI or any subsidiary and who do not receive regular long-
term cash compensation as consultants).
Effective on June 16, 2020 the Board instituted an annual common stock award for all the directors under which they will receive $7,000 in value of newly
issued shares of common stock, par value $0.01 per year annually for three years, as long as they are serving as a director at the annual appointment date.
Additionally, the directors will receive a $3,000 cash payment per year annually for three years, as long as they are serving as a director at the annual
appointment date.
Effective on April 3, 2020 the Board instituted an annual stock options award program for the Chairman of the Board under which he/she will be awarded
options to purchase $20,000 worth of shares of common stock, par value $0.01 at an exercise price determined by the close on April 2 or the last trading
day prior to April 3.
Prior to April 3, 2020, the Company maintained a quarterly and an annual stock options award program for all the directors under which they will be
awarded options to purchase $5,000 worth of shares of common stock, par value $0.01 per quarter at an exercise price determined by the close on the last
day of the quarter. Additionally, the directors that served on a committee received options to purchase $10,000 worth of shares of common stock, par value
$0.01 annually, per committee served, at an exercise price determined by the close on the last day of the year.
57
Director Compensation Table for Fiscal 2021
The following table summarizes the compensation paid to each director in the fiscal year ended December 31, 2021:
J. Melville Engle
Charles Nuzum Sr.
Daniel Handley
Greg St. Clair Sr.
Nancy Chung-Welch
Christina Jenkins
Raymond Vennare
Richard Gabriel
Fees Paid or
Earned in
Cash
Stock
Awards (1)
Option
Awards
Total
$
$
$
$
$
$
$
$
9,999 $
- $
15,454 $
8,455 $
24,668 $
13,111 $
7,778 $
2,333 $
44,447(2) $
76,668(3) $
39,003(4) $
49,000(5) $
55,003(6) $
38,452(7) $
25,102(8) $
6,000(9) $
- $
- $
- $
- $
- $
- $
- $
- $
54,446
76,668
54,457
57,455
79,671
51,563
32,880
8,333
(1) Represents the actual compensation cost granted during 2021 as determined pursuant to FASB ASC 718, Stock Compensation.
(2) Reflects 19,395 shares of common stock received in 2021 for serving on the Board and 20,428 shares of common stock received on January 4,
2022 for 2021 service on the Board and the Merger & Acquisition Committee.
(3) Reflects 27,147 shares of common stock received in 2021 for serving on the Board and 43,775 shares of common stock received on January 4,
2022 for 2021 service on the Board and the Audit, Compensation and Governance Committees.
(4) Reflects 19,395 shares of common stock received in 2021 for serving on the Board and 14,709 shares of common stock and $5,455 in cash
received on January 4, 2022 for 2021 service on the Board and the Governance Committee.
(5) Reflects 27,147 shares of common stock received in 2021 for serving on the Board and 14,709 shares of common stock and $5,455 in cash
received on January 4, 2022 for 2021 service on the Board and the Audit Committee.
(6) Reflects 19,395 shares of common stock received in 2021 for serving on the Board and 31,517 shares of common stock and $11,669 in cash
received on January 4, 2022 for 2021 service on the Board and the Audit, Compensation and Merger & Acquisition Committees.
(7) Reflects 19,436 shares of common stock received in 2021 for serving on the Board and 14,709 shares of common stock and $5,445 in cash on
January 4, 2022 for 2021 service on the Board and the Merger & Acquisition Committee.
(8) Reflects 9,512 shares of common stock received in 2021 for serving on the Board and 14,709 shares of common stock and $5,445 in cash on
January 4, 2022 for 2021 service on the Board and the Governance Committee.
(9) Mr. Gabriel resigned from the Board effective May 1, 2021. Mr. Gabriel was awarded 4,959 shares of common stock for serving on the Board.
ITEM 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER
MATTERS.
Equity Compensation Plan Information
The following table presents the equity compensation plan information as of December 31, 2021:
Number of
securities
to be issued upon
exercise of
outstanding
restricted stock,
warrants and
options
(a)
Weighted-
average
exercise
price of
outstanding
options,
warrants
(b)
Number of
securities
remaining
available for
future issuance
under
equity
compensation
plans (excluding
securities reflected
in
column (a)
(C)
Equity compensation plans approved by security holders (1)
Equity compensation plans not approved by security holders
1,804,537 $
- $
4.83
-
1,015,187
-
(1) Consists of outstanding options under the 2008 Equity Incentive Plan and the 2012 Stock Incentive Plan. The remaining share authorization under
the 2008 Equity Incentive Plan was rolled over to the current 2012 Stock Incentive Plan.
58
Security Ownership of Certain Beneficial Owners and Management
The following table sets forth as of December 31, 2021 certain information regarding beneficial ownership of our common stock by:
●
●
●
Each person known to us to beneficially own 5% or more of our common stock;
Each executive officer who in this Annual Report Form 10-K are collectively referred to as the “Named Executive Officers;”
Each of our directors; and
● All of our executive officers (as that term is defined under the rules and regulations of the SEC) and directors as a group.
We have determined beneficial ownership in accordance with Rule 13d-3 under the Exchange Act. Beneficial ownership generally means having sole or
shared voting or investment power with respect to securities. Unless otherwise indicated in the footnotes to the table, each stockholder named in the table
has sole voting and investment power with respect to the shares of common stock set forth opposite the stockholder’s name. We have based our calculation
of the percentage of beneficial ownership on 65,911,001 shares of our common stock outstanding on March 13, 2022. Unless otherwise noted below, the
address for each person or entity listed in the table is c/o Predictive Oncology Inc., 2915 Commers Drive, Suite 900, Eagan, Minnesota 55121.
Name of Beneficial Owner
Officers and Directors
J. Melville Engle (2)
Carl Schwartz (3)
Bob Myers (4)
Chuck Nuzum (5)
Gregory St. Clair (6)
Daniel Handley (7)
Christina Jenkins (8)
Raymond Vennare
Nancy Chung-Welch (9)
Richard L. Gabriel (10)
Amount and
Nature of
Beneficial
Ownership
Percent
of
Class
70,689
2,265,099
70,689
117,911
73,177
71,020
34,145
24,221
95,887
89,355
All directors and executive officers as a group (10 persons)
3,010,536
59
0.26%
3.44%
0.11%
0.18%
0.11%
0.11%
0.05%
0.04%
0.15%
0.14%
4.54%
1. Under Rule 13d-3, a beneficial owner of a security includes any person who, directly or indirectly, through any contract, arrangement,
understanding, relationship, or otherwise has or shares: (1) voting power, which includes the power to vote, or to direct the voting of shares; and
(2) investment power, which includes the power to dispose or direct the disposition of shares. Certain shares may be deemed to be beneficially
owned by more than one person (if, for example, persons share the power to vote or the power to dispose of the shares). In addition, shares are
deemed to be beneficially owned by a person if the person has the right to acquire the shares (for example, upon exercise of an option) within 60
days of the date as of which the information is provided. In computing the percentage ownership of any person, the amount of shares outstanding
is deemed to include the number of shares beneficially owned by such person (and only such person) by reason of these acquisition rights. As a
result, the percentage of outstanding shares of any person as shown in this table does not necessarily reflect the person’s actual ownership or
voting power with respect to the number of shares of common stock actually outstanding.
Includes options to purchase 125,139 shares that are exercisable within 60 days of December 31, 2021.
Includes (i) 2,091,695 shares owned directly, and (ii) 173,404 shares issuable upon exercise of options held by Dr. Schwartz that are exercisable
within 60 days of December 31, 2021.
Includes options to purchase 47,478 shares that are exercisable within 60 days of December 31, 2021.
4
Includes options to purchase 40,277 shares that are exercisable within 60 days of December 31, 2021.
5.
Includes options to purchase 26,623 shares that are exercisable within 60 days of December 31, 2021.
6.
Includes options to purchase 32,846 shares that are exercisable within 60 days of December 31, 2021.
7.
Includes options to purchase 72,326 shares that are exercisable within 60 days of December 31, 2021.
8.
9.
Includes options to purchase 40,277 shares that are exercisable within 60 days of December 31, 2021.
10. Includes options to purchase 72,326 shares that are exercisable within 60 days of December 31, 2021.
2.
3.
ITEM 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS, AND DIRECTOR INDEPENDENCE.
The Audit Committee has the responsibility to review and approve all transactions to which a related party and we may be a party prior to their
implementation, to assess whether such transactions meet applicable legal requirements.
One of our former directors, Richard L. Gabriel, is the Senior Vice President of Research & Development for Predictive Oncology, and the President of
TumorGenesis, a division of Predictive Oncology. He accepted the management positions as of May 1, 2021, which coincides with the date he resigned as a
Board member. While Mr. Gabriel was a Board member he served as a director of GLG Pharma (“GLG”).
60
GLG and we have a partnership agreement with Helomics for the purpose of bringing together their proprietary technologies to build out personalized
medicine platform for the diagnosis and treatment of women’s cancer. There has been no revenue or expenses generated by this partnership to date.
Richard L. Gabriel had also contracted as the Chief Operating Officer for TumorGenesis our wholly-owned subsidiary. As of May 1, 2021, Mr. Gabriel
resigned from the contracted position to become part of management for the Company. Mr. Gabriel received $13,500 in monthly cash payments, while
contracting.
ITEM 14. PRINCIPAL ACCOUNTING FEES AND SERVICES.
In connection with the audit of the fiscal 2021 and 2020 financial statements, we entered into an engagement agreement with Baker Tilly US, LLP (2021,
2020), which sets forth the terms by which they will perform audit services for us.
The following table represents aggregate fees billed to us for the fiscal years ended December 31, 2021 and December 31, 2020, by Baker Tilly US, LLP,
respectively, our principal accountants. All fees described below were approved by the Audit Committee. None of the hours expended on the audit of the
2021 and 2020 financial statements were attributed to work performed by persons who were not employed full time on a permanent basis by Baker Tilly
US, LLP.
Audit Fees (1)
Audit-Related Fees (2)
Tax Fees (3)
All Other Fees (4)
2021
2020
396,246 $
-
28,265
99,537
524,048 $
306,235
27,461
22,250
37,415
393,361
$
$
(1) Audit Fees were principally for services rendered for the audit and/or review of our consolidated financial statements. Also, includes fees for
services rendered in connection with the filing of registration statements and other documents with the SEC, the issuance of accountant consents
and comfort letters.
(2) Audit-Related Fees were not incurred in 2021, and in 2020 consisted of fees related to providing predecessor auditor with required representations
related to registration statements filed in 2020.
(3) Tax Fees consist of fees billed in the indicated year for professional services performed by Baker Tilly US, LLP with respect to tax compliance
during 2021.
(4) Other Fees in 2021 consisted of fees for auditing zPREDICTA for 2020 and 2019, and for reviewing zPREDICTA for the three and nine months
ended September 30, 2020 and September 30, 2021 related to the acquisition of zPREDICTA by the Company. In 2020, other fees related to
consulting services performed by Baker Tilly US, LLP provided prior to Baker Tilly US, LLP's engagement as the Company's independent
registered public accounting firm. All services were provided prior to April 1, 2020 and were related to the audit closing process for the year
ended December 31, 2019 as further described in the Company's Form 8-K filing on April 30, 2020.
61
ITEM 15. EXHIBITS, FINANCIAL STATEMENT SCHEDULES.
PART IV
The following exhibits and financial statements are filed as part of, or are incorporated by reference into, this report:
(1) Financial Statements
The following financial statements are filed with this Annual Report and can be found beginning at page F-1 of this report:
● Report of Independent Registered Public Accounting Firm, PCOAB Firm ID #23 dated March 31, 2022;
● Consolidated Balance Sheets as of December 31, 2021 and December 31, 2020;
● Consolidated Statements of Net Loss for the Years Ended December 31, 2021 and December 31, 2020;
● Consolidated Statements of Stockholders’ Equity for the Years Ended December 31, 2021 to December 31, 2020;
● Consolidated Statements of Cash Flows for the Years Ended December 31, 2021 and December 31, 2020; and
● Notes to Consolidated Financial Statements.
(2) Financial Statement Schedules
All schedules for which provision is made in the applicable accounting regulations of the SEC have been omitted because the information required
to be shown in the schedules is not applicable or is included elsewhere in the financial statements and Notes to Financial Statements.
(3) Exhibits
See “Exhibit Index” following the signature page of this Form 10-K for a description of the documents that are filed as Exhibits to this Annual
Report on Form 10-K or incorporated by reference herein.
62
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this Annual Report on Form 10-
K to be signed on its behalf by the undersigned, thereunto duly authorized.
SIGNATURES
Dated: March 31, 2022
Predictive Oncology Inc.
By
/s/ J. Melville Engle
J. Melville Engle
Chief Executive Officer
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.
Signatures
Title
/s/ J. Melville Engle
J. Melville Engle
/s/ Bob Myers
Bob Myers
/s/ Chuck Nuzum
Chuck Nuzum
/s/ Daniel E. Handley
Daniel E. Handley
/s/ Gregory St. Clair Sr.
Gregory St. Clair Sr.
/s/ Nancy Chung-Welch
Nancy Chung-Welch
/s/ Raymond Vennare
Raymond Vennare
/s/ Christina Jenkins
Christina Jenkins
Chief Executive Officer
(Principal executive officer)
Chief Financial Officer
(Principal financial and accounting officer)
Director
Director
Director
Director
Director
Director
63
March 31, 2022
March 31, 2022
March 31, 2022
March 31, 2022
March 31, 2022
March 31, 2022
March 31, 2022
EXHIBIT INDEX
PREDICTIVE ONCOLOGY INC.
FORM 10-K
Exhibit
Number
Description
2.1
Agreement and Plan of Merger dated November 24, 2021 by and among the Company, Golden Gate Acquisition, Inc., zPredicta, Inc.
and Tom Kelly, as Representative (Filed on December 1, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein
by reference). Exhibit 2.1
3.1
Certificate of Incorporation (Filed on December 19, 2013 as an exhibit to our Current Report on Form 8-K and incorporated herein by
reference). Exhibit 3.1
3.2
3.3
3.4
3.5
Certificate of Amendment to Certificate of Incorporation to effect reverse stock split and reduction in authorized share capital filed with
the Delaware Secretary of State on October 20, 2014. (Filed on October 24, 2014 as an exhibit to our Current Report on Form 8-K and
incorporated herein by reference.) Exhibit 3.2
Certificate of Amendment to Certificate of Incorporation regarding increase in share capital, filed with the Delaware Secretary of State
on July 24, 2015. (Filed on June 30, 2015 as an appendix to our Information Statement on Schedule 14C and incorporated herein by
reference.) Exhibit 3.3
Certificate of Amendment to Certificate of Incorporation to increase authorized share capital, filed with the Delaware Secretary of State
on September 16, 2016. (Filed on September 16, 2016 as an exhibit to our Current Report on Form 8-K and incorporated herein by
reference.) Exhibit 3.4
Certificate of Amendment to Certificate of Incorporation to effect reverse stock split and reduction in authorized share capital, fled with
the Delaware Secretary of State on October 26, 2016. (Filed on October 27, 2016 as an exhibit to our Current Report on Form 8-K and
incorporated herein by reference.) Exhibit 3.5
3.6
Certificate of Amendment to Certificate of Incorporation regarding increase in share capital, filed with the Delaware Secretary of State
on January 26, 2017. (Filed on January 27, 2017 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.)
Exhibit 3.6
3.7
3.8
3.9
Certificate of Amendment to Certificate of Incorporation to effect reverse stock split, filed with the Delaware Secretary of State on
January 2, 2018. (Filed on January 2, 2018 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.)
Exhibit 3.7
Certificate of Amendment to Certificate of Incorporation to effect name change, filed with the Delaware Secretary of State on February
1, 2018. (Filed on February 6, 2018 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 3.8
[Intentionally omitted.]
3.10
Second Amended and Restated Bylaws as of June 10, 2019. (Filed on June 13, 2019 as an exhibit to our Current Report on Form 8-K
and incorporated herein by reference.) Exhibit 3.10
3.11
Form of Certificate of Designation of Preferences, Rights and Limitations of Series B Convertible Preferred Stock. (Filed on August 20,
2015 as an exhibit to our Registration Statement on Form S-1 (File No. 333-198962) and incorporated herein by reference.) Exhibit 3.11
64
3.12
Certificate of Designation of Preferences, Rights and Limitations of Series C Convertible Preferred Stock. (Filed on November 29, 2017
as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 3.12
3.13
Certificate of Amendment to Certificate of Incorporation dated March 22, 2019. Filed on March 22, 2019 as an exhibit to our Current
Report on Form 8-K and incorporated herein by reference. Exhibit 3.13
3.14
Certificate of Designation Of Preferences, Rights And Limitations of Series D Convertible Preferred Stock. (Filed on April 1, 2020 as an
exhibit to our Annual Report on Form 10-K and incorporated herein by reference.) Exhibit 3.14
3.15
Certificate of Designation of Preferences, Rights and Limitations of Series E Convertible Preferred Stock Effective June 13, 2019. (Filed
on June 19, 2019 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 3.15
3.16
Certificate of Amendment of Certificate of Incorporation, changing name from Precision Therapeutics Inc. to Predictive Oncology Inc.
(Filed on June 13, 2019 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 3.16
3.17
3.18
Certificate of Amendment of Certificate of Incorporation, amending number of shares of common stock and preferred stock, effecting a
reverse stock split. (Filed on October 28, 2019 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.)
Exhibit 3.17
Certificate of Amendment to the Certificate of Incorporation, doubling number of shares of common stock and preferred stock due to
stock split. (Filed on August 19, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit
3.18
4.1
Form of specimen certificate evidencing shares of Series B Convertible Preferred Stock. (Filed on August 10, 2015 as an exhibit to our
Registration Statement on Form S-1 (File No. 333-198962) and incorporated herein by reference.) Exhibit 4.1
4.2
Investor Warrant issued November 28, 2017. (Filed on November 29, 2017 as an exhibit to our Current Report on Form 8-K and
incorporated herein by reference.) Exhibit 4.2
4.3
Series E Warrant Agency Agreement by and between Skyline Medical Inc. and Corporate Stock Transfer, Inc. dated January 9, 2018.
(Filed on January 10, 2018 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 4.3
4.4
Form of Series E Warrant Certificate. (Filed on January 10, 2018 as an exhibit to our Current Report on Form 8-K and incorporated
herein by reference.) Exhibit 4.4
4.5
Common Stock Purchase Warrant issued to L2 Capital, LLC dated September 28, 2018. (Filed on October 4, 2018 as an exhibit to our
Current Report on Form 8-K and incorporated herein by reference.) Exhibit 4.5
4.6
Common Stock Purchase Warrant issued to Peak One Opportunity Fund, LP dated September 28, 2018. (Filed on October 4, 2018 as an
exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 4.6
4.7
Form of Unit Purchase Option issued February 27, 2019. (Filed on March 1, 2019 as an exhibit to our Current Report on Form 8-K and
incorporated herein by reference.) Exhibit 4.7
4.8
Form of Common Stock Purchase Warrant issued March 29, 2019. (Filed on April 2, 2019 as an exhibit to our Current Report on Form
8-K and incorporated herein by reference.) Exhibit 4.8
65
4.9
Form of Unit Purchase Option for the Purchase of Units issued March 29, 2019. (Filed on April 2, 2019 as an exhibit to our Current
Report on Form 8-K and incorporated herein by reference.) Exhibit 4.9
4.10
Common Stock Purchase Warrant Issued to Oasis Capital, LLC dated September 27, 2019. (Filed on September 30, 2019 as an exhibit to
our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 4.10
4.11
Form of Specimen Common Stock Certificate. (Filed on October 3, 2019 as an exhibit to our Registration Statement on Form S-3 (File
No. 333-234073) and incorporated herein by reference.) Exhibit 4.11
4.12
Form of Common Stock Purchase Warrant Issued on or about October 1, 2019. (Filed on October 10, 2019 as an exhibit to our Current
Report on Form 8-K and incorporated herein by reference.) Exhibit 4.12
4.13
Common Stock Purchase Warrant issued to Oasis Capital, LLC dated February 5, 2020. (Filed on February 7, 2020 as an exhibit to our
Current Report on Form 8-K and incorporated herein by reference.) Exhibit 4.13
4.14*
Description of Registrant’s Securities.
4.15
Common Stock Purchase Warrant issued to Oasis Capital, LLC dated March 6, 2020. (Filed on April 6, 2020 as an exhibit to our
Registration Statement on Form S-3 (File No. 333-237581) and incorporated herein by reference.) Exhibit 4.15
4.16
Common Stock Purchase Warrant issued to Oasis Capital, LLC dated April 5, 2020. (Filed on April 6, 2020 as an exhibit to our
Registration Statement on Form S-3 (File No. 333-237581) and incorporated herein by reference.) Exhibit 4.16
4.17
Form of Common Stock Purchase Warrant issued June 29, 2020. (Filed on June 26, 2020 as an exhibit to our Current Report on Form 8-
K and incorporated herein by reference.) Exhibit 4.17
4.18
Form of Helomics Common Stock Purchase Warrant issued April 4, 2019. (Filed on January 24, 2019 as Annex H on Form S-4/A (File
No. 333-228031) and incorporated herein by reference.) Exhibit 4.18
4.19
Form of Common Stock Purchase Warrant issued January 12, 2021. (Filed on January 12, 2021 as an exhibit to our Current Report on
Form 8-K and incorporated herein by reference.) Exhibit 4.19
4.20
Form of Common Stock Purchase Warrant issued January 19, 2021. (Filed on January 21, 2021 as an exhibit to our Current Report on
Form 8-K and incorporated herein by reference.) Exhibit 4.20
4.21
Form of Common Stock Purchase Warrant issued January 21, 2021. (Filed on January 26, 2021 as an exhibit to our Current Report on
Form 8-K and incorporated herein by reference.) Exhibit 4.21
4.22
Form of Placement Agent Warrant to H.C. Wainwright & Co., LLC or its designees in connection with certain financing transactions in
2020 and 2021. (Filed on January 29, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.)
Exhibit 4.22
4.23
Form of Common Stock Purchase Warrant dated February 10, 2021. (Filed on February 12, 2021 as an exhibit to our Current Report on
Form 8-K and incorporated herein by reference.) Exhibit 4.23
4.24
Form of Common Stock Purchase Warrant dated February 23, 2021. (Filed on February 22, 2021 as an exhibit to our Current Report on
Form 8-K and incorporated herein by reference.) Exhibit 4.24
4.25
Form of Common Stock Purchase Warrant dated June 16, 2021. (Filed on June 16, 2021 as an exhibit to our Current Report on Form 8-
K and incorporated herein by reference.) Exhibit 4.25
66
4.26
Form of Placement Agent Warrant dated June 16, 2021. (Filed on June 16, 2021 as an exhibit to our Current Report on Form 8-K and
incorporated herein by reference.) Exhibit 4.26
10.1
Office Lease Agreement between the registrant and Roseville Properties Management Company, as agent for Lexington Business Park,
LLC. (Filed on November 12, 2008 as an exhibit to our Registration Statement on Form S-1 and incorporated herein by reference.)
Exhibit 10.1
10.2
Employment Agreement with Robert Myers dated August 11, 2012. (Filed on November 5, 2012 as an exhibit to our Registration
Statement on Form S-1 and incorporated herein by reference.)** Exhibit 10.2
10.3
Amended Lease with Roseville Properties Management Company, Inc. dated January 29, 2013. (Filed on February 8, 2013 as an exhibit
to our Registration Statement on Form S-1 (except for Exhibit 10.19, by incorporation by reference from the Schedule 13D/A filed by
Dr. Herschkowitz and other parties on November 8, 2012) and incorporated herein by reference.) Exhibit 10.3
10.4
Amended and Restated 2012 Stock Incentive Plan. (Filed on March 22, 2019 as an exhibit to our Current Report on Form 8-K and
incorporated herein by reference.) Exhibit 10.4
10.5*
Form of Stock Option Agreement for Employees under Amended and Restated 2012 Stock Incentive Plan.**
10.6*
Form of Stock Option Agreement for Executive Officers under Amended and Restated 2012 Stock Incentive Plan.**
10.7*
Form of Stock Option Agreement for Directors under Amended and Restated 2012 Stock Incentive Plan.**
10.8
10.9
10.10
10.11
10.12
Amendment to Employment Agreement by and between the Issuer and Bob Myers dated August 20, 2018** (Filed on April 1, 2019 as
an exhibit to our Annual Report on Form 10-K and incorporated herein by reference.) Exhibit 10.8
Equity Purchase Agreement by and between the Issuer and Oasis Capital, LLC dated October 24, 2019. (Filed on October 25, 2019 as an
exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.9
Registration Rights Agreement by and between the Issuer and Oasis Capital, LLC dated October 24, 2019. (Filed on October 25, 2019 as
an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.10
Securities Purchase Agreement by and among the Company and the Investors dated March 15, 2020. (Filed on March 16, 2020 as an
exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.11
Registration Rights Agreement by and among the Company and the Investors dated March 15, 2020. (Filed on March 16, 2020 as an
exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.12
10.13
Form of Securities Purchase Agreement dated January 8, 2021, by and between Predictive Oncology Inc. and certain Purchasers. (Filed
on January 12, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.13
10.14
Form of Securities Purchase Agreement dated January 19, 2021, by and between Predictive Oncology Inc. and certain Purchasers. (Filed
on April 6, 2020 as an exhibit to our Registration Statement on Form S-3 (File No. 333-237581) and incorporated herein by reference.)
Exhibit 10.14
67
10.15
Form of Securities Purchase Agreement dated January 21, 2021, by and between Predictive Oncology Inc. and certain Purchasers. (Filed
on January 21, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.15
10.16
10.17
10.18
Form of Securities Purchase Agreement dated February 10, 2021, by and between Predictive Oncology Inc. and certain Purchasers.
(Filed on February 12, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.16
Form of Securities Purchase Agreement dated February 18, 2021, by and between Predictive Oncology Inc. and certain Purchasers.
(Filed on February 22, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.17
Form of Registration Rights Agreement dated February 18, 2021, by and between Predictive Oncology Inc. and certain Purchasers.
(Filed on February 22, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.18
10.19
Transition and Separation Agreement by and between the Company and Carl Schwartz dated March 19, 2021. (Filed on March 23,
2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.19
10.20
Agreement and Release by and between the Company and Carl Schwartz dated March 19, 2021. (Filed on March 23, 2021 as an exhibit
to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.20
10.21
Offer Letter by and between the Company and J. Melville Engle dated March 19, 2021.** (Filed on March 23, 2021 as an exhibit to our
Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.21
10.22
Employment Agreement by and between the Company and J. Melville Engle dated effective as of March 19, 2021** (Filed on April 7,
2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.22
10.23
2021 Long Term Incentive Plan** (Filed on May 20, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by
reference.) Exhibit 10.23
10.24
Form of Securities Purchase Agreement, dated June 14, 2021, by and between Predictive Oncology Inc. and certain Purchasers. (Filed
on June 16, 2021 as an exhibit to our Current Report on Form 8-K and incorporated herein by reference.) Exhibit 10.24
14.1
Code of Ethics. (Filed on April 16, 2012 as an exhibit to our Annual Report on Form 10-K and incorporated herein by reference.)
Exhibit 14.1
21.1*
Subsidiaries of the Registrant.
23.1*
Consent of Independent Registered Public Accounting Firm: Baker Tilly US, LLP
31.1*
Certification of principal executive officer required by Rule 13a-14(a)
31.2*
Certification of principal financial officer required by Rule 13a-14(a)
32.1*
Section 1350 Certification
101.INS*
Inline XBRL Instance Document – the instance document does not appear in the Interactive Data File because its XBRL tags are
embedded within the Inline XBRL 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*
Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)
*Filed herewith.
**Compensatory Plan or arrangement required to be filed pursuant to Item 15(b) of Form 10-K.
68
The audited consolidated financial statements for the periods ended December 31, 2021 and December 31, 2020 are included on the following pages:
INDEX TO FINANCIAL STATEMENTS
Financial Statements:
Report of Independent Registered Public Accounting Firm, PCAOB Firm ID # 23
Consolidated Balance Sheets
Consolidated Statements of Net Loss
Consolidated Statements of Stockholders’ Equity
Consolidated Statements of Cash Flows
Notes to Consolidated Financial Statements
69
Page
F-1
F-3
F-4
F-5
F-8
F-10
REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
To the shareholders and the board of directors of Predictive Oncology Inc.:
Opinion on the Financial Statements
We have audited the accompanying consolidated balance sheets of Predictive Oncology Inc. (the "Company") as of December 31, 2021 and 2020, the
related consolidated statements of net loss, stockholders’ equity, and cash flows for the years ended December 31, 2021 and 2020, and 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, 2021 and 2020, and the results of their operations and their cash flows for the years
ended December 31, 2021 and 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 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 provides a reasonable basis
for our opinion.
Critical Audit Matter
The critical audit matter communicated below is a matter arising from the current period audit of the consolidated financial statements that was
communicated or required to be communicated to the audit committee and that: (1) relates to accounts or disclosures that are material to the consolidated
financial statements and (2) involved our especially challenging, subjective, or complex judgments. The communication of the critical audit matter does not
alter in any way our opinion on the consolidated financial statements, taken as a whole, and we are not, by communicating the critical audit matter below,
providing a separate opinion on the critical audit matter or on the account or disclosure to which it relates.
F-1
Critical Audit Matter Description
zPREDICTA, Inc. Acquisition – Fair Value of Intangible Assets
As discussed in Note 2 to the consolidated financial statements, the Company accounted for the zPREDICTA, Inc. acquisition as a business combination
and allocated the purchase price amongst the tangible and intangible assets acquired and liabilities assumed. Auditing the accounting for the acquisition
was complex due to the significant estimation uncertainty in determining the fair values of identifiable intangible assets, which consisted primarily of
developed technology and customer relationships totaling approximately $3.7 million.
We identified the fair value of intangible assets related to developed technology and customer relationships recorded in connection with the zPREDICTA,
Inc. acquisition as a critical audit matter. The fair value estimates were based on underlying assumptions about future performance of the acquired business,
which involves significant estimation uncertainty. The significant assumptions used to form the basis of the fair value of the developed technology included
obsolescence factors, revenue growth rates, earnings metrics, and discount rates. The significant assumptions used to form the basis of the fair value of the
customer relationships included customer margins, revenue growth rates, attrition rates and discount rates. These significant assumptions are forward-
looking and could be affected by future economic and market conditions.
How We Addressed the Matter in Our Audit
The primary procedures we performed to address this critical audit matter included substantively testing, with the assistance of firm personnel with
expertise in the application of fair value and valuation methodologies, the appropriateness of the judgements and assumptions used in management’s
process for determining the fair value of the identifiable intangibles, which included the following procedures:
● Obtained management’s purchase price allocation detailing fair values assigned to the acquired tangible and intangible assets.
● Obtained the valuation report prepared by a valuation specialist engaged by management to assist in the purchase price allocation, including
determination of fair values assigned to acquired identifiable intangible assets, and examined valuation methods used and qualifications of
specialist.
●
●
●
Evaluating the appropriateness of the valuation methodologies used, as well as assumptions regarding the customer margins, attrition rates and
discount rates related to customer relationships and the obsolescence factor and discount rates for technology, among other valuation assumptions.
Examined the completeness and accuracy of the underlying data supporting the significant assumptions and estimates used in the valuation report,
including historical and projected financial information.
Performing inquiries of personnel at zPREDICTA, Inc. that were highly involved in the development of the forecasts to evaluate the reasonableness
of revenue and margin forecasts as well as examining a sample of customer revenue contracts to support the reasonableness of the revenue forecast.
●
Comparing the significant assumptions used by management to current industry and economic trends.
We have served as the Company's auditor since 2020.
/s/Baker Tilly US, LLP
Minneapolis, Minnesota
March 31, 2022
F-2
PART 1. FINANCIAL INFORMATION
Item 1. Financial Statements
Current Assets:
Cash and cash equivalents
Accounts Receivable
Inventories
Prepaid Expense and Other Assets
Total Current Assets
Fixed Assets, net
Intangibles, net
Lease Right-of-Use Assets
Other Long-Term Assets
Goodwill
Total Assets
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED BALANCE SHEETS
ASSETS
December 31,
2021
December 31,
2020
$
$
$
28,202,615 $
354,196
387,684
513,778
29,458,273
2,511,571
3,962,118
814,454
167,065
6,857,790
43,771,271 $
1,021,774 $
-
1,262,641
129,480
186,951
639,662
3,240,508
25,415
239,664
3,505,587
-
792
678,332
256,878
289,535
289,490
1,514,235
3,822,700
3,398,101
1,395,351
116,257
2,813,792
13,060,436
1,372,070
4,431,925
2,588,047
294,382
53,028
597,469
9,336,921
235,705
845,129
10,417,755
-
792
656,146
167,649,028
(128,040,282)
40,265,684
198,048
110,826,949
(108,383,108)
2,642,681
LIABILITIES AND STOCKHOLDERS' EQUITY
Current Liabilities:
Accounts Payable
Notes Payable – Net of Discounts of $0 and $244,830
Accrued Expenses and other liabilities
Derivative Liability
Deferred Revenue
Lease Liability – Net of Long-Term Portion
Total Current Liabilities
Other Long Term Liabilities
Lease Liability, long-term portion
Total Liabilities
Stockholders’ Equity:
Preferred Stock, 20,000,000 authorized inclusive of designated below
Series B Convertible Preferred Stock, $.01 par value, 2,300,000 authorized, 79,246 and 79,246 shares
outstanding
Common Stock, $.01 par value, 200,000,000 and 100,000,000 authorized, 65,614,597 and 19,804,787
outstanding
Additional Paid-in Capital
Accumulated Deficit
Total Stockholders' Equity
Total Liabilities and Stockholders' Equity
$
43,771,271 $
13,060,436
See Notes to Consolidated Financial Statements
F-3
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED STATEMENTS OF NET LOSS
Revenue
Cost of goods sold
Gross profit
General and administrative expense
Operations expense
Sales and marketing expense
Loss on goodwill impairment
Loss on impairment intangibles
Loss on impairment of software acquired
Total operating loss
Other income
Other expense
Loss on early extinguishment of debt
Gain on derivative instruments
Gain on notes receivables associated with asset purchase
Net loss before income tax benefit
Income tax benefit
Net loss
Deemed dividend
Net loss attributable to common shareholders
Loss per common share - basic and diluted
Weighted average shares used in computation - basic and diluted
See Notes to Consolidated Financial Statements
F-4
$
$
$
$
Year Ended December 31,
2020
2021
1,420,680 $
487,024
933,656
10,932,125
2,698,565
774,530
2,813,792
2,893,548
1,249,727
(20,428,631)
184,528
(239,631)
-
164,902
-
(20,318,832)
(661,658)
(19,657,174) $
-
(19,657,174) $
1,252,272
447,192
805,080
10,351,973
2,351,709
584,937
12,876,498
-
-
(25,360,037)
843,440
(2,427,026)
(1,996,681)
1,765,907
1,290,000
(25,884,397)
-
(25,884,397)
554,287
(26,438,684)
(0.36) $
(2.21)
54,876,044
11,950,154
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY
Series B Preferred
Series D Preferred
Series E Preferred
Common Stock
Shares Amount
Shares
Amount
Shares
Amount
Shares
Amount
Additional
Paid-In
Capital
Accumulated
Deficit
Total
79,246 $
792
3,500,000
$
35,000
258
$
3
4,056,652
$
40,567
$ 93,653,667
$ (82,498,711) $ 11,231,318
1,583,481
15,835
2,307,043
2,322,878
30,000
300
40,950
41,250
260,000
2,600
455,223
457,823
46,875
468
119,532
116,951
170,000
1,700
265,628
(258)
(3)
1,398,607
13,986
(13,983)
62,373
(3,500,000)
(35,000)
350,004
3,500
31,500
1,390,166
13,902
(13,149)
1,396,826
13,968
591,949
1,079,719
10,797
1,661,970
120,000
116,951
267,328
-
62,373
-
753
605,917
1,672,767
1,274,826
12,748
1,682,237
1,694,985
1,865,953
1,865,953
F-5
Balance at
12/31/2019
Shares issued
pursuant to CEO
note conversion and
accrued interest and
exchange agreement
Inducement shares
issued pursuant to
promissory note
extension
Issuance of shares
and prefunded
warrants pursuant to
March 2020 private
placement
Inducement shares
issued pursuant to
2020 convertible
debt and warrants
Warrants issued
pursuant to 2020
convertible debt
Shares issued
pursuant to note
conversions - bridge
loan
Shares issued
pursuant to series E
preferred stock
conversions
Warrants issued
pursuant to 2020
convertible debt
Shares issued
pursuant to series D
preferred stock
conversions
Issuance of shares
from prefunded
warrant exercises
Issuance of shares
pursuant to May
2020 offering, net
Shares issued in
connection with asset
purchase agreement
Exercise of warrants
and issuance of new
warrants June 2020,
net
Repricing and
Reclassification of
warrants issued
pursuant to
convertible debt
Repricing and
Reclassification of
June 2020 warrants
Exercise of warrants
Shares issued
pursuant to Equity
Line
Shares issued
pursuant to
convertible debt
Share issuance to
consultant and other
Vesting expense and
option repricing
Net loss
Balance at 12/31/20
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY (continued)
Series B Preferred
Series D Preferred
Series E Preferred
Common Stock
Shares Amount
Shares Amount
Shares
Amount
Shares
Amount
122,000
1,220
Additional
Paid-In
Capital
803,455
190,930
Accumulated
Deficit
Total
4,231,073
42,311
4,849,037
2,212,359
22,124
1,006,230
202,199
2,022
428,184
721,269
(25,884,397)
$ (108,383,108) $
721,269
(25,884,397)
2,642,681
803,455
192,150
4,891,348
1,028,354
430,206
79,246 $
792
- $
-
-
$
-
19,804,787
$ 198,048
$ 110,826,949
F-6
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY
Balance at 12/31/2020
Shares issued pursuant to agreement with
former CEO related to accrued interest
Issuance of shares and warrants pursuant
to Shelf offerings, net
Issuance of shares and warrants pursuant
to February 2021 private placement, net
Exercise of warrants
Shares issued pursuant to convertible debt
Issuance of shares and warrants pursuant
to June 2021 direct placement, net
Shares issued pursuant to transition
agreement with former CEO
Shares issued pursuant to Equity Line
Share issuance to consultant and other
Vesting expense and option repricing
Net loss
Balance at 12/31/2021
Series B Preferred
Common Stock
Shares
Amount
79,246 $
Shares
792 19,804,787 $
Amount
Additional
Paid-In
Capital
Accumulated
Deficit
Total
198,048 $ 110,826,949 $ (108,383,108) $ 2,642,681
100,401
1,004
142,569
143,573
13,488,098
134,881 14,877,611
15,012,492
9,043,766
5,269,059
1,107,544
90,438 15,974,301
4,461,169
52,702
502,936
11,075
16,064,739
4,513,871
514,011
15,520,911
155,209 19,291,087
19,446,296
400,000
647,504
174,954
57,573
-
792 65,614,597 $
79,246 $
4,000
6,475
1,750
564
-
-
675,590
205,193
704,412
(19,657,174) (19,657,174)
656,146 $ 167,649,028 $ (128,040,282) $ 40,265,684
(4,000)
669,115
203,443
703,848
-
See Notes to Consolidated Financial Statements
F-7
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED STATEMENTS OF CASH FLOWS
Cash flow from operating activities:
Net loss
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
Vesting expense
Equity instruments issued for management, consulting, and other
Amortization of debt discount
Gain on valuation of equity-linked instruments
Benefit from release of valuation allowance
Gain on note receivable associated with asset purchase agreement
Gain on extinguishment of PPP loan
Debt extinguishment costs
Loss on goodwill impairment
Loss on intangible impairment
Loss on impairment of acquired software
Loss on fixed asset disposal
Changes in assets and liabilities:
Accounts receivable
Inventories
Prepaid expense and other assets
Accounts payable
Accrued expenses
Deferred revenue
Other liabilities
Net cash used in operating activities:
Cash flow from investing activities:
Acquisition of zPREDICTA, net of cash acquired
Purchase of fixed assets
Proceeds from sale of fixed assets
Acquisition of intangibles
Loan activities
Net cash used in investing activities
Cash flow from financing activities:
Proceeds from issuance of common stock, net
Proceeds from exercise of warrants into common stock
Proceeds from debt issuance
Repayment of debt
Payment penalties
Proceeds from issuance of stock pursuant to equity line
Issuance of common stock, prefunded warrants, warrants and exchange of warrants, net
Repurchase of common stock upon vesting of restricted stock units
Other liabilities
Net cash provided by financing activities
Net increase in cash and cash equivalents
Cash and cash equivalents at beginning of year
Cash and cash equivalents end of year
See Notes to Consolidated Financial Statements
F-8
Year Ended
December 31,
2021
2020
$
(19,657,174) $
(25,884,397)
1,340,301
715,938
205,193
244,830
(164,902)
(661,658)
-
-
-
2,813,792
2,893,548
1,249,727
5,858
(20,769)
(98,149)
(194,363)
(350,296)
(499,563)
54,548
(85,790)
(12,208,929)
(9,590,214)
(910,429)
-
(51,893)
(55,000)
(10,607,536)
50,523,527
4,513,871
-
(4,162,744)
(1,073,470)
675,590
-
(11,526)
(124,500)
50,340,748
27,524,283
678,332
28,202,615 $
1,024,848
721,269
450,901
1,246,541
(1,765,907)
-
(1,290,000)
(541,867)
1,996,681
12,876,498
-
-
120,577
69,913
(94,715)
(245,526)
(1,688,572)
700,966
12,644
32,414
(12,257,732)
-
(298,379)
193,321
(62,398)
-
(167,456)
-
1,935,855
2,761,867
(1,472,389)
(247,327)
4,891,348
5,057,919
-
25,416
12,952,689
527,501
150,831
678,332
$
PREDICTIVE ONCOLOGY INC.
CONSOLIDATED STATEMENTS OF CASH FLOWS continued
Non-cash transactions
Bridge loan conversion into common stock
Warrants issued pursuant to debt issuance
Shares issued pursuant to CEO note conversion and accrued interest and exchange agreement
Shares issued pursuant to former CEO per agreement related to accrued interest
Shares issued pursuant to convertible debt
Fixed assets acquired for notes receivable and common stock
Increase to operating lease right of use asset and lease liability due to new and modified leases
Put and conversion derivative from debt issuance and modification
Shares issued pursuant to debt
Series D preferred stock conversions
Inducement shares issued pursuant to convertible debt
Fixed assets acquired for financing arrangements
Series E preferred stock conversion
Cash paid during the period for:
Interest paid on debt
See Notes to Consolidated Financial Statements
F-9
Year Ended
December 31,
2021
2020
-
-
-
143,573
-
-
77,128
-
-
-
514,011
-
-
267,328
179,324
2,322,878
-
1,028,354
2,962,767
1,417,077
636,563
140,555
35,000
-
113,192
13,983
$
690,508 $
145,831
PREDICTIVE ONCOLOGY INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
NOTE 1 — SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Nature of Operations and Continuance of Operations
Predictive Oncology Inc., (the “Company” or “Predictive” or “we”) filed with the Secretary of State of Delaware a Certificate of Amendment to its
Certificate of Incorporation to change the corporate name to Predictive Oncology Inc. on June 10, 2019, trading under the new ticker symbol “POAI,”
effective June 13, 2019.
The Company operates in four primary business areas: first, application of artificial intelligence (“AI”) in our precision medicine business, to provide AI-
driven predictive models of tumor drug response to improve clinical outcomes for patients and to assist pharmaceutical, diagnostic, and biotech industries
in the development of new personalized drugs and diagnostics primarily through its wholly owned subsidiary Helomics Holding Corporation (“Helomics”);
second, tumor-specific in vitro models for oncology drug discovery and research through its newly acquired wholly-owned subsidiary, zPREDICTA; third,
contract services and research focused on solubility improvements, stability studies, and protein production, primarily with our Soluble Biotech subsidiary,
and; fourth, production of the United States Food and Drug Administration (“FDA”)-cleared STREAMWAY System for automated, direct-to-drain medical
fluid waste disposal and associated products through its incorporated division Skyline.
The Company had cash and cash equivalents of $28,202,615 as of December 31, 2021. As of December 31, 2021, there was no outstanding debt. The
Company believes that its existing capital resources will be sufficient to support its operating plan for the next twelve months and beyond. However, the
Company may also seek to raise additional capital to support its growth through additional debt, equity or other alternatives or a combination thereof. The
Company currently expects to use cash on hand to fund capital and equipment investments, research and development, potential acquisitions and its
operations, and expects such sources to be sufficient to fund its requirements over that time.
Coronavirus Outbreak
The current COVID-19 worldwide pandemic has presented substantial public health challenges. In response to the crisis, emergency measures have been
imposed by governments worldwide, including mandatory social distancing and the shutdown of non-essential businesses. These measures have adversely
impacted the global economy, disrupted global supply chains and created significant volatility and disruption of financial markets, and our business and
operations have been and will likely continue to be materially and adversely affected. For example, our contract manufacturer for the STREAMWAY®
System has been forced to change locations, thereby delaying our order fulfillment for parts. We have also reduced on-site staff at several of our facilities,
resulting in delayed production, less efficiency, and our sales staff is unable to visit with hospital administrators who are our customers and potential
customers. In addition, COVID-19 has impacted the Company’s capital and financial resources, including our overall liquidity position and outlook. For
instance, our accounts receivable has slowed while our suppliers continue to ask for pre-delivery deposits. Ultimately, the extent of the impact of the
COVID-19 pandemic on our future operational and financial performance will depend on, among other matters, the duration and intensity of the pandemic;
the level of success of global vaccination efforts; governmental and private sector responses to the pandemic and the impact of such responses on us; and
the impact of the pandemic on our employees, customers, suppliers, operations and sales, all of which are uncertain and cannot be predicted. These factors
may remain prevalent for a significant period of time even after the pandemic subsides, including due to a continued or prolonged recession in the U.S. or
other major economies. Even in areas where "stay-at-home" restrictions, masking and social distancing measures have been lifted and the number of
COVID-19 cases have declined, some jurisdictions may re-impose these measures as and if variant strains emerge or cases rise. The impacts of the
COVID-19 pandemic, as with any adverse public health developments, could have a material adverse effect on our business, results of operations, liquidity
or financial condition and heighten or exacerbate risks described in this Annual Report on Form 10-K.
F- 10
Recently Adopted Accounting Standards
The Company considers the applicability and impact of all Accounting Standards Updates (“ASUs”) issued by the Financial Accounting Standards Board
(the “FASB”). Recently issued ASUs not listed below either were assessed and determined to be not applicable or are currently expected to have no impact
on the condensed consolidated financial statements of the Company.
In June 2016, the FASB issued ASU 2016-13, “Financial Instruments – Credit Losses.” This ASU added a new impairment model (known as the current
expected credit loss (“CECL”) model) that is based on expected losses rather than incurred losses. Under the new guidance, an entity recognizes as an
allowance its estimate of expected credit losses. The CECL model applies to most debt instruments, trade receivables, lease receivables, financial guarantee
contracts, and other loan commitments. The CECL model does not have a minimum threshold for recognition of impairment losses and entities will need to
measure expected credit losses on assets that have a low risk of loss. As a smaller reporting company pursuant to Rule 12b-2 of the Securities Exchange
Act of 1934, as amended, these changes become effective for the Company on January 1, 2023. Management is currently evaluating the potential impact of
these changes on the consolidated financial statements of the Company.
Accounting Policies and Estimates
The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America (“U.S. GAAP”)
requires management to make estimates and assumptions that affect the reported amounts of assets, liabilities, revenues and expenses and disclosure of
contingent assets and liabilities at the date of the financial statements and during the reporting period. Actual results could materially differ from those
estimates.
Reclassifications
Certain reclassifications have been made to the prior years’ financial statements to conform to the current year presentation. The reclassifications had no
effect on previously reported results of operations, cash flows or stockholders’ equity.
Cash and cash equivalents
The Company considers all highly liquid instruments with maturities when purchased of three months or less to be cash equivalents. The Company places
its cash with high quality financial institutions and believes its risk of loss is limited to amounts in excess of that which is insured by the Federal Deposit
Insurance Corporation.
Receivables
Receivables are reported at the amount the Company expects to collect on balances outstanding. The Company provides for probable uncollectible amounts
through charges to earnings and credits to the valuation allowance based on management’s assessment of the current status of individual accounts.
Amounts recorded in accounts receivable on the consolidated balance sheet include amounts billed and currently due from customers. The amounts due are
stated at their net estimated realizable value. An allowance for doubtful accounts is maintained to provide for the estimated amount of receivables that will
not be collected. The Company reviews customers’ credit history before extending unsecured credit and establishes an allowance for uncollectible accounts
based upon factors surrounding the credit risk of specific customers, historical trends and other information. Invoices are generally due 30 days after
presentation. Accounts receivable over 30 days is generally considered past due. The Company does not accrue interest on past due accounts receivables.
Receivables are written off once all collection attempts have failed and are based on individual credit evaluation and specific circumstances of the
customer. The allowance for doubtful accounts balance was $0 as of both December 31, 2021 and 2020.
F- 11
Fair Value Measurements
As outlined in Accounting Standards Codification (“ASC”) 820, Fair Value Measurement, fair value is the price that would be received to sell an asset or
paid to transfer a liability in an orderly transaction between market participants at the measurement date. The accounting standards ASC 820 establishes a
three-level fair value hierarchy that prioritizes information used in developing assumptions when pricing an asset or liability as follows:
Level 1 – Observable inputs such as quoted prices in active markets;
Level 2 – Inputs other than quoted prices in active markets, that are observable either directly or indirectly; and
Level 3 – Unobservable inputs where there is little or no market data, which requires the reporting entity to develop its own assumptions.
The Company uses observable market data, when available, in making fair value measurements. Fair value measurements are classified according to the
lowest level input that is significant to the valuation.
The fair value of the Company’s investment securities, which consist of cash and cash equivalents, was determined based on Level 1 inputs. The fair value
of the Company’s derivative liabilities and debt were determined based on Level 3 inputs. The Company generally uses Black Scholes method for
determining the fair value of warrants classified as liabilities on a recurring basis. In addition, the Company uses the Monte Carlo method and other
acceptable valuation methodologies when valuing the conversion feature and other embedded features classified as derivatives on a recurring basis. See
Note 7 – Derivatives. When performing quantitative testing related to goodwill impairment analysis, the Company estimates the fair values of its reporting
units using discounted cash flows. To determine fair values, the Company is required to make assumptions about a wide variety of internal and external
factors. Significant assumptions used in the impairment analysis include financial projections of free cash flow (including significant assumptions about
operations including the rate of future revenue growth, capital requirements, and income taxes), long-term growth rates for determining terminal value and
discount rates. The majority of the inputs used in the discounted cash flow model are unobservable and thus are considered to be Level 3 inputs. See Note
10 – Goodwill and Intangibles.
The acquisition of zPREDICTA was accounted for as a business combination using the acquisition method of accounting. This method requires, among
other things, that assets acquired and liabilities assumed be recognized at fair value as of the acquisition date. The fair value for the assets acquired and the
liabilities assumed are based on information knowable and determined by management as of the acquisition date. The majority of the inputs used in the
discounted cash flow model, the relief-from-royalty method under the income approach, the distributor method under the income approach and the multi-
period excess earnings method under the income approach, each are unobservable and thus are considered to be Level 3 inputs. See Note 2 – zPREDICTA
Acquisition.
Inventories
Inventories are stated at the lower of cost or net realizable value, with cost determined on a first-in, first-out basis.
Fixed Assets
Fixed assets are stated at cost less accumulated depreciation. Depreciation of fixed assets is computed using the straight-line method over the estimated
useful lives of the respective assets. Estimated useful asset life by classification is as follows:
Computers, software and office equipment
Leasehold improvements (1)
Manufacturing tooling
Laboratory equipment
Demo equipment
(1) Leasehold improvements are amortized over the shorter of the useful life or the remaining lease term.
F- 12
Years
3 - 10
2 - 5
3 - 7
4 - 10
3
Upon retirement or sale of fixed assets, the cost and related accumulated depreciation or amortization are removed from the balance sheet and the resulting
gain or loss is reflected in operations. Maintenance and repairs are charged to operations expense as incurred.
Long-lived Assets
Finite-lived intangible assets consist of patents and trademarks, licensing fees, developed technology, acquired software and customer relationships, and are
amortized over their estimated useful life. Accumulated amortization is included in intangibles, net in the accompanying consolidated balance sheets.
The Company reviews finite-lived identifiable intangible assets for impairment in accordance with ASC 360, Property, Plant and Equipment, whenever
events or changes in circumstances indicate the carrying amount may not be recoverable. Events or changes in circumstances that indicate the carrying
amount may not be recoverable include, but are not limited to, a significant change in the medical device marketplace and a significant adverse change in
the business climate in which the Company operates.
The Company prepared an undiscounted cash flow as of December 31, 2021 to evaluate long-lived assets based on a triggering event per ASC 360. The
Company concluded that the undiscounted cash flows did not support the carrying values of its Helomics asset group at December 31, 2021. The Company
determined the value of the intangibles and the software license acquired were fully impaired as of December 31, 2021 and recognized and impairment loss
of $2,893,548 for its long-lived intangible assets and $1,249,727 for the acquired software. The Company concluded there was no impairment of its other
finite lived tangible assets as of December 31, 2021. See Note 10 – Intangible Assets and Goodwill.
The Company also prepared an undiscounted cash flow as of December 31, 2020 to evaluate long-lived assets based on a triggering event at that time. The
Company concluded that the undiscounted cash flows of the long-lived assets exceeded the carrying values. The Company concluded there was no
impairment of its finite lived assets as of December 31, 2020.
Goodwill
In accordance with ASC 350, Intangibles – Goodwill and Other, goodwill is calculated as the difference between the acquisition date fair value of the
consideration transferred and the fair value of net assets acquired. Goodwill is an asset representing the future economic benefits arising from other assets
acquired in a business combination. Goodwill is not amortized but is tested on an annual basis for impairment at the reporting unit level as of December 31,
or whenever events or changes in circumstances indicate that the carrying amount may not be fully recoverable.
To determine whether goodwill is impaired, annually or more frequently if needed, the Company performs a multi-step impairment test. The Company first
has the option to assess qualitative factors to determine if it is more likely than not that the carrying value of a reporting unit exceeds its estimated fair
value. The Company may also elect to skip the qualitative testing and proceed directly to the quantitative testing. When performing quantitative testing, the
Company first estimates the fair values of its reporting units using discounted cash flows. To determine fair values, the Company is required to make
assumptions about a wide variety of internal and external factors. Significant assumptions used in the impairment analysis include financial projections of
free cash flow (including significant assumptions about operations including the rate of future revenue growth, capital requirements, and income taxes),
long-term growth rates for determining terminal value and discount rates. Comparative market multiples are used to corroborate the results of the
discounted cash flow test. These assumptions require significant judgement. Pursuant to ASU 2017-04, Simplifying the Test for Goodwill Impairment, the
single step is to determine the estimated fair value of the reporting unit and compare it to the carrying value of the reporting unit, including goodwill. To the
extent the carrying amount of goodwill exceeds the implied goodwill, the difference is the amount of the goodwill impairment. The Company also
completes a reconciliation between the implied equity valuation prepared and the Company’s market capitalization. The majority of the inputs used in the
discounted cash flow model are unobservable and thus are considered to be Level 3 inputs. The inputs for the market capitalization calculation are
considered Level 1 inputs. See Note 3 – Intangible Assets and Goodwill.
F- 13
Leases – At inception of a contract a determination is made whether an arrangement meets the definition of a lease. A contract contains a lease if there is
an identified asset and the Company has the right to control the asset. Operating leases are recorded as right-of-use (“ROU”) assets with corresponding
current and noncurrent operating lease liabilities on our consolidated balance sheets. Financing leases are included within fixed assets with corresponding
current liability within other current liabilities and noncurrent liability within other long-term liabilities on our consolidated balance sheets.
ROU assets represent our right to use an underlying asset for the duration of the lease term and lease liabilities represent our obligation to make lease
payments arising from the lease. Recognition on the commencement date is based on the present value of lease payments over the lease term using an
incremental borrowing rate. Leases with a term of 12 months or less at the commencement date are not recognized on the balance sheet and are expensed as
incurred.
The Company has lease agreements with lease and non-lease components, which are accounted for as a single lease component for all asset classes. Leases
are accounted for at a portfolio level when similar in nature with identical or nearly identical provisions and similar effective dates and lease terms.
Revenue Recognition
The Company recognizes revenue when it satisfies a performance obligation by transferring control of the promised goods or services to its customers, in
an amount that reflects the consideration the Company expects to be entitled to in exchange for those goods or services. Sales taxes are imposed on the
Company’s sales to nonexempt customers. The Company collects the taxes from the customers and remits the entire amounts to the governmental
authorities. Sales taxes are excluded from revenue and expenses.
Revenue from Product Sales
The Company has medical device revenue consisting primarily of sales of the STREAMWAY System, as well as sales of the proprietary cleaning fluid and
filters for use with the STREAMWAY System. This revenue stream is reported within both the domestic and international revenue segments. The Company
sells its medical device products directly to hospitals and other medical facilities using employed sales representatives and independent contractors.
Purchase orders, which are governed by sales agreements in all cases, state the final terms for unit price, quantity, shipping and payment terms. The unit
price is considered the observable stand-alone selling price for the arrangements. The Company sales agreement, and Terms and Conditions, is a dually
executed contract providing explicit criteria supporting the sale of the STREAMWAY System. The Company considers the combination of a purchase order
and acceptance of its Terms and Conditions to be a customer’s contract in all cases.
Product sales for medical devices consist of a single performance obligation that the Company satisfies at a point in time. The Company recognizes product
revenue when the following events have occurred: (1) the Company has transferred physical possession of the products, (2) the Company has a present
right to payment, (3) the customer has legal title to the products, and (4) the customer bears significant risks and rewards of ownership of the products.
Based on the shipping terms specified in the sales agreements and purchase orders, these criteria are generally met when the products are shipped from the
Company’s facilities (“FOB origin,” which is the Company’s standard shipping terms). As a result, the Company determined that the customer is able to
direct the use of, and obtain substantially all of the benefits from, the products at the time the products are shipped. The Company may, at its discretion,
negotiate different shipping terms with customers which may affect the timing of revenue recognition. The Company’s standard payment terms for its
customers are generally 30 to 60 days after the Company transfers control of the product to its customer. The Company allows returns of defective
disposable merchandise if the customer requests a return merchandise authorization from the Company.
F- 14
Customers may also purchase a maintenance plan for the medical devices from the Company, which requires the Company to service the STREAMWAY
System for a period of one year subsequent to the one-year anniversary date of the original STREAMWAY System invoice. The maintenance plan is
considered a separate performance obligation from the product sale, is charged separately from the product sale, and is recognized over time (ratably over
the one-year period) as maintenance services are provided. A time-elapsed output method is used to measure progress because the Company transfers
control evenly by providing a stand-ready service. The Company has determined that this method provides a faithful depiction of the transfer of services to
its customers.
All amounts billed to a customer in a sales transaction for medical devices related to shipping and handling, if any, represent revenues earned for the goods
provided, and these amounts have been included in revenue. Costs related to such shipping and handling billing are classified as cost of goods sold. This
revenue stream is reported under the Skyline reportable segment.
Revenue from Clinical Testing
Clinic diagnostic testing is comprised of our Tumor Drug Response Testing (ChemoFx) and Genomic Profiling (BioSpeciFx) tests. The Tumor Drug
Response Testing test determines how a patient’s tumor specimen reacts to a panel of various chemotherapy drugs, while the Genomic Profiling test
evaluates the expression and/or status of a particular gene related to a patient’s tumor specimen. Revenues are recognized when control of the promised
goods or services is transferred to customers, in an amount that reflects the consideration the Company expects to be entitled to in exchange for those goods
or services. The estimated uncollectible amounts are generally considered implicit price concessions that are a reduction in revenue. Helomics’ payments
terms vary by the agreements reached with insurance carriers and Medicare. The Company’s performance obligations are satisfied at one point in time
when test reports are delivered.
For service revenues, the Company estimates the transaction price which is the amount of consideration it expects to be entitled to receive in exchange for
providing services based on its historical collection experience using a portfolio approach as a practical expedient to account for patient contracts as
collective groups rather than individually. The Company monitors its estimates of transaction price to depict conditions that exist at each reporting date. If
the Company subsequently determines that it will collect more consideration than it originally estimated for a contract with a patient, it will account for the
change as an increase to the estimate of the transaction price, provided that such downward adjustment does not result in a significant reversal of
cumulative revenue recognized.
The Company recognizes revenue from these patients when contracts as defined in ASC 606, Revenue from Contracts with Customers are established at the
amount of consideration to which it expects to be entitled or when the Company receives substantially all of the consideration subsequent to the
performance obligations being satisfied. The Company’s standard payment term for hospital and patient direct bill is 30 days after invoice date. This
revenue stream is reported under the Helomics segment.
CRO Revenue
Contract revenues are generally derived from studies conducted with biopharmaceutical and pharmaceutical companies. The specific methodology for
revenue recognition is determined on a case-by-case basis according to the facts and circumstances applicable to a given contract. The Company typically
uses an input method that recognizes revenue based on the Company’s efforts to satisfy the performance obligation relative to the total expected inputs to
the satisfaction of that performance obligation. For contracts with multiple performance obligations, the Company allocates the contract’s transaction price
to each performance obligation on the basis of the standalone-selling price of each distinct good or service in the contract. Advance payments received in
excess of revenues recognized are classified as deferred revenue until such time as the revenue recognition criteria have been met. Payment terms are net
30 from the invoice date, which is sent to the customer as the Company satisfies the performance obligation relative to the total expected inputs to the
satisfaction of that performance obligation. This revenue stream is reported under the Helomics and zPREDICTA segments.
F- 15
Variable Consideration
The Company records revenue from distributors and direct end customers in an amount that reflects the transaction price it expects to be entitled to after
transferring control of those goods or services. The Company’s current contracts do not contain any features that create variability in the amount or timing
of revenue to be earned.
Warranty
The Company generally provides one-year warranties against defects in materials and workmanship on product sales and will either repair the products or
provide replacements at no charge to customers. As they are considered assurance-type warranties, the Company does not account for them as separate
performance obligations. Warranty reserve requirements are based on a specific assessment of the products sold with warranties where a customer asserts a
claim for warranty or a product defect.
Contract Balances
The Company records a receivable when it has an unconditional right to receive consideration after the performance obligations are satisfied. As of
December 31, 2021 and 2020, accounts receivable totaled $354,196 and $256,878, respectively.
The Company’s deferred revenues related primarily to our zPREDICTA contract research revenue and maintenance plans of our Skyline Medical operating
segment. As of December 31, 2021 and 2020, deferred revenue was $186,951 and $53,028, respectively.
Practical Expedients
The Company has elected the practical expedient not to determine whether contracts with customers contain significant financing components as well as
the practical expedient to recognize shipping and handling costs at point of sale.
Valuation and accounting for stock options and warrants
The Company determines the grant date fair value of options and warrants using a Black-Scholes option valuation model based upon assumptions
regarding risk-free interest rate, expected dividend rate, volatility and estimated term.
The fair value of each option and warrant grant is estimated on the grant date using the Black-Scholes option valuation model with the following
assumptions:
Expected dividend yield
Expected stock price volatility
Risk-free interest rate
Expected life (years)
Expected dividend yield
Expected stock price volatility
Risk-free interest rate
Expected life (years)
For the Year Ended December 31,
2021
0.0%
-
-
10
0.0%
84.8%
-
Stock Options
89.6%
1.66%
82.6%
0.13%
Warrants
0.69%
5.5
82.6%
0.135%
5/
2020
0.0%
-
-
10
0.0%
-
-
87%
1.78%
87%
0.79%
5.5
84.8%
0.93%
0.42%
5/
F- 16
Research and Development
Research and development costs are charged to operations as incurred. Research and development costs were $315,850 and $372,710 for the years ended
2021 and 2020, respectively.
Other Expense
Other expense consisted primarily of interest expense, payment penalties, amortization of original issue discounts, and loss on debt extinguishment
associated to the Company’s notes payable.
Offering Costs
Costs incurred which are direct and incremental to an offering of the Company’s securities are deferred and charged against the proceeds of the offering,
unless such costs are deemed to be insignificant in which case they are expensed as incurred.
Income Taxes
The Company accounts for income taxes in accordance with ASC 740, Income Taxes (“ASC 740”). Under ASC 740, deferred tax assets and liabilities are
determined based on the differences between the financial reporting and tax bases of assets and liabilities and net operating loss and credit carryforwards
using enacted tax rates in effect for the year in which the differences are expected to impact taxable income. Valuation allowances are established when
necessary to reduce deferred tax assets to the amounts expected to be realized.
The Company reviews income tax positions expected to be taken in income tax returns to determine if there are any income tax uncertainties. The
Company recognizes tax benefits from uncertain tax positions only if it is more likely than not that the tax positions will be sustained on examination by
taxing authorities, based on technical merits of the positions. The Company has identified no income tax uncertainties.
Under Internal Revenue Code Section 382, certain stock transactions which significantly change ownership could limit the amount of net operating
carryforwards that may be utilized on an annual basis to offset taxable income in future periods. The Company has not yet performed an analysis of the
annual net operating loss carryforwards and limitations that are available to be used against taxable income. Consequently, the limitation, if any, could
result in the expiration of the Company’s loss carryforwards before they can be utilized. The Company has not analyzed net operating loss carryforwards
under Section 382 to date. As a result of the Helomics acquisition, there may be significant limitation to the net operating loss. In addition, the current NOL
carryforwards might be further limited by future issuances of our common stock.
Tax years subsequent to 2001 remain open to examination by federal and state tax authorities due to unexpired net operating loss carryforwards.
Credit Risk
Financial instruments which potentially subject the Company to concentrations of credit risk consist principally of cash. The Company places its cash with
high credit quality financial institutions and, by policy, generally limits the amount of credit exposure to any one financial institution. As of December 31,
2021. the Company did not have credit risk for cash amounts held in a single institution that are in excess of amounts issued by the Federal Deposit
Insurance Corporation.
Risks and Uncertainties
The Company is subject to risks common to companies in the medical device and biopharmaceutical industries, including, but not limited to, development
by the Company or its competitors of new technological innovations, dependence on key personnel, protection of proprietary technology, and compliance
with regulations of the Food and Drug Administration, Clinical Laboratory Improvement Amendments, and other governmental agencies.
F- 17
The Company has evaluated all of its activities and concluded that no other subsequent events have occurred that would require recognition in the
consolidated financial statements or disclosure in the notes to the consolidated financial statements, except as described above and in Note 16 – Subsequent
Events.
NOTE 2 – zPREDICTA ACQUISITION
On November 24, 2021, the Company entered into an Agreement and Plan of Merger (the “Agreement”) among the Company, a wholly-owned subsidiary
of the Company (the “Merger Sub”), zPREDICTA, and a representative for certain parties who held interests in zPREDICTA. Also on November 24, 2021,
the Company acquired zPREDICTA through the merger of Merger Sub with and into zPREDICTA, with zPREDICTA surviving as a wholly-owned
subsidiary of the Company.
As consideration for the acquisition, the stockholders and certain holders of interests in zPREDICTA as of immediately prior to the transaction collectively
received consideration of approximately $10.0 million in cash. The Agreement contains customary and negotiated representations, warranties, and
indemnity provisions.
The acquisition costs of $895,297 related to the acquisition are presented in legal, accounting and consulting expenses within general and administrative
expenses in the accompanying consolidated statements of net loss.
The following table summarizes the acquisition date fair values of assets acquired and liabilities assumed, and the consideration transferred:
Cash consideration
Assets acquired:
Cash
Accounts receivable
Prepaid expenses
Intangible assets
Liabilities assumed:
Accrued expenses
Deferred tax liability
Deferred revenue
Goodwill
$
10,015,941
425,727
76,549
25,733
3,780,000
(408,825)
(661,658)
(79,375)
$
6,857,790
The purchase price allocation has been derived from estimates. The Company’s judgements used to determine the estimated fair value assigned to each
class of assets acquired and liabilities assumed can materially affect the consolidated operations of the consolidated Company. The total purchase price has
been allocation to identifiable assets acquired and liabilities assumed based upon valuation studies and procedures performed to date. The fair value and
useful life for the intangible assets are (a) tradename $80,000 b) developed technology $3,500,000 and c) customer relationships $200,000 with useful lives
of 4 years, 10 years and 10 years, respectively all using a straight-line method.
The Company acquired zPREDICTA through a non-taxable reverse triangular merger combination. As part of purchase accounting there was $3,780,000 in
fair value assigned to purchased intangibles which the Company established a related deferred tax liability as a result of the stock merger combination that
offset the acquired deferred assets including NOL’s and other temporary timing differences.
Identifiable Intangible Assets
The Company acquired intangible assets related to trademarks for the acquired zPREDICTA trade name with an estimated fair market value of $80,000.
The fair values of the asset were determined by the relief-from-royalty method under the income approach. The Company determined the asset is a finite
lived asset. The useful life of the tradename has a remaining useful life of 4 years as of December 31, 2021.
The Company acquired intangible assets with a useful life of 10 years and an estimated value of $200,000 related to customer relationships stemming from
stable and predictable cash flow streams associated with customers. zPREDICTA’s customer base includes contract research partnerships with
pharmaceutical, diagnostic, biotechnology, and research companies. The customer relationships were valued using the distributor method under the income
approach.
F- 18
The Company acquired intangible assets with a useful life of 10 years and an estimated value of $3,500,000 related to developed technology stemming
from the 3D tumor model technology. Since the model technology was identified as the primary asset, this technology was valued using the multi-period
excess earnings method under the income approach.
Goodwill
Goodwill of $6,857,790 was recognized in the zPREDICTA acquisition and represents the excess of the consideration transferred over the fair values of
assets acquired and liabilities assumed and represents the future economic benefits and synergies arising from the transaction. None of the goodwill will be
deductible for income tax purposes. See Note 10 – Goodwill and Intangibles.
Financial Results
The financial results of zPREDICTA since the acquisition date have been included in the Company’s accompanying consolidated statements of net loss.
Pro Forma
The following pro forma information presents the combined results of operations of the Company and zPREDICTA as if the acquisition of zPREDICTA
had been completed on January 1, 2020, with adjustments to give effect to pro forma events that are directly attributable to the acquisition.
Revenue
Net loss attributable to common shareholders
2021
Unaudited
2020
Unaudited
$
$
2,429,786 $
(18,878,432) $
1,815,560
(26,946,564)
The primary adjustments include the inclusion of the revalued amortization for zPREDICTA intangible assets. The unaudited pro forma results do not
reflect any operating efficiencies or potential cost savings which may result from the consolidation of operations. Accordingly, these unaudited pro forma
results are presented for informational purposes only and are not necessarily indicative of what the actual results of operations of the combined company
would have been if the acquisition had occurred at the beginning of those respective time periods, nor are they indicative of future results of operations.
There are certain portions of purchase accounting, specifically Section 382 for Tax Loss Carryforwards, which take place after a company has undergone a
shift in ownership, that the Company has not completed yet and may have a significant impact on the financial statements.
NOTE 3 – INVENTORIES
Inventories are stated at the lower of cost or net realizable value, with cost determined on a first-in, first-out basis. Inventory balances consist of the
following:
Finished goods
Raw materials
Work-In-Process
Total
December 31,
2021
December 31,
2020
$
$
193,287 $
183,410
10,987
387,684 $
95,898
151,366
42,271
289,535
F- 19
NOTE 4 – STOCKHOLDERS’ EQUITY, STOCK OPTIONS AND WARRANTS
Authorized Shares
At the special meeting on August 17, 2021, the stockholders approved a proposal to increase the number of authorized shares of common stock to
200,000,000 shares of common stock, $0.01 par value. The amendment to the certificate of incorporation to affect this increase was filed on August 17,
2021.
2021 Offerings
In January and February 2021, the Company completed a series of five offerings, all of which were priced at-the-market under applicable NASDAQ rules.
The first four offerings were registered direct offerings of common stock under its shelf registration statement, and in each such case, in a concurrent
private placement, the Company also issued such investors one warrant to purchase common stock for each two shares purchased in the transaction.
Following those four offerings, the Company completed a private placement of common stock, with each investor receiving one warrant to purchase
common stock for each two shares purchased in the transaction. In June 2021, the Company completed a registered direct offering of common stock and
warrants. The warrants became exercisable on the effective date of an increase in the number of shares of the Company’s authorized common stock, which
occurred on August 17, 2021, and expire three years after the initial exercise date. In each case, each such investor warrant is exercisable immediately upon
issuance and will expire five and one-half years from the issue date. In each case, the Company paid to the placement agent an aggregate fee equal to 7.5%
of the aggregate gross proceeds received by the Company in the offering and a management fee equal to 1% of the aggregate gross proceeds received by
the Company in the offering and reimbursed the placement agent for certain non-accountable and out-of-pocket expenses. In addition, the Company
granted to the placement agent, or its assigns warrants to purchase 7.5% of the shares sold to investors in the offering at an exercise price equal to 125% of
the price of the shares in the transaction, with a term of five years for the registered direct offerings (three years for the June 2021 offering) or five and one-
half years for the private placement.
These 2021 offerings were as follows:
Exercise
Price per
Share –
investor
Warrants
Exercise
Price per
Share –
Placement
Agent
Placement
Agent
Gross
Proceeds of
Net
Proceeds of
Offering
Offering
Sale Price
per Share*
Investor
Warrants
Shares
Warrants
Warrants
0.80
3,650,840 $
2,200,000 $
0.842 1,825,420 $
Offering Closing Date
January 12, 2021 (registered
direct)
January 21, 2021 (registered
direct)
January 26, 2021 (registered
direct)
February 16, 2021 (registered
direct)
February 23, 2021 (private
placement)
June 16, 2021 (registered
direct)
Total
* Sale price includes one share and a warrant to purchase one-half share (or one whole share in the case of the June 16, 2021 offering).
1.375 15,520,911 $
26,786,843
1.25 1,164,068 $
2,853,958
15,520,911 $
38,057,775
1.75 2,111,144 $
1.95 4,521,883 $
1.20 1,707,485 $
1.00 1,100,000 $
9,043,766 $
4,222,288 $
3,414,970 $
316,672 $
678,282 $
165,000 $
273,813 $
256,123 $
2.00
2.00
1.20
1.00
1.0525 $ 3,074,007 $ 2,731,767
1.25 $ 2,200,000 $ 1,932,050
1.50 $ 4,097,964 $ 3,668,687
2.1875 $ 7,389,004 $ 6,679,989
2.4375 $ 17,635,344 $ 16,064,739
1.71875 $ 21,341,252 $ 19,446,296
$ 55,737,571 $ 50,523,528
F- 20
2021 Warrant Exercises
During the year ended December 31, 2021, the holders of outstanding investor warrants have exercised such warrants for the total purchase of 5,269,059
shares at a weighted average exercise price of $0.86 per share, for total proceeds of $4,513,871.
Equity Line
On October 24, 2019, the Company entered into an equity purchase agreement with an investor, providing for an equity financing facility. Upon the terms
and subject to the conditions in the purchase agreement, the investor is committed to purchase shares having an aggregate value of up to $15,000,000 of the
Company’s common stock for a period of up to three years. The Company issued to the investor 104,651 commitment shares at a fair market value of
$450,000 for entering into the agreement. From time to time during the three-year commitment period, provided that the closing conditions are satisfied,
the Company may provide the investor with put notices to purchase a specified number of shares subject to certain limitations and conditions and at
specified prices, which generally represent discounts to the market price of the common stock. During the year ended December 31, 2020, the Company
issued 4,231,073 shares of common stock valued at $4,891,348 pursuant to the equity line. As of December 31, 2021, there was $9,113,829 of remaining
available balance under the equity line, subject to shareholder approval required for additional purchases, as well as requirements for market conditions
including trading volume and stock price, and subject to other limitations. During the year ended December 31, 2021, the Company issued 647,504, shares
of its common stock valued at $675,590 pursuant to the equity line.
Series D Preferred Stock
In April 2019, the Company issued 3,500,000 shares of Series D preferred stock to Helomics as part of its acquisition of Helomics. Each share of Series D
preferred stock is subject to automatic conversion, whereby each such share converts automatically on a 10:1 basis into a share of the Company’s common
stock upon the earlier of (1) the consummation of any fundamental transaction (e.g., a consolidation or merger, the sale or lease of all or substantially all of
the assets of Predictive or the purchase, tender or exchange offer of more than 50% of the outstanding shares of voting stock of Predictive,) or (2) the one-
year anniversary of the issuance date. On April 4, 2020, 3,500,000 shares of Series D convertible preferred stock were converted into 350,004 shares of
common stock.
Series E Convertible Preferred Stock
In June through September 2019, the Company entered into a private placement securities purchase agreement with investors for shares of Series E
convertible preferred stock. The Company issued 258 preferred shares. Each preferred shareholder had the right to convert each Series E convertible
preferred share into 0.056857% of the issued and outstanding shares of common stock immediately prior to conversion for each share of Series E
convertible stock, beginning six months after the initial close date of June 13, 2019. On the date that is 12 months after the initial closing date, the
Company has the option to convert the preferred shares into common stock upon the same terms and limitations as the above optional conversion. The
preferred shares included a contingent beneficial conversion amount of $289,935, representing the intrinsic value of the shares at the time of issuance. The
Company determined the Series E convertible preferred stock should be classified as permanent equity and the beneficial conversion feature amount was
accreted through the earliest redemption date of December 13, 2019.
F- 21
During the first quarter of 2020, 50 shares of Series E convertible preferred stock were converted into 141,191 shares of common stock. In May 2020, we
notified the holders of our Series E Convertible Preferred Stock of our election to convert the outstanding shares of Series E Stock into common stock
effective on June 13, 2020 pursuant to the terms of the Series E Stock. Prior to the conversion, there were 207.7 shares of Series E Stock outstanding. Each
share of Series E Stock converted into 0.056857% of the issued and outstanding shares of common stock immediately prior to conversion; therefore, the
207.7 outstanding shares of Series E Stock on June 13, 2020 converted into 1,257,416 shares of common stock equal to 11.8% of the outstanding shares of
common stock as of June 12, 2020.
March 2020 Private Placement
On March 18, 2020, we sold and issued to private investors (i) 260,000 shares of common stock, at a sale price of $2.121 per share; (ii) prefunded warrants
to acquire 1,390,166 shares of common stock, sold at $2.12 per share and exercisable at an exercise price of $0.001 per share; (iii) Series A warrants to
acquire 1,650,166 shares of Common Stock at $1.88 per share, exercisable immediately and terminating five and one-half years after the date of issuance;
and (iv) Series B warrants to acquire 1,650,166 shares of Common Stock at $1.88 per share, exercisable immediately and terminating two years after the
date of issuance. See below for amendment dated September 23, 2020.
In addition, and in lieu of common shares, the investors also purchased prefunded warrants to purchase 1,390,166 shares of common stock at a purchase
price of $2.12 per prefunded warrant, which represents the per share offering price, minus the $0.0001 per share exercise price of each such prefunded
warrant. As a result of the prefunded warrants exercise price being of a nominal amount, these warrants were included as outstanding shares within our
earnings per share calculation during the period from purchase through to exercise during the second quarter 2020.
The sale of the offering shares, prefunded warrants and A and B warrants resulted in gross proceeds of $3,498,612 and net proceeds of $3,127,818 after
deducting the placement agent fees and estimated offering expenses payable by the Company. The Company agreed to use the net proceeds from the
offering for general corporate purposes. The offering closed on March 18, 2020, subject to the satisfaction of customary closing conditions.
Effective September 23, 2020, the Company amended the terms of A and B warrants. Earlier in September, the Company notified the holders of the
warrants that the Company would accept an exercise price therefor of $0.8457, amended from the original exercise price of $1.88 per share. The
amendment also modified the settlement provisions of the warrants under certain circumstances; this change resulted in a classification change from
derivative liability to equity classification. See Note 7 –– Derivatives for discussion of A, B and agent warrants accounted for as derivative liabilities prior
to September 23, 2020.
Dr. Schwartz Note Exchange
Effective as of April 21, 2020, the Company and Carl Schwartz, entered into an exchange agreement relating to a promissory note of the Company dated
January 31, 2020 issued by the Company in the principal amount of $2,115,000. Pursuant to the exchange agreement, Dr. Schwartz was issued 1,583,481
shares of newly issued common stock at an exchange rate of $1.43 per share. See Note 5 – Notes Payable.
May 2020 Registered Direct Offering and Concurrent Private Placement of Warrants
During May 2020, the Company entered into a securities purchase agreement with certain accredited investors for a registered direct offering of 1,396,826
shares of common stock, par value $0.01 per share. In a concurrent private placement, the Company also issued such investors warrants to purchase up to
an aggregate of 1,396,826 shares of common stock. The shares and the warrants were sold at a combined offering price of $1.575 per share and associated
warrant. Each warrant is exercisable immediately upon issuance at an exercise price of $1.45 per share and will expire five and one-half years from the
issue date. The sale of the offering shares and associated warrants resulted in gross proceeds of $2,200,001 and net proceeds of $1,930,100 after deducting
the placement agent fees and offering expenses payable by the Company. The Company used the net proceeds from the offering to repay certain
indebtedness and agreed to use the remaining net proceeds from the offering for general corporate purposes. The offering closed on May 8, 2020.
F- 22
Acquisition from Soluble Therapeutics and BioDtech
On May 27, 2020, the Company entered into an Asset Purchase Agreement with InventaBioTech, Inc. (“InventaBioTech”) and two of its subsidiaries,
Soluble Therapeutics, Inc. (“Soluble”), and BioDtech, Inc. (“BioDtech”), and simultaneously completed the acquisition of substantially all of Soluble’s and
BioDtech’s assets. In exchange, the Company issued 125,000 shares of common stock and waived all existing claims that the Company has or may have
against InventaBioTech (f/k/a CytoBioscience, Inc.), including the nonpayment of $1,290,000 owing by InventaBioTech to the Company. All of the shares
issued in the acquisition were deposited into escrow, with 25,000 released upon the six-month anniversary of the closing, 25,000 released upon the nine-
month anniversary of the closing, and the remaining shares released on May 26, 2021. Notwithstanding the foregoing, all or some of the escrow shares may
be released and returned to the Company for reimbursement in the event that the Company suffers a loss against which InventaBioTech, Soluble, and
BioDtech have indemnified the Company pursuant to the Agreement. The Company is also entitled to reclaim 10,000 of the shares if, within six months of
the closing, the Company is unable to successfully obtain ownership of all of Soluble’s interest under its license agreement with the UAB Research
Foundation. As a result of the acquisition, which was treated as an asset acquisition, the Company recognized fixed assets of $1,492,500.
June 2020 Warrant exercise and issuance
During June 2020, the Company entered into an agreement with certain accredited institutional investors to immediately exercise for cash an aggregate of
1,396,826 of the warrants issued in connection with the May 2020 Registered Direct Offering, exercisable immediately at the exercise price of $1.45 per
share of common stock plus an additional $0.125 for each new warrant to purchase up to a number of shares of common stock equal to 100% of the number
of shares issued pursuant to the exercise of the existing warrants. The new warrants are exercisable immediately and have a term of five and one-half years
and an exercise price per share equal to $1.80. The Company received $2,130,701 in gross proceeds and net proceeds of $1,865,800 after deducting the
placement agent fees and offering expenses payable by the Company.
Effective on September 23, 2020, the Company amended the terms of warrants to purchase up to 1,396,826 shares of the Company’s common stock, par
value $0.01 per share. The amendment modified the settlement provisions of the warrants under certain circumstances; this change resulted in a
classification change from derivative liability to equity classification.
Acquisition of Quantitative Medicine
On July 1, 2020, the Company entered into an Asset Purchase Agreement with Quantitative Medicine LLC (“QM”), a Delaware limited liability company
and its owners and simultaneously completed the acquisition of substantially all of QM’s assets owned by Seller. QM is a biomedical analytics and
computational biology company that developed a novel, computational drug discovery platform called CoRE. CoRE is designed to dramatically reduce the
time, cost, and financial risk of discovering new therapeutic drugs by predicting the main effects of drugs on target molecules that mediate disease. In
exchange for QM’s assets, including CoRE, the Company provided consideration in the form of 954,719 shares of common stock, which, when issued, had
a fair value of $1,470,267. One half of the shares issued, or 477,359 shares were deposited and held in escrow upon issuance, while 207,144 of the
remaining shares were issued to Carnegie Mellon University (“CMU”) in satisfaction of all pre-closing amounts owed to CMU under a technology
licensing agreement that was assumed by the Company on the closing date. Half of the shares held in escrow were released on the six-month anniversary of
the closing date, and the other half was released on the one-year anniversary of the closing date.
F- 23
Warrants Issued in Connection with Helomics Acquisition
Effective on September 14, 2020, the Company amended the terms of warrants to purchase up to 1,424,506 shares of the Company’s common stock, par
value $0.01 per share, which were issued to certain holders in connection with the Company’s merger transaction with Helomics on April 4, 2019. In
September 2020, the Company notified the holders of the warrants that the Company will accept an exercise price of $0.845, equal to the last reported per
share price of Common Stock on the NASDAQ Capital Market on September 11, 2020, amended from the original exercise price of $10.00 per share (as
adjusted for a one-for-ten (1:10) reverse stock split that was effective on October 29, 2019). The value of the amendment was determined based on the
increase in the fair value on the date of modification using the Black Scholes method and equaled $554,287. The amendment was accounted for as a
deemed dividend and increased the loss attributable to the common shareholders when calculating earnings per share. The Warrants were issued on April 4,
2019 to holders of warrants in Helomics; the Warrants expire on April 4, 2024. See Note 8 – Loss per Share.
Equity Incentive Plan
The Company has an equity incentive plan, which allows issuance of incentive and non-qualified stock options, stock appreciation rights, stock awards,
restricted stock, restricted stock units and performance awards to employees, directors and consultants of the Company, where permitted under the plan.
The exercise price for each stock option is determined by the market price on the date of issuance. Vesting requirements are determined by the Board of
Directors when granted and currently range from immediate to three years. Options outstanding under this plan have a contractual life of ten years.
At the special meeting on August 17, 2021, the stockholders approved a proposal to increase the reserve shares of common stock authorized for issuance
under the Amended and Restated 2012 Stock Incentive Plan by 1,500,000 to 3,250,000 reserve shares.
Options and Warrants
ASC 718, Compensation – Stock Compensation, (“ASC 718”) requires that a company that issues equity as compensation needs to record compensation
expense on its statements of net loss that corresponds to the estimated cost of those equity grants. ASC 718 requires companies to estimate the fair value of
stock-based payment awards on the date of grant using an option-pricing model or other acceptable means.
The Company determines the grant date fair value of options and warrants using a Black-Scholes option valuation model based upon assumptions
regarding risk-free interest rate, expected dividend rate, volatility and estimated term. See Note 1 – Summary of Significant Accounting Policies –
Accounting Policies and Estimates.
The following summarizes transactions for stock options and warrants for the periods indicated:
Stock Options
Warrants
Number of
Shares
Average
Exercise
Price
Number of
Shares
Average
Exercise
Price
Outstanding at December 31, 2019
766,424 $
11.34
2,171,610 $
Issued
Forfeited
Exercised
319,851
(72,728)
-
1.03
10.58
-
8,097,468
(128,710)
(2,786,992)
Outstanding at December 31, 2020
1,013,547 $
5.41
7,353,376 $
Issued
Forfeited
Expired
Exercised
147,230
(92,593)
-
(5,313)
1.06
8.64
-
0.74
29,640,801
-
(25,233)
(5,269,059)
Outstanding at December 31, 2021
1,062,871 $
4.83
31,699,885 $
F- 24
15.26
1.55
95.11
0.79
1.99
1.44
-
10.00
0.86
1.66
At December 31, 2021, 949,615 stock options are fully vested and currently exercisable with a weighted average exercise price of $5.27 and a weighted
average remaining term of 8.14 years. There are 31,725,118 warrants that are fully vested and exercisable. At December 31, 2020, 977,420 stock options
are fully vested and currently exercisable with a weighted average exercise price of $5.29 and a weighted average remaining term of 8.76 years. There were
7,353,376 warrants that are fully vested and exercisable as of December 31, 2020. Stock-based compensation recognized in 2021 and 2020 was $146,714
and $780,269, respectively. The Company has $70,324 of unrecognized compensation expense related to non-vested stock options that are expected to be
recognized over the next 19 months.
The following summarizes the status of options and warrants outstanding at December 31, 2021:
Range of Exercise Prices
Options:
0.72 – 1.10
$1.15 – 1.64
$2.610 – 8.41
$10.10 – 5,962.50
Total
Warrants:
$0.80-1.72
$1.80 – 2.18
$2.25 – 10.00
$10.71 – 22.50
Total
Weighted
Average
Remaining
Life
9.31
8.36
8.15
5.99
3.31
4.50
3.37
2.94
Shares
335,876
356,673
214,937
155,385
1,062,871
21,468,599
8,451,287
1,555,778
224,221
31,699,885
Stock options and warrants expire on various dates from August 2022 to November 2031.
Stock Options and Warrants Granted by the Company
The following table is the listing of outstanding stock options and warrants as of December 31, 2021 by year of grant:
Stock Options:
Year
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
Total
Shares
F- 25
114
146
84
394
9,174
214,555
78,325
314,963
303,199
141,917
1,062,871
Price
$1.54 – $1,500.00
1.54 – 5,962.50
1.54 – 3,468.75
1.54 – 862.50
1.54 – 42.50
1.54 – 21.00
1.54 – 13.50
1.54 – 7.50
0.73 – 3.48
0.72 – 1.47
$0.72 – $5,962.50
Warrants:
Year
2017
2018
2019
2020
2021
Total
Shares
108,435
196,946
1,690,286
2,010,144
27,694,074
31,699,885
Price
$10.71 – $22.50
8.36 – 13.125
0.845 – 11.80
0.845 – 2.992
0.80 – 2.992
$0.80 – $22.50
NOTE 5– NOTES RECEIVABLE
The Company had a secured promissory note receivable from CytoBioscience for $1,112,524 (“2017 Promissory Note”), plus interest paid monthly at the
per annum rate of (8%) on the principal amount. Unpaid principal and unpaid accrued interest on the note were due and payable on February 28, 2020. In
2019, CytoBioscience and its parent company, InventaBioTech, paid interest in the first quarter due through April 2019. The Company had not received
any payments from CytoBioscience since the first quarter of 2019. The Company had evaluated the feasibility of repayment and concluded that it was
probable that the Company would be unable to collect all amounts due according to the contractual terms of the receivable. During 2019, the Company
recorded a valuation allowance of $1,037,524 related to the notes receivable balance. During 2019, the Company also recorded a loss on this note for the
uncollected balance.
On May 27, 2020, the Company entered into an Asset Purchase Agreement with InventaBioTech, Inc. (“InventaBioTech”) and two of its subsidiaries,
Soluble Therapeutics, Inc. (“Soluble”), and BioDtech, Inc. (“BioDtech”), and simultaneously completed the acquisition of substantially all of Soluble’s and
BioDtech’s assets. In exchange, the Company issued 125,000 shares of common stock and waived all existing claims that the Company has or may have
against InventaBioTech (f/k/a CytoBioscience, Inc.). Prior to the completion of the transaction, InventaBioTech owed the Company approximately
$1,290,000 under the 2017 Promissory Note, which was secured by certain intellectual property and equipment useful in CRO. In connection with the asset
purchase agreement, the Company recognized a gain on the note previously determined to be uncollectable of $1,290,000 and recognized fixed assets of
$1,492,500.
NOTE 6 – NOTES PAYABLE
The balances of notes payable were as follows:
2018 Investor loan
Promissory note 2019
Promissory note 2020
Total Notes Payable, gross
Less: Unamortized discount
Total Notes Payable, net
Secured Notes and Repayment in Full
Due Date
March 31, 2021
March 27, 2021
March 31, 2021
December 31, 2021
$
$
December 31,
2020
1,721,776
1,490,833
1,464,146
4,676,755
244,830
4,431,925
- $
-
-
-
-
- $
In September 2018, the Company issued convertible secured promissory notes to two private investors in the original principal amount of an aggregate
$2,297,727 (together, the “2018 Investor Note”) in exchange for cash proceeds of $2,000,000. As additional consideration for the 2018 Investor Note, the
Company issued an aggregate 65,000 shares of its common stock as inducement shares plus warrants to acquire up to an aggregate 107,178 shares of
common stock at an exercise price of $11.55 per share. Pursuant to a security agreement between the Company and the investors, the Company granted to
the investors a security interest in its assets to secure repayment of the note. The 2018 Investor Note accrued interest at a rate of 8% per annum. In February
2019, the Company entered into a forbearance agreement with the 2018 Investor Note investors pursuant to which, among other things, the investors agreed
to forbear on their rights to accelerate the 2018 Investor Note based on an event of default and a claimed event of default. In connection with such
forbearance, an additional $344,659 in principal and an additional 16,667 common shares were issued to the investors. In September 2019, the 2018
Investor Note of one investor was paid in full. On March 19, 2020, the Company and the L2 Capital, LLC (“L2”) agreed to extend the note maturity to June
28, 2020. The Company and L2 further agreed to extend the due date to July 15, 2020 and then in July 2020 agreed to extend to September 30, 2020.
Effective September 30, 2020, L2 and the Company agreed to extend to March 31, 2021.
F- 26
Each investor received the right to convert all or any part of its portion of the 2018 Investor Note into shares of the Company’s common stock at a
discounted price, subject to certain limitations. During the year ended December 31, 2020, L2 converted $267,328 of the principal balance, and received
170,000 shares of the Company’s common stock.
During September 2019, the Company issued a secured promissory note with a principal amount of $847,500 (the “2019 Investor Note”) to Oasis Capital,
LLC (“Oasis”), an affiliate of L2, in exchange for cash proceeds of $700,000. As additional consideration for the loan, the Company issued an aggregate
8,857 shares of its common stock to Oasis plus warrants to acquire up to 68,237 shares of the Company’s common stock at an exercise price of $6.21 per
share. The warrants are exercisable beginning on the sixth month anniversary of the effective date through the fifth-year anniversary thereof. The 2019
Investor Note accrued interest at a rate of 8% per annum. On March 19, 2020, the Company entered into an agreement to extend the due date the 2019
Investor Note from March 2020 to June 27, 2020. The Company increased the principal amount due on the 2019 Investor Note by $300,000 and issued
30,000 shares of its common stock as consideration for the extension. The change in value resulting from the extension exceeded 10% and as a result the
extension was accounted for as an extinguishment under ASC 470, Debt. During the first quarter of 2020, the Company incurred a $300,000 loss on debt
extinguishment related to the extension of the note. The Company and Oasis further agreed to extend the due date of the note to July 15, 2020 and then
agreed to extend to September 30, 2020. The change in value resulting from the extension to September 30, 2020 exceeded 10% and as a result the
extension was accounted for as an extinguishment under ASC 470, Debt. During the third quarter of 2020, the Company incurred a $345,000 loss on debt
extinguishment related to the extension of the 2019 Investor Note to September 30, 2020. Effective September 30, 2020, Oasis and the Company agreed to
further extend the maturity date of the 2019 Investor Note to March 31,2021. The change in value resulting from the extension to March 31, 2021 exceeded
10% and as a result the extension was accounted for as an extinguishment under ASC 470, Debt. During the third quarter of 2020, the Company incurred a
$690,000 loss on debt extinguishment related to the extension of the note to March 31, 2021. Further, the parties agreed that the note shall be convertible
into shares of the Company’s common stock, at a conversion price equal to the lesser of (i) $1.00 and (ii) 70% of the lowest VWAP (as defined in the note)
of the Company’s common stock during the twenty (20) Trading Day (as defined) period ending on either (i) the last complete Trading Day prior to the
conversion date or (ii) the conversion date, as determined by the holder in its sole discretion upon such conversion (subject to adjustment). During the
fourth quarter of 2020, Oasis converted $525,000 in outstanding principal of the 2019 Investor Note in exchange for 1,136,448 shares of the Company’s
common stock. No payment penalties were paid in relation to payments on this promissory note during the year ended December 31, 2020 and $320,542 in
payment penalties were accrued but not paid as of December 31, 2020. As of December 31, 2020, the remaining balance on the promissory note was
$1,490,833 with $244,830 unamortized discount.
On February 5, 2020, the Company issued a secured promissory note with a principal amount of $1,450,000 (the “2020 Investor Note”) to Oasis. Net
proceeds of $400,000 were received for each of the first, second, and third tranches on February 5, 2020, March 5, 2020, and April 5, 2020, respectively.
The Company granted to Oasis a security interest in its assets to secure repayment of the note. The 2020 Investor Note accrued interest at a rate of 8% per
annum. Subject to certain limitations, the outstanding principal amount of the note and interest thereon were convertible at the election of the investor into
shares of the Company’s common stock at a conversion price equal to $2.589. The conversion price was amended effective September 30, 2020 to a
variable price equal to 70% of the lowest VWAP (as defined in the note) of Company’s common stock during the twenty (20) Trading Day (as defined in
the note) period ending on either (i) the last complete Trading Day prior to the conversion date or (ii) the conversion date, as determined by the holder in its
sole discretion upon such conversion (subject to adjustment). The note contains a conversion feature and a put which were determined to be derivatives and
are discussed further below. Effective July 15, 2020, the Company and Oasis agreed to amend the maturity date of the note to September 30, 2020. The
change in value resulting from the amendment to maturity to September 30, 2020 exceeded 10% and as a result the amendment was accounted for as an
extinguishment under ASC 470, Debt. During the third quarter of 2020, the Company incurred a $172,500 loss on debt extinguishment related to the
amendment of the note to September 30, 2020. Effective September 30, 2020, the investor and the Company agreed to further extend the maturity date of
the 2020 Investor Note to March 31, 2021. The change in value resulting from the extension to March 31, 2021 exceeded 10% and as a result the extension
was accounted for as an extinguishment under ASC 470, Debt. During the third quarter of 2020, the Company incurred a $345,000 loss on debt
extinguishment related to the extension of the note to March 31, 2021. As additional consideration, the Company issued to Oasis warrants to purchase
94,631, 92,700 and 92,700 shares of the Company’s common stock at the closing of the first, second and third tranches, respectively. The warrants are
exercisable beginning on the sixth month anniversary of the issuance date at an exercise price equal $2.992 per share. The Company also issued 46,875
shares of its common stock to Oasis at the closing of the first tranche. During the fourth quarter of 2020, Oasis converted $503,354 in outstanding principal
in exchange for 1,075,911 shares of the Company’s common stock. No payment penalties were paid in relation to payments on this promissory note during
the year ended December 31, 2020 and $314,011 in payment penalties were accrued but not paid as of December 31, 2020. As of December 31, 2020, the
outstanding balance on the promissory note was $1,464,146 with no remaining unamortized discount.
F- 27
On March 1, 2021, the Company used $5,906,802 of the proceeds of the private placement on February 23, 2021, described below under “2021 Offerings”,
to repay in full the outstanding principal and interest and applicable premium amounts under the 2018 Investor Note, the 2019 Investor Note and the 2020
Investor Note.
Dr. Schwartz Notes
In November 2018, Dr. Schwartz made a loan to the Company with a principal balance of $370,000. As of December 31, 2018, one promissory note was
held with a principal balance of $370,000 and an unamortized discount of $63,028. From November 30, 2018 through July 15, 2019, Dr. Schwartz made
numerous loans to the Company in the total amount of $1,920,000 under two promissory notes. As consideration for these amounts, Dr. Schwartz received
promissory notes and warrants to purchase 22,129 shares of the Company’s common stock at $8.36 per share. Further, beginning on February 1, 2019 and
the first day of each calendar month thereafter while the note remained outstanding, a number of additional warrants were issued. Beginning in October
2019, the Company and Dr Schwartz began to renegotiate the note. Due to the negotiations, the Company did not issue any additional warrants because
they would be cancelled under the new deal.
During January 2020, the Company entered into an exchange agreement with Dr. Schwartz. Under the exchange agreement, the two outstanding notes were
cancelled and in exchange a new promissory note in the amount of $2,115,000 bearing 12% interest per annum and maturing on September 30, 2020 was
issued. In addition to the promissory note, Dr. Schwartz received 50,000 shares of the Company’s common stock. All warrants issued under the prior
promissory notes were cancelled under the exchange agreement; no rights and obligations remain under the cancelled notes. The Company determined that
the exchange agreement had, in substance, occurred at December 31, 2019.
Effective as of April 21, 2020, the Company and Carl Schwartz, entered into an exchange agreement relating to a promissory note of the Company dated
January 31, 2020 issued by the Company in the principal amount of $2,115,000. The note bore twelve percent (12%) interest per annum and had a maturity
date of September 30, 2020. The accrued interest on the note through April 21, 2020 was $77,878, resulting in a total balance of $2,192,878 in principal
and accrued interest on the Note as of such date. Dr. Schwartz and the Company agreed to exchange the note for newly issued shares of common stock of
the Company at market value. Pursuant to the exchange agreement, Dr. Schwartz was issued 1,583,481 shares of newly issued common stock at an
exchange rate of $1.43 per share, equal to the closing price of the common stock on April 21, 2020. Dr. Schwartz agreed (1) not to sell or otherwise transfer
766,740 shares for three months after the date of the exchange agreement, and (2) not to sell or otherwise transfer the remaining 766,741 shares for six
months after the date of the exchange agreement. In 2021, the Company determined that due to a calculation error, the balance of the 2020 Schwartz Note
should have been higher by $143,573 at the time of the exchange agreement, and on February 24, 2021, the Company issued an additional 100,401 shares
to Dr. Schwartz.
F- 28
Short Term Borrowings
The Company entered into short-term borrowings with an investor. The maturity date of the notes is six months after the dates of issuance with interest
rates of 8% payable at maturity. Repayment of such notes is subject to a premium. During year ended December 31, 2020, the Company issued short term
notes for a total of $1,098,684 for cash proceeds of $1,020,000 and repaid $1,459,973 of principal using a portion of proceeds from the equity financing
facility. Payment penalties of $247,327 were paid in relation to payments on these short-term borrowings during the year ended December 31, 2020. There
were no amounts outstanding under the short-term borrowings as of December 31, 2020.
April 2020 Paycheck Protection Program
On April 20, 2020, the Company entered into a promissory note with Park State Bank, which provides for an unsecured loan of $541,867 pursuant to the
Paycheck Protection Program (the “PPP”) under the Coronavirus Aid, Relief, and Economic Security Act and applicable regulations (the “CARES Act”).
The promissory note has a term of 2 years with a 1% per annum interest rate. Payments are deferred for 6 months from the date of the promissory note and
the Company can apply for forgiveness of all or a portion of the promissory note after 60 days for covered use of funds.
Pursuant to the terms of the PPP, the promissory note, or a portion thereof, may be forgiven if proceeds are used for qualifying expenses as described in the
CARES Act, such as payroll costs, costs used to continue group health care benefits, mortgage interest payments, rent and utilities. The Company has used
all proceeds for qualifying expenses. The Company received forgiveness for the loan under the Paycheck Protection Program and recognized a gain in other
income for the full amount of the loan during the fourth quarter of 2020.
NOTE 7 - DERIVATIVES
The Company concluded the September 2018 Investor Note contained a conversion feature which is an embedded derivative and required bifurcation. The
embedded derivative’s value was determined using the discounted stock price for the 20-trading days preceding the balance sheet date and the assumption
of conversion on that date, as management believed it was probable that the notes would be convertible based on management’s expectation that additional
financing would be required. During the year ended December 31, 2020, the maximum number of conversions was reached. The Company recognized an
unrealized gain for the corresponding change in fair value of $50,989 for the year ended December 31, 2020. The fair value of the derivative liability
related to the bridge loan was zero as of December 31, 2020.
The Company concluded the Promissory Note 2020 contained a conversion feature and a put each of which was an embedded derivative and are required to
be bifurcated. In accordance with ASC 815, Derivatives and Hedging, the Company combined these two embedded derivatives into a single derivative and
determined the fair value to record within the derivative liability on the consolidated balance sheet. At inception, the fair value of the derivative liability
was $68,796, $52,125 and $20,542 for the first, second and third tranches, respectively. During the year ended December 31, 2020, the Company
recognized a gain of $87,923 on the change in the fair value of the derivative liability. As a result of the repayment of the note as of March 1, 2021, the
embedded derivative had a fair value of zero prior to the repayment. The Company recorded a gain on the fair value of the derivative of $104,529 during
the year ended December 31, 2021. As of December 31, 2020, the fair value of the derivative liability was $104,529.
The Company concluded the A, B and agent warrants issued in connection with the March 2020 Private Placement discussed above are a derivative
liability due to certain features of the warrants which could, in certain circumstances, result in the holder receiving the Black Scholes value of the
outstanding warrants in the same type of consideration as the common stockholders. As a result, in those circumstances, the amount of consideration would
differ from that provided to holders of common stock, therefore, the warrants were classified as a liability. At inception, the A, B and agent warrants had a
fair value of $2,669,995. During the third quarter of 2020, the A and B warrants were amended as discussed in Note 6 - Notes Payable above. As a result of
this amendment, the warrants no longer represented a liability to the Company and were reclassified to equity. Prior to reclassification, a gain on the change
in fair value of $700,910 was recorded during the year ended December 31, 2020. As of December 31, 2021, the fair value of the agent warrants was
determined to be $41,336 and the Company recorded a loss on the change in fair value of $7,683 during the year ended December 31, 2021. As of
December 31, 2020, the fair value of the agent warrants was determined to be $33,654 and the Company recorded a gain on the change in fair value of
$69,479 during the year ended December 31, 2020.
F- 29
The Company concluded the warrants and agent warrants issued in connection with the May 2020 Offering discussed above are a derivative liability due to
certain features of the warrants which could, in certain circumstances, result in the holder receiving the Black Scholes value of the outstanding warrants in
the same type of consideration as the common stockholders. As a result, in those circumstances, the amount of consideration would differ from that
provided to holders of common stock, therefore, the warrants were classified as a liability. At inception, the warrants and agent warrants had a fair value of
$1,324,184. The Company recorded a loss on the change in fair value of the warrants of $460,065 during the year ended December 31, 2020. During June
2020, the investors exercised the warrants and exchanged the warrants for shares of common stock as discussed above. The fair value of the agent warrants
was determined to be $33,819 and $42,646 as of December 31, 2021 and as of December 31, 2020, respectively. The Company recorded a loss on the
change in fair value of the agent warrants of $8,827 during the year ended December 31, 2021 and a gain on the change in fair value of the agent warrants
of $48,675 during the year ended December 31, 2020.
In connection with the June 2020 Warrant exercise and issuance, the Company concluded the warrants and agent warrants issued in connection with the
June 2020 Warrant exercise and issuance, discussed above, are a derivative liability due to certain features of the warrants which could, in certain
circumstances, result in the holder receiving the Black Scholes value of the outstanding warrants in the same type of consideration as the common
stockholders. As a result, in those circumstances, the amount of consideration would differ from that provided to holders of common stock, therefore, the
warrants were classified as a liability. At inception, the warrants and agent warrants had a fair value of $1,749,721. During the year ended December 31,
2020, the June warrants were amended. As a result of this amendment, the warrants no longer represented a liability to the Company and were reclassified
to equity. Prior to reclassification, the Company recorded a gain on the change in fair value of the warrants of $834,520 during the year ended December
31, 2020. The Company recorded a loss on the change in fair value of the agent warrants of $12,797 during the year ended December 31, 2021 and a gain
on the change in fair value of the agent warrants of $79,045 during the year ended December 31, 2020. The fair value of the agent warrants was $45,498
and $32,701 as of December 31, 2021 and as of December 31, 2020, respectively.
On September 30, 2020, the Promissory Note 2019 was amended. The Company concluded the Promissory Note 2019 contained a conversion feature
which is an embedded derivative and is required to be bifurcated. In accordance with ASC 815, Derivatives and Hedging, the Company determined the fair
value to record within the derivative liability on the consolidated balance sheet. At inception, the fair value of the derivative liability was $495,100. As a
result of the repayment of the note as of March 1, 2021, the embedded derivative had a fair value of zero prior to the repayment. The Company recorded a
gain on the fair value of the derivative of $89,680 during the year ended December 31, 2021. The Company recorded a gain on the change in fair value of
the derivative liability of $405,420 during the year ended December 31, 2020. As of December 31, 2020, the fair value of the derivative liability was
$89,680.
F- 30
The table below discloses changes in value of the Company’s embedded derivative liabilities discussed above.
Derivative liability balance at December 31, 2019
Derivative instrument recognized for A, B and Agent Warrants
Derivative instrument related to Promissory Note 2020
Derivative instrument recognized for May 2020 Warrants
Derivative instrument recognized for June 2020 Warrants
Derivative instrument related to Promissory Note 2020
Reclassification of Warrant liabilities to Equity on exercise
Reclassification of Warrant liabilities to Equity
Derivative instrument related to September 30 debt amendments
Gain recognized to revalue derivative instrument at fair value
Derivative liability balance at December 31, 2020
Gain recognized to revalue derivative instrument at fair value
Derivative liability balance at December 31, 2021
NOTE 8 - LOSS PER SHARE
$
$
$
50,989
2,669,995
120,921
1,324,184
1,749,721
20,542
(1,701,756)
(2,669,408)
495,100
(1,765,906)
294,382
(164,902)
129,480
The following table presents the shares used in the basic and diluted loss per common share computations:
Year Ended
December 31,
2021
2020
Numerator:
Net loss attributable to common shareholders per common share: basic and diluted calculation
$
(19,657,174) $
(26,438,684)
Denominator:
Weighted average common shares outstanding-basic
Effect of diluted stock options, warrants and preferred stock (1)
Weighted average common shares outstanding-diluted
Loss per common share-basic and diluted
54,876,044
-
54,876,044
(0.36) $
11,950,154
-
11,950,154
(2.21)
$
(1) The following is a summary of the number of underlying shares outstanding at the end of the respective periods that have been excluded from the
diluted calculations because the effect on loss per common share would have been anti-dilutive:
Options
Warrants
Convertible debt
Preferred stock: Series B
NOTE 9 – INCOME TAXES
Year Ended December 31,
2020
2021
1,062,871
31,699,885
-
79,246
1,013,547
7,353,376
1,107,544
79,246
The provision for income taxes consists of an amount for taxes currently payable and a provision for tax consequences deferred to future periods. Deferred
income taxes are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets
and liabilities and their respective tax bases. Deferred income tax assets and liabilities are measured using enacted tax rates expected to apply to taxable
income in the years in which those temporary differences are expected to be recovered or settled.
F- 31
The Company recognized an income tax benefit of $661,658 in our consolidated statement of net loss related to the release of valuation allowance as a
result of the zPREDICTA business combination. However, due to the cumulative operating losses, the Company determined that a 100% valuation
allowance for the net deferred tax assets at December 31st is appropriate.
Actual income tax benefit differs from statutory federal income tax benefit as follows:
Statutory federal income tax benefit
State tax benefit, net of federal taxes
Foreign tax benefit
Foreign operations tax rate differential
State rate adjustment
Nondeductible/nontaxable items
Goodwill impairment
NOL adjustments
Other
Valuation allowance increase
Total income tax benefit
Deferred taxes consist of the following:
Deferred tax assets:
Noncurrent:
Inventory
Compensation accruals
Accruals and reserves
Deferred revenue
Charitable contribution carryover
Derivatives
Intangibles
Right of use asset
NSQO compensation
NOL and credits
Total deferred tax assets
Deferred tax liabilities:
Noncurrent:
Depreciation
Total deferred tax liabilities
Net deferred tax assets
Less: valuation allowance
Total
Year Ended December 31,
2020
2021
4,266,955 $
793,282
-
-
5,153
(260,768)
(605,420)
(612,588)
150,083
(3,075,039)
661,658 $
5,434,463
578,746
62,146
(44,120)
65,112
(268,968)
(2,762,014)
(1,141,662)
(461,020)
(1,462,683)
-
$
$
December 31, 2021
December 31,
2020
$
- $
58,829
50,537
26,198
1,095
27,859
700,876
18,543
1,602,429
82,814,111
85,300,477
7,196
63,846
162,628
11,641
4,331
63,145
295,941
13,861
1,738,217
80,038,356
82,400,860
(120,353)
(120,353)
(295,775)
(295,775)
85,180,124
(85,180,124)
- $
82,105,085
(82,105,085)
-
$
The Company has determined, based upon its history, that it is probable that future taxable income may be insufficient to fully realize the benefits of the net
operating loss (“NOL”) carryforwards and other deferred tax assets. As such, the Company has determined that a full valuation allowance is warranted.
Future events and changes in circumstances could cause this valuation allowance to change.
F- 32
The acquired NOL carryforwards from zPREDICTA experienced an ownership change as defined in Section 382 of the Internal Revenue Code as a result
of the merger. In addition, the Company experienced an ownership change in 2019 with the Helomics acquisition as well as December 2013. As a result,
the ability to utilize the Company’s NOLs is limited. The Company may have experienced additional ownership changes since December 2013, but a
formal study has not yet been performed. The general limitation rules allow the Company to utilize its NOLs subject to an annual limitation that is
determined by multiplying the federal long-term tax-exempt rate by the Company’s value immediately before the ownership change.
At December 31, 2020, the Company had $297,735,754 of gross NOLs to reduce future federal taxable income, the majority of which are expected to be
available for use in 2021, subject to the Section 382 limitation described above. The federal NOL’s of $261,455,216 expire beginning in 2022 if unused and
$36,280,538 will carryforward indefinitely. The Company also had $222,290,524 of gross NOLs to reduce future state taxable income at December 31,
2020. The state NOL’s will expire beginning in 2021 if unused. The Company dissolved its Belgium subsidiary in 2020 and all carryforward tax losses will
be eliminated on the final 2020 Belgium tax return filed. The Company's net deferred tax assets, which include the NOLs, are subject to a full valuation
allowance. At December 31, 2020, the federal, state, and foreign valuation allowances were $59,913,739, $22,191,346, and $0, respectively.
At December 31, 2021, the Company had $308,990,822 of gross NOLs to reduce future federal taxable income, the majority of which are expected to be
available for use in 2022, subject to the Section 382 limitation described above. The federal NOL’s of $259,490,005 expire beginning in 2023 if unused and
$49,500,817 will carryforward indefinitely. The Company also had $227,277,399 of gross NOLs to reduce future state taxable income at December 31,
2021. The state NOL’s will expire beginning in 2022 if unused. The Company's net deferred tax assets, which include the NOLs, are subject to a full
valuation allowance. At December 31, 2021, the federal and state valuation allowances were $62,034,750 and $23,145,374 respectively.
Tax years subsequent to 2001 remain open to examination by federal and state tax authorities due to unexpired net operating loss carryforwards.
The Company reviews income tax positions expected to be taken in income tax returns to determine if there are any income tax uncertainties. The
Company recognizes tax benefits from uncertain tax positions only if it is more likely than not that the tax positions will be sustained on examination by
taxing authorities, based on technical merits of the positions. The Company has identified no income tax uncertainties.
The Company recognizes interest and penalties on unrecognized tax benefits as well as interest received from favorable tax settlements within income tax
expense. At December 31, 2021 and 2020, the Company recorded no accrued interest or penalties related to uncertain tax positions.
NOTE 10 – Goodwill and Intangibles
Intangible Assets
Finite-lived intangible assets consist of patents and trademarks, licensing fees, developed technology, acquired software and customer relationships, and are
amortized over their estimated useful life. Amortization expense was $374,328 and $313,709 in 2021 and 2020, respectively. Accumulated amortization is
included in intangibles, net in the accompanying consolidated balance sheets. The Company reviews finite-lived identifiable intangible assets for
impairment in accordance with ASC 360, Property, Plant and Equipment, whenever events or changes in circumstances indicate the carrying amount may
not be recoverable. Events or changes in circumstances that indicate the carrying amount may not be recoverable include, but are not limited to, a
significant change in the medical device marketplace and a significant adverse change in the business climate in which the Company operates.
F- 33
As of December 31, 2021, there were $3,962,118 in net intangibles as compared to $3,398,101 in net intangibles as of December 31, 2020.
The components of intangible assets were as follows:
December 31, 2021
December 31, 2020
Patents & Trademarks
Developed Technology
Customer Relationships
Tradename
Total
Accumulated
Amortization Impairment
Gross
Carrying
Costs
$
453,314 $
6,382,000
645,000
478,000
Gross
Carrying
Costs
(230,572) $
401,421 $
(432,733) (2,485,725) 3,463,542 2,882,000
445,000
(410,000)
398,000
(29,344)
$ 7,958,314 $ (1,102,649) $ (2,893,548) $ 3,962,118 $ 4,126,421 $
Net
Carrying
Amount
(37,083)
(370,740)
197,917
77,917
222,742 $
- $
The following table outlines the estimated future amortization expense related to intangible assets held as of December 31, 2021:
Year ending December 31,
2022
2023
2024
2025
2026
Thereafter
Total
Impairment of Long-Lived Assets
Accumulated
Amortization
Net
Carrying
Amount
(211,110) $
190,311
(252,175) 2,629,825
185,417
(259,583)
392,548
(5,452)
(728,320) $ 3,398,101
Expense
411,609
411,610
411,610
409,526
391,610
1,926,153
3,962,118
$
$
The Company reviews long-lived assets, including property and equipment and intangible assets with estimable useful lives, for impairment whenever
events or changes in circumstances indicate that the carrying amount of such an asset may not be recoverable.
The recoverability of an asset to be held and used is determined by comparing the carrying amount to the estimated undiscounted future cash flows
expected to be generated by the asset. If the carrying amount of the asset exceeded its estimated undiscounted future cash flows, the Company recorded an
impairment charge in the amount by which the carrying amount of the asset exceeds its fair value, which is determined by either a quoted market price, if
any, or a value determined by utilizing discounted cash flow techniques.
The Company prepared an undiscounted cash flow as of December 31, 2021 to evaluate long-lived assets based on a triggering event per ASC 360. The
Company concluded that the undiscounted cash flows did not support the carrying values of its Helomics asset group at December 31, 2021. The Company
determined the value of the intangibles and the software license acquired were fully impaired as of December 31, 2021 and recognized and impairment loss
of $2,893,548 for its long-lived intangible assets and $1,249,727 for the acquired software. The Company concluded there was no impairment of its other
finite lived tangible assets as of December 31, 2021. No impairment charges were incurred during 2020.
Goodwill
In accordance with ASC 350, Intangibles – Goodwill and Other, goodwill is calculated as the difference between the acquisition date fair value of the
consideration transferred and the fair value of net assets acquired. Goodwill is an asset representing the future economic benefits arising from other assets
acquired in a business combination. Goodwill is an indefinite-lived asset and is not amortized. Goodwill is tested for impairment annually at the reporting
unit level, or whenever events or circumstances present an indication of impairment.
F- 34
In the Helomics acquisition, the Company recorded goodwill of $23,790,290. The goodwill was recorded to the Helomics segment which represents a
single reporting unit. As a part of the annual impairment testing as of December 31, 2019, the Company had the option to assess qualitative factors to
determine if it was more likely than not that the carrying value of a reporting unit exceeded its estimated fair value. The Company believed a qualitative
testing approach was not appropriate and, therefore, proceeded to the quantitative testing. When performing quantitative testing, the Company first
estimated the fair value of the Helomics reporting unit using discounted cash flows. To determine fair values, the Company was required to make
assumptions about a wide variety of internal and external factors. Significant assumptions used in the impairment analysis included financial projections of
free cash flow (including significant assumptions about operations including the rate of future revenue growth, capital requirements, and income taxes),
long-term growth rates for determining terminal value, and discount rates for the Helomics reporting unit. Comparative market multiples were also used to
corroborate the results of the discounted cash flow test. These assumptions required significant judgment and actual results may differ from assumed and
estimated amounts.
In testing goodwill for impairment as of September 30, 2020, the Company performed a quantitative impairment test, including computing the fair value of
the Helomics reporting unit and comparing that value to its carrying value. Based upon the Company’s quantitative goodwill impairment test, the Company
concluded that goodwill was impaired as of the testing date of September 30, 2020. Pursuant to ASU 2017-04, Simplifying the Test for Goodwill
Impairment, the single step is to determine the estimated fair value of the reporting unit and compare it to the carrying value of the reporting unit, including
goodwill. To the extent the carrying amount of goodwill exceeds the implied goodwill, the difference is the amount of the goodwill impairment. The
quantitative review as of September 30, 2020 resulted in $2,997,000 of impairment expense related to goodwill.
When evaluating the fair value of Helomics reporting unit the Company used a discounted cash flow model and market comparisons. Key assumptions
used to determine the estimated fair value included: (a) expected cash flow for the 20-year period following the testing date (including net revenues, costs
of revenues, and operating expenses as well as estimated working capital needs and capital expenditures); (b) an estimated terminal value using a terminal
year growth rate of 3.0% determined based on the growth prospects of the reporting unit; and (c) a discount rate of 25% based on management’s best
estimate of the after-tax weighted average cost of capital. The discount rate included a Company specific risk premium of 10% for risks related to the term
of the forecasts.
In testing goodwill for impairment as of December 31, 2020, the Company performed a quantitative impairment test, including computing the fair value of
the Helomics reporting unit and comparing that value to its carrying value. Based upon the Company’s annual goodwill impairment test, the Company
concluded that goodwill was impaired as of the testing date of December 31, 2020. The Company’s annual impairment test as of December 31, 2020
resulted in $9,879,498 of impairment expense related to goodwill. A decrease in the growth rate of 0.5% or an increase of 0.5% to the discount rate would
reduce the fair value of Helomics reporting unit by approximately an additional $588,000 and $988,000, respectively. As of December 31, 2020, the
cumulative impairment recorded was $20,976,498.
When evaluating the fair value of Helomics reporting unit the Company used a discounted cash flow model. Key assumptions used to determine the
estimated fair value in 2020 included: (a) expected cash flow for the 10-year period following the testing date (including net revenues, costs of revenues,
and operating expenses as well as estimated working capital needs and capital expenditures); (b) an estimated terminal value using a terminal year growth
rate of 5.0% determined based on the growth prospects of the reporting unit; and (c) a discount rate of 14.0% based on management’s best estimate of the
after-tax weighted average cost of capital. The discount rate included a Company specific risk premium of 1.0% for risks related to the term of the
forecasts. The Company further used a probability weighting of various forecasts to address forecast risk.
F- 35
During the third quarter of 2021, the Company concluded that potential impairment indicators were present and that an impairment assessment was
warranted for goodwill. In testing goodwill for impairment as of September 30, 2021, the Company performed a quantitative impairment test, including
computing the fair value of the Helomics reporting unit and comparing that value to its carrying value. Based upon the Company’s quantitative goodwill
impairment test, the Company concluded that goodwill was fully impaired as of September 30, 2021.
The quantitative review as of September 30, 2021 resulted in $2,813,792 of impairment expense related to goodwill. As of September 30, 2021, the
cumulative impairment recorded was $23,790,290.
When evaluating the fair value of Helomics reporting unit the Company used a discounted cash flow model and market comparisons. Key assumptions
used to determine the estimated fair value included: (a) expected cash flow for the 10-year period following the testing date (including net revenues, costs
of revenues, and operating expenses as well as estimated working capital needs and capital expenditures); (b) an estimated terminal value using a terminal
year growth rate of 4.0% determined based on the growth prospects of the reporting unit; and (c) a discount rate of 15% based on management’s best
estimate of the after-tax weighted average cost of capital. The Company further used a probability weighting of various forecasts to address forecast risk.
Goodwill of $6,857,790 was recognized in the zPREDICTA acquisition and represents the excess of the consideration transferred over the fair values of
assets acquired and liabilities assumed and represents the future economic benefits and synergies arising from the transaction. None of the goodwill will be
deductible for income tax purposes. See Note 2 – zPREDICTA acquisition.
The following tables present changes in the carrying value of goodwill our consolidated balance sheet:
Goodwill balance at December 31, 2019
Impairment
Goodwill balance at December 31, 2020
Impairment
Acquisition of zPREDICTA
Goodwill balance at December 31, 2021
$
$
$
15,690,290
(12,876,498)
2,813,792
(2,813,792)
6,857,790
6,857,790
The majority of the inputs used in the discounted cash flow model are unobservable and thus are considered to be Level 3 inputs. The inputs for the market
capitalization calculation are considered Level 1 inputs. The Company will continue to monitor its reporting units to determine whether events and
circumstances warrant further interim impairment testing.
NOTE 11 – LEASES
Our corporate offices are located in Eagan, Minnesota. The lease as amended has a three-year term ended January 31, 2021. We lease 5,773 square feet at
this location, of which 2,945 square feet is used for office space and 2,828 is used for manufacturing. The lease was amended subsequent to December 31,
2020 for one additional year until January 31, 2022, and has a second amended six-month term until July 31, 2022. Management and the landlord have
orally agreed to further extensions as needed.
The offices of our Helomics subsidiary are located in Pittsburgh, Pennsylvania. The lease, as amended, has a three-year term ending February 28, 2023. We
lease 17,417 square feet at this location, of which approximately 1,000 square feet are used for office space and 16,417 square feet is used for laboratory
operations.
zPREDICTA’s offices are located in San Jose, California. We lease approximately 1,236 square feet at this location. The lease is month-to-month tenancy.
Soluble Biotech’s offices are located in Birmingham, Alabama. We lease approximately 4,314 square feet at this location. The lease is effective through
August 25, 2025.
TumorGenesis’s offices are located in Salem, Massachusetts. We lease approximately 1,450 square feet at this location. The lease is effective through May
31, 2023.
F- 36
Skyline Medical Europe’s offices were located in Belgium. The Company leased around 2,000 square feet at this location, 750 square feet of which is used
for storage and 1,250 square feet is used for office space. The lease was terminated in the fourth quarter of 2020.
Lease expense under operating lease arrangements was $595,669 and $565,581 for 2021 and 2020, respectively.
The following table summarizes other information related to the Company’s operating leases:
Weighted average remaining lease term – operating leases in years
Weighted average discount rate – operating leases
December 31, 2021
1.69
8%
December 31, 2020
2.33
8%
The Company’s lease obligation as of December 31, 2021 which includes expected lease extensions that are reasonable certain of renewal, are as follows:
2022
2023
2024
2025
Total lease payments
Less interest
Present value of lease liabilities
NOTE 12 – Property, Plant and Equipment
Fixed Assets
The Company’s fixed assets consist of the following:
Computers, software and office equipment
Laboratory equipment
Leasehold improvements
Manufacturing tooling
Demo equipment
Total
Less: Accumulated depreciation
Total fixed assets, net
$
$
751,345
188,931
71,420
48,552
1,060,248
180,922
879,326
December 31,
2021
December 31,
2020
$
$
517,488 $
3,456,091
428,596
121,120
56,614
4,579,909
2,068,338
2,511,571 $
1,862,669
2,811,011
315,297
108,956
56,614
5,154,547
1,331,847
3,822,700
Upon retirement or sale or fixed assets, the cost and related accumulated depreciation are removed from the balance sheet and the resulting gain or loss is
reflected in operations expense. Maintenance and repairs are expensed as incurred.
The Company prepared an undiscounted cash flow as of December 31, 2021 to evaluate long-lived assets based on a triggering event per ASC 360. The
Company concluded that the undiscounted cash flows did not support the carrying values of its Helomics asset group at December 31, 2021. The Company
determined the value of the intangibles and the software license acquired were fully impaired as of December 31, 2021 and recognized and impairment loss
of $2,893,548 for its long-lived intangible assets and $1,249,727 for the acquired software. The Company concluded there was no impairment of its other
finite lived tangible assets as of December 31, 2021.
F- 37
Depreciation expense was $965,973 and $711,139 in 2021 and 2020, respectively.
NOTE 13 – SEGMENTS
The Company has determined its reportable segments in accordance with ASC 280, Segment Reporting. Factors used to determine the Company’s
reportable segments include the availability of separate financial statements, the existence of locally based leadership across geographic regions, the
economic factors affecting each segment, and the evaluation of operating results at the segment level. The Chief Operating Decision Maker (“CODM”)
allocates the Company’s resources for each of the reportable segments and evaluates their relative performance. Each reportable segment listed below has
separate financial statements and locally based leadership that are evaluated based on the results of their respective segments. It should be noted that the
reportable segments below have different products and services. The financial information is consolidated and evaluated regularly by the CODM in
assessing performance and allocating resources.
During the third quarter of 2020, the Company considered, whether under ASC 280-10-50-3, there was a change in its reportable segments. As a result of
the formation of the new Soluble subsidiary, the Company believes the Soluble business represents a reportable segment. Soluble signed its first contract
during the third quarter of 2020. The Company also believes it is appropriate to combine our Skyline Medical and Skyline Europe entities into a single
reportable segment based on the changes to our physical presence and intent to sign future contracts through the US entity. Finally, the Company believes
the Helomics business continues to be a reportable segment.
The Company has four reportable segments: Helomics, zPREDICTA, Soluble and Skyline. See discussion of revenue recognition in Note 1 – Summary of
Significant Accounting Policies for a description of the products and services recognized in each segment. The reported financial information below has
been reclassified to conform to the current presentation. This information is intended to assist investors in making comparisons of the Company’s historical
financial information with future financial information.
The table below summarizes the Company’s segment reporting as of and for years ended December 31, 2021 and 2020.
Year Ended December 31, 2021
Skyline
Helomics
Soluble
$
Revenue
Depreciation and Amortization
Impairment expense – goodwill
Impairment expense – intangibles
Impairment expense – acquired software
$
Net loss
1,169,811 $
(30,002)
-
-
-
(520,822) $
13,367 $
(886,642)
(2,813,792)
(2,893,548)
(1,249,727)
(11,326,948) $
233,293 $
(366,713)
-
-
-
(1,251,564) $
zPREDICTA Corporate
90 $
(40,625)
-
-
-
531,446 $
Total
1,420,680
(1,340,301)
(2,813,792)
(2,893,548)
(1,249,727)
(7,089,286) $ (19,657,174)
4,119 $
(16,319)
-
-
-
Assets
Skyline
Helomics
Soluble
zPREDICTA Corporate
$
906,977 $
1,802,792 $
1,742,445 $
10,782,568 $
28,536,489 $
Total
43,771,271
December 31, 2021
F- 38
Revenue
Depreciation and Amortization
Impairment expense
Net loss
$
$
1,185,214 $
(38,310)
-
(1,132,251) $
64,188 $
(761,105)
(12,876,498)
(15,112,131) $
2,870 $
(184,071)
-
(671,367) $
Total
1,252,272
(1,024,848)
(12,876,498)
(8,968,648) $ (25,884,397)
- $
(41,362)
-
Skyline
Year Ended December 31, 2020
Soluble
Helomics
Corporate
Assets
Skyline
Helomics
December 31, 2020
Soluble
Corporate
$
1,191,439 $
9,773,902 $
1,883,585 $
211,510 $
Total
13,060,436
In 2021, substantially all the Company revenues were located or derived from operations in the United States. As of December 31, 2021, all of the
Company’s long-lived assets were located within the United States.
NOTE 14 – RELATED PARTY TRANSACTIONS
The Audit Committee has the responsibility to review and approve all transactions to which a related party and the Company may be a party prior to their
implementation, to assess whether such transactions meet applicable legal requirements.
One of the Company’s former directors, Richard L. Gabriel, is the Chief Operating Officer of GLG Pharma (“GLG”) and serves as a director of that firm.
The Company and GLG have a partnership agreement for the purpose of bringing together their proprietary technologies to build out personalized medicine
platform for the diagnosis and treatment of women’s cancer. There has been no revenue or expenses generated by this partnership to date.
Richard L. Gabriel was also contracted as the Chief Operating Officer for TumorGenesis. Through April 1, 2019, Mr. Gabriel received $12,000 per month
pursuant to a renewable six-month contract. On May 1, 2019, Mr. Gabriel executed a one-year contract with renewable three-month periods to continue as
the Chief Operating Officer for TumorGenesis, receiving $13,500 in monthly cash payments.
Effective May 1, 2021, Richard Gabriel resigned as a member of the Company’s Board of Directors. Mr. Gabriel’s resignation is in connection with his
assuming a management position with the Company, and not due to any disagreements with the Company on any of our operations, policies or practices.
NOTE 15 – RETIREMENT SAVINGS PLANS
The Company has a pre-tax salary reduction/profit-sharing plan under the provisions of Section 401(k) of the Internal Revenue Code, which covers
employees meeting certain eligibility requirements. During 2019 and 2018, the Company matched 100% of the employee’s contribution up to 4.0% of their
earnings. The employer contribution was $127,953 and $119,555 in 2021 and 2020, respectively. There were no discretionary contributions to the plan in
2021 and 2020.
NOTE 16 – SUBSEQUENT EVENTS
Equity Line Agreement
During the first quarter of 2022 through March 28, the Company issued 120,000 shares of its common stock valued at $86,885 pursuant to the equity line.
F-39
Description of Registrant’s Securities
Exhibit 4.14
As of March 25, 2022, Predictive Oncology Inc. (the “Company”) has one class of securities registered under Section 12 of the Securities Exchange Act of
1934, as amended (the “Exchange Act”), namely, our common stock, par value $0.01 per share (“Common Stock”).
Description of Common Stock
The following description of our Common Stock is a summary and does not purport to be complete. It is subject to and qualified in its entirety by reference
to our Certificate of Incorporation, as amended (the “Certificate of Incorporation”), our Second Amended and Restated Bylaws, as amended (the
“Bylaws”), and the Certificate of Designation of Preferences, Rights and Limitations applicable to each series of our Preferred Stock (as defined below)
(collectively, the “Certificates of Designation”), each of which are incorporated by reference as an exhibit to the Annual Report on Form 10-K of which this
Exhibit 4.1 is a part. We encourage you to read the Certificate of Incorporation, the Bylaws, the Certificates of Designation, and the applicable provisions
of the General Corporation Law of the State of Delaware (the “DGCL”) for additional information.
Authorized Capital Stock. Our authorized capital stock consists of 200,000,000 shares of Common Stock, and 20,000,000 shares of preferred stock, $0.01
par value per share (“Preferred Stock”). Out of the Preferred Stock, as of December 31, 2021, 2,300,000 shares have been designated Series B Convertible
Preferred Stock, of which 79,246 shares were outstanding
The outstanding shares of our Common Stock and Preferred Stock are fully paid and nonassessable.
The Series B Convertible Preferred Stock is convertible into Common Stock at the option of its holders on a 1:1 basis, subject to a 4.99% beneficial
ownership blocker.
Blank Check Preferred Stock. Our Board of Directors is authorized, subject to any limitations prescribed by law, to provide for the issuance of the shares of
Preferred Stock in series and, by filing a certificate pursuant to the applicable law of the State of Delaware, to establish from time to time the number of
shares to be included in each such series, and to fix the designation, powers, preferences and rights of the shares of each such series and any qualifications,
limitations or restrictions thereon. The number of authorized shares of Preferred Stock may be increased or decreased (but not below the number of shares
thereof then outstanding) by the affirmative vote of the holders of a majority of the outstanding shares of Common Stock without a vote of the holders of
the Preferred Stock, or of any series thereof, unless a vote of any such holders is required pursuant to the certificate or certificates establishing the series of
Preferred Stock.
Voting Rights. The holders of our Common Stock are entitled to one vote for each outstanding share of Common Stock owned by that shareholder on every
matter properly submitted to the shareholders for their vote. Shareholders are not entitled to vote cumulatively for the election of directors.
Dividend Rights. Subject to the dividend rights of the holders of any outstanding series of preferred stock, holders of our Common Stock are entitled to
receive ratably such dividends and other distributions of cash or any other right or property as may be declared by our Board of Directors out of our assets
or funds legally available for such dividends or distributions.
Liquidation Rights. In the event of any voluntary or involuntary liquidation, dissolution or winding up of our affairs, holders of our Common Stock would
be entitled to share ratably in our assets that are legally available for distribution to shareholders after payment of liabilities and after the satisfaction of any
liquidation preference owed to the holders of any Preferred Stock.
Conversion, Redemption and Preemptive Rights. Holders of our Common Stock have no conversion, redemption, preemptive, subscription or similar
rights.
Bylaws. Certain provisions of our Bylaws could have anti-takeover effects. These provisions are intended to enhance the likelihood of continuity and
stability in the composition of our corporate policies formulated by our Board of Directors. In addition, these provisions also are intended to ensure that our
Board of Directors will have sufficient time to act in what our Board of Directors believes to be in the best interests of our Company and our shareholders.
Nevertheless, these provisions could delay or frustrate the removal of incumbent directors or the assumption of control of us by the holder of a large block
of Common Stock, and could also discourage or make more difficult a merger, tender offer, or proxy contest, even if such event would be favorable to the
interest of our shareholders. These provisions are summarized below.
Advance Notice Provisions for Raising Business or Nominating Directors. Sections 2.09 and 2.10 of our Bylaws contain advance-notice
provisions relating to the ability of shareholders to raise business at a shareholder meeting and make nominations for directors to serve on our
Board of Directors. These advance-notice provisions generally require shareholders to raise business within a specified period of time prior to a
meeting in order for the business to be properly brought before the meeting.
Number of Directors and Vacancies. Our Bylaws provide that the exact number of directors shall be determined from time to time solely by
resolution adopted by the affirmative vote of a majority of the entire Board of Directors. The Board of Directors is divided into three classes, as
nearly equal in number as possible, designated: Class I, Class II and Class III (each, a “Class”). In the case of any increase or decrease, from time
to time, in the number of directors, the number of directors in each class shall be apportioned as nearly equal as possible. Except as otherwise
provided in the Certificate of Incorporation, each director serves for a term ending on the date of the third annual meeting of the Company’s
stockholders following the annual meeting at which such director was elected; provided, that the term of each director shall continue until the
election and qualification of a successor and be subject to such director’s earlier death, resignation or removal. Vacancies on the Board of
Directors resulting from death, resignation, removal or otherwise and newly created directorships resulting from any increase in the number of
directors may be filled solely by a majority of the directors then in office (although less than a quorum) or by the sole remaining director.
2
Listing. Our Common Stock is traded on the Nasdaq Capital Market under the trading symbol “POAI”.
Warrants. As of December 31, 2021, 31,699,885 shares of our common stock were issuable upon the exercise of outstanding warrants to purchase common
stock, with exercise prices ranging from $.80 to $22.50 per share and a weighted average exercise price of $1.66 per share. Generally, warrants expire after
periods ranging from three years to five and a half years after issuance. Substantially all of the warrants issued to investors have a provision that permits a
net exercise in the event that a registration statement is not effective with respect to the shares.
Options. As of December 31, 2021, 1,062,871 shares of our common stock were issuable upon the exercise of stock options to purchase common stock,
with exercise prices ranging from $.72 to $5,962.50 per share and a weighted average exercise price of $4.83 per share. Generally, options expire on the
ten-year anniversary of the issue date.
3
PREDICTIVE ONCOLOGY INC.
SUBSIDIARIES OF THE REGISTRANT
Exhibit 21.1
Subsidiary
Jurisdiction of Incorporation
Helomics Holding Corporation
TumorGenesis Inc.
Soluble Biotech Inc.
Skyline Medical, Inc.
Helomics Intermediate Corporation
Helomics Corporation
zPredicta, Inc.
Delaware
Delaware
Delaware
Delaware
Delaware
Delaware
Delaware
CONSENT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
We consent to the incorporation by reference in the Registration Statements on Form S-1 (File No. 333-239207, 333-252584, and 333-252585);
Form S-3 (File No. 333-221966, 333-228908, 333-235441, 333-237581, 333-239851, 333-254309 and 333-255582); Form S-4 (File No. 333-228031); and
Form S-8 (File No. 333-169556, 333-175565, 333-186464, 333-188510, 333-198378, 333-213742, 333-216711, 333-230704, 333-250149, and 333-
259264) of Predictive Oncology Inc. (the “Company”) of our report dated March 31, 2022, relating to the consolidated financial statements, which report
expresses an unqualified opinion on the consolidated financial statements for the year ended December 31, 2021, appearing herein.
Exhibit 23.1
/s/ Baker Tilly US, LLP
Minneapolis, Minnesota
March 31, 2022
I, J. Melville Engle, certify that:
1.
I have reviewed this annual report on Form 10-K of Predictive Oncology Inc.;
CERTIFICATION
Exhibit 31.1
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to
make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period
covered by this report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material
respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4. The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as
defined in Exchange Act Rules 13a-15(e) and 15-d-15 (e)) and internal control over financial reporting (as defined in Exchange Act Rules
13a-15(f) and 15d-15(f)) for the registrant and have:
a. Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our
supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to
us by others within those entities, particularly during the period in which this report is being prepared;
b. Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed
under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of
financial statements for external purposes in accordance with generally accepted accounting principles;
c. Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions
about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such
evaluation; and
d. Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s
most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is
reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial
reporting, to the registrant’s auditors and the audit committee of the registrant’s Board of Directors (or persons performing the equivalent
functions):
a. All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which
are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
b. Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s
internal control over financial reporting.
Date: March 31, 2022
/s/ J. Melville Engle
J. Melville Engle
Chief Executive Officer (Principal Executive Officer)
I, Bob Myers, certify that:
1.
I have reviewed this annual report on Form 10-K of Predictive Oncology Inc.;
CERTIFICATION
Exhibit 31.2
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to
make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period
covered by this report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material
respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4. The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as
defined in Exchange Act Rules 13a-15(e) and 15-d-15 (e)) and internal control over financial reporting (as defined in Exchange Act Rules
13a-15(f) and 15d-15(f)) for the registrant and have:
a. Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our
supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to
us by others within those entities, particularly during the period in which this report is being prepared;
b. Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed
under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of
financial statements for external purposes in accordance with generally accepted accounting principles;
c. Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions
about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such
evaluation; and
d. Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s
most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is
reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial
reporting, to the registrant’s auditors and the audit committee of the registrant’s Board of Directors (or persons performing the equivalent
functions):
a. All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which
are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
b. Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s
internal control over financial reporting.
Date: March 31, 2022
/s/ Bob Myers
Bob Myers
Chief Financial Officer (Principal Financial Officer)
CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER AND PRINCIPAL FINANCIAL OFFICER PURSUANT TO 18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
In connection with the Annual Report on Form 10-K of Predictive Oncology Inc. (the “Company”) for the year ended December 31, 2021 as filed with the
Securities and Exchange Commission on the date hereof (the “Report”), I, J. Melville Engle, Chief Executive Officer, and I, Bob Myers, Chief Financial
Officer, of the Company, certify, pursuant to § 906 of the Sarbanes-Oxley Act of 2002, 18 U.S.C. § 1350, that to our knowledge:
1. The Report fully complies with the requirements of Section 13(a) of the Securities Exchange Act of 1934 (15 U.S.C. 78m); and
2. The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the
Exhibit 32.1
Company.
Date: March 31, 2022
/s/ J. Melville Engle
J. Melville Engle
Chief Executive Officer
(Principal Executive Officer)
/s/ Bob Myers
Bob Myers
Chief Financial Officer
(Principal Financial Officer)
PREDICTIVE ONCOLOGY INC.
STOCK OPTION AGREEMENT
(Employee)
Exhibit 10.5
This STOCK OPTION AGREEMENT (the “Agreement”) is made and entered into effective as of [●], between Predictive Oncology Inc., a
Delaware corporation (the “Company”) and the undersigned employee (“Employee”).
BACKGROUND
A. Employee has either been hired to serve as an employee to the Company or the Company desires to induce Employee to continue to serve the
Company as an employee.
B. The Company has adopted the Amended and Restated 2012 Stock Incentive Plan (the “Plan”), pursuant to which shares of common stock of
the Company have been reserved for issuance under the Plan. Employee and the Company desire to enter into this Agreement for the granting
of stock options.
NOW, THEREFORE, the parties hereto agree as follows:
1. Grant of Option; Purchase Price. Subject to the terms and conditions herein set forth, the Company hereby irrevocably grants to Employee
the right and option, hereinafter called the “Option”, to purchase from the Company all or any part of any aggregate of [●] shares (the
“Shares”) of common stock, $0.01 par value of the Company (the “Common Stock”). The purchase price of the Shares covered by the Option
shall be $[●] per Share.
2. Exercise and Vesting of Option. The Option shall be exercisable only to the extent that all, or any portion thereof, has vested in Employee.
Except as otherwise provided herein, the Option shall vest ratably over a period of eight (8) quarters in equal quarterly installments, beginning
on [●], and continuing on the first quarter after the date of this Agreement and through each subsequent anniversary date (the “Vesting Date”)
until the Option is fully vested, as set forth in the following schedule:
No. of Shares To Be Vested
Vesting Date
In the event that Employee ceases to be employed by the Company, for any reason or no reason, prior to any Vesting Date, that portion of the
Option scheduled to vest on such Vesting Date, and all portions of the Option scheduled to vest in the future, shall not vest and all of Employee’s rights to
and under such non-vested portions of the Option shall terminate.
3. Termination of Employment. Except as provided in Section 5 below, in the event that Employee ceases to be employed by the Company, for
any reason or no reason, with or without cause, prior to any Vesting Date, that part of the Option scheduled to vest on such Vesting Date, and
all parts of the Option scheduled to vest in the future, shall not vest and all of Employee’s rights to and under such non-vested parts of the
Option shall terminate.
1
4. Term of Option. To the extent vested, and except as otherwise provided in this Agreement, the Option shall be exercisable for ten (10) years
from the date of this Agreement; provided, however, that, except as provided in Section 5 below, in the event Employee or his/her legal
representative shall have three (3) months from the date of such termination of his/her position as an employee to exercise any part of the
Option vested pursuant to Section 2 of this Agreement. Upon the expiration of such three (3) month period, except as provided in Section 5
below, or, if earlier, upon the expiration date of the Option as set forth above, the Option shall terminate and become null and void.
5. Death of Employee. In the event of Employee’s death, the person designated in Employee’s will, or in the absence of such designation,
Employee’s legal representative may, in like manner, exercise the Option to the extent of the number of Shares which were vested at the time of
his/her death, but such right shall expire unless exercised by such designated person or legal representative, within the earlier of (i) six (6)
months after the death of Employee, or (ii) the expiration of the Option.
6. Method of Exercising Option. Subject to the terms and conditions of this Agreement, the Option may be exercised, in whole or in part, by
giving written notice to the Company, specifying the number of Shares to be purchased and accompanied by the full purchase price for such
shares. Any such notice shall be deemed given when received by the Company at its corporate headquarters. The option price shall be payable
(a) in United States dollars upon exercise of the option and may be paid by cash, uncertified or certified check or bank draft; (b) by delivery of
shares of Common Stock in payment of all or any part of the option price, which shares shall be valued for this purpose at the Fair Market
Value (as defined below) on the date such option is exercised; or (c) by instructing the Company to withhold from the Shares issuable upon
exercise of the Option Shares in payment of all or any part of the exercise price and/or any related withholding tax obligations consistent with
Section 13, which shares shall be valued for this purpose at the Fair Market Value or in such other manner as may be authorized from time to
time by the Board of Directors. All Shares that shall be purchased upon the exercise of the Option as provided herein shall be fully paid and
non-assessable.
7. Rights of Option Holder. Employee as holder of the Option, shall not have any of the rights of a shareholder with respect to the Shares
covered by the Option except to the extent that one or more certificates for such Shares shall be delivered to him or her upon the due exercise
of all or any part of the Option.
8. Limitations on Transferability. Except as otherwise provided below, the Option shall not be transferred, pledged or assigned other than by
will or by the laws of decent and distribution, or pursuant to a qualified domestic relations order as defined by the Internal Revenue Code of
1986, as amended (the “Code”) or Title I of the Employee Retirement Income Security Act, or the rules there under, and the Company shall not
be required to recognize any attempted assignment of such rights. Notwithstanding the preceding sentence, the Option may be transferred by
Employee to Employee’s spouse, children, grandchildren or parents (collectively, the “Family Members”), to trusts for the benefit of Family
Members, to partnerships or limited liability companies in which Family Members are the only partners or shareholders, or to entities exempt
from federal income taxation pursuant to Section 501(c)(3) of the Code. During Employee’s lifetime, the Option may be exercised only by him
or her, by his/her guardian or legal representative or by the transferees permitted by the preceding sentence.
2
9. No Continued Employment or Right to Corporate Assets. Nothing contained in this Agreement shall be deemed to grant Employee any
right to continue in the employ of the Company for any period of time or to any right to continue his/her present or any other rate of
compensation, nor shall this Agreement be construed as giving Employee, Employee’s beneficiaries or any other person any equity or interests
of any kind in the assets of the Company or creating a trust of any kind or a fiduciary relationship of any kind between the Company and any
such person.
10. Securities Law Matters. Employee acknowledges that the Shares to be received by him or her upon exercise of the Option may not have been
registered under the Securities Act of 1933 or the Blue Sky laws of any state (collectively, the “Acts”). If such Shares have not been so
registered, Employee acknowledges and understands that the Company is under no obligation to register, under the Acts, the Shares received by
him or her or to assist him or her in complying with any exemption from such registration if he or she should at a later date wish to dispose of
the Shares. Employee acknowledges that if not then registered under the Acts, the Shares shall bear a legend restricting the transferability
thereof, such legend to be substantially in the following form:
“The shares represented by this certificate have not been registered or qualified under federal or state securities laws. The shares may not be
offered for sales, sold, pledged or otherwise disposed of unless so registered or qualified, unless an exemption exists or unless such
disposition is not subject to the federal or state securities laws, and the Company may require that the availability or any exemption or the
inapplicability of such securities laws be established by an opinion of counsel, which opinion of counsel shall be reasonably satisfactory to
the Company.”
11. Employee Representations. Employee hereby represents and warrants that Employee has reviewed with his/her own tax advisors the federal,
state, and local tax consequences of the transactions contemplated by this Agreement. Employee is relying solely on such advisors and not on
any statements or representation of the Company or any of its agents. Employee understands that he or she will be solely responsible for any tax
liability that may result to him or her as a result of the transactions contemplated by the Agreement. The Option, if exercised, will be exercised
for investment and not with a view to the sales or distribution of the Shares to be received upon exercise thereof.
12. Adjustment. In the event of any recapitalization, stock dividend, stock split, combination of shares or other change in the Common Stock, the
number of Shares then subject to the Option shall be adjusted in proportion to the change in outstanding shares of Common Stock. In the event
of any such adjustments, the purchase price of the Option shall be adjusted as and to the extent appropriate, in the discretion of the Board, to
provide Employee with the same relative rights before and after the adjustment.
13. Withholding.
a. The Company shall have the right to withhold from or to collect as a condition of payment, any taxes required by law to be withheld. At any
time when Employee is required to pay to the Company an amount required to be withheld under applicable income tax laws upon exercise of
the Option, Employee may satisfy this obligation in whole or in part by electing (the “Election”) to have the Company withhold, from such
Shares, shares of the Common Stock having a value up to the minimum amount of withholding taxes required to be collected on the
transaction. The value of the shares to be withheld shall be based on the Fair Market Value of the Common Stock on the date that the amount
of tax to be withheld shall be determined (Tax Date”).
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b. Each Election must be made before the Tax Date. The Committee may disapprove of any Election, may suspend or terminate the right to make
elections, or may provide with respect to the Option that the right to make Elections shall not apply to the Option. An Election is irrevocable.
14. Sale, Merger, Exchange or Liquidation. In the event of an acquisition of the Company through the sale of substantially all of the Company’s
assets or through a merger, exchange, reorganization or liquidation of the Company or a similar event as determined by the Board (collectively a
“transaction”), the Board shall be authorized, in its sole discretion, to take any and all action it deems equitable under the circumstances,
including but not limited to any one or more of the following:
a.
b.
c.
d.
providing that the Option shall terminate and the Employee shall receive, in lieu of any Shares they would be entitled to receive under the
vested portion of the Option, such stock, securities or assets, including cash, as would have been paid to Employee if the Option had been
exercised and Employee had received Common Stock immediately before such transaction (with appropriate adjustment for the purchase price,
if any).
providing that Employee shall receive, with respect to each share of Common Stock under the vested portion of the Option as of the effective
date of any such transaction, at the determination of the Board, cash, securities or other property, or any combination thereof, in an amount
equal to the excess, if any, of the Fair Market Value of such Common Stock on a date within ten days before the effective date of such
transaction over the Option purchase price, and that the Option shall be cancelled.
providing Employee a substantially equivalent stock option (taking into account the transaction and the number of shares or other equity issued
by such successor entity) with respect to the equity of the entity succeeding the Company by reason of such transaction.
providing that all unvested portions of the Option shall be void and deemed terminated, or, in the alternative, for the acceleration or waiver of
the vesting of the Option.
The Board may restrict the rights of Employee under this Section 14 to the extent necessary to comply with Section 16(b) of the 1934 Act, the
Internal Revenue Code of 1986, as amended, or any other applicable law or regulation. The grant of the Option shall not limit in any way the right or
power of the Company to make adjustments, reclassifications, reorganizations or changes of its capital or business structure or to merge, exchange or
consolidate or to dissolve, liquidate, sell or transfer all or any part of its business or assets.
15. Definition of Fair Market Value. For purposes of this Agreement, the “Fair Market Value” of a Share at a specified date shall be the amount
which the Board of Directors determines in good faith to be 100% of the fair market value of such a share as of the date in question.
Notwithstanding the foregoing:
a.
If such shares are listed on a U.S. securities exchange, then the Fair Market Value shall be determined by reference to the last sale price of a
Share on such U.S. securities exchange on the applicable date. If such U.S. securities exchange is closed for trading on such date, or if the
Common Stock does not trade on such date, then the last sale price used shall be the one on the date the Common Stock last traded on such
U.S. securities exchange.
4
b.
c.
If such shares are publicly traded but are not listed on a U.S. securities exchange, then Fair Market Value shall be determined by reference to
the trading price of a share of Common Stock on such date (or, if the applicable market is closed on such date, the last date on which the
Common Stock was publicly traded), be a method consistently applied by the Committee.
If such shares are not publicly traded, then the Committee’s determination will be based upon a good faith valuation of the Company’s
Common Stock as of such date, which shall be based upon such factors as the Committee deems appropriate. The valuation shall be
accomplished in a manner that complies with Code Section 409A.
16. General.
a. The Option is granted pursuant to the Plan and is governed by the terms thereof. In the event of any conflict between the terms of this
Agreement and the terms of the Plan, the terms of the Plan shall control. The Company shall at all times during the term of the Option reserve
and keep available such number of Shares as will be sufficient to satisfy the requirements of this Agreement.
b. Nothing herein expressed or implied is intended or shall be construed as conferring upon or giving to any person, firm. Or corporation other
than the parties hereto, any rights or benefits under or by reason of this Agreement.
c. Each party hereto agrees to execute such further documents as may be necessary or desirable to effect the purposes of this Agreement.
d. This Agreement may be executed in any number of counterparts, each of which shall be deemed an original, but all of which shall constitute
one and the same agreement.
e. This Agreement, in its interpretation and effect, shall be governed by the laws of the State of Minnesota applicable to contracts executed and to
be performed therein.
[Signature page follows]
5
IN WITNESS WHEREOF, the undersigned have executed this Agreement as of the date first written above.
[Signature page to Stock Option Agreement]
PREDICTIVE ONCOLOGY INC.
By______________________________
Its______________________________
EMPLOYEE:
________________________________
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PREDICTIVE ONCOLOGY INC.
NON-QUALIFIED STOCK OPTION AGREEMENT
(Executive)
Exhibit 10.6
This STOCK OPTION AGREEMENT (the “Agreement”) is made and entered into effective as of [●] between Predictive Oncology Inc., a
Delaware corporation (the “Company”) and [●] (“Employee”).
BACKGROUND
A. Employee has either been hired to serve as an employee to the Company or the Company desires to induce Employee to continue to serve the
Company as an employee.
B. The Company has adopted the Amended and Restated 2012 Stock Incentive Plan (the “Plan”), pursuant to which shares of common stock of
the Company have been reserved for issuance under the Plan.
NOW, THEREFORE, the parties hereto agree as follows:
1. Grant of Option; Purchase Price. Subject to the terms and conditions herein set forth, the Company hereby irrevocably grants from the
Plan to Employee the right and option, hereinafter called the “Option”, to purchase all or any part of an aggregate of the number of
shares of common stock, $0.01 par value, of the Company (the “Shares”) set forth at the end of this Agreement after “Number of
Shares” at the price per Share set forth at the end of this Agreement after “Purchase Price.”
2. Exercise and Vesting of Option. The Option shall be exercisable only to the extent that all, or any portion thereof, has vested in
Employee. Except as provided herein in Sections 5 and 6 hereof, the Options shall vest in equal installments of [●] shares quarterly
over two years, beginning on [●], with the last installment vesting on [●] (each such date is hereinafter referred to singularly as a
“Vesting Date” and collectively as “Vesting Dates”), so long as Employee remains an employee of the Company.
3. Termination of Employment. Except as provided in Section 5 below, in the event that Employee ceases to be employed by the
Company, for any reason or no reason, with or without cause, prior to any Vesting Date, that part of the Option scheduled to vest on
such Vesting Date, and all parts of the Option scheduled to vest in the future, shall not vest and all of Employee's rights to and under
such non-vested parts of the Option shall terminate.
4. Term of Option. To the extent vested, and except as otherwise provided in this Agreement, the Option shall be exercisable for ten (10)
years from the date of this Agreement; provided, however, that, except as provided in Section 5 below, in the event Employee ceases
to be employed by the Company, for any reason or no reason, Employee or his/her legal representative shall have three (3) months
from the date of such termination of his/her position as an employee to exercise any part of the Option vested pursuant to Section 3 of
this Agreement. Upon the expiration of such three (3) month period, except as provided in Section 5, or, if earlier, upon the expiration
date of the Option as set forth above, the Option shall terminate and become null and void.
1
5. Termination of Employment. For certain definitions in this Section 5, reference is made to the Employment Agreement dated August
11, 2012, as amended on August 20, 2018, between the Employee and the Company (as it may be amended or restated from time to
time, the “Employment Agreement”).
a.
b.
c.
In the event of a termination of employment of Employee by the Company without Cause (as defined in the Employment
Agreement) or by Employee for Good Reason (as defined in the Employment Agreement), (i) any unvested portion of the
Option shall immediately vest, and (ii) the Option shall be exercisable until the earlier of (A) five (5) years after the date of
such termination or (B) the expiration of the Option.
In the event of Employee’s voluntary termination of his employment or death on or after [●] (which will be considered his
retirement age), (i) the entire Option shall immediately vest in full to the extent not already vested and (ii) the Option shall be
exercisable by Employee or his estate or legal representative through the full remaining term of the Option.
In the event of Employee’s death, Employee’s estate or his legal representative, as the case may be, may exercise the Option
to the extent of the number of Shares which were vested at the time of his death, but such right shall expire unless exercised
by Employee’s estate or legal representative within the earlier of (i) twelve (12) months after the death of Employee, or (ii)
the expiration of the Option.
6. Change in Control. “Change in Control” has the meaning provided in the Plan. Notwithstanding anything to the contrary contained
herein, in the event of a Change in Control of the Company, the Option shall become fully vested upon the effective date of such
event, and shall remain exercisable for the remainder of the term of the Option.
7. Method of Exercising Option. Subject to the terms and conditions of this Agreement and the Plan, the Option may be exercised, in
whole or in part, by written notice to the Company. Such notice shall state the election to exercise the Option, the number of Shares in
respect of which it is being exercised, the method of exercise, and shall be signed by the person or persons exercising the Option. The
Employee may exercise the Option by (i) paying to the Company in cash the full exercise price; (ii) arranging for a broker to sell
Shares and immediately thereafter pay to the Company the full exercise price; or (iii) delivering Shares previously owned by
Employee, the total market value of which equals the full exercise. Applicable tax withholding may be paid by any method permitted
under the Plan. Upon proper exercise, the Company shall deliver a certificate or certificates representing such Shares as soon as
practicable after the notice shall be received. All Shares that shall be purchased upon the exercise of the Option as provided herein
shall be fully paid and non-assessable.
8. Rights of Option Holder. Employee, as holder of the Option, shall not have any of the rights of a shareholder with respect to the
Shares covered by the Option except to the extent that one or more certificates for such Shares shall be delivered to him or her upon
the due exercise of all or any part of the Option.
2
9. Limitations on Transferability. The Option shall not be transferred, pledged or assigned except, in the event Employee's death, by will
or the laws of descent and distribution to the limited extent provided in the Plan, or pursuant to a qualified domestic relations order as
defined by the Internal Revenue Code of 1986, as amended (the “Code”) or Title I of the Employee Retirement Income Security Act,
or the rules there under, and the Company shall not be required to recognize any attempted assignment of such rights. Notwithstanding
the preceding sentence, the Option may be transferred by Employee to Employee's spouse, children, grandchildren or parents
(collectively, the “Family Members”), to trusts for the benefit of Family Members, to partnerships or limited liability companies in
which Family Members are the only partners or shareholders, or to entities exempt from federal income taxation pursuant to Section
501(c)(3) of the Code. During Employee's lifetime, the Option may be exercised only by him or her, by his/her guardian or legal
representative or by the transferees permitted by the preceding sentence.
10. No Continued Employment or Right to Corporate Assets. Nothing contained in this Agreement shall be deemed to grant Employee any
right to continue in the employ of the Company for any period of time or to any right to continue his/her present or any other rate of
compensation, nor shall this Agreement be construed as giving Employee, Employee’s beneficiaries or any other person any equity or
interests of any kind in the assets of the Company or creating a trust of any kind or a fiduciary relationship of any kind between the
Company and any such person.
11. Securities Law Matters. Employee acknowledges that the Shares to be received by him or her upon exercise of the Option may not have
been registered under the Securities Act of 1933 or the Blue Sky laws of any state (collectively, the “Acts”). If such Shares have not
been so registered, Employee acknowledges and understands that the Company is under no obligation to register, under the Acts, the
Shares received by him or her or to assist him or her in complying with any exemption from such registration if he or she should at a
later date wish to dispose of the Shares. Employee acknowledges that if not then registered under the Acts, the Shares shall bear a
legend restricting the transferability thereof, such legend to be substantially in the following form:
“The shares represented by this certificate have not been registered or qualified under federal or state securities laws. The shares
may not be offered for sale, sold, pledged or otherwise disposed of unless so registered or qualified, unless an exemption exists or
unless such disposition is not subject to the federal or state securities laws, and the Company may require that the availability or
any exemption or the inapplicability of such securities laws be established by an opinion of counsel, which opinion of counsel shall
be reasonably satisfactory to the Company.”
12. Employee Representations. Employee hereby represents and warrants that Employee has reviewed with his/her own tax advisors the
federal, state, and local tax consequences of the transactions contemplated by this Agreement. Employee is relying solely on such
advisors and not on any statements or representation of the Company or any of its agents. Employee understands that he or she will be
solely responsible for any tax liability that may result to him or her as a result of the transactions contemplated by this Agreement. The
Option, if exercised, will be exercised for investment and not with a view to the sale or distribution of the Shares to be received upon
exercise thereof.
3
13. General.
a. The Option is granted pursuant to the Plan and is governed by the terms thereof. In the event of any conflict between the
terms of this Agreement and the terms of the Plan, the terms of the Plan shall control. The Company shall at all times during
the term of the Option reserve and keep available such number of Shares as will be sufficient to satisfy the requirements of
this Agreement.
b. Nothing herein expressed or implied is intended or shall be construed as conferring upon or giving to any person, firm, or
corporation other than the parties hereto, any rights or benefits under or by reason of this Agreement.
c. Each party hereto agrees to execute such further documents as may be necessary or desirable to affect the purposes of this
Agreement.
d. This Agreement may be executed in any number of counterparts, each of which shall be deemed an original, but all of which
shall constitute one and the same agreement.
e. This Agreement, in its interpretation and effect, shall be governed by the laws of the State of Delaware applicable to
contracts executed and to be performed therein.
[Signature page follows]
4
IN WITNESS WHEREOF, the undersigned have executed this Agreement as of the date first written above.
[Signature page to Non-Qualified Stock Option Agreement]
NUMBER OF SHARES:
____________________
PREDICTIVE ONCOLOGY INC.
PURCHASE PRICE:
____________________ per share
By:___________________
Its:___________________
EMPLOYEE:
By:___________________
Its:___________________
5
PREDICTIVE ONCOLOGY INC.
NON-QUALIFIED STOCK OPTION AGREEMENT
(Director)
Exhibit 10.7
This STOCK OPTION AGREEMENT (the “Agreement”) is made and entered into effective as of [ ● ], between Predictive
Oncology Inc., a Delaware corporation (the “Company”) and [●]. (“Director”).
BACKGROUND
A. Director is serving as a member of the board of directors of the Company (the “Board”) and the Company desires to reward Director for
his/her services to the Company as a member of the Board for the quarter ended [●], and as a member of the [Committee Name] of the
Board for the year ended [●].
B. The Company has adopted the Amended and Restated 2012 Stock Incentive Plan (as amended, the “Plan”), pursuant to which shares of
common stock of the Company have been reserved for issuance under the Plan.
NOW, THEREFORE, the parties hereto agree as follows:
1. Grant of Option; Purchase Price. Subject to the terms and conditions herein set forth, the Company hereby irrevocably grants from the
Plan to Director the right and option, hereinafter called the “Option,” to purchase all or any part of an aggregate of the number of
shares of common stock, $0.01 par value, of the Company (the “Shares”) set forth at the end of this Agreement after “Number of
Shares” at the price per Share set forth at the end of this Agreement after “Purchase Price.”
2. Exercise and Vesting of Option. The Option shall vest immediately and shall be exercisable for the remaining term of the Option.
3. Term of Option. The Option shall be exercisable for ten (10) years from the date of this Agreement. In the event that Director ceases to
be a director of the Company, for any reason or no reason, the Director retains all of Director’s rights to and under the Option.
4. Death of Director. In the event of Director’s death, the person designated in Director’s will, or in the absence of such designation,
Director’s legal representative may, in like manner, exercise the Option.
5. Change in Control. “Change in Control” has the meaning provided in the Plan. Notwithstanding anything to the contrary contained
herein, in the event of a Change in Control of the Company, the Option shall become fully vested upon the effective date of such event,
and shall remain exercisable for the remainder of the term of the Option.
1
6. Method of Exercising Option. Subject to the terms and conditions of this Agreement and the Plan, the Option may be exercised by
written notice to the Company. Such notice shall state the election to exercise the Option, the number of Shares in respect of which it is
being exercised, the method of exercise, and shall be signed by the person or persons exercising the Option. The Director may exercise
the Option by (i) paying to the Company in cash the full exercise price; (ii) arranging for a broker to sell Shares and immediately
thereafter pay to the Company the full exercise price; (iii) delivering Shares previously owned by Director, the total market value of
which equals the full exercise; or (iv) instructing the Company to withhold from the Shares issuable upon exercise of the Option Shares
in payment of all or any part of the applicable exercise price. Applicable tax withholding may be paid by any method permitted under
the Plan. Upon proper exercise, the Company shall deliver a certificate or certificates representing such Shares as soon as practicable
after the notice shall be received. All Shares that shall be purchased upon the exercise of the Option as provided herein shall be fully
paid and non-assessable.
7. Rights of Option Holder. Director, as holder of the Option, shall not have any of the rights of a shareholder with respect to the Shares
covered by the Option except to the extent that one or more certificates for such Shares shall be delivered to him or her upon the due
exercise of all or any part of the Option.
8. Limitations on Transferability. The Option shall not be transferred, pledged or assigned except, in the event Director’s death, by will or
the laws of descent and distribution to the limited extent provided in the Plan, or pursuant to a qualified domestic relations order as
defined by the Internal Revenue Code of 1986, as amended (the “Code”) or Title I of the Employee Retirement Income Security Act, or
the rules there under, and the Company shall not be required to recognize any attempted assignment of such rights. Notwithstanding the
preceding sentence, the Option may be transferred by Director to Director’s spouse, children, grandchildren or parents (collectively, the
“Family Members”), to trusts for the benefit of Family Members, to partnerships or limited liability companies in which Family
Members are the only partners or shareholders, or to entities exempt from federal income taxation pursuant to Section 501(c)(3) of the
Code. During Director’s lifetime, the Option may be exercised only by him or her, by his/her guardian or legal representative or by the
transferees permitted by the preceding sentence.
9. No Continued Membership or Right to Corporate Assets. Nothing contained in this Agreement shall be deemed to grant Director any
right to continue as a member of the Board for any period of time or to any right to continue his/her present or any other rate of
compensation, nor shall this Agreement be construed as giving Director, Director’s beneficiaries or any other person any equity or
interests of any kind in the assets of the Company or creating a trust of any kind or a fiduciary relationship of any kind between the
Company and any such person.
2
10. Securities Law Matters. Director acknowledges that the Shares to be received by him or her upon exercise of the Option may not have
been registered under the Securities Act of 1933 or the Blue Sky laws of any state (collectively, the “Acts”). If such Shares have not
been so registered, Director acknowledges and understands that the Company is under no obligation to register, under the Acts, the
Shares received by him or her or to assist him or her in complying with any exemption from such registration if he or she should at a
later date wish to dispose of the Shares. Director acknowledges that if not then registered under the Acts, the Shares shall bear a legend
restricting the transferability thereof, such legend to be substantially in the following form:
“The shares represented by this certificate have not been registered or qualified under federal or state securities laws. The shares may
not be offered for sale, sold, pledged or otherwise disposed of unless so registered or qualified, unless an exemption exists or unless
such disposition is not subject to the federal or state securities laws, and the Company may require that the availability or any
exemption or the inapplicability of such securities laws be established by an opinion of counsel, which opinion of counsel shall be
reasonably satisfactory to the Company.”
11. Director Representations. Director hereby represents and warrants that Director has reviewed with his/her own tax advisors the federal,
state, and local tax consequences of the transactions contemplated by this Agreement. Director is relying solely on such advisors and not
on any statements or representation of the Company or any of its agents. Director understands that he or she will be solely responsible
for any tax liability that may result to him or her as a result of the transactions contemplated by this Agreement. The Option, if
exercised, will be exercised for investment and not with a view to the sale or distribution of the Shares to be received upon exercise
thereof.
12. General.
a. The Option is granted pursuant to the Plan and is governed by the terms thereof. In the event of any conflict between the terms
of this Agreement and the terms of the Plan, the terms of the Plan shall control. The Company shall at all times during the term
of the Option reserve and keep available such number of Shares as will be sufficient to satisfy the requirements of this
Agreement.
b. Nothing herein expressed or implied is intended or shall be construed as conferring upon or giving to any person, firm, or
corporation other than the parties hereto, any rights or benefits under or by reason of this Agreement.
c. Each party hereto agrees to execute such further documents as may be necessary or desirable to effect the purposes of this
Agreement.
d. This Agreement may be executed in any number of counterparts, each of which shall be deemed an original, but all of which
shall constitute one and the same agreement.
e. This Agreement, in its interpretation and effect, shall be governed by the laws of the State of Minnesota applicable to contracts
executed and to be performed therein.
[Signature page follows]
3
IN WITNESS WHEREOF, the undersigned have executed this Agreement as of the date first written above.
[Signature page to Non-Qualified Stock Option Agreement]
NUMBER OF SHARES:
____________________
PREDICTIVE ONCOLOGY INC.
PURCHASE PRICE:
____________________ per share
By:___________________
Its:___________________
DIRECTOR:
By:___________________
Its:___________________
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