2021 Q1 Form 10-K Financial Statement

#000143774922005677 Filed on March 09, 2022

View on sec.gov

Income Statement

Concept 2021 Q1 2021 2020 Q4
Revenue $110.4K $385.5K $250.0K
YoY Change -84.58% -78.86% -7.41%
Cost Of Revenue
YoY Change
Gross Profit
YoY Change
Gross Profit Margin
Selling, General & Admin $1.070M $3.577M $830.0K
YoY Change 114.0% 62.6% 97.62%
% of Gross Profit
Research & Development $602.8K $15.55M $760.0K
YoY Change -25.48% 536.3% 72.73%
% of Gross Profit
Depreciation & Amortization $4.517K $38.52K $20.00K
YoY Change 354.43% 95.98%
% of Gross Profit
Operating Expenses $1.674M $19.13M $1.590M
YoY Change 27.7% 312.27% 84.88%
Operating Profit -$1.564M -$18.75M
YoY Change 162.74% 565.5%
Interest Expense $755.00 $1.286K $0.00
YoY Change -33.89% -99.1%
% of Operating Profit
Other Income/Expense, Net $1.298K $175.5K
YoY Change -432.82% -224.25%
Pretax Income -$1.560M -$18.57M -$1.340M
YoY Change 160.0% 527.38% 127.12%
Income Tax $0.00
% Of Pretax Income
Net Earnings -$1.563M -$18.57M -$1.340M
YoY Change 162.35% 527.79% 127.12%
Net Earnings / Revenue -1415.34% -4817.19% -536.0%
Basic Earnings Per Share -$0.29 -$3.04
Diluted Earnings Per Share -$292.7K -$3.044M -$349.9K
COMMON SHARES
Basic Shares Outstanding 5.332M 6.100M
Diluted Shares Outstanding

Balance Sheet

Concept 2021 Q1 2021 2020 Q4
SHORT-TERM ASSETS
Cash & Short-Term Investments $20.84M $11.42M $9.880M
YoY Change 9372.73% 15.63% 3428.57%
Cash & Equivalents $20.84M $11.42M $9.884M
Short-Term Investments
Other Short-Term Assets $120.0K $156.2K $170.0K
YoY Change 71.43% -8.09% 70.0%
Inventory
Prepaid Expenses
Receivables $0.00 $49.01K $180.0K
Other Receivables $0.00 $0.00 $0.00
Total Short-Term Assets $20.96M $11.63M $10.24M
YoY Change 2487.13% 13.57% 2188.39%
LONG-TERM ASSETS
Property, Plant & Equipment $143.2K $156.9K $147.7K
YoY Change 1390.05% 4.63% 1292.99%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $10.00K $11.01K $10.00K
YoY Change 0.0% 10.1% 0.0%
Total Long-Term Assets $154.2K $167.9K $158.8K
YoY Change 647.91% 11.96% 634.41%
TOTAL ASSETS
Total Short-Term Assets $20.96M $11.63M $10.24M
Total Long-Term Assets $154.2K $167.9K $158.8K
Total Assets $21.12M $11.80M $10.39M
YoY Change 2441.48% 13.54% 2116.75%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $232.5K $2.058M $267.7K
YoY Change -68.62% 662.05% 75.37%
Accrued Expenses $36.62K $3.378M $359.3K
YoY Change -98.09% 838.29% -80.59%
Deferred Revenue
YoY Change
Short-Term Debt $0.00 $0.00 $0.00
YoY Change
Long-Term Debt Due $180.0K $0.00 $180.0K
YoY Change 1700.0% -100.0% 1700.0%
Total Short-Term Liabilities $451.9K $5.435M $810.3K
YoY Change -83.07% 571.03% -59.81%
LONG-TERM LIABILITIES
Long-Term Debt $10.00K $0.00 $10.00K
YoY Change -50.0% -100.0% -66.67%
Other Long-Term Liabilities $2.000M
YoY Change
Total Long-Term Liabilities $10.00K $2.000M $10.00K
YoY Change -50.0% 19900.0% -66.67%
TOTAL LIABILITIES
Total Short-Term Liabilities $451.9K $5.435M $810.3K
Total Long-Term Liabilities $10.00K $2.000M $10.00K
Total Liabilities $464.1K $7.435M $825.0K
YoY Change -82.78% 795.83% -59.62%
SHAREHOLDERS EQUITY
Retained Earnings -$47.37M -$45.81M
YoY Change 9.04% 6.9%
Common Stock $67.94M $55.30M
YoY Change 64.9% 40.56%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $20.65M $4.362M $9.569M
YoY Change
Total Liabilities & Shareholders Equity $21.12M $11.80M $10.39M
YoY Change 2441.48% 13.54% 2116.75%

Cashflow Statement

Concept 2021 Q1 2021 2020 Q4
OPERATING ACTIVITIES
Net Income -$1.563M -$18.57M -$1.340M
YoY Change 162.35% 527.79% 127.12%
Depreciation, Depletion And Amortization $4.517K $38.52K $20.00K
YoY Change 354.43% 95.98%
Cash From Operating Activities -$1.621M -$11.20M -$1.540M
YoY Change 352.02% 307.06% 450.0%
INVESTING ACTIVITIES
Capital Expenditures $0.00 $47.72K -$160.0K
YoY Change -69.57% 1500.0%
Acquisitions
YoY Change
Other Investing Activities
YoY Change
Cash From Investing Activities $0.00 -$47.72K -$160.0K
YoY Change -69.57% 1500.0%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net $9.400M
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities $12.58M $12.78M 0.000
YoY Change 4134.47% 2.21%
NET CHANGE
Cash From Operating Activities -$1.621M -$11.20M -1.540M
Cash From Investing Activities $0.00 -$47.72K -160.0K
Cash From Financing Activities $12.58M $12.78M 0.000
Net Change In Cash $10.96M $1.540M -1.700M
YoY Change -17909.64% -83.96% 486.21%
FREE CASH FLOW
Cash From Operating Activities -$1.621M -$11.20M -$1.540M
Capital Expenditures $0.00 $47.72K -$160.0K
Free Cash Flow -$1.621M -$11.24M -$1.380M
YoY Change 352.02% 286.75% 411.11%

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<table border="0" cellpadding="0" cellspacing="0" style="width: 100%; text-indent: 0px;"><tbody><tr style="vertical-align: top;"><td style="width: 45pt;"> <p style="margin: 0pt; text-align: justify; font-family: Times New Roman; font-size: 10pt;"><b><em style="font: inherit;">1.</em></b></p> </td><td style="width: auto;"> <p style="margin: 0pt; text-align: justify; font-family: Times New Roman; font-size: 10pt;"><b>Description of Business and Recent Developments</b></p> </td></tr> </tbody></table> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p> <p style="font-family:Times New Roman;font-size:10pt;font-variant:normal;margin:0pt;">GeoVax Labs, Inc. (“GeoVax” or the “Company”), is a clinical-stage biotechnology company developing immunotherapies and vaccines against infectious diseases and cancers using novel vector vaccine platforms. GeoVax’s product pipeline includes ongoing human clinical trials in COVID-<em style="font: inherit;">19</em> and head and neck cancer. Additional research and development programs include preventive vaccines against Zika Virus, hemorrhagic fever viruses (Ebola, Sudan, Marburg, and Lassa) and malaria, as well as immunotherapies for solid tumors. Certain of our vaccine development activities have been, and continue to be, financially supported by the U.S. Government. This support has been both in the form of research grants and contracts awarded directly to us, as well as indirect support for the conduct of preclinical animal studies and human clinical trials.</p> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p> <p style="font-family:Times New Roman;font-size:10pt;font-variant:normal;margin:0pt;"><i>GEO-<em style="font: inherit;">CM04S1</em> License</i> -- In <em style="font: inherit;"> November 2021, </em>GeoVax entered into a license agreement with City of Hope (the “COH License”), granting GeoVax exclusive rights to further develop and commercialize GEO-<em style="font: inherit;">CM04S1</em> (formerly referred to as <em style="font: inherit;">COH04S1</em>). GEO-<em style="font: inherit;">CM04S1,</em> a synthetic, attenuated modified vaccinia Ankara (sMVA) vector expressing Spike and Nucleocapsid antigens of the SARS-CoV-<em style="font: inherit;">2</em> virus, was initially developed at COH for immunocompromised patients.</p> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p> <p style="font-family:Times New Roman;font-size:10pt;font-variant:normal;margin:0pt;">GEO-<em style="font: inherit;">CM04S1</em> is being studied in an ongoing Phase <em style="font: inherit;">2</em> clinical trial to evaluate its safety and immunogenicity, compared to the Pfizer mRNA-based vaccine, in patients who have previously received either an allogeneic hematopoietic cell transplant, an autologous hematopoietic cell transplant or chimeric antigen receptor (CAR) T cell therapy. GEO-<em style="font: inherit;">CM04S1</em> is the only COVID-<em style="font: inherit;">19</em> vaccine that includes both SARS-CoV-<em style="font: inherit;">2</em> spike and nucleocapsid proteins to advance to a Phase <em style="font: inherit;">2</em> trial in cancer patients. Such vaccines also tend to produce an immune response quickly – in less than <em style="font: inherit;">14</em> days – with only mild side effects. The trial is also the <em style="font: inherit;">first</em> to compare an investigational multi-antigenic COVID-<em style="font: inherit;">19</em> vaccine to the current Food and Drug Administration (FDA)-approved mRNA vaccine from Pfizer/BioNTech in people who are immunocompromised. Such patients have often shown a weak antibody response after receiving currently available COVID-<em style="font: inherit;">19</em> vaccines.</p> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p> <p style="font-family:Times New Roman;font-size:10pt;font-variant:normal;margin:0pt;">In <em style="font: inherit;"> December 2021, </em>patient enrollment began for the Phase <em style="font: inherit;">2</em> portion of a Phase <em style="font: inherit;">1/2</em> trial of GEO-<em style="font: inherit;">CM04S1,</em> to study its use as a universal booster vaccine to current FDA-approved vaccines. GeoVax believes that the GEO-<em style="font: inherit;">CM04S1</em> vaccine, when administered as a heterologous booster, will provide additional recognition elements to the immune system over a homologous boost from mRNA vaccines such as those developed by Moderna or Pfizer, which are directed only toward SARS-CoV-<em style="font: inherit;">2</em> Spike protein. The <em style="font: inherit;">COH04S1</em> vaccine’s MVA backbone <em style="font: inherit;"> may </em>be more effective at inducing COVID-<em style="font: inherit;">19</em> immunity since MVA strongly induces T cell responses even in a background of immunosuppression. In addition, GEO-<em style="font: inherit;">CM04S1</em> targeting of both Spike and Nucleocapsid antigens, <em style="font: inherit;"> may </em>offer greater protection against the significant sequence variation observed with the Spike antigen.</p> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p> <p style="font-family:Times New Roman;font-size:10pt;font-variant:normal;margin:0pt;"><i>Gedeptin</i>®<i> License</i> -- In <em style="font: inherit;"> September 2021, </em>GeoVax entered into an Assignment and License Agreement with PNP Therapeutics, Inc. (the “PNP License), whereby GeoVax expanded its immuno-oncology pipeline and added a new technology platform through the acquisition of exclusive rights to Gedeptin®, a novel patented product for the treatment of solid tumors through a gene therapy strategy known as GDEPT (Gene-Directed Enzyme Prodrug Therapy). In GDEPT, a vector is used to selectively transduce tumor cells with a nonhuman gene, which expresses an enzyme that can convert a nontoxic prodrug into a potent antitumor compound. A Phase <em style="font: inherit;">1/2</em> clinical trial is currently enrolling to evaluate the safety and efficacy of repeat cycles of Gedeptin therapy in patients with recurrent head and neck squamous cell carcinoma (HNSCC), with tumors accessible for injection and <em style="font: inherit;">no</em> curable treatment options. The FDA has granted Gedeptin Orphan Drug status for the treatment of HNSCC and the initial stage of the ongoing clinical trial is being funded by the FDA pursuant to its Orphan Products Clinical Trials Grants Program. GeoVax’s license to Gedeptin includes rights to expand its use to all human diseases and/or conditions including, but <em style="font: inherit;">not</em> limited to, cancers.</p> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p> <p style="font-family:Times New Roman;font-size:10pt;font-variant:normal;margin:0pt;">GeoVax is incorporated under the laws of the State of Delaware and our principal offices are located in the metropolitan Atlanta, Georgia area.</p> <p style="font-family:'Times New Roman';font-size:10pt;font-variant:normal;margin:0pt;"> </p>
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