2023 Q2 Form 10-Q Financial Statement

#000155837023008839 Filed on May 09, 2023

View on sec.gov

Income Statement

Concept 2023 Q2 2023 Q1
Revenue $0.00 $0.00
YoY Change -100.0%
Cost Of Revenue
YoY Change
Gross Profit
YoY Change
Gross Profit Margin
Selling, General & Admin $7.399M $7.329M
YoY Change 13.59% 23.51%
% of Gross Profit
Research & Development $12.89M $12.02M
YoY Change -13.4% -11.93%
% of Gross Profit
Depreciation & Amortization $22.00K $30.00K
YoY Change -24.14% 0.0%
% of Gross Profit
Operating Expenses $20.29M $19.34M
YoY Change -5.19% -1.19%
Operating Profit -$20.29M -$19.34M
YoY Change -5.19% 13.92%
Interest Expense $1.121M $769.0K
YoY Change 75.16% 1273.21%
% of Operating Profit
Other Income/Expense, Net -$40.00K -$7.000K
YoY Change -766.67% -125.0%
Pretax Income -$24.28M -$15.71M
YoY Change 10.61% -7.36%
Income Tax $0.00 $0.00
% Of Pretax Income
Net Earnings -$24.28M -$15.71M
YoY Change 10.61% -7.36%
Net Earnings / Revenue
Basic Earnings Per Share -$1.37 -$0.08
Diluted Earnings Per Share -$1.37 -$0.08
COMMON SHARES
Basic Shares Outstanding 200.9M 200.7M
Diluted Shares Outstanding 200.7M

Balance Sheet

Concept 2023 Q2 2023 Q1
SHORT-TERM ASSETS
Cash & Short-Term Investments $183.1M $111.2M
YoY Change 94.14% 4.64%
Cash & Equivalents $183.1M $97.26M
Short-Term Investments $0.00 $13.94M
Other Short-Term Assets $6.875M $7.689M
YoY Change 100.03% 70.22%
Inventory
Prepaid Expenses
Receivables $2.000K $0.00
Other Receivables $0.00 $0.00
Total Short-Term Assets $190.0M $118.9M
YoY Change 94.09% 4.81%
LONG-TERM ASSETS
Property, Plant & Equipment $40.00K $62.00K
YoY Change -73.51% -65.56%
Goodwill
YoY Change
Intangibles
YoY Change
Long-Term Investments
YoY Change
Other Assets $20.00K $36.00K
YoY Change -76.19% -65.71%
Total Long-Term Assets $1.795M $1.984M
YoY Change -29.16% -26.76%
TOTAL ASSETS
Total Short-Term Assets $190.0M $118.9M
Total Long-Term Assets $1.795M $1.984M
Total Assets $191.8M $120.9M
YoY Change 90.98% 4.07%
SHORT-TERM LIABILITIES
YoY Change
Accounts Payable $4.553M $4.903M
YoY Change 166.88% 69.3%
Accrued Expenses $13.76M $13.94M
YoY Change -22.1% 4.84%
Deferred Revenue
YoY Change
Short-Term Debt $579.0K $1.004M
YoY Change
Long-Term Debt Due $290.0K $282.0K
YoY Change
Total Short-Term Liabilities $20.79M $22.36M
YoY Change 3.46% 32.41%
LONG-TERM LIABILITIES
Long-Term Debt $39.74M $39.57M
YoY Change 61.95% 62.11%
Other Long-Term Liabilities $8.482M $4.760M
YoY Change 349.5% 128.96%
Total Long-Term Liabilities $48.22M $44.33M
YoY Change 82.48% 67.35%
TOTAL LIABILITIES
Total Short-Term Liabilities $20.79M $22.36M
Total Long-Term Liabilities $48.22M $44.33M
Total Liabilities $69.01M $66.69M
YoY Change 48.35% 53.75%
SHAREHOLDERS EQUITY
Retained Earnings -$777.5M -$753.2M
YoY Change 10.66% 10.65%
Common Stock $879.1M $786.3M
YoY Change 16.18% 4.34%
Preferred Stock
YoY Change
Treasury Stock (at cost)
YoY Change
Treasury Stock Shares
Shareholders Equity $101.6M $33.03M
YoY Change
Total Liabilities & Shareholders Equity $191.8M $120.9M
YoY Change 90.98% 4.07%

Cashflow Statement

Concept 2023 Q2 2023 Q1
OPERATING ACTIVITIES
Net Income -$24.28M -$15.71M
YoY Change 10.61% -7.36%
Depreciation, Depletion And Amortization $22.00K $30.00K
YoY Change -24.14% 0.0%
Cash From Operating Activities -$19.90M -$20.29M
YoY Change 56.8% 5.21%
INVESTING ACTIVITIES
Capital Expenditures
YoY Change
Acquisitions
YoY Change
Other Investing Activities $14.00M -$804.0K
YoY Change -52.14% -104.17%
Cash From Investing Activities $14.00M -$804.0K
YoY Change -52.14% -104.17%
FINANCING ACTIVITIES
Cash Dividend Paid
YoY Change
Common Stock Issuance & Retirement, Net
YoY Change
Debt Paid & Issued, Net
YoY Change
Cash From Financing Activities 91.48M 44.05M
YoY Change 12821.05% 73.07%
NET CHANGE
Cash From Operating Activities -19.90M -20.29M
Cash From Investing Activities 14.00M -804.0K
Cash From Financing Activities 91.48M 44.05M
Net Change In Cash 85.58M 22.96M
YoY Change 395.72% -9.73%
FREE CASH FLOW
Cash From Operating Activities -$19.90M -$20.29M
Capital Expenditures
Free Cash Flow
YoY Change

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<p style="font-family:'Times New Roman','Times','serif';font-size:10pt;padding-bottom:12pt;margin:0pt;"><b style="font-weight:bold;">1. Nature of business</b></p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;padding-bottom:12pt;text-indent:36pt;background:#ffffff;margin:0pt;">Verastem, Inc. (the “Company”) is a late stage development biopharmaceutical company, with an ongoing registration directed trial, committed to advancing new medicines for patients battling cancer. The Company’s pipeline is focused on novel anticancer agents that inhibit critical signaling pathways in cancer that promote cancer cell survival and tumor growth, particularly RAF/ MEK inhibition and FAK inhibition.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;padding-bottom:12pt;text-indent:36pt;background:#ffffff;margin:0pt;">The Company’s most advanced product candidates, avutometinib and defactinib, are being investigated in both preclinical and clinical studies for the treatment of various solid tumors, including, but not limited to low-grade serous ovarian cancer (“LGSOC”), non-small cell lung cancer (“NSCLC”), colorectal cancer (“CRC”), pancreatic cancer, and melanoma. The Company believes that avutometinib may be beneficial as a therapeutic as a single agent or when used together in combination with defactinib, other agents, other pathway inhibitors or other current and emerging standard of care treatments in cancers that do not adequately respond to currently available therapies.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-indent:36pt;background:#ffffff;margin:0pt 0pt 12pt 0pt;">On September 24, 2018, the Company’s first commercial product, COPIKTRA® (duvelisib), was approved by the U.S. Food and Drug Administration (the “FDA”) for the treatment of adult patients with certain hematologic cancers including relapsed or refractory chronic lymphocytic leukemia/ small lymphocytic lymphoma after at least two prior therapies and relapsed or refractory follicular lymphoma after at least two prior systemic therapies. On August 10, 2020, the Company and Secura Bio, Inc. (“Secura”) entered into an asset purchase agreement (“Secura APA”). Pursuant to the Secura APA, the Company sold to Secura its exclusive worldwide license, including certain related assets for the research, development, commercialization, and manufacture in oncology indications of products containing COPIKTRA (duvelisib). The transaction closed on September 30, 2020. Refer to <i style="font-style:italic;">Note 14. License, collaboration, and commercial agreements</i> for a detailed discussion of the Secura APA.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-indent:36pt;margin:0pt 0pt 12pt 0pt;">The condensed consolidated financial statements include the accounts of Verastem Securities Company and Verastem Europe GmbH, wholly-owned subsidiaries of the Company. All financial information presented has been consolidated and includes the accounts of the Company and its wholly-owned subsidiaries. All intercompany balances and transactions have been eliminated in consolidation.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-indent:36pt;margin:0pt 0pt 12pt 0pt;">The Company is subject to the risks associated with other life science companies, including, but not limited to, possible failure of preclinical testing or clinical trials, competitors developing new technological innovations, inability to obtain marketing approval of the Company’s product candidates, avutometinib and defactinib, market acceptance and commercial success of the Company’s product candidates, avutometinib and defactinib, following receipt of regulatory approval, and, protection of proprietary technology and the continued ability to obtain adequate financing to fund the Company’s future operations. If the Company does not obtain marketing approval and successfully commercialize its product candidates, avutometinib and defactinib, following regulatory approval, it will be unable to generate product revenue or achieve profitability and may need to raise additional capital.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-indent:36pt;margin:0pt 0pt 12pt 0pt;">The Company has historical losses from operations and anticipates that it may continue to incur operating losses as it continues the research and development of its product candidates. As of March 31, 2023, the Company had cash, cash equivalents, and investments of $111.2 million, and an accumulated deficit of $753.2 million. The Company expects its existing cash resources will be sufficient to fund its planned operations through at least 12 months from the date of issuance of these condensed consolidated financial statements.</p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;text-indent:36pt;margin:0pt;">The Company expects to finance the future development costs of its clinical product portfolio with its existing cash, cash equivalents, and investments, through potential future milestones and royalties received pursuant to the Secura APA, through the loan and security agreement with<span style="background:#ffffff;"> Oxford Finance LLC (“Oxford”),</span> or through other strategic financing opportunities that could include, but are not limited to collaboration agreements, future offerings of its equity, or the incurrence of debt. However, there is no guarantee that any of these strategic or financing opportunities will be </p><p style="font-family:'Times New Roman','Times','serif';font-size:10pt;margin:0pt 0pt 12pt 0pt;">executed or executed on favorable terms, and some could be dilutive to existing stockholders. If the Company fails to obtain additional future capital, it may be unable to complete its planned preclinical studies and clinical trials and obtain approval of certain investigational product candidates from the FDA or foreign regulatory authorities.</p>
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CY2023Q1 us-gaap Concentration Risk Credit Risk Financial Instruments Off Balance Sheet Risk
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