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DCPH Price Correlated With Financials For Deciphera Pharmaceuticals

Free historical financial statements for Deciphera Pharmaceuticals Inc. See how revenue, income, cash flow, and balance sheet financials have changed over 17 quarters since 2018. Compare with DCPH stock chart to see long term trends.

DCPH Stock Compared to Quarterly

DCPH Income Statement

Revenue, Net:29223000
Revenue Per Share:0.4413
Cost of Goods & Services Sold:382000
Selling, General & Admin Expense:28321000
Research & Development Expense:47412000
Total Operating Expenses:76115000
Operating Income:-46892000
Net Income:-46892000
Earnings Per Share, Basic:-0.8
Shares Outstanding, Basic Avg:66216509

DCPH Cash Flow

Operating Activities Net Income:
Depreciation, Depletion & Amortization:783000
Change in Accounts Receiveable:2561000
Net Cash from Operations:-51352000
Net Cash from Operations Per Share:-0.7755
Net Cash from Financing Activities:83000
Property, Plant & Equipment Purchases:0
Net Cash from Investing Activities:59652000
Net Change in Cash & Equivalents:8383000

DCPH Balance Sheet

Cash and Cash Equivalents:95332000
Accounts Receivable, Net:23151000
Total Current Assets:319835000
Property, Plant & Equipment, Net:7821000
Total Assets:385464000
Accounts Payable:17801000
Total Short-Term Liabilities:86670000
Total Liabilities:113899000

Insider Trading

SEC Form 4
Brightstar Associates LLC   10% Owner
1,478,978 sh at $10
Nature of the Business and Summary of Significant Accounting Policies Nature of the Business

Deciphera Pharmaceuticals, Inc. (the Company) is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines to improve the lives of people with cancer. Leveraging its proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology, the Company designs kinase inhibitors to target the switch pocket region of the kinase with the goal of developing potentially transformative medicines. Through its patient-inspired approach, the Company seeks to develop a broad portfolio of innovative medicines to improve treatment outcomes. QINLOCK, the Company's switch-control kinase inhibitor, was engineered using its proprietary drug discovery platform and developed for the treatment of fourth-line GIST. QINLOCK is approved in Australia, Canada, China, the European Union (EU), Hong Kong, Switzerland, Taiwan, the United States (U.S.), and the United Kingdom (U.K.) for the treatment of fourth-line GIST. The Company wholly owns QINLOCK and all of its drug candidates with the exception of a development and commercialization out-license agreement for QINLOCK in Greater China. In addition to QINLOCK, the Company has identified and advanced multiple product candidates from its platform into clinical studies, including vimseltinib and DCC-3116.

The Company is subject to risks and uncertainties common to companies in the biotechnology industry, including, but not limited to, development by competitors of new technological innovations, dependence on key personnel, market acceptance and the successful commercialization of QINLOCK or any of the Company's current or future drug candidates for which it receives marketing approval, protection of proprietary technology, ability to complete late-stage clinical trials, ability to obtain and maintain regulatory approvals, compliance with government regulations, the impact of the novel coronavirus (COVID-19) pandemic on its operations, and the ability to secure additional capital to fund operations. QINLOCK and the Company's drug candidates currently under development will require significant additional research and development efforts, including extensive preclinical and/or clinical testing and regulatory approval. In addition to supporting its research and development efforts, the Company will be required to invest in the Company's commercial capabilities and infrastructure, to support its commercialization of QINLOCK, the Company's first approved drug, and any current or future drug candidate for which the Company obtains marketing approval. These efforts require significant amounts of additional capital, adequate personnel and infrastructure, and extensive compliance-reporting capabilities. Even if the Company's drug development and commercialization efforts are successful, it is uncertain when, if ever, the Company will realize sufficient revenue to result in a profit from product sales of QINLOCK or any current or future drug candidates for which it receives marketing approval.

The full extent to which the COVID-19 pandemic, or the future outbreak of any other highly infectious or contagious diseases, may impact the Company's business, including its preclinical studies, clinical trial operations, or commercialization efforts will depend on continuously changing circumstances, which are highly uncertain and cannot be predicted at this time, such as the duration of such pandemic including future waves of infection, new strains of the virus that causes COVID-19, or the impact of effective vaccines, the actions taken to contain the pandemic or mitigate its impact, and the direct and indirect economic effects of the pandemic and containment measures, among others. The Company is continuing to monitor the long-term impact of COVID-19, if any, on its financial condition and results of operations. The ongoing fluidity of this situation precludes an

Data imported from Deciphera Pharmaceuticals Inc SEC filings. Check original filings before making any investment decision.