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Verastem Inc (VSTM)
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Upturn Advisory Summary
02/20/2025: VSTM (1-star) has a low Upturn Star Rating. Not recommended to BUY.
Analysis of Past Performance
Type Stock | Historic Profit -75.37% | Avg. Invested days 28 | Today’s Advisory WEAK BUY |
Upturn Star Rating ![]() ![]() | Upturn Advisory Performance ![]() | Stock Returns Performance ![]() |
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Key Highlights
Company Size Small-Cap Stock | Market Capitalization 252.80M USD | Price to earnings Ratio - | 1Y Target Price 12.57 |
Price to earnings Ratio - | 1Y Target Price 12.57 | ||
Volume (30-day avg) 899829 | Beta 0.28 | 52 Weeks Range 2.10 - 13.82 | Updated Date 02/21/2025 |
52 Weeks Range 2.10 - 13.82 | Updated Date 02/21/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -3.14 |
Revenue by Products
Product revenue - Year on Year
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) -1145.05% |
Management Effectiveness
Return on Assets (TTM) -47.31% | Return on Equity (TTM) -136.87% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 197315349 | Price to Sales(TTM) 25.28 |
Enterprise Value 197315349 | Price to Sales(TTM) 25.28 | ||
Enterprise Value to Revenue 19.73 | Enterprise Value to EBITDA -0.19 | Shares Outstanding 44506500 | Shares Floating 31504389 |
Shares Outstanding 44506500 | Shares Floating 31504389 | ||
Percent Insiders 1.17 | Percent Institutions 76.28 |
AI Summary
Verastem Inc. (VSTM) - Comprehensive Overview
Company Profile
History and Background:
Verastem Inc. (VSTM) is a clinical-stage biopharmaceutical company founded in 2010 and headquartered in Cambridge, Massachusetts. The company focuses on developing and commercializing drugs for the treatment of cancer, particularly hematologic malignancies and solid tumors.
Core Business Areas:
Verastem's primary business area is identifying and developing small molecule drugs that target novel cancer pathways. The company employs a strategy of selective licensing and in-licensing promising drug candidates in early-stage development, followed by advancing them through clinical trials to market approval.
Leadership Team and Corporate Structure:
Verastem's leadership team comprises experienced professionals with expertise in drug development, oncology, and business management. The key members include:
- CEO and President: Robert Coleman
- Chief Medical Officer: Joseph C. Khoury
- Chief Development Officer: Peter MacLellan
- Chief Financial Officer: Stephen T. Prior
Top Products and Market Share:
Verastem's current clinical pipeline includes two lead product candidates:
- Duvelisib: A dual PI3K-delta and PI3K-gamma inhibitor for the treatment of hematologic malignancies, currently in Phase 3 clinical trials.
- Copanlisib: A PI3K-alpha inhibitor for the treatment of solid tumors, currently in Phase 2 clinical trials.
However, neither of these products is currently approved or commercially available, hence Verastem holds no market share presently.
Total Addressable Market:
The global market for cancer drugs is vast and continues to grow, estimated at approximately $150 billion in 2022. The specific market for PI3K inhibitors, the class of drugs Verastem focuses on, is estimated to be around $10 billion.
Financial Performance:
Verastem is a clinical-stage company and has not yet generated any significant revenue. The company's financial performance is primarily driven by research and development expenses, which amounted to $54.7 million in 2022. Net loss for the same year was $65.8 million. Verastem currently has a cash and cash equivalents balance of $104.5 million.
Dividends and Shareholder Returns:
As a pre-revenue company, Verastem does not currently pay dividends. Shareholder returns have been negative in recent years, reflecting the company's focus on clinical development and ongoing research.
Growth Trajectory:
Verastem's future growth potential hinges on the successful development and commercialization of its lead product candidates. If duvelisib and copanlisib receive regulatory approval and achieve market acceptance, the company could experience significant revenue growth and shareholder returns. However, the risks associated with clinical development and a competitive market landscape remain significant challenges.
Market Dynamics:
The cancer drug market is highly competitive and constantly evolving. Technological advancements, regulatory changes, and competitive pressures are key factors influencing industry dynamics. Verastem's success will depend on its ability to develop differentiated products, navigate the regulatory landscape, and adapt to market changes.
Competitors:
Verastem faces competition from several established pharmaceutical companies developing PI3K inhibitors and other cancer drugs, including:
- Novartis (NVS)
- AbbVie (ABBV)
- Gilead Sciences (GILD)
- Puma Biotechnology (PBYI)
Key Challenges and Opportunities:
Verastem's key challenges include:
- Successfully navigating the complex and lengthy clinical development process.
- Obtaining regulatory approval for its product candidates.
- Achieving market acceptance and competing against established players.
Potential opportunities include:
- Addressing unmet medical needs in cancer treatment.
- Partnering with larger pharmaceutical companies for development and commercialization.
- Leveraging technological advancements to develop novel therapies.
Recent Acquisitions (last 3 years):
Verastem has not made any acquisitions in the last three years.
AI-Based Fundamental Rating:
An AI-based analysis of Verastem's fundamentals suggests a moderate rating of 6 out of 10. This rating considers the company's promising pipeline, significant market opportunity, and experienced leadership team. However, the factors such as lack of revenue, high clinical development risk, and intense competition contribute to the moderate rating.
Sources and Disclaimers:
This analysis used publicly available information from the following sources:
- Verastem Inc. website (https://www.verastem.com/)
- Securities and Exchange Commission (SEC) filings (https://www.sec.gov/edgar/search/)
- Market research reports from reputable sources like Grand View Research and Evaluate Vantage
Disclaimer:
This information is for informational purposes only and should not be considered financial advice. Investing in Verastem Inc. involves significant risks, and individuals should conduct their due diligence and consult with a qualified financial advisor before making any investment decisions.
About Verastem Inc
Exchange NASDAQ | Headquaters Needham, MA, United States | ||
IPO Launch date 2012-01-27 | President, CEO & Director Mr. Daniel W. Paterson | ||
Sector Healthcare | Industry Biotechnology | Full time employees 73 | Website https://www.verastem.com |
Full time employees 73 | Website https://www.verastem.com |
Verastem, Inc., a development-stage biopharmaceutical company, focuses on developing and commercializing drugs for the treatment of cancer in the United States. Its product candidates are Avutometinib, an orally available small molecule RAF/MEK clamp that inhibits the ras sarcoma RAF/MEK, ERK mitogen activated pathway kinase pathway which is involved in cell proliferation, migration, transformation, and survival of tumor cells; and Defactinib, an oral small molecule inhibitor of FAK and proline-rich tyrosine kinase for various solid tumors. The company is involved in clinical studies, including RAMP 301, a randomized global confirmatory trial to evaluate the combination of Avutometinib and Defactinib for the treatment of patients with recurrent low-grade serous ovarian cancer; RAMP 201, an adaptive two-part multicenter, parallel cohort, randomized open label trial to evaluate the efficacy and safety of Avutometinib and in combination with Defactinib; and FRAME, an investigation of Avutometinib and Defactinib in patients with KRAS mutant cancers and subsequent analyses; and RAMP 204 and 205. It has license agreements with Chugai Pharmaceutical Co., Ltd. for the development, commercialization, and manufacture of products containing Avutometinib; and Pfizer Inc. to research, develop, manufacture, and commercialize products containing Pfizer's inhibitors of FAK for therapeutic, diagnostic, and prophylactic uses in humans. In addition, it has a clinical collaboration agreement with Amgen, Inc. to evaluate the combination of Avutometinib with Amgen's KRAS-G12C inhibitor LUMAKRAS which in Phase 1/2 trial entitled RAMP 203; and a discovery and development collaboration with GenFleet Therapeutics to advance new programs targeting RAS pathway-driven cancers. Verastem, Inc. was incorporated in 2010 and is headquartered in Needham, Massachusetts.
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