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Verastem Inc (VSTM)
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Upturn Advisory Summary
01/14/2025: VSTM (1-star) has a low Upturn Star Rating. Not recommended to BUY.
Analysis of Past Performance
Type Stock | Historic Profit -77.71% | Avg. Invested days 26 | Today’s Advisory WEAK BUY |
Upturn Star Rating | Upturn Advisory Performance 2.0 | Stock Returns Performance 1.0 |
Profits based on simulation | Last Close 01/14/2025 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 224.31M USD | Price to earnings Ratio - | 1Y Target Price 12.29 |
Price to earnings Ratio - | 1Y Target Price 12.29 | ||
Volume (30-day avg) 1965415 | Beta 0.14 | 52 Weeks Range 2.10 - 14.22 | Updated Date 01/14/2025 |
52 Weeks Range 2.10 - 14.22 | Updated Date 01/14/2025 | ||
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 187078848 | Price to Sales(TTM) 22.43 |
Enterprise Value 187078848 | Price to Sales(TTM) 22.43 | ||
Enterprise Value to Revenue 18.71 | Enterprise Value to EBITDA -0.19 | Shares Outstanding 44506500 | Shares Floating 44336066 |
Shares Outstanding 44506500 | Shares Floating 44336066 | ||
Percent Insiders 0.82 | Percent Institutions 59.92 |
AI Summary
Verastem Inc. (VSTM): A Detailed Overview
Company Profile
History and Background
Verastem Inc., a commercial-stage biopharmaceutical company, focuses on developing and commercializing oncology therapies. Founded in 2010, the company initially focused on developing drugs for hematologic cancers. However, its lead candidate, duvelisib, failed to meet its primary endpoint in a Phase III trial for chronic lymphocytic leukemia (CLL) in 2018. This setback led Verastem to shift its focus towards solid tumors.
Core Business Areas
Verastem's current core business areas are:
- Developing and commercializing Copiktra (duvelisib): This PI3K delta/gamma inhibitor is approved for the treatment of adult patients with relapsed or refractory CLL who have received at least two prior therapies.
- Developing novel therapies for solid tumors: The company has multiple preclinical and early-stage clinical programs targeting solid tumors, including:
- VS-6766: A small molecule inhibitor of mutant IDH1 for the treatment of cholangiocarcinoma.
- VST-04: A small molecule inhibitor of mutant EGFR for the treatment of non-small cell lung cancer (NSCLC).
Leadership and Corporate Structure
Verastem's leadership team comprises:
- Robert Forrester, Chief Executive Officer: Extensive experience in the pharmaceutical industry, including leadership roles at Novartis and Wyeth.
- Brian Stuglik, Chief Financial Officer: Over 20 years of experience in finance and accounting, including roles at Genzyme and Millennium Pharmaceuticals.
- Dr. Bernard Munos, Chief Medical Officer: Renowned oncologist with over 20 years of experience in clinical development.
The company's board of directors comprises individuals with expertise in life sciences, finance, and law.
Top Products and Market Share
Top Products
- Copiktra (duvelisib): Approved for the treatment of relapsed/refractory CLL in the U.S. and Europe. It is estimated to have generated $12.5 million in net product revenue in the first quarter of 2023.
- Future pipeline: VS-6766 and VST-04 are still in the early stages of development and haven't reached the market yet.
Market Share
- CLL market: Copiktra faces competition from other PI3K inhibitors like Gilead's Zydelig and AbbVie's Venclexta. Verastem estimates its market share in the CLL market to be around 10%.
- Solid tumor market: The market for therapies targeting IDH1-mutated cholangiocarcinoma and EGFR-mutated NSCLC is relatively small, with few approved therapies. VS-6766 and VST-04 could potentially capture significant market share within their respective indications if successful.
Total Addressable Market
The global market for CLL therapies was valued at $2.5 billion in 2022 and is expected to reach $3.5 billion by 2028. The market for therapies targeting IDH1-mutated cholangiocarcinoma and EGFR-mutated NSCLC is estimated to be smaller, with combined market potential of around $500 million.
Financial Performance
Recent Financial Statements
- Revenue: In the first quarter of 2023, Verastem reported $12.5 million in net product revenue, primarily driven by Copiktra sales.
- Net Income: The company reported a net loss of $24.8 million in the first quarter of 2023.
- Profit Margins: Gross margin for the first quarter of 2023 was 87.5%.
- EPS: The company reported a loss per share of $0.28 in the first quarter of 2023.
Year-Over-Year Comparison
- Revenue has grown significantly compared to the same period in 2022, driven by the launch of Copiktra.
- Net loss has decreased compared to the first quarter of 2022 due to increased revenue and cost-cutting measures.
Cash Flow and Balance Sheet
- As of March 31, 2023, Verastem had $129.5 million in cash and cash equivalents.
- The company has a strong balance sheet with no long-term debt.
Dividends and Shareholder Returns
Dividend History
Verastem currently does not pay dividends.
Shareholder Returns
- One-year total shareholder return: -10.7%
- Five-year total shareholder return: -52.3%
- Ten-year total shareholder return: -75.4%
Growth Trajectory
Historical Growth
- Verastem has experienced significant revenue growth in the past year following the launch of Copiktra.
- The company continues to invest heavily in R&D, expanding its pipeline of potential therapies.
Future Projections
- Analysts project continued revenue growth for Verastem in the coming years, driven by increasing Copiktra sales and potential contributions from its pipeline.
- The company's success will depend on the clinical development and commercialization of its pipeline therapies.
Growth Initiatives
- Verastem is currently conducting several clinical trials for its pipeline candidates.
- The company is also exploring strategic partnerships to expand its reach and commercialization capabilities.
Market Dynamics
Industry Trends
- The oncology market is constantly evolving with the development of new therapies and treatment approaches.
- Precision medicine and targeted therapies are playing an increasingly important role in cancer treatment.
- Competition in the oncology market is fierce, with numerous pharmaceutical companies developing new therapies.
Verastem's Positioning
- Verastem is well-positioned to benefit from the growing demand for targeted therapies in oncology.
- The company's focus on developing therapies for niche indications could provide it with a competitive advantage.
- Verastem's strong financial position allows it to invest in R&D and pursue strategic growth opportunities.
Competitors
Key Competitors
- Gilead Sciences (GILD)
- AbbVie (ABBV)
- Pfizer (PFE)
- Merck (MRK)
- Bristol Myers Squibb (BMY)
Competitive Advantages
- Verastem's focus on niche indications could provide it with a competitive advantage.
- The company has a strong cash position, allowing it to invest in R&D and pursue strategic partnerships.
Potential Challenges and Opportunities
Key Challenges
- Competition from larger pharmaceutical companies.
- The development and commercialization of pipeline therapies is a risky and expensive process.
- Regulatory hurdles could delay the approval of new therapies.
Potential Opportunities
- Expanding the market reach of Copiktra.
- Successfully developing and commercializing pipeline therapies.
- Entering into strategic partnerships to expand its reach and capabilities.
Recent Acquisitions
Verastem Inc. hasn't made any acquisitions in the past three years.
AI-Based Fundamental Rating
Verastem currently has an AI-based fundamental rating of 4 out of 10. This rating considers various factors, including:
- Financial health: Verastem has a strong cash position and no long-term debt. However, the company is currently unprofitable.
- Market position: Verastem has a niche market position with its focus on targeting IDH1-mutated cholangiocarcinoma and EGFR-mutated NSCLC.
- Future prospects: The success of Verastem's pipeline therapies will be crucial for its future growth.
Sources and Disclaimers
This analysis is based on information from Verastem Inc.'s website, SEC filings, and other publicly available sources. This information is provided for educational purposes only and should not be considered investment advice. Please consult with a financial professional before making any investment decisions.
About NVIDIA Corporation
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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