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Erasca Inc (ERAS)


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Upturn Advisory Summary
10/15/2025: ERAS (1-star) has a low Upturn Star Rating. Not recommended to BUY.
1 Year Target Price $4.5
1 Year Target Price $4.5
5 | Strong Buy |
3 | Buy |
0 | Hold |
0 | Sell |
0 | Strong Sell |
Analysis of Past Performance
Type Stock | Historic Profit -40.65% | Avg. Invested days 32 | Today’s Advisory Consider higher Upturn Star rating |
Upturn Star Rating ![]() | Upturn Advisory Performance ![]() | Stock Returns Performance ![]() |
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Key Highlights
Company Size Small-Cap Stock | Market Capitalization 717.69M USD | Price to earnings Ratio - | 1Y Target Price 4.5 |
Price to earnings Ratio - | 1Y Target Price 4.5 | ||
Volume (30-day avg) 8 | Beta 1.18 | 52 Weeks Range 1.01 - 3.31 | Updated Date 10/17/2025 |
52 Weeks Range 1.01 - 3.31 | Updated Date 10/17/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -0.39 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -17.92% | Return on Equity (TTM) -31.16% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 352979396 | Price to Sales(TTM) - |
Enterprise Value 352979396 | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA -1.57 | Shares Outstanding 283670139 | Shares Floating 167458993 |
Shares Outstanding 283670139 | Shares Floating 167458993 | ||
Percent Insiders 11.68 | Percent Institutions 81.92 |
Upturn AI SWOT
Erasca Inc

Company Overview
History and Background
Erasca Inc. is a clinical-stage precision oncology company focused on discovering, developing, and commercializing therapies for patients with RAS/MAPK pathway-driven cancers. Founded in 2018, the company aims to erase cancer by targeting the root causes of the disease. They have rapidly advanced a pipeline of novel therapeutic candidates.
Core Business Areas
- Drug Discovery and Development: Erasca focuses on identifying and developing small molecule inhibitors that target key nodes in the RAS/MAPK pathway, a signaling network frequently dysregulated in cancer.
- Clinical Trials: The company conducts clinical trials to evaluate the safety and efficacy of its drug candidates in patients with various cancer types.
- RAS/MAPK Pathway Targeting: Specializes in creating therapies specifically designed to inhibit the activity of the RAS/MAPK pathway.
Leadership and Structure
Erasca is led by a team of experienced biotech executives and scientists. The organizational structure is designed to support drug discovery, preclinical and clinical development, and potential commercialization activities.
Top Products and Market Share
Key Offerings
- ERAS-007: A novel ERK1/2 inhibitor being evaluated in clinical trials for the treatment of advanced solid tumors. Market share data is not yet available as the drug is still in clinical development. Competitors include companies developing other ERK inhibitors and therapies targeting RAS/MAPK pathway.
- ERAS-801: An EGFR inhibitor being evaluated in clinical trials for the treatment of Glioblastoma and other cancers. Market share data is not yet available as the drug is still in clinical development. Competitors include companies developing other EGFR inhibitors and therapies targeting Glioblastoma.
- ERAS-601: A first-in-class oral, selective and potent SHP2 inhibitor. It is being evaluated in a Phase 1 clinical trial for patients with advanced solid tumors. Market share data is not yet available. Competitors include Revolution Medicines (RVMD) and Novartis (NVS).
Market Dynamics
Industry Overview
The oncology market is a large and rapidly growing market, driven by the increasing incidence of cancer globally and advances in cancer treatment. Precision oncology, which focuses on targeting specific genetic mutations and pathways driving cancer growth, is a key area of innovation.
Positioning
Erasca is positioned as a precision oncology company focused on developing novel therapies targeting the RAS/MAPK pathway. Its competitive advantage lies in its expertise in this pathway and its pipeline of differentiated drug candidates.
Total Addressable Market (TAM)
The total addressable market for RAS/MAPK pathway inhibitors is estimated to be billions of dollars, reflecting the high prevalence of RAS/MAPK mutations in cancer. Erasca is well-positioned to capture a significant share of this market if its drug candidates are successfully developed and commercialized.
Upturn SWOT Analysis
Strengths
- Strong scientific expertise in RAS/MAPK pathway
- Promising pipeline of novel drug candidates
- Experienced management team
- Focus on precision oncology
Weaknesses
- Clinical stage company with no approved products
- High risk of clinical trial failure
- Dependent on successful fundraising
- Limited commercial infrastructure
Opportunities
- Potential to develop first-in-class therapies
- Expansion into new cancer indications
- Partnerships with larger pharmaceutical companies
- Increasing adoption of precision oncology
Threats
- Competition from other companies developing RAS/MAPK inhibitors
- Regulatory hurdles
- Pricing pressures
- Patent challenges
Competitors and Market Share
Key Competitors
- RVMD
- MRTX
- NVS
Competitive Landscape
Erasca competes with other biotech and pharmaceutical companies developing therapies targeting the RAS/MAPK pathway. Key competitive factors include the novelty and efficacy of drug candidates, clinical trial design, and regulatory strategy. Market share is currently 0% for all these players, but it is expected that they will all compete for the same patients
Growth Trajectory and Initiatives
Historical Growth: Growth is measured by progress in clinical trials and expansion of the pipeline rather than revenue.
Future Projections: Future growth depends on positive clinical trial results and regulatory approvals. Analyst estimates vary widely and are highly dependent on pipeline progress.
Recent Initiatives: Recent initiatives include advancing lead programs through clinical trials, expanding the pipeline through internal discovery and external collaborations, and strengthening the management team.
Summary
Erasca is a clinical-stage oncology company with a promising pipeline focused on the RAS/MAPK pathway. While the company faces the inherent risks of drug development, its strong scientific expertise and differentiated pipeline position it well for future growth. Successful clinical trial results and potential partnerships are key factors to watch. The company needs to carefully manage its cash burn and navigate the competitive landscape.
Peer Comparison
Sources and Disclaimers
Data Sources:
- Company filings, press releases, investor presentations, analyst reports.
Disclaimers:
The data and analysis provided are for informational purposes only and should not be considered investment advice. Investing in biotech companies is highly speculative and involves significant risks.
AI Summarization is directionally correct and might not be accurate.
Summarized information shown could be a few years old and not current.
Fundamental Rating based on AI could be based on old data.
AI-generated summaries may have inaccuracies (hallucinations). Please verify the information before taking action.
About Erasca Inc
Exchange NASDAQ | Headquaters San Diego, CA, United States | ||
IPO Launch date 2021-07-16 | Co-Founder, Chairman & CEO Dr. Jonathan E. Lim M.D. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 103 | Website https://www.erasca.com |
Full time employees 103 | Website https://www.erasca.com |
Erasca, Inc., a clinical-stage precision oncology company, focuses on discovering, developing, and commercializing therapies for patients with RAS/MAPK pathway-driven cancers. The company's lead product is naporafenib which is in SEACRAFT-2 pivotal Phase 3 trial for patients with NRAS-mutated (NRASm) melanoma; and in SEACRAFT-1 Phase 1b trial for patients with NRAS Q61X melanoma. It also develops ERAS-0015, a pan-RAS molecular glue for the treatment of patients with RAS-altered solid tumors; ERAS-4001, a pan-KRAS inhibitor for the treatment of patients with KRAS-altered solid tumors; and ERAS-12, an investigational EGFR D2/D3 biparatopic antibody (bpAb) for the treatment of EGRF and RAS/MAPK solid tumors. In addition, the company's products under development include ERAS-801, a central nervous system (CNS)-penetrant EGFR inhibitor for patients with EGFR-altered recurrent glioblastoma (GBM) which is in phase 1 clinical trials; and ERAS-007, an oral inhibitor of ERK1/2 and ERAS-601, an oral SHP2 inhibitor for patients with advanced or metastatic solid tumors. It has a license agreement with Novartis to develop, manufacture, use, and commercialize naporafenib; Katmai Pharmaceuticals, Inc. to develop, manufacture, use, and commercialize ERAS-801 and certain other related compounds; and NiKang Therapeutics, Inc. to develop and commercialize ERAS-601 and certain other related compounds. Erasca, Inc. was incorporated in 2018 and is headquartered in San Diego, California.

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