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Erasca Inc (ERAS)



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Upturn Advisory Summary
08/14/2025: ERAS (1-star) has a low Upturn Star Rating. Not recommended to BUY.
1 Year Target Price $5.29
1 Year Target Price $5.29
5 | Strong Buy |
3 | Buy |
0 | Hold |
0 | Sell |
0 | Strong Sell |
Analysis of Past Performance
Type Stock | Historic Profit -62.58% | Avg. Invested days 25 | 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 445.36M USD | Price to earnings Ratio - | 1Y Target Price 5.29 |
Price to earnings Ratio - | 1Y Target Price 5.29 | ||
Volume (30-day avg) 8 | Beta 1.07 | 52 Weeks Range 1.01 - 3.31 | Updated Date 08/15/2025 |
52 Weeks Range 1.01 - 3.31 | Updated Date 08/15/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -0.39 |
Earnings Date
Report Date 2025-08-12 | When - | Estimate -0.12 | Actual -0.12 |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -22.16% | Return on Equity (TTM) -45.82% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 194124118 | Price to Sales(TTM) - |
Enterprise Value 194124118 | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA -1.57 | Shares Outstanding 283670016 | Shares Floating 198473973 |
Shares Outstanding 283670016 | Shares Floating 198473973 | ||
Percent Insiders 11.68 | Percent Institutions 83.94 |
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, Erasca aims to erase cancer by creating therapies that target key oncogenic drivers.
Core Business Areas
- Drug Discovery and Development: Focused on developing novel therapies that directly inhibit RAS/MAPK pathway proteins and/or suppress upstream receptor tyrosine kinase signaling.
- Clinical Trials: Conducting clinical trials to evaluate the safety and efficacy of its investigational therapies in various cancer indications.
- Commercialization Planning: Preparing for the potential commercial launch of its products, including manufacturing, marketing, and distribution strategies.
Leadership and Structure
Jonathan E. Lim, M.D., serves as the Chairman, CEO, and Co-Founder. The company has a management team with expertise in drug development, oncology, and business strategy. Erasca has a Board of Directors overseeing the strategic direction.
Top Products and Market Share
Key Offerings
- ERAS-007 (CDK4/6 Inhibitor): A CDK4/6 inhibitor in clinical development for solid tumors. Competitors include Eli Lilly (Verzenio), Pfizer (Ibrance), and Novartis (Kisqali).
- ERAS-601 (SHP2 Inhibitor): A SHP2 inhibitor in clinical development for solid tumors. Competitors include Revolution Medicines (RMC-4630).
- ERAS-3490 (KRAS G12C inhibitor): A KRAS G12C inhibitor, designed to overcome the limitations of existing inhibitors in this class. Competitors: Amgen (Lumakras) and Mirati (Krazati).
Market Dynamics
Industry Overview
The oncology drug market is a large and rapidly growing market. Increased cancer incidence, aging populations, and technological advances in diagnostics and treatment are driving market growth.
Positioning
Erasca is positioned as a precision oncology company focused on RAS/MAPK pathway-driven cancers, differentiating itself through its portfolio of novel inhibitors and combination strategies.
Total Addressable Market (TAM)
The TAM for targeted cancer therapies is estimated to be in the tens of billions of dollars annually. Erasca's focus on RAS/MAPK pathway-driven cancers positions it to capture a significant portion of this market, if successful in clinical trials and commercialization.
Upturn SWOT Analysis
Strengths
- Strong pipeline of novel drug candidates targeting RAS/MAPK pathway
- Experienced management team with expertise in oncology drug development
- Potential for first-in-class or best-in-class therapies
- Focus on combination strategies to address drug resistance
Weaknesses
- Clinical trial risk and uncertainty
- High cash burn rate associated with drug development
- Reliance on successful clinical trial outcomes
- Competition from established pharmaceutical companies
Opportunities
- Potential for strategic partnerships and collaborations
- Expansion into new cancer indications
- Approval and commercialization of multiple drug candidates
- Advancements in precision medicine and biomarker discovery
Threats
- Clinical trial failures
- Regulatory hurdles and delays
- Competition from other drug developers
- Changes in reimbursement policies
Competitors and Market Share
Key Competitors
- LLY
- PFE
- NVS
- AMGN
- MRTX
- RVSN
Competitive Landscape
Erasca faces intense competition from established pharmaceutical companies and other biotech companies developing therapies for RAS/MAPK pathway-driven cancers. Its success will depend on demonstrating superior efficacy, safety, and convenience in clinical trials.
Growth Trajectory and Initiatives
Historical Growth: Historical growth is characterized by investment in R&D.
Future Projections: Future growth is contingent on clinical trial success and regulatory approvals.
Recent Initiatives: Advancing clinical trials for ERAS-007, ERAS-601, and ERAS-3490. Presenting clinical data at medical conferences. Expanding the pipeline through internal discovery efforts.
Summary
Erasca is a clinical-stage biotech company with a promising pipeline focused on RAS/MAPK pathway-driven cancers. Its future hinges on successful clinical trial outcomes and regulatory approvals, and it faces significant competition from larger players. The company's strength lies in its targeted approach and experienced team, while its weaknesses include high cash burn and clinical trial risk. Overall, Erasca is a high-risk, high-reward investment.
Peer Comparison
Sources and Disclaimers
Data Sources:
- Company Filings (SEC)
- Investor Presentations
- Press Releases
- Analyst Reports
Disclaimers:
This analysis is for informational purposes only and should not be considered investment advice. The information provided is based on publicly available data and is subject to change. Investing in biotech companies involves significant risks, including the risk of losing your entire investment.
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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