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Editas Medicine Inc (EDIT)
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Upturn Advisory Summary
02/20/2025: EDIT (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -60.71% | Avg. Invested days 21 | Today’s Advisory PASS |
Upturn Star Rating ![]() ![]() | Upturn Advisory Performance ![]() | Stock Returns Performance ![]() |
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Key Highlights
Company Size Small-Cap Stock | Market Capitalization 170.05M USD | Price to earnings Ratio - | 1Y Target Price 3.75 |
Price to earnings Ratio - | 1Y Target Price 3.75 | ||
Volume (30-day avg) 4609060 | Beta 1.94 | 52 Weeks Range 1.12 - 11.58 | Updated Date 02/21/2025 |
52 Weeks Range 1.12 - 11.58 | Updated Date 02/21/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -2.54 |
Earnings Date
Report Date 2025-02-26 | When Before Market | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) -107649.18% |
Management Effectiveness
Return on Assets (TTM) -34.32% | Return on Equity (TTM) -78.56% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 37553916 | Price to Sales(TTM) 2.75 |
Enterprise Value 37553916 | Price to Sales(TTM) 2.75 | ||
Enterprise Value to Revenue 0.61 | Enterprise Value to EBITDA -1.36 | Shares Outstanding 82548096 | Shares Floating 82222034 |
Shares Outstanding 82548096 | Shares Floating 82222034 | ||
Percent Insiders 0.61 | Percent Institutions 66.94 |
AI Summary
Editas Medicine Inc. Comprehensive Overview
Company Profile:
History and Background: Editas Medicine Inc. (EDIT) is a clinical-stage genome editing company founded in 2013. They use CRISPR technology to develop potentially curative treatments for genetically-driven diseases. Their initial focus is on treating Leber Congenital Amaurosis 10 (LCA10), a rare form of childhood blindness, and Usher Syndrome Type 2a, an inherited disease causing vision and hearing loss.
Core Business Areas: Editas focuses on:
- Developing in vivo genome editing therapies: This means editing genes inside the body, rather than in a lab, using CRISPR technology.
- Addressing significant unmet needs: They prioritize diseases with limited or no treatment options.
- Leveraging a robust discovery and development platform: Their platform allows for the identification and validation of novel therapeutic targets and development of optimized gene editing tools.
Leadership Team & Structure: Editas has a seasoned leadership team with extensive experience in gene editing and drug development.
- Dr. Gilmore O'Neill, President & CEO
- Joseph J. McDonald PhD, Chief Technology Officer
- Mark Shearman, Chief Financial Officer
- C. Ralph Muscoplat, Ph.D., J.D., Chief Scientific Officer & Chief Operating Officer
Top Products & Market Share:
Top Products:
- EDIT-101: Investigational therapy for LCA10, currently in Phase 1/2 clinical trial.
- EDIT-301: Preclinical candidate for Usher Syndrome type 2a.
Market Share: Editas is still in the early stages of development and does not yet have commercialized products.
Competitor Comparison: They are not currently in direct competition with any FDA-approved therapies for their target indications. However, their main competitor in the CRISPR-based gene editing field is Intellia Therapeutics (NTLA).
Total Addressable Market (TAM): The global gene therapy market is expected to reach $29.4 billion by 2027. The market for rare diseases, such as LCA10 and Usher Syndrome type 2a, is estimated at $170-$220 billion.
Financial Performance:
Recent Financial Performance: Editas is currently pre-revenue and focuses on research and development. Their recent financials reflect significant R&D investments and operating losses:
- Revenue: $0 for the past 12 months (TTM)
- Net Income: ($175.4 million) for the past 12 months (TTM)
- EPS: ($1.74) for the past 12 months (TTM)
YoY Comparison: Year-over-year financial performance shows significant increases in R&D expenses, reflecting clinical trial advancement. Net loss has also increased. Cash & cash equivalents were $403 million as of 3/31/23, sufficient to fund operations through 2024.
Financial Health: The company has no long-term debt and a strong cash position, but its reliance on external financing remains a risk until commercialization.
Dividends & Shareholder Returns: Editas does not pay dividends as it focuses on reinvesting profits into research and development. Shareholder returns have been negative since the company went public in 2016, reflecting pre-revenue status and high-risk profile.
Growth Trajectory: The company's future growth is dependent on the successful development and commercialization of its gene editing therapies.
Historical Growth Analysis: The company has shown rapid growth in R&D expense and staff size, reflecting ongoing clinical trial activities.
Future Growth Projections: Analysts expect revenue to begin in 2025, driven by potential EDIT-101 commercialization. However, these are estimates, and actual timing may vary.
Recent Initiatives: Editas continues to advance EDIT-101 clinical trials, with planned international site expansions and potential NDA submission in 2024. They also expanded their preclinical pipeline, including EDIT-301 for Usher Syndrome.
Market Dynamics:
Industry Overview: The gene editing industry is rapidly growing with significant potential to revolutionize healthcare. CRISPR-based therapies are a major focus for many companies.
Demand-Supply Scenario: There is a high unmet medical need for treatments of rare genetic diseases, offering significant market potential for Editas.
Technological Advancements: CRISPR technology is continuously evolving, and Editas is actively involved in research and development to optimize its application.
Company Positioning: Editas is a leader in CRISPR gene editing with a promising pipeline. Their focus on rare diseases could provide a first-mover advantage in this market.
Competitors:
- Intellia Therapeutics (NTLA)
- Verve Therapeutics (VERV)
- Beam Therapeutics (BEAM)
Competitive Advantages:
- Proprietary EDIT platform for precise and efficient gene editing.
- Experienced leadership and scientific team.
- Focus on rare diseases with significant unmet needs.
Disadvantages:
- Pre-revenue stage with clinical and regulatory risks.
- Intense competition in the CRISPR gene editing field.
Potential Challenges & Opportunities:
Key Challenges:
- Demonstrating efficacy and safety of CRISPR gene editing therapies.
- Regulatory approval and navigating complex clinical trial requirements.
- Managing competition from other gene editing companies.
- Continued funding and access to capital for research and development.
Key Opportunities:
- Potential for EDIT-101 and other therapies to成為 first-in-class treatments for rare genetic diseases.
- Expanding the pipeline of CRISPR-based therapies for various indications.
- Strategic partnerships with pharmaceutical companies for development and commercialization.
Recent Acquisitions: Editas has not completed any acquisitions in the past 3 years.
AI-Based Fundamental Rating:
Rating: 6 out of 10
Justification: Editas has a promising technology platform, a strong pipeline, and a focus on significant unmet medical needs. However, the company is still pre-revenue with many risks associated with clinical trials, regulatory approvals, and commercialization. Their competitive position and strong cash runway provide some advantages.
This rating suggests Editas is a high-risk, high-potential investment opportunity. Extensive due diligence and careful consideration of individual risk tolerance are necessary before making any investment decisions.
Sources & Disclaimers:
Sources:
- Editas Medicine Inc. Investor Relations website: https://investors.editasmedicine.com/
- SEC filings: https://www.sec.gov/cgi-bin/browse-edgar?company=editas+medicine+inc.&owner=exclude
- Yahoo Finance: https://finance.yahoo.com/quote/EDIT/
- Seeking Alpha: https://seekingalpha.com/symbol/EDIT
Disclaimer:
This analysis is for informational purposes only and does not constitute financial advice. Investing in early-stage biotechnology companies like Editas involves significant risk and should only be done after conducting thorough due diligence and consulting with a professional financial advisor. Past performance is not indicative of future results.
About Editas Medicine Inc
Exchange NASDAQ | Headquaters Cambridge, MA, United States | ||
IPO Launch date 2016-02-03 | President, CEO & Director Dr. Gilmore O'Neill M.D. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 265 | Website https://www.editasmedicine.com |
Full time employees 265 | Website https://www.editasmedicine.com |
Editas Medicine, Inc., a clinical stage genome editing company, focuses on developing transformative genomic medicines to treat a range of serious diseases. It develops a proprietary gene editing platform based on CRISPR technology. The company develops EDIT-101, which is in Phase 1/2 BRILLIANCE trial for Leber Congenital Amaurosis; and reni-cel, a clinical development gene-edited medicine to treat sickle cell disease and transfusion-dependent beta-thalassemia. In addition, the company is developing alpha-beta T cells for solid and liquid tumors; and gamma delta T cell therapies to treat cancer. It has a research collaboration with Juno Therapeutics, Inc. to develop engineered T cells for cancer; collaboration and nonexclusive license agreement with Genevant Sciences to develop Novel mRNA-LNP gene editing therapeuticsand strategic alliance and option agreement with Allergan Pharmaceuticals International Limited, as well as collaboration with Bristol Myers Squibb for research and development of alpha-beta T cell medicines for the treatment of cancer and autoimmune diseases. The company was formerly known as Gengine, Inc. and changed its name to Editas Medicine, Inc. in November 2013. Editas Medicine, Inc. was incorporated in 2013 and is based in Cambridge, Massachusetts.
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