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- $531.0MMarket Cap
- 54.95%1-Year Change
- BiotechnologyIndustry
Editas Medicine (EDIT)
Key Performance
More- Earnings Score: 56
- Momentum Score: 51
- True Yield: N/A
- Financial Health Score: 4
Latest Research & News
CRISPR Therapeutics vs. Editas Medicine: Which Gene Editing Stock Is a Better Buy in 2026?
The article compares two gene-editing biotech companies: CRISPR Therapeutics, which has FDA-approved CASGEVY therapy and stronger financials, versus Editas Medicine, which focuses on in vivo gene editing but lacks FDA approval and has a weaker balance sheet. CRISPR Therapeutics is recommended as the better 2026 investment due to its commercial-stage advantage, stronger cash position, and lower financial risk, despite Editas offering potentially greater upside if successful.
05/31/2026, 12:11 PM • The Motley Fool
Neutrolis Appoints Caren Deardorf as Chief Business & Strategy Officer
Neutrolis Inc., a clinical-stage biotech company focused on treating autoimmune and inflammatory diseases, announced the appointment of Caren Deardorf as Chief Business & Strategy Officer. Deardorf brings over 30 years of executive leadership experience in commercialization and product launches, previously serving as Chief Commercial & Strategy Officer at Editas Medicine, Magenta Therapeutics, and Ohana Biosciences. She will lead business development and commercial strategy as Neutrolis advances its NTR-1011 candidate following positive Phase 1a results.
04/15/2026, 2:00 PM • GlobeNewswire
Editas Medicine Announces Fourth Quarter and Full Year 2025 Results and Business Updates
Editas Medicine reported Q4 2025 financial results with a net loss of $5.6 million ($0.06 per share), down from $45.4 million in Q4 2024. The company's lead candidate EDIT-401 demonstrated >90% mean LDL-C reduction in preclinical studies and remains on track for IND/CTA submission by mid-2026, with first-in-human trials in HeFH patients expected to begin later in 2026. The company maintains a strong cash position with runway into Q3 2027.
03/09/2026, 7:00 AM • GlobeNewswire
The global genome editing market is projected to grow from $9.39 billion in 2025 to $23.66 billion by 2031, driven by increased funding, CRISPR advancements, and AI integration. However, off-target effects and regulatory hurdles pose significant challenges. Key developments include AI-enhanced editing systems achieving 95% reduction in off-target effects and expansion into agricultural biotechnology.
01/22/2026, 4:56 AM • GlobeNewswire
Gene Therapies for Cancer Treatment Market Projects USD 238.77 Billion at 39.94% CAGR by 2034
The global gene therapies for cancer treatment market is expected to grow from $8.28 billion in 2024 to $238.77 billion by 2034, with a 39.94% CAGR. North America currently dominates the market, with CAR-T cell therapy leading market share and significant innovations driving growth.
11/17/2025, 10:00 AM • GlobeNewswire
Healthcare Innovation Accelerates as Four Converging Forces Drive Early Intervention Focus
Healthcare companies are advancing precision medicine through gene therapy, AI diagnostics, and innovative treatments targeting age-related conditions, with several firms making significant breakthroughs in areas like longevity biotechnology and personalized care.
09/25/2025, 9:15 AM • Benzinga
The global gene editing market is projected to grow from USD 6.09 billion in 2024 to USD 15.46 billion by 2032, driven by CRISPR technology advances, therapeutic applications, and significant research funding, with North America leading market development.
09/02/2025, 6:00 AM • GlobeNewswire
Two biotech companies, Editas Medicine and Sarepta Therapeutics, are experiencing severe challenges that make them unattractive investment options. Editas Medicine lacks marketable products and has a history of abandoned projects, while Sarepta Therapeutics is dealing with patient deaths related to its gene therapy treatment Elevidys.
06/27/2025, 8:15 AM • The Motley Fool
Peers
Statistics
MoreInformation as of 06/02/2026
Company Profile
Editas Medicine, Inc., a clinical stage genome editing company, focuses on developing transformative genomic medicines to treat a range of serious diseases. The company develops a proprietary gene editing platform based on CRISPR technology. Its lead program is EDIT-401, a one-time therapy designed to reduce LDL cholesterol through the upregulation of the LDL receptor to treat hyperlipidemia. The company also develops therapies to treat Sickle cell disease and transfusion-dependent beta thalassemia; and in vivo gene editing medicines indicated for other cells and tissues. It has a research collaboration with Juno Therapeutics, Inc. to develop alpha-beta T-cell experimental medicines for the treatment of solid and liquid tumors, and autoimmune disease. 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.
Key Executives
- Gilmore O'Neill
- Linda C. Burkly
- Amy Parison
- George McDonald Church
- Gregory Whitehead
Current Ownership Distribution
- Institutions951.2M (77.63%)
- Mutual Funds261.4M (21.33%)
- Insiders12.8M (1.05%)
- Other0 (0.00%)