StockNews.AI
EDIT
StockNews.AI
7 hrs

Editas Medicine Reports In Vivo Proof-of-Concept Data for EDIT-401 at the European Society of Gene and Cell Therapy (ESGCT) 32nd Annual Congress

1. EDIT-401 shows ≥90% LDL-C reduction in preclinical studies. 2. Therapy utilizes CRISPR/Cas9 technology for efficient gene editing. 3. Durable LDL-C reduction maintained over three months in mouse models. 4. Presentation at ESGCT Congress highlights innovative gene editing approaches. 5. Editas aims to commercialize transformative medicines for serious diseases.

5m saved
Insight
Article

FAQ

Why Bullish?

The strong efficacy data for EDIT-401 suggests potential market success. Historical trends show positive price movements following successful trial results in biotech.

How important is it?

The article presents critical preclinical findings that could enhance EDIT's market position and investment appeal.

Why Long Term?

If proven effective in later trials, EDIT-401 could lead to significant market adoption and revenue. Preclinical success often influences investor confidence in longer-term prospects.

Related Companies

CRSPNTLAVCELPGEN
CAMBRIDGE, Mass., Oct. 09, 2025 (GLOBE NEWSWIRE) -- Editas Medicine, Inc. (Nasdaq: EDIT), a pioneering gene editing company, today reported in vivo preclinical proof-of-concept data for EDIT-401, an experimental, potential best-in-class, one-time therapy to significantly reduce LDL-cholesterol (LDL-C), at the 32nd Annual European Society of Gene and Cell Therapy (ESGCT) Congress in Seville, Spain. The Company shared results from preclinical studies demonstrating potent and durable reductions in LDL-C through upregulation of the LDL receptor (LDLR). Key EDIT-401 Data Presented includes: Robust efficacy data: ≥90% LDL-C reduction in non-human primates achieved within 48 hours of a single dose of EDIT-401; ≥90% LDL-C reduction in mice with high baseline LDL-C and reduced LDLR functionOptimized therapeutic strategy: CRISPR/Cas9 nuclease and dual gRNAs with LNP delivery disrupt negative regulatory elements in the 3' UTR, increasing mRNA stability enabling potent LDLR upregulation≥6-fold mean increase in LDLR protein in the NHP liver, requiring only a moderate level of functional editing of LDLR alleles Durable effect: LDL-C reduction maintained in mouse models in a three-month study “The in vivo proof-of-concept data presented today reinforce the potential impact of our differentiated upregulation strategy. In preclinical non-human primate studies, EDIT-401 achieved robust efficacy data with a ≥90% mean LDL-C reduction. These data strengthen our conviction that EDIT-401 represents a novel therapeutic approach with the potential to significantly improve outcomes for people living with high LDL cholesterol,” said Linda C. Burkly, Ph.D., Executive Vice President and Chief Scientific Officer, Editas Medicine. Abstracts are available to registrants on the ESGCT website. The presentation will also be posted to the “Posters & Presentations” section of the Company’s website at the time of the presentation and will remain accessible following the event.Oral Presentation Details: Title: A transformative LDL cholesterol-lowering in vivo CRISPR gene editing medicine that functionally upregulates LDLR in mice and non-human primatesSession Date and Time: Thursday, October 9, 5:00 p.m. CEST / 11:00 a.m. ET  Session Title: 9A: Gene Editing II, Ex Vivo ApplicationsRoom: Parallel APresenter: Linda Burkly, Ph.D., Executive Vice President and Chief Scientific Officer, Editas Medicine Final Abstract Number: OR069 About Editas Medicine As a pioneering gene editing company, Editas Medicine is focused on translating the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of transformative in vivo medicines for people living with serious diseases around the world. Editas Medicine aims to discover, develop, manufacture, and commercialize durable, precision in vivo gene editing medicines for a broad class of diseases. Editas Medicine is the exclusive licensee of Broad Institute’s Cas12a patent estate and Broad Institute and Harvard University’s Cas9 patent estates for human medicines. For the latest information and scientific presentations, please visit www.editasmedicine.com.

Related News