2025-08-08 • musculardystrophynews.com
FSHD patients sought for first clinical trial testing EPI-321
2025-08-08 • musculardystrophynews.com
FSHD patients sought for first clinical trial testing EPI-3212025-08-07 • musculardystrophynews.com
DYNE-251 for DMD granted FDA breakthrough therapy designation2025-08-06 • businesswire.com
Epicrispr Biotechnologies Doses First Patient in First-in-Human Clinical Trial of EPI-321 for Facioscapulohumeral Muscular Dystrophy2025-08-06 • drugdiscoverynews.com
FDA grants Breakthrough Therapy designation to Duchenne muscular dystrophy therapeutic2025-08-05 • thepharmaletter.com
Hansa Biopharma supportive data from treatment with imlifidase in DMD2025-08-05 • globenewswire.com
Dyne Therapeutics Announces FDA Breakthrough Therapy Designation for DYNE-251 in Duchenne Muscular Dystrophy (DMD)2025-08-04 • fingerlakes1.com
New York launches Empire AI medical projects to target ALS and muscular dystrophy2025-07-30 • biospace.com
Genethon to Launch Pivotal Trial in Europe of GNT0004 a Low-Dose Microdystrophin Gene Therapy for Duchenne Muscular Dystrophy2025-07-30 • neurologylive.com
EMA Issues Negative Opinion for Sarepta’s Gene Therapy Elevidys2025-07-30 • PR Newswire
MyHealthTeam Launches myMDteam Focused on Muscular Dystrophy2025-07-26 • medscape.com
EMA Says No to Duchenne Gene Therapy Elevidys2025-07-24 • biospace.com
Precision BioSciences Receives FDA Orphan Drug Designation for PBGENE-DMD for the Treatment of Duchenne Muscular Dystrophy2025-07-24 • cgtlive.com
FDA Revokes Sarepta’s Platform Technology Designation for Muscular Dystrophy Gene Therapy Vector Following Patient Deaths2025-07-22 • newsweek.com
FDA Suspends Muscular Dystrophy Drug After 3 Patient Deaths2025-07-22 • pharmalive.com
Sarepta Therapeutics Issues Statement on Fda Clinical Hold on Elevidys2025-07-22 • fiercebiotech.com
Sarepta LGMD trials all hit by FDA hold amid newly surfaced safety concerns over gene therapy2025-07-22 • in.investing.com
FDA places clinical hold on Sarepta’s gene therapy trials for muscular dystrophy2025-07-20 • washingtonpost.com
Gene therapy maker Sarepta tells FDA it won't halt shipments despite patient deaths2025-07-19 • bostonglobe.com
Sarepta Therapeutics crisis is huge blow to Duchenne families, company2025-07-19 • investopedia.com
Sarepta Therapeutics Stock Tumbles on Report of Third Death in Clinical Trial2025-07-19 • musculardystrophynews.com
Dosing begins in gene therapy trial for DMD-linked heart disease2025-07-19 • kumc.edu
First cardiovascular gene therapy trial in U.S. for people with Duchenne muscular dystrophy begins at KU Medical Center2025-07-18 • prnewswire.co.uk
Facioscapulohumeral Muscular Dystrophy Market Gearing Up for Outstanding Expansion Across the 7MM During the Forecast Period (2025-2034) | DelveInsight2025-07-17 • stocktitan.net
Precision BioSciences Highlights New Preclinical Data for PBGENE-DMD Further Supporting Advancement of Novel Gene Editing Approach for the Treatment of Duchenne Muscular Dystrophy Towards Clinic2025-07-16 • PR Newswire
Springbok Analytics Publishes Predictive Disease Progression Model for Muscular Dystrophy2025-07-12 • stocktitan.net
Capricor Therapeutics Provides Regulatory Update on Deramiocel BLA for Duchenne Muscular Dystrophy2025-07-10 • PR Newswire
REGENXBIO Announces Publication of Preclinical Results Demonstrating Functional Benefits of Novel Microdystrophin Construct in RGX-202 Investigational Gene Therapy for Duchenne Muscular Dystrophy2025-07-10 • PR Newswire
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