Greenstone Biosciences Receives NIH R61 Grant to Advance Cardiac Fibrosis Therapeutics for Duchenne Muscular Dystrophy Business Wire (Press Release) 00:36
Cardiomyopathy in Duchenne muscular dystrophy is focus of nearly $2M grant Newswise (Press Release) 16:21 Tue, 04 Aug
Bloodstream-delivered cell therapy slows muscle decline in young people with Duchenne muscular dystrophy, phase 3 trial finds Clinical Services Journal 09:24 Tue, 04 Aug
STAT Plus: Pharmalittle: We’re reading about an FDA panel nixing a Duchenne drug, FTC suing Hims & Hers, and more STAT 14:18 Thu, 30 Jul
MRI-derived 3D lower limb muscle shape as a biomarker for disease severity in Duchenne muscular dystrophy Nature.com 13:18 Thu, 30 Jul
Court orders home care, breathing machine for Duchenne patient Beka Shonia Georgia Today 08:46 Thu, 30 Jul
The Lancet Publica Ensayo Histórico Sobre Terapia Para Distrofia Muscular de Duchenne Newswise (Press Release) 17:41 Wed, 29 Jul
The Lancet Publishes Landmark Trial of Duchenne Muscular Dystrophy Therapy Newswise (Press Release) 17:10 Wed, 29 Jul
FDA Advisers Meet Today on a Cell Therapy for the Heart Disease That Now Kills Most Duchenne Patients Medical Daily 12:00 Wed, 29 Jul
STAT Plus: Pharmalittle: We’re reading about FDA views on a Duchenne drug, GSK cost savings, and more STAT 14:30 Tue, 28 Jul
Capricor Therapeutics shares tumble after FDA reviewers raise concerns over Duchenne therapy Proactive Investors (US) 15:59 Mon, 27 Jul
STAT Plus: Ahead of hearing, FDA questions the efficacy of Capricor’s Duchenne drug STAT 14:14 Mon, 27 Jul
NOX4 inhibition may protect hearts affected by Duchenne muscular dystrophy News-Medical.Net 18:42 Fri, 17 Jul
Earlier Intervention May Improve Motor Function in Duchenne Muscular Dystrophy Newswise (Press Release) 15:49 Thu, 09 Jul
Satellos Bioscience Duchenne Drug Candidate's Interim Data Boosts Confidence Benzinga 14:37 Wed, 08 Jul Article paywall
CureDuchenne Launches 'A Cure Can't Wait' PSA Campaign, Using the Power of a Birthday to Inspire Public Action for Duchenne Muscular Dystrophy PR Newswire (Press Release) 13:06 Wed, 08 Jul
Grünenthal receives FDA designations for tegacorat in Duchenne muscular dystrophy PharmaTimes 10:28 Wed, 08 Jul
Grünenthal receives FDA Orphan Drug and Rare Pediatric Disease Designations for Tegacorat for the Treatment of Duchenne Muscular Dystrophy Pressat (Press Release) 10:02 Wed, 08 Jul
