FDA Accepts Biologics License Application for Duchenne Muscular Dystrophy Cardiomyopathy Treatment
1. CAPR's BLA for deramiocel received FDA acceptance and priority review. 2. PDUFA action date set for August 31, 2025, indicating a clear path ahead. 3. Exclusive distribution rights for deramiocel granted to NS Pharma. 4. Deramiocel addresses unmet needs for Duchenne muscular dystrophy patients. 5. Clinical data shows deramiocel's potential for significant therapeutic impact.