FDA Grants Orphan Drug Designation to EPI-321, Epic Bio’s Novel Genetic Medicine Candidate for Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD)
– Potential one-time therapy for the treatment of FSHD includes a novel non-cutting dCas protein delivered via a single AAV – – EPI-321 is the only therapy designed to target the epigenetic root cause of the disease – – Company on track for clinical initiation in first half of 2024 – SOUTH SAN FRANCISCO, Calif. … Read more