Epicrispr secures $90M after early data on epigenetic FSHD treatment | 2026-08-11 on August 12, 2026 AAV vector DUX4 protein, human EPI-321 Epicrispr epigenetic editing Muscular Dystrophy, Facioscapulohumeral Scientific Study Series C +
Epicrispr raises $90M to rewrite treatment of rare muscle disease on August 11, 2026 DUX4 protein, human EPI-321 Epicrispr epigenetic editing Fidelity Management & Research FOXD3 gene Genus Phalacrocorax (organism) muscle mass Muscular Dystrophy, Facioscapulohumeral Sanofi Ventures Series C +
How one biotech is using 'digital twins' to study a muscle disease therapy on June 29, 2026 digital twins EPI-321 Epicrispr Biotechnologies epigenetic editing gains lean muscle muscle disease therapy Muscular Dystrophy, Facioscapulohumeral +