Epicrispr raises $90M to rewrite treatment of rare muscle disease

Epicrispr Biotechnologies raised $90 million in a Series C round to advance its epigenetic therapy EPI-321 for facioscapulohumeral muscular dystrophy, a rare muscle disease with no approved treatments.

The funding, co‑led by Octagon Capital and Janus Henderson Investors, supports pivotal clinical development of EPI-321 and broader investments in Epicrispr’s epigenetic editing platform.

Early clinical data from an ongoing Phase 1/2 trial show that EPI-321 increased lean muscle mass in FSHD patients after a single infusion, with no serious adverse events reported.

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Epicrispr bags $90M to rewrite treatment of rare muscle disease

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