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epigenetics
Biotech
Epicrispr bags $90M to rewrite treatment of rare muscle disease
The round positions the biotech to advance a pipeline of epigenetic medicines led by an early-phase facioscapulohumeral muscular dystrophy prospect.
Nick Paul Taylor
Aug 11, 2026 10:30am
Scribe records upsized $129M IPO to fund genetic med trials
Jul 24, 2026 4:00am
Scribe aims for $96M IPO to fund lipid-lowering genetic meds
Jul 20, 2026 9:48am
Scribe notes IPO plan to push lipid-lowering meds through clinic
Jul 6, 2026 7:54am
Epicrispr gene silencer enhances muscle in muscular dystrophy
Jun 26, 2026 10:40am
Anti-aging biotech NewLimit nabs $435M to rejuvenate old cells
Jun 2, 2026 1:00pm
