
Entrada Therapeutics unveils pipeline advances for Duchenne and myotonic dystrophy therapies

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Entrada Therapeutics Inc. has announced advancements in its pipeline for treating Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1). The DMD program includes candidates ENTR-601-44 and ENTR-601-45, with clinical data expected in 2026, and ENTR-601-50 authorized for a Phase 1⁄2 study in the U.K. The DM1 program, in partnership with Vertex, is in the multiple ascending dose phase, with completion expected in early 2026. The company is also exploring accelerated approval pathways and plans to initiate global registrational studies.
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