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ENVISION phase 3 study of SRP-9001 in ambulatory and non-ambulatory Duchenne muscular dystrophy

jRCT2033230274Phase 3Not yet recruiting

Sponsor
Sarepta Therapeutics
Start
Sep 2023
Modality
Gene Therapies
01

Overview

Phase 3, randomised, double-blind trial of delandistrogene moxeparvovec in Duchenne muscular dystrophy (DMD) (2 arms), sponsored by Sarepta Therapeutics. Primary endpoint: Change from baseline in Performance of Upper Limb total score. Planned start Sep 2023; status: not yet recruiting.

02

Drugs

delandistrogene moxeparvovec
03

Conditions

Duchenne muscular dystrophy (DMD)

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