Trial intelligence / Profile preview

EXPEDITION long-term follow-up after delandistrogene moxeparvovec

jRCT2053240056Phase 3Not yet recruiting

Sponsor
Sarepta Therapeutics
Start
Aug 2024
Modality
Gene Therapies
01

Overview

Phase 3, open-label, single-arm trial of delandistrogene moxeparvovec in Duchenne muscular dystrophy (DMD), sponsored by Sarepta Therapeutics. Primary endpoint: Treatment-emergent adverse events. Planned start Aug 2024; status: not yet recruiting.

02

Drugs

delandistrogene moxeparvovec
03

Conditions

Duchenne muscular dystrophy (DMD)

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