Trial intelligence / Profile preview

EXPEDITION long-term follow-up of delandistrogene moxeparvovec in Duchenne muscular dystrophy

2023-505043-39-00Phase 3Authorised

Sponsor
Sarepta Therapeutics
Start
Mar 2024
Modality
Gene Therapies
Countries
11
01

Overview

Phase 3, open-label, single-arm trial of delandistrogene moxeparvovec in Duchenne muscular dystrophy (DMD), sponsored by Sarepta Therapeutics. Primary endpoint: Number of participants with treatment-emergent adverse events, serious adverse events, and adverse events of special interest. Planned start Mar 2024; status: authorised.

02

Drugs

delandistrogene moxeparvovec
03

Conditions

Duchenne muscular dystrophy (DMD)

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Study design & results

Available in the Gosset platform where reported.

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Available in the Gosset platform where reported.

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