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EMBARK Phase 3 Study of SRP-9001 in Duchenne Muscular Dystrophy

2019-003374-91Phase 3Completed

Sponsor
Sarepta Therapeutics
Start
Sep 2021
Modality
Gene Therapies
Countries
1
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Overview

Phase 3, randomised, double-blind trial in Duchenne muscular dystrophy (DMD) comparing SRP-9001 with Placebo (2 arms). Primary endpoint: Change in NSAA total score from Baseline to Week 52 (Part 1). Started Sep 2021; status: completed.

02

Drugs

delandistrogene moxeparvovec
03

Conditions

Duchenne muscular dystrophy (DMD)

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