A Long-term Follow-up Study of Participants Who Received Delandistrogene Moxeparvovec (SRP-9001) in a Previous Clinical Study

Enrolling by invitation · Phase 3

Conditions studied: Duchenne Muscular Dystrophy

In brief

The purpose of this study is to provide a single clinical study with a uniform approach to monitoring long-term safety and efficacy in participants who received delandistrogene moxeparvovec in a previous clinical study. No study drug will be administered as part of this study.

Key facts

Study ID
NCT05967351
Run by
Sarepta Therapeutics, Inc.
People needed
400
Starts
2023-09-27
Expected to finish
2033-10-31
Last updated by the study team
2026-02-06

Who can join

Age: any. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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