Study to Evaluate the Safety and Effectiveness of ELEVIDYS in Participants With Duchenne Muscular Dystrophy Treated in a Post-Marketing Setting
Starting soon · Phase 4
Conditions studied: Duchenne Muscular Dystrophy
In brief
The primary objective of this study is to evaluate acute liver injury (ALI) rates associated with ELEVIDYS with the addition of sirolimus as an adjunct prophylactic immunosuppression agent.
Key facts
- Study ID
- NCT07542314
- Run by
- Sarepta Therapeutics, Inc.
- People needed
- 20
- Starts
- 2026-07-31
- Expected to finish
- 2027-03-31
- Last updated by the study team
- 2026-05-26
Who can join
Age: 4 and older. Sex: male. Healthy volunteers: not accepted.
Full record on ClinicalTrials.gov
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