CompletedPhase 2NCT04179409
A 48-Week, Open Label, Study to Evaluate the Efficacy and Safety of AMONDYS 45, EXONDYS 51, VYONDYS 53 in Subjects With DuchenneMuscular Dystrophy Carrying Eligible DMD Duplications.
Studying Duchenne muscular dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Kevin Flanigan
- Principal Investigator
- Kevin Flanigan, MDNationwide Children's Hospital
- Intervention
- Amondys 45(drug)
- Enrollment
- 3 enrolled
- Eligibility
- MALE
- Timeline
- 2020 – 2023
Study locations (1)
- Nationwide Children's Hospital, Columbus, Ohio, United States
Collaborators
Sarepta Therapeutics, Inc.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT04179409 on ClinicalTrials.govOther trials for Duchenne muscular dystrophy
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