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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Defining Endpoints in Becker Muscular DystrophyBecker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseActive, not recruitingNot stated2026-09-03NCT05257473

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Research sitesCityCountryLinked trials
John Walton Muscular Dystrophy Research CentreNewcastle upon TyneUnited Kingdom1
Kennedy Krieger InstituteBaltimoreUnited States41
Nationwide Children's HospitalColumbusUnited States309
University of AucklandAucklandNew Zealand4
University of California, IrvineOrangeUnited States29
University of Colorado Anschutz Medical CampusAuroraUnited States142
University of IowaIowa CityUnited States284
University of Kansas Medical CenterKansas CityUnited States240
University of MinnesotaMinneapolisUnited States325
Virginia Commonwealth UniversityRichmondUnited States156
Washington University School of MedicineSt LouisUnited States895