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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Biomarker Development for Muscular DystrophiesBecker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, facioscapulohumeral muscular dystrophy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseRecruitingNot stated2025-11-24NCT05019625

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Research sitesCityCountryLinked trials
Boston Children's HospitalBostonUnited States343
Brigham and Women's HospitalBostonUnited States511
Massachusetts General HospitalBostonUnited States20
University of PittsburghPittsburghUnited States137
Wake Forest UniversityWinston-SalemUnited States22