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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Clinical Trial Readiness to Solve Barriers to Drug Development in FSHDCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, facioscapulohumeral muscular dystrophy, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseActive, not recruitingNot stated2026-09-17NCT03458832