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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Safety and Dystrophin Expression of SPOT-03 in Duchenne Muscular Dystrophy (DMD) PatientsCongenital, 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 diseaseRecruitingEarly phase 12026-05-07NCT07188012

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Research sitesCityCountryLinked trials
Shanghai Children's Medical CenterShanghaiChina4