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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Calcium Channel Blocker in Myotonic Dystrophy Type 1Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseNot yet recruitingPhase 12025-12-09NCT07075965

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University of Rochester189

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