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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Nemaline Myopathy Clinical Research Network (NM-CTRN)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Thomsen and Becker disease, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular diseaseNot yet recruitingNot stated2025-01-14NCT06774703