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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
3 Year Follow up on ANO5 PatientsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Disease Progression, Muscular Disorders, Atrophic, Pathologic Processes, Pathological Conditions, Signs and Symptoms, hereditary disease, limb-girdle muscular dystrophy, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseActive, not recruitingNot stated2026-08-12NCT05206617