Funding: Grosserer L. F. Foghts Foundation

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
3 Year Follow up on ANO5 Patients	Congenital, 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 disease	Active, not recruiting	Not stated	2026-08-12		NCT05206617

Clinical trials