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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
UK SMA Patient RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Kennedy disease, Spinal Muscular Atrophies of Childhood, X-linked disease, autosomal recessive distal spinal muscular atrophy 1, central nervous system disorder, hereditary disease, inherited neurodegenerative disorder, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, proximal spinal muscular atrophy, spinal cord disorder, spinal muscular atrophyRecruitingNot stated2026-08-20NCT04292574

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Research sitesCityCountryLinked trials
John Walton Muscular Dystrophy Research CentreNewcastle upon TyneUnited Kingdom3