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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Clinical, Molecular and Imaging Biomarkers in Spinal and Bulbar Muscular Atrophy (SBMA)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Kennedy disease, X-linked disease, central nervous system disorder, hereditary disease, inherited neurodegenerative disorder, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, spinal cord disorder, spinal muscular atrophyRecruitingNot stated2026-08-13NCT04944940

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Research sitesCityCountryLinked trials
National Institutes of Health Clinical CenterBethesdaUnited States800