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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Long-Term Follow-up Study for Patients From AVXS-101-CL-101Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Spinal Muscular Atrophies of Childhood, Spinal Muscular Atrophy Type I, central nervous system disorder, hereditary disease, inherited neurodegenerative disorder, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, spinal cord disorder, spinal muscular atrophyActive, not recruitingNot stated2026-09-22NCT03421977

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OrganizationsLinked trials
Novartis Gene Therapies2

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Research sitesCityCountryLinked trials
Nationwide Children's HospitalColumbusUnited States309