Washington Unviersity School of Medicine in Saint Louis

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Long-term Follow-up Study of Patients Receiving Onasemnogene Abeparvovec-xioi	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Juvenile Spinal Muscular Atrophy, Muscular Atrophy, Spinal, Type II, 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, proximal spinal muscular atrophy, spinal cord disorder, spinal muscular atrophy	Active, not recruiting	Phase 3	2026-09-24		NCT04042025

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