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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Long-term Extension of GTX-102 in Angelman SyndromeAbnormalities, Multiple, Angelman syndrome, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Imprinting Disorders, central nervous system disorder, chromosomal disorder, hereditary disease, movement disorder, nervous system disorderActive, not recruitingPhase 32026-09-09NCT06415344

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OrganizationsLinked trials
Ultragenyx Pharmaceutical Inc24

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