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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Gene Therapy for Crigler Najjar Syndrome Type I (AlphaCN)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Crigler-Najjar syndrome, Nutritional and Metabolic Diseases, hereditary disease, hereditary hyperbilirubinemia, inborn errors of metabolism, metabolic diseaseRecruitingPhase 1 / Phase 22025-01-13NCT06641154

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