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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Gene Therapy for Severe Crigler Najjar SyndromeCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Crigler-Najjar syndrome, Nutritional and Metabolic Diseases, hereditary disease, hereditary hyperbilirubinemia, inborn errors of metabolism, metabolic diseaseRecruitingNot applicable2023-03-28NCT03466463

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OrganizationsLinked trials
Genethon6

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Research sitesCityCountryLinked trials
AMCAmsterdamNetherlands1
ASST Papa Giovanni XXIIIBergamoItaly21
Azienda Ospedaliera Universitaria Federico IINaplesItaly33
Hopital Antoine BeclereClamartFrance3