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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type CBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Niemann-Pick disease, Niemann-Pick disease type C, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, histiocytosis, inborn errors of metabolism, lymphatic system disorder, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, non-Langerhans cell histiocytosis, sphingolipidosisRecruitingNot stated2026-08-31NCT05588167

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Research sitesCityCountryLinked trials
National Institutes of Health Clinical CenterBethesdaUnited States800