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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
NGGT006 Gene Therapy for Homozygous Familial HypercholesterolemiaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, familial hypercholesterolemia, hereditary disease, homozygous familial hypercholesterolemia, hyperlipidemia, hyperlipoproteinemia, inborn errors of metabolism, metabolic diseaseRecruitingEarly phase 12026-09-03NCT06125847

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Research sitesCityCountryLinked trials
First Affiliated Hospital of Xian Jiaotong UniversityXi'anChina4