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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
GSD VI and GSD IX Natural HistoryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Glycogen Storage Disease, Type IXA2, Nutritional and Metabolic Diseases, disorder of glycogen metabolism, glycogen storage disease IXa1, glycogen storage disease IXa2, glycogen storage disease IXb, glycogen storage disease IXc, glycogen storage disease VI, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, metabolic diseaseRecruitingNot stated2026-05-05NCT04454216

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OrganizationsLinked trials
Duke University446

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Research sitesCityCountryLinked trials
Duke UniversityDurhamUnited States160