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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study Observing Disease Progression in a Patient With Hutchinson-Gilford Progeria Syndrome (HGPS)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, laminopathy, metabolic disease, progeroid syndromeNot yet recruitingNot stated2026-09-24NCT07839351

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OrganizationsLinked trials
Bundang CHA Hospital10

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Research sitesCityCountryLinked trials
Bundang CHA medical centerSeongnam-siSouth Korea4