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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
European Cystinosis Cohort 2Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, cystinosis, hereditary disease, inborn errors of metabolism, lysosomal storage disease, metabolic diseaseNot yet recruitingNot stated2026-09-17NCT07680751

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Research sitesCityCountryLinked trials
AP-HP_ Hôpital Charles FoixIvry-sur-SeineFrance1