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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
European Cystinosis CohortCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, cystinosis, hereditary disease, inborn errors of metabolism, lysosomal storage disease, metabolic diseaseRecruitingNot stated2026-07-07NCT05901077