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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Orphan Europe Carbaglu® Surveillance ProtocolBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, nervous system disorder, urea cycle disorderRecruitingNot stated2024-02-07NCT03409003