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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of MZE782 in Adults With PKUBrain 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, phenylketonuriaRecruitingPhase 22026-10-08NCT07694440
A Phase 2 Study of MZE829 in Adults With APOL1 Kidney DiseaseProteinuric Kidney DiseaseRecruitingPhase 22026-07-27NCT06830629