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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Prospective Sub-Study of the Global Hypophosphatasia RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hypophosphatasia, inborn errors of metabolism, inborn metal metabolism disorder, metabolic diseaseRecruitingNot stated2026-02-09NCT05234567

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Alexion Pharmaceuticals, Inc.48

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