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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Registry of Patients With HypophosphatasiaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hypophosphatasia, inborn errors of metabolism, inborn metal metabolism disorder, metabolic diseaseEnrolling by invitationNot stated2026-09-04NCT02306720

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OrganizationsLinked trials
Alexion Pharmaceuticals, Inc.48

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Research sitesCityCountryLinked trials
Leicester Royal InfirmaryLeicesterUnited Kingdom8