Clinical Trials on Metal Metabolism, Inborn Errors
Total 9956 results
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La Jolla Pharmaceutical CompanyPRA Health SciencesCompletedHereditary HemochromatosisUnited States, Australia, France, United Kingdom
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Novartis PharmaceuticalsCompletedTransfusional HemosiderosisEgypt, Spain, United Kingdom, Jordan
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San Filippo Neri General HospitalCompletedHereditary HemochromatosisItaly
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Bond BiosciencesTerminatedHereditary HemochromatosisAustralia
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Protagonist Therapeutics, Inc.CompletedHereditary HemochromatosisUnited States, Canada
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Rennes University HospitalMinistry of Health, FranceCompletedGenetic HemochromatosisFrance
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Novartis PharmaceuticalsCompletedIron Overload | Hereditary HemochromatosisUnited States, Germany, Italy, Australia, Canada, France
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University Hospital, LilleCompleted
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Sanquin Research & Blood Bank DivisionsRadboud University Medical Center; Maastricht University Medical Center; Atrium... and other collaboratorsUnknownHereditary HemochromatosisNetherlands
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Alexion PharmaceuticalsCompletedHypophosphatasia | Bone DiseaseUnited States
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University of MiamiHRSA/Maternal and Child Health BureauCompletedPhenylketonuria | Inborn Errors of Metabolism | GalactosemiaUnited States
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Interregionale Blutspende SRKEnrolling by invitationHereditary Hemochromatosis | HyperferritinemiaSwitzerland
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Swiss Federal Institute of TechnologyInstituto de Investigação em ImunologiaCompletedIron Metabolism Disorders | Iron Overload | PolyphenolsPortugal, Switzerland
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Prothya BiosolutionsActive, not recruiting
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Sciotec Diagnostic Technologies GmbHNot yet recruitingFructose IntoleranceAustria
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Augusta UniversityUniversity of Iowa; Teikyo UniversityRecruitingFructose IntoleranceUnited States
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Augusta UniversityUnknownFructose IntoleranceUnited States
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Rennes University HospitalCompletedHemochromatosis Type 1France
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Novartis PharmaceuticalsCompletedIron OverloadUnited Kingdom, Italy, Oman, United Arab Emirates, Lebanon, Thailand, Egypt
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Mayo ClinicNational Institute of Neurological Disorders and Stroke (NINDS)Enrolling by invitationCongenital Disorders of GlycosylationUnited States
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University of Wisconsin, MadisonNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Stanford...Completed
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LipomedCompletedHemochromatosisEgypt, Turkey
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Orphatech Pharmaceuticals, GmbHWithdrawnMolybdenum Cofactor Deficiency Type AAustralia
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Murdoch Childrens Research InstituteMelbourne Health; Austin Health; Royal Brisbane and Women's Hospital; The University... and other collaboratorsCompletedHereditary HaemochromatosisAustralia
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Rennes University HospitalCompletedHereditary Hemochromatosis C282Y HomozygousFrance
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Origin BiosciencesCompletedMolybdenum Cofactor Deficiency, Type AUnited States, Spain, Israel, Norway, Turkey, United Kingdom
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LipomedCompleted
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University of LausanneCompletedGlucose Metabolism Disorders | Fructose Metabolism, Inborn Errors | Hereditary Fructose Intolerance
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Origin BiosciencesCompletedMolybdenum Cofactor Deficiency, Type AUnited States, Australia, Netherlands, United Kingdom, Tunisia
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Novartis PharmaceuticalsCompletedTransfusional HemosiderosisUnited States
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Maastricht University Medical CenterPfizerCompleted
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Augusta UniversityTerminatedDietary Fructose IntoleranceUnited States
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University of LausanneUniversity of LiegeCompletedHereditary Fructose IntoleranceBelgium
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Medical University of ViennaActive, not recruitingBone Diseases, Metabolic | Bone | HypophosphatasiaAustria
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Mayo ClinicCompletedHemochromatosisUnited States
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Nantes University HospitalCompletedHypobetalipoproteinemiaFrance
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Rennes University HospitalCompleted
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Vanderbilt University Medical CenterHarvard UniversityRecruitingAlbright Hereditary Osteodystrophy | PseudohypoparathyroidismUnited States
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University of LausanneRecruiting
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Assistance Publique - Hôpitaux de ParisCompletedInborn Errors of MetabolismFrance
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CENTOGENE GmbH RostockRecruitingInborn Errors of MetabolismPakistan
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University of LausanneCompletedInborn Errors of MetabolismSwitzerland
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CENTOGENE GmbH RostockCompletedInborn Errors of Metabolism | BiomarkerEgypt, Sri Lanka, Albania, Romania, Georgia, India, Lithuania, Pakistan
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Universitaire Ziekenhuizen KU LeuvenUnknownLipid Metabolism, Inborn ErrorsBelgium
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Massachusetts General HospitalRecruiting
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Vanderbilt University Medical CenterRecruitingPseudohypoparathyroidism Type 1a | Albright Hereditary Osteodystrophy | PseudohypoparathyroidismUnited States
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Ashley ShoemakerEnrolling by invitationPseudohypoparathyroidism Type 1a | Albright Hereditary Osteodystrophy | PseudohypoparathyroidismUnited States
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Vanderbilt University Medical CenterMassachusetts General HospitalCompletedPseudohypoparathyroidism Type 1a | Albright Hereditary OsteodystrophyUnited States