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Clinical Trials on Urea Cycle Disorders, Inborn
Total 7042 results
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AkesoAD Pharmaceuticals Co., Ltd.CompletedHeterozygous Familial HypercholesterolemiaChina
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Fundación Hipercolesterolemia FamiliarCompletedFamilial HypercholesterolemiaSpain
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Organon and CoCompletedHeart Disease | Lipid Metabolism, Inborn Errors
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Nantes University HospitalCompletedFamilial HypobetalipoproteinemiaFrance
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Nantes University HospitalCompletedStudy of cardiovAscular Contrasted Phenotypes in Patients With FamIliaI hypercholesteRolemia (SAFIR)Homozygous Familial HypercholesterolemiaFrance
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The Medicines CompanyCompletedHomozygous Familial HypercholesterolemiaUnited States, Netherlands, South Africa
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Regeneron PharmaceuticalsCompletedHomozygous Familial HypercholesterolemiaUnited States, Netherlands, Canada
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Rennes University HospitalCompleted
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Madrigal Pharmaceuticals, Inc.CompletedHeterozygous Familial HypercholesterolemiaDenmark
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Central South UniversityCompletedHomozygous Familial HypercholesterolemiaChina
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CymaBay Therapeutics, Inc.CompletedHomozygous Familial HypercholesterolemiaCanada, France, Netherlands, Norway
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Merck Sharp & Dohme LLCTerminatedHyperlipoproteinemia Type II | Homozygous Familial Hypercholesterolemia
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Japan Tobacco Inc.CompletedType II HyperlipidaemiaNetherlands
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metaX Institut fuer Diatetik GmbHGreat Ormond Street Hospital for Children NHS Foundation Trust; Birmingham...Not yet recruitingAlkaptonuria | Homocystine; Metabolic Disorder | Tyrosinemia, Type I | Tyrosinemia, Type II | Tyrosinemia, Type III | MSUD (Maple Syrup Urine Disease)
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University of PittsburghNational Institute of Neurological Disorders and Stroke (NINDS); Rare Diseases...RecruitingPyruvate Dehydrogenase Complex Deficiency DiseaseUnited States
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METAFORA biosystemsAssistance Publique - Hôpitaux de Paris; European Commission; Ministry for Health... and other collaboratorsCompletedMovement Disorders | Intellectual Disability | Seizures | Ataxia | Glut1 Deficiency Syndrome | De Vivo DiseaseFrance
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Hospital Universitari Vall d'Hebron Research InstituteUniversidad de MurciaUnknownCongenital Heart Diseases | Antithrombin III Deficiency | Congenital Disorder of Glycosylation | Conotruncal DefectsSpain
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CENTOGENE GmbH RostockWithdrawnMetabolic Disorders | Tyrosinosis | Hepatorenal Tyrosinemia | Fumarylacetoacetase Deficiency | Fah DeficiencyGermany, Sri Lanka, India
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Assistance Publique - Hôpitaux de ParisRecruitingX-linked HypophosphatemiaFrance
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Wuerzburg University HospitalKyowa Kirin, Inc.Completed
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Hospices Civils de LyonCompleted
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Kyowa Hakko Kirin Pharma, Inc.Kyowa Kirin Co., Ltd.CompletedX-linked HypophosphatemiaUnited States, Canada
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Peking Union Medical College HospitalUnknownX-linked HypophosphatemiaChina
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University of AarhusAarhus University Hospital; University of East Anglia; Kolding SygehusCompleted
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Zeria PharmaceuticalCompletedPrimary Hypophosphatemic RicketsJapan
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Neurogene Inc.RecruitingNeuronal Ceroid Lipofuscinosis CLN5United States, United Kingdom
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Polaryx Therapeutics, Inc.Not yet recruitingJuvenile Neuronal Ceroid Lipofuscinosis
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REGENXBIO Inc.Active, not recruitingNeuronal Ceroid Lipofuscinosis Type 2United Kingdom
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University of RochesterBatten Disease Support and Research Assocation (BDSRA)CompletedJuvenile Neuronal Ceroid LipofuscinosisUnited States
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StemCells, Inc.CompletedNeuronal Ceroid LipofuscinosisUnited States
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Ultragenyx Pharmaceutical IncTerminatedGlycogen Storage Disease Type IIIUnited States, Netherlands
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Organon and CoBayerCompletedHypercholesterolemia | Familial Hypercholesterolemia | Homozygous Sitosterolemia
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Organon and CoCompletedPrimary Hypercholesterolemia | Homozygous Familial Hypercholesterolemia
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HDL TherapeuticsMedStar Heart and Vascular InstituteUnknownHomozygous Familial Hypercholesterolemia | HoFHUnited States
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Assistance Publique - Hôpitaux de ParisCompletedCongenital Disorders of GlycosylationFrance
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University College, LondonAegerion Pharmaceuticals, Inc.CompletedPercutaneous Coronary Intervention | Familial Hypercholesterolemia | Cardiac Event
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Amsterdam Molecular TherapeuticsThe Clinical Trial CompanyCompletedFamilial Lipoprotein Lipase DeficiencyCanada
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Isfahan University of Medical SciencesCompletedTangier Disease | Body Mass Index Quantitative Trait Locus 8 Disorder
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Children's Hospital of PhiladelphiaActive, not recruitingMaple Syrup Urine DiseaseUnited States
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University Hospital, ToursInstitut National de la Santé Et de la Recherche Médicale, FranceCompletedPKU | HyperphenylalaninemiaFrance
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Institut Investigacio Sanitaria Pere VirgiliRecruitingFamilial Hypercholesterolemia | Familial Hypercholesterolemia - Homozygous | Familial Hypercholesterolemia - HeterozygousSpain
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Vanderbilt University Medical CenterHarvard UniversityRecruitingAlbright Hereditary Osteodystrophy | PseudohypoparathyroidismUnited States
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The Rogosin InstituteRecruitingHomozygous Familial HypercholesterolemiaUnited States
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National Heart, Lung, and Blood Institute (NHLBI)Completed
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Novartis PharmaceuticalsActive, not recruitingFamilial Hypercholesterolemia - HomozygousGreece, Lebanon, Turkey, France, Canada, Malaysia, Netherlands, United States
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Fresenius Medical Care Deutschland GmbHCompletedCardiovascular Diseases | Dyslipidemias | Hypercholesterolemia, FamilialGermany
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The Medicines CompanyCompletedElevated Cholesterol | Heterozygous Familial HypercholesterolemiaUnited States, Canada, Czechia, Denmark, Netherlands, South Africa, Spain, Sweden
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AstraZenecaCompletedHomozygous Familial Hypercholesterolemia (HoFH)Malaysia, Canada, Taiwan, Belgium, Denmark, Israel
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National Heart, Lung, and Blood Institute (NHLBI)CompletedBlood Disease | Hemochromatosis
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University of RochesterNational Heart, Lung, and Blood Institute (NHLBI)CompletedBlood Disease | Hemochromatosis