Search clinical trials for: Metabolism, Inborn Errors
Total 15939 results
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Spruce BiosciencesRecruitingCongenital Adrenal Hyperplasia | 21-OHDUnited States
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University Children's Hospital, ZurichUniversity Children's Hospital Basel; UChildrenVienna; Insel Gruppe AG, University...RecruitingPhenylketonuriasSwitzerland
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Universitair Ziekenhuis BrusselRecruitingIrritable Bowel SyndromeBelgium
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University Hospital, RouenNot yet recruiting
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University Hospital, Strasbourg, FranceRecruiting
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Adrenas Therapeutics IncRecruitingCongenital Adrenal HyperplasiaUnited States
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University of PecsNot yet recruitingIrritable Bowel Syndrome | Lactose Intolerance | Lactose MalabsorptionHungary
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ModernaTX, Inc.RecruitingGlycogen Storage DiseaseUnited States, Canada
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University College, LondonRecruitingOrnithine Transcarbamylase DeficiencyUnited Kingdom
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University Hospital Center of MartiniqueRecruiting
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University of Texas Southwestern Medical CenterRecruitingGlucose Metabolism Disorders | Epilepsy | Glucose Transporter Type 1 Deficiency Syndrome | Glut1 Deficiency Syndrome 1 | Glut1 Deficiency Syndrome 1, Autosomal Recessive | Glucose Transporter Protein Type 1 Deficiency Syndrome | Glucose Transport DefectUnited States
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University of Erlangen-Nürnberg Medical SchoolRecruitingPompe Disease (Late-onset) | Pompe Disease | Pompe's Disease Juvenile Onset | Pompe Disease Infantile-OnsetGermany
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University of AarhusRecruiting
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Assistance Publique - Hôpitaux de ParisCanon Medical Systems, USARecruiting
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Assistance Publique - Hôpitaux de ParisRecruitingAtherosclerosis | Familial HypercholesterolemiaFrance
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Children's Hospital of Orange CountyUltragenyx Pharmaceutical IncRecruitingInflammation | Mucopolysaccharidoses | Cardiac Disease | Carotid DiseaseUnited States
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Children's Mercy Hospital Kansas CityRecruiting
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University of California, San FranciscoNot yet recruitingCystinuriaUnited States
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Ohio State UniversityUniversity of HoustonRecruitingRefractive Errors | Down SyndromeUnited States
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TakedaRecruiting
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Chang Gung Memorial HospitalRecruitingFabry DiseaseTaiwan
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Vitaflo International, LtdRecruitingPhenylketonurias | PKU | Maple Syrup Urine Disease | Homocystinuria | Glutaric Acidemia I | Hereditary TyrosinemiaUnited Kingdom
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Inozyme PharmaNot yet recruitingGeneralized Arterial Calcification of Infancy | Autosomal Recessive Hypophosphatemic Rickets | Ectonucleotide Pyrophosphatase/phosphodiesterase1 Deficiency | ATP-Binding Cassette Subfamily C Member 6 Deficiency
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Eunice Kennedy Shriver National Institute of Child...RecruitingCHILD Syndrome | Smith Lemli Opitz Syndrome | Lathosterolosis | DesmosterolosisUnited States
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Tang-Du HospitalAir Force Military Medical University, ChinaNot yet recruiting
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Recordati Rare DiseasesTarget PharmaSolutions, Inc.RecruitingPropionic Acidemia | Methylmalonic Acidemia | HyperammonemiaUnited States
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First Affiliated Hospital Xi'an Jiaotong UniversitySimcere CompanyRecruitingCerebral Infarction | G6PD DeficiencyChina
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Taipei Veterans General Hospital, TaiwanNot yet recruitingGlycogen Storage Disease Type II
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National Human Genome Research Institute (NHGRI)RecruitingDiabetes | Undiagnosed Diseases | Inherited Metabolic Disorders | Batten's Disease | Tay SachsUnited States
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Massachusetts General HospitalEuropean Leukodystrophy AssociationRecruitingRestless Legs Syndrome | AdrenoleukodystrophyUnited States, Netherlands
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University of LausanneRecruiting
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Dicerna Pharmaceuticals, Inc., a Novo Nordisk companyRecruitingPrimary Hyperoxaluria Type 3 | Primary Hyperoxaluria Type 2 | Primary Hyperoxaluria Type 1 | Primary HyperoxaluriaUnited States, Canada, Lebanon, Turkey, United Kingdom, Germany, Italy, Japan, Poland, Spain, United Arab Emirates
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Aspa TherapeuticsRecruitingCanavan DiseaseUnited States
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Radboud University Medical CenterDutch Kidney FoundationRecruiting
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Hong Kong Children's HospitalRecruitingGlycogen Storage Disease Type IBHong Kong
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Alnylam PharmaceuticalsRecruitingPrimary Hyperoxaluria Type 1France, Spain, United States, Israel, Belgium, Switzerland, Germany, United Kingdom, Italy, Canada
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National Taiwan University HospitalRecruiting
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Duke UniversityRecruiting
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Stephen G. Kaler, MDRecruitingMenkes Disease | Occipital Horn SyndromeUnited States
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Viking Therapeutics, Inc.RecruitingAdrenomyeloneuropathy Form (AMN) of X-linked Adrenoleukodystrophy (X-ALD)United States, France, Germany, Italy, United Kingdom
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National Institute of Diabetes and Digestive and...RecruitingPrimary Hyperparathyroidism | Pseudohypoparathyroidism | Parathyroid Cancer | Inheritable Bone Diseases | Multiple Endocrine Neoplasia, Type 1United States
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University Medical Centre LjubljanaNot yet recruitingPhenylketonurias | Nutritional and Metabolic Diseases
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Fred Hutchinson Cancer CenterNational Cancer Institute (NCI); National Heart, Lung, and Blood Institute... and other collaboratorsRecruitingCongenital Amegakaryocytic Thrombocytopenia | Paroxysmal Nocturnal Hemoglobinuria | Diamond-Blackfan Anemia | Shwachman-Diamond Syndrome | Bone Marrow Failure Syndrome | Hereditary Sideroblastic Anemia | Hematologic Neoplasm With Germline GATA2 Mutation | Hematologic Neoplasm With Germline SAMD9... and other conditionsUnited States
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Second Affiliated Hospital, School of Medicine,...RecruitingClinical Features and OutcomeChina
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Second Affiliated Hospital, School of Medicine,...Recruiting
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Peking University Third HospitalNot yet recruitingFamilial Hypercholesterolemia
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Mackay Memorial HospitalSanofi Taiwan Co. LtdRecruiting
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Second Affiliated Hospital, School of Medicine,...RecruitingSingle Nucleotide Polymorphism | Hyperuricemia | Gout | Gut Microbiota | Uric Acid | Genetic Loci | FecesChina
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Eunice Kennedy Shriver National Institute of Child...RecruitingTurner Syndrome | Galactosemia | Ovarian Disfunction | Post-menarcheal Adolescents | Variations in Sex Characteristics | Differences in Sex DevelopmentUnited States
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Shenzhen People's HospitalRecruitingEvaluate the Efficacy and Safety of IBI306 in Subjects With Homozygous Familial HypercholesterolemiaLipid Metabolism Disorders | Familial Hypercholesterolemia - Homozygous | Proprotein Convertase Subtilisin/Kexin 9China