Search clinical trials for: Metabolic abnormalities
Total 76763 results
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University of LeipzigRhythm Pharmaceuticals, Inc.RecruitingChild Obesity | Hunger | Gene AbnormalityGermany
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Leiden University Medical CenterThe Dutch Brain Foundation (funding)Not yet recruitingCerebral Amyloid Angiopathy
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Regeneron PharmaceuticalsNot yet recruitingNon-transfusion Dependent Beta-thalassemia (NTDT)
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Umraniye Education and Research HospitalRecruitingPreterm Birth | Fetal Growth Retardation | Preeclampsia | Gestational Diabetes | Gestational HypertensionTurkey
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AstraZenecaRecruitingCarpal Tunnel Syndrome | Amyloidosis | Polyneuropathy | Hereditary Transthyretin AmyloidosisRussian Federation
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Jiangsu HengRui Medicine Co., Ltd.Not yet recruitingGout With Hyperuricemia in Adults
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QED Therapeutics, Inc.RecruitingChildren With HypochondroplasiaUnited States, Australia, Norway, Portugal, Singapore, Spain
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Nido Biosciences, Inc.RecruitingSpinal and Bulbar Muscular Atrophy | Kennedy's DiseaseKorea, Republic of, Denmark, Italy, United Kingdom
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University of FloridaUniversity of Rwanda; World VisionRecruitingFetal Growth Retardation | Infant MalnutritionRwanda
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Tisento TherapeuticsNot yet recruitingMitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS Syndrome)United States, Australia, Italy, Germany, Canada, United Kingdom
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Vanderbilt University Medical CenterAminu Kano Teaching HospitalNot yet recruitingMalnutrition | Sickle Cell Disease
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Institute of Liver and Biliary Sciences, IndiaRecruitingGlycogen Storage DiseasesIndia
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Alnylam PharmaceuticalsRecruitingCerebral Amyloid AngiopathyCanada
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GeneCradle IncRecruitingPompe Disease (Late-onset)China
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Laval UniversityRecruitingFamilial Hypercholesterolemia | Cholesterol, Elevated | Nutrition, HealthyCanada
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Clinuvel Europe LimitedRecruiting
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University College, LondonWashington University School of Medicine; University of Washington; Alzheimer... and other collaboratorsNot yet recruitingAlzheimer Disease | Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) | Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 2 (Disorder) | Autosomal Dominant Alzheimer Disease Due to Mutation of Amyloid Precursor Protein (Disorder)
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Lawson Health Research InstituteGreenstone Biosciences, Inc.Not yet recruitingCardiovascular Diseases | Heart Failure | Cardiomyopathies | Congenital Heart Disease | Cerebrovascular Accident | Arrythmia | Cardiometabolic Syndrome
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Institut Mutualiste MontsourisRecruitingCarpal Tunnel Syndrome | Knee Prosthesis | ATTR Amyloidosis | Cardiopathy | Hip Prosthesis | Lumbar Spine StenosisFrance
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Harmony Biosciences, LLCRecruiting
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University of California, San FranciscoNot yet recruitingESRD | Dysequilibrium Syndrome | Hyperkalemia | Metabolic AcidosisUnited States
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AstraZenecaRecruiting
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MemorialCare Health SystemDexCom, Inc.RecruitingHyperinsulinism | Hypoglycemia NeonatalUnited States
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OctapharmaRecruiting
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Fondazione SISA (Societa Italiana per lo Studio...RecruitingFamilial Hypercholesterolemia | Genetic DisorderItaly
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Cliniques universitaires Saint-Luc- Université...RecruitingRare Diseases | Inborn Errors of MetabolismBelgium
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Alnylam PharmaceuticalsRecruitingHereditary Amyloidosis, Transthyretin-Related | Asymptomatic Carrier StateFrance
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Karamanoğlu Mehmetbey UniversityRecruitingWolff-Parkinson-White SyndromeTurkey
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Emory UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Recruiting
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TakedaNot yet recruitingHereditary Angioedema (HAE)
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John Paul II Hospital, KrakowRecruitingTransthyretin AmyloidosisPoland
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Pharvaris Netherlands B.V.RecruitingHereditary Angioedema | Hereditary Angioedema Type I | Hereditary Angioedema Type II | Hereditary Angioedema Types I and II | Hereditary Angioedema Attack | Hereditary Angioedema With C1 Esterase Inhibitor Deficiency | Hereditary Angioedema - Type 1 | Hereditary Angioedema - Type 2 | C1 Esterase Inhibitor... and other conditionsUnited States, Puerto Rico
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Fondation Ophtalmologique Adolphe de RothschildNot yet recruitingAlbinism, Ocular
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Cairo UniversityNot yet recruitingMolar Incisor Hypomineralization
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AstraZenecaRecruitingTransthyretin Amyloidosis Cardiomyopathy, Heart Failure With Preserved Ejection FractionRussian Federation
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Jirair Krikor BedoyanUltragenyx Pharmaceutical IncRecruitingPyruvate Dehydrogenase Complex DeficiencyUnited States
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Rigshospitalet, DenmarkNot yet recruitingBrain Diseases | Genetic Diseases, Inborn | Metabolism, Inborn Errors | Brain Diseases, Metabolic | Phenylketonurias | Brain Diseases, Metabolic, Inborn | Amino Acid Metabolism, Inborn Errors | Metabolic DiseaseDenmark
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Istituto Auxologico ItalianoRecruiting
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Medical University of ViennaUniversity of Vienna; Griffith UniversityRecruiting
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Centre Hospitalier Sud FrancilienNot yet recruiting
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NGGT (Suzhou) Biotechnology Co., Ltd.Not yet recruitingPhenylketonurias
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Lundquist Institute for Biomedical Innovation at...Not yet recruitingMucopolysaccharidosis III | Sanfilippo SyndromeUnited States
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Maastricht University Medical CenterRecruitingQuality of Life | Tuberous Sclerosis | Basal Cell Nevus Syndrome | Cutis Laxa | Epidermolysis Bullosa | Ichthyosis | Ectodermal Dysplasia | Albinism | Birt-Hogg-Dube Syndrome | Palmoplantar KeratosesNetherlands
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University of PisaFondazione C.N.R./Regione Toscana "G. Monasterio", Pisa, ItalyRecruitingPregnancy Complications | Pregnancy Related | Pre-Eclampsia | Fetal Growth Retardation | Fetal Complications | Gestational Diabetes | Pregnancy Disease | ECG Electrode Site ReactionItaly
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Hospital do CoracaoUniversity of Sao Paulo; Instituto Dante Pazzanese de Cardiologia; National Institute...Not yet recruiting
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Chiesi Farmaceutici S.p.A.ICON plcNot yet recruiting
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Caroline Michaela KistorpSanofiNot yet recruitingChronic Kidney Diseases | Fabry DiseaseDenmark
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The University of QueenslandNot yet recruitingAtaxia TelangiectasiaAustralia
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Eisai Co., Ltd.RecruitingAlzheimer's DiseaseJapan
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National Taiwan University HospitalRecruiting