- ICH GCP
- US Clinical Trials Registry
- Search trials
Clinical Trials on Hereditary+Antithrombin+Deficiency+Type+2
Total 10729 results
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KalVista Pharmaceuticals, Ltd.Completed
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ShireHalozyme TherapeuticsCompletedHereditary AngioedemaUnited States
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ShireCompletedHereditary AngioedemaUnited States
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ShireCompletedAngioedemaUnited States
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ShireCompletedHereditary AngioedemaUnited States
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ShireCompletedHereditary AngioedemaUnited States
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KalVista Pharmaceuticals, Ltd.CompletedHereditary AngioedemaUnited Kingdom
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BioCryst PharmaceuticalsCompletedHereditary AngioedemaUnited Kingdom
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Pharming Technologies B.V.CompletedHereditary AngioedemaUnited States, Canada, Czechia, Italy, Macedonia, The Former Yugoslav Republic of, Romania, Serbia
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BioCryst PharmaceuticalsCompletedHereditary AngioedemaUnited Kingdom
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Massachusetts General HospitalShire Human Genetic Therapies, Inc.CompletedHereditary AngioedemaUnited States
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BioCryst PharmaceuticalsCompleted
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Pharming Technologies B.V.CompletedHereditary AngioedemaUnited States, Bulgaria, Canada, Hungary, Israel, Italy, Macedonia, The Former Yugoslav Republic of, Poland, Romania, Serbia, South Africa
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CSL BehringCompletedHereditary AngioedemaUnited States, Canada
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CSL BehringCompletedHereditary AngioedemaBulgaria, United States, Poland, Spain, Hungary, United Kingdom, Russian Federation, Macedonia, The Former Yugoslav Republic of, Argentina, Australia, Canada, Czech Republic, Israel, Romania, Sweden
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BioCryst PharmaceuticalsCompletedHereditary AngioedemaUnited Kingdom
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Mathias Ried-LarsenCompletedDiabetes Mellitus, Type 2 | Type 2 Diabetes Mellitus | Type2 Diabetes | Type2 Diabetes MellitusDenmark
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The Hospital for Sick ChildrenCompletedX-linked Lymphoproliferative Syndrome Type 2 (XLP-2)Canada
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BioCryst PharmaceuticalsCompletedHereditary Angioedema | Prophylaxis | HAEAustria, Denmark, France, Germany, Hungary, Israel, Italy, North Macedonia, Poland, Switzerland, United Kingdom, United States, Australia, Hong Kong, Korea, Republic of, New Zealand, Serbia, Slovakia, South Africa, Spain
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Pharming Technologies B.V.CompletedHereditary Angioedema | Genetic DisordersNetherlands, Romania
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Pharming Technologies B.V.CompletedGenetic DisordersNetherlands
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Pharming Technologies B.V.CompletedHereditary Angioedema | Angioneurotic EdemaNetherlands
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Pharming Technologies B.V.CompletedHereditary Angioedema | Genetic Disorders | Angioneurotic EdemaNetherlands, Romania
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Vastra Gotaland RegionOctapharmaWithdrawn
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BioCryst PharmaceuticalsApproved for marketingHereditary Angioedema | Prophylaxis | HAE
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University Hospital, GrenobleTerminatedHealthy Volunteers | Hereditary AngioedemaFrance
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Pharming Technologies B.V.CompletedGenetic DisordersNetherlands
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Northern Care Alliance NHS Foundation TrustBrighter ABCompletedDiabetes type1 | Diabetes type2United Kingdom
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University Hospital, AkerUniversity of OsloUnknownDiabetes Mellitus Type 2 | Hypovitaminosis DNorway
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CSL BehringRecruiting
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King Edward Medical UniversityCompletedDiabetes Mellitus, Type 2 | Vitamin D Deficiency | Insulin Resistance
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Penn State UniversityWithdrawn
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University of WashingtonCompletedObesity | Type 2 Diabetes Mellitus | Insulin Resistance | Metabolic Disease | Androgen DeficiencyUnited States
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Oregon Health and Science UniversityCompletedTrifunctional Protein Deficiency | Very Long Chain Acyl Coa Dehydrogenase Deficiency | Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Carnitine Palmitoyltransferase Deficiency 2United States
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Pamukkale UniversityBakirkoy Dr. Sadi Konuk Research and Training HospitalCompletedType2 Diabetes | Self Efficacy | Self Management | Cholesterol; Lipidosis | High Density Lipoprotein Deficiency | Motivational Interview | Tele-nursing | LDL - Low Density Lipoprotein Receptor DisorderTurkey
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Istituti Clinici Scientifici Maugeri SpACompletedHereditary AngioedemaItaly
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University Hospital, GrenobleCompletedHereditary AngioedemaFrance
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Steno Diabetes Center CopenhagenThe Novo Nordisk Foundation Center for Basic Metabolic Research; Department... and other collaboratorsCompletedDiabetes Mellitus, Type 2 | Metabolic Disease | Sucrase Isomaltase Deficiency | Sucrose Intolerance CongenitalGreenland
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Hoffmann-La RocheCompletedHaemophilia A | Moderate Hereditary Factor VIII Deficiency Disease Without Inhibitor | Severe Hereditary Factor VIII Deficiency Disease Without InhibitorItaly
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AlexionRecruitingWolman Disease | Cholesterol Ester Storage Disease | Lysosomal Acid Lipase Deficiency | Acid Cholesteryl Ester Hydrolase Deficiency, Type 2 | Acid Lipase Deficiency | LIPA Deficiency | LAL-DeficiencyFrance, Belgium, United States, Spain, Germany, Greece, Israel, Italy, Slovenia, United Kingdom, Brazil, Canada, Denmark, Australia, Croatia, Czechia, Ireland, Mexico, Netherlands, Poland, Portugal, Saudi Arabia
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Eli Lilly and CompanyActive, not recruitingGlucose Metabolism Disorders | Diabetes Mellitus, Type 2 | Diabetes Mellitus | Endocrine System Diseases | Type2 Diabetes | Metabolic Disease | T2DM (Type 2 Diabetes Mellitus) | T2DUnited States, India, Australia, United Kingdom, Mexico, Brazil, Israel, France, Italy
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Hanmi Pharmaceutical Company LimitedUnknownType2 Diabetes Mellitus | Type1 Diabetes MellitusUnited States
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German Federal Institute for Risk AssessmentUniversity of Vienna; Heidelberg University; University of Jena; University of... and other collaboratorsNot yet recruitingCardiovascular Diseases | Obesity | Diabetes Mellitus, Type 2 | Bone Loss | Dietary Exposure | Sustainability | Vitamin Deficiency | Mineral Deficiency | ExposureGermany, Austria
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Chinese University of Hong KongCompletedType 2 Diabetes Mellitus | Type2 Diabetes | ObeseHong Kong
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Rigshospitalet, DenmarkUnknownCarbohydrate Metabolism, Inborn Errors | Metabolism, Inborn Errors | Lipid Metabolism, Inborn Errors | Glycogen Storage Disease Type II | Glycogen Storage Disease Type V | VLCAD Deficiency | Glycogen Storage Disease Type III | Phosphoglycerate Kinase Deficiency | Neutral Lipid Storage Disease | Carnitine... and other conditionsDenmark
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Scripps HealthJ. Craig Venter InstituteCompletedLi-Fraumeni Syndrome | Hereditary Cancer Syndromes | TP53 Gene Germline Mutation CarrierUnited States
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National Cancer Institute (NCI)CompletedColorectal Neoplasm | Hereditary NonpolyposisUnited States
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Oregon Health and Science UniversityCompletedTrifunctional Protein Deficiency | Carnitine Palmitoyltransferase 2 Deficiency | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
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Foundation For Rare Disease ResearchInstitute for Asthma & Allergy; Virant Diagnostics, Inc.; MedBio Reference Laboratories...Not yet recruitingAngioedema | Urticaria | C1 Inhibitor Deficiency | Angioedemas, Hereditary | Mastocytosis | Indolent Systemic Mastocytosis | Systemic Mastocytoses | ACE Inhibitor-Induced Angioedema
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Washington University School of MedicineRecruitingHypertension | Diabetes Mellitus, Type 2 | Vitamin D DeficiencyUnited States