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Clinical Trials on Hereditary Disorder
Total 146468 results
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Radboud University Medical CenterJacques and Gloria Gossweiler FoundationCompletedHereditary Spastic Paraplegia | Strumpell DiseaseNetherlands
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National Institute of Neurological Disorders and...TerminatedHereditary Spastic ParaplegiaUnited States
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University of Campinas, BrazilConselho Nacional de Desenvolvimento Científico e Tecnológico; Cristália Produtos...CompletedHereditary Spastic ParaplegiaBrazil
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National Human Genome Research Institute (NHGRI)CompletedHNPCC | Hereditary Nonpolyposis Colon CancerUnited States
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Myriad Genetic Laboratories, Inc.Completed
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Centre Hospitalier Régional Metz-ThionvilleCompletedPseudophakic Bullous Keratopathy | Fuchs' Endothelial Corneal Dystrophy | Descemet Membrane Endothelial Keratoplasty | Graft DetachmentFrance
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Stanford UniversityUniversity of Pennsylvania; University of California, Davis; Oregon Health and... and other collaboratorsRecruitingFuchs' Endothelial Dystrophy | Fuchs Dystrophy | FuchsUnited States
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Michael D. Straiko, MDLions VisionGift Research; Eye Bank Association of AmericaRecruitingFuchs Endothelial DystrophyUnited States
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Trefoil Therapeutics, Inc.CompletedFuchs' Endothelial Dystrophy | Fuchs Dystrophy | FuchsUnited States
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University of Illinois at ChicagoWithdrawn
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Hanny Al-Samkari, MDRecruitingHereditary Hemorrhagic TelangiectasiaUnited States
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National Human Genome Research Institute (NHGRI)CompletedTelangiectasia, Hereditary Hemorrhagic | Osler-Rendu-Weber Disease | Osler-Rendu DiseaseUnited States
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National Center for Research Resources (NCRR)University of VermontCompletedTelangiectasia, Hereditary Hemorrhagic
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University Hospital, EssenPhilipps University Marburg Medical Center; University Hospital, Aachen; German...Active, not recruitingHereditary Hemorrhagic Telangiectasia | Dental DiseasesGermany
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GlaxoSmithKlineTerminatedTelangiectasia, Hereditary HemorrhagicUnited States, Canada
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Oslo University HospitalCompletedHereditary Factor VIII Deficiency Disease With InhibitorNorway
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St George's, University of LondonTerminatedEndometrial Cancer | Hereditary Non-polyposis Colon Cancer (hmsh2, hmlh1, hpms1, hpms2)United Kingdom
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ProQR TherapeuticsActive, not recruitingEye Diseases | Neurologic Manifestations | Eye Diseases, Hereditary | Sensation Disorders | Vision Disorders | Blindness | Leber Congenital Amaurosis | Leber Congenital Amaurosis 10 | Retinal Disease | Eye Disorders CongenitalUnited States, Belgium, Brazil, Canada, France, Germany, Italy, Netherlands, United Kingdom
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Brigham and Women's HospitalEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedGenetic Predisposition to Disease | Hereditary DiseaseUnited States
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Cornea Research Foundation of AmericaWithdrawnFuchs' Endothelial DystrophyUnited States
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Federal University of São PauloEye Clinic Day Hospital, São PauloUnknownKeratoconus | Cornea | Bullous Keratopathy | Corneal Dystrophy
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Shanghai Vitalgen BioPharma Co., Ltd.Not yet recruitingBietti Crystalline DystrophyChina
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Beijing Tongren HospitalRecruitingBietti Crystalline DystrophyChina
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OctapharmaRecruiting
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Hospital Universitari Vall d'Hebron Research InstituteHospital Universitario La PazNot yet recruitingHereditary Angioedema With C1 Esterase Inhibitor DeficiencySpain
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CSL BehringCompletedHereditary Angioedema Types I and IIBulgaria, Hungary, Poland, Romania
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CSL BehringCompletedHereditary Angioedema Types I and IIGermany
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Ultragenyx Pharmaceutical IncCompletedHereditary Inclusion Body Myopathy (HIBM)United States
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Beijing Tongren HospitalRecruitingBietti's Crystalline DystrophyChina
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Marian Macsai, MDRecruitingFuchs' Endothelial DystrophyUnited States
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State Scientific Centre of Coloproctology, Russian...The Loginov MCSC MHD; Pirogov National Medical and Surgical Center; Moscow City... and other collaboratorsRecruitingColorectal Cancer | Lynch Syndrome | Hereditary Colorectal Cancer | MSIRussian Federation
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CSL BehringCompletedHereditary Angioedema Types I and IIUnited States, Spain, Australia, Canada, Czechia, Hungary, Israel, Italy, Romania, United Kingdom
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Santen Inc.ActualEyes Inc.Active, not recruitingFuchs Endothelial Corneal DystrophyUnited States, France, India
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Massachusetts General HospitalBroad Institute; Laboratory for Molecular MedicineCompletedGenetic Predisposition to Disease | Hereditary DiseaseUnited States
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ProQR TherapeuticsTerminatedEye Diseases | Neurologic Manifestations | Eye Diseases, Hereditary | Sensation Disorders | Vision Disorders | Blindness | Leber Congenital Amaurosis | Leber Congenital Amaurosis 10 | Retinal Disease | Eye Disorders CongenitalUnited States, Belgium
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Unity Health TorontoThe Ottawa HospitalCompletedEpistaxis | Hereditary Hemorrhagic Telangiectasia (HHT)Canada
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University of California, San DiegoCompletedHereditary Hemorrhagic Telangiectasia (HHT)United States
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University of California, San DiegoCompletedHereditary Hemorrhagic Telangiectasia (HHT)United States
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University of California, San DiegoGenentech, Inc.WithdrawnHereditary Hemorrhagic Telangiectasia (HHT) | Nosebleeds
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Maastricht University Medical CenterNot yet recruitingIntraocular Pressure | Fuchs' Endothelial Dystrophy | Pseudophakic Bullous Keratopathy
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Xuanwu Hospital, BeijingRecruitingGait | Motor FunctionChina
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NYU Langone HealthRecruitingHereditary Sensory and Autonomic Neuropathies | Familial Dysautonomia (Riley-Day Syndrome) | Hereditary Sensory and Autonomic Neuropathy 3United States, Israel
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University Hospital, GrenobleCompletedHereditary AngioedemaFrance
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IRCCS Fondazione Stella MarisCompletedHereditary Spastic Paraplegia | Spastic Paraplegia Type 11Italy
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Fox Chase Cancer CenterNational Cancer Institute (NCI)CompletedColorectal Cancer | Hereditary Non-polyposis Colon CancerUnited States
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Assistance Publique - Hôpitaux de ParisCompletedRhabdomyolysis Linked to a Hereditary Disease of MetabolismFrance
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University of SouthamptonUnknownKeratoconus | Fuchs Dystrophy | Corneal DiseaseUnited Kingdom
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Clinic for Special ChildrenRecruitingMyopathy | Myopathy; Hereditary | Myopathies, Nemaline | TNNT1-associated Myopathy | Infantile-onset Nemaline Rod Myopathy | Myopathy, Rod | Amish Nemaline Myopathy | Nemaline Myopathy 5 | NEM5 | Genetic Muscle Disease | Recessive Hereditary Disorder (Autosomal) | ANMUnited States
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Kowa Research Institute, Inc.RecruitingFuchs Endothelial Corneal DystrophyUnited States, Germany, Spain, Canada, United Kingdom, Denmark
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Centre Hospitalier Universitaire de BesanconCompletedCataract | Keratoconus | Fuchs' Endothelial DystrophyFrance