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- US Clinical Trials Registry
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Clinical Trials on Hereditary Eye Disease in United States
Total 147830 results
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Sling Therapeutics, Inc.Active, not recruitingEye Diseases | Endocrine System Diseases | Thyroid Diseases | Thyroid Eye Disease | Graves Ophthalmopathy | Exophthalmos | Orbital Diseases | Thyroid Associated Ophthalmopathy | Graves Orbitopathy | Proptosis | IGF1R | HashimotoUnited States, Spain, Italy, United Kingdom, Canada
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Kubota Vision Inc.Food and Drug Administration (FDA)CompletedStargardt DiseaseUnited States, United Kingdom, Germany, Spain, Brazil, Canada, Denmark, France, Italy, Netherlands, South Africa
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University of Wisconsin, MadisonTerminated
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Topcon Medical Systems, Inc.CompletedNormal Healthy Subjects With No Known Ocular Diseases | Glaucomatous Eyes | Eyes With Retinal DiseasesUnited States
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Moorfields Eye Hospital NHS Foundation TrustBayerCompletedRetinitis Pigmentosa | Macular OedemaUnited Kingdom
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GenSight BiologicsCompletedOptic, Atrophy, Hereditary, LeberUnited Kingdom, United States, France, Germany, Italy
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GenSight BiologicsCompletedOptic, Atrophy, Hereditary, LeberUnited Kingdom, United States, Germany, Italy, France
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National Human Genome Research Institute (NHGRI)CompletedOculocutaneous AlbinismUnited States
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University of California, San FranciscoUniversity of Washington; California Institute of TechnologyRecruiting
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Spark Therapeutics, Inc.Children's Hospital of Philadelphia; University of IowaActive, not recruitingLeber Congenital Amaurosis | Inherited Retinal Dystrophy Due to RPE65 MutationsUnited States
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St. Jude Children's Research HospitalRecruitingGlaucoma, Congenital | Retinoblastoma | Cataracts Infantile | LeucocoriaUnited States
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McMaster UniversityIcahn School of Medicine at Mount Sinai; Edward-Elmhurst Health SystemCompletedChalazion Unspecified Eye, Unspecified Eyelid | Chalazion Left Eye, Unspecified Eyelid | Chalazion Right Eye, Unspecified Eyelid | Chalazion Both EyesUnited States, Canada
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Complement TherapeuticsRecruitingEye Diseases | Macular Degeneration | Retinal Degeneration | Geographic Atrophy | Dry Age-related Macular Degeneration | Retinal Disease | Macular AtrophyUnited Kingdom, United States
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National Eye Institute (NEI)CompletedAlbinism | Albinism, Oculocutaneous | Albinism, OcularUnited States
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National Eye Institute (NEI)National Human Genome Research Institute (NHGRI)Completed
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GlaxoSmithKlineTerminatedGraves OphthalmopathyUnited Kingdom
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Weill Medical College of Cornell UniversityNovartisWithdrawnDry Eye | Dry Eye Syndromes | Dry Eyes ChronicUnited States
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ProQR TherapeuticsRecruitingEye Diseases | Neurologic Manifestations | Retinal Degeneration | Retinal Dystrophies | Sensation Disorders | Vision Disorders | Blindness | Leber Congenital Amaurosis | Leber Congenital Amaurosis 10 | Retinal Disease | Eye Disorders CongenitalBelgium, Brazil, Canada, Germany, Italy, Netherlands, United Kingdom
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Johns Hopkins UniversityTerminatedDiabetic Retinopathy | Stargardt Disease | Macular Degeneration (Age Related)United States
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National Human Genome Research Institute (NHGRI)Terminated
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National Human Genome Research Institute (NHGRI)Recruiting
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Nidek Co. LTD.CompletedCataract | Normal Non-fluency | Aphakic Eye | Eyes With Corneal AbnormalityUnited States
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Topcon Medical Systems, Inc.CompletedNormal Healthy Subjects With No Known Ocular Diseases | Glaucomatous Eyes | Eyes With Retinal DiseasesUnited States
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Johns Hopkins UniversityNovartisEnrolling by invitationMultiple Sclerosis | Retinal Degeneration | Visual Acuity | Tomography, Optical CoherenceUnited States
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Gemini Therapeutics, Inc.TerminatedMacular Degeneration | Retinal Degeneration | Geographic Atrophy | Dry Age-related Macular Degeneration | Retinal DiseaseUnited States
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Ohio State UniversityAlcon ResearchCompletedContact Lens | Astigmatism of Both EyesUnited States
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Jaeb Center for Health ResearchDepartment of Health and Human Services; Food and Drug Administration (FDA); Conquering...RecruitingGyrate Atrophy | Gyrata of Choroid and Retina; Atrophy | Ornithine-δ-aminotransferase | OAT | Chorioretinal DegenerationUnited States, Canada, Finland, France, United Kingdom, Germany, Brazil
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Southern California College of Optometry at Marshall...RecruitingAqueous Tear Deficiency | Meibomian Gland Dysfunction of Bilateral Eyes (Disorder)United States
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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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Nova Southeastern UniversityRecruitingGlaucoma, Suspect | Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System | Congenital Coloboma of the Optic Nerve | Optic Nerve Head Pits, Bilateral CongenitalUnited States
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NightstaRx Ltd, a Biogen CompanyEnrolling by invitationChoroideremia | X-Linked Retinitis PigmentosaUnited States, United Kingdom, Netherlands, Germany, France, Brazil, Canada, Denmark, Finland
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OcugenRecruitingRetinitis Pigmentosa | Leber Congenital AmaurosisUnited States
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COA Research Foundation, INCAllerganTerminated
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Massachusetts General HospitalBroad Institute; Laboratory for Molecular MedicineCompletedGenetic Predisposition to Disease | Hereditary DiseaseUnited States
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Memorial Sloan Kettering Cancer CenterActive, not recruitingHearing Loss | Intraocular RetinoblastomaUnited States
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Vanderbilt-Ingram Cancer CenterNational Cancer Institute (NCI)RecruitingCancer Survivor | Retinoblastoma | Unilateral Retinoblastoma | Intraocular Retinoblastoma | Biological SiblingUnited States, Canada
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Pharvaris Netherlands B.V.Active, not 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, Poland, Germany, Austria, Bulgaria, Canada, Ireland, Italy, United Kingdom
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Children's Cancer and Leukaemia GroupUnknown
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Pro-Change Behavior SystemsRecruitingMental Health Issue | Hereditary CancerUnited States
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Boston Children's HospitalCureAP4 FoundationRecruitingHereditary Spastic Paraplegia | SPG50 | SPG47 | SPG51 | SPG52 | AP4-related Hereditary Spastic Paraplegia | Early Onset Hereditary Spastic Paraplegia | SPG4 | SPG3A | SPG15 | SPG11United States
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Brandon Eye Associates, PAActive, not recruiting
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Imperial College LondonRecruitingEvaluation of High Dose Prednisolone Pharmacokinetics in the Acute and Chronic Setting (EHD-Pred PK)Vasculitis | Asthma | Thyroid Eye Disease | Inflammatory Disease | COPD Exacerbation AcuteUnited Kingdom
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Jaeb Center for Health ResearchFoundation Fighting BlindnessRecruitingRetinitis Pigmentosa | Inherited Retinal DegenerationUnited States, United Kingdom, France, Finland, Israel, Netherlands, Switzerland, Australia, Canada, Brazil, Mexico
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Massachusetts General HospitalCompletedHereditary Sensory and Autonomic Neuropathy Type IUnited States
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QLT Inc.CompletedLCA (Leber Congenital Amaurosis) | RP (Retinitis Pigmentosa)Canada, United States, Germany, Netherlands, United Kingdom
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Indiana UniversityRecruitingPigmentary Retinopathy | Pentosan Polysulfate Sodium Maculopathy | Pigmentary Maculopathy | Toxic Maculopathy | Interstitial Cystitis, ChronicUnited States
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QLT Inc.CompletedLCA (Leber Congenital Amaurosis) | RP (Retinitis Pigmentosa)United States, Canada, Germany, Netherlands, United Kingdom
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Liminal BioSciences Ltd.CompletedDiabetes | Inflammation and FibrosisUnited Kingdom
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Rhythm Pharmaceuticals, Inc.CompletedBardet-Biedl Syndrome | POMC DeficiencyNetherlands, United States, Germany, Canada, Puerto Rico, United Kingdom
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Eunice Kennedy Shriver National Institute of Child...CompletedUrogenital Abnormalities | Mental Retardation | Wilm's Tumor | WAGR Syndrome | AniridiaUnited States