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Leber congenital amaurosis

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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-6 of 6 results.
Natural History Study of Patients With Leber Congenital Amaurosis Associated With Mutations in RPE65
Status: Recruiting
Last Changed: Jul 16, 2019
First Received: Mar 22, 2016
Disease(s): Leber Congenital Amaurosis
Locations: Kellogg Eye Center, Ann Arbor, Michigan, United States
Moorfields Eye Hospital, London, United Kingdom
Long-Term Follow-Up Gene Therapy Study for Leber Congenital Amaurosis OPTIRPE65 (Retinal Dystrophy Associated With Defects in RPE65)
Status: Recruiting
Last Changed: Jul 16, 2019
First Received: Oct 27, 2016
Disease(s): Leber Congenital Amaurosis (LCA), Eye Diseases, Eye Diseases, Hereditary, Retinal Diseases
Intervention(s): AAV OPTIRPE65
Locations: Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom
A Study to Evaluate Efficacy, Safety, Tolerability and Exposure After a Repeat-dose of Sepofarsen (QR-110) in LCA10 (ILLUMINATE)
Status: Recruiting
Last Changed: Jul 16, 2020
First Received: Apr 12, 2019
Disease(s): Leber Congenital Amaurosis 10, Blindness, Leber Congenital Amaurosis, Vision Disorders, Sensation Disorders, Neurologic Manifestations, Eye Diseases, Eye Diseases, Hereditary, Eye Disorders Congenital, Retinal Disease
Intervention(s): sepofarsen, Sham
Locations: University of Miami - Bascom Palmer Eye Institute, Miami, Florida, United States
University of Iowa, Iowa City, Iowa, United States
Columbia University Medical Center, New York, New York, United States
Casey Eye Institute - Oregon Health & Science University, Portland, Oregon, United States
University of Pennsylvania - Center for Advanced Retinal & Ocular Therapeutics, Philadelphia, Pennsylvania, United States
... and 13 other locations.
Single Ascending Dose Study in Participants With LCA10
Status: Recruiting
Last Changed: Jun 17, 2020
First Received: Mar 13, 2019
Disease(s): Blindness, Leber Congenital Amaurosis 10, Vision Disorders, Eye Diseases, Eye Diseases, Hereditary, Eye Disorders Congenital, Retinal Disease, Retinal Degeneration
Intervention(s): AGN-151587
Locations: Bascom Palmer Eye Institute, Miami, Florida, United States
Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, United States
W.K. Kellogg Eye Center - University of Michigan, Ann Arbor, Michigan, United States
Casey Eye Institute - OSHU, Portland, Oregon, United States
Natural History Study of CEP290-Related Retinal Degeneration
Status: Recruiting
Last Changed: Jul 07, 2020
First Received: Jan 10, 2018
Disease(s): Blindness, Leber Congenital Amaurosis 10, Vision Disorders, Eye Diseases, Eye Diseases, Hereditary, Eye Disorders Congenital, Retinal Disease, Retinal Degeneration
Locations: Bascom Palmer Eye Institute, Miami, Florida, United States
Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, United States
W.K. Kellogg Eye Center, Ann Arbor, Michigan, United States
Casey Eye Institute - OHSU, Portland, Oregon, United States
Universite Pierre et Marie Curie, Paris, France
... and 3 other locations.
Inherited Retinal Degenerative Disease Registry
Status: Recruiting
Last Changed: Dec 13, 2018
First Received: May 06, 2015
Disease(s): Eye Diseases Hereditary, Retinal Disease, Achromatopsia, Bardet-Biedl Syndrome, Bassen-Kornzweig Syndrome, Batten Disease, Best Disease, Choroidal Dystrophy, Choroideremia, Cone Dystrophy, Cone-Rod Dystrophy, Congenital Stationary Night Blindness, Enhanced S-Cone Syndrome, Fundus Albipunctatus, Goldmann-Favre Syndrome, Gyrate Atrophy, Juvenile Macular Degeneration, Kearns-Sayre Syndrome, Leber Congenital Amaurosis, Refsum Syndrome, Retinitis Pigmentosa, Retinitis Punctata Albescens, Retinoschisis, Rod-Cone Dystrophy, Rod Dystrophy, Rod Monochromacy, Stargardt Disease, Usher Syndrome
Locations: Foundation Fighting Blindness, Columbia, Maryland, United States