Biallelic RPE65 Mutation-associated Retinal Dystrophy
Showing 1 - 25 of >10,000
Biallelic RPE65 Mutation-associated Retinal Dystrophy Trial in Beijing (FT-001 Low Dose, FT-001 Mid Dose, FT-001 High Dose)
Recruiting
- Biallelic RPE65 Mutation-associated Retinal Dystrophy
- FT-001 Low Dose
- +2 more
-
Beijing, Beijing, ChinaPeking Union Medical College Hospital
May 11, 2023
Confirmed Biallelic RPE65 Mutation-associated Retinal Dystrophy Trial in United States (AAV2-hRPE65v2,voretigene
Active, not recruiting
- Confirmed Biallelic RPE65 Mutation-associated Retinal Dystrophy
- AAV2-hRPE65v2,voretigene neparvovec-rzyl
-
Los Angeles, California
- +9 more
Oct 22, 2021
Retinal Dystrophy, PRPF31 Mutationassociated Retinal Dystrophy, RP11 Trial in Dallas (VP-001)
Recruiting
- Retinal Dystrophy
- +2 more
-
Dallas, TexasRetina Foundation of the Southwest
Jun 5, 2023
Natural History of PRPF31 Mutation-Associated Retinal Dystrophy
Recruiting
- Retinitis Pigmentosa
- +4 more
-
San Francisco, California
- +4 more
Oct 5, 2022
Inherited Retinal Dystrophy Due to RPE65 Mutations, Leber Congenital Amaurosis Trial in Iowa City, Philadelphia
Active, not recruiting
- Inherited Retinal Dystrophy Due to RPE65 Mutations
- Leber Congenital Amaurosis
- AAV2-hRPE65v2,voretigene neparvovec-rzyl
-
Iowa City, Iowa
- +1 more
Dec 9, 2021
Amaurosis of Leber, Retinal Diseases Trial in Gainesville, Philadelphia (rAAV2-CBSB-hRPE65)
Active, not recruiting
- Amaurosis of Leber
- Retinal Diseases
- rAAV2-CBSB-hRPE65
-
Gainesville, Florida
- +1 more
Dec 13, 2021
Subjects Who Received Voretigene Neparvovec-rzyl (AAV2-hRPE65v2)
Active, not recruiting
- Inherited Retinal Dystrophy Due to RPE65 Mutations
- AAV2-hRPE65v2
- (no location specified)
Dec 9, 2021
Leber Congenital Amaurosis Trial in Philadelphia (voretigene neparvovec-rzyl)
Completed
- Leber Congenital Amaurosis
- voretigene neparvovec-rzyl
-
Philadelphia, PennsylvaniaThe Children's Hospital of Philadelphia
Oct 30, 2020
Leber Congenital Amaurosis Associated With Mutations in RPE65
Recruiting
- Leber Congenital Amaurosis
-
Ann Arbor, Michigan
- +1 more
Apr 7, 2022
Neurodegenerative Disease, Hereditary, Mitochondrial Diseases, Optic Atrophy Trial in Buffalo (Mutation analysis)
Recruiting
- Neurodegenerative Disease, Hereditary
- +2 more
- Mutation analysis
-
Buffalo, New YorkUBMD Pediatrics
Mar 3, 2022
Neurodegenerative Disease, Hereditary, Mitochondrial Diseases, Optic Atrophy Trial in Buffalo (Mutation analysis)
Recruiting
- Neurodegenerative Disease, Hereditary
- +2 more
- Mutation analysis
-
Buffalo, New YorkUBMD Pediatrics
Mar 3, 2022
Bietti's Crystalline Dystrophy Trial in Beijing (ZVS101e)
Recruiting
- Bietti's Crystalline Dystrophy
-
Beijing, Beijing, ChinaPeking University Third Hospital
Feb 2, 2023
Cell Collection to Study Eye Diseases
Recruiting
- Retinal Disease
- +3 more
-
Bethesda, MarylandNational Institutes of Health Clinical Center
Jan 23, 2023
Best Disease and Other Retinal Degenerative Diseases.
Active, not recruiting
- Retinal Disease
- +4 more
-
Rochester, MinnesotaMayo Clinic
Jan 4, 2022
LCA5 Trial (AAV8.hLCA5)
Not yet recruiting
- LCA5
- AAV8.hLCA5
- (no location specified)
Nov 22, 2022
Objective Perimetry Using Chromatic Multifocal Pupillometer
Recruiting
- Retinal Dystrophies
- +2 more
-
Tel HaShomer, IsraelSheba Medical Center
Jan 15, 2023
Phenotypic Description of Atypical Clinical Forms of PLA2G6
Enrolling by invitation
- Neuroaxonal Dystrophy, Atypical
-
Clermont-Ferrand, France
- +6 more
Jun 29, 2022
Study of BEST1 Vitelliform Macular Dystrophy
Recruiting
- Best Vitelliform Macular Dystrophy
- Retinitis Pigmentosa
- Natural History Study
-
New York, New York
- +2 more
Mar 30, 2023
Retinal Imaging in Patients With Inherited Retinal Degenerations
Recruiting
- Retinitis Pigmentosa
-
San Francisco, CaliforniaDepartment of Ophthalmology Retinal Degenerations Clinic, UCSF
Sep 23, 2021
Rate of Progression in EYS Related Retinal Degeneration
Active, not recruiting
- Retinitis Pigmentosa
- Eye Diseases
-
San Francisco, California
- +19 more
Feb 3, 2022
To Evaluate the Scaling Clinical Study of AAV2-RPE65 Gene Therapy Agent (LX101) in Patients With Congenital Amaurosis (LCA)
Not yet recruiting
- To Evaluate the Scaling Clinical Study of AAV2-RPE65 Gene Therapy Agent (LX101) in Patients With Congenital Amaurosis (LCA)
- (no location specified)
Aug 29, 2023
Macular Edema, Inherited Retinal Dystrophy, Laser Retinopathy Trial in Rome (subthreshold treatment with micropulsed laser)
Not yet recruiting
- Macular Edema
- +2 more
- subthreshold treatment with micropulsed laser
-
Rome, RM, ItalyIRCSS Fondazione G:B:Bietti
Jul 27, 2023