Retinal Dystrophies

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Information
Disease name
Retinal Dystrophies
Disease ID
Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT04123626 Active, not recruiting Phase 1/Phase 2 A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Gene October 7, 2019 June 7, 2022
NCT04945772 Completed Phase 2 Efficacy and Safety of MCO-010 Optogenetic Therapy in Adults With Retinitis Pigmentosa [RESTORE] July 13, 2021 January 18, 2024
NCT01546181 Completed Retinal Imaging by Adaptive Optics in Healthy Eyes and During Retinal and General Diseases October 2010 June 15, 2017
NCT02983305 Completed N/A Optical Head-Mounted Display Technology for Low Vision Rehabilitation June 26, 2017 November 21, 2018
NCT03763227 Completed Phase 2 Intravitreal Ranibizumab (Lucentis®) in the Treatment of Non-leaking Macular Cysts in Retinal Dystrophy July 24, 2015 August 29, 2019
NCT03843840 Completed Dual Wavelength OCT February 15, 2019 October 21, 2020
NCT06162585 Enrolling by invitation Non-Interventional Long Term Follow-up Study of Participants Previously Enrolled in the RESTORE Study December 8, 2023 September 2027
NCT06455826 Not yet recruiting Phase 1 MAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects (Wallaby) June 2024 November 2025
NCT06319872 Not yet recruiting Phase 1 The Effects of Disulfiram (Antabuse®) on Visual Acuity in Patients With Retinal Degeneration April 15, 2024 April 15, 2025
NCT02014389 Recruiting Evaluation of Objective Perimetry Using Chromatic Multifocal Pupillometer December 1, 2013 December 31, 2026
NCT05294978 Recruiting EyeConic: Qualification for Cone-Optogenetics July 1, 2021 December 2024
NCT05573984 Recruiting Natural History of PRPF31 Mutation-Associated Retinal Dystrophy July 7, 2022 April 30, 2027
NCT03853252 Recruiting N/A iPS Cells of Patients for Models of Retinal Dystrophies November 3, 2014 November 2024
NCT06177977 Recruiting N/A SS-HH-OCT as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs) March 1, 2024 December 2026
NCT03592017 Unknown status N/A Performance of Long-wavelength Autofluorescence Imaging October 1, 2018 July 30, 2022
NCT04855045 Unknown status Phase 2/Phase 3 An Open-label, Dose Escalation and Double-masked, Randomized, Controlled Trial Evaluating Safety and Tolerability of Sepofarsen in Children (<8 Years of Age) With LCA10 Caused by Mutations in the CEP290 Gene. March 23, 2021 December 2023
MeSH unique ID (MeSH (Medical Subject Headings))
D058499