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Retinal Dystrophies clinical trials

View clinical trials related to Retinal Dystrophies.

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NCT ID: NCT06455826 Not yet recruiting - Eye Diseases Clinical Trials

MAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects (Wallaby)

Start date: June 2024
Phase: Phase 1
Study type: Interventional

A Phase 1 Open-Label, Multiple Ascending Dose Study to Evaluate the Safety and Tolerability of Intravitreally Administered VP-001 in Participants with Confirmed PRPF31 Mutation-Associated Retinal Dystrophy

NCT ID: NCT06319872 Not yet recruiting - Clinical trials for Alcohol Use Disorder

The Effects of Disulfiram (Antabuse®) on Visual Acuity in Patients With Retinal Degeneration

Start date: April 15, 2024
Phase: Phase 1
Study type: Interventional

Oral disulfiram (Antabuse®) has been shown to improve image-forming vision in animal models with retinal degeneration due to its ability to decrease Retinoic Acid synthesis and consequently reduce hyperactivity in the inner retina. The investigator will aim to evaluate the impact of oral disulfiram on the vision of patients with retinal degeneration who are being treated with the drug in the management of their concurrent alcohol use disorder.

NCT ID: NCT06212297 Recruiting - Clinical trials for Inherited Retinal Dystrophy

Fellow-eye Study (FE) of LX101 in Subjects With Inherited Retinal Dystrophy

Start date: September 12, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Up to nine subjects who have participated in the earlier LX101 clinical study, and who meet all study eligibility criteria, will receive LX101 administration in the previously uninjected, contralateral eye to evaluate the safety of bilateral, sequential subretinal administration of LX101.

NCT ID: NCT06196827 Active, not recruiting - Clinical trials for Inherited Retinal Dystrophy Associated With RPE65 Mutations

Safety and Tolerability of LX101 for Inherited Retinal Dystrophy Associated With RPE65 Mutations

Start date: July 2, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to evaluate the safety, tolerability and efficacy of LX101 in subjects with biallelic RPE65 mutation-associated inherited retinal dystrophy.

NCT ID: NCT06177977 Recruiting - Retinal Dystrophies Clinical Trials

SS-HH-OCT as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs)

SS-HH-OCT
Start date: March 1, 2024
Phase: N/A
Study type: Interventional

The goal of this observational study is to utilize a novel imaging system designed for high-resolution retinal imaging of neonates, infants and children to identify the signs of photoreceptor development and degeneration in children with early-onset inherited retinal dystrophies (EORDs). Participants will have research imaging with SS-HH-OCT at the time of clinically-indicated eye examinations or procedures. The investigators aim to establish the basis for utilization of OCT imaging in earlier diagnosis and disease monitoring in children with EORDs. This work will set data reference standards and IRD endpoints that can be used in clinical trials.

NCT ID: NCT06162585 Enrolling by invitation - Clinical trials for Retinitis Pigmentosa

Non-Interventional Long Term Follow-up Study of Participants Previously Enrolled in the RESTORE Study

REMAIN
Start date: December 8, 2023
Phase:
Study type: Observational

This study will be conducted following Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Eligible subjects will be consented to return for scheduled study visits for this study following their completion in study NTXMCO-002 (RESTORE). They will not receive a second treatment with MCO-010 (or a repeated sham injection) in this study

NCT ID: NCT05976139 Recruiting - Macular Edema Clinical Trials

Micropulsed Laser in Patients With Macular Oedema in Retinal Dystrophies

Start date: September 6, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether subthreshold treatment with micropulsed laser can be effective in resolving macular edema in patients with inherited retinal dystrophy. Visits will be performed after 1, 3, 6, 9, 12, 18, and 24 months after treatment. Laser treatment will be performed on the day of the first visit, and its repetition at subsequent visits between months 3 and 12 will be evaluated. Evaluations of treatment effects will include: - comprehensive ophthalmologic examination - multifocal electroretinogram - OCT examination - OCT-angiography examination - retinography Primary endpoint. - central retinal thickness, measured by OCT

NCT ID: NCT05902962 Recruiting - Retinal Dystrophy Clinical Trials

SAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects

Platypus
Start date: April 20, 2023
Phase: Phase 1
Study type: Interventional

A Phase 1 Open-Label, Single Arm Dose Escalation Study to Evaluate the Safety and Tolerability of Intravitreally Administered VP-001 in Participants with Confirmed PRPF31 Mutation-Associated Retinal Dystrophy

NCT ID: NCT05858983 Recruiting - Clinical trials for Biallelic RPE65 Mutation-associated Retinal Dystrophy

Gene Therapy in Subjects With Biallelic RPE65 Mutation-associated Retinal Dystrophy

Start date: November 30, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this clinical trial is to evaluate the safety, tolerability and efficacy of subretinal administration of FT-001 in subjects with biallelic RPE65 mutation-associated retinal dystrophy.

NCT ID: NCT05820100 Completed - Clinical trials for Retinitis Pigmentosa

Observational Study to Assess the Reliability and Validity of the MLYMT and MLSDT

Start date: April 25, 2023
Phase:
Study type: Observational

This is a prospective Multi-Center Observational Study to assess the reliability and validity of the Multi-Luminance Y-Mobility Test (MLYMT) and Multi-Luminance Shape Discrimination Study (MLSDT) Main Outcome Measures: (i) Performance scores in normal and severely visually impaired subjects with a clinical diagnosis of retinitis pigmentosa (RP) on MLYMT and MLSDT at multiple luminance levels and (ii) reliability and content validity of MLYMT and MLSDT.