Retinal Disease

National Eye Institute Biorepository for Retinal Diseases

Genotype-Phenotype Study of Patients With Plaquenil -Induced Retinal Toxicity, With Evaluation of the ABCA4 Gene

A Efficacy and Safety Study of Ranibizumab 10mg/ml Injection (Incepta) in Patients With Diabetic Macular Edema

Cell Collection to Study Eye Diseases

Modified Soft Contact Lens During Vitrectomy

Study to Evaluate the Long-Term Safety of Ultevursen in Participants With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene

Smartphone Screening for Eye Diseases

Optimize Pediatric OCT Imaging

Study to Evaluate Ultevursen in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene

Stem Cell Ophthalmology Treatment Study II

Study to Evaluate Sepofarsen in Subjects With Leber Congenital Amaurosis (LCA) Type 10 (HYPERION)

The Genetics Navigator: Evaluating a Digital Platform for Genomics Health Services

P200TxE Diseased Eye Image Collection

AI-Assisted Interpretation of Ultra-Widefield Retinal Images

Collecting Data on Retinal Blood Blood Flow and Blood Vessel Shape/Appearance Using an Investigational Device, XyCAM CRE, and to Then Compare Those Images With Images Collected From a Patient's Routine Clinical Examination.

Establishment of a Multimodal Standard Database for Inflammation-related Ophthalmopathy

A Repeat-Dose, Open-Label, Two Arm Safety and Efficacy Study of Two Doses of VP-001 Administered Intravitreally in Participants With Confirmed PRPF31 Mutation-Associated Retinal Dystrophy, Including Participants Previously Treated With VP001

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

Inherited Retinal Degenerative Disease Registry

COmparison of Clarus and Optos Ultrawide Field Imaging Systems for Inherited Retinal Disease