CONE-ROD DYSTROPHY

This study tests a new treatment called OpCT-001 for people with inherited eye diseases like retinitis pigmentosa and Usher syndrome, which cause vision loss. The treatment involves injecting special cells into the eye to replace damaged light-sensing cells. The study has two par…

This early study tests a single injection of ACDN-01 into the eye for people with Stargardt disease or related vision loss caused by ABCA4 gene mutations. The main goal is to check safety and find the best dose. Up to 15 adults with advanced vision loss will take part. The therap…

This study is a prescreening step to find people with a specific genetic eye condition called ABCA4-related retinopathy, which includes Stargardt disease and cone-rod dystrophy. About 50 participants will undergo genetic testing and eye exams to see if they qualify for future tri…

This registry collects health information from people with inherited retinal diseases to help researchers better understand these conditions. Participants create an online profile and can update it over time. The goal is to speed up research and connect people with clinical trial…

This study uses a special camera called adaptive optics to take detailed pictures of the back of the eye in people with outer retinal diseases, such as age-related macular degeneration and retinitis pigmentosa. The goal is to develop new ways to diagnose and track these diseases.…

This study looks at whether people with retinitis pigmentosa and similar eye diseases experience short-term improvements in vision after using a device that delivers mild electrical stimulation to the eye. The device is already approved in Europe to slow vision loss. Researchers …