Condition: Retinitis Pigmentosa · Sponsor: Ocugen
This is a Phase 3 study to Assess the Efficacy, Safety and Tolerability of OCU400 in patients with retinitis pigmentosa (RP) associated with RHO mutations and patients with any other RP associated mutation with a clinical phenotype of RP. This is a multicenter, assessor blinded and randomized study which will enroll 140 subjects. Study has completed enrollment of all 140 subjects.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Associated Retina Consultants | Phoenix, Arizona, United States | — |
| University of Southern Califormia | La Jolla, California, United States | — |
| University of Southern California, Roski Eye Insitute | Los Angeles, California, United States | — |
| Advanced Research, LLC. | Deerfield Beach, Florida, United States | — |
| Bascom Palmer Eye Institute, University of Miami, Miller School of Medicine | Miami, Florida, United States | — |
| Erie Retina Research LLC | Erie, Pennsylvania, United States | — |
| Vanderbilt Eye Institute | Nashville, Tennessee, United States | — |
| Retina Consultants of Texas | Bellaire, Texas, United States | — |
| Retina Foundation of the Southwest | Dallas, Texas, United States | — |
| Baylor College of Medicine | Houston, Texas, United States | — |
| Valley Retina Institute | McAllen, Texas, United States | — |
| Gundersen Health System | La Crosse, Wisconsin, United States | — |
+ 5 more locations — full list on the registry record.
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