Study Summary
This intermediate-size patient population expanded access program is to provide access to investigational product OCU400 for up to 75 patients with Retinitis Pigmentosa (RP) outside of the ongoing clinical trial Phase 3 program for patients who do not have access to alternative Food and Drug Administration (FDA)-approved products for treatment of the disease.
Want to learn more about this trial?
Request More InfoInterventions
OCU400DRUG
Participants will receive a subretinal injection of OCU400 modifier gene therapy product.
Study Locations
| Facility | City | State | Country |
|---|---|---|---|
| Associated Retina Consultants | Phoenix | Arizona | United States |
| Advanced Research | Deerfield Beach | Florida | United States |
| Erie Retina Research | Erie | Pennsylvania | United States |
| Gundersen Health | La Crosse | Wisconsin | United States |