NCT03626207
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Eye Diseases, Hereditary, +5 more
- Locations
-
- Site JP00001 Kobe, Hyōgo, Japan
Clinical trial condition
Explore clinical trials studying Retinitis Pigmentosa. Study availability and eligibility vary by location and protocol.
NCT03626207
NCT04319809
NCT04925687
NCT00447993
NCT04604899
NCT03349242
NCT03073733
NCT02661711
NCT02110225
NCT02140164