Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History of PRPF31 Mutation-Associated Retinal DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaActive, not recruitingNot stated2026-04-13NCT05573984

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
PYC Therapeutics5

7 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
Centre For Eye Research Australia (CERA) - Retinal Gene Therapy UnitEast MelbourneAustralia1
Lions Eye InstituteNedlandsAustralia2
Oregon Health and Science University - Casey Eye InstitutePortlandUnited States1
Retina Foundation of the SouthwestDallasUnited States1
University of California San FranciscoSan FranciscoUnited States144
University of Florida HealthJacksonvilleUnited States5
University of Michigan Kellogg Eye CenterAnn ArborUnited States9