RP Cure Tracker

Trials / NCT04285398

Prospective Natural History Study of Retinitis Pigmentosa

Underway, not enrolling N/A Natural history / observational

Sponsor
SparingVision
Treatment
Ophthalmic examinations; Mobility Test
Gene
PDE6A, PDE6B, RHO
Conditions
Retinitis Pigmentosa
Ages
18 Years to no upper limit
Enrollment
82 participants
Started
2020-02-12
Main results expected
2026-06-30
Results posted
Not yet
Record last updated
2025-05-22

What the study is testing

This is natural history study of rods and cones degenerations in patients with Retinitis Pigmentosa (RP) caused by pathogenic mutations in RHO, PDE6a or PDE6b gene mutations.

Where it runs

France (1)
United States (1)

Open on ClinicalTrials.gov for contacts and eligibility