Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Retinitis pigmentosa 37

MONDO:0012625

Any retinitis pigmentosa in which the cause of the disease is a mutation in the NR2E3 gene.

Also known as: NR2E3 retinitis pigmentosa, RP37, retinitis pigmentosa 37, retinitis pigmentosa caused by mutation in NR2E3, retinitis pigmentosa type 37

26 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (679) Nervous system disorder (231) Hereditary disease (176) Eye disorder (102) Retinal disorder (85) Retinitis pigmentosa (81) Inherited retinal dystrophy (40) Retinal degeneration (40) Perceptual disorders (22) Human disease (14)
Trials to join now! 12 Not yet recruiting 3 Not yet finished but already full! 1 Completed 8 Terminated 2
Sort by
  • Can a single eye injection restore sight in genetic blindness?

    ⭐️ CURE ⭐️ Ongoing

    This trial tests an experimental gene therapy called OCU400 in people with retinitis pigmentosa or Leber congenital amaurosis, which are inherited conditions that cause progressive vision loss and can lead to blindness. The therapy is given as a single injection into the eye, wit…

    Phase: PHASE1, PHASE2 • Sponsor: Ocugen • Aim: ⭐️ CURE ⭐️

    Last updated Aug 02, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space