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Prospective Natural History Study of Retinitis Pigmentosa (PHENOROD2)

Type: Observational

Status of the trial: Active, Recruiting

Orphan Drug Recognition: Yes


  • Opening Date: 2020-02-01
  • Closing Date: 2020-03-01


Inclusion: RP with mutations affecting the RHO, PDE6A and PDE6B genes Visual acuity ≥ 20/200 for at least one eye Binocular Visual field diameter ≥ 5° as measured on the Goldmann III-4e isopter

Exclusion: Patients with any other gene mutation known to be involved in RP Patients with other ocular disorder likely to impact the visual function Pregnant or breastfeeding women

More information

Children: No

Adults: Yes

Funder Type: private

HCP: Other investigators

Within ERN-EYE members

Principal investigators

Other investigators


  • Retinal Rare Eye Diseases (WG1)


* indicates required

This ERN is supported by: