Clin2
NCT07710196Possibly a fitRecruiting

NPI-001 for preserving vision in usher syndrome

Retinitis Pigmentosa (RP)Usher Syndrome

Part of Brain & nervous system, Ear, nose & throat, Eyes & vision, Genetic & congenital clinical trials.

This study tests a 24-month treatment with NPI-001, an oral medication, to see if it can slow the loss of light-sensing cells in the retina for people with retinitis pigmentosa tied to Usher syndrome. It aims to preserve remaining vision and delay further damage.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
80 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have retinitis pigmentosa (RP) associated with Usher syndrome.
  • You have some healthy retina tissue left in both eyes—specifically, an EZ width of at least 500 microns that includes the fovea (the sharp vision area).
  • You see enough points on a special eye test (MAIA microperimetry) to show that your vision is stable enough.
  • Your other medications have been at a steady dose for at least a month.
  • If you could become pregnant, you must be willing to use birth control during the 24-month trial.
  • You haven't had eye surgery in the last 2 months, and you don't have other eye diseases like glaucoma or diabetic retinopathy.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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