Clin2
NCT05874310Possibly a fitRecruiting

Gene therapy trial for RPGR-related vision loss

X-Linked Retinitis Pigmentosa

Part of Eyes & vision clinical trials.

This early study tests a gene therapy designed for people whose vision problems are caused by an RPGR genetic change. It may help slow or improve the eye disease by treating the underlying cause.

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

Phase
Early Phase 1
Enrollment
18 people
Ages
8 years to 45 years
Study type
Interventional

Who can take part

  • Be able and willing to follow all study visit and testing instructions
  • Be a male age 8 to 45 when you sign consent
  • Have a confirmed genetic change (variant) in the RPGR gene
  • Do not have other inherited retinal genetic causes of vision loss
  • Have not had any prior gene therapy to the eye (or any prior gene therapy product)

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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