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NCT07681778Possibly a fitNot yet recruiting

Gene therapy for inherited retinal degeneration from RDH12 mutations

Leber Congenital AmaurosisLeber Congenital Amaurosis (LCA)

Part of Eyes & vision clinical trials.

This trial tests an experimental gene therapy (OPGx-RDH12-1001) injected under the retina to treat a rare form of inherited vision loss called LCA caused by RDH12 gene mutations. It aims to see if the treatment is safe and tolerable for people with advanced vision loss.

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

Phase
Phase 1/Phase 2
Enrollment
10 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 12 years or older.
  • You have a vision loss condition called LCA caused by a specific genetic change (RDH12 mutation), confirmed by a blood test.
  • Your vision in at least one eye is 20/200 or worse (for adults) or 20/40 or worse (for others).
  • You have not had any gene therapy before.
  • You are healthy enough for eye surgery and do not have active eye infections, recent eye surgery, or conditions that make surgery risky.
  • Women who can get pregnant must use contraception for one year after treatment; men must use contraception for 180 days.

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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