Clin2
NCT05966493Possibly a fitRecruiting

Lufepirsen gel for persistent corneal epithelial defects

Persistent Corneal Epithelial Defect

Part of Eyes & vision clinical trials.

This Phase 2 trial tests whether a treatment gel called NEXAGON (lufepirsen) can improve healing and safety in people with a persistent corneal problem called PCED that hasn’t gotten better despite standard non-surgical treatments. You may be a candidate if your defect has lasted at least 2 weeks and hasn’t improved recently, and if you don’t have certain eye infections or other eye conditions.

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

Phase
Phase 2
Enrollment
84 people
Ages
2 years and older
Study type
Interventional

Who can take part

  • Have PCED in the study eye lasting at least 2 weeks
  • Your PCED has not improved after at least one standard non-surgical eye treatment
  • Your PCED has shown no clinical improvement in the 2 weeks before starting the study
  • Be able to give written consent (or assent, if applicable)
  • If you can become pregnant: be at least 1 year past menopause, surgically unable to become pregnant, or have a negative urine pregnancy test

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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