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Clinical Trial ● Currently Recruiting Phase III NCT07519902

An Efficacy and Safety Study of Cenegermin Ophthalmic Solution Compared With Vehicle in the Treatment of PCED

An Efficacy and Safety Study of Cenegermin Ophthalmic Solution Compared With Vehicle in the Treatment of PCED — Recruiting • Phase III • NCT07519902.

📅 16 Jul 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07519902
Start
2026-06-02
Completion
2027-12
ClinicaliQ Trial Snapshot
  • An Efficacy and Safety Study of Cenegermin Ophthalmic Solution Compared With Vehicle in the Treatment of PCED — Recruiting • Phase III • NCT07519902.
  • Cenegermin eye drops versus placebo for treating persistent corneal erosion, measuring complete healing at four weeks.

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What This Trial Is Studying

This is a phase 3, randomized, multicenter, double-masked, parallel group, vehicle-controlled prospective clinical trial to evaluate the safety and efficacy of cenegermin in inducing complete epithelial healing in participants with PCED. The primary objective is the evaluation of complete epithelial healing after 4 weeks of treatment. The study is comprised of 3 periods: an 8-week initial treatment period (Day 1 to Week 8), an 8-week extension treatment period (Week 9 to Week 16), and a 24-week follow-up period (Week 17 to Week 40). Conditions: Persistent Corneal Epithelial Defect Interventions: Cenegermin,…

Full Trial Details
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Eligibility criteria, protocol, and results when available
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