drugset / Trial / NCT07625124

A Phase 2 Study of RCI001 Ophthalmic Solution in Participants With Dry Eye Disease

NCT07625124 ↗

Phase 2 Not yet recruiting 200 enrolled Rudacure
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2 clinical study designed to evaluate the safety and efficacy of 0.25% RCI001 Ophthalmic Solution compared with placebo in participants with dry eye disease. The study will enroll adults with dry eye disease. After a 2-week run-in period with placebo ophthalmic solution, eligible participants will be randomly assigned to receive either 0.25% RCI001 Ophthalmic Solution or placebo ophthalmic solution in both eyes for 4 weeks. Study treatment will be administered either twice daily or four times daily, depending on the assigned dosing regimen. The main purpose of the study is to determine whether RCI001 improves the signs and symptoms of dry eye disease compared with placebo. The primary assessments include total corneal fluorescein staining and ocular discomfort at Day 28. Safety will be assessed through eye examinations, visual acuity, intraocular pressure, drop comfort, and adverse event monitoring.

Timeline

Start
2027-09-01
Primary completion
2028-06-30
Completion
2028-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject RCI001 Unknown 0.25 % Topical

Indications