drugset / Trial / NCT07068958

A Study Evaluating the Efficacy and Safety of RCI001 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye

NCT07068958 ↗

Phase 2 Not yet recruiting 200 enrolled ORA, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this study is to evaluate the safety and efficacy of 0.25% RCI001 Ophthalmic Solution twice a day (BID) and four times a day (QID) compared to placebo (vehicle) in the treatment of the signs and symptoms of dry eye. The secondary objective of this study is to evaluate the optimal dosing frequency of 0.25% RCI001 Ophthalmic Solution (BID versus QID) in the treatment of the signs and symptoms of dry eye.

Timeline

Start
2025-08-01
Primary completion
2025-11-01
Completion
2025-11-01

Drugs

EvaluationDrugModalityDoseRoute
Subject RCI001 Unknown 0.25 % Other

Indications