Overview

A Study Evaluating the Efficacy of SAR 1118 (0.1%, 1.0%, 5.0%) Ophthalmic Solution in Subjects With Dry Eye Conducted in a Controlled Adverse Environment (CAE)

Status:
Completed
Trial end date:
2010-02-18
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the efficacy of three different concentrations (0.1%, 1.0%, 5.0%) of SAR 1118 Ophthalmic Solution compared to placebo in the treatment of dry eye.
Phase:
Phase 2
Details
Lead Sponsor:
Shire
Treatments:
Lifitegrast
Ophthalmic Solutions
Pharmaceutical Solutions