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Safety and Efficacy of KPI-121 Compared to Placebo in Subjects With Dry Eye Disease — STRIDE 2  

Dry Eye Syndromes Clinical Trial

Official title:
A Phase 3, Double-Masked, Randomized, Controlled Study of KPI-121 0.25% Ophthalmic Suspension Compared to Vehicle in Subjects With Dry Eye Disease

Clinical Trial Summary

The primary purpose of this study is to determine the efficacy and safety of KPI-121 0.25% ophthalmic suspension compared to vehicle (placebo) in subjects who have a documented clinical diagnosis of dry eye disease. The product will be studied over 14 days, with 1-2 drops instilled in each eye four times daily (QID).

Clinical Trial Description

This is a Phase 3, multi-center, double-masked, randomized, vehicle-controlled, parallel-group study designed to evaluate the safety and efficacy of KPI-121 0.25% ophthalmic suspension versus vehicle in subjects with dry eye disease. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02819284
Study type Interventional
Source Kala Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 3
Start date June 2016
Completion date September 2017
View Details
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