Last updated on August 2018

Dry Eye Study


Brief description of study

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 Study Identifier: TX211431

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Oculus Research, Inc.

4170 Fayetteville Rd Raleigh, NC United States
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