A Study to Evaluate Efficacy and Safety of Lifitegrast in Subjects With Dry Eye (OPUS-3)
Status: | Completed |
---|---|
Conditions: | Ocular, Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/11/2019 |
Start Date: | November 6, 2014 |
End Date: | October 5, 2015 |
A Phase 3, Multicenter, Randomized, Double-masked, and Placebo-controlled Study Evaluating the Efficacy and Safety of a 5.0% Concentration of Lifitegrast Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye Disease and History of Recent Artificial Tear Use
Evaluate the efficacy and safety of Lifitegrast in subjects with dry eye disease and a recent
history of artificial tear use.
history of artificial tear use.
Inclusion Criteria:
- Patient-reported history of Dry Eye Disease in both eyes.
- Use of over the counter artificial tears within the past 30 days.
- A negative urine pregnancy test for females and willingness to use adequate birth
control throughout the study.
- Able and willing to comply with all study procedures.
Exclusion Criteria:
- Presence of an ocular condition that could affect the study parameters such as active
ocular infections, ocular inflammation, glaucoma, or diabetic retinopathy;.
- Unwilling to stop wearing contact lenses during the study.
- LASIK or other ocular surgical procedures within 12 months prior to or during the
study.
- Use of prohibited medications
- Significant medical conditions that could affect the study parameters.
We found this trial at
41
sites
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