Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Suspension in Patients With Dry Eye Disease
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/6/2019 |
Start Date: | June 2015 |
End Date: | January 2016 |
This study will evaluate the safety, efficacy, tolerability, and systemic pharmacokinetics of
3 different doses of topical ophthalmic AGN-223575 suspension compared to AGN-223575 vehicle
in patients with dry eye disease.
3 different doses of topical ophthalmic AGN-223575 suspension compared to AGN-223575 vehicle
in patients with dry eye disease.
Inclusion Criteria:
- Signs and symptoms of dry eye disease
- Has used RESTASIS and/or artificial tears in both eyes twice a day for at least 60
days.
Exclusion Criteria:
- History of glaucoma, or ocular hypertension
- Diagnosis of ocular infection
- Use of contact lenses in the past 14 days or expected use during the study
- Use of any topical ophthalmic medications in the past 30 days
- Use of corticosteroids in the past 30 days.
We found this trial at
28
sites
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