Expired Study
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Andover, Massachusetts 01810


Purpose:

The purpose of this study is to compare the safety and efficacy of RX-10045 to placebo for the treatment of the signs and symptoms of dry eye.


Criteria:

Inclusion Criteria: - Be at least 18 years of age; - Have provided written informed consent; - Have a history of dry eye for at least 6 months prior to enrollment; - Have a history of use or desire to use eye drops for dry eye symptoms within the past 6 months; - Demonstrate a response when exposed to the CAE. Exclusion Criteria: - Have an on-going ocular infection, or active ocular inflammation - Have worn contact lenses within 72 hours of Visit 1 or have anticipated use of contact lenses during the study; - Have contact lens-induced dry eye; - Have previously had laser in situ keratomileusis (LASIK) surgery; - Be using or have anticipated use of temporary punctual plugs during the study; - Have best corrected visual acuity > +0.7 in both eyes; - Be a woman who is pregnant, nursing or planning a pregnancy; - Have a known allergy and/or sensitivity to the test article or its components; - Be currently using any medication known to cause ocular drying that is not used on a stable dosing regimen for at least 30 days


NCT ID:

NCT00799552


Primary Contact:

Principal Investigator
Gail Torkildsen, MD
Ophthalmic Research Associates, Andover, MA


Backup Contact:

N/A


Location Contact:

Andover, Massachusetts 01810
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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