Expired Study
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Andover, Massachusetts 01810


Purpose:

The objective of the Phase 2 study is to compare the safety and efficacy of cis-UCA Ophthalmic Solutions to placebo for the treatment of the signs and symptoms of dry eye.


Criteria:

Key Inclusion Criteria: - Be at least 18 years of age; - Provide written informed consent; - Have a subject reported history of dry eye; - Have a history of use or desire to use eye drops. Key Exclusion Criteria: - Have any clinically significant eye findings that require therapeutic treatment, and/or in the opinion of the Investigator may interfere with study parameters; - Have worn contact lenses within 7 days of Visit 1 or anticipate using contact lenses during the study; - Have previously had laser-assisted in situ keratomileusis (LASIK) surgery within the last 12 months; - Have used Restasis® within 30 days of Visit 1; - Have any planned ocular and/or lid surgeries over the study period; - Be a woman who is pregnant, nursing or planning a pregnancy; - Be unwilling to submit a urine pregnancy test at Visit 1 and Visit 4 (or early termination visit) if of childbearing potential; - Have a known allergy and/or sensitivity to the study drug or its components; - Have a condition or be in a situation which the Investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study; - Be currently enrolled in an investigational drug or device study or have used an investigational drug or device within 30 days of Visit 1; - Be unable or unwilling to follow instructions, including participation in all study assessments and visits.


NCT ID:

NCT02326090


Primary Contact:

N/A


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: November 18, 2019

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