Last updated on November 2019

Lacripep in Subjects With Dry Eye Associated With Primary Sj gren's Syndrome


Brief description of study

The objective of this study is to evaluate the efficacy and safety of two strengths of Lacripep ophthalmic solution versus placebo administered three times daily for four weeks in subjects with a diagnosis of Dry Eye associated with documented Primary Sjgren's Syndrome

Detailed Study Description

This is a multi-center, randomized, placebo-controlled, double-masked, parallel-group study. Subjects will be randomized into three treatment groups: 0.005%, or 0.01% Lacripep, or placebo in a 1:1:1 ratio.

Clinical Study Identifier: NCT03226444

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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