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Lacripep™ in Subjects With Dry Eye Associated With Primary Sjögren's Syndrome

Dry Eye Clinical Trial

Official title:
A Double-Masked, Randomized, Multi-Center Phase 2 Study to Evaluate the Efficacy and Safety of Lacripep™ in Subjects With Dry Eye Associated With Primary Sjögren's Syndrome

Clinical Trial Summary

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 Sjögren's Syndrome

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03226444
Study type Interventional
Source TearSolutions, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date June 30, 2017
Completion date December 27, 2019
View Details
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