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Ocular Tolerability of Voclosporin Ophthalmic Solution Versus Restasis® in Subjects With Dry Eye Disease

Dry Eye Clinical Trial

Official title:
An Investigator-Masked, Randomized, Parallel-Group Study of the Ocular Tolerability of Voclosporin Ophthalmic Solution Versus Restasis® in Subjects With Dry Eye Disease

Clinical Trial Summary

Evaluate the tolerability, efficacy and safety of VOS versus Restasis® in subjects with mild to moderate Dry Eye Disease (DED).

Clinical Trial Description

This is a Phase 2, multi-center, Investigator-masked, randomized, parallel-group study to evaluate the tolerability, efficacy and safety of VOS versus Restasis® over a 28-day treatment period in subjects with mild to moderate DED. Approximately 90 subjects will be randomized to either VOS or Restasis® at approximately 7 centers located in the US ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03597139
Study type Interventional
Source Aurinia Pharmaceuticals Inc.
Contact
Status Completed
Phase Phase 2
Start date August 13, 2018
Completion date December 13, 2018
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