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Clinical Trial Summary

The objective of this study is to compare the safety and efficacy of BRM421 Ophthalmic Solution to placebo for the treatment of the signs and symptoms of dry eye.


Clinical Trial Description

This is a multi-center, double-masked, randomized, vehicle-controlled, phase 2 study in approximately 150 subjects. (75 per treatment arm). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03066219
Study type Interventional
Source BRIM Biotechnology Inc.
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Status Completed
Phase Phase 2
Start date February 7, 2017
Completion date June 28, 2017

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