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Safety and Efficacy of BRM421 for Dry Eye Syndrome Treatment

Dry Eye Syndrome Clinical Trial

Official title:
A Multi-Center, Randomized, Double Masked, Placebo Controlled Clinical Study to Assess the Safety and Efficacy of BRM421 Ophthalmic Solution in Subjects With Dry Eye Using a Controlled Adverse Environment (CAE®) Model

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, placebo-controlled, phase 2/3 study with approximately 200 subjects. (around 100 subjects per treatment arm). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04343287
Study type Interventional
Source BRIM Biotechnology Inc.
Contact
Status Completed
Phase Phase 2/Phase 3
Start date January 15, 2020
Completion date June 23, 2020
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