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Study of TOP1630 for Dry Eye Syndrome — THEIA-1  

Dry Eye Syndrome Clinical Trial

Official title:
A Multi-Center, Randomized, Double Masked, Placebo Controlled Clinical Study to Assess the Efficacy and Safety of TOP1630 0.1% Ophthalmic Solution Compared to Placebo in Subjects With Moderate to Severe Dry Eye Syndrome

Clinical Trial Summary

In subjects with Dry Eye Syndrome (DES):

The primary objective of this study is to confirm the efficacy of TOP1630 0.1% Ophthalmic Solution TID OU compared to placebo treatment at Day 29 on pre-specified sign and symptom endpoints in subjects with moderate to severe DES.

Clinical Trial Description

This study is designed to assess the efficacy and safety of TOP1630 ophthalmic solution in subjects with Dry Eye Syndrome (DES).

Eligible subjects will be randomized double masked to either TOP1630 or placebo for a duration of 28 days' treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03833388
Study type Interventional
Source Topivert Pharma Ltd
Contact
Status Completed
Phase Phase 2/Phase 3
Start date February 13, 2019
Completion date May 14, 2019
View Details
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