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Clinical Trial Summary

Qlaris' Phase 2 clinical trial investigating the safety, tolerability, and ocular hypotensive efficacy of QLS-111 in normal tension glaucoma patients.


Clinical Trial Description

A randomized, active- and vehicle-controlled, multi-site, double-masked study to evaluate the safety and tolerability of QLS-111 versus vehicle in subjects with NTG. Primary objective is to evaluate the ocular and systemic safety and tolerability of 2 concentrations of QLS-111 compared to vehicle control. Secondary objective is to evaluate the ocular hypotensive efficacy of 2 concentrations of QLS-111 with once daily morning (QAM), once daily evening (QPM), and twice daily (BID) dosing versus vehicle with QAM, QPM, and BID dosing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06030193
Study type Interventional
Source Qlaris Bio, Inc.
Contact Lisa Brandano
Phone 9789302103
Email lbrandano@qlaris.bio
Status Not yet recruiting
Phase Phase 2
Start date June 10, 2024
Completion date March 7, 2025

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