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Qlaris Study of QLS-111 in Combination With a PGA for OAG and/or OHT Patients

Glaucoma Clinical Trial

Official title:
A Pilot, Double-masked, Vehicle-controlled, Randomized Study to Evaluate the Safety and Tolerability of QLS-111 Versus Vehicle in Combination With Latanoprost Treatment in Subjects With Open-angle Glaucoma and/or Ocular Hypertension

Clinical Trial Summary

Qlaris Phase 2 clinical study investigating the safety, tolerability, and ocular hypotensive efficacy of QLS-111 in combination with latanoprost in open-angle glaucoma (OAG) and/or ocular hypertension (OHT) patients.

Clinical Trial Description

Pilot, double-masked, vehicle-controlled, randomized, prospective parallel study of 14-day once daily evening (QPM) dosing, followed by 14-day twice daily (BID) dosing of an investigational product (IP), QLS-111, or vehicle as concomitant therapy with monotherapy latanoprost a PGA treatment that is administered QPM. Both eyes (OU) will be dosed. The study is comprised of seven (7) visits and approximately 28 days of IP dosing. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06249152
Study type Interventional
Source Qlaris Bio, Inc.
Contact Lisa Brandano
Phone 9789302103
Email lbrandano@qlaris.bio
Status Recruiting
Phase Phase 2
Start date April 21, 2024
Completion date October 5, 2024
View Details
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