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Clinical Trial Summary

This is a phase 3 part A study to confirm the efficacy in reduction of intraocular pressure and safety of PHP-201 ophthalmic solution in patients with primary open-angle glaucoma or ocular hypertension.


Clinical Trial Description

As a selective ROCK inhibitor, PHP-201 is designed to alleviate the side effects, which are the disadvantages of existing intraocular pressure reducing agents, while exhibiting sufficient intraocular pressure-lowering effect in glaucoma patients. This clinical trial aims to provide a new therapeutic option by evaluating the efficacy and safety of PHP-201 0.5% in patients with primary open-angle glaucoma or ocular hypertension who require intraocular pressure reduction therapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04863365
Study type Interventional
Source pH Pharma
Contact Younyoung Hwang
Phone +82 31 779 5301
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date November 2021
Completion date November 2025

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