At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Prospective, Double-masked, Randomized, Multi-center, Active-controlled, Parallel-group 12-month Study Assessing the Safety and Ocular Hypotensive Efficacy of PG324 Ophthalmic Solution Compared to AR-13324 Ophthalmic Solution, 0.02% and Latanoprost Ophthalmic Solution, 0.005% in Subjects With Elevated Intraocular Pressure
In Brief
A Phase 3 clinical trial evaluating PG324 Ophthalmic Solution 0.02%/0.005%, Netarsudil (AR-13324) Ophthalmic Solution 0.02%, and 1 other intervention for Open-angle Glaucoma and Ocular Hypertension. Completed, enrolled 718 participants across 1 site.
Detailed Summary
To evaluate ocular hypotensive efficacy and safety of PG324 Ophthalmic Solution compared to Netarsudil (AR-13324) Ophthalmic Solution and Latanoprost Ophthalmic Solution. Following completion of the Month 12 study visit procedures, subjects will be offered the opportunity to participate in a 2-month observational (i.e., non-interventional) trial extension.
Study Details
Timeline
Interventions
1 drop once daily (QD), in the evening (PM) in both eyes (OU)
1 drop once daily (QD), in the evening (PM) in both eyes (OU)
1 drop once daily (QD), in the evening (PM) in both eyes (OU)