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PG-234 ( A Phase III Study: 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.

To read more about this study click here.

For additional information of if you think you may be a candidate for this trial click here.

Study Coordinator (Marvin Martinez): mmartinez@saeye.com