Overview

Safety and Efficacy of T-2345 Compared to Xalatan in Subjects With Primary Open Angle Glaucoma or Ocular Hypertension

Status:
Completed
Trial end date:
2015-01-01
Target enrollment:
Participant gender:
Summary
This is a Phase 3 study to evaluate the safety and efficacy of T-2345 dosed to one of both eyes once daily for 84 days compared to Xalatan dosed to one of both eyes once daily for 84 days in patients with elevated eye pressure.
Phase:
Phase 3
Details
Lead Sponsor:
Nephron Pharmaceuticals Corporation
Treatments:
Latanoprost
Ophthalmic Solutions
Pharmaceutical Solutions