Overview

OPC-1085EL in the Treatment of Primary Open Angle Glaucoma or Ocular Hypertension in Chinese Subjects

Status:
Recruiting
Trial end date:
2024-04-01
Target enrollment:
Participant gender:
Summary
It is a phase III, multi-center, randomized, single-blind (to evaluator), parallel, and positive-controlled clinical trial evaluating the efficacy and safety of OPC-1085EL in the treatment of primary open angle glaucoma or ocular hypertension in Chinese subjects. It is planned that 240 subjects (120 in each group) will be randomly assigned to receive OPC-1085EL or 0.005% latanoprost ophthalmic solution (latanoprost) at a ratio of 1:1.
Phase:
Phase 3
Details
Lead Sponsor:
Otsuka Beijing Research Institute
Treatments:
Carteolol
Latanoprost
Ophthalmic Solutions
Pharmaceutical Solutions