drugset / Trial / NCT07661329

A Comparative, Randomized, Investigator-blind, Active-controlled, Parallel-group, Multicenter, Clinical Endpoint Study

NCT07661329

Phase 3 Recruiting 600 enrolled YS Life Science Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is to establish non-inferiority of a preservative free formulation of Bimatoprost ophthalmic solution 0.01% (YSBP) of YS Life Science Co., Ltd. compared to LUMIGAN® (bimatoprost ophthalmic solution) 0.01% of AbbVie INC in subjects with primary open angle glaucoma (POAG) or ocular hypertension.

Timeline

Start
2026-06-02
Primary completion
2027-11-01
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 0.01 % Other