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Study identifier: NCT07661329 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Primary Open Angle Glaucoma (POAG) · Ocular Hypertension (OH)  ·  Sponsor: YS Life Science Co., Ltd.

PhasePhase 3
Planned participants600
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (16)

National Clinical TrialsBeverly Hills, California, United StatesNot Yet Recruiting
United medical research instituteInglewood, California, United StatesNot Yet Recruiting
Eye research foundation, Inc.Newport Beach, California, United StatesRecruiting
Visionary Eye Research InstituteNewport Beach, California, United StatesNot Yet Recruiting
North Bay Eye AssociatesPetaluma, California, United StatesNot Yet Recruiting
Advanced research, LLCBoynton Beach, Florida, United StatesNot Yet Recruiting
Quantum clinical trialsMiami Beach, Florida, United StatesNot Yet Recruiting
Advanced research, LLCWeston, Florida, United StatesNot Yet Recruiting
Clayton Eye Clinical ResearchMorrow, Georgia, United StatesNot Yet Recruiting
Coastal Research Associates, LLCRoswell, Georgia, United StatesNot Yet Recruiting
The eye care instituteLouisville, Kentucky, United StatesNot Yet Recruiting
Tekwani vision centerSt Louis, Missouri, United StatesNot Yet Recruiting

+ 4 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07661329