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Study identifier: NCT04890106 Synced from ClinicalTrials.gov · July 30, 2026
● Completed

Bioequivalence Study With Clinical Endpoint Comparing Bimatoprost Ophthalmic Solution 0.01% to LUMIGAN® In The Treatment of Chronic Open-Angle Glaucoma

Condition: Glaucoma, Open-Angle  ·  Sponsor: Mankind Pharma Limited

PhasePhase 3
Planned participants310
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a randomized, double-masked, two-treatment, single-period, parallel design, multiple dose at multiple clinical trial sites designed to demonstrate bioequivalence with clinical endpoint in subjects with chronic open-angle glaucoma or ocular hypertension in both eyes. Test Product - Bimatoprost Ophthalmic Solution, 0.01% of Mankind Pharma Limited, India Reference Product - LUMIGAN® (Bimatoprost Ophthalmic Solution) 0.01% of Allergan, Inc.,

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

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

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Locations (9)

CBCC Global Research Site:011Bakersfield, California, United States
CBCC Global Research Site 016Mission Hills, California, United States
CBCC Global Research Site 017Newport Beach, California, United States
CBCC Global Research Site: 012Newport Beach, California, United States
CBCC Global Research Site 013Pasadena, California, United States
CBCC Global Research Site 019Petaluma, California, United States
CBCC Global Research Site 015San Diego, California, United States
CBCC Global Research Site 020Pembroke Pines, Florida, United States
CBCC Global Research Site 018Houston, Texas, United States

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Source record: clinicaltrials.gov/study/NCT04890106