Delray Beach, Florida 33484

  • Ocular Hypertension


This study evaluates the duration of intraocular pressure (IOP)-lowering effect and safety of as needed administrations of Bimatoprost sustained release (SR) in participants with open-angle glaucoma (OAG) or ocular hypertension (OHT) who are not adequately managed with topical IOP-lowering medication for reasons other than medication efficacy.


Inclusion Criteria: • Diagnosis of either Diagnosis of either open angle glaucoma (OAG) (i.e., primary OAG, pseudoexfoliation glaucoma, pigmentary glaucoma) or ocular hypertension requiring intraocular pressure-lowering treatment Exclusion Criteria: - Concurrent or anticipated enrollment in another investigational drug or device study or participation in such a study within 2 months prior to enrolling in this study - Previous administration with Bimatoprost SR in the study eye



Primary Contact:

Study Director
Saumya Nagar

Clinical Trials Registry Team
Phone: 1-877-277-8566

Backup Contact:


Location Contact:

Delray Beach, Florida 33484
United States

Study Coordinator
Phone: 561-498-3664

Site Status: Recruiting

Data Source:

Date Processed: September 15, 2021

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