Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Open-angle Glaucoma or Ocular Hypertension



Status:Recruiting
Conditions:High Blood Pressure (Hypertension), Ocular
Therapuetic Areas:Cardiology / Vascular Diseases, Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:3/31/2019
Start Date:February 28, 2019
End Date:July 17, 2023
Contact:Clinical Trials Registry Team
Email:IR-CTRegistration@allergan.com
Phone:1-877-277-8566

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A Phase 3b Study to Evaluate the Duration of Effect of Bimatoprost SR in Participants With Open-Angle Glaucoma or 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 enrollment in another Allergan Bimatoprost SR study
We found this trial at
12
sites
Danbury, Connecticut 06810
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Danbury, CT
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Austin, Texas 78731
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Austin, TX
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Cranberry Township, Pennsylvania 16066
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Cranberry Township, PA
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Eugene, Oregon 97401
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Eugene, OR
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Kansas City, Missouri 64133
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Kansas City, MO
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Kansas City, Missouri 64154
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Kansas City, MO
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Nashville, Tennessee 37205
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Nashville, TN
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Nashville, TN
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Newport Beach, California
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Newport Beach, CA
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Pasadena, California 91107
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Pasadena, CA
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Poughkeepsie, New York 12603
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Poughkeepsie, NY
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San Antonio, TX
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