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 |
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.
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
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