At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Efficacy and Safety of Bimatoprost SR in Patients With Open-angle Glaucoma or Ocular Hypertension
In Brief
A Phase 3 clinical trial evaluating Bimatoprost SR, Active Comparator: Timolol 0.5%, and 2 other interventions for Glaucoma, Open-Angle and Ocular Hypertension. Completed, enrolled 594 participants across 106 sites in 14 countries.
Detailed Summary
This study will evaluate the efficacy and safety of bimatoprost SR in participants with open-angle glaucoma or ocular hypertension. The study includes a 12-month treatment period with an 8-month extended follow-up.
Study Details
Timeline
Interventions
Bimatoprost SR administered in the study eye on Day 1, Week 16, and Week 32.
Timolol 0.5% administered once in the morning and once in the evening for up to 20 months.
Sham administered on Day 1, Week 16, and Week 32.
Timolol vehicle administered once in the morning and once in the evening for up to 20 months.