drugset / Trial / NCT00457795

24-hour IOP-lowering Effect of Brimonidine 0.1%

NCT00457795

Phase 4 Completed 15 enrolled Allergan
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of brimonidine 0.1% three-times daily in patients with glaucoma or ocular hypertension

Timeline

Start
2006-12
Primary completion
2009-02
Completion
2009-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Brimonidine Small molecule 0.1 %