drugset / Trial / NCT01111890

Comparison of the Efficacy of AZARGA® Versus COSOPT® in Patients With Open-Angled Glaucoma or Ocular Hypertension

NCT01111890

Phase 4 Completed 70 enrolled Alcon Research
RandomizedParallel-groupSingle-blindTreatment

Summary

Subjects are dosed twice daily at 9AM and 9PM for 12 weeks. The primary efficacy variable is the mean change in Intraocular Pressure (IOP) from baseline to 12 weeks. Secondary efficacy variable: % IOP ≤ 18 millimeters mercury (mmHg). Exploratory endpoint: Ocular discomfort scale after first dose.

Timeline

Start
2010-04
Primary completion
2011-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Brinzolamide Small molecule 1 %
Comparator Dorzolamide Small molecule 2 %
Background Timolol Other / unclassified 0.5 %