drugset / Trial / NCT01263444

Safety and Efficacy of Adding AZARGA® Adjunctive to Prostaglandin Therapy

NCT01263444

Phase 4 Completed 47 enrolled Alcon Research
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the safety and efficacy of adding AZARGA® as a single agent to prostaglandin monotherapy in patients with either ocular hypertension or primary open-angle glaucoma.

Timeline

Start
2011-03
Primary completion
2013-04
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Brinzolamide Small molecule 1 % Topical
Subject Timolol Other / unclassified 0.5 % Topical
Background Bimatoprost Other / unclassified Topical
Background Latanoprost Small molecule Topical
Background Tafluprost Other / unclassified Topical
Background Travoprost Other / unclassified Topical