drugset / Trial / NCT01230736

Safety and Efficacy of Changing to DuoTrav From Prior Therapy

NCT01230736

Phase 4 Completed 105 enrolled Alcon Research
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study to assess the safety and efficacy of changing to DuoTrav® from prior bimatoprost 0.03%/timolol 0.5% (used concomitantly or in a fixed combination) pharmacotherapy in uncontrolled patients with open-angle glaucoma or ocular hypertension.

Timeline

Start
2010-10
Primary completion
2011-02
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Timolol Other / unclassified 0.5 % Topical
Subject Travoprost Other / unclassified 0.004 % Topical

Indications