drugset / Trial / NCT01510145

Efficacy of Changing to TRAVATAN® From Prior Therapy

NCT01510145

Phase 4 Completed 191 enrolled Alcon Research
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to assess the efficacy and tolerability of TRAVATAN® solution without BAK (benzalkonium chloride) after changing from prior latanoprost 0.005% ophthalmic solution monotherapy in subjects with open-angle glaucoma or ocular hypertension due to tolerability issues.

Timeline

Start
2012-02
Primary completion
2013-05
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Travoprost Other / unclassified 0.004 % Other