drugset / Trial / NCT00150267

A 5-Year Postmarketing Safety Study Of Xalcom In Patients With Open Angle Glaucoma Or Ocular Hypertension

NCT00150267

Phase 3 Completed 976 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To estimate the frequency of patients with ocular/periorbital adverse events. To identify any possible long-term adverse consequences of increased iris pigmentation and to follow serious adverse events throughout the study period.

Timeline

Start
2002-02
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Xalacom Unknown