drugset / Trial / NCT00300443

Safety and Efficacy Study of Bimatoprost in Patients With Glaucoma or Ocular Hypertension

NCT00300443

Phase 2/3 Completed 561 enrolled Allergan
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of bimatoprost in patients with glaucoma or ocular hypertension

Timeline

Start
2005-12
Primary completion
2007-06
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 0.01 %
Subject Bimatoprost Other / unclassified 0.0125 %
Subject Bimatoprost Other / unclassified 0.03 %

Indications