drugset / Trial / NCT00972777

Efficacy of Besifloxacin Ophthalmic Suspension in the Treatment of Bacterial Conjunctivitis

NCT00972777

Phase 2/3 Completed 474 enrolled Bausch & Lomb Incorporated
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is being conducted to evaluate the clinical and microbial efficacy of besifloxacin ophthalmic suspension compared with vehicle in the treatment of bacterial conjunctivitis. This study was conducted as a phase IIb study and continued with further enrollment as a phase III study.

Timeline

Start
2009-10
Primary completion
2010-10
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Besifloxacin Small molecule 0.6 % Topical