drugset / Trial / NCT01740388

Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis

NCT01740388

Phase 3 Terminated 136 enrolled Bausch & Lomb Incorporated
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the clinical and microbial efficacy of besifloxacin ophthalmic suspension, 0.6% (Besifloxacin) administered BID for 3 days compared to vehicle in the treatment of bacterial conjunctivitis.

Timeline

Start
2013-02
Primary completion
2013-07
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Besifloxacin Small molecule 0.6 % Other