Trial intelligence / Profile preview

Safety of Besivance in Bacterial Conjunctivitis

NCT01175590Phase 3Completed

Sponsor
Bausch + Lomb
Start
Jun 2010
Primary completion
Dec 2011
Modality
Small Molecules
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in bacterial conjunctivitis (BC) comparing Besivance with Vehicle (2 arms). Primary endpoints: Ocular Treatment Emergent Adverse Events at 7 days and Non-Ocular Treatment-Emergent Adverse Events at 7 days. Started Jun 2010; status: completed.

02

Drugs

besifloxacin
03

Conditions

bacterial conjunctivitis (BC)

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