drugset / Trial / NCT00210964

Ceftobiprole in Hospital Acquired Pneumonia

NCT00210964

Phase 3 Completed 781 enrolled Basilea Pharmaceutica
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the clinical cure rate of ceftobiprole medocaril (the water-soluble prodrug \[form\] of ceftobiprole) referred to as ceftobiprole versus a comparator in the treatment of patients with nosocomial pneumonia.

Timeline

Start
2005-04
Primary completion
2007-05
Completion
2007-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ceftazidime Small molecule 2 g Intravenous
Subject Ceftobiprole Small molecule 500 mg Intravenous
Comparator Linezolid Other / unclassified 600 mg Intravenous

Indications