drugset / Trial / NCT01371838

A Study to Evaluate the Efficacy and Safety of Intravenous Ceftaroline Versus Intravenous Ceftriaxone in the Treatment of Adult Hospitalised Patients With Community-Acquired Bacterial Pneumonia in Asia

NCT01371838 ↗

Phase 3 Completed 848 enrolled Pfizer Forest Laboratories · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This purpose of this study is to Evaluate the Efficacy and Safety of Intravenous Ceftaroline Versus Intravenous Ceftriaxone in the Treatment of Adult Hospitalised Patients With Community-Acquired Bacterial Pneumonia in Asia.

Timeline

Start
2011-12
Primary completion
2013-05
Completion
2013-05

Outcome

Met primary endpoint

paper 217 (84%) of 258 patients in the ceftaroline fosamil group and 178 (74%) of 240 patients in the ceftriaxone group were clinically cured PMID 25539586 ↗

paper difference 9·9%, 95% CI 2·8-17·1 PMID 25539586 ↗

paper The superiority of ceftaroline fosamil was consistent across all preplanned patient subgroup analyses PMID 25539586 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ceftaroline fosamil Other / unclassified 600 mg Intravenous
Comparator Ceftriaxone Other / unclassified 2 g Intravenous

Indications