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

Study identifier:D3720C00002

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase III, Multicentre, Randomised, Double-Blind, Comparative 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

Medical condition

Community-Acquired Bacterial Pneumonia, Lung Infection of Individual not Recently Hospitalized

Phase

Phase 3

Healthy volunteers

No

Study drug

Ceftaroline, Ceftriaxone

Sex

All

Actual Enrollment

848

Study type

Interventional

Age

18 Years - 150 Years

Date

Study Start Date: 01 Dec 2011
Primary Completion Date: 01 May 2013
Study Completion Date: 01 May 2013

Study design

Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Nov 2014 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

Forest Laboratories Inc

Inclusion and exclusion criteria