Status:

COMPLETED

Comparative Study of Ceftaroline vs. Ceftriaxone in Adult Subjects With Community-Acquired Pneumonia

Lead Sponsor:

Forest Laboratories

Conditions:

Bacterial Pneumonia

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to determine whether ceftaroline is effective and safe in the treatment of Community-Acquired Pneumonia

Detailed Description

The purpose of this study is to determine whether ceftaroline is effective and safe in the treatment of Community-Acquired Pneumonia. Clinical trials for this study is held in many countries

Eligibility Criteria

Inclusion

  • Subjects are required to meet the following inclusion criteria:
  • Community-acquired pneumonia
  • initial hospitalization, or treatment in an emergency room or urgent care setting
  • infection would require initial treatment with IV antimicrobials.

Exclusion

  • Subjects must NOT meet any of the following exclusion criteria:
  • CAP suitable for outpatient therapy with an oral antimicrobial agent
  • respiratory tract infections not due to community-acquired bacterial
  • Non-infectious causes of pulmonary infiltrates
  • Pleural empyema
  • Infection with an atypical organism
  • History of any hypersensitivity or allergic reaction to any ß-lactam antimicrobial
  • History of any hypersensitivity or allergic reaction to clarithromycin or any macrolide/ ketolide

Key Trial Info

Start Date :

January 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2009

Estimated Enrollment :

606 Patients enrolled

Trial Details

Trial ID

NCT00621504

Start Date

January 1 2008

End Date

June 1 2009

Last Update

March 14 2017

Active Locations (168)

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Page 1 of 42 (168 locations)

1

Investigational site

Los Angeles, California, United States, 90015

2

Investigational Site

Pasadena, California, United States, 91105

3

Investigational Site

Sacramento, California, United States, 95817

4

Investigational Site

San Diego, California, United States, 92114