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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00035269
Other study ID # M12600071
Secondary ID A5951056
Status Completed
Phase Phase 3
First received May 2, 2002
Last updated April 25, 2011
Start date December 2001
Est. completion date May 2003

Study information

Verified date April 2011
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This study will treat patients who have a community-acquired pneumonia that is due to a specific bacteria (S. pneumoniae)


Recruitment information / eligibility

Status Completed
Enrollment 230
Est. completion date May 2003
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 13 Years and older
Eligibility Other specific inclusion/exclusion criteria may apply. In order to determine eligibility, further examination by the investigator is necessary.

Inclusion Criteria:

- Patients must have the signs and symptoms of pneumonia, with a chest xray showing a pneumonia.

- The patient must have S. pneumoniae (a specific bacteria) growing in sputum or blood to continue treatment.

Exclusion Criteria:

- Patients cannot have taken more than one day of another antibiotic before entering this study.

- Patients with HIV and a low CD4 count are excluded.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Antibiotic


Locations

Country Name City State
Slovakia Research Center Bratislava
Spain Research Center Barcelona
Spain Research Center Barcelona
Spain Research Center Barcelona
Spain Research Center Girona
Spain Research Center Madrid
Spain Research Center Madrid
Spain Research Center Madrid
Spain Research Center Mataro Barcelona
Spain Research Center Mostoles Madrid
Taiwan Research Center Kaohsiung
Taiwan Research Center Taoyuan
United States Research Center Ann Arbor Michigan
United States Research Center Baltimore Maryland
United States Research Center Baton Rouge Louisiana
United States Research Center Charlottesville Virginia
United States Research Center Columbus Ohio
United States Research Center Dallas Texas
United States Research Center Fleetwood Pennsylvania
United States Research Center Hackensack New Jersey
United States Research Center Harrogate Tennessee
United States Research Center Hershey Pennsylvania
United States Research Center Houston Texas
United States Research Center Jackson Tennessee
United States Research Center Jacksonville Florida
United States Research Center Knoxville Tennessee
United States Research Center Los Angeles California
United States Research Center Lubbock Texas
United States Research Center Memphis Tennessee
United States Research Center Memphis Tennessee
United States Research Center Memphis Tennessee
United States Research Center Naples Florida
United States Research Center Nashville Tennessee
United States Research Center Newark New Jersey
United States Research Center Ninety Six South Carolina
United States Research Center Richmond Virginia
United States Research Center Royal Oak Michigan
United States Research Center Savannah Georgia
United States Research Center Seattle Washington
United States Research Center Somerville New Jersey
United States Research Center Spartanburg South Carolina
United States Research Center Springfield Illinois
United States Research Center Springfield Missouri
United States Research Center Staten Island New York
United States Research Center Stony Brook New York
United States Research Center Zanesville Ohio

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Countries where clinical trial is conducted

United States,  Slovakia,  Spain,  Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary To assess the microbiologic efficacy of linezolid in the treatment of patients with pneumonia caused by penicillin-resistant Streptococcus pneumoniae (PRSP).
Primary Additionally, microbiologic efficacy will be assessed in all pneumonia patients infected with S pneumoniae SP) and in those infected with penicillin-sensitive (PSSP) and penicillin-intermediate (PISP) S pneumoniae.
Secondary To assess clinical efficacy and safety in pneumonia patients infected with S pneumoniae.
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