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COMPLETEDPhase 3NCT01045902

BAY12-8039, iv/Oral Pulmonary Abscess/Aspiration Pneumonia

The purpose of this trial is to determine the efficacy and safety of Moxifloxacin in comparison to Sulbactam/Ampicillin in the treatment of pulmonary abscesses and aspiration pneumonia.

Lead sponsor: Bayer•15 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Bayer

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Male or female patients aged 18 years or above
•The primary diagnosis is community or hospital acquired primary pulmonary abscess or aspiration pneumonia, requiring initial parenteral treatment

Exclusion Criteria

•Known hypersensitivity to fluoroquinolones and/or ß-lactams
•Patients with mechanical ventilation lasting more than 48 hours prior to enrollment, with poststenotic pneumonia, infarction pneumonia, pulmonary tuberculosis, lung abscess/pneumonia with concomitant endocarditis

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: January 11, 2010Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE3

Enrollment139

Start dateFeb 2001

Last updatedJan 11, 2010

Condition

Pneumonia, Aspiration Lung Abscess

Locations shown

Mannheim, Baden-Wurttemberg

Nuremberg, Bavaria

Regensburg, Bavaria

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 11, 2010Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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