Overview

Doripenem in the Treatment of Ventilator-Associated Pneumonia

Status:
Completed
Trial end date:
2006-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to compare the clinical response rate of doripenem versus comparator in patients with ventilator-associated pneumonia (VAP).
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Collaborator:
Peninsula Pharmaceuticals, Inc.
Treatments:
Doripenem
Criteria
Inclusion Criteria:

- Patient has received mechanical ventilation for > 24 hours

- Presence of a new or progressive infiltrate on chest x-ray

Exclusion Criteria:

- Believed at study entry to have ventilator-associated pneumonia caused solely by
pathogen(s) resistant to certain antibiotics

- History of moderate or severe hypersensitivity reactions to certain antibiotics