The purpose of this study is to compare the clinical cure rate of ceftobiprole medocaril versus a comparator in the treatment of patients with nosocomial pneumonia.
Official Title
A Phase III Randomized Double-Blind Study of Ceftobiprole Versus Comparator in the Treatment of Nosocomial Pneumonia
Conditions
- Pneumonia
Study Type
Interventional
Study Design
Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Further Details
- Primary Outcomes: Clinical cure rate (the ratio of the number of clinically cured subjects to the total number of patients in the population) at 7 to 14 days after the end of therapy.
- Secondary Outcomes: Microbiological eradication rate at 7-14 days after the end of therapy; Clinical cure rate and microbiological relapse at late follow-up visit; All deaths due to pneumonia within 30 days after randomization
Study Start
March 2005
Eligibility & Criteria
- Ages Eligible for Study: 18 Years and above
- Genders Eligible for Study: Both
Inclusion Criteria:
- Patients suffering from nosocomial pneumonia or ventilator-associated pneumonia
- Female patients must be postmenopausal for at least 1 year, surgically sterile, or practicing an effective method of birth control, before entry and throughout the study, and have a negative serum or urine pregnancy test at the screening
Exclusion Criteria:
- Known or suspected hypersensitivity to any related antibiotic medications
- Any known or suspected condition or concurrent treatment that would be contraindicated by the prescribing information
- Treatment with any investigational drug within 30 days before enrollment
- Prior enrollment to this study
Total Enrolment
770 (expected)
Contact Details
- Nambour Qld, 4560, Australia; Not yet recruiting
- Bedford Park/Adelaide, 5042, Australia; Recruiting
- Fremantle Wa, 6160, Australia; Recruiting
- Parkville, 3052, Australia; Not yet recruiting
- Southport, 4215, Australia; Recruiting
- Bedford Park, 5042, Australia; Recruiting
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