The purpose of this research study is to measure the levels of ceftobiprole in the blood and urine during and after administration of four doses of ceftobiprole. Safety of the drug will also be evaluated.
Patients will receive an intravenous dose of ceftobiprole infused over 4 hours. Multiple blood samples will be obtained to determine the concentration of ceftobiprole in the plasma. Pharmacokinetic parameters such as clearance and volume of distribution will be calculated. 1000mg every 8hours or every 12 hours
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
33
Ceftobiprole, 1G q12h as 4 hour infusions, on Day 1 and Ceftobiprole, 1G as single 4 hour infusion on Day 2
Ceftobiprole, 1G q8h as 4 hour infusions, on Day 1 and Ceftobiprole, 1G as single 4 hour infusion on Day 2
Unnamed facility
Birmingham, Alabama, United States
Unnamed facility
Chicago, Illinois, United States
Unnamed facility
Beech Grove, Indiana, United States
Unnamed facility
Omaha, Nebraska, United States
Pharmacokinetics (to measure the levels of ceftobiprole in the blood and urine) during dosing and 24 hours after last dose
Time frame: 3 days
Safety will be evaluated throughout the study.
Time frame: 7 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Aalst, Belgium
Unnamed facility
Edegem, Belgium
Unnamed facility
Greenfield Park, Quebec, Canada
Unnamed facility
Jerusalem, Israel
Unnamed facility
Gwangju, South Korea
Unnamed facility
Incheon, South Korea
...and 3 more locations