Pharmacokinetics of Ceftaroline in Subjects 12 to 17 Years of Age
Completed · Phase 1
Conditions studied: Infection
In brief
The purpose of this study is to determine the pharmacokinetics of ceftaroline in pediatric subjects
Key facts
- Study ID
- NCT00633126
- Run by
- Forest Laboratories
- People needed
- 9
- Starts
- 2008-03-01
- Expected to finish
- 2009-02-01
- Last updated by the study team
- 2017-03-14
Who can join
Age: 12 and older, up to 17. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Hospitalized and receiving antibiotic therapy for treatment of a suspected infection of any type
- Body mass index (weight [kg]/height squared [m2]) of no more than 30
- Males and females between 12 and 17 years of age, inclusive
You may not qualify if…
- History of any hypersensitivity or allergic reaction to any β-lactam antimicrobial
- Past or current history of epilepsy or seizure disorder
- Critically ill or unstable patients
Where it is running
- Investigational Site — Louisville, Kentucky, United States
- Investigational Site — Durham, North Carolina, United States
- Investigational site — Akron, Ohio, United States
- Invetigational Site — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
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