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Clinical Trial Summary

The primary focus of the study is the evaluation of the safety of treatment with moxifloxacin in a pediatric population 3 months to <18 years old. Approximately 450 pediatric subjects with a complicated intra-abdominal infection will be enrolled in the study and treated with either moxifloxacin intravenously and orally if switched to oral therapy or ertapenem (intravenously) and, if switched to oral therapy, amoxicillin/clavulanate.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01069900
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date July 21, 2010
Completion date January 21, 2015

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