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Clinical Trial Summary

The purpose of the study is to describe the clinical efficacy of CUBICIN therapy in patients with superficial and deep post-surgical Gram-positive wound infections


Clinical Trial Description

A multi-center, single-arm, open-label, non-comparative study to describe the clinical efficacy of CUBICIN therapy in patients with superficial and deep post-surgical Gram-positive wound infections. Adjunctive treatment with aztreonam and/or metronidazole could be given for Gram-negative and/or anaerobic organisms. Patients are to be treated for a period of 7-14 days as specified in the package insert. An evaluation is to be performed on the day CUBICIN treatment is completed (assessment for outcome of cure, improved, failure or unable to evaluate). A follow-up is required for patients with an Investigator response of 'Improved' at the end of treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00651131
Study type Interventional
Source Cubist Pharmaceuticals LLC
Contact
Status Terminated
Phase Phase 4
Start date June 1, 2004
Completion date March 1, 2005

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