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The purpose of this study is to determine the clinical efficacy, safety, and tolerability of a 250 mg BID oral dose of JNJ-32729463 compared with linezolid in subjects with complicated skin and skin structure infections (cSSSIs).
Allocation: Randomized, Control: Active Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Complicated Skin and Skin Structure Infections
JNJ-32729463, linezolid, JNJ-32729463 placebo, linezolid placebo
Furiex Research Site
Furiex Pharmaceuticals, Inc
Published on BioPortfolio: 2014-08-27T03:13:28-0400
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The study is now completed
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Misunderstanding among individuals, frequently research subjects, of scientific methods such as randomization and placebo controls.
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