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Clinical Trial Summary

The purpose of this study is to describe the single dose pharmacokinetics of total radioactivity in plasma and whole blood following PO administration of [14C] TR-701 in healthy adult male subjects.


Clinical Trial Description

This study will be an open-label, single-dose study of the absorption, metabolism, and excretion of 200 mg [14C]-TR-701 (approximately 100 μCi) administered orally following at least an 8-hour fast. Subjects will receive a single dose of 200 mg [14C] TR 701 (approximately 100 μCi) administered as an oral solution.

The dose will be administered following at least an 8-hour fast and followed by a 4-hour fast from food, not including water. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01442831
Study type Interventional
Source Trius Therapeutics LLC
Contact
Status Completed
Phase Phase 1
Start date September 9, 2010
Completion date September 22, 2010

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