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Clinical Trial Summary

This is an open-label, 2-cohort study to evaluate the absolute bioavailability, absorption, distribution, metabolism and excretion of TD-1473 in healthy male subjects. Subjects in cohort 1 will receive a single oral dose of TD-1473 and a single intravenous bolus dose of [14C]-TD-1473. Subjects in cohort 2 will receive a single oral dose of [14C]-TD-1473 only.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03408470
Study type Interventional
Source Theravance Biopharma
Contact
Status Completed
Phase Phase 1
Start date January 31, 2018
Completion date February 21, 2018

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