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Clinical Trial Summary

The objective of this study is to determine the mass balance and routes of excretion of total radioactivity after a single oral 200 mg dose of [14C]rogaratinib given as a solution. For further clinical development, human mass balance data are required to elucidate the absorption, distribution, metabolism, and excretion (ADME) of rogaratinib.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03484585
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 1
Start date April 6, 2018
Completion date August 9, 2018

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