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Clinical Trial Summary

Evaluate the potential effect of hepatic or renal impairment on the pharmacokinetics, safety and tolerability of BAY 1841788 (ODM-201).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02894385
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 1
Start date September 13, 2016
Completion date December 15, 2017

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