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Clinical Trial Summary

This study is to investigate the pharmacokinetic (PK) and safety of M2951 (Bruton's tyrosine kinase [BTK] inhibitor) in participants with different degrees of hepatic impairment compared to participants with normal hepatic function.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04546789
Study type Interventional
Source Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
Contact
Status Completed
Phase Phase 1
Start date September 30, 2020
Completion date May 16, 2021

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