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Clinical Trial Summary

The primary objective of this study was to assess the steady-state zanubrutinib pharmacokinetics (PK) when co-administered with moderate and strong cytochrome P450 family 3 subfamily A (CYP3A) inhibitors.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04551963
Study type Interventional
Source BeiGene
Contact
Status Completed
Phase Phase 1
Start date November 15, 2020
Completion date February 21, 2022

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