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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of ibrutinib + venetoclax (I+V) and ibrutinib monotherapy regimens in which dosing of ibrutinib is either proactively reduced or reactively modified in response to adverse events (AEs).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05963074
Study type Interventional
Source Janssen Research & Development, LLC
Contact Study Contact
Phone 844-434-4210
Email Participate-In-This-Study@its.jnj.com
Status Recruiting
Phase Phase 2
Start date January 31, 2024
Completion date March 19, 2029

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