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Clinical Trial Summary

The purpose of this study is to compare the efficacy and safety of fixed duration pirtobruitinib (LOXO-305) with VR (Arm A) compared to VR alone (Arm B) in patients with CLL/SLL who have been previously treated with at least one prior line of therapy. Participation could last up to five years.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04965493
Study type Interventional
Source Eli Lilly and Company
Contact Patient Advocacy
Phone 1-855-LOXO-305
Email clinicaltrials@loxooncology.com
Status Recruiting
Phase Phase 3
Start date September 20, 2021
Completion date January 2027

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