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Clinical Trial Summary

This study consists of 2 parts: Phase 1b and Phase 2. Phase 1b will evaluate the safety and tolerability of the combination of idelallisib with the anti-CD37 monoclonal antibody BI 836826 in participants with relapsed/refractory chronic lymphocytic leukemia (R/R CLL), and establish the high recommended Phase 2 combination dose (highRP2D) as well as an alternate lower recommended Phase 2 combination dose (lowRP2D). Phase 2 will determine the rates of complete response (CR) and of minimal residual disease (MRD) negativity with the combination at the highRP2D and the lowRP2D in participants with R/R CLL.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02538614
Study type Interventional
Source Gilead Sciences
Contact
Status Terminated
Phase Phase 1
Start date December 29, 2015
Completion date July 5, 2017

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