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Clinical Trial Summary

This multicenter, double-blind, randomized, placebo-controlled study will evaluate the safety of a single infusion of tocilizumab versus placebo, administered in addition to standard premedications (antipyretic, antihistamine, and corticosteroid) prior to the first infusion of obinutuzumab administered in combination with oral chlorambucil to participants with previously untreated B-CLL who have comorbidities. All eligible participants will be treated with a total of 6 cycles of obinutuzumab + chlorambucil (cycle length = 28 days).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02336048
Study type Interventional
Source Hoffmann-La Roche
Contact
Status Terminated
Phase Phase 1
Start date June 26, 2015
Completion date September 21, 2018

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