The purpose of this trial is to determine 1. Disease stabilization/response rate after six 21-day cycles of ibrutinib 2. Remission status after six, twelve and 20 21-day cycles of ibrutinib
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
14
1st Department of Medicine, Cologne University Hospital
Cologne, Germany
Response Rate
Time frame: after 6 cycles (each cycle is 21 days) of Ibrutinib
Remission status
Time frame: Remission status after six, twelve and 20 21-day cycles of ibrutinib
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