16
Participants
Start Date
August 31, 2014
Primary Completion Date
November 30, 2016
Study Completion Date
December 31, 2016
Ibrutinib
Participants will receive ibrutinib capsules 560 milligram (mg) orally, once daily on a 28-day cycle up to 7 cycles or until disease progression (or relapse if the participant achieved a complete response \[CR\]), unacceptable toxicity, or end of treatment, whichever occurs first.
Fukuoka
Isehara
Kobe
Kyoto
Nagoya
Osaka
Sendai
Tokyo
Lead Sponsor
Janssen Pharmaceutical K.K.
INDUSTRY