19
Participants
Start Date
May 1, 2018
Primary Completion Date
November 29, 2021
Study Completion Date
November 29, 2021
Ibrutinib
Participants will receive 420 mg (3 \* 140 mg capsules) oral ibrutinib once daily starting on Week 1 Day 1, unless they have intervening unacceptable toxicity or meet other criteria for participants discontinuation.
Anjo Kosei Hospital, Anjo-shi
Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Bunkyō City
Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima
Tokai University Hospital, Isehara
Osaka Women's and Children's Hospital, Izumi
Kobe City Medical Center General Hospital, Kobe
National Hospital Organization Kumamoto Medical Center, Kumamoto
Kurashiki Central Hospital, Kurashiki
Gunmaken Saiseikai Maebashi Hospital, Maebashi
Japanese Red Cross Nagoya Daiichi Hospital, Nagoya
The Hospital of Hyogo College of Medicine, Nishinomiya
Okayama University Hospital, Okayama
Osaka City University Hospital, Osaka
Hokkaido University Hospital, Sapporo
National Center for Child Health and Development, Setagaya Ku
Lead Sponsor
Janssen Pharmaceutical K.K.
INDUSTRY