38
Participants
Start Date
September 22, 2014
Primary Completion Date
March 12, 2021
Study Completion Date
March 12, 2021
azacitadine
75 mg/m2 by IV infusion or subcutaneous dosing
venetoclax
Step-up doses of venetoclax to the designated cohort dose
rituximab / IDEC-C2B8
375 mg/m2 on Week 6
rituximab / IDEC-C2B8
500 mg/m2 Week 10 Day 1 and thereafter
Nagoya City University Hospital /ID# 129278, Nagoya
Tohoku University Hospital /ID# 129275, Sendai
NHO Nagoya Medical Center /ID# 129222, Nagoya
Aichi Cancer Center Hospital /ID# 129061, Nagoya
University of Fukui Hospital /ID# 165801, Yoshida-gun
National Hospital Organization Kyushu Cancer Center /ID# 149741, Fukuoka
Kyushu University Hospital /ID# 163202, Fukuoka
Kobe City Medical Center General Hospital /ID# 170919, Kobe
Kindai University Hospital /ID# 169554, Osakasayama-shi
Osaka University Hospital /ID# 169862, Suita-shi
National Cancer Center Hospital /ID# 129044, Chuo-ku
The Cancer Institute Hospital Of JFCR /ID# 129277, Koto-ku
Toranomon Hospital /ID# 148229, Minato-ku
NTT Medical Center Tokyo /ID# 166281, Shinagawa-ku
Lead Sponsor
Collaborators (1)
Genentech, Inc.
INDUSTRY
AbbVie
INDUSTRY