40
Participants
Start Date
January 15, 2018
Primary Completion Date
December 31, 2019
Study Completion Date
December 31, 2019
Rituximab
The administration of rituximab at 375 mg/m\^2/day by intravenous infusion on Day 1 of each 21-day cycle with up to 6 cycles. Dose modifications are not permitted.
Research Site, Nagoya
Research Site, Toyoake
Research Site, Matsuyama
Research Site, Maebashi
Research Site, Ōta
Research Site, Shibukawa
Research Site, Fukuyama
Research Site, Sapporo
Research Site, Kobe
Research Site, Isehara
Research Site, Sendai
Research Site, Sayama
Research Site, Izumo
Research Site, Mibu
Research Site, Shimotsuke
Research Site, Chuo-ku
Research Site, Koto-ku
Research Site, Shibuya-ku
Research Site, Shinagawa-ku
Research Site, Akita
Research Site, Fukuoka
Research Site, Fukushima
Research Site, Ibaraki
Research Site, Kumamoto
Research Site, Kyoto
Research Site, Nagasaki
Research Site, Okayama
Research Site, Osaka
Research Site, Yamagata
Lead Sponsor
SymBio Pharmaceuticals
INDUSTRY