The purpose of this study is to investigate the antitumor effect and safety of the product for relapsed or refractory indolent B-cell non-Hodgkin's lymphomas.
The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been renamed to Bayer Schering Pharma AG, Germany.Bayer Schering Pharma AG, Germany is the sponsor of the trial.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
45
0,3mCi/kg
0,4mCi/kg
Unnamed facility
Nagoya, Aichi-ken, Japan
Unnamed facility
Kashiwa-shi, Chiba, Japan
Unnamed facility
Maebashi, Gunma, Japan
Unnamed facility
Kanazawa, Ishikawa-ken, Japan
Best overall response rates (the percentage of patients who achieved PR or better response)
Time frame: After 9 weeks or 13 weeks
The incidence of critical toxicity
Time frame: During treatment period
Safety evaluation
Time frame: During treatment period
Complete response (CR or CRu) rates
Time frame: After 9 weeks or 13 weeks
Progression-free survival (PFS)
Time frame: After end of study
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Isehara-shi, Kanagawa, Japan
Unnamed facility
Kyoto, Kyoto, Japan
Unnamed facility
Sendai, Miyagi, Japan
Unnamed facility
Chuo-ku, Tokyo, Japan
Unnamed facility
Shinjuku-ku, Tokyo, Japan