scholarly journals Efficacy and safety of sirukumab in Japanese patients with moderate to severe rheumatoid arthritis inadequately controlled by disease modifying anti-rheumatic drugs: Subgroup analysis of a phase 3 study

2018 ◽  
Vol 28 (6) ◽  
pp. 941-949
Author(s):  
Tsutomu Takeuchi ◽  
Yoshiya Tanaka ◽  
Hisashi Yamanaka ◽  
Masayoshi Harigai ◽  
Toshikazu Nakano ◽  
...  
2017 ◽  
Vol 28 (4) ◽  
pp. 583-591 ◽  
Author(s):  
Yoshiya Tanaka ◽  
Tatsuya Atsumi ◽  
Koichi Amano ◽  
Masayoshi Harigai ◽  
Taeko Ishii ◽  
...  

2017 ◽  
Vol 44 (11) ◽  
pp. 1285-1290 ◽  
Author(s):  
Shinichi Imafuku ◽  
Hitoe Torisu-Itakura ◽  
Atsushi Nishikawa ◽  
Fangyi Zhao ◽  
Gregory S. Cameron ◽  
...  

2021 ◽  
Author(s):  
Tatsuya Atsumi ◽  
Yoshiya Tanaka ◽  
Tsukasa Matsubara ◽  
Koichi Amano ◽  
Naoki Ishiguro ◽  
...  

ABSTRACT Objectives To evaluate the efficacy and safety of filgotinib for Japanese patients with rheumatoid arthritis (RA) and limited or no prior methotrexate (MTX) exposure. Methods Data up to 24 weeks were analysed for 71 Japanese patients from a 52-week global Phase 3 study. Patients with RA and limited or no prior MTX exposure were randomised in a 2:1:1:2 ratio to filgotinib 200 mg plus MTX, filgotinib 100 mg plus MTX, filgotinib 200 mg, or MTX. Maximum MTX dose was 15 mg/week. Primary endpoint was proportion achieving 20% improvement in American College of Rheumatology criteria (ACR20) at Week 24. Results Week 24 ACR20 rates in Japanese patients were 82.6%, 90.9%, 83.3%, and 80.0% for filgotinib 200 mg plus MTX, filgotinib 100 mg plus MTX, filgotinib 200 mg, and MTX, respectively. Greater ACR20 rates with filgotinib vs MTX occurred at Week 2. Greater proportions receiving filgotinib vs MTX achieved DAS28-CRP <2.6 at Weeks 12 and 24. Adverse event rates were comparable across treatments and between the Japanese and overall populations. Conclusions While Week 24 ACR20 rates were similar, filgotinib provided faster responses and higher remission rates vs MTX. In Japanese patients with RA and limited or no prior MTX exposure, filgotinib was generally well tolerated.


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