The aim of this study is to examine the efficacy and adverse events in the following 3 groups in rheumatoid arthritis patients: 1. Sarilumab treatment for 12 months 2. Tocilizmab treatment for 12 months 3. Abatacept treatment for 12 months
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
90
To examine the effects of salirumab in RA patients
To examine the effects of tocilizmab in RA patients
To examine the effects of abatacept in RA patients
Yukio Nakamura
Matsumoto, Nagano, Japan
RECRUITINGChange from Baseline Values of DAS28-CRP
Assessment of efficacy in rheumatoid arthritis patients for 1 year treated by salirumab (N=30), tocilizumab (N=30), or abatacept (N=30).
Time frame: Baseline and 1 year
Assessment of adverse event in rheumatoid arthritis patients for 1 year treated by salirumab (N=30), tocilizumab (N=30), or abatacept (N=30).
Time frame: at 1 year
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