An open-label, PhaseⅢ study to evaluate the efficacy and safety of MRA in patients with RA
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
8mg/kg/4 weeks
Chugoku region
Chugoku, Japan
Chukyo region
Chukyo, Japan
Hokkaido region
Hokkaido, Japan
Hokuriku region
Hokuriku, Japan
Frequency of ACR 20% improvement at the final visit
Time frame: throughout study
Time course of the frequency of ACR 20%, 50% and 70% improvement,time course of individual items within the ACR core set.
Time frame: throughout study
Time course of DAS28 to the final visit.
Time frame: throughout study
Time course of steroid sparing effect from first visit to final visit.
Time frame: throughout study
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Kansai region
Kansai, Japan
Kanto region
Kanto, Japan
Kousinetsu region
Kousinetsu, Japan
Kyushu region
Kyushu, Japan
Sikoku region
Sikoku, Japan
Tohoku region
Tōhoku, Japan