The purpose of the study is to assess the efficacy on joint damage and safety in RA patients treated with DMARDs in a double blind, placebo controlled study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
123
oral
oral
Unnamed facility
Chyugoku Region, Japan
Unnamed facility
Hokkaido Region, Japan
Unnamed facility
Hokuriku Region, Japan
Unnamed facility
Kansai Region, Japan
Unnamed facility
Radiographic progression of structural joint damage
Time frame: 52 Weeks
Signs and symptoms of rheumatoid arthritis
Time frame: 52 Weeks
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Kanto Region, Japan
Unnamed facility
Kyushu Region, Japan
Unnamed facility
Shin-etsu Region, Japan
Unnamed facility
Tohoku Region, Japan