This study consists of a 28-week placebo-controlled double-blind inter-group efficacy study in steroid refractory Lupus Nephritis patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
64
Unnamed facility
Chubu Region, Japan
Unnamed facility
Hokkaido Region, Japan
Unnamed facility
Hokuriku Region, Japan
Unnamed facility
Kansai Region, Japan
Unnamed facility
Kanto Region, Japan
Change of Lupus Nephritis - Disease Activity Index total score
proteinuria, RBC-urine, serum creatinine, anti ds-DNA antibody, complement (C3)
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Unnamed facility
Shikoku Region, Japan
Unnamed facility
Tohoku Region, Japan