The purpose of this study is to compare the effect of blisibimod plus standard of care versus placebo plus standard of care alone on the proportion of subjects achieving improvement in renal disease parameters.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Blisibimod administered subcutaneously
Placebo administered subcutaneously
The proportion of subjects to achieve the proteinuria threshold
Time frame: Week 24
The proportion of subjects who progress to end-stage renal disease
Time frame: approximately 5 years
Change from baseline in serum immunoglobulins IgA, IgG and IgM, plasma cells and B cell subsets
Time frame: Week 24
Number of Participants with Adverse Events
Time frame: Week 24
Change from baseline in serum creatinine
Time frame: Week 24
Change from baseline in eGFR
Time frame: Week 24
The proportion of subjects requiring the addition of corticosteroid or other therapy
Time frame: Week 24
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