The purpose of the study is to assess the safety and tolerability of daily intravenous NI-0401 treatment, compared to matching placebo. And to assess the ability of NI-0401 to modulate the CD3 complex on T-cells.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
40
0.05 mg up to 10 mg
Placebo
Safety and tolerability of intravenous NI-0401 .
Time frame: 24 weeks
Immunological response defined as the percent change in the modulation of the CD3 complex on T-cells
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