The purpose of this study is to assess the safety, tolerability, immunogenicity and pharmacokinetics of single escalating doses of VIS410 in healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
41
DaVita Clinical Research
Minneapolis, Minnesota, United States
Safety assessment
Incidence of adverse events
Time frame: 120 days post-infusion
Pharmacokinetic analysis
Serum concentration-time profile
Time frame: 56 days post-infusion
Immunogenicity
Detect and measure anti-drug antibodies to VIS410
Time frame: 120 days post-infusion
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