This single-center, randomized, placebo-controlled, double-blind, multiple ascending dose study will evaluate the safety, pharmacokinetics and immunogenicity of MCAF5352A in healthy volunteers. Subjects will be randomized to receive either MCAF5352A or placebo on Days 1, 15 and 29.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
23
Unnamed facility
Québec, Quebec, Canada
Safety: Incidence of adverse events
Time frame: approximately 5 months
Pharmacokinetics: Area under the concentration-time curve
Time frame: Pre-dose and 5 time points up to 14 days post-dose
Immunogenicity: Serum MCAF5252A antibodies
Time frame: Days 1, 29, 50, 78, 106 and 134
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