This is a phase 1 study in which healthy volunteers will receive VIR-2482 or placebo and will be assessed for safety, pharmacokinetics, and immunogenicity of VIR-2482 in preventing Influenza A illness.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
100
Investigative Site
Brisbane, Queensland, Australia
Number of participants with treatment-emergent adverse events.
Time frame: Up to 12 months post-dose
Number of participants with abnormalities in vital signs.
Time frame: Up to 12 months post-dose
Number of participants with abnormalities in electrocardiogram (ECG).
Time frame: Up to 12 months post-dose
Number of participants with abnormalities in clinically significant laboratory findings.
Time frame: Up to 12 months post-dose
Concentrations of VIR-2482 in serum
Time frame: Up to 12 months post-dose
Incidence of anti-drug antibody (ADA) to VIR-2482
Time frame: Up to 12 months post-dose
Titers (if applicable) of anti-drug antibody (ADA) to VIR-2482
Time frame: Up to 12 months post-dose
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