The study will evaluate the safety, tolerability, and immunogenicity of VAX-31 in adults ≥50 years of age.
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Serotype-specific OPA geometric mean titers (GMT)
Timeframe: 1 month after VAX-31 vaccination
Serotype-specific OPA geometric mean fold rise (GMFR) from baseline
Timeframe: 1 month after VAX-31 vaccination
Percentage of subjects reporting solicited local adverse events (AE) (redness, swelling, and pain at injection site)
Timeframe: up to 7 days after vaccination
Percentage of subjects reporting solicited systemic AE (fever, headache, fatigue, muscle pain, and joint pain)
Timeframe: up to 7 days after vaccination
Percentage of subjects reporting unsolicited AE
Timeframe: up to 31 days after vaccination
Percentage of subjects reporting new onset of chronic illness (NOCI), medically attended AE (MAAE), and serious adverse events (SAE)
Timeframe: up to 6 months after vaccination