This is a single-centre, open-label, first-in-human, single ascending dose and multiple dose study to assess the safety, reactogenicity, and immunogenicity of the SC-Ad6-1 investigational product when administered via the intramuscular (IM), intranasal (IN) or inhaled (IH) route in healthy volunteers.
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Number of participants with solicited local and systemic adverse events for 7 days Following Each Dose
Timeframe: 7 days following each dose
Incidence and severity of adverse events (AEs), including withdrawals due to safety or tolerability reasons
Timeframe: Up to 106 days following first dose
Humoral response to SARS-CoV-2 as measured by neutralizing antibodies using wild-type virus assay
Timeframe: Up to 106 days following first dose