Human parainfluenza viruses (HPIVs) are a major health concern in infants and young children under 5 years of age, causing serious respiratory tract disease. The purpose of this study is to test the safety of and immune response to a new HPIV vaccine in healthy infants, children, and adults.
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Frequency of vaccine-related reactogenicity events (REs) that occur during the acute monitoring phase of the study (Days 0 to 10 for adult and seropositive groups, Days 0 to 28 for seronegative groups)
Timeframe: Throughout study
Quantifying the amount of vaccine virus shed by each recipient
Timeframe: Throughout study
Determining the amount of serum antibody and mucosal antibody induced by the vaccine in each recipient
Timeframe: Throughout study