The purpose of this study is to learn about the safety, tolerability and immune effects of a pneumococcal vaccine in toddlers. Participants will take part in this study for approximately 6 or 8 months depending on which group they are assigned to. During this time participants will have 2 clinic visits and 1 phone visit for the 1-Dose group, or 3 clinic visits and 1 phone visit for the 2-Dose group. At these clinic visits, participants will be asked if any side effects were experienced. The participants will also have to give blood samples during some clinic visits.
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Percentage of participants reporting prespecified local reactions within 7 days after each dose
Timeframe: 7 days after each dose
Percentage of participants reporting prespecified systemic events within 7 days after each dose
Timeframe: 7 days after each dose
Percentage of participants reporting Adverse Events (AEs) within 1 month after the last assigned vaccination
Timeframe: From signing of ICD to 1 month after last assigned vaccination
Percentage of participants reporting Serious Adverse Events (SAEs) within 6 months after vaccination
Timeframe: From signing of ICD to 6 months after last assigned vaccination