The main objective of this study is to evaluate the safety, reactogenicity, and immunogenicity of the mRNA-1647 vaccine administered according to a 3-study injection schedule in healthy cytomegalovirus (CMV)-seronegative and CMV-seropositive Japanese adults 18 to 40 years of age in the United States.
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Number of Participants With Solicited Local and Systemic Adverse Reactions (ARs)
Timeframe: Up to Day 176 (7 days after each injection)
Number of Participants With Unsolicited Adverse Events (AEs)
Timeframe: Up to Day 197 (28 days after each injection)
Number of Participants With Medically-Attended AEs (MAAEs)
Timeframe: Day 1 through 6 months after the last injection (up to Day 347)
Number of Participants With Serious AEs (SAEs)
Timeframe: Day 1 through End of Study (EOS) (up to Day 347)
Number of Participants With AEs of Special Interest (AESIs)
Timeframe: Day 1 through EOS (up to Day 347)