This study aims to evaluate the safety and tolerability of clesrovimab compared to palivizumab as assessed by the proportion of participants experiencing adverse events (AEs).
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Number of Participants With Solicited Injection-site Adverse Events (AEs) in RSV Season 1
Timeframe: Up to 5 days after each dose in RSV Season 1 (Up to ~33 days)
Number of Participants With Solicited Daily Body Temperatures With Fever in RSV Season 1
Timeframe: Up to 5 days after each dose in RSV Season 1 (Up to ~33 days)
Number of Participants With Solicited Systemic AEs in RSV Season 1
Timeframe: Up to 5 days after each dose in RSV Season 1 (Up to ~33 days)
Number of Participants With Anaphylaxis/Hypersensitivity AEs of Special Interest (AESI) in RSV Season 1
Timeframe: Up to 42 days in RSV Season 1
Number of Participants With Rash AESI in RSV Season 1
Timeframe: Up to 42 days in RSV Season 1
Number of Participants With Nonserious AEs in RSV Season 1
Timeframe: Up to 42 days in RSV Season 1
Number of Participants With Serious AEs (SAEs) Through the Duration of Participation in RSV Season 1
Timeframe: Up to 365 days in RSV Season 1