The overall objective of the MEDI-534 clinical development program is to evaluate the safety, efficacy and tolerability of MEDI-534 for the prevention of serious RSV and PIV3 disease in young infants.
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Number of Participants With Solicited Adverse Events (SEs) After Dose 1
Timeframe: Days 0-28 after Dose 1 (Dose 1 was on Day 0)
Number of Participants With SEs After Dose 2
Timeframe: Days 0-28 after Dose 2 (Dose 2 was on Day 48-64)
Number of Participants With SEs After Dose 3
Timeframe: Days 0-28 after Dose 3 (Dose 3 was 48-64 days after Dose 2)
Number of Participants With Adverse Events (AEs) After Dose 1
Timeframe: Days 0-28 after Dose 1 (Dose 1 was on Day 0)
Number of Participants With AEs After Dose 2
Timeframe: Days 0-28 after Dose 2 (Dose 2 was on Day 48-64)
Number of Participants With AEs After Dose 3
Timeframe: Days 0-28 after Dose 3 (Dose 3 was 48-64 days after Dose 2)
Number of Subjects With Medically-attended Lower Respiratory Illnesses (MA-LRIs)
Timeframe: Days 0 to 180 days after final dose or the end of the RSV season, whichever was later
Number of Participants With Serious Adverse Events (SAEs)
Timeframe: Days 0-28 after any dose
Number of Participants With Significant New Medical Conditions (SNMCs)
Timeframe: Day 0 through 180 days after the final dose or through the end of the RSV season, whichever was later