BENITIONSClinical Trial Intelligence

Study to Evaluate the Safety, Reactogenicity, and Effectiveness of mRNA-1273.214 SARS-CoV-2 (COVID-19) Vaccine in Infants

2상 조기 종료 NCT05584202

대상 질환SARS-CoV-2
임상 단계2상
스폰서ModernaTX, Inc.
상태조기 종료
참여자 수68 명
중재(약물)mRNA-1273.214
시작일2022년 9월 30일
완료일2024년 11월 15일
결과 공개일2025년 11월 26일

요약

The study evaluated the safety, tolerability, reactogenicity, and effectiveness of mRNA-1273.214 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in infants aged 12 weeks to \< 6 months.

Number of Participants With Solicited Local and Systemic Adverse Reactions (ARs) After First Injection

Day 1 up to 7 days after first vaccination (up to Day 8) · Participants

mRNA-1273.214 5 μg First Injection (Solicited Safety Set)23 Participants
mRNA-1273.214 10 μg First Injection (Solicited Safety Set)7 Participants
mRNA-1273.214 5 μg First Injection (Solicited Safety Set)8 Participants
mRNA-1273.214 10 μg First Injection (Solicited Safety Set)3 Participants
mRNA-1273.214 5 μg First Injection (Solicited Safety Set)1 Participants
mRNA-1273.214 10 μg First Injection (Solicited Safety Set)0 Participants

Number of Participants With Solicited Local and Systemic ARs After Second Injection

Day 57 up to 7 days after second vaccination (up to Day 64) · Participants

mRNA-1273.214 5 μg Second Injection (Solicited Safety Set)18 Participants
mRNA-1273.214 10 μg Second Injection (Solicited Safety Set)6 Participants
mRNA-1273.214 5 μg Second Injection (Solicited Safety Set)7 Participants
mRNA-1273.214 10 μg Second Injection (Solicited Safety Set)2 Participants
mRNA-1273.214 5 μg Second Injection (Solicited Safety Set)1 Participants
mRNA-1273.214 10 μg Second Injection (Solicited Safety Set)0 Participants

Number of Participants With Unsolicited Adverse Events (AEs) After Any Injection

Day 1 up to 28 days after any vaccination (up to Day 85) · Participants

mRNA-1273.214 5 μg (Safety Set)24 Participants
mRNA-1273.214 10 μg (Safety Set)8 Participants

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전체 임상

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