BENITIONSClinical Trial Intelligence

A Study to Evaluate the Safety and Immunogenicity of mRNA-1975 and mRNA-1982 Against Lyme Disease in Participants 18 Through 70 Years of Age

1/2상 완료 NCT05975099

대상 질환Lyme Disease
임상 단계1/2상
스폰서ModernaTX, Inc.
상태완료
참여자 수807 명
중재(약물)mRNA-1975, mRNA-1982
시작일2023년 7월 26일
완료일2025년 5월 30일
결과 공개일2026년 7월 30일

요약

The purpose of this study is to evaluate the safety and immunogenicity in parallel of heptavalent mRNA-1975 and monovalent mRNA-1982 against Lyme disease in healthy adult participants.

Number of Participants With Solicited Local and Systemic Adverse Reactions (ARs) Within 7 Days After Day 1 Injection

Up to 7 days after Day 1 injection · Participants

mRNA-1975 Dose Level 170 Participants
mRNA-1975 Dose Level 280 Participants
mRNA-1975 Dose Level 382 Participants
mRNA-1975 Dose Level 491 Participants
mRNA-1982 Dose Level 164 Participants
mRNA-1982 Dose Level 277 Participants

Number of Participants With Solicited Local and Systemic ARs Within 7 Days After Day 57 Injection

Up to 7 days after Day 57 injection · Participants

mRNA-1975 Dose Level 179 Participants
mRNA-1975 Dose Level 280 Participants
mRNA-1975 Dose Level 390 Participants
mRNA-1975 Dose Level 496 Participants
mRNA-1982 Dose Level 170 Participants
mRNA-1982 Dose Level 282 Participants

Number of Participants With Solicited Local and Systemic ARs Within 7 Days After Day 169 Injection

Up to 7 days after Day 169 injection · Participants

mRNA-1975 Dose Level 181 Participants
mRNA-1975 Dose Level 287 Participants
mRNA-1975 Dose Level 381 Participants
mRNA-1975 Dose Level 492 Participants
mRNA-1982 Dose Level 176 Participants
mRNA-1982 Dose Level 282 Participants

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