BENITIONSClinical Trial Intelligence

A Study to Evaluate the Immunogenicity and Safety of mRNA-1283 COVID-19 Vaccine Boosters

Фаза 2 Завершено NCT05137236

ЗаболеваниеSARS-CoV-2
ФазаФаза 2
СпонсорModernaTX, Inc.
СтатусЗавершено
Участники540 участн.
ВмешательствоmRNA-1283, mRNA-1283.211, mRNA-1273, mRNA-1283.529
Дата начала6.12.2021
Дата завершения23.03.2023
Публикация результатов17.07.2025

Кратко

The main goal of Part A of this study is to assess the safety, reactogenicity, and immunogenicity of the study vaccine candidates. The main goal of Part B of this study is to assess the safety, reactogenicity, and immunogenicity of the mRNA-1283.529 booster vaccine candidate.

Parts A and B: Number of Participants With Solicited Local and Solicited Systemic Reactogenicity Adverse Reactions (ARs)

Up to Day 7 · Participants

Part A: mRNA-1283 Low Dose30 Participants
Part A: mRNA-1283 Medium Dose40 Participants
Part A: mRNA-1283 High Dose37 Participants
Part A: mRNA-1283.211 Low Dose28 Participants
Part A: mRNA-1283.211 High Dose29 Participants
Part A: mRNA-127346 Participants

Parts A and B: Number of Participants With Unsolicited AEs

Up to Day 28 · Participants

Part A: mRNA-1283 Low Dose13 Participants
Part A: mRNA-1283 Medium Dose9 Participants
Part A: mRNA-1283 High Dose11 Participants
Part A: mRNA-1283.211 Low Dose12 Participants
Part A: mRNA-1283.211 High Dose7 Participants
Part A: mRNA-12738 Participants

Parts A and B: Number of Participants With Serious Adverse Events (SAEs), Medically Attended AEs (MAAEs), AEs Leading to Withdrawal From Study Participation and AEs of Special Interest (AESIs)

Day 1 to Day 366 · Participants

Part A: mRNA-1283 Low Dose2 Participants
Part A: mRNA-1283 Medium Dose1 Participants
Part A: mRNA-1283 High Dose2 Participants
Part A: mRNA-1283.211 Low Dose3 Participants
Part A: mRNA-1283.211 High Dose3 Participants
Part A: mRNA-12732 Participants

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