Phase 1/2 randomized, observer-blind clinical trial of a first-generation, mRNA-based vaccine against seasonal influenza and COVID-19 in healthy adults

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Authors: Amanda K. Rudman Spergel, Carole Henry, Raffael Nachbagauer, Paulina Kapłonek, Eleanor Astley, Andrei Avanesov, Harry L. Bertera, Lizbeth Carmona, Deniz Cizmeci, Avi Collins, Alan Embry, Ruiting Guo
+11 more Xuezhou Mao, Alicia Pucci, Sarah Shao, Jessica Shih-Lu-Lee, Wen-Han Yu, Daniel C. Brune, Laurence Chu, Muhammad Irfan, Galit Alter, Jintanat Ananworanich, Christine A. Shaw
Cited by: 4
References: 23

Abstract

A multicomponent vaccine against seasonal influenza and COVID-19 could reduce disease burden in adults by providing simultaneous protection in a single-dose regimen. The first-generation, mRNA-based, multicomponent mRNA-1073 vaccine, combining antigens encoded by mRNA-1010 (influenza) and mRNA-1273 (COVID-19) vaccines, was investigated in a phase 1/2 clinical trial. This stratified, observer-blinded study randomly assigned healthy adults (18–75 years) to receive mRNA-1073 (25-µg, 50-µg, or 100-µg) + placebo, mRNA-1273 (50-μg) + placebo, mRNA-1010 (50-μg) + placebo, or co-administered mRNA-1010 (50-μg) + mRNA-1273 (50-μg) on day 1. Primary study objectives were safety and reactogenicity. Secondary study objectives assessed humoral immunogenicity against vaccine-matched influenza and SARS-CoV-2 strains at day 29 and all evaluable time points through day 181. An exploratory objective was to further characterize immune responses across the study vaccines. Overall, 550 participants were randomly assigned to receive study vaccination. mRNA-1073 exhibited dose-dependent reactogenicity. Most solicited adverse reactions were grade 1 or 2 in severity; no grade 4 events, serious adverse events related to study vaccination, or deaths were reported. A single dose of mRNA-1073 elicited durable immune responses through 6 months against all vaccine-matched influenza and SARS-CoV-2 strains. Systems serology analysis indicated that mRNA-1073 induced robust, balanced antibody responses with comparable immune profiles to mRNA-1010 + mRNA-1273. mRNA-1073 had an acceptable safety profile and elicited durable immune responses against all vaccine-matched influenza and SARS-CoV-2 strains, supporting ongoing evaluations of mRNA-based multicomponent vaccines that simultaneously protect against seasonal influenza and COVID-19 in a single dose.Registration: ClinicalTrials.gov identifier: NCT05375838 (https://clinicaltrials.gov/study/NCT05375838).

Fields of Study & Subjects

SARS-CoV-2 and COVID-19 Research Influenza Virus Research Studies Immune responses and vaccinations

Publication details

Journal / source
Human Vaccines & Immunotherapeutics
Publisher
Informa UK Limited
Volume
22
Issue
1
Pages
2589644–2589644
Publication date
2 February 2026
Language
EN