An mRNA-based seasonal influenza vaccine in adults: Results of two phase 3 randomized clinical trials and correlate of protection analysis of hemagglutination inhibition titers

The safety, immunogenicity, and efficacy of the original formulation of the investigational mRNA-1010 vaccine for seasonal influenza were investigated in two randomized, active-controlled, phase 3 trials in adults (NCT05415462 and NCT05566639), and the results were used to evaluate hemagglutination inhibition (HAI) titers as correlates of risk and protection against influenza-like illness. mRNA-1010 (50-µg) demonstrated an acceptable reactogenicity and safety profile among the >14,000 adult participants vaccinated in both trials. The efficacy profile of mRNA-1010 was generally reflective of immunogenicity findings, with higher immune responses against influenza A strains and lower responses against influenza B strains relative to an active comparator (licensed inactivated influenza vaccine). An analysis of HAI titers as a correlate of protection against influenza infection provided support for its use as a surrogate endpoint for mRNA-1010, similar to licensed influenza vaccines. These findings support further optimization and development of mRNA-1010 against seasonal influenza.

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Publication Details

Journal
Human Vaccines & Immunotherapeutics
Published
2025-04-02
DOI
https://doi.org/10.1080/21645515.2025.2484088
Citations
16
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
21.67

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article

An mRNA-based seasonal influenza vaccine in adults: Results of two phase 3 randomized clinical trials and correlate of protection analysis of hemagglutination inhibition titers

Honghong Zhou, Chong Ma, Bryony Hicks, Jignesh Vakil et al.
16 citations
Human Vaccines & Immunotherapeutics
Influenza Virus Research Studies
21.67
article

An mRNA-based seasonal influenza vaccine in adults: Results of two phase 3 randomized clinical trials and correlate of protection analysis of hemagglutination inhibition titers

Honghong Zhou, Chong Ma, Bryony Hicks, Jignesh Vakil, Katie C. Hall, Raffael Nachbagauer, Andrei Avanesov, Mieke Soens, Evelyn Du, Jacqueline Miller, Boris Kandinov, Kristi Schaefers, Lingyi Zheng, Conrado J. Llapur, Alicia Pucci, David J. Ensz, Sinead Rudden, Jia Guo, Yoonyoung Park, Jintanat Ananworanich, Wenmei Huang, Carlos Fierro, Brandon Essink
article en
16 citations

Abstract

The safety, immunogenicity, and efficacy of the original formulation of the investigational mRNA-1010 vaccine for seasonal influenza were investigated in two randomized, active-controlled, phase 3 trials in adults (NCT05415462 and NCT05566639), and the results were used to evaluate hemagglutination inhibition (HAI) titers as correlates of risk and protection against influenza-like illness. mRNA-1010 (50-µg) demonstrated an acceptable reactogenicity and safety profile among the >14,000 adult participants vaccinated in both trials. The efficacy profile of mRNA-1010 was generally reflective of immunogenicity findings, with higher immune responses against influenza A strains and lower responses against influenza B strains relative to an active comparator (licensed inactivated influenza vaccine). An analysis of HAI titers as a correlate of protection against influenza infection provided support for its use as a surrogate endpoint for mRNA-1010, similar to licensed influenza vaccines. These findings support further optimization and development of mRNA-1010 against seasonal influenza.

Human Vaccines & ImmunotherapeuticsVol. 21(1)
Moderna Therapeutics (United States) (US), Mayo Clinic in Arizona (US), Velocity Clinical Research (United States) (US), Meridian Clinical Research (US), Micropharma (Canada) (CA), Johnson County Clin-Trials (United States) (US)
Moderna
Good health and well-being
Openalex Percentile: Top 0%
Influenza Virus Research Studies
21.67
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