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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

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

Research output: Contribution to journalArticlepeer-review

17 Scopus 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.

Original languageEnglish
Article number2484088
JournalHuman Vaccines and Immunotherapeutics
Volume21
Issue number1
DOIs
StatePublished - 2025
Externally publishedYes

Keywords

  • Seasonal influenza
  • correlate of protection
  • immunogenicity
  • mRNA vaccine
  • reactogenicity
  • safety

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