Moderna mRNA flu vaccine outperforms standard shot in Phase 3 trial
Moderna's mRNA-based flu vaccine has demonstrated superior efficacy over traditional flu shots in a Phase 3 clinical trial. Results published in the New England Journal of Medicine indicate that the mRNA vaccine reduced influenza illness by approximately 27% more than a standard-dose vaccine. The trial, which enrolled thousands of participants across multiple countries, compared Moderna's candidate to licensed flu vaccines. The company plans to submit the data to the U.S. Food and Drug Administration (FDA), which is expected to make a decision on approval in August. If authorized, this would be the first mRNA flu vaccine to enter the market, leveraging the same platform technology used in Moderna's COVID-19 vaccine. The findings mark a significant step in applying mRNA technology to seasonal influenza prevention, potentially offering improved protection and faster adaptation to circulating strains.
Key facts
- Moderna's mRNA flu vaccine reduced flu illness by about 27% more than a standard-dose vaccine.
- Results were published in the New England Journal of Medicine.
- The trial was a Phase 3 study comparing the mRNA vaccine to standard-dose flu vaccines.
- The FDA is expected to make a decision on approval in August.
- This would be the first mRNA flu vaccine if authorized.
- The vaccine uses the same mRNA platform as Moderna's COVID-19 vaccine.
- The trial enrolled thousands of participants across multiple countries.
- mRNA technology may allow faster adaptation to circulating flu strains.
Entities
Institutions
- Moderna
- U.S. Food and Drug Administration
- New England Journal of Medicine
Sources
- Quartz —