Moderna today announced promising interim phase 3 clinical trial findings for its next-generation COVID vaccine, which offers the potential for a longer shelf life and paves the way for a combination mRNA vaccine against flu and COVID.
The mRNA-1283 vaccine showed a higher immune response—including in seniors—than its currently licensed vaccine, called mRNA-1273.222. Response was higher against Omicron BA.4/BA.5 as well as the original SARS-CoV-2 virus.
The trials enrolled more than 12,000 people ages 12 and older in the United States, Canada, and the United Kingdom. Researchers also found the mRNA 1283 had a similar safety profile as Moderna's currently licensed vaccine.
"The storage, shelf life and pre-filled syringe presentation of mRNA-1283 could alleviate healthcare provider burden and potentially increase access into new settings to serve public health," the company said in its statement.
In a separate statement on the status of its mRNA vaccines portfolio, Moderna said clinical trials of its combination flu-COVID vaccine (mRNA 1083) in people ages 50 and older is fully enrolled and that it expects data this year. The US Food and Drug Administration has granted it fast-track designation.