Moderna today reported promising relative vaccine efficacy (rVE) findings from a phase 3 trial of its seasonal mRNA flu vaccine candidate compared to a standard-dose licensed flu vaccine in adults ages 50 years and older.
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In a press release, the company said its candidate flu vaccine, called mRNA 1010, showed superior results, with an rVE of 26.6% in the overall study population (95% confidence interval, 16.7% to 35.4%).
Moderna also reported strong rVE against each of the three individual strains: H1N1 (29.6%), H3N2 (22.2%), and B/Victoria (29.1%). It added that subgroup analysis showed a consistently strong rVE point estimate across all age-groups, risk factors, and previous vaccination status. Also, the rVE in people ages 65 years and older was 27.4%.
Large trial spanned 11 countries.
The trial enrolled nearly 41,000 adults ages 50 and older across 11 countries. The company said that the new findings, which will be presented at an upcoming medical conference and submitted for peer-reviewed publication, follow earlier phase 3 trial findings that showed superior seroconversion rates and geometric mean titer ratios against all strains in the vaccine compared to high- and standard-dose seasonal flu vaccines.
Stephane Bancel, MBA, Moderna’s chief executive officer, said the strong phase 3 efficacy results are a significant milestone in the company’s effort to reduce the flu burden in older adults.
“The severity of this past flu season underscores the need for more effective vaccines," he said. "An mRNA-based flu vaccine has the potential advantage to more precisely match circulating strains, support rapid response in a future influenza pandemic, and pave the way for COVID-19 combination vaccines."