Moderna has announced its combined flu and Covid vaccine has generated strong immune responses in early-stage trials.

Interim results from its phase 1/2 studies found the vaccine (mRNA-1083) generated antibody levels similar to or greater than flu vaccines as well as similar results to the standalone Moderna Covid jab.

Related Article: Government seeks pharmacists' views to underpin first-ever men’s health strategy

It plans to start a phase 3 trial of the combined vaccine in adults over the age of 50 later this year, a statement from the company said.

They will be aiming for regulatory approval in 2025, a spokesperson said.

The early tests suggested the vaccine appeared effective against A and B strains of flu when compared with widely used flu vaccines produced by Sanofi and GSK.

It was also found to be safe and tolerated with rates of adverse effects similar to those that had been reported with the Moderna Covid-19 vaccine.

Related Article: Vaping trends stall following regulation announcement

Stéphane Bancel, chief executive officer at Moderna said: ‘Flu and Covid-19 represent a significant seasonal burden for individuals, providers, healthcare systems and economies.

‘Combination vaccines offer an important opportunity to improve consumer and provider experience, increase compliance with public health recommendations, and deliver value for healthcare systems.’

Related Article: NHSE to ‘expand’ community pharmacy RSV vaccine offer

Other companies are also in the process of developing combined flu and Covid-19 vaccines including Pfizer/BioNTech and Novavax.

This article first appeared on our sister title Pulse.