FDA authorizes Moderna and Pfizer’s updated COVID-19 booster shots

By Jane Byrne contact

- Last updated on GMT

© GettyImages/Tang Ming Tung
© GettyImages/Tang Ming Tung

Related tags: Moderna, COVID-19, Fda, Food and drug administration, Pfizer

The US regulator has granted emergency authorization for Pfizer-BioNTech’s and Moderna’s Covid booster shots that target the highly contagious BA.5 omicron subvariant.

Pfizer’s modified booster secured an emergency use authorization (EUA) from the US Food and Drug Administration (FDA) for people aged 12 and older, while Moderna's shot was given an EUA for use in individuals aged 18 and up.

The bivalent vaccines or 'updated boosters' contain two messenger RNA (mRNA) components of SARS-CoV-2 virus, one of the original strain of SARS-CoV-2 and the other one in common between the BA.4 and BA.5 lineages of the omicron variant of SARS-CoV-2.

The FDA said the BA.4 and BA.5 lineages of the omicron variant are currently causing most cases of COVID-19 in the US and are predicted to circulate this fall and winter. In fact, BA.5 accounts for over 88% of all new COVID cases in the US, according to data​ from the US Centers for Disease Control and Prevention (CDC).

Supporting evidence 

In June, the FDA's Vaccines and Related Biological Products Advisory Committee voted overwhelmingly to include an omicron component in COVID-19 booster vaccines.

For each bivalent COVID-19 vaccine, the agency said it based its decision on the totality of available evidence, including extensive safety and effectiveness data for each of the monovalent mRNA COVID-19 vaccines.

The regulator said it also relied on safety and immunogenicity data obtained from a clinical study of a bivalent COVID-19 vaccine that contained mRNA from omicron variant BA.1 lineage that is similar to each of the vaccines being authorized, and nonclinical data obtained using a bivalent COVID-19 vaccine that contained mRNA of the original strain and mRNA in common between the BA.4 and BA.5 lineages of the omicron variant.

Close collaboration with vaccine producers

“The FDA has been planning for the possibility that the composition of the COVID-19 vaccines would need to be modified to address circulating variants. We sought input from our outside experts on the inclusion of an omicron component in COVID-19 boosters to provide better protection against COVID-19.

"We have worked closely with the vaccine manufacturers to ensure the development of these updated boosters was done safely and efficiently. The FDA has extensive experience with strain changes for annual influenza vaccines. We are confident in the evidence supporting these authorizations,”​ said Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research.

Pfizer-BioNTech said they are also planning to submit an application for an omicron-adapted bivalent vaccine for children aged five through to 11 years of age to the FDA in early October. And the companies are working with the FDA to prepare an application for an omicron-adapted bivalent vaccine in children aged six months to four years of age as well.

Related topics: Markets & Regulations

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