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CDC signs off on updated Covid-19 boosters

The updated COVID-19 boosters are formulated to better protect against the most recently circulating COVID-19 variant,” Walensky said in a statement. “They can help restore protection that has waned since previous vaccination and were designed to provide broader protection against newer variants. This recommendation followed a comprehensive scientific evaluation and robust scientific discussion. If you are eligible, there is no bad time to get your COVID-19 booster and I strongly encourage you to receive it.”
The updated boosters have instructions that tell our cells to make antibodies against two strains of the virus that causes Covid-19: the original strain and the BA.4 and BA.5 Omicron subvariants, which share the same spike.
Pfizer/BioNTech’s updated vaccine is a 30-microgram dose authorized for people 12 and older. Moderna’s updated vaccine is a 50-microgram dose authorized for people 18 and older.
The CDC said in the statement that it “also expects to recommend updated COVID-19 boosters for other pediatric groups” in the coming weeks.
People are eligible for the updated boosters as long as they have completed all primary doses in their vaccine series. The committee recommended that the new boosters be given at least two months after the last dose of any Covid-19 vaccine and up to three months after an infection.
The new formulations do not replace shots for the primary series.
I just would like to remind the committee that every year, we use influenza vaccines that are based on new strains without clinical studies being done,” said Dr. Melinda Wharton, associate director for vaccine policy at the CDC’s National Center for Immunization and Respiratory Diseases.
Dr. Doran Fink, deputy director of the FDA’s Division of Vaccines and Related Products Applications, said, “I do appreciate the amount of discomfort that I’m hearing from committee members who are being asked to take this leap with the Covid vaccines that they haven’t been asked to make previously with the Covid vaccines.
“FDA felt very comfortable with the approach of extrapolating the safety and effectiveness or rather the known and potential benefits,” Fink said. “We recognize that we’ve taken a different path than the regulatory authorities have in Europe and Canada.”
New analyses on the cost-effectiveness of the boosters suggest that the US could save at least $63 billion in medical costs between August and March 31 if as many people get these boosters as got flu shots during the 2021-22 season.
In the studies that looked at the shot targeting BA.1 along with the original, the boosters broadened immunity against many variants, and they were proven to be better than the older single-strain boosters because they made higher levels of antibodies.
Moderna presented tantalizing data suggesting that the two-strain shots it developed against the Beta variant might extend the length of protection people get from their vaccines, which currently drops off significantly after about four months. It said a study on these results was being prepared for publication

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