Moderna Asks FDA to Authorize Variant-Specific COVID Vaccine

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Moderna Asks FDA to Authorize Variant-Specific COVID Vaccine
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Moderna released study results today showing its new Omicron-specific booster increased antibodies against the coronavirus by a factor of 5, even against some of the newer and more worrisome variants.

The booster in development contains both Moderna’s original COVID-19 vaccine and one specifically designed to target the more recent BA.4 and BA.5 Omicron subvariants.

The announcement comes at a time when the proportion of BA.4 and BA.5 subvariants in the United States is growing. These two strains now account for about 35% of those circulating in the U.S., according toBA.4 and BA.5"represent an emergent threat to global public health," Stéphane Bancel, chief executive officer of Moderna, stated in a.

The combination vaccine was not as strong against all Omicron variants though, showing that antibodies against BA.4 and BA.5 were approximately three times lower than against the older BA.1 variant. The late-stage study shows that 1 month after giving the shot to people already vaccinated and boosted, this new booster created"potent neutralizing antibody responses" against BA.4 and BA.5 in all who got the shot, regardless of prior infection, the company

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