FDA withdraws EUA for AstraZeneca's Evusheld

The Food and Drug Administration has withdrawn emergency use authorization for AstraZeneca’s Covid-19 antibody cocktail Evusheld as the treatment is not expected to neutralize the currently dominant XBB.1.5 subvariant of omicron.

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The FDA had limited Evusheld’s use earlier this month for the same reason and the agency’s Thursday announcement sent U.S. shares of London-based AstraZeneca down 1.31% to $65.75.

Omicron subvariant XBB.1.5 has been spreading rapidly in the country since December and it made up nearly half of all U.S. Covid cases last week, according to government data.

[Interesting. For immune suppressed individuals, this pretty much leaves them with only infusions of antibodies as their therapeutic response, unless something else has been approved as of late. — Ed]

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