FDA limits use of sotrovimab for COVID-19 in some US regions
The US Food and Drug Administration is continually monitoring how authorized and approved treatments for COVID-19 are affected by changing variants - currently Omicron and the Omicron sub-variants, such as BA.2.
As a result, on Friday, considering the most recent data available, the FDA announced that sotrovimab is no longer authorized for use at this time in the following states and territories:
- Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, and Vermont (Health and Human Services [HHS] Region 1)
- New Jersey, New York, Puerto Rico, and the Virgin Islands (HHS Region 2)
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