By Joe Hoppe

 

GlaxoSmithKline PLC's monoclonal antibody treatment for the coronavirus, sotrovimab, has been limited in use by the U.S. Food and Drug Administration, the federal agency said late Wednesday.

The pharmaceutical giant's product shouldn't be used to treat patients with mild-to-moderate infections in places where the disease is likely to have been caused by a variant that isn't susceptible to the drug, the FDA said.

GlaxoSmithKline's partner Vir Biotechnology Inc. has previously said sotrovimab retains its neutralizing of the activity of the emerging BA.2 form of the Omicron variant of the coronavirus.

The FDA said it will monitor conditions to determine whether the drug should be used in certain geographic regions.

Shares at 1011 GMT were down 4.2 pence, or 0.3%, at 1,545.8 pence.

 

Write to Joe Hoppe at joseph.hoppe@wsj.com

 

(END) Dow Jones Newswires

February 24, 2022 05:29 ET (10:29 GMT)

Copyright (c) 2022 Dow Jones & Company, Inc.
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