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Vir Biotechnology to Participate in the Morgan Stanley 20th Annual Global Healthcare Conference

Vir Biotechnology to Participate in the Morgan Stanley 20th Annual Global Healthcare Conference
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US Food and Drug Administration Revises Emergency Use Authorization for Sotrovimab Due to Omicron BA 2 Subvariant

SAN FRANCISCO, March 25, 2022 GlaxoSmithKline plc and Vir Biotechnology, Inc. today announced that the US Food and Drug Administration has amended the Emergency Use Authorization Fact. | March 25, 2022

Data Suggest Sotrovimab Retains Neutralizing Activity Against Omicron Subvariant BA 2

Data Suggest Sotrovimab Retains Neutralizing Activity Against Omicron Subvariant BA 2
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