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Vir Biotechnology Provides Corporate Update and Reports First Quarter 2022 Financial Results

Vir Biotechnology Provides Corporate Update and Reports First Quarter 2022 Financial Results
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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

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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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GSK and Vir Biotechnology Announce United States Government Agreement to Purchase Additional Supply of Sotrovimab, Authorized for the Early Treatment of COVID-19

– 600,000 additional doses to be supplied to the US government for distribution in Q1 2022, enabling further access to sotrovimab nationwide – – Brings total number of doses. | January 11, 2022

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Vir Biotechnology Announces New Research Describing the Structural Basis of SARS-CoV-2 Omicron Immune Evasion and Receptor Engagement

Vir Biotechnology Announces New Research Describing the Structural Basis of SARS-CoV-2 Omicron Immune Evasion and Receptor Engagement - read this article along with other careers information, tips and advice on BioSpace

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