Sotrovimab

Sotrovimab Entwicklungsbezeichnung VIR-7831 ist ein von VIR Biotechnology und GlaxoSmithKline GSK entwickelter Arzneistoff zur ambulanten Behandlung von COVID-19Es handelt sich um einen gegen SARS-CoV-2 gerichteten monoklonalen Antikörper mit zweifacher Wirkungsweise. A Phase 3 randomized multi-center open label study to assess the efficacy safety and tolerability of monoclonal antibody VIR-7831 sotrovimab given intramuscularly versus intravenously for the treatment of mildmoderate coronavirus disease 2019 COVID-19 in high-risk non-hospitalized patients.

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Australias purchase of sotrovimab has been supported by the Science.

. Sotrovimab is approved for emergency use in the US Singapore and Canada however Australia is the first OECD country to issue a formal regulatory approval for sotrovimab. Präklinische Daten deuten darauf hin dass Sotrovimab sowohl das Eindringen. As with all products procured for the Stockpile this treatment will be provided to states and territories as needed.

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Us Government Contracts For Approximately 1 Billion Usd Now In Place To Purchase Sotrovimab Further Expanding Acc Us Government Government State Government