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Phase 2 dose-ranging study of the virologic efficacy and safety of the combination COVID-19 antibodies casirivimab and imdevimab in the outpatient setting

2021-11-10

Abstract excerpt

<h4>Summary</h4> <h4>Background</h4> The monoclonal antibody combination casirivimab and imdevimab (REGEN-COV ® ) reduced viral load, hospitalisation, or death when administered 1:1 as an intravenous (IV) dose ≥1200 mg in a phase 3 COVID-19 outpatient study. Availability of subcutaneous (SC) and/or lower IV doses should increase accessibility and/or drug supplies for patients. <h4>Methods</h4> This is a double-bli...

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Literature Corpus work
9605a092-6eeb-5538-bdc7-d6c673d929f3
DOI
10.1101/2021.11.09.21265912
Open publication

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Phase 2 dose-ranging study of the virologic efficacy and safety of the combination COVID-19 antibodies casirivimab and imdevimab in the outpatient settingDOI 10.1101/2021.11.09.21265912
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