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Complete map of SARS-CoV-2 RBD mutations that escape the monoclonal antibody LY-CoV555 and its cocktail with LY-CoV016
The 3 references without a DOI — listed, not checked
no DOI — not checkedUS Food and Drug Administration. Emergency use authorization (EUA) for bamlanivimab 700 mg and estevimab 1,400 mg IV administered together. Center for Drug Use and Evaluation (CDER), 2021 [cited 2021 Jul 22]. https://www.fda.gov/media/145802/download
no DOI — not checkedHensley MK, Bain WG, Jacobs J, Nambulli S, Parikh U, Cillo A, Intractable COVID-19 and prolonged SARS-CoV-2 replication in a CAR-T-cell therapy recipient: a case study. Clin Infect Dis. 2021;ciab072.
no DOI — not checkedEuropean Medicines Agency. Assessment report Eli Lilly. Company Limited use of bamlanivimab and etesevimab for the treatment of COVID-19, 2021 [cited 2021 Jun 2]. https://www.ema.europa.eu/en/documents/referral/eli-lilly-company-limited-antibody-combination-bamlanivimab/etesevimab-covid19-article-53-procedure-assessment-report_en.pdf
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