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The anti–SARS-CoV-2 monoclonal antibody (mAb) bamlanivimab received emergency use authorization based on interim results of an industry-funded study (BLAZE-1; NEJM JW Infect Dis Jan 2021 and N Engl J Med 2020 Oct 28; [e-pub]) in which 577 outpatients (mean age, 45) with mild to moderate COVID-19 (67% with at least 1 risk factor for severe COVID-19) were randomized to receive a single infusion of placebo, one of three doses of bamlanivimab (700 mg, 2800 mg, or 7000 mg), or a combination of 2800 mg bamlanivimab plus 2800 mg etesevimab (a neutralizing anti–SARS-CoV-2 mAb that targets an epitope on the spike protein distinct from that of bamlanivimab). Change from baseline in log viral load (the primary outcome) was assessed at treatment day 11…