Developed on unprecedented timelines similar to the COVID-19 vaccines, monoclonal antibody therapies – once seen as central to the fight against SARS-CoV-2 – have only played a limited role so far since the US emergency use approvals of Regeneron and Eli Lilly’s products.
Now armed with new data, and seeking expanded emergency use authorizations (EUAs), that looks set to change soon; but the companies will still face challenges to the treatments truly assisting
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