Regeneron Asks FDA to Approve Emergency Use of REGN-COV2 for COVID-19
Regeneron Pharmaceuticals said that it submitted a request to the FDA seeking emergency-use authorization for its REGN-COV2 investigational antibody combination for the treatment of COVID-19. REGN-COV2 is a combination of two monoclonal antibodies, REGN10933 and REGN10987, which has been designed to block infectivity of SARS-CoV-2.
The disclosure came the same day that Eli Lilly announced that it submitted an EUA request to the FDA for its neutralising IgG1 monoclonal antibody LY-CoV555 for use in higher-risk patients who have been recently diagnosed with mild-to-moderate COVID-19.