Evusheld has become the latest COVID-19 antibody drug to lose federal authorization after it was deemed ineffective against the dominant versions of the virus. The U.S. Food and Drug Administration (FDA) on Thursday withdrew its emergency use authorization for Evusheld, a two-dose cocktail of monoclonal antibodies meant to provide protection to those who have a…
FDA Pulls Authorization for Evusheld, Says It’s Ineffective Against New COVID Mutations
AstraZeneca’s COVID-19 Prevention Jab Granted Emergency Authorization for Immune Compromised
December 9, 2021
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The U.S. Food and Drug Administration (FDA) on Dec. 8 issued an emergency use authorization for an AstraZeneca COVID-19 antibody drug designed to help prevent infection in people with compromised immune systems. The drug, called Evusheld, is a combination of two long-acting synthetic antibodies: tixagevimab and cilgavimab, which are derived from B-cells donated by patients who have recovered from the…
FDA Grants Eli Lilly’s Experimental COVID-19 Antibody-Drug Emergency Use Authorization
Eli Lilly’s COVID-19 antibody-drug has been granted emergency use authorization by the Food and Drug Administration (FDA), widening access to a therapy that has shown improvement in treating patients with mild to moderate cases of the CCP virus. Data from a late-stage trial last month showed that Eli Lilly’s combination therapy of two antibodies, bamlanivimab and…
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