FDA issued an EUA for New Long-Acting Monoclonal Antibodies for Pre-exposure Prevention of COVID-19 in patients with moderate to severely compromised immune systems or a history of severe adverse reactions to a COVID-19 vaccine
Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for AstraZeneca’s Evusheld (tixagevimab co-packaged with cilgavimab and administered together) for the pre-exposure prophylaxis (prevention) of COVID-19 in certain adults and pediatric individuals (12 years of age and older weighing at least 40 kilograms [about 88 pounds]). The product is only authorized