FDA Issues EUA for Bamlanivimab and Etesevimab for COVID-19 Treatment

On February 9, 2021, the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for bamlanivimab and etesevimab administered together for the treatment of mild to moderate COVID-19 in adults and pediatric patients (12 years of age or older weighing at least 40 kilograms [about 88 pounds]) who test positive for SARS-CoV-2 and who are at high risk for progressing to severe COVID-19. The authorized use includes treatment for those who are 65 years of age or older or who have certain chronic medical conditions.

The safety and effectiveness of this investigational therapy for use in the treatment of COVID-19 continues to be evaluated.

Read the FDA announcement.

Posted 2/10/21