Effective January 24, 2022, the FDA updated the Emergency Use Authorization (EUA) fact sheets for two COVID-19 monoclonal antibody treatments: bamlanivimab plus etesevimab (Eli Lilly) and casirivimab plus imdevimab (Regeneron, also known as REGEN-COV). Neither of these treatments are authorized for use anywhere in the U.S. due to their ineffectiveness against the dominant Omicron variant. Sites are directed to immediately stop administering these therapeutics as they do not retain EUA.
Ph: (443) 281-9157
Fax: (410) 582-8728
801 Landmark Dr.
Glen Burnie, MD 21061
Contact Us
Mon-Fri: 8:30AM-6:30PM
Sat: 9:00AM-2:00PM
Rob Lee
8 weeks ago
The user didn't write a review, and has left just a rating.