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In February 2021, the FDA issued an emergency use authorization (EUA) for bamlanivimab and etesevimab administered together for the treatment of mild to moderate COVID-19 in people twelve years of age or older weighing at least 40 kilograms (88 lb) who test positive for SARS‑CoV‑2 and who are at high risk for progressing to severe COVID-19.
On 16 April 2021, the FDA revoked the emergency use authorization (EUA) for the investigational monoclonal antibody therapy bamlanivimab, when administered alone, to be used for the treatment of mild-to-moderate COVID-19 in adults and certain pediatric patients. [69]
Sep. 17—Kaiser Permanente has opened a new monoclonal antibody infusion site at its West Oahu facility to meet growing demand from qualified COVID-19 patients. The infusion center, Kaiser's ...
While COVID-19 lands more people in hospitals, doctors are turning to monoclonal antibodies to help keep people out. Governor Greg Abbott was one of the latest political leaders to test positive ...
The advantage of active monoclonal antibody therapy is the fact that the immune system will produce antibodies long-term, with only a short-term drug administration to induce this response. However, the immune response to certain antigens may be inadequate, especially in the elderly.
Apr. 15—The Henry Ford Health System is receiving additional supplies of monoclonal antibodies from the federal government in an effort to hold down COVID-19 hospitalizations that are ...
This list of over 500 monoclonal antibodies includes approved and investigational drugs as well as drugs that have been withdrawn from market; consequently, the column Use does not necessarily indicate clinical usage. See the list of FDA-approved therapeutic monoclonal antibodies in the monoclonal antibody therapy page.