The Food and Drug Administration has issued an emergency use authorization for the first injectable monoclonal antibody medication for pre-exposure prevention of COVID-19 for some adults and children 12 years and older.
The pre-exposure therapy, Evusheld by AstraZeneca, is authorized for those individuals who are not currently infected with the COVID-19 virus and who have not recently been exposed to an individual infected with COVID-19.
The authorization also requires that individuals either have moderate to severely compromised immune systems due to a medical condition or due to taking immunosuppressive medications or treatments, or have a history of having severe adverse reactions to a COVID-19 vaccine and/or component(s) of those vaccines.
“Vaccines have proven to be the best defense available against COVID-19,” said Patrizia Cavazzoni, M.D., director of the FDA’s Center for Drug Evaluation and Research in a press release from the Georiga Department of Public Health. “However, there are certain immune-compromised individuals who may not mount an adequate immune response to COVID-19 vaccination, or those who have a history of severe adverse reactions to a COVID-19 vaccine and therefore cannot receive one and need an alternative prevention option. Today’s action authorizes the use of the combination of two monoclonal antibodies to reduce the risk of developing COVID-19 in these individuals.”
To learn more about the pre-exposure monoclonal antibody therapy, speak with your physician or visit the District 2 Public Health website.
