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Administration of anti–SARS-CoV-2 monoclonal antibodies after FDA deauthorization

08.29.22 | JAMA Network

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About The Study: Hospitals and health systems administered more than 158,000 anti–SARS-CoV-2 monoclonal antibodies (mAbs) doses in early 2022 despite Food and Drug Administration (FDA) deauthorization because of a lack of efficacy against the Omicron variant. Medicare payments for mAb administration range from $450 to $750 per dose, indicating that spending on these deauthorized treatments likely exceeds $71 million. The findings suggest that the use of deauthorized mAb products was widespread, even though patients had a minimal likelihood of benefit.

Authors: Timothy S. Anderson, M.D., M.A.S., of Beth Israel Deaconess Medical Center in Boston, is the corresponding author.

To access the embargoed study: Visit our For The Media website at this link https://media.jamanetwork.com/

(doi:10.1001/jamanetworkopen.2022.28997)

Editor’s Note: Please see the article for additional information, including other authors, author contributions and affiliations, conflict of interest and financial disclosures, and funding and support.

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JAMA Network Open

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Jim Michalski
JAMA Network
Jim.Michalski@jamanetwork.org

How to Cite This Article

APA:
JAMA Network. (2022, August 29). Administration of anti–SARS-CoV-2 monoclonal antibodies after FDA deauthorization. Brightsurf News. https://www.brightsurf.com/news/1EOP4VQL/administration-of-antisars-cov-2-monoclonal-antibodies-after-fda-deauthorization.html
MLA:
"Administration of anti–SARS-CoV-2 monoclonal antibodies after FDA deauthorization." Brightsurf News, Aug. 29 2022, https://www.brightsurf.com/news/1EOP4VQL/administration-of-antisars-cov-2-monoclonal-antibodies-after-fda-deauthorization.html.