Intravenous bamlanivimab use associates with reduced hospitalization in high-risk patients with mild to moderate COVID-19

Author:

Ganesh RavindraORCID,Pawlowski Colin F.ORCID,O’Horo John C.,Arndt Lori L.,Arndt Richard F.ORCID,Bell Sarah J.,Bierle Dennis M.ORCID,Borgen Molly Destro,Hanson Sara N.,Heyliger AlexanderORCID,Larsen Jennifer J.,Lenehan Patrick J.,Orenstein Robert,Puranik Arjun,Speicher Leigh L.,Tulledge-Scheitel Sidna M.,Venkatakrishnan A.J.,Wilker Caroline G.,Badley Andrew D.ORCID,Razonable Raymund R.ORCID

Funder

Mayo Clinic

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference28 articles.

1. An EUA for bamlanivimab-a monoclonal antibody for COVID-19;JAMA,2020

2. An EUA for bamlanivimab etesevimab for COVID-19;Med Lett Drugs Ther,2021

3. An EUA for casirivimab imdevimab for COVID-19;Med Lett Drugs Ther,2020

4. Jones BE, et al. LY-CoV555, a rapidly isolated potent neutralizing antibody, provides protection in a non-human primate model of SARS-CoV-2 infection [preprint]. https://doi.org/10.1101/2020.09.30.318972 Posted on bioRxiv October 9, 2020

5. Coronavirus (COVID-19) update: FDA revokes emergency use authorization for monoclonal antibody bamlanivimab. News release. U.S. Food and Drug Administration; April 16, 2021. Accessed April 24, 2021. https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-revokes-emergency-use-authorization-monoclonal-antibody-bamlanivimab

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