Pulmonary Medicine

Monoclonal Antibody Treatment for COVID-19 Receives FDA Authorization


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Host: Linda Bernstein, Pharm.D.

The U.S. Food and Drug Administration has granted Eli Lilly and Company’s trial vaccine for COVID-19 an Emergency Use Authorization, or EUA. On this episode of The Drug Report, learn more about this monoclonal antibody and how the company plans on distributing it.

Published November 30, 2020

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Pulmonary MedicineBy ReachMD