SILVER SPRING, Md., Nov. 21, 2020 /PRNewswire/ -- Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for casirivimab and imdevimab to be administered together for the treatment of mild to moderate COVID-19 in adults and pediatric patients (12 years of...
from PR Newswire: https://ift.tt/35Sb63n
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