U.S. Allowing First Emergency Use of COVID-19 Antibody Drug
U.S. health officials have allowed emergency use of the first antibody drug to help the immune system fight COVID-19.
The Food and Drug Administration has cleared the experimental drug from Eli Lilly for people 12 and older with mild or moderate COVID-19 not requiring hospitalization.
Tests of it are continuing, but the drug does not seem to help patients with more serious illness.
It is similar to a treatment President Trump received after contracting the virus last month.
The government previously reached an agreement to buy and supply much of the early production of the drug.
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