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Eli Lilly Alzheimer s Drug Gains FDA Breakthrough Status
Eli Lilly Alzheimer s Drug Gains FDA Breakthrough Status
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Lilly Covid Antibody Combo Gets U S Emergency Authorization
Lilly Covid Antibody Combo Gets U.S. Emergency Authorization Bloomberg 2/10/2021 Riley Griffin © Bloomberg Eli Lilly & Co. corporate headquarters stand in Indianapolis, Indiana, U.S., on Monday, May 21, 2012. (Bloomberg) Eli Lilly & Co.’s combination antibody drug for Covid-19 was cleared for emergency use by U.S. regulators, providing doctors with a treatment option that is expected to be better able to combat new coronavirus mutations. The Food and Drug Administration authorized the treatment for use in Covid-positive adults and children 12 and older who are at high risk of developing severe forms of the disease or progressing to the hospital, according to a fact sheet posted Tuesday by the agency.
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