Gilead's remdesivir gets U.S. FDA approval for hospitalized COVID-19 patients

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The FDA approved Gilead’s antiviral drug remdesivir for treating patients hospitalized with COVID-19, making it the first and only drug approved for the disease in the U.S. $GILD

- The U.S. Food and Drug Administration on Thursday approved Gilead Sciences Inc’s antiviral drug remdesivir for treating patients hospitalized with COVID-19, making it the first and only drug approved for the disease in the United States.

Remdesivir has been available under an FDA emergency use authorization since May, after a study led by the National Institutes of Health showed it reduced hospital stays by five days. Remdesivir, which will be sold under the brand name Veklury, costs $3,120 for a five-day treatment course, or $2,340 for government purchasers such as the Department of Veterans Affairs. Shares of Gilead rose 4.3% in after hours trading to $63.30.Remdesivir has become the standard of care for patients hospitalized with severe COVID-19 even though it has not been shown to improve survival.

The company said Veklury has regulatory approvals or temporary authorizations in about 50 additional countries.

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