Regeneron receives emergency use authorization from the FDA

November 23, 2020
Regeneron receives emergency use authorization from the FDA

Another experimental COVID-19 drug is approved to treat severe cases of COVID-19 infection

Regeneron is the latest pharma company to receive the Food and Drug Administration’s emergency use authorization for its experimental COVID-19 vaccine.

The company was granted a EUA for the same drug that President Trump was administrated when he was declared positive for infection.

Multiple studies showed that the drug is effective when it is administrated shortly after diagnosis. Now, it will be used in severe cases of infection.

Regeneron has doses to treat 80,000 patients by the end of November, and the number will increase to 300,000 by the end of January 2021.

According to data from Johns Hopkins, the US has the largest death toll, with more than 12 million confirmed cases.

Following the news, Regeneron stock price traded 3.9% higher.

Sources: bbc.com

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