[Image source=EPA Yonhap News]

[Image source=EPA Yonhap News]

View original image

[Asia Economy New York=Correspondent Baek Jong-min] Remdesivir, which has attracted attention as a treatment for the novel coronavirus infection (COVID-19), has received emergency use authorization from the U.S. Food and Drug Administration (FDA).


U.S. President Donald Trump announced this on the 1st (local time) at the White House Oval Office together with Daniel O'Day, CEO of Gilead. President Trump added that remdesivir will be distributed to hospitals starting from the 4th.


O'Day, CEO of Gilead, the manufacturer of remdesivir, also announced that they will donate enough remdesivir for 1.5 million people.


Remdesivir was originally developed as an Ebola treatment, but it rapidly emerged as a treatment after showing effectiveness in clinical trials for COVID-19.



Gilead's stock price fell 4.8% that day but rose about 2% based on the news released after the market closed.


This content was produced with the assistance of AI translation services.

© The Asia Business Daily(www.asiae.co.kr). All rights reserved.

Today’s Briefing