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Comment by dragonwriter

> If this study was only conducted on patients who were already hospitalized I don't think it is a cohort that represents Remdesivir's intended users.

That's the scope of the authorized investigatory use in the US, so unless you think the Trump Administration is simultaneously promoting and sabotaging it, I think it's the intended target:

“VEKLURY® (remdesivir) is authorized for use under an EUA only for the treatment of adult and pediatric patients hospitalized with suspected or laboratory-confirmed COVID-19, and for whom use of an intravenous (IV) agent is clinically appropriate. VEKLURY must be administered via IV infusion.”

https://www.remdesivir.com/us/?gclsrc=aw.ds&&gclid=CjwKCAjwi...

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