adonis
Footballguy
Except we were told by NP that they hadn't filed for an EUA, and that the advice given by both the MHRA and FDA was that they weren't interested in approving a drug for emergency use for a mild-moderate population, or on the results from a mild-moderate population.Wow, you all are crazy. It was a no news call. Nothing has changed for the most part.
Could this NOT have been determined by a $#$%@# phone call at some point, oh, I don't know, over the past two months? I'll supply a script.
"Hey Guys, it'd your buddy NP over at Cytodyn. We're working with a drug that has had good success against Covid in the mild to moderate population. Is there any chance that even good data in this group could lead to emergency use authorization? Oh...no? Ok, thanks."
Bam. Months of investors hopes being strung along gone.