NRX is supposed to submit the USFDA EUA application for Aviptadil/Zeysimi, right? I think that RLF may go thru Swiss/ EU/ EMA. Thats what I got from go's post. Trials in Switzerland with sites approved. Turkey?
I may have expressed it wrong, but I'll be happy to explain it again: With the following reason, FDA does not issue an EUA anyway. When the vaccination rate in the USA reduces the number of seriously ill patients, a point in time has been reached certainly when there is no longer EMERGENCY ! .... and without an emergency there is no EUA ! It's as simple as that ! Relief then does not need an approval furthermore that takes many months or even years! Do you really think Relief will wait that long?
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