Replies to post #163462 on Cytodyn Inc (CYDY)

[DonDonDonDon]

FDA rushed so much , when Dr Fauci from the WH asked openly for EUA for this mostly worthless drug Remdesivir , FDA issued EUA 2-3 days later.

Remdesivir had stat sig with a p value of less than .001 on its primary endpoint on its whole trial which consisted of more than 1,000 patients. Rem also came close to stat sig with mortality on its whole trial with a p value of .059. Leronlimab isn't even in the same ballpark. All we have to judge leronlimab is a few cherrypicked data points.