Philippines (FDA), Brazil (Albert Einstein), Macle
Post# of 142806
I tend to agree with you #EvilRabbit...I do not see this letter from the FDA taking them off course from impartially testing and reviewing the effectiveness of Leronlimab in Covid-19. i.e. FDA's position on Leronlimab in today's letter is nothing new to them.
I tend to believe that the FDA have themselves in a corner with Leronlimab with: their own protocols; reliance on P values; turning down the "4 Dose" protocol at the outset (and perhaps for CD18); failure to disclose today that Cytodyn has filed a follow-up study based upon the learnings (Age, 4 Dose...), failure to see in the interim review or request to see the interim CD-12 results (and missed or did not see the age imbalance).
I firmly believe in the science of Leronlimab, the data & the lives saved. Cytodyn has great momentum elsewhere and this defensive play by the FDA will be seen for what it is soon enough.
GLTA
GLTA