Cytodyn Inc (CYDY)

[Rockleo]

Guys....Give me 5 minutes of uninterrupted time..To show you how the FDA sabotaged the CYDY CD 12 Trial ..

CD12 was to evaluate Leronlimab for severely ill to Critical Covid patients..For which there is no treatment available at present..!!!

In an Adaptive Trial like CD 12.. The Data Safety Monitoring Board ..DSMB.. is privy to the unblinded results..!!!

They could see the Mortality benefit of Leronlimab on Critically ill patients
78% Day 7..
82% Day14..
50% Day21..
31% Day 28..

They could have seen that CYDY was correct in asking for Leronlimab to have 4 weekly injections..Instead of only 2.. Stopping at Day 7 ..AS THE FDA INSISTED..

Why did the DSMB not do its job..??

The answer lies with Dr Frederick Hayden..A consultant with GILEAD Sciences (Remdesivir).. That the FDA put on the 3 member Panel..!!!

If this is not conflict of interest..What is..??