not to beat a dead horse, info for the newbies -
Post# of 148109
the FDA also had significant data that leronlimab also had an 8+ year long safety record that was safer than aspirin, and an 8+ year long efficacy record of keeping HIV at bay at the time in nearly 1000 patients of all walks of life. even had a celebrity patient (my favorite guy in the world). and not just patients but some of the people were the worst, drug addicted, homeless, irresponsible life choice, drug resistant people on the planet, getting positive results in HIV. yeah that good.
its not like cytodyn made some pie in the sky exclamation about some drug in early development they had a hypothesis on. they also had "anecdotal" ( hate that phrase ) data that leronlimab had taken covid people off of respirators when nothing else could, and rather quickly. EUA should have been granted immediately regardless of the CEO. instead they put a HALT to the emergency use status - a crime in itself , ordered a trial, and quashed it completely with horrendous trial design. 82% showed recovery in the first two weeks, but not allowed to keep taking the drug and collapsed by the 28th day of the trial, and many died. 2 weeks on and 2 weeks off, see what happens. food and water for 2 weeks, no food and water for the next 2 weeks - lets see who is thirty and hungry...all of them?.
would like to see any other trial for anything designed like this. a joke. FDA not looking out for the protection of anybody but themselves and those that can enrich them.
odd because if cytodyn became the savior of the pandemic, the very same money would still flow to the FDA. we are here 100% aware of this, this info is for the newbies. need to keep repeating this so new eyes can see it.