Cytodyn Inc (CYDY)

[misiu143]

FDA had more then enough of safety data on leronlimab by this time , not to withhold treatment for severe /critical patients after 7 days , especially when Dr Patterson showed them results of Rantes in severe patients , and that Rantes are still high at 14 days , so more treatment is needed with SC drug with half life of 10 days..and not just to stop it at 7 days..

By then after evaluating HIV treatment with 350 mg , FDA requested to start 525 and 700 mg , and this was finished by the time covid came. Safety was know to FDA.

And by this time FDA already had dose justification and safety for cancers with 350 , 525 and 700 mg.

I bet if we will be Gilead we will not have this problems..

All imo.