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CytoDyn Inc CYDY
(Total Views: 658)
Posted On: 06/03/2020 2:22:30 PM
Post# of 153903
Posted By: HCIT
Re: nmbr1stckpckr #36484
nmbr1stckpckr, I put it this way. I think the FDA is asking for no more EINDS is because they want CYDY to finish both trials and wants us to put these or any new Doctors asking the FDA for an IND for their respective patients into one or the other of our 2 Covid trials instead of INDS.

Now, if one of these patients progresses further towards ARDS, they will have the permission from the FDA to give them the drug rather than a placebo to save their live/lives. I can't see the FDA purposely saying no to that. I would put it this way to the FDA, "are you telling me Mr. FDA that you won't allow the patient to come off of a placebo and let him/her or them to die? Mr. FDA, what if it was you that had Covid-19 and you we're on a placebo, wouldn't you want your government agency to allow you access to Leronlimab? How could they say no, IMO that's like committing murder don't ya know

Anyway, thanks for your replies on this subject and thank you for your much better language - GLTU and all us longs

HCIT













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