News Focus
News Focus
icon url

3X Charm

03/23/22 7:32 PM

#206090 RE: stockorus #206089

If NP’ s dredged trial data was meaningful in any scientific way, some company would have made a run at acquiring CYDY. It is not , the FDA says it’s not and so does the market. Clinging to NP lies and frauds is a recipe for investing disaster.
icon url

HyGro

03/23/22 9:04 PM

#206091 RE: stockorus #206089

It is a DONE deal. FDA Statement has closed down any consideration of the CD10 and CD12 trials. No EUA. Now the FDA Letter is forbidding the company from the claiming they were successful and forcing the company to pull all of NPs past false statements. And then there is the SEC and DOJ investigation into the Cytodyn's CoV trials and communications.

That's about as dead as any trial as I've ever seen. Not even a zombie left.

Google FDA Statistical Guidance, should get you there.
icon url

misiu143

03/24/22 11:35 AM

#206102 RE: stockorus #206089

Stockorus , do you still have a short statement/voice from Dr Lalezary how they asked FDA for 4 doses of leronlimab for CD12 , but for no reason FDA refused , FDA changed their protocol to two doses only..
I saved someplace but I cant find it , can you please post it again..!!!!!

Yes , it should be post again and again to show how FDA sabotage our CD12 , but we still showed at 14 days with critical patients 82% mortality benefit ABOVE all these toxic drugs with minimal efficacy they approved..

But I guess , as we know by now from the FDA executive from the Veritas video....Vaccine MUST be , and will be mandated , then company makes billions every year , " RECURRENT REVENUE " and they giving HUNDREDS of MILLIONS to FDA every year..

Yes good enough reason to sabotage a study of a great drug...

Yes , leronlimab should be approve ASAP , it is needed , people are dying..

All IMO.