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Wow! Trick is definitely the right word. You conducted MILLIONS of scenarios? I have to go with the FDA on this one. The FDA approved OLE and eIND. You can conduct two million scenarios and not find one that the FDA would allow doctors to give a drug they knew failed a trial.
CYDY is currently under priced, the market is correcting that. Looks to be headed to $7 this week. $30 to $50 with positive announcement $100 with approval
NP always seems very confident when he talks about three digits. The reason for this is obvious, CytoDyn is obviously in talks with a BP. All the rumors today about a buy out is starting make sense.
Shares being sold??!! CYDY is up 200% in the last two months!!! Investors are buying.
Three fingers. CYDY is going to triple digits after approval. That's just common knowledge, everyone knows that, the only question left is how far into triple digits. Covid with HIV will definitely break $200.
"leronlimab is the miracle cure for covid" we have something in common, I also feel Leronlimab is the miracle cure for covid.
Dr. Harish Seethamraju, M.D. Montefiore-Einstein Scientists, at Montefiore hospital in New York
Did Samsung get paid by OWS? Are ongoing logistics for CD12 approval going on at this very moment? Could be OWS is coordinating with Samsung to start production on Leronlimab?
The smart shorts covered, there's not very many of those.
The sharks are the longs that will take their money.
Tick tock..times running out to cover, CYDY about to leg up again.
Now you're catching on. CYDY is up over 700% in anticipation of CD12 results. Over 40 thousand new investors. The market is saying the trial is positive. Me personally I'm going with FDA, the FDA approved OLE and eIND, they have seen the data, they will approve the trial.
NOPE If the trial was heading for failure the FDA would not let the trial continue. The trial although complete is still actively recruiting but the big change is the FDA required the plecebo to be stopped and Leronlimab administered to ALL patients. This is after the FDA had access to CD12 data. The FDA will not allow a drug to continue if they had knowledge it failed.
CD12-OLE-EIND-XW013K6 = EUA
Are you talking about the patent for Leronlimab to not only be a treatment for cancer but to PREVENT cancer? Absolutely incredible, not only treat but prevent cancer.
3 fingers... CYDY will be three figures after approval. Judging by a sudden influx of buying the market is suggesting CD12 will be approved.
Nah, tocilizumab trial data shows Leronlimab mortality under 18%. With these numbers CD12 will be approved.
News leak??
If top line results are good we could get a PR anytime, tomorrow, Monday, next week, the week after. Nobody knows what's going on behind the scenes.
CD12 will get Leronlimab FDA approval
I'm looking forward to the ride. It's going to be an exciting year to be a CYDY shareholder!
FDA is probably drafting their next PR as we speak, Leronlimab is approved for Covid
CD12-OLE-EIND-MEDICARE CODES = EUA
CD12... trial is complete...data at any moment...place your bets
Did it strike a nerve to hear Leronlimab will be approved? Medicare codes, OLE, eIND, and now following in the identical track as Lilly for approval. It's looking good for CYDY. 3 billion in revenue coming in 2021
Makes sense, a big pharma company getting preferential treatment over a small company. Now that's out of the way Leronlimab will get approval.
"COVID-19 Long-Hauler Therapy Space Beginning to Take Shape | BioSpace" https://www.biospace.com/article/covid-19-long-hauler-therapies-space-beginning-to-take-shape/
So you're saying medicare was informed by the FDA that Leronlimab will be approved? That's the reason for the medicare codes? That could be I'm sure government agencies communicate internally.
The FDA approved Leronlimab for OLE and eIND, AFTER having looked at CD12 data. They would not have approved that if what you're saying had any fact.
This is all fiction based on nothing more than your opinion. The trial is blind, you nor anyone else has the data from the trial.
OLE EIND = EUA
That's only your opinion and you're 100% wrong. The FDA determines what is approved not kgromax
The FDA has approved OLE and eIND for LERONLIMAB, this is an indication of a successful CD12 trial. There's no way the FDA would have given OLE and eIND if the trial failed.
Thanks for making point, FOMO ran it up because investors know this stock is going parabolic. The same FOMO shorts and flippers are desperately showing now.
CYDY went to $10 without approval it's going past $100 after approval.
So your "expect" is based on nothing, only your opinion?? So essentially hoping and praying for no approval? The FDA expects Leronlimab to be approved, that's the only logical reason they would have allowed eIND'S to resume. Is your opinion the FDA is wrong to allow eIND for Leronlimab?
But who knows..maybe the FDA will see the sad talk on message boards, feel sorry for the shorts and help them out, that's always a possibility.
What type of analysis is "expect"? How did CYDY get to $10 without an approval? If it can get to $10 without approval do you expect it to go much higher after approval?
Thanks to Leronlimab there are hundreds less. After approval that number will be in the thousands.
That's where your getting confused. The long term trend line from the 52 week bottom is up over 700%, that's an incredible gain! The 52 week low was .79 cents.
That you tube channel also has a paid subscription you can look into.
I heard the wall socket was the style used in the Philippines. That would mean NP was in the Philippines finalizing contracts to sell Leronlimab.
I think the wall socket is a much more important subject.