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This is to easy, discussion over. Cytodyn did not fail a thing, it won it just needs a stamp of approval, ink pad ready
Show me proof---all I'm asking and we close the conversation - PROOF THAT CYTODYN FAILED???? Cytodyn will get an EUA, wait and see
Oh man, I gotta really laugh-
Did the FDA say anything about failure?
Did Cytodyn say they failed?
Show me one stitch of evidence that it failed, not your opinion, show me something factual besides a hit piece without an author
Door kicks in-
Anybody know who did Bobby Lupo????
Anybody have proof that Cytodyn failed the trial???
Anybody????
Come on man, show me some stuff, when did Cytodyn fail the study??
Anybody???
FDA say it???
Who said it?
Where's the proof???
Was a pumper? So he pumped Cytodyn for what type of gain? I guess you didn't hear but he "pumped" again today with a letter to the FDA.
Interesting take on Dr. Yo, being like a sidekick.
Let me remind you, these two are doctors who took and oath. They don't have to "pump" anything, financially I'm sure they live comfortably.
Have anything that shows Dr.Paterson is delusional? Google searches? Criminal records? You claimed DR Agresti was sued right? Where you right about that?
How can all the doctors and hospitals involved in the Cytodyn trials be wrong? Hmmmmm, highly doubt that. So, evidence of the failure ive been asking about?
Well, Egypt hasn't met Dr. Patterson and Leronlimab yet, speaking of denial, why makes you think Leronlimab will not get the EAU that it is so well deserved after it passed the trial? Not one bit of evidence that showed it failed
Dr. Paterson explains it in 1 tweet- To those that call Leronlimab a failure are dead wrong- I guess you know more than he does about medicine? I challenge anyone to show me proof of failure. You can't produce a stitch of facts or any documentation of it so lets move on and watch Cytodyn do its thing and save some lives.
Dr Jay Lalezari has just written a letter to @DrWoodcockFDA at the FDA about the strategic importance of #Leronlimab CD12 results and posted it over on his Quest Clinical Research website. Here’s a link to the pdf:https://t.co/1e7OlvrvBP
— Kevin G. O'Neill (@kgo81) March 16, 2021
Nadda, nothing, zero response. Funny thing, no one can produce a bit of proof, evidence or anything for that matter than Leronlimab failed, amazing. But, they will just keep saying it did.
Misiu, I agree with you. Frustrating when the punishment handed down is so lean it's a crime.
Yes sir, files and about 110 emails and screenshots- Cytodyn will get what it deserves - approvals with the FDA. I'll do whatever I can to bring this to light with the FDA and the SEC when called upon.
Misiu, investigations take time. Wherever the evidence takes you, you then have to seek proof through various means to prove that an individual(s) has suffered either a loss or harm. Then you have to identify the person(s) involved as to what capacity. This can take a great amount of time through computer forensics, telephone records, geo graphing , interviews and document reviews. There's no doubt in my mind that Cytodyn would prosecute if the evidence and proof is presented to them. I highly doubt that it is on their to do list.
Sometimes you get lucky, someone has a history or bad blood with someone involved and they provide all the evidence and testimony you need, done deal.
There's a huge difference between lawsuits and criminal activity to gain profit. Cytodyn and the shareholders would sign criminal complaints to make sure justice would be served. Again, Cytodyn and shareholders suffered great financial losses on 6/30, this won't just go away without someone taking the fall for it.
I'll ask again, obviously I won't get an answer but I'll waist a post on it- where is the cold hard proof of this alleged epic fail? How did Cytodyn fail? When? If you have any information, Ill ask again, send it to me. I also would like to know how accurate is the information that you are getting? More specifically, how honest are people that gave you this information? Send this to me and I'll give it the attention it deserves.
I'm almost positive that that's our boy. If it is, I will dig, dig and dig as deep as I have to to link him to it. Once all the evidence is collected and if ties are uncovered, that info will be in Naders mailbox within hours. Like I said, Cytodyn was hurt that day, Cytodyn will return the favor with a little help.
Any proof of those allegations? I highly doubt Cytodyn is a scandal, fraud or anything else thats assumed. Statements like that require some facts or at least proof. There's none. Cytodyn will win FDA approvals no doubt.
JLA, an investigation of the 6/30 hit is on, this I can assure you. Cytodyn shareholders suffered tremendous loses that day. I'm working on that as well.
I think it's time I start investigating these law firms and find out exactly where they are getting the initial push from, not a problem at all to achieve. This is the 200th time this is being done to Cytodyn, no doubt there's a person or person(s) lighting the fire.
Thanks C- I'm on a mission not to boost SP but to save some lives. Like we've all been saying 125K more would be alive today if Leronlimab was allowed to do it's thing.
All is great in CYDY land!!!!! In fact, about to get better!!! I have a meeting ( face to face) scheduled with a very powerful lawmaker who I've worked with before in DC. My boots will be on the ground this Friday at 7 am in DC for other work BUT lunch will be interesting. So far, he seems really interested in the FACTS which I will gladly make him aware of, he'll run the ball into the end zone. Like I said before, being in the Federal sector has it's perks- this is the one favor I'm calling into all my contacts- LOOK AT LERONLIMAB!
Oh, yeah, things are great in CYtodyn land, see below:
1. When leronlimab was used in addition to “commonly used COVID-19 treatments” a clear benefit was seen in the primary endpoint of all-cause mortality at day 28 with an absolute risk reduction of death of 6.5% with a relative risk reduction of death of 28.1% (N = 309, p = .0319).
2. When leronlimab was used in combination with dexamethasone, a clear benefit was seen in the primary endpoint of all-cause mortality at day 28 with an absolute risk reduction of death of 5.7% with a relative risk reduction of 26.2% (N=233, p=.055)
3. The mean length in hospital stay was decreased by 5.5 days in the critically ill population (p = .005)
4. Mortality status at day 28 when leronlimab was used in addition to “commonly used COVID-19 treatments” in the critically ill population with an age < 65 showed a clear mortality benefit with an absolute risk reduction of death of 20.9% with a relative risk reduction of death of 73% (N=40, p=.03)
5. Leronlimab, when given to critically ill patients on dexamethasone, showed a clear mortality benefit at day 28 with a 6.5% absolute reduction (corresponding to a 23.5% relative reduction) in death risk (N=35, p=.04)
6. Length of hospital stay in critically ill patients < 65-years-old showed a clear benefit with a reduction of 6.8 days (N=44, p=.006)
In addition, there were no safety signals seen in the leronlimab group versus placebo. Based on this data, the company is continuing its regulatory talks with the FDA, MHRA, Health Canada, the Philippines, and Brazil. The data supports the use of leronlimab worldwide and shows superiority to dexamethasone which is the current Standard of Care (SOC).
Oh question, is there any documents or facts that you may have that support your claim of Leronlimab being saline? How about that it failed?
Just shoot those over to me, I'll make them available to my contacts
This is exactly what is going to happen with Cytodyn:
Patient testimonials and letters written to Dr. Woodcock regarding a drug to treat Muscular Dystrophy changed the outcome. After parsing a 12 patient trial that many in the FDA said showed no efficacy of the drug eteplirsen, Woodcock pushed (and pushed hard) succeedingin getting approval.
"Patients, their parents, their congressmen, and drug maker Sarepta Therapeutics all lobbied the FDA hard for approval, writing heartbreaking letters and flooding public hearings to beg for access to the treatment.
I'm hoping for this week, I'm sure the guy has quite a busy schedule.
Pulled some strings, called in some favors, looking to get a conference call with Andrew Tantillo, Acting Associate Commissioner for Legislative Affairs from the FDA. Wonder of he knows what's going on? I'll certainly ask!!
I have no doubt. I know how federal agencies work, they are easily swayed by political pressure and media attention, I bet that EUA comes through in no time.
I just sent the article over to a very good friend at FOX and CNBC. Her response was " wow". She is going to reach out to Nader!!!
Show me proof that it missed endpoints- not a post, show me facts
Portage, I'm a visual type of person, show me evidence it failed. Just one shred. In my world, it's all about evidence- you have zero. Leronlimab did not fail a thing, the trial proves its better than anything else out there. Thats a fact and there's evidence, see the difference?
I don't think we'll have to wait that long. Imagine if the press was to do a story on how other drugs that scored worse than Leronlimab in trials got approved and Leronlimab was denied? Can you imagine if the general public found out that if Leronlimab was approved based on the facts and figures of the trial, 125K people would still be alive? Now, imagine of a heavy hitting politician knew about what transpired at the FDA? Imagine a activist group getting wind of Leronlimab not being approved because of big pharma influence? Imagine if the rumor of paid big pharma bashers was to be proven true? Do you think the FDA would then do a 180??? I do. Media influence in todays society especially corruption does wonders for the good guy.
Thats in phase 1, has some safety concerns and is for mild to moderate. Apples to oranges when it comes to Leronlimab
BUT better than any other drug out there, wait until the FDA takes another look at Leronlimab, I'll bet you'll see a PR with a picture of an approved stamp on a cover letter.
Find me one stitch of paper or a link that says " failed". Leronlimab performed much better than any other drug in severe to critical. It will get an EUA as soon as the FDA cuts the corruption and BP influence out of the equation.
His words were either weekly or every two weeks as per the CC
I have several friends I've reached out to regarding if a EUA needs to be filed for or can it be given without the paperwork. Seems like a 50-50 split. One friend told me he's heard of conditional EUA's awarded then followed by the necessary filing. We can only wait and see.
Dad, let me remind you of this:
17:50 Drs. Mahboob Rahman Harish Seethamraju, Nicolas Agresti, Chris Recknor, Kush Dhody, Kazem Kazempour, believe the results are very strong to warrant conditional EUA while Cytodyn generates more data. We are working on all avenues for this immediate conditional EUA while we conduct a small 140 patient trial to support our data. That protocol for the 140 patients has been submitted and would be conducted at the same sites as the CD12 trial so things could go very quickly.
This is far from being over regardless of what's posted on here- the EUA can come with the flip of a switch
Nader is nothing but a spokesperson within the Cytodyn wheel. It's the hired guns doing the heavy lifting.
Oh really? The SEC never announces an investigation? Truly an ignorant statement, I've dealt with the SEC before on many levels, I deal with many, many federal agencies on a daily basis, it's my bread and butter so telling me about investigations and everyone else falls on deaf ears.
All of your statements are not facts but opinion, so really means nothing.
So, Cytodyn is needed in the EU now? Amazing, i guess triple digits are a reality
Another bogus investigation. If there was anything to investigate the SEC would have launched it. This is just simply a " cast the line out" to see if we can get enough shareholders on board to even try and build a case. This will go nowhere just like the others and their record as a law firm is not very impressive at all. Cytodyn will prevail with FDA approval, they will do a 180 because there's quite a few politicians now asking " how could a drug with these numbers NOT get approved? " wait and see.
means absolutely nothing. When VIR is told to stop their trial from the DSMC, I don't care what their cap is, they are finished. Lucky if they last another week into the trials. Cytodyn on the other hand has continued and completed their trial without DSMC interference, just praise. FDA will do a 180 and approve this soon in my opinion.
They can only wish to do so. Cytodyn will be the SOC for severe to critical.
After this statement from the DSMC that drug is due to fail and Cytodyn will take the mild to moderate treatments as well
"Although VIR-7831 met the initial pre-specified criteria to continue to the next phase of the trial, early sensitivity analyses of the first 300 patients enrolled in the trial have ‘raised concerns’ over the potential benefit of the drug in this setting.
As a result, the independent data and safety monitoring board (DSMB) has recommended that enrolment for the VIR-7831 arm of the trial should be paused while the data matures"
Bye bye
A lot of responses to Dr. Woodcocks twitter account! I think she's aware of Leronlimab,a lot of pro leronlimab tweets!
Thats what Leronlimab does! Thanks for the great news!
I had to travel for work wifi was spotty at best- that's where I've been to all asking