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Really? Why is there an " add to basket" icon for Leronlimab. they do sales to. Check it out....
https://www.creativebiolabs.net/Anti-Human-CCR5-Therapeutic-Antibody-13791.htm?gclid=Cj0KCQjwo-aCBhC-ARIsAAkNQiulB1-5KHaiEK1IBFudK3aG4M650bx3CyGVNd51_fJllUgHEMhaE2oaAlIsEALw_wcB
It's very obvious, like I said, getting ready for sales
Google this:
creative biolabs leronlimab
Looks like they are getting ready for sales. Cytodyn well on it's way based on todays intel I've received, looks like a definitive winner
Don, I deliver but no pizzas, with my intel, it took about 4.7 minutes to determine that Cytodyns offices are occupied, phones are on and lease is good.
C-20- thank you friend.
Another key finding as of today:
Punch this in google
"buy leronlimab creative biolabs"
When an accusation is made and it needs proof positive evidence to prove it's true right?
Like If I told you that Leronlimab will soon be for sale, would you believe me? No right?
But if while being asked during questioning and you asked me- Can I buy Leronlimab?
My answer would be yes.
You would say- BS I dont believe you
Then the right thing for me to say is, Oh it's true, google this:
"buy leronlimab creative biolabs"
OMG, there's your proof right?
So I'm not lying- so yes, a hardy boys nancy drew investigation is required to prove false statements
Anyone have an answer to my previous post??
There was some posts about Cytodyn that made some accusations and I wonder if anyone came up with anything in regards to
An info on the supposed failure?
Any info on the offices being empty? The lease? ( someone was going to see if their lease was active)
Info on the " street" email address? ( cytodyn was accused of using a street email address????)
I would guess at this point these accusations were false??
There was some posts about Cytodyn that made some accusations and I wonder if anyone came up with anything in regards to
An info on the supposed failure?
Any info on the offices being empty? The lease? ( someone was going to see if their lease was active)
Info on the " street" email address? ( cytodyn was accused of using a street email address????)
I would guess at this point these accusations were false??
Directly from my email to the FDA requesting if a conditional EUA exists, i guess it does- end of story
With respect to the emergency use of an unapproved product, the Secretary, to the extent practicable given the applicable circumstances described in subsection (b)(1), shall, for a person who carries out any activity for which the authorization is issued, establish such conditions on an authorization under this section as the Secretary finds necessary or appropriate to protect the public health, including the following:
(ii)Appropriate conditions designed to ensure that individuals to whom the product is administered are informed—
It was added March 19th, confirmed already-
What about this recent bombshell, notice the word APPROVED:
CODES FOR APPROVED MONOCLONAL ANTIBODIES
The 10 codes for approved monoclonal antibodies represent four specific types: Bamlanivimab, Etesevimab, Leronlimab, and REGN-COV2. Note that Leronlimab is injected subcutaneously, while the other three substances are administered intravenously via either central or peripheral vein. Three codes for non-specific approved monoclonal antibody substances via intravenous or subcutaneous injection are also included. This will allow for the coding of other monoclonal substances that may be developed in the future to treat COVID-19.
The codes are:
XW013K6: Introduction of Leronlimab Monoclonal Antibody into Subcutaneous Tissue, Percutaneous Approach, New Technology Group 6
LOL...OK. Can't twist this one, it's an SRO which was added March 19th, it's not an "update" it's just another step towards Leronlimabs approval
Where I got it is not important but we're on our way. read the meaning of an SRO, I would say the FDA is working on some sort of approval and regulation with Cytodyn
Wrong, just added March 19th, read the meaning of an SRO, didn't expect this to not be chewed up and twisted by some but IT'S SIGNIFIANT, take it any way you want it. Leronlimab is well on its way
Cytodyn has been added to the FDA's SRO list on March 19th, clearly well on our way to approval of some sort
SRO meaning :An organization that does not have a record of sales of FDA-regulated products will be deemed to be significantly regulated if its operations are predominately in fields regulated by FDA, or if its research, development, or other business activities are reasonably expected to result in the development of products that are regulated by FDA.
This is interesting-one of the law firms "investigating" Cytodyn quotes the article by Paul Santos. They are basing their investigation on a guy who does not know the biotech industry and has ties at AF? I'm really starting to feel that AF himself is feeding these lawfirms. We all know AF has ties to PS. This calls for an in depth investigation as to where the law firms are getting leads from.
On March 5, 2021, CytoDyn issued a press release providing an update on its product "Vyrologix (leronlimab-PRO 140), a CCR5 antagonist with the potential for multiple therapeutic indications." The press release stated, in part, that "the Phase 3 trial of leronlimab for the treatment of severe-to-critical patients with COVID-19 demonstrated continued safety, substantial improvement in the survival rate, and faster hospital discharge in critically ill COVID-19 patients." Although the press release touted purportedly positive results, industry observers and analysts quickly characterized the Company's press release as misleading. For example, on March 8, 2021, Seeking Alpha published an article by Paul Santos entitled "CytoDyn: Parsing Failure." The article asserted that Cytodyn's "leronlimab Phase 3 trial on COVID-19 severe-to-critical patients failed . . . to meet both its primary endpoint and all secondary endpoints with any statistical significance" and described the Company as having effectively "buried" the results in its press release. Santos noted that "[a] normal biotech company would have stated this clearly, both in its PR titles and in their text bodies. Cytodyn, however, did something else."
Really? So the building is occupied, and you're saying the Cytodyn offices are empty?
Lets look at this logically, obviously they are operational.
So, Do you have access to the building and grounds?
You heard wrong, I've had many conversations with the Cytodyn staff and I can swear from their offices, I guess when I dialed and they picked up, I'd venture to say they were within their four walls. Any proof of the Leronlimab FDA failure yet? Find out why there's no case number assigned to the "lawsuit" , got a docket number? Why did the first attorney drop the case?
So where did you hear that the offices were empty?
Just in case met me remind you, there's a COVID pandemic. The Federal bldg i work in has been empty as well, staff working in the field or from home. In todays modern tech world, Nader and the Cytodyn team can work from home and not miss a beat.
laughing, that case is closed and done with, see the date? May of 2020? Like I said, these law firms are digging themselves in deep, wait and see how Cytodyn spins the lawsuit arrow going the other way.
A what? A class action lawsuit that doesnt even have a court assigned case number? LOL..please.
The case number on top is NOT assigned by the court system, that's in house.
Cytodyn won't announce a frivolous suit by a bunch of ambulance chasing attorneys that have zero merit and will be tossed by mid week
They will announce lawsuits against AF along with a signed criminal complaint soon along with many others who will be named in the biggest takedown of naked shorting very soon
What If I told you that one attorney already bailed on that suit and another claim filed was found to be deficient? The new attorney will drop this case as well, guaranteed. It' nice to have connections in the court system, we can get public information quickly.
Cytodyn will not even blink on this one, I bet the judge laughs at this.
I gather great factual information from experts, including a former FDA official. I evaluate and base my decision based on facts gathered and how the experts see the data. The FDA has NOT stopped Leronlimab from being used, in fact, I'd like to see how many lives have been saved outside the trial when the drug was administered as compassionate use like the letter I posted earlier.
Your qualifications are?
But the HUGE difference is the trial results, drugs with much worse numbers were approved, no argument there.
Another letter written to Dr. Woodcock, must be even another quack doctor huh? From my intel, Woodcock is receiving letters from Doctors by the hundreds every day.
Dear Dr. Woodcock,
My name is Dr. Joe Campbell and have been a practicing Anesthesiologist in Hattiesburg MS since 1987 and have been the Chairman of the Anesthesia department in our regional medical center for decades.
Mississippi has been hit particularly hard by the Covid pandemic because of our population’s abundance of comorbidities, (hypertension, diabetes and obesity) low compliance in mask wearing and general distrust of the vaccines.
Because of this, we have a larger proportion of critical Covid patients under 65 on ventilators than the rest of the country. We have used decadron on our critically ill patients since it was shown to be advantageous earlier in the pandemic, but as you know, no real advances have been made in the critically ill population since then.
Last year I became aware of Pro-140 (Lorinlimab), a monoclonal antibody that blocks the CRR5 receptor that is currently on track for treatment of HIV. At the suggestion of Dr. Bruce Patterson (who is formally from Stanford), it was repurposed by the drug maker Cytodine for treatment of critically ill Covid patients.
As you probably know, Cytodine’s CD12 trial results of Pro-140 were recently revealed. The study was small and unfortunately, the placebo arm had a much lower average age that distorted the overall mortality results. However, if the data is adjusted for age, a statistically significant mortality improvement in ventilator patients occurred, particularly in patients under age 65.
The study also showed a statistically significant 6 day shorter length of stay in these critical patients.
The fact that Pro-140 could achieve statistical significance with such small numbers is telling. The safety profile from the 1000 plus HIV patients also indicates extreme safety.
I have used Pro-140 on one patient with good results via compassionate use, but this is not a viable route of medication acquisition given all the paperwork involved.
Please have your statisticians review the CD12 study for age adjusted mortality and consider granting a conditional EUA to use on critically ill Covid patients on ventilators (which would be in addition to the current SOC.)
Of note since Pro-140 modulates the immune response and doesn’t directly engage the virus, it should be effective in patients who are infected by the new mutated forms of the virus.
A conditional emergency use approval of Pro 140 (while the drug continues testing) could save thousands of lives and not endanger anyone as there are no known side effects of the drug.
Thank you got your time.
Sincerely,
Dr. Joe Hand Campbell, Jr.
Chairman Department of Anesthesiology
Forrest General Hospital
Hattiesburg, MS
Board of Directors
Hattiesburg Clinic
LOL..not convinced thats why Cytodyn still has OLE's and an eIND in place, ongoing trials and more importantly guidance from the FDA but they are not convinced? LMAO...seems like they are convinced it works and fast tracking. See ya in the winners circle really soon
Yes, put out by a harvard study and doctor, google it. Cytodyn is not mentioned in it
Proof of the "failure"? Funny, thats not how the people who are medical professionals see it, including one in Washington. Leronlimab will be a household name soon. On another note, the feds are quite aware of AF as well, I shined a beam of light on that, it's being looked into
Right, yeah OK, huh huh...quack doctors trying to make a few bucks by treating:
an ongoing low level of inflammation in the brain
an autoimmune condition in which the body makes antibodies that attack the brain
decreased blood flow to the brain, due to abnormalities of the autonomic nervous system
difficulty making enough energy molecules to satisfy the needs of the brain and body.
Inflammation of the lungs
Imagine that?
Leronlimab will save these long haulers as well, in phase 2 and kicking arse
Every drug that has been given a billing code has been approved, what makes you think Leronlimab won't be approved, I'd say the odds are better than ever, we have doctors writing into the FDA with praise and asking for approval. Just a reminder, the OLE's and eIND are still in full swing, Doctors are using it, that's a great sign, no? BTW, find any documentation or facts to support your statement that Leronlimab failed?
Dr. Sanjay Gupta? Yep, listed as a shareholder- see attached:
https://www.cytodyn.com/investors/sec-filings/all-sec-filings/content/0001193125-16-448171/d66206ds1.htm?TB_iframe=true&height=auto&width=auto&preload=false
Agreed.
Does anyone remember who posted that Dr. Nicholas Agresti was sued for malpractice? He's the doctor who treated 4 patients with Leronlimab and published a paper on his findings.
Dont blink- Cytodyn is going to shock everyone soon based on what I'm seeing on the boards from posters who have hooks.
HAHAHA - this is a joke like the other FAKE investigations. Guess who I just got off the phone with? A pseudo non existent firm, like I said before, I'll never show my cards or my capabilities. It's all a short tactic. BTW, working on getting me some proof of the Leronlimab FAKE failure accusation that I asked for 18 times?
Really? Any solid proof the Cytodyn is hurting for funding? Bankruptcy? Where's the proof????? The link I posted totally debunks your theory, comes from a former FDA official. Leronlimab is well on it's way to being a huge name.
The three finger event will happen soon. If Cytodyn gets the EUA here in the US and in other countries, gets HIV then the three finger event gets escalated to a four finger event. Don't blink and don't kid yourself, Cytodyn has made a tremendous amount of headway. Now compiled with shareholders and doctors writing the FDA, I'm not going to be surprised when the SP goes parabolic. You'd be surprised at how fast things change with a phone call from the right person to Woodcock.
I'm in DC now, lunch tomorrow. Hope to make some headway and open some dialogue between the FDA and lawmakers.
I've heard and can confirm there's an active investigation of the 6/30 events. It was brought up to the SEC by a state senator and it hinges on the pumping of Gilead and a leaked video. It all ties into the same person. Cytodyn I'm sure is aware of it as well
Wrong link but here you go, see below. I clarified this with a former FDA official- conditional means that the safety and efficiency of the drug are continued to be monitored while in use- so there you have it, a conditional EUA is real. It's not named that way but it exists.
https://www.fda.gov/media/144412/download
Wrong again as usual- as of yesterday-date at the top
https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section360bbb-3&num=0&edition=prelim
BTW, find those documents or a link that Leronlimab failed? It's obvious that your statement is false.
The fact is that it's better than any other treatment for severe to critical so therefore I would say it won. Cytodyns EUA is imminent
Really? How do you know I havent sold? Assuming doesnt work with me. I may be here for other reasons- maybe I see that Leronlimab can save lives? Could be another reason, like deep undercover stuff too..ya never know