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Hello, Dr M! Question for you and/or Dr Rock (or anyone else):
I read about a young, healthy adult who developed transverse myelitis after receiving one dose of the Moderna vaccine.
Question: Do you think this is a condition that Leronlimab could mitigate or repair?
Thanks!
Great post, C-20, 100%! And it looks like Dr M has been on fire the last 2 days; hope this portends a great week.
GO CYDY, let's save some lives!
Thanks, RTBhub, I read what the lawyers had to say and it seems to boil down to their summary paragraph - "don’t call subgroup analyses from failed studies “really strong” results."
My initial thoughts:
1, Subgroup or not, why didn't these 3 lawyers acknowledge the amazing success of LL in reducing mortality after 7 and 14 days? Subgroup, large group, whatever, have they ever seen better results? If you're looking for something, anything to fight a virus in a pandemic, why would you NOT get excited about such a strong - and completely SAFE - drug like LL?
2. Why didn't these lawyers question why Cytodyn gave only 2 injections and not 4? Since they mention NP's alluding to the possible results at 3 weeks and 4 weeks, why didn't they say something like, "Yes, NP did raise an interesting point, I wonder why they were limited to just 2 doses?"
3. Why didn't these lawyers acknowledge our subgroup was overly weighted by 3:1 with the most vulnerable (elderly) patients? Did they not find it at all noteworthy that LL treated the sickest with such great success?
4. Instead of dropping dynamite (FDA letters) on minnows (CYDY), did these 3 lawyers ever castigate the FDA for allowing Pfizer and etc to slide on not releasing their vaccine safety data? Did they ever question why Pfizer was allowed to roll their control and test groups into one large bloc of patients, something that is NEVER supposed to happen? Did they ever criticize the FDA for approving Remdesivir? Did they ever admonish the FDA for not approving any other therapeutics besides Remdesivir, a decision that has led to 100's of thousands of deaths and untold suffering?
Amazing how these lawyers can't see the forest for the trees. They hold a small start-up biotech with no commercial footprint and no access to patients to the most grammatically correct phrasing in a Proactive video with an audience in the hundreds while keeping their mouths shut about the most abominable handling of a viral pandemic in history.
On a more positive note, we're 1 week closer to the Big PR, so hang in there and GO CYDY!
Have to disagree with you on this, C-20. When you say -
"maybe people will start to realize what has been a viable drug all this time but has been held up for political reasons,"
- I think the last two years of how the FDA/CDC and the tech/news media have responded to the pandemic does not bode well for a public awakening.
When the media and health bureaucracies politicize the science, hide the vax safety data, hide the hospital data, and de-platform anyone who counters the CDC/FDA narrative, the awakening will be a slow glacial thaw, at best.
I hope I'm wrong. But right now, I think the best and only options CYDY has are to either get traction (approvals) in another large nation, or team up with a big pharma.
Science and clinical/statistical efficacy are not enough. The reality is BP and govt bureaucrats hold all the cards and, caring only about revenue streams and power, are irredeemably corrupt.
Great post, Dr M! And to follow up, I'm pasting in an article I just read re: how Ivermectin was sabotaged back in the fall/winter of 2020. If you just substitute "Leronlimab" (or any other effective COVID 19 therapeutic), everything rings true.
Article:
LIVERPOOL, England (LifeSiteNews) — Providence will occasionally place a man at a key juncture of history, a position of great moment where the fate of millions lies in his hands.
Andrew Hill, M.D., was just such a man, in just such a position. In October 2020 he was asked by the WHO to review the rapidly accumulating evidence that Ivermectin was a safe and effective treatment for COVID.
To say there was a lot riding on Hill’s findings was an understatement. If it turned out that this generic drug, cheap to manufacture and already widely available, could knock out COVID, then it could be rapidly deployed. Countless lives could be saved.
Hill seemed eminently qualified for his assigned task. A?senior visiting Research Fellow?in the Pharmacology Department at Liverpool University, he had been researching viruses and their treatments for 30 years. He was also, not incidentally, an advisor to the Bill and Melinda Gates Foundation as well as the Clinton Foundation.
No one would call Dr. Hill’s competence to perform such an evaluation into question. But, as we have seen throughout the COVID pandemic, competence is no substitute for character. Or for courage.
As Hill assembled his data, he was more and more impressed by what he found. He made a presentation to the NIH with other advocates of Ivermectin and spoke in favor of its use. On December 29, 2020, he wrote on Twitter that “Ivermectin is showing effects on viral clearance, hospitalization and survival across a wide range of randomized trials in different countries.” He even admitted that if his 58-year-old brother got COVID, he would give him Ivermectin.
He told the front-line doctors with whom he had been collaborating up to this point, who themselves had saved thousands of lives by using Ivermectin, that his report was almost ready. They were anxiously awaiting its release. And they weren’t the only ones.
Big Pharma was watching too. They had developed an?experimental gene therapy?to treat COVID. But this “vaccine”—as they were careful to refer to it—could not be approved by the FDA if there was an effective therapeutic drug available. If WHO said that Ivermectin was safe and effective, they stood to lose hundreds of billions of dollars in sales.
Dr Hill’s report, when it came out on January 18, 2021, was chock-full of evidence that this cheap, widely available drug was the weapon that humanity needed to defeat COVID. But instead of reaching the obvious conclusion, he punted: “Ivermectin should be validated in larger appropriately controlled randomized trials before the results are sufficient for review by regulatory authorities.”
As soon as Hill published his paper—in a preprint, rather than a refereed scholarly journal—as if on cue, a massive campaign to discredit Ivermectin was unleashed.
The front-line doctors were shocked and heartbroken. Why did Hill effectively kill the most promising therapeutic drug for treating COVID? Who had gotten to Hill? Who had forced this wrenching conclusion on him?
Dr. Tess Lawrie?has now answered?that question. In a brilliant?18-minute video?(also available on Rumble?here) she recounts her interactions with Andrew Hill, including video of a final Zoom call in which she begs him to rewrite the conclusion of his paper and save lives: “Come out in support of Ivermectin,” she pleads. “You know the science supports it. We can save lives. People are dying unnecessarily.” ?
Dr. Hill hems and haws and finally—with guilt written all over his face—says he will come out in favor of Ivermectin “in six weeks. … I’m doing everything I can.”
Dr. Lawrie replies, “You’re not doing everything you can. Doing everything you can would involve saying to those people who are paying you that, ‘I’m not going to support this.’”
Hill didn’t come out in favor of Ivermectin in six weeks—or ever. Instead, he went full anti-Ivermectin. On October 1, 2021, we find him on Twitter advertising a lecture he was slated to give. It was entitled “Effects of Bias and Potential Medical Fraud in the Promotion of Ivermectin.’” The sell-out was complete.
So who were “those people,” as Dr. Lawrie calls them, who were paying Hill? She asks him repeatedly to tell her who pressured him to alter his conclusion. Again and again Hill bobs and weaves, telling her that he’s in “a tricky situation.” He finally admits, while looking away from the camera in embarrassment, that “Unitaid” had a hand in making revisions to his paper.
Now Unitaid happens to be the very health-related NGO that helped to sponsor Hill’s meta-analysis in the first place. His paymasters, if you will.
And Unitaid is a very big deal: an affiliate of the World Health Organization, it has awarded billions of dollars of research grants since its founding in 2006.?And on January 12, 2021, just a few days before Andrew Hill torpedoed Ivermectin, Unitaid awarded another grant. It shoveled out?$40 million in funding?to Dr. Hill’s other paymasters, the University of Liverpool for a “long-acting medicines centre.”
Millions of families have had to bury a loved one because a cheap, safe, therapeutic drug called Ivermectin was denied to them. Instead, we had to become human guinea pigs for experimental gene therapy so Big Pharma can reap huge profits from guaranteed government contracts with zero liability for vaccine-related side-effects and deaths.
One of the most galling facts about this entire episode is that we all know, perfectly well, what the Andrew Hills and Anthony Faucis would do someone they loved or valued came down with COVID. After all, Hill himself admitted that if his 58-year-old brother came down with COVID he would give him Ivermectin.
They know it works. That’s why hundreds of Congressmen and their staffers have taken it. And that’s why Joe Rogan and Aaron Rodgers have taken it.?
But don’t you dare ask your doctor for it. He’ll tell you it’s a horse de-wormer.
—————————
Steven W.?Mosher?is the President of the Population Research Institute and the author of the Politically Incorrect Guide to Pandemics (Regnery Press, available for pre-order now)
Great find, money! Looks like the only current treatment options for triple neg breast cancer are surgery, chemo, radiation therapy, and Trodelvy.
And since we seem to have beaten Trodelvy's avg survival duration by at least two weeks - and combined with LL's lack of SAE's - we're looking good if we hear LL has added another 2 mths to the survival average.
Hoping and praying for some great updated results!
Appreciate all your posts, LABZ, thanks for all your enthusiasm and research.
I find it pretty amazing that after 2 + years of COVID 19 and its variants, every national health bureaucracy still marches in lockstep re: vax and lockdowns as the only arrow in the quiver. And this despite the vax efficacy that continues to drop and the SAE's that continue to rise.
Meanwhile...the world's absolute best, safest hope for those suffering the most from COVID continues to gather refrigerated dust.
So, what singular event will break the logjam? An EUA in some foreign nation? Macron or Trudeau or Biden being saved by LL? How about the CEO of Pfizer or J&J being saved by LL, would that do it?
This is really an Allen in Wonderland pandemic (Allen also swims on the UPenn women's team). People die, the world wails in panic, and Leronlimab sits in the stands with a beer.
Madness.
Good Morning, Dr M! Question: Do you find it strange that Brazil is experiencing such high infection rates during their summer? Doesn't the COVID virus spread more readily during the colder, less humid months than during the warmer, more humid days of summer?
Money, if you or other business-savvy posters have time - I'd like to know your thoughts on the 8k bond financing - and also on David Welch, who I don't think I've heard of before today. Could you tell me why you think he might be a good pick for CEO - and why you think might be in the running for the job?
Appreciate your knowledge and posts!
Three Questions on Time:
1. Is there a typical or "usual" amount of time it takes for a small biopharma like CYDY to negotiate a partnership deal?
2. If so, how long does it "usually" take? 30 days, 60, 90 or more?
3. And does a Buyout typically require more negotiation time? Any estimate on that?
BONUS QUESTION: Which has precedence - an NDA that pauses all PR's to investors - or the legal requirement that any material news be reported within 4 business days?
These animal results sure sound good! Is this data from a recent study?
Thanks for the detailed reply, Buddyboy20! I didn't know Cytodyn was able to "reconstruct their trial information, by researching the HIV trial site information." That is great news, I thought Amarex held all the cards.
In retrospect, Nadar must have been in a very difficult spot before he went public with the revelations on the failures of our CRO. The shareholders were screaming for BLA submission, but Amarex, apparently, always had enough plausible excuses/lies to keep stringing NP and the board along.
I'm sure NP didn't want to believe that a CRO could so thoroughly obfuscate and botch things up that it would, in retrospect, look deliberate.
To debtors prison for Amarex,
Onward CYDY!!!!!!!!
Worst case question: what happens if large swaths of Phase 3 data were not saved by Amarex and/or deliberately destroyed? Would Cytodyn have to redo the entire Phase 3 trial?
And could that have been the point all along, to delay CYDY as long as possible?
Sounds too sick to consider. Then again, we are talking the reach and power of BP. If they could leverage their influence to suppress excellent/cheap therapeutics the last 2 years - and let hundreds of thousands suffer and die - would they not be capable of scheming with a CRO to sabotage CYDY?
Sincerely hope I'm wrong.
I get it, Cytodyn doesn't have the money or influence of a BP.
I've been incredibly naive about gov't agencies and pharma companies up until I discovered CYDY almost 2 years ago.
Just can't believe our own gov't health agency can be so corrupt.
Leronlimab could be the closest thing we have to a medical miracle, and our own health agencies do everything they can to bury it.
Guess we need to show such incredible results that another country takes notice and says the hell with the FDA, we want it.
Re: this mAb called bebtelovimab (EUA authorized today to treat mild to moderate cases of the coronavirus), does anyone know how their study results compare with out NEWS2 results from 18 months ago? Wasn't NEWS2 also a mild-to-moderate COVID cohort?
I got the following off the YMB for side effects:
"Possible side effects of bebtelovimab include itching, rash, infusion-related reactions, nausea and vomiting. Serious and unexpected adverse events including hypersensitivity, anaphylaxis and infusion-related reactions have been observed with other SARS-CoV2 monoclonal antibodies and could occur with bebtelovimab."
Would it be fair to say our mAb is at least as good as Eli Lily's mAB, but Leronlimab is a much safer drug?
Does bebtelovimab have ANY advantage over Leronlimab?
A partnership with Qilu sounds plausible, but is this something to root for? Is China not notorious for stealing/copying intellectual property?
Qilu may present themselves as a private company, but the CCP controls all.
Don't want to be a killjoy, but I would feel much better partnering with a BP outside a communist nation.
Posted by "M" on YMB:
"drD22 minutes ago
I have been waiting to tell the longs about a second end stage cancer patient I now have for whom I advocated to get Leronlimab even after Dr Nader stated they were stopping right to try . Yesterday she asked me to tell her story as she wants all of you to know and thank you for helping saving her life . She’s 44y/0 and has end stage ovarian cancer . She is the mother of 3 boys under the age of 13 . After her little one was born 4 years ago she was diagnosed with ovarian cancer . Since then , she has had 157 chemotherapies and 10 radiation therapies and 2 major surgeries to literally “scrape” the tumors and metastasis from her abdominal cavity and mesenterium.
Has been sent to hospice 5 times in the past year . Yesterday was her Leronlimab #10 monotherapy. Yesterday her MRI showed shrinkage of all her Metastasis on her liver and mesenterium. Her pain in her pelvis that she’s had for 4 years is gone since Leronlimab #2 . Her ascites from mesenterium weeping is almost resolved . She says she feels better for the first time in 4 years . I will be posting her story with with her name and pictures on twit not2shabbe as per her request . Her oncologist is stunned and elated as he had told her he couldn’t give her anymore chemo and sent her again to hospice .
So yes , Know what you Own longs and thank you for making this miracle happen . Her 3 little kids were crying for joy and cheering yesterday and all of you helped this happen . It was Christmas yesterday for this family ?? of Life arrived ."
Thank God for her recovery, and GO CYDY!!!!!!!!!!!!!!!!!
I think it's unfair to blame NP for everything. Look how the FDA stacked the deck against therapeutics for the pandemic. Look how our CRO sabotaged the data. There have been and continue to be major BP and govt forces aligned against CYDY, and I don't think it would have mattered who was driving the ship.
Some may not like NP's style, but when dealing with corrupt govt organizations on a tilted playing field, it's hard to fairly judge.
Thanks for all the replies, it sounds like most think a partnership is the reason for the silence. Don't know how long this whole partnership dance lasts, but Chuckles is right, the silence is deafening.
Then again, so was the reaction from my brother - who I told 15 months ago that $5.00 was a great entry price - when we went sub-50 cents.
Maybe tomorrow, maybe next month, looking forward to some game-changing news!
moneycrew and Chuckles and C-20 and LABZ and etc - what do you think the most likely reason for the cnx'd conf call and continued silence is?
- Negotiations in progress for a partnership on one indication (NASH)?
- Negotiations for a company buyout?
- No imminent partnership or buyout, just getting the new house in order and adopting a more restrained practice of issuing PR's?
Just wondering where the business evidence points and if/where there is consensus on the continued silence.
Thanks!
My guess on why the FDA pulled the mAb treatments is they were a perceived reason/excuse for people not to get vaxxed. I don't have any proof, other than the entire history of the FDA/CDC the last two years, i.e., it's BP vaccines or nothing, no therapeutics allowed.
Strange, though, that at this late stage of the vaccine game - after so many billions have been earned and the vaccines are actually showing negative efficacy against Covid (Israel) - that they would ban these mAbs now. It can't be for safety, not if they still allow the vaccines.
Then again, the FDA/CDC can do anything they want, they lie and kill and sleep just fine, no 3 AM FBI Swat Team visits for them!
Hoping this is the week for some AMAZING good news.
And if you're reading any of these ihub messages, N.P., good luck and God Bless you and your family, thank you for all your passion and hard work!
Just saw where Oxford researchers announced a new super-mutant HIV strain has been detected in the Netherlands.
I've also been reading where some new COVID strains have been detected, most recently the BA.2 variant, more stealthy and possibly more infectious than the current player.
But from what I understand, LL doesn't care about new strains of HIV or COVID, it just blocks the CCR5 receptor and doesn't allow attachment.
Is that not a hell of a weapon?
Is there any other drug in the world that can do these things...and also fight cancer and NASH and about 87 more lethal conditions?
The length of time it takes the FDA (and the world) to approve Leronlimab is directly proportional to bureaucratic malfeasance and Big Pharma rot.
Had the FDA done the right thing and approved LL for an EUA, we wouldn't now be seeing headlines like this:
Wed Feb 2, 2022 - 10:19 am EST
LONDON (LifeSiteNews) – Britain’s Office for National Statistics (ONS) has released data indicating that children who received the COVID-19 jabs have suffered a death rate 54 times greater than that of their un-jabbed counterparts.
FDA/CDC/NIH/Fauci, how much blood is on their hands?
We're starting to find out.
Great summary post, Dr M!
I'd love to see you restate this info for Sen Ron Johnson when he holds his next Covid hearing.
It really infuriates when I read comments about how CYDY shareholders - for the most part, American citizens - shouldn't call, critique, or complain to the FDA.
Whatever their titles, FDA bureaucrats works for us, and we'll question their words and actions for any reason or none. They are not kings, we are not serfs, and hopefully, someday soon, those who promulgated the lethal double standard for safe therapeutic (LL) vs unsafe therapeutics (remdesivir) and vaccines will be prosecuted to the maximum legal extent.
Nadar's strength:
This undoubtedly has been said before, but it just occurred to me that the only way a team voluntarily gives up a player with a strong or rare talent is when they can either replace that member, or the player's talent is no longer needed.
So for team Cytodyn, I believe Nadar himself had said that his greatest talent was raising money, this is what made him unique/valuable for CYDY.
Therefore, since he was released, it could very well be that either they have another CEO lined up who's just as adept at raisin g money - OR they don't need that money-raising skill set anymore because of an impending partnership worth a lot of $$.
Go CYDY!
I hear your frustration, Emergcy. I've been invested since March 2020, so I'm coming up on two years and, unfortunately, an ugly SP decline.
But I'm not going to sell. Not to take management off the hook, but since I'm not a business guy, since I don't know what really went on in those Vancouver halls, I can't fairly judge NP's reign.
However, after doing a lot of research into our government's response to COVID 19 - after being dumbfounded by their active suppression of safe and effective therapeutics and witnessing how worthless/dangerous big pharma drugs get quickly approved - I'm fairly convinced we could have put the Tom Brady of CEO's in charge, and we'd be in the same boat re: approvals.
I don't know what it will take to smash the FDA/CDC/NIH corruption - hearing Fauci announce a series of vaccines for 6 month old babies gives me little hope - but if there's one drug that can soar, it's Leronlimab. I don't want a buyout, not yet, but I do hope we get a strong partner for an indication like NASH. I really despise Pfizer and all the rest, but a BP may be the only way in.
Regardless, always enjoy your posts. Good luck!
Prediction for tomorrow, pop or drop?
Question re: Quiet Period
I just read on the yahoo board the following comment from 'suacier:'
"During a quiet period, a publicly listed company cannot conduct any pr’s or make any announcements about anything that could cause a normal investor to change their position on the company's stock, like BUY."
Does any corporate legal or stock expert know if this is true?
If so, it sure seems to fit Cytodyn right now, especially considering how often they communicated in the past.
Was anyone else dreading a Friday PM bad news PR?
Fortunately, I was yet again proved wrong. And at this point, given the cnx'd webcast and no PR's or Proactives, I'm 60-70% convinced the next announcement won't be just good, it'll be the inflection point for NP's predicted climb toward $100 +
Question: is there actually an SEC mandated "quiet period" that prohibits publicly traded companies from communicating with shareholders while they're in negotiations for partnerships or other like events? Is the company prohibited from releasing ANY press release during this period, even something not related to the pending event(s)?
Should be an interesting week!
And if the quiet continues, the pressure only builds.
Plummeting SP, scheduled webcast, cancelled webcast, no explanation, expecting a screaming SP dive only to see a 26% rise on big volume...
This week gets my vote (no dropbox) as the strangest week in CYDY history, at least since March 2020.
Excellent summary of current situation, the following is from the Reddit "Leronlimab_Times" board and was written by "FireLife619:"
"Samsung:
The bad: We owe $13.5M and were notified by Samsung to make commercially reasonable efforts. Samsung MAY terminate the agreement within 45 days.
The good: Management notified them in writing their intent to commence the agreement before day 45.
The ugly: Manipulators love this. They will pound this narrative forever and try and put the company in a hostile environment on why they’re not answering to share holders.
The truth: Samsung has liked the Covid-19 results in the past and understands the commercial value of Leronlimab.
Personal belief: I don’t think Samsung terminates the contract. I believe there will be a new arrangement made to keep both parties in a relationship.
Sec:
The bad: Posters at YMB have claimed they reached out to SEC about comments. In the 10Q it now lists mTNBC. The last person I remember doing this with the SEC (to the best of my ability) was affiliated with IncellDx and had 200K promissory notes with them.
The Good: the company has previous PRs comparing the approved mTNBC drug and the chemotherapy data. We just need significant data soon.
The ugly: Manipulators will demand to see the data.
The truth: It “could” be a new application and it MAY be 60 days. We will find out soon. However, many share holders note that we are shooting ourselves in the foot. Maybe some share holders are impatient, maybe some are not actual share holders and they want to know the data, so big pharma can manipulate theirs to keep extending the goal post. Bottom line is, the FDA said our drug is slightly better than an approved drug in Oncology that was bought for $21B. Shareholders know that’s just (1) of our 32+ indications.
Amarex:
The bad: we already know they screwed us. And now we may have in question of a $6.5M bond, something that could be delayed for several months if the company doesn’t have it.
The good: Naders proactive video was really him being proactive. He said we had about $8M and the last time he re-assured us, we didn’t go bankrupt at the end of the year. A loss the narrative was told all year didn’t happen.
The ugly: They will continue to use the bankruptcy narrative.
The truth: We have 187-200M shares to raise money and pay everyone.
Nash:
The good: “In November and December 2021, interim preliminary results were announced regarding the Company’s Phase 2 NASH, 14-week open-label, 350 mg weekly dose, clinical trial. In January 2022, the Company announced it met its primary endpoint in proton density fat fraction (“PDFF”) and its secondary endpoint in cT1 in this trial. This clinical trial compared the changes from baselines in these endpoints in 22 patients.”
The ugly: Manipulators said we didn’t hit end points when we did. They claimed the company didn’t announce 700Mg results because the results were bad.
The truth: Historically, 700Mg have yielded better results than 350Mg. Also, WE DON’T HAVE THE RESULTS YET. “The Company is evaluating the results of the other part of the trial, in which 50 patients received a 700 mg weekly dose of either leronlimab or a placebo in a double-blind, randomized”
Personal belief: I feel we are raising money as little as possible. We only want to have about $6-10M on hand. The reason is because once we potentially get an approval, we will have the ability to buy back a huge amount of our shares so the dilution is minimal and then we will still have about 100M to negotiate partnerships.
Highlights:
“The Company believes that material uncertainties related to the ultimate regulatory approval of leronlimab for commercial sale have been significantly reduced”
"Revenue recognized was approximately $225.0 thousand and $266.0 thousand for the three and six months ended November 30, 2021, respectively..." (est $491K)
“In December 2021, the Company hired Darshana Jani, M.S., as Vice President, Clinical Biosciences, who has over 25 years of industry experience in pharmaceutical drug development, including designing and developing a variety of regulatory compliant biological and bioanalytical methods and assay platforms in therapeutic areas for hematology, oncology, neurology, and auto-immune disease. She has successfully contributed to numerous IND and BLA submissions in the U.S. and internationally”
This lady sounds like our female version of Chris Recknor. We drafted another MVP.
Last but not least: “The Company intends to seek additional funding through equity or debt offerings, licensing agreements, supply and distribution agreements, and strategic alliances to implement its business plan.“
The last proactive video, NP said he would go Fund Raise. Go NASH!"
Thanks FireLife619!
Just entered my Major Buy of 3k shares.
THAT should turn this around!
For what it's worth - and given my medical/business acumen, that's not very much - but I think the fact that NP didn't specifically mention the 700 mg NASH results - coupled with the fact that he emphasized the NASH partnership talks - I interpret that as a positive combination. Hopefully, results look to be strong enough at 700 mg that Cytodyn has some serious partnership suitors.
Back to running silent, more depth charges on the way!
Pfizer to the rescue once again!
https://www.theepochtimes.com/covid-antiviral-pills-cause-life-threatening-reactions-when-used-with-many-common-meds-fda_4186839.html/?utm_source=partner&utm_campaign=TheLibertyDaily
Unbelievable the kind of life-saving and market potential a SAFE, efficacious molecule like Leronlimab has. I know Big Pharma wants to crush Cytodyn because our product would actually work (and not sicken/kill the patient), but then I wonder what they would do with LL if they succeed in breaking Cytodyn.
Would LL ever see the light of day? I bet the very first thing Pfizer or other BP would do would be to put all their financial guys into a room and see what would make more money: the status quo of crappy pharmaceuticals with little efficacy and lots of side effects, or selling Leronlimab to actually help people live.
Eisenhower was right, but also wrong. His experience was with the military-industrial complex, but I wonder if the medical-industrial complex has actually maimed/killed even more Americans than the last 50 years of war.
Anyone cold today?
Here, this ought to make your blood boil:
https://rumble.com/embed/voaxg5/?pub=qdzr7
In short, it's a methodical, logical, very reasoned presentation by the Canadian Covid Care Alliance showing the outrageous violations propagated by Pfizer in its mRNA 'vaccine' trials.
Incredibly enlightening. And the reason it should make every CYDY shareholder's blood boil is everything mentioned in that unsigned hit-piece FDA 'letter' that came out last spring applies 100x more to Pfizer's 'study.' They hid negative results, they purposely skewed the demographics of their population groups, they used incorrect/misleading endpoints - according to the video, the Pfizer sham of a 'study' did practically EVERYTHING wrong. And DELIBERATELY so.
Just nauseating what misery Pfizer/BP/Government have caused with these 'vaccines' (that only result in an Absolute Risk Reduction of catching Covid by 0.83%). Almost as nauseating is the HUGE double standard on display, how Pfizer's junk science vaccine study sailed right through while CYDY's amazing/promising and SAFE results were torpedoed.
Fire all the bastards, the whole BP-Govt cabal makes me sick and they have literally sickened the world. Amazing NP & Co have made it this far, the FDA corruption they face is enormous. May God help the victims of Covid and the 'vaccines,' and may God help us all.
Merry Christmas to All, and to All a Good Night!
The big question I have with Amarex - is why?
Why did Amarex - a seemingly well-respected operation - so thoroughly botch the job assigned to it by Cytodyn, then lie about it for years?
Why would the owners of Amarex destroy their own company . . .when all they had to do was do their job?
Very sorry about losing your younger brother, Hook. We will keep him in our prayers.
It sounds like you and your wife got Covid at about the same time as my wife and I, I'm just getting over it now and my wife is a few days behind. Strange how the virus hits some so hard and others its more of a glancing blow. May God Bless you both with speedy recoveries!
The Perfect Covid Storm needs to meet Leronlimab, the Perfect Covid Slayer:
https://andmagazine.com/talk/2021/12/20/the-covid-vaccines-are-a-myth/
Can't wait for the results of our 4-shot series. Wouldn't it be amazing if LL was the champion that put Covid on the mat?
And wouldn't it be even more amazing if saving the world from COVID...was just the beginning?
Excellent question, Mr Cranium!
"Another point, why in the hell isn't the whole globe going after China and what they did to this world( rhetorical question)."
However, the trail to the CCP and Wuhan lab also runs to the slimy rock over the hole occupied by the troll named "I Am Science." He thinks very highly of himself, as all trolls do, and he also has a fine collection of skulls from his AZT and AIDS testing-on-orphans days. The sand flies eating beagle pups alive might be the edge he needs to win Time's Man of the Year.
Disgusting how every supposedly civilized government kowtows to the CCP (and Fauci/FDA/NIH/CDC). Just shows you how important a free press is, and it also shows how most nations, including ours, only allow state-approved narratives.
Amazing Cytodyn has made it this far. Our little company is the lone salmon swimming upstream against the bears of big pharma and the sky-high dams of the FDA.
GO CYDY!!!!!!