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Vax killer, COVID killer, Big Pharma slayer,
I like them all.
Leronlimab,
the Fat Man of atomic therapeutics!
"All this is really sickening what is done to us the people during this pandemic .."
Agree, Dr M. But it's more than sickening, it's evil, and this latest push to "get vaccinated or get fired" is beyond the pale.
My brother (PhD in physics, impeccable career supporting top secret DOD programs) has been told to get vaxed or get out by 21 Sep. And I just heard about a Marine with 10 years service who refused to get vaxed, so his commander called him and said 'get it - or we will suspend your pay.' The man has a family, so he relented. Multiply these stories times x-million and this is the country we've become:
'Take an experimental vaccine with an absolute risk reduction from 0.3% to 1.1%...take an experimental vaccine that was never tested on animals...take an experimental vaccine that was developed from research gleaned from aborted human beings...take an experimental vaccine that has a higher chance of getting young people admitted to a hospital with adverse side effects than than those same young people getting admitted for COVID...get jabbed or you're gone.'
THIS is America?
THIS is liberty?
This is fear-driven emotion and herd-driven pseudo-science driven by politicians wallowing in power and corporations gorging on greed.
People in authority should be flogged for their abuse of authority. What's happened, what is happening, is absolute madness.
And COMPLETELY Un-American.
Good Evening, Dr Rock! Just wondering if you had any thoughts on the amazing Ivermectin results out of Uttar Pradesh?
"The active caseload in Uttar Pradesh is down to 269, while the percentage of active cases against the total confirmed cases is 0 per cent.
The active caseload, which was at a high of 3,10,783 in April, has reduced by over 99 per cent.
And this state is one of the five lowest COVID cases of all states in India despite having only a low vaccination rate of 5.8% fully vaccinated compared to the USA that has 54% fully vaccinated. "
Also amazing are the results out of Kerala (a tiny state located in southern India) that relied more on vaccines and less on Ivermectin; they've reported a significant increase in COVID-19 cases.
Any thoughts??
Thanks for the good SP news, JPG77! It's been a while.
And just as we shoot the messenger with bad news, we reward those who bring something good.
You may pick up your prize in the ihub lobby, 2 free tickets to the Concert of the Shorts. Earplugs included, should be a hell of a wail.
Agree 100%, Pinseekr, the "why" of pursuing vaccines vs therapeutics is the 100 billion dollar question. But because so many nations jumped on the Vax wagon, they made this hundred billion dollar question into the trillion dollar question vis-a-vis national economic lockdowns.
Amazing the horrendous avalanche this "Max Vaccine" policy has triggered: loss of freedom from NZ and AUS to Europe and the US, eternal masking, stunted social growth for kids, more depression, even more obesity, citizens dividing into "pro" and "anti" vax camps - guess we didn't have enough division already - and then there's the loss of trust and confidence in health agencies, scientists, doctors, employers, etc.
Politics and profits drove the response to this, and straight from the White House, the dictatorial response will only get worse.
Honestly, you could say drugs like Leronlimab really could help save not just lives, but liberty and freedom, too. Incredibly, though, the big question seems to be - will therapeutics be allowed to succeed.
The answer must eventually be yes, because Israel gives a glimpse as to where this Max Vax policy leads: More variants, more infections, more sickness and death.
So here's a thought: to both fight COVID 19 and restore US prestige, let's load a few Buffs with Leronlimab and - nation by nation, deliver a few million vials. Sort of like Teddy Roosevelts Great White Fleet tour from 1907, I think the first B-52 was flying back then.
Good points, Pinseekr.
My question is: if the medical-scientific leaders have known for decades that "vaccines drive variants" much like antibodies can breed resistance, why did the world ignore therapeutics to instead attack COVID 19 with vaccines?
I know - and believe - the reason was a mix of potential windfall profits for big pharmas plus political maneuvering, but I can't believe all the leading medical and science journals and colleges were silent on this fundamental error.
Have our people and institutions really been so corrupted?
Maybe we can chalk much of it up to google/twitter/facebook/etc threatening to deplatform anyone who criticizes the vaccine strategy.
Last question: why did the polio and chicken pox vaccines not drive variants the way the COVID vaccines seemingly have done? Just different kinds of viruses?
Can you explain this more? I don't get why - just because there is an effective therapeutic like LL - why would that prevent an EUA for a vaccine.
Don't therapeutics and vaccines have different goals, i.e., we get vaccinated to hopefully inoculate ourselves against something we haven't got yet, but we take a therapeutic after we get it.
So why would the success of LL hold back the EUA of a vaccine?
Thanks!
Good Evening, Dr! Question: Can you tell me why someone would be denied Leronlimab under Right to Try? Is it because the company can't afford to give away the drug?
I guess that makes sense, because if word got out about LL, they might very well exhaust their supply and not have enough for the Brazil trials. Is that the reason?
Question for our MD's and scientists:
- Someone on the reddit/CYDY posted a list of autoimmune diseases that might be treatable with Leronlimab
- Then,I read the following on another reddit page unrelated to Leronlimab or CYDY:
"There is a question about whether these new vaccines, which also focus on the spike protein, will also cause autoimmune disorders. The problem is that autoimmune disorders take time to develop and to show up. It may also take a long time before doctors and scientists can link the sudden rise in autoimmune disorders with these vaccines. Usually, in a vaccine trial you closely monitor your trial group for years and years. This allows you to identify the signals. With the current program of injecting millions of people, there will be no clear way to link causation to the vaccines and an increase in autoimmune disorders may just fly under the radar. We may not know for a very long time or never."
So, my question: Do you think Leronlimab might have a future in combating autoimmune diseases, and if so - do you think we're in for a possible huge increase in autoimmune diseases via the vaccines?
Thanks, LABZ! I can hold out, I'll ration my peaches and rainwater till the glorious arrival of the USS CYDY, and prime a depth charge for U-13D.
No prisoners!
Thanks for the update, daemon57! I'm down to my last rusty can of peaches, and the sharks have stopped making reservations at my life raft, they're just lining up.
Rumors or news, telegraph what you can!
Question for moneycrew (and others): I have no experience (as a stockholder) with a small bio company like CYDY when it "partners up" with a big fish like Roche. I assume everything is in the details - what are the terms of the partnership, what indication(s) are covered, what's the reimbursement - but to my question - do you have an expectation of what a "typical" big pharma partnership for one of indications might do to the share price?
Does teaming up with a big pharma result in a synergistic effect on the SP, i.e., does the agreement itself typically exceed the monetary sum of its parts?
2 Questions for Black Ops (and others):
1. Do you think the daily selling pressure for the past few months - and perhaps the last year or more - is coming from an organized group of traders/brokers funded by one or more big pharma companies?
2. And if so, is this illegal?
I know there are reasons to be contrary on CYDY - this applies to every company in the world - but given all the success LL has shown against AIDS and cancer and COVID 19 - and given all the other indications now being explored and its amazing safety profile - $1.30ish seems an absurdly low price.
Thoughts?
Thanks, Dr! I assume these results strengthen CYDY's case for LL to warrant "Breakthrough Designation" status for certain cancers?
Good Morning, Dr Misiu! Question: After the success of Leronlimab against AIDS in the Phase 3 trial 3 years ago - and after the FDA said try it all again with a higher dose - do you know if Cytodyn ever considered going for an AIDS treatment approval in another country?
Hasn't this been Cytodyn's strategy with Covid? In other words, since the FDA didn't give us an EUA to fight Covid, we're trying to sell to the Philippines, Brazil, Canada, etc.
Do you know if NP ever thought about using this same strategy to sell LL to fight AIDS overseas?
And I wonder how the FDA would react to that. Would the mammoth bureaucracy hold a grudge against Cytodyn?
Finally, I hope and pray your son's X-rays look good today!
Great summary, Dr M!
All I can add is a boatload of frustration and incredulity:
We have invested in what appears to be the most promising, most safe and effective therapeutic in the world, a drug that has already saved AIDS patients could very well help millions across many varied diseases and pathologies, a drug that could have ended lockdowns and mandates and economic collapse and kids in masks...and we're valued at $1.40/share?
Well done, medical bureaucrats.
Well done, FDA.
I don't believe in karma. But I do believe in smashing federal bureaucracies into entities that actually hold their people accountable for what they do and don't do.
Am I reading this Pfizer contract right?
I got this from a link from "Jan Kowalski", he was replying to Dr Malone on the latter's twitter feed:
— Jan Kowalski Bunga🇵🇱💯🇵🇱 (@JanKowBunga) August 8, 2021
For Dr Misiu and her son - if anyone on this board prays the rosary, you can join me "in spirit" in about 30 minutes to ask for complete recovery.
(Also any other sick family/friends).
The letter states "...will be carried out in 35 brazilian research centers with 612 patients who are hospitalized and in need of oxygenation support, aims to prevent the disease from evolving into a more severe case, requiring invasive mechanical ventilation."
Yes, Brazil approved! Someone just sent me the "Biomm SA" Relevant Fact letter confirming this, I've been waiting for the image to arrive so I can post it here.
"ANVISA approved, on this date, the start of phase 3 clinical study of the monoclonal antibody leronlimab in Brazil."
The letter was dated today, 2 Aug 2021
Great News!!
Agree 100%, jimmy667! No one attacks a worthless target. And from the attacks I see, they have shifted from Leronlimab being worthless to our leadership being worthless and/or corrupt.
And when I see some "longs" off this and other discussion boards join the attacks and support the 13d group - and they do this either NOT KNOWING what the 13d's specific agenda is, or they do this KNOWING that the 13d will squander our limited resources on BUYING Incelldx and slaughtering shareholder value - that only confirms the forces aligned against CYDY are desperate.
They know LL works. They want it cheap - or they are being paid by big pharma people who want it off the market (or in their own arsenal).
They will destroy the company to maximize their personal gain.
I would buy more if I could, but I've been maxed out in CYDY for months.
The next few months are critical, this is a great buy-in opportunity, and let's launch those trials in Brazil. Leronlimab works!
Daemon57, just want to say thanks for your continual reality-based optimism and excellent posts, both are much appreciated.
Let’s hope CYDY starts the week with a Brazilian flavored bang!
And when a federal agency like the FDA intentionally lies to or misleads Americans about the efficacy of HCQ/zinc and Ivermectin, and refuses to let COVID longhaulers continue their LL treatment after it eases their pain, clears their minds, and lets them walk again - is intentionally causing suffering and death for hundreds of thousands of Americans also a felony?
Or does this felony thing only work one way.
Ah, to be king just for a day....
Fantastic info, Dr M, thanks!
And that video of the young woman with Long Hauler's proves once again, this time with intimate force, how simply pathetic the FDA has been.
The FDA approved lousy drugs with bad side effects for no other apparent reason than to make money for Big Pharmaceutical companies.
They mocked or ignored the impressive efficacy and safety of ivermectin and HCQ/Zinc because, apparently, there's insufficient profit margin for the BP's.
They supported useless mask mandates and economic/school shutdowns which devastated families and businesses and lives.
They have pushed potentially dangerous and lethal high-profit "vaccines" that only raise the Absolute Risk Reduction by 0.3% - 1% for a virus that more than 99% of the general population survives.
And now, Long-haulers can't get the only drug that helps them live???
EVERYTHING the FDA has done in this pandemic has been stupid and wrong and continues to be stupid and wrong. And Nadar is the bad guy?
Disgusting.
Thanks, Lawman. $ounds like I should have been a lawyer.
Agree 100%, Rabbit. I'm not much on the behind-the-scenes corporate stuff, but from what I've read, I don't trust these 13D guys AT ALL. I thoroughly respect Dr Patterson, but after reading about how he's trying to sell his company to CytoDyn, that's a huge red flag. I want a BOD that have no ulterior or alternative motives, and though he might have some great scientific acumen re: biomarkers and testing that could really help us judge how and how well LL is working, that is an entirely different issue.
I support what Dr Patterson brings to the scientific table, but not to the management table. And I'm just not impressed with anyone else in that 13D group at all. In fact, with some, I'm disgusted. WAY too much baggage.
I'm staying with Nadar!
Great find, daemon57, thanks for posting! This article should be mandatory reading for all CYDY shareholders.
Leronlimab works. Leronlimab is safe. Millions need it, Big Pharma wants it, and many will spread whatever FUD they can to get in cheap.
Everything else is noise.
Agree 100%, Killer.
The only way to move the FDA is with political pressure, someone like Sen Rand Paul or Ron Johnson. And the only way to get these senators to act is via public outcry and constituent pressure.
As for NP and others warning us shareholders to keep quiet and don't bother the FDA, that's just a tactical response on his part, he doesn't want to burn the FDA bridge.
But if people are suffering and dying needlessly and we have a safe drug that works, we HAVE to speak out. FDA double standards MUST be exposed. To keep silent is morally wrong.
I agree with you, Dr M: when the sharks are circling, we shouldn't be changing our captain and crew...unless they're bringing the USS Iowa and a boatload of Marines. Then again, as another poster said, maybe this will light even a hotter fire under our CEO and current BOD, though I'm not sure how much hotter things could get.
Will hopefully have some good and/or surprising news this week!
Happy July 4th + 1, Dr Rock!
But I do have a slight disagreement with your last statement, i.e., CYDY doesn't need just one lucky break...we just need a level playing field.
Given that, we will simultaneously mitigate suffering, save lives, and blow away many ineffective/expensive and dangerous drugs.
Hoping for a great CYDY week!
Happy Independence Day, Americans!
And thank God for our founding fathers and Bill of Rights, this is the only place in the world where we can debate the merits of LL or anything else without fear of imprisonment.
$1.70 or not, always be grateful!
Good Evening, Black Ops, wherever you are,
do you have any thoughts on the 13d situation?
Have you seen this type of thing before, a slate of new people put together to change the CE and BOD?
I think Janet Woodcock would be a great choice for CYDY CEO,
she believes if a drug is safe and shows promise, that it
should be used during a pandemic.
Patients, not p-values!
What more could you ask?
Legal question about the 13D Group: If and when they reveal their plan for running Cytodyn, are they legally bound to follow it?
Because if not - "Whoa, we had no idea the company was in such bad shape!" - will we not be told whatever will garner the most votes for their Group? I mean, not that people ever shade the truth to get a few votes, but -
“If you like your health care plan, you’ll be able to keep your health care plan, period.”
"If you like your doctor, you will be able to keep your doctor, period.”
"We’ll lower premiums by up to $2,500 for a typical family per year.”
"Read my lips, no new taxes."
So here's a big point in N.P.'s favor: We know him, his shortcomings and talents and history, and we know he'll do all he can for the shareholder, e.g., no reverse split. I also love his transparency and enthusiasm and grit, he does not easily retreat.
It's not fair, C-20, I blew all my dry powder months ago because I knew CYDY was way undervalued at $3.00. I also knew it way undervalued last June at $8.00. So all I can do now is read posts telling me what a great time to buy this is, but all I can do is hold my empty musket and watch.
And completely agree!
Oh, and nice to see a finish in the green, is this the start of the inevitable advance?
Thank you Dr M and Swordsman, I think the "biggest" thing LL has going for it (besides safety) is it crosses the blood-brain barrier.
Not pretending I really know what the hell that means, but given that mental fogginess/impairment is a primary complaint of most longhaulers, I think LL will be in a class by itself in treating their symptoms.
Today's share price sky is a little dim, but the horizon looks incredibly bright!!!
Good Morning, Dr Misiu and Dr Rock and other MD's/scientists in our midst,
I got this quote off the reddit/cydy board:
"Looks like our LH trial has 2 major completing trial, one by Puretech Health with 168 patients and the other is NIH sponsored 900 patients."
Question: Does anyone know if the drug(s) being used in these 2 other trials are in any way like our LL? Are they monoclonal antibodies?
Just wondering how they might stack up against our wonder drug.
Thanks!
RESPECT THE ROCK!
Just as the FDA sees no reason to approve Leronlimab, I see no reason for us to approve of our current, monolithic FDA.
In other words, why not 50 FDA's?
Yes, it sounds like a mess. But it's the mess of federalism, it's how our states get to run things like schools and budgets for themselves.
Specifically, just as every state has the freedom to craft their own pandemic response - some with severe lockdowns, others with barely none - let's let the people of each state create their own drug administration. Sounds like even more bureaucracy, but unlike today's FDA, we would have COMPETITION between the states and state-run FDA's.
So if Texas saw a drug like Leronlimab? "Hey, it's safe and might work, what do we got to lose?" And if a state like NY wanted to be ultra conservative by outlawing HCQ/zinc and ivermectin, well, let them. And let the people vote with their feet.
The point is, a federal FDA has no self-correcting mechanism. Every bad decision goes uncorrected/unpunished, so the only antidote is competition. In the end, our institutions have to serve the people, but over time, unelected bureaucrats and giant bureaucracies have proven themselves progressively more unresponsive and corrupt.