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Whosonfirst, that is all phantasy. First the FDA has to be forced to release Leronlimab, since they know that what we need this best medication to save 1000sands of lives instead using their mediocre products.
Learning53, it is just your opinion, nothing is true, until the FDA gets investigated and prosecuted for mis-management.
Here Today, the FDA are looking for something or every thing, to drag this out for weeks and month to find no end point at all, to conclude that they found no end point and can not approve this best medication to save lives.
rockleo, wow, this message was very powerful. It is a good description of this man fauci.
Respect, for your courage.
W#hat is the FDA doing with CytoDyn/Leronlimab, after studying and improving the injection formula from 350 mg to 700 mg and could not find any other improvements.
Are they after the secret chemical ingredients??
Is that why it takes so long to release LLeronlimab to the doctors and Hospitals to start saving lives?
Is any one here to save lives, raise you right arm.
Or are you just here for the profits???
How about getting some heat to the greedy FDA, to approve Leronlimab, since they have many reasons to study and re-excamen the product since July 2020
They did not find anything to improve Lerolimab.
That is why it takes so long
The money printing machines of the federal reserve bank running full steam, day and night, just to keep up with the cost of fighting the virus in every state at the hospitals.
The cost of saving lives are enormous and depends on the quality of the products.
Some patients being treated with Leronlimab are leaving the hospitals in 3 days, others stay in beds for many weeks.
All these trillions of dollars are added to the trillions we already spent.
Of course, we the taxpayers have to pay for all of that.
mercurio, it is not Nader who does screw up some vague items in filing.
It is the FDA with their arrogant power, that is responsible for delaying the approval of many superior product in comparison to all BPH products.
The FDA, by mis-managing approval services, makes them guilty for 100sands of citizens lives destroyed.
misiu143, thanks for the explanation, that Leronlimab does not stop the virus covid-19 directly. You are more familiar with medical researches and work in the medical field.
An other question is, "why do doctors and hospitals want Leronlimab for treatment of their patient so urgently, to make empty beds available faster with Leronlimab treatments than any other product"?
I read on this board, that patients get discharged within 2 to 3 days and send home, being treated with Leronlimab, while other patients treated with the usual big farmacy products have to wait longer and longer and eventual
demise.
I do realize, that each case is different, depending on severity.
Do you have at least some negative feelings about the FDA not wanting to approve Leronlimab since July 2020 when they promised it, but renegt on it?
misiu143, the reason I have been asking you about Leronlimab, is that my only focus on this board is to free CYTODYN/Leronlimab from the claws of the FDA mainly to save lives by the 1000sands.
What ever the FDA has been doing this year, with approving mediocre products, that did not make a difference in the death rate or new infections at all.
Early approval of Leronlimab in 2020 would have been miraculous in reducing the spread of the virus every where in the world.
Kids would bee at school right now, entertainments would have their normal spectators, the economy would be blooming.
The mis-management of the FDA is deplorable, criminal, murderous IMHO and has to be investigated.
But who is going to prosecute now?????
misiu143, if Leronlimab is not as effective as these new injections, why is the FDA is so afraid to release Leronlimab for a whole year now?????
Where did you learn, that Leronlimab has to be injected every week to keep
the patient healthy???
These new BF injections have not been around long enough to be so sure, that one injection is enough to save the person for let`s say a year?
you are some what confusing.
JLA Ins, You have the correct idea, the SEC and the justice department should investigate these boards, that would bring out a lot law infractions
called criminal activities, why we can not reduce the daily death number of
covid-19 infected citizens.
The news papers and other media can not lie about numbers since the numbers are being reported first by doctors and hospitals.
I am talking about Leronlimab and other medical products that are most effective against the covid-19 virus, and being held captive by the FDA.
Yes, investigate and start prosecutions.
Mountainman5, I strongly agree, the FDA has to stop holding Leronlimab captive for almost a year. They plainly ignore the power of Leronlimab over the horrible covid-19 virus.
Our president has no power. He has to listen to his party.
Covid-19 death rate is at the highest now, but restaurents and enter tainment centers, can open with the usual safety restrictions.
How can that be possible, when last year every place was shut down with only 1/3 of the death rate.
It is time, Leronlimab is being released by the FDA to save many lives.
This is the CYDY board, the subject is Leronlimab, the medicine that could put a stop to the covid-19 dilemma.
Most posters hitting around the bush, calling Leronlimab "ll", or Nader Pourhassan "NP".
I would bet, that many here do not even know all the abbreviations.
Leronlimab, the best of the best is being kid-napped by the FDA and held captive for all kind of reasons, like improvement of the medical formula, a change from 350 mg per shot to 700 mg per shot or a new study of the science with hundreds of new patient being studied for treatment of the virus, double and triple new studies since 2019 and before, the time when leronlimab was curing the AIDS virus paqtiets each patient with AIDS had to struggle with the beurocratic paper work for permission to be treate with Leronlimab, since the FDA did not want to approve Leronlimab at that time either.
Rockleo, lot of respect in return to you for the important information.
I am scheduled for a virus injection on the 25th of May at Kaiser Hospital
in Panorama City, Los Angeles.
I have no idea whose injection they are going to give me. I made up my mind, if is the one from Phyzer Co. , I will post pone my injection day, until they offer me one from Humana.
Number1Stocker, everything is fine with me what you are saying at this time, because there is no other way than the FDA way.
I don`t know if you were already here at IHUB last year 2020 Jan. to July?
Jan. 2020 CYDY was presented to the FDA for effectiveness and safety.
Two weeks later, the response was, "our studies show, that this product will be ready for approval in July.
Every one waited eagerly for July 2020. July 2020 came and went by without any news from the FDA.
Instead 2 month later, the FDA wanted new studies and an improvement of Leronlimab from 350 mg to 700 mg injection.
Of course, this new approach from the FDA was just a sign, that approval and release to doctors and hospitals would be strong competition to big pharmacies.
moneycrew, the data of Leronlimab is irrelevant, the study of Leronlimabs science, the yearlong improvement study by the FDA are irrelevant all together.
Leronlimab was a perfect, ready product to save patients from death over the virus infection.
It was ready with the 350 mg injection for virus patients.
It did not need the improvement study by the FDA from 350 mg to 700 mg.
This is as good as I can describe it plain English.
Why does no one under stand, that the FDA is wrong to keep Leronlimab away from doctors and hospitals?
For all the new posters here, Leronlimab is a perfect, ready to treat covid-19 infected patients in a very short time span, specially serious ill patients with little hope of staying alive.
The FDA is keeping this accomplished medication away from the public, pretending to study the science of this product and to improve it.
So far, there has not been intentions to approve this product, that does not need improvement.
???????
BreezeWoodAcres, in my opinion fauci is a criminal, shielding the big pharmacies from competition, like Leronlimab and other perfect medications against the virus.
Fauci is the highest paid official in our government, but he contradicts himself every week or so, starting with saying "face masks do not work", "we do not have to be afraid of the virus".
Just a few examples. He tells the FDA what to do.
The FDA and fauci are responsible for thousands of corona virus deaths, by keeping effective medications locked away, by faking they need to research more of the science and other none-sense.
Dr fauci and FDA are in charge now, to determine which stock will be approved in order not to have any kind of competition, like Leronlimab.
This regime change will not tolerate Law and Order.
Mountainman, your hope with LERONLIMAB sound exciting.
When do you believe the revolutionization of this medication will occur?
This year or next year?
BreezeWoodAcres, you are a great commentator in deed, with a few others almost equal. Depending how much time you have to prepare for.
Leronlimab is on our minds and it is still being deprived willfully and criminally from us and a lot of poor souls suffering from painfully from the corona disease, waiting for Leronlimab.
Rush L. tore into mr. faucy at his ""friday open line" talk show today, showing all of fauci`s contradiction from Jan. 2020 until today.
This man fauci talks up a storm, but makes it his life task to oppose any
great medication that could stop the spread of this awful corona disaster.
We will waitand wait and wait>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>
Leronlimab is ready and was ready for a long time. Very efficient, very safe and almost no side effects. The best medication to do the stop of spreading the covit-19 virus all over.
The FDA and co-horts believe every one here is retarded and with a new regieme in place they can not be prosecuted for man-slaughter for not approving any good product that comes along to save lives.
It is soo obvious, that the FDA are dragging their feet on approving good products, unless they come from a known big pharmacy.
Dr. fauci and the FDA are corrupt, but can not be prosecuted any more, because regime change is law less and corrupt besides.
kgromax, for its effectiveness and safety with little side effects, Leronlimab is looked at by the FDA as an evil medication, that would bring the end to the corona virus disaster.
It is very sad, specially now there is no one willing to prosecute crime.
Dr fauci and the FDA painted themselves into a corner by not allowing Leronlimab to be approved.
Leronlimab, a safe and effective medication against the corona virus, would have already put an end to death of many victims.
Now the FDA and cohorts can safely be accused of manslaughter of 20 to 30,000sands by willingly and intentionally ignoring CYDY, but approving other companies products half as effective with side effects.
The longer the FDA waits to approve Leronlima, the higher the fines will be.
GLTA
SansBS, thank you, for waking up to the truth, that the FDA, mr. fauci and the big pharmacies have put them selves into position of criminal wrong doing, by with holding support for a perfect medication, that would have done an end to the worst calamity that hit this earth.
The "ifs" and the "whens" and hope for Leronlimab`s approval have been speculated on this board for a long time.
My conclusion is, that the FDA has no intension to approve CYDY`s highly perfect medication against the corona virus at any time right now.
Approving Leronlimab would replace all other big pharmas half as good products and the revenue would flow the other way, our way.
What can be done about that?
A court order, accusing the FDA of 10,000 and more death from the virus, for neglecting willfully the approval of a perfect medication, Leronlimab.
Are you dreaming of that Leronlimab will be approved by the FDA?
The FDA promised approval in JULY 2020.
It never happened.
GLTA
I agree, Dr. Leo, I have no business meddling within your researches.
It doesn`t make much sense to me either, but then, my mind is not that over crowded like a doctors.
Sorry, for that.
PersianLeo, at least you have some kind of idea, what is going on with the FDA, regarding to CYDY never approval.
Rockleo, data review of 389 patients will take 6 month IMHO.
This is after my experience in the past with the FDA.
After that review they will find an other reason for some more reviews.
I was ready to say the same, but could not remember that long article about 6 month waiting time for the FDA concerning CytoDyn enlisting new patients for more studies.
Keep on dreaming. This week end and next week end two more week ends.
The FDA, mr. fauci and all the big pharmacies have no use for a perfect medication like Leronlimab.
Do not even mention Leronlimab, CytoDyn or CYDY at all. It may hurt your feelings.
I just bought a few more CYDY shares on the dip, but will not sell any of them for a long time.
Yesterday, we the US, broke the world record in total new corona virus death in one day.
It looks more and more like population control by our government and world wide.
Some of the side effects of big pharmacy injections is, that women cant have children any more.
This is really sad.
dadbrotheroftwins, aaaaaaaai can answer this easy question.
Where there is demand, there is supply.
CytoDyn had a long wait to get ready for any one who wants Leronlimab.
I am sure, there are more than one manufacturer-supplier to jump in at a moments notice.
The problem is always the same problem, problem, problem with the FDA and others.
The FDA will not let Leronlimab escape from their prison, they will not free this valuable medication, they rather face death eye to eye to overfill their coffers with profits, profits and profits again.
If it would be myself, that had been banished, I would fully understand.
I have been getting away with a lot angry postings.