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Although, it did not meet the endpoints in the CD12 trial, it did prove it was very effective. It just needed to have either one or two more doses for some patients. This trial design error will not happen in the next trials. Anyone familiar with this drug, is very impressed with its efficacy. The trial design failed, not the molecule. The trial did not benefit from adaptive design, like some favored companies received. Error corrected, now we are moving on.
If it goes lower, I will pick up some more. Thanks for your concern.
Crap, now I have sell! Thanks for telling me.
This company has never been in a better position, than it is right now. The drug's contact, with the medical world, is growing exponentially. Soon, the politics of things, will turn into the masses demanding better protection from their governments. The company is more flush with money, than they have ever been. You must decide, if this investment is causing you too much stress, then sell it, and move on. Personally, I think it would be a mistake.
Very nicely put!
When does not being toxic, have anything to do efficacy?
Yeah but, but, what if we had a distributor, in country, to take care of that? Does that change anything? If we had a distributor under agreement to work with the Philippines government, does that change how your narrative works?
Have patience, exponential growth, and awareness are in progress. Soon, even you, will see positive changes.
Perhaps you can place a dollar value, either on a person's life, or on their care while on a ventilator. Maybe we can take these figures and show them to that person's loved ones. Please, explain how you obtain you figures. Thank you in advance.
Are you suggesting that a stock photo, that you found on the internet, is indicative of the only dosage size that has been put into a vial? LOL! Go find your own pictures.
I think that might be outdated.
Thank you.
One vial per injection (350 mg). Two injections per treatment. Therefore, four vials for two treatments.
Thank you, for your reply. However, it would be nice to show that patients treated, with Leronlimab, for their Covid-19, do not have residual inflammation and virus. That they do not become Long-haulers. There seems to be a lot of people,treated by big pharma drugs, that have residual inflammation and Covid-19.
It would be interesting to see some hard data, on patients treated with Leronlimab, on any long haul symptoms. It would be nice to see the protocol for these trials.
IMHO
I believe Dr Randy said that the Philippine government authorized the hospitals to stock , up to, 100 vials per institution. That will treat a lot of celebrities. There are almost 1000 hospitals in the country. Maybe, some non-celebrities might get treated, as well. IMHO. GLTUA.
Corruption in the FDA and Big Pharma? Say it isn't so!
https://www.seattleorganicrestaurants.com/vegan-whole-food/institutional-corruption-of-pharmaceuticals-how-FDA-cannot-be-trusted-with-public-safety.php
Well spoken. It is very sad that they had to go outside the USA to find a government, with enough balls, to serve their people. Instead of serving themselves. It makes me ashamed of my government.
On the bright side, as an investor, the Philippines will unlock the shackles, placed on this wonderful, eloquent drug, and make us wealthy. It won't be next week, but it will happen sooner than most people think.
The entire Philippines medical community is about to get a close up, and personal example of what this amazing molecule will do. The explosion is started!
This is amazing news! I think it has left most everybody speechless! It made my heart skip a beat!
Is that because the, so called, vaccines are really therapeutics with no safety information?
I did not realize that. That would be very unfortunate. Please, would you explain more?
Exactly, get receptor occupancy quicker. Lower the viral load quicker. Add dosing for weeks three and four, if needed.
Maybe that will give the opportunity to try the IV first and go to increased dosage, as needed. Are there any limitations to dosing? It may surprisingly effective.
Is that the code to start the short attack? The post from Clay Trader, with no link.
Email this with question to Mahoob?
Obviously, not enough! IMO
I will give that some thought. Thank you!
Here is a copy of my email to Janet Woodcock. I tried to keep it simple and quick to read. It didn't even get a canned acknowledgement.
Dear Ms Woodcock,
As a citizen, of the USA, I am requesting that you consider EUA for Vyrologix (Leronlimab) for use against Covid-19. I am asking, based on these points:
1) Is it safe? Yes, its safety profile is unmatched.
2) Does it offer benefit? Yes, it offers statistically significant benefit over Dexamethasone, for serious and critical patients. Additionally, it shortens hospital stay by six days.
3) Can it save lives? Yes, it can. Although, the critical patient group was small, it shows that it can save lives that would have been lost under the current standard of care. This has been reinforced through EINDs and OLE.
Again, this treatment is proven safe, offers benefit, and can save lives. In the interest of advancing beneficial care, the decision should be simple. Please, grant this treatment an EUA, while gathering more clinical evidence of its benefit.
Outstanding! Thank you!
I have sent my email to Janet Woodcock, citing that this treatment fulfills her description for EUA. It is safe. It offers benefit. It can save lives.
One bee is not scary. A thousand bees, in unison, can strike fear into the bravest heart. Make your voices heard. Nobody else will speak your mind!
Thank you.
I enjoy your posts. Misiu143, Ohm20 and yourself give very valuable information on this drug, this company and the real world that they can help. When I first ran across what this wonderful drug is capable of, I thought it was too good to be true. After I studied it, I jumped in and will not sell, until we either go broke or succeed.
GLTUA
I have been following this board for a few months. I just signed up to respond to this post. It is an excellent idea. Therefore, I did email my Congressman the following: Does the FDA work for the big pharmaceutical companies? Why have they only authorized moderately safe and moderately effective/ineffective treatments for Covid-19? Leronlimab is a safe and effective treatment that can save a lot of lives. Yet, it is being slow walked by the FDA. Do they not care about the death rate? Are they aware that people are dying? Please turn some, much needed government attention to this swamp. Look at who is really calling the shots. They have a lot of blood on their hands. Please see what can be done about getting our population some safe and effective treatment. Put forth some due diligence on this matter. You will see.