Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
I am confident he did, hopefully the forces that make the decision regarding purchases want to provide leronlimab for the general population as well.
Do you think they'll wait until he's discharged to make the announcement, or perhaps sooner?
What does the Brazil government have in place regarding purchasing medicine from other countries? Do they require EUA or something similar, or do they paddle their own boat?
My patience with this matter has long gone away. I try to stay with the positive, and hope enough money is offered for a BO it gets done. A BO I feel would be best, especially if there were revenue streams in place, as that would lessen the chance of leronlimab being put on the shelf.
I personally hoping for a BO or partnership. NP will not leave on his own, and only if he gets his millions will he relinquish control. I feel neither one will happen unless there is revenue, and if multiple countries purchase leronlimab, the bidding will start imo.
Would love official word or news article from Philippines paper confirming what we have read on face book.
I believe until positive info from 28 in Philippines or official confirmatiom of ex-prez receiving leronlimab, something that gives confidence that Philippenes will buy, then shorts will have their way.
Misiu143, when current administration for Philippines says "follow the rules" does he mean no EUA unless one is given by country of company, (in CytoDyn's case the FDA), or do you think he is just referring to individuals who may try to take this as an opportunity for self enrichment? I believe the later, but I you have some insight, I would appreciate it,
I pray for Brazils citizens sake that leronlimab is brought in. There is no other theraputic that can come close to what leronlimab can do. Regardless whether you think it is "saline" or whatever, too many people are dying not to try it imo. As human beings we need to have compassion. What is there to lose? They're dying as it is now.
Would you take part in a trial if you were critically ill, and there was a 50-50 chance you wouldn't get the drug that was saving lives around the world?
I agree, but what would it look like if FDA demanded more trials and US citizens are dying, when in "3rd world countries" people's lives were being saved by a US drug?
What is point of trials when revenue is coming in? That's what I meant. When more than one country purchases, wouldn't data from recovered patients suffice for phase 4 confirmatory trial?
What becomes of CD16,CD17 if Philippenes buy 100,000 vials followed by Brazil purchase?
If we could have official declaration from Philippines govt, I believe that would push sp up. I believe the reports, but buyers need to hear it too.
How much does Dr Randy Nicolas influence their government? I am so glad he has stepped forward like this, but for someone like me, I wonder if it makes a difference. Is it possible for a decision to purchase 100,000 vials be based on a small group of doctors doing an interview. I would like for a public acknowledgement from NP or Philippines or news organization that leronlimab was used for former president, (even though I am confident it was), then I would believe an order is more likely as I don't think they would provide leronlimab for him and not the people imo.
Even at 200-600 per day, if their stay was 6 days less, that is 1200-3600 savings which would pay for it. And oh by the way, they would have 82% better chance to live imagine that!
Sad that other countries put citizens health before politics, procedure and power, and US citizens are allowed to suffer when FDA is supposed to be the best in world with health concerns for our country imo.
Thank you misiu143. I felt that some stipulations that are in place would have to be revised to give EUA as well. I was hoping you thought so as well because I didn't know how a mass CSP could be implemented. If they move forward with this, perhaps Brazil might follow suit, which would be great for their citizens imo. Then that could provide impetus for countries like Canada and Europe.
Misiu143, if it as you say that leronlimab was used, what chance would it be for them to use CSP for all 100,000 vials and distribute it to hospitals? Is that feasible?
I thought I heard NP mumble something to the effect that Philippenes had said they might go off of eIND as basis for CSP. Did I hear wrong? If so then Brazil might do the same.
Misiu143 I just fear that as good as this news is, that rather than having the FDA make a decision regarding EUA, they may rescind eIND even before CD16 or CD17 if they felt that it would stop CSP in Philippines. I'm not sure if eIND has a direct effect with the CSP, but I believe the FDA will stop at nothing if they feel that a US company is trying to market a drug without their approval. How beneficial is irrelevant, I believe it is all about power and money.
Misiu143 do you doubt that FDA knows efficacy of leronlimab? All these individuals you mention trying to help those who are sick, and FDA I feel surely has to know yet are apparently more interested in procedure than people's lives. I asked a question earlier that wasn't answered, do you think FDA might rescind eIND if they thought it was being used to get CSP so as to avoid potential liability?
Dieselpro or misiu142 could FDA rescind eIND? If what is being rumoured that eIND will be basis of CSP which will gives sales (revenue) for a as yet unapproved drug to a US company, could it be done to remove any potential liability on FDA's part?
I wonder as something similar may take place with Brazil, and maybe other cou tries and then stopping it would be impossible.
Will CYDY have revenue by July 4th?
I thought he said something like that, but are 4 shots going to be used for EUA? Isn't it different than CD12. I understood that's what is being used.
How are OLE patients doing. Would FDA accept results of these in making a determination of EUA and saying only phase 4 confirmatory needed, not CD16 or CD17?
Daemon57 if BO what price? I think this is real possibility, but truth, CYDY has no "approved" drug yet. Do you think it would happen before EUA somewhere, or is it possible the BP is waiting on assured revenue before making the offer?
Misiu143 I was shocked as well hearing about Dr Rahman. Perhaps a BO is close and he won'the be needed for BLA and he was aware of this. I listened closely a second time, and when BO conversation was going on, NP seemed pleased about it. Perhaps it is in the cards. I believe it would be best for patients who need it and shareholders, if done right.
Philippines also said the same thing, but now they indicate that an eIND would be sufficient. Maybe Brazil could use the same process, or perhaps because leronlimab has received a designation for fast track approval for covid might do the trick. Many people are dying in Brazil, and I'm sure they are desperate for help. Peoples lives matter, not money in the pocket of the FDA from BP is the way I see it. Has NP been a disaster as a CEO, goes without question, but leronlimab will save lives if given the opportunity, and even you know that.
Absolutely! If they just had the pr that was put out at 4 and highlighted that since the Philippines was willing to use eIND as an reason to consider such a large purchase of potentially 100,000 vials, it might have even gone up more.Dr Rahnan leaving could have been in an 8k if they felt necessary, but the CC wasn't needed in the least imo.
I can see the news now. New therapeutic from US saving lives in other countries, but FDA wants more trials. I bet that would go over great.
If Philippines and Brazil give EUA what does anybody think FDA would do? Especially if other countries follow suit?
I hate this turn of events, but hopefully there can be another Dr who can be brought in. Leronlimab is too good not to get it into the human population for all the different indications that it can treat.
Dieselpro, yes csp approval for 100,000 vials would be great, and hopefully just the beginning. This CC was about as troubling as I've ever heard, but bottom line is revenue. If they use eIND for approval, then buy leronlimab, perhaps Brazil would do something similar. They would probably get a lot more, then I believe other countries may use the same logic imo.
Sp not based on CC's. Revenue is the driving force, and as much negative feelings I have for NP, when leronlimab has sales of 100,000 vials to the Philippines, I believe that is just the start imo. As the old saying goes, "granny bar the door".
The pr says negotiating for 100,000 vials of additional leronlimab with Philippines under csp rules as well as 28 additional patients. From what I understand, that is sales, correct. CYDY is not giving it away or they would not be negotiating. Perhaps Brazil is next.
True thought, hopefully they have experienced enough of FDA's poor recommendations, and will decide what is best for their citizens based on leronlimab's results against covid for critical patients, who desperately need it in several countries imo.
The efficacy against so many indications I believe is what is holding a lot of things up. I'm sure any country that is going to give EUA will not only look at covid testing, but also the cancer, NASH, and HIV. Possible situation may be "it's hard to believe" may be what is being said and so rather than take that first step, they would rather wait on FDA to give their blessing imo.
C-20 I am not a NP fan either, and I agree we're being slow rolled by FDA. Do or anybody think MHRA or Europe or Canada will he affected by FDA's inaction in this matter?