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.
My wish is that we have 3 news releases on one day: sales contract with the Philippines signed, very positive results of CD12 with reduction of mortality bigger than 50% and stop of trading on this day due to uplisting to NASDAQ. Results: Gap opening with 15$. House of shorters collapsing. Many of the shorters disappear forever due to bankruptcy and can't continue with their destructive "business".
I heard from Janet a very comprehensive interview 2 months ago. Yes, she mentioned LL, but she expressed her preference for BP. She likes very much these powerful BP- companies. The small companies haven't got in her opinion enough financial power to succeed with their developments. Means for me: small company be innovative but then sell to BP for a fraction of value as you will not survive FDA's approval process. In this way the BP business is very well protected.
For BP FDA approves even drugs which reduces the stay in hospital only by 1 day while CD10 wasn't good enough.
It seems for me that only MM selling and buying among themselves. Very little turnover, very little money needed but still great effect.
Thank you for your answer. I would be happy if I am wrong. Only i still miss to believe into their honesty when i think what i learned how they delay HIV.
Maybe Rockleo could tell us: if the results of CD12 are as good as we expect, how far could/would FDA go to delay us even for an EUA for another 3 to 6 months? What reason could they invent to please BP for further Donations? Any experience, any phantasy? Don't tell me that lives count.
Few years ago when this board was high because the coming buyout by Gilead for HIV, I said numerous times that I as CEO of Gilead I wouldn't waste my money and buy CYDY for many Billion $ when I have the chance to keep my cash- cow running for many years for spending continuouselyfew $ to break CYDY's neck. Some donations to FDA in addition made it happen as we see. Now for Covid we got Remdestodeath. Same story.
Why is this club of shorters shorting without any fear and worries and continue like there is no tomorrow? By no means they can cover the 27++Mio shares until the results are out. Are they stupid? No!! I think they behave like this as they get paid for it. The bill is paid by big uncle. Every week delay of LL brings others Billions of $ profit.
Maybe they are not as desperate as we want to believe. What if uncle BP pays the bill? 290 Mio $ is the earning of few hours for BP, not more than a tip.
Something G&S will not like to read. He bashes in the worst Nader for at least 4 years. He has been qualifying Nader constantly as incapable and as the worst CEO.
Ok, will remember.
I saw today on TV elderly people driving their car, just stopping for a moment, not getting out of the car, get vaccinated while sitting in the car and then move on.
Is this responsible to vaccinate like distributing a burger in a drive-in? For me, this is irresponsible crazy. Everybody who gets vaccinated should be watched for at least 30 minutes nearby....but I am not a doctor, just one who will wait for another 3 to 6 months until becomes vaccinated and buy in the meantime, if possible, a shot Leronlimab. When I will be back in Malaysia I might even fly over to Manila to buy LL in case elsewhere not possible to buy.
Some of you smart guys have to complain about everything. Most of the names in pharma are complicated. Who cares? Its something you have hopefully never even ones a lifetime in use. Who cares then about names. Or will you use it as perfume?
except the faster enrollment CD12 we got nothing to eat for the next 2 months. EUA will have no data for 6 weeks as no unblinding will take place. Our hope is Philippines. BLA continues to disappoint and delays month by month. Others are great potentials for future 12 to 18 months.
Low expectations until mid of February. High expectations until end of 2021. FDA and BP ARE the major roadblocks.
Thanks. Very clear to me.
Only those ones who are new with stock are surprised. Watching the share price of this company and listening to its CC for more than 4 years, I knew we will sink after CC. It was almost always like this. 90% of these calls had "no meat".
I expect this stock not to go up before mid of January, maybe we have to wait until the second week of February.
The future potential is great, but how it will play out, we will have to continue to watch.
Dear Rockleo, you are one of our few real experts on this board. The BLA- application process for HIV irritates me the most. Yesterday during the CC at the time of 28,50 NP said for me very clearly that CYDY didn't have the right and accepted procedure in place to measure the receptor occupancy. May I kindly ask you to answer the following questions:
1) Does this mean that the medical team didn't know what is the FDA- accepted procedure to measure the occupancy? Tests for such expensive trials should be very well clarified in advance and not 2 years after finishing phase 3.
2) I assume that all the blood samples taken during the trial are refrigerated and available. This might be several 1000 blood- samples. How fast can be such testing performed? I believe Nader knows this requirement for a very long time - at least since August 20.
Taking into account what I heard about BLA yesterday, I would believe that a BLA filing for FDA is several months and not weeks away and for UK/Canada at least many weeks. The chance to see an FDA- HIV BLA approval in 2021 isn't very high. Maybe the chance is better in other countries. I believe Gilead will not agree and empower the FDA to approve this HIV- BLA already in 2021.
It will be already a miracle if FDA approves Leronlimab for Covid 19 now during the next 2 to 3 months. Maybe the grant us a EUA the next 1 to 2 months.
Great results are one side of the coin, the other side is very big money.
As we have to assume that the research- and management team are at least very intelligent people, such questions like:
They also need the contemporaneous SOC data in order to declare endpoint(s) met or not.
AND: who decides what contemporaneous trials should be used? NWBO as it suits them? Or perhaps the RAs, each on its own or them all together?
were clarified already at least in June and July. Everybody knew these questions will need answers. This is no reason for delay. There is something else. I don't know but maybe they time it with the quarterly report?
yes, tons of buying from tons of shares sold by warrant holders. I think the warrant owners are unloading their shares, make a profit, and buying the shares using their warrants. I think this will continue and even intensifying during the next days until the extension period for the warrants is over.
I experienced this last year with CYDY. This period lasted in this case even several months. No share price move up is likely.
We can only hope for the positive PR then it could be over very fast.
What does this mean?? Appeared at "Targeted Oncology"
Search Results for DCVax
Results for "DCVax"
New content coming soon, please check back later.
TV showed today horrific pictures about dead bodies in hospitals in Texas. Nurses crying that even doctors don't want to treat patients anymore. This might have been made up as a show on purpose, who knows, I never believe anything anymore.
So thought I will check some figures hoping that least the following basic figures are correct:
USA: population 328 Mio/current daily Covid-infected persons 200 000/ total infected persons 12 Mio/ total dead persons 254 000
Texas: 29 Mio/13700/1,15 Mio/ 20872
Germany: 83 Mio/23600/914000/13900
Austria: 8,8 Mio/6700/242000/2328
Based on these basic figures I made my calculations:
USA: 609 daily infected persons per 1 Mio inhabitants/ 21,7 dead persons per 1 Mio infected persons
Texas: 472/18,2
Germany: 284/15,2
Austria: 760/9,6
One can come to many different conclusions. Some of mine are the following:
1)Austria is the worst in this small group in terms of the number of infections.
2)Germany is much better than the USA and his neighbour Austria
3)Austria might have an "easy-to fight" virus (joke!) or more robust/healthy people (I don't believe) or just a much better accessible health care system than all other countries. Compare 9,6 with 21,7 dead persona per 1 Mio infected persons. I believe that top-class health care is everywhere the same, but not everywhere one can afford to get adequate treatment.
Not only BLM but also PLM (poor life matters). Like always, the poorest are suffering the most.
I am a firm believer that when LL is finally applied, this death- toll can be reduced by 70% and we have 90% fewer long hauliers, and consequently, the pandemic is gone.
Unfortunately, I have to believe that BP wants to make money and not get people healthier, and FDA is the BP- Protection. Means we will not get LL anytime soon, most likely not before March/April 2021.
Sad to acknowledge after being with Cytodyn for more than 4 years.
PS: I don't believe in vaccination as a solution to our problems before the end of 2021. If I am wrong, I will be happy. I don't trust BP, and I don't trust the FDA. Just see what scrap they have approved (e.g. Remdesivir and others)
These pharma companies are deadly sick. Who is going to stop pharma and FDA?
I guess one of us both is very wrong. Why do you want to ask Pfizer for the efficiency result?
These are the facts they published:
1) 44000 volunteers
2) 50% vaccinated
3) later they find 170 of the 40 000 got COVID
4) out of the 170 infected persons 162 were in the placebo group
5) 162/170 = 95%
6) 170/44000 = 386 out of 100 000 got sick
7) in which time frame it is not written. The waited 1 week? 5 weeks?
8) USA has currently 170 000 daily new cases at a population of 328 Mio which gives the USA a daily rate of 170 000/328 000 000 = 52 infections per day and 100 000 people.
9) if the test got a number of 386 sick people, then they waited for 386/52 = 7,4 days;
10)we don't know where the people came from.
This is accurate science?
a) a sample of 170 people?
b) observing 7 days?
Does FDA give approval on this? Indeed, very accurate, very scientific!!
GOD may beware me from such pharma scientists and FDA!!
By the way: 52 is a very low rate.
I read this article before. It is a shame and offence for every serious and honest scientist to conclude out of such data efficiency of 95%. Is this how science is working in the pharma industry? This is a solid fake story!
The only serious and well-proven results are (and will be) provided so far from CYDY for its LL. Why they are the only well-proven pharma company? Because BP, in my opinion, is doing everything to prevent and delay LL to get to sick people LL and take big profits away from BP.
FDA is the big BP- profit- protection institution.
Being played takes 2 parties: a CROOK and an IDIOT!
FDA gets now with Biden as president a "double lead" as Kessler comes back. More of the same (Hahn and Kessler)old. What should now change? Even more "food" needed! This is the first joke!
We can only hope that this kind of "doctor" is getting to lose his license because he is totally out of picture. He is a shame for the community of medical doctors.
The message he gave, if true, follows his image. I dont like this either, but let's not follow his words but his actions. Maybe he will have tomorrow a serious word with Kickeriki from FDA and will push Therapeuticals which we need more urgent than Vacincation.
NP is not a credible person but we know Mr. HAHN and Mr. Fauci is credible. You know what? If I have a choice among these 3 persons, my choice would be NP.
One aspect I believe, with crooks you better send a crook for dealing.
EMA (=FDA of European Union) is investigating Remdesivir because of severe kidney damages. Good luck Mr. President with your doctors.
Regeneron will not work and help Trump. Therefore in 10 to 15 days, Trump will be a severe and critical condition. What will they give him then? LL! A few days later Trump will tell his famous doctors to go to hell as they let him aölmost die giving him Regeneron instead of LL.
End of the story! Likelihood? Very high!
PS: Why they don't give Trump the fantastic drug Remdesivir? Why not the even better Plasma? One can clearly see what sh.t show is going on!
I am very glad you joined the board and give us your insights and opinions. Too many crooks on this board.
For 4 years this has been a very competent board, but 1 year ago crooks hi-jacked the board and since then spitting continuously their sh.t.
Please don't go away. Thanks!
You might despise who you like. You are not important to them. The fact is, these guys got 84% of the acceptance of their shareholders.
NP has his issues, like all CEOs and other managers, never met in 45 years a perfect one, many have only a perfectly shiny surface on which people judge. Nevertheless, I like NP and I believe he will be even more successful. Take note, he was successful in the last years and he will be successful in the next few years and I will stay with him and make another fortune.
By the way, do you like the CEO of FDA, Mr. Hahn, who in my opinion bent his spine under pressure and approved Remdesivir and Plasma? Do you like such people? Would be he your CEO of choice which you wouldn't despise?
Despite my extremely low expectations for this CC, this CC was almost a lethal shocking theatre. Why the hell does NP hold such CC? I got used over many years to his poor CCs. This one was one of his worst! It will not be easy, even for him, to top it in the future.
It was a total failure in terms of content and tone.
#What does he want to achieve with this CC? to pi.. off even the own longterm loyal shareholders? We all know that LL is super! We, the longterm shareholders, don't need the 10th repetition of stories. I feel ashamed for such performance and to keep great doctors away from their work for telling us stories we have heard and read for months. If I have enough credit for talking truth, I don't need others to talk instead of me.
#Who is the audience of his CC? There are no scientists in the audience. There are very few experts but the majority is and will be shareholders with no or very little bioscience background. How many people does this CC reach?
#What is the expectation of his audience, what do they want to hear? We got enough bla bla and misleading information for the last few months, we are not interested in blaming shorters, we are not interested what others (Remdesivir) not achieved, we are interested after many months on hard facts without misleading information!
Listening to this CC I don't know should I feel sorry for NP and his team because of the hopeless helpless incompetence or should I feel sorry for me? I got taught many years ago by an expert that LL is a Superdrug and in the meantime, the evidence is so strong that I even can follow that to a certain extent. So, I need to stay because I believe in LL but not anymore in this team.
Examples:
#NASDAQ: apart from misleading information- they wanted to make us believe that uplisting will take place in August, I hoped always for September, but now it will rather take us into November or even later. I consider it as irresponsible to assume we will stay above 4,0 $ and to say if we need for 3$ additional equity we can organize it. Jesus! Is NASDAQ valuable or not for CYDY? If yes then take the credit facility and secure the uplisting! Is this a game for kindergarten??
#EUA for M&M: Most of us were made believing that we try to get an approval for EUA. Now we learn that FDA isn't interested at all in M&M (every S&C was once an M&M). And I fall from the chair: NP says he supports this view. Did he get crazy? He even doesn't fight for it! FDA approved the shit Remdesivir! For what? GILEAD failed with the mortality rate and got approved for M&M! Now we should believe to get EUA approval from FDA and MRHA based on reasonable interim results for S&C in November?
#HIV- combo/BLA: That FDA is playing NP for years is one thing, but that NP is even praising them for this game is another. We got more than 1 year ago phase 3 approved and still have no valid BLA application? Is there anyone who believes we get HIV license in 2021? For me, it is clear that people with HAART resistance are dying and need LL but GILEAD doesn't want this approval. The BLA- game will be continued for maybe years.
My Summary:
*the CC was shockingly poor in all terms
*NASDAQ uplisting is played by the management irresponsible
*BLA for HIV: we get played by FDA. We can not expect any valid BLA application this year and a license before June 2021
*EUA for S&C: maybe in November/December, but who knows how long it will take as FDA is in favor of BP with money (Remdesivir without anything positive results for people but with side effects took them few days to approve) and not with us tiny fish.
*NASH, TNBC, several kinds of Cancers: good interim results in 20221, but nothing "bankable" before 2022
*We know and heard again that LL is super and has a bright future
*What can we expect for CYDY? The company could be indeed extremely valuable, my son called it the Amazon of Biotech, but with this team, it will take many years and if we get a buyout, the real value will never play out.
NP did very well not to combine with Remdesivir.- God Thanks!!
LL would have covered the sh.t and Gilead would have said: "look our Remdesivir works!"
If Lily performs such a trial with a mix of drugs, I just wonder as they should know better: combine sh.t with sh.it, the outcome is sh.t.
Amateur you are smart enough to know that. So why you recommend such stupid trial? What agenda do you have? Maybe NP is just smarter than those who complain about him.
The shorters have increased their efforts in the last few weeks by 100%. I think the last figure for shorted shares was around 25 Mio. I would understand that these additional 12 Mio shares were used to drive us successful further down where we are.
The great short runs of the past were very well organized and successful and even involved Wallstreet Journal. I assume they have also their info- channels to NASDAQ and know that our uplisting is many weeks away from now and the can continue to short without any risk. There might be also an info channel via Gilead to FDA about the approval process and so they can work without a net.
25 Mio shares they cant cover without driving the price to the sky. They must be very sure about what they can do.
Any experienced opinion about this?
Dear Misiu, thank you for your kind answer and professional opinion. Doctors should have the choice to take what is best to help people.
If FDA is thinking that one criterion for approval is also the price of the drug then they are very wrong. The market (people, insurance companies, doctors,...) will decide what is the value of life and what are the short-term and long-term costs of treatment.
Maybe the cheapest and best would be any way to let the people above 60 to die and not to treat. Being 67, I recognize that many think like this.
When I can buy LL, I will do so as I have plans for another 25 years.
Saltz, I read your posts with great interest and respect for many years. Regarding this post, I have a very different view and as I am not a doctor- med I would like to ask Misue about her opinion to your and my view as a practitioner:
1) I understand that you say we don't get approval for M&M as LL would be of no use for M&M as it is by far too expensive. I wonder why so many of the real experts are looking at the results for M&M and even discuss Phase 3 if it is useless for M&M?? Why to waste money for Phase 2 and Phase 3?
2) I think between M&M and S&C we have a transition time of several days: during the first 3 days, we should treat the person with Antiviral drugs, eg. Hydroxychloroquine and Zinc and Quercin. Then the person might shift into the mode when the immune system COULD start to kill the person and ONLY LL can help. So far I have not heard about any other successful drug (sh.t, like Redemsivir we all know, is a fake)for S&C. Your idea is to give only LL to people who are already in the hospital and in the emergency room, just before dying, risking longterm damages. You wouldn't be my doctor of trust!
3) Only the doctor can decide when M&M shifts into S&C mode. And here it starts the problem. Why not permit LL for M&M and prevent the risk to move into S&C. If the doctor could decide, then we have "tomorrow" an normal life and no one needs lockdowns and no one needs to die because of COVID.
4)I even would say we don't need vaccines. In my country, very few people take a vaccine against flue. My last flue vaccination was in 1972. I consider flue vaccination as a waste of money and it is highly useless. If I have medicine like LL, I will not get a vaccination although I am 67. If I get once get COVID I would ask for antiviral (like described above) and if it doesn't get better I would ask for LL.
5)Maybe I would take LL even for prevention.
6)I consider LL as the fast track back to normal life. It seems no one is interested in normal life anymore.
It will be the joke of the century when now UK approves LL and the corrupted BPFDA clan in USA will be left behind. All available injections of LL, developed in USA and produced in S-Korea, will be consumed abroad in UK and EU. Will then someone wake up in USA?
Mr. Fraudi says whatever he gets paid for, like Mr. Chicken!
Thanks, very much appreciated.