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Really need to tie in some papers being published soon. Voting no until we get approvals. Isn’t it funny how T/A guy has a word ion his name that he complains about all the time. Hope for approvals. Hope for BLA etc.
Says posted September 05, 2020. Did you get it hot off the press? Great job let’s see if the competency level at FDA and NIH can comprehend this article. Very straight forward
Can see the shorts and AF coming out in force tomorrow with Fife story. Hold on
What I find kinda interesting is how CYDY is a week away from getting approvals in U.K. and meeting with FDA next week. So after yesterday’s CC and all the great news, SEC files charges against FIFE and Iliad who financed us to the tune of $28.5 million. Does anyone else see the connection to this. One day after one of the most positive CC with numerous catalysts right around the corner. Something very fishy about this. So all or most of the marbles seem to rely on getting approved right away. What will become of the funding and contracts written by Iliad, now that Fife is under investigation by SEC
Posters crack me up no approvals on yesterday’s call more of the same. Look in the mirror. Stop with the nonsense. This drug is on a fast track to stardom and approvals are very close. Are you seriously distorted by past mistakes? Things are moving forward as fast as possible. However we are at the mercy no more of the slow rolling FDA, beholden to BP. Once this gets approved in U.K., the FDA will be revamped. Chaos rules in the current administration. Lies being told in order to save their interests in BP. Truth is we all know that Leronlimab cannot be stopped. Too much forward momentum and in two weeks time, looking back all the mistakes will be forgotten when stock price takes off. NADER=GOAT
Fumbles don’t always go down as turnovers. We are right where we need to be. Advancing to the next level is what we are waiting on. All indications are stacked in the right direction. We hit the board in U.K. before all this talk about rushing vaccines out by November 1st we good. COVID is unfortunately something that happened that might open the door to a world of promising Leronlimab for multiple indications. Two weeks time should have some of the biggest questions answered. Then we ride fast and furious to the top.
Few more weeks of shorts before this rocket flies. My original prediction was by Columbus Day we would have confirmed results of CD-12. Looking like right on the money. As far as uplist, just don’t see it happening. Maybe after approvals come in. HIV looks like we finally will get some traction on moving forward. Voting No on additional shares until something is approved. Talk about putting the cart before the horse. Papers will coincide with U.K. approval around 9/21. All IMO
Most questions came from some serious players from finance sector hoping to get more info from Mulholland on uplist. To me it would appear that there is some serious interest amongst institutional players that see this company has a ton of potential. Just waiting on the sidelines with boatloads of dollars. The drive towards the end zone before was ground and pound. But now it seems like there is an aerial attack as well as some trick plays being mixed in as we go for the touchdowns. We are in the red zone and a few more plays will get us to the desired results. Progress is happening. How many other trials have been shut down already for not meeting endpoints in safety or efficacy. How many trials have had there endpoints changed or criteria made less challenging? Yet here we are inches away from approval based on appropriate trials double blinded with outstanding results no safety issues and 150% better results in NEWS2. FDA sees the bull charging and will have no choice to approve before U.K. or it’s lights out for whatever credibility they have left. The easy bar was set by approving Remdesivir and CP so now they are trapped. Good luck to the shorts trying to spin this positive CC into a nothingburger.
Nader is insane. Definition of insanity doing the same thing over and over and expecting different results. Someone please notify Bellevue on of their patients has escaped. He is not bashful for one thing. How can you reward yourself with no approvals no revenues, fumbled BLA, many missed timelines, e mails not sent or fax machines checked and the list goes on and on. Science is great, Leronlimab is great. If all of this is true why are we not on everyone’s radar? Use of those shares would be better utilized for a great PR firm with connections to major media outlets and possibly a hire who has a connection to the higher ups at the FDA.
Just doesn’t seem right that all along those 100 million shares that were voted on to supposedly hold off hostile takeover(lol) and the possibility of no financing or approvals came through we were led to believe that a very small portion might be needed as to not dilute shareholders positions. And now only 6weeks later, we are asked as shareholders to increase authorization of those shares to reward those in charge who have yet to get anything across the finish line. When does this accountability come to the forefront. Those shares need to be authorized based on performance. Of course with slight exception to entice the best people for the advisory committee, but for the others absolutely not. Do your damn job and get something done already
Wow feel like we was robbed. Sure wish I could compensate myself like that. It’s like being held hostage vote yes or we won’t be able to give ourselves more compensation and help ourselves out with goodies. Lots of big balls to mess up on so many fronts without any profits to ask for more. How’s about performance related. Isn’t that what compensation should be based on ? Doing the job right. Not missing paperwork. Meeting timelines. Can someone answer this rationally because it would appear that there will be plenty of no votes on this one
No credibility lost great drug great team just fighting an uphill battle. The more we get beat down, the stronger we come back fighting. Can you feel the momentum moving in the right direction. At any moment greatness can be achieved. FDA can be heroes, UK heroes all it takes is someone to have the guts to approve Leronlimab for EUA and let the drug take it from there.
Read last line says NOT. I’ve been here for long haul may not agree with everyone as I’m sure there are two sides to each coin but I’ve lost plenty more on the Jets than I can stand to lose on here. If this is a home run I will be here. If it is a strike out oh well it is penny land. It’s not about the money as much it is about saving the world from Covid. The world is full of good actors. But the forces of good can not seem to rise to the top with all the negative forces trying to stomp them out. Looking forward to rest of the week. The waters are choppy and there are tons of sharks circling the boat(shorts) waiting for blood to drop. I will stand firm and continue to take a stand for the best drug available Leronlimab
Wow that’s it I’m selling all my shares I can’t believe it. Thanks for bringing this all to light justda. Don’t know where I would be without your DD. Excellent wait for it NOT.
Nasdaq uplist share price $5.95.
Expecting huge news on Wednesday hitting a trifecta. Sorry that’s at Saratoga. As far as CC smooth as cream cheese Nader will fudge things up. He has an impressive streak going unlike EF Hutton when they spoke people listened. My new Lambo has slowly been turned into a 2002 Toyota Camry.
Putting on my crash helmet for this weeks drop. All talk no action CEO just doesn’t get it. The pep rallies fall short all the time with no significant information. All indications would seem that unfulfilled promises and timelines will be pushed back and the only news we will look forward to will be CD-12 which unless it’s a home run will not encourage FDA to grant EUA. So far every PR that has been put out has been met with silence. IMO we have the science, we have the results, we have the catalysts, but no traction due to being traded on otc and not in the big leagues. Miracles can happen but the probability seems to get lower and lower as the days pass.
I find it ironic that Descovy for prep advertises during Two and a Half Men show and Charlie Sheen is taking Leronlimab for years. We have very little publicity, no money for media except for Proactive, and are not known by many except stockholders and a few others. Two trials stellar results and not a peep. As mentioned on another board 9/14 there will be a groundswell mentioning Leronlimab and Cydy on Facebook, Twitter, social media to bring awareness as well as info being given to long hauler groups who are desperate for help in getting rid of their ongoing symptoms. Sure hope this massive CC brings some good news, especially in light of the FDA pushing miracle vaccines before phase III trials are complete granting EUA to them.
Who knows maybe after conference call Nader will announce his resignation. That should make a whole bunch of people on this ihub platform very happy. No names mentioned but you know who you are. All IMO and best of luck
This is the stacked deck that others have talked about. FDA and BP are winners and then bogus vaccines next
So there it is your head to head with Remdesivir. They did a phase III with many more patients. Sets the bar for a phase III for Leronlimab. Whether we are better at 3days and drug does the wonder 3 as Dr BP states it will not matter. Need a much larger phase 3 and then it’ll be to wait for S/C results that need to be far superior to the almighty Remdesivir.
So why wait til September 02 to hear this: already know the answers.
#1&2 Topline info sent and we are waiting for a response yada,yada,yada
#3 Cancer basket trial with many indications(22) currently enrolling moving forward
#4 HIV sub in US & UK Sept 4 written response to questions from our original RTF
#5 HIV cure just starting intend to enroll Yada,yada, yada
#6 Nash timeline many years Yada yada yada but we are hopeful
#7 Potential other trials? Anything and everything under the sun and hopefully something will get approved
#8 Scietific advisory board The best of the best but being CEO I don’t listen to them
#9 Nasdaq soon lol very soon lol like never no revenue no sales no approvals
So why wait til September 2 all questions answered today
So let’s see it took how many weeks for M2M data to come out with the results? Now it’s sent off to theFDA to review all the data. They are not gonna say ok we will go by what you say without checking it especially that it is a new drug to market and all the other screw ups so far in announcing SOCs that are just not that good. Same with S/C. Results will come out and will be vetted again by FDA. We know that in the FDAs statements that they would expedite all drugs that showed safety and efficacy as compared to the current SOC. Of course Nader should refrain from giving timelines and stop flubbing just give facts as he receives them. No news is good news if the only news that comes out is not as spectacular as some seem to believe. Science is one thing but once there is doubt due to serious issues being brought up then credibility becomes an issue. Shorts will always be here. They feed off this stock and all the hype without execution. It buys them time which they know they have with all the delays and missed timeframes that are forever blurred out on proactive. Covid is not going anywhere fast as schools reopen and people go back to living their lives. Sometimes the only way the rookie gets is chance is by luck. Someone is underperforming or gets hurt. Let’s just see if we get our break too.
Trump, Fauci and FDA signed NDAs to reveal anything to do with the word Leronlimab or the company CYDY. That is the reason nothing has been said. Looks like BP is the only thing they are allowed to mention or give OWS money and airtime to. Hearing any NEWS from across the pond or another country might be the best chance for our once in a lifetime drug. The word is getting out there but it is slow and not enough to influence the share price or get many new investors on board. Silence is golden but also deafening and watching paint dry is even worse. In for the long haul and approvals to follow. GLTA
What a great country I tell you. So president will announce a Covid test that can give results in 5 minutes for $750 million and then once you find out you are positive you can hope to be treated with an IV drip of Remdesivir to get out of hospital 4 days early or get an infusion of CP and hope the blood isn’t tainted to get antibodies that may protect you from the virus depending on the level of the plasma that is being transfused.
Anyone know what time NPs flight to Dulles airport lands?
What’s plain to see is as time drags on there is less of a chance for any EUA without at least a phase III for M2M something should have come about by now. Second the Nasdaq should have been in contact and as of now the uplist would appear doubtful. UK and others will only follow FDA approval. A lot of talks on therapeutics but that’s all it is. Vaccines are the king unfortunately and we all know how that will be rushed and more than likely produce less than stellar results for a mutating virus. The hope is for something positive to come from Sept 4 questions fromFDA re : HIV and the results from SC trial. Until then we will drift in the abyss and have to fight the lies and distortions created by the FAKE NEWS.
There are posters on this board who gather tons of information to INFORM. A ton of posts are mere speculation as to timeframes and share price and end with IMO. And a lot is banter between posters. I find it educational, informative, humorous at times and ludicrous often. Once again Dr NP cannot just randomly put out information as he likes. There are as he said proofreading a by legal team to make sure PRs are on the up and up. Those of you that choose to engage with the slimy media see firsthand the agenda. Lies and distortions, cut and paste, edits to the truth all in order to stop the inevitable which is the science and results of Leronlimab. Nader said trust in the science and fundamentals. If not sell the stock. Watching a pot of water boil doesn’t get the water to boil faster. Hang in there if you are a believer and know that the trials will be completed and the results will be what they will be.
Isn’t it really obvious that every time there is a bit of good news, there is a counter hit coordinated by the likes of AF, WSJ, and Stat. We really have the best drug cause everyone fired off all the artillery they can to prevent Leronlimab from ever making it to the big league. This is a war that we are fighting in against many fronts from an incompetent FDA, a clueless administration that touts bleach, compounds in a flower, and CP with no trial data. Amazing how this country is run by the shills who are paid by BP to silence the small players by spewing and spinning false narratives cause that’s all they have. Bring in science bring in safety and efficacy bring in results of properly conducted trials that were performed to spec with no funny business like changing endpoints and moving goalposts. I can only say that this drug really needs to be used outside of the USA because the swamp was never drained when this administration took over. Only big players with cash allowed at this party. No lobbyists need not apply. CYDY stands on science.
Been involved in many NDA’s before. So much info is held close to the vest. Sure when price increases or decreases everyone is quick to assume someone knows something. That’s not how it is all the time. Sure Kodak was a fine example of this and look at all the problems this created. There is enough going on behind the scenes right now that would make your head spin. Like many on here have said they are in long term and believe in the science. Let’s keep it that way. Eventually things have a way of working out. GLTA
Next PR will be on Thursday announcing cD 12 completed interim enrollment 195 with clock starting for results on mortality at 28 day. Expect results out by end of September. And the beat goes on. Next week 2 big announcements re: uplist and update on talk with FDA re: HIV BLA IMO of course
No news 10% down day
Too bad cuz in a head to head trial, there would be no doubt and all this current SOC bs could’ve been put to rest instead of hundreds of thousands dying needlessly
On may 18, press release for phase 3 protocol three arm comparative trial of Leronlimab, Resmidever, and comparative and combination trial of Leronlimab and Remdesivir was to be conducted. What ever happened to this? Had this trial been conducted it would have shown Leronlimab to be a slam dunk as the best treatment for Covid. Yet nothingburger. Why
Another losing day down 10%
Let’s revue what just happened. Leronlimab was not mentioned by Trump. Plasma was. Does that really hurt Leronlimab? Look how many Drs in the medical field are questioning this and it’s effectiveness. There are lots of problems with it. It reminds me of the NBA lottery draft. So big deal you lose the #1 pick who turned out to be a dud and you enddd up with the #2 pick. We are still in the game with a highly prized pick that no one can compare to us right now. This announcement wasn’t an all in win or go home. Too much hype and speculation that we would be named. Our time is very soon. Ask yourself this question? Did all the other players get mentioned either? Stay with the real facts and not justdafacts. Some TA commenters make it out to be game over put a nail in the coffin for CYDY. Far from the truth. You can only slow down the freight train for so long. We will be successful albeit in another country but it is coming.
Any timeframe on publishing Dr BP papers
So let’s see if we had two PR released this morning, DR BP, Dr Yo & Dr Drew this afternoon discussing Leronlimab and OWS letter and an early evening thriller Proactive video with king Nader, I’m sure this trifecta of good news should bring us down to about $2 tmorrow. Don’t know how this game works but I’m long and strong so bring what you have and I will buy on the dips. GLTA
As the expression goes Drive For Show, Putt For Dough. Let’s see if this puppy can exceed that and get a hole in one. All we need is one more pin Rodney. Steady calculations and a sharp eye on the ball will get Leronlimab to the 18th hole with a huge lead. Can anyone else feel the need for this drug to get us back up and running. For shame that so many die each day unnecessarily as FDA delays. To all the DRS a shout out and thank you for your tremendous work. And to those who go the extra yard bringing tremendous knowledge, research and debunking bs myths appreciate you. You know who you are. Let’s rock and roll
FDA= NO WAY. Conspiracy theories grow. Better shot going outside of USA for approval. IMO of course. The crystal ball get mighty cloudy when those who look to line their pockets are involved. What a lie. It appears that even convalescent plasma is now the bone of contention with the NIH. How obvious is it that the favorites will be the ones these lifers decide on regardless of results.