I wouldn't claim to know any more about what's going to happen on Wednesday's call than anyone else. I bought in around February of 2019 and have continued to increase my shares with the exception of a small amount I sold to cover the cost of some home renovations. I'm up a good bit. Even after the great bull*$#& collapse from $10 to $3-ish, because I'm an expert investor*.
*Not true about being an expert, just lucky I think
So what do I think is going to happen on the call Wednesday? Great question and thank you so much for asking me...
Details of the current discussions with MHRA in regards to fast track approval for COVID-19
Would it be written that way if the MHRA had already told us to bugger off?
(Please award me appropriate points for using "bugger", which I'm only 85% sure is a term used in the UK. Bollocks if not.)
I still think this is the best possible route to revenue at this moment. They developed NEWS2 and we crushed it. They also have a good bit of Covid still. I'm no mathematishionist* but that adds up to a win in my book. I'll also wager that they're at least a little less corrupt than the FDA and can see a f*$&ing gift horse when it presents itself. Also don't sleep in Israel. They wouldn't normally be in the top 5 of countries approached so there are reasons and relationships driving that which can make all the difference.
*Medical term
Status of Emergency Use Approval for COVID-19, CD10 trial in U.S.
I believe this portion of the call will go like this:
NP: The FDA has been amazing so far and they have asked us for some data around the trial that we are providing by sometime next week. After we submit that data we expect feedback within 1-2 weeks and we are thankful for the (corrupt and pathetic*) FDA's efforts in helping bring this important product to market. Can-kicking down the road in other words.
*My words, but I think we an all agree that there's some shenanigans occurring right now within the FDA
Detail discussions of the cancer results and discussions from invited guest (from Creative MicroTech) on the leronlimab potential in all cancers based on current results in the last 1 year
This is actually pretty exciting. Aren't we awaiting a breakthrough designation on the basket cancers? They, meaning Creative MicroTech, have apparently been involved for a little while now and if patients are continuing to end up with 0 circulating tumor cells than watch out!
HIV – BLA submission in U.S. and U.K.
Spoiler alert because Cytodyn wants it and they've asked for it and they've not been responded to yet. At least in the US. Try to keep it in your pants as we don't get any substantial news on this front from the states. But maybe we get a nugget or two from the UK. I mean, for crying out loud the evidence is substantial at this point. We just need someone who isn't "conflicted" to look at it.
HIV – cure project
How great would it be if they've already injected a few patients?! I know this kind of trial depends on when they're scheduled for their transplant but I have to imagine this makes all the news sites if it's successful so I'm anxious to see it get underway.
NASH timeline
I think they're finally ready to start really sinking money into this. Sucks that a fully funded, revenue generating company would have probably been further along but we aren't here to turn a $79/share stock into $94. We're trying to usher this "penny" OTC stock into the stratosphere for a much greater return. Dem's the breaks.
Potential other trials
Clearly it's not anything of substance if we're just talking "potential". I'd love an MS or Alzheimer's trial as much as the next guy but I'm banking on the fact that these sorts of things are too fringe to be happening any time soon.
Scientific Advisory Board
Wait! We have a science board?! I had no idea!!!
Kidding, of course. This is a tremendous idea that will pay off significantly over time. I can't imagine there's any meat on this bone right now though,as they just started announcing people. I'm guessing we just added another one or two people at this point.
NASDAQ uplist
People really have their you know what's in a wad over this. Nasdaq folks appear to be behind their traditional timelines right now. But even then they explain publicly that the time for the company to respond to questions is a 1-2 week process and the time that NASDAQ takes to process that information is another 1-2 weeks. So we are well within that timeframe and looking at another week or so before we can reasonably expect an answer without any other variables getting involved.
But here's the thing. We qualify. There's no reason we shouldn't be accepted. Same for HIV BLA. We qualify. There's no real reason we shouldn't be accepted.
When it comes to Covid I'm as annoyed as the rest of you about exposure but consider that almost nobody posting about Covid treatments is really an expert about what's going on. If you start googling monoclonal antibodies you will find a lot of information about everything but Leronlimab. Hell, even stat news has an article on the first page because they understand how to abuse the system and show up in searches. People who do the laziest of DD will not easily find Cytodyn or learn much of substance about Leronlimab. It perpetuates itself.
The MINUTE we get an authorization in another country (which is my prediction for how it will go, by the way) we will be contracting with them to sell over 1 BILLION DOLLARS in inventory. That's all we need. The media will follow. The share price will rise. The approvals will follow. The share price will rise. The reserving/purchase of 2021's stock will happen and that will be far more than 1 Billion dollars. The share price will rise. The agreements to increase production will happen. Me spending an absurd amount of money on a bottle of wine to celebrate will happen. Gloating to AF on twitter and calling him a failed Dbag will happen. You get the point. I'll be drunk and pretending like I knew all along exactly how it would go while conveniently forgetting that I predicted we'd be at $20+ weeks ago.
Long. Strong. And about to get the friction on.
*Not true about being an expert, just lucky I think
So what do I think is going to happen on the call Wednesday? Great question and thank you so much for asking me...
Details of the current discussions with MHRA in regards to fast track approval for COVID-19
Would it be written that way if the MHRA had already told us to bugger off?
(Please award me appropriate points for using "bugger", which I'm only 85% sure is a term used in the UK. Bollocks if not.)
I still think this is the best possible route to revenue at this moment. They developed NEWS2 and we crushed it. They also have a good bit of Covid still. I'm no mathematishionist* but that adds up to a win in my book. I'll also wager that they're at least a little less corrupt than the FDA and can see a f*$&ing gift horse when it presents itself. Also don't sleep in Israel. They wouldn't normally be in the top 5 of countries approached so there are reasons and relationships driving that which can make all the difference.
*Medical term
Status of Emergency Use Approval for COVID-19, CD10 trial in U.S.
I believe this portion of the call will go like this:
NP: The FDA has been amazing so far and they have asked us for some data around the trial that we are providing by sometime next week. After we submit that data we expect feedback within 1-2 weeks and we are thankful for the (corrupt and pathetic*) FDA's efforts in helping bring this important product to market. Can-kicking down the road in other words.
*My words, but I think we an all agree that there's some shenanigans occurring right now within the FDA
Detail discussions of the cancer results and discussions from invited guest (from Creative MicroTech) on the leronlimab potential in all cancers based on current results in the last 1 year
This is actually pretty exciting. Aren't we awaiting a breakthrough designation on the basket cancers? They, meaning Creative MicroTech, have apparently been involved for a little while now and if patients are continuing to end up with 0 circulating tumor cells than watch out!
HIV – BLA submission in U.S. and U.K.
Spoiler alert because Cytodyn wants it and they've asked for it and they've not been responded to yet. At least in the US. Try to keep it in your pants as we don't get any substantial news on this front from the states. But maybe we get a nugget or two from the UK. I mean, for crying out loud the evidence is substantial at this point. We just need someone who isn't "conflicted" to look at it.
HIV – cure project
How great would it be if they've already injected a few patients?! I know this kind of trial depends on when they're scheduled for their transplant but I have to imagine this makes all the news sites if it's successful so I'm anxious to see it get underway.
NASH timeline
I think they're finally ready to start really sinking money into this. Sucks that a fully funded, revenue generating company would have probably been further along but we aren't here to turn a $79/share stock into $94. We're trying to usher this "penny" OTC stock into the stratosphere for a much greater return. Dem's the breaks.
Potential other trials
Clearly it's not anything of substance if we're just talking "potential". I'd love an MS or Alzheimer's trial as much as the next guy but I'm banking on the fact that these sorts of things are too fringe to be happening any time soon.
Scientific Advisory Board
Wait! We have a science board?! I had no idea!!!
Kidding, of course. This is a tremendous idea that will pay off significantly over time. I can't imagine there's any meat on this bone right now though,as they just started announcing people. I'm guessing we just added another one or two people at this point.
NASDAQ uplist
People really have their you know what's in a wad over this. Nasdaq folks appear to be behind their traditional timelines right now. But even then they explain publicly that the time for the company to respond to questions is a 1-2 week process and the time that NASDAQ takes to process that information is another 1-2 weeks. So we are well within that timeframe and looking at another week or so before we can reasonably expect an answer without any other variables getting involved.
But here's the thing. We qualify. There's no reason we shouldn't be accepted. Same for HIV BLA. We qualify. There's no real reason we shouldn't be accepted.
When it comes to Covid I'm as annoyed as the rest of you about exposure but consider that almost nobody posting about Covid treatments is really an expert about what's going on. If you start googling monoclonal antibodies you will find a lot of information about everything but Leronlimab. Hell, even stat news has an article on the first page because they understand how to abuse the system and show up in searches. People who do the laziest of DD will not easily find Cytodyn or learn much of substance about Leronlimab. It perpetuates itself.
The MINUTE we get an authorization in another country (which is my prediction for how it will go, by the way) we will be contracting with them to sell over 1 BILLION DOLLARS in inventory. That's all we need. The media will follow. The share price will rise. The approvals will follow. The share price will rise. The reserving/purchase of 2021's stock will happen and that will be far more than 1 Billion dollars. The share price will rise. The agreements to increase production will happen. Me spending an absurd amount of money on a bottle of wine to celebrate will happen. Gloating to AF on twitter and calling him a failed Dbag will happen. You get the point. I'll be drunk and pretending like I knew all along exactly how it would go while conveniently forgetting that I predicted we'd be at $20+ weeks ago.
Long. Strong. And about to get the friction on.
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