Ticker on Fox just said Trump announcement coming at 5:30 EST. Don’t know if they changed the time, but I will certainly be tuned in early.

I heard Meadows say that too. Hopefully he was just emphasizing the delay in FDA. But our results did come out weeks ago (seams like months now). Although they did submit the EUA just 11-12 days ago, I was under the impression that the results were shared with FDA and even Big Pharma when they originally came out. If so FDA knew about results before the EUA. Who knows!

CNN, CNBC, etc... are all parrots. They repeat what the see on other stations. The Ex-FDA guy suggested it might be plasma and then Washington Post ran with it, then CNBC, then CNN. That’s how fake news takes off.
Plasma would NOT be a breakthrough! They have been doing it for months and the FDA just pulled it this past week. IMO

Mark Meadows on Fox Sunday did say that what Trump was going to talk about should have been announce a couple of weeks ago when Wallace asked him about Trump complaint that FDA is dragging its feet.
So I seriously doubt he is y’all about Plasma.
IMO

A lot of hype about Ivermectin. Australia paper says it’s a cure in 48 hours. But further review shows you have to take 120mg, when normal dose is 3-15mg. No trials have been done, so doubt (hope) this isn’t the big news

That wouldn’t be a Major breakthrough on therapeutics
It’s been there, it’s been pulled by FDA. Don’t see that being brought back would be a Major Breakthrough
IMO

Sad news on Holly the other day. Cancer has spread to much. Going into Hospice care. My prayers go out to her and her family. Unfortunately this is the path of many of our women today. I don’t know if Leronlimab will be the all out cure for this cancer, but we definitely need to keep up the fight to find it. And before the net sayers and Shorters attack the drug for the failure, please know the science of LL. It is not a chemotherapy drug. It helps to prevent the metastases of cancer cells. In Holly’s case, it was too late. God Bless her for trying and look over her family.

As far as Viral load, Dr BP is talking about viral load in the blood. This doesn’t happen until the vascular tissue in the lungs starts to weaken after the Cytokene storm and basically your are in Severe/Critical condition. So I don’t think there would be any viral load in any Mild/Moderate patient. I believe BP even said as much during one of the YouTube videos. Now in the Severe/critical trial, that would be important to know and I would think that info would be supplied to the FDA

BP said, on Dr Yo, he didn’t know him, but that doesn’t mean that someone doesn’t know them both

This from MisterS on another board:

“ They just announced P value day 3 is less then .03 and 14 day is leas then .02. I looked up P value online and this is what it states:

“ A P value <0.05 is perceived by many as the Holy Grail of clinical trials (as with most research in the natural and social sciences). It is greatly sought after because of its power to persuade the clinical community to accept or not accept a new treatment into practice.””

FDA will take notice. IMO

I agree, we have been complaining about lack of media attention for weeks. This would have been a GREAT opportunity to hit up all of the Media companies. “The drug is Leronlimab and We now actually have Significant Trial Data, we are Cytodyn”. Let the world know who we are, get interest going. But so far....crickets. You have to make yourself be heard in this day and age. Maybe they will this afternoon, maybe they have plans in the works, but from past experience it’s doubtful. We need a REAL PR FIRM NOW! This should have been a no brainer.

The hypocrisy is overwhelming. This is Nevada Governor buying Hydroxy at a Walgreens In May after exposed to someone with Covid. This is AFTER he put a Band on the sale of it in March.

http://360newslasvegas.com/sisolak-took-hydroxychloroquine-after-cv19-exposure/?fbclid=IwAR1OFaI1Yj_XxzygnS6rrgn3eAvzp9OByVWGVX3tU7Hm77NnUg4rkMNgx_0

I have said before, I don’t know how truly effective it is, but the safety record of it and the success proclaimed by hundreds of Doctors who prescribe it has convinced me that if my family or I get Covid, we will take the drug! Not suggesting anyone else do the same, but until something like Leron is available, that will be my choice. There are several large studies that say it works and several that say it doesn’t. IMO

Even more interesting, if the US believes Hydroxychloroquine is useless, WHY are we sending 2 million doses to Brazil????? Would that not be an insult to our southern friends, a slap in the face perhaps?

https://www.usnews.com/news/health-news/articles/2020-06-01/us-sends-2-million-doses-of-hydroxychloroquine-to-brazil?src=usn_fb

Yeah, Fauci says it doesn’t work, but here ya go!

I am as disappointed as everyone about the S2C DSMC not leading to EUA, but the bigger trial is the M2M. If, and that’s a big if, it shows that Leron can substantially lead to less patients progressing into Severe/critical, then it will become the standard of care for anyone getting Covid. And with less progression, there will be much fewer Severe/critical to treat. That is my hope! Get Covid, go to hospital, get a shot then go home. Sounds familiar

https://www.cytodyn.com/investors/news-events/press-releases/detail/456/cytodyn-receives-positive-dsmc-recommendation-for

May have been financially beneficial to exercise this transaction prior to the Stock Price taking off? This could be a GOOD sign. Not a tax lawyer or accountant, but could be true.

Awesome follow-up, thanks!!!

Yeah, there’s no appendix saying what those Codes are so I don’t know. Hope that’s it

Unless he’s trying to set up an incredible trap for Shorts, this makes little sense! And even if it was a trap for Shorts (which I doubt), a lot of people will lose a lot of money. Not cool! If someone with more experience in these type of transactions has a better explanation, I would love to hear it.

This is very interesting and perhaps a bit concerning. Not sure of all the inner workings of his compensation package, but I can understand getting the 323k shares, but I’m not sure why he then sold 157k shares at 4.97. Especially knowing that the results of both trials will be coming out in next couple of weeks. I expect another article from AF tomorrow about this! ??

I just forwarded this video to Senator Cassidy of Louisiana. He will be on TV tomorrow (I believe FoxNews Sunday) and urged him to watch it. We need more public and media interest in Leronlimab so the FDA can’t suppress or delay our results at the behest of Gilead.
Hope it works!

I agree, the serious side effects of Maraviroc make it less desirable for long term treatment and in that race I would bet on Leron all day (all though there are a lot of HIV patients who are taking it). And the short term Side effects of nausea and diarrhea also favor Leron but the benefit of po form will be still be advantageous. It will be interesting to see just how effective it is with COVID. I read that Leron covers the CCR5 surface by 108%, basically overlaps it, not sure how well Maraviroc bonds and whether that will even be a factor in Covid. I also saw that Leron is not cross-resistant with Maraviroc with HIV (cells become resistant to Maraviroc but not Leron) but not sure if that will make a difference with COVID either. I’m just glad we will be able to bring Leron to the public for Covid first. Hopefully the Gold Standard!

Maraviroc, Pfizer’s CCR5 antagonist, starts Phase 1 trials for COVID in September. It expects to be completed by December. Biggest plus for it is that it is in a Pill form and already in use for HIV. Don’t know how well it will compare with Leron, but will no doubt be a competitor. Hopefully we get approval in few weeks and become the standard that they will have to compare their drug to. And by then, hopefully our HIV treatment will be off and running as well as Breast cancer indication (the bigger market). I would assume if we are successful there, Pfizer will start their own trials for that as well.

https://clinicaltrials.gov/ct2/show/NCT04435522

Senator Bill Cassidy is a fellow physician from Louisiana, I saw that he is going to be on national TV this weekend (I think it is FoxNews Sunday). So I sent him a detailed email about Leronlimab and asked that he sheds some lite on the drug to the country. I invited him to do some research into Lero and be the first politician to bring the drug to the media before it hits big in the next week or two. We need the media to start taking notice to lessen the chance of FDA or Big Pharma keeping it in a box. Hopefully Optimistic!

Whosonfirst, read my follow up post #99984

While my jury is still out on the effectiveness of Hydroxychloroquine, I can tell you without a shadow of a doubt that if I, or my family members get the Rona, I/we will be taking the combination with Zithromax and Zinc.
Those drugs have been used by more than 60 million people with very minimal side effects. So I have no problem taking it. I have seen too many patients and friends with the disease....it ain’t pretty.
That is, until Leronlimab gets approved!

Thank you! You are helping me make my point. I’m an anesthesiologist, I Don’t prescribe medications for any Covid patients (although I do take care of them). My point is, Data can be manipulated in many ways. That’s why all results need to be peered reviewed. I hope for, and believe we will see very good results when they come out. I believe in the science. But it will all need to be peer reviewed. Bottom line, don’t believe everything you read!

I am a Physician and of all the people I have written Hydroxychloroquine and Arithromycin to, ZERO have progressed to point where they need ventilation

Raises Trump discussing it towards the end of last week, Mark Meadows was on TV this past Sunday saying same thing. Here is just one article about it

https://nypost.com/2020/07/26/new-covid-19-treatments-may-be-days-away-wh-chief-of-staff/

Food for thought. The administration said there would be strong, great news coming out later this week about therapeutics. So far HGEN and Moderna have already been in the news this week and it was that big. So I doubt either of those are their big news. NP schedules Conference call for Thursday, not on a Friday afternoon (as one probably would with bad news). IF the administrations “great” news is about Leronlimab, I would expect either a press release, or announcement from Trump, on Thursday morning with NP’s follow-up conference call to discuss implications, possible licensing arrangements, manufacturing, etc....
To schedule a conference call 4 days out, you must be expecting, or know, what’s going to happen over those four days. Hopefully optimistic and as always IMO

Grip, I’m a physician in Las Vegas and would live to partake in the celebratory Wine and Cigar along with you!
Go long!

All I have is my control number. Don’t know the password so had to sign in as guess ??

Shareholder meeting
https://computershare.lumiagm.com/?fromUrl=285700571

Shareholder meeting
https://computershare.lumiagm.com/?fromUrl=285700571