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This has nothing to do with the drug or the marketing of their stock. Rather it was due to a lack of internal controls because they had a lack of staff to separate their duties. They have fixed the situation by hiring more staff and have agreed to pay the fine. It's a nothing burger! Nice try though!
Thank you Dr. Jerry for the update.
But didn't RLTF-100 state they would extend their monitoring of the trial participants to 60 days to track deaths? That trial has already been unblinded.
Any news from the trial hospitals with expanded access? I would think a doctor in one of those hospitals would be singing the praises of Leronlimab to his co-workers and maybe even the media. I would think that Nader has gotten some feedback too and I wish he would mention it in one of his calls or videos.
Is it confirmed that a $10 million convertible note was converted into stock recently?
Dr. Patterson tweeted this yesterday, maybe try that and see if it works.
brucep
@brucep13
Anti-histamines are helping long haulers because of possible mast cell involvement!!! #incelldx #CCR5 #longhauler
Dr. Patterson Tweeted this today:
@brucep13
Anti-histamines are helping long haulers because of possible mast cell involvement!!! #incelldx #CCR5 #longhauler
Does anyone know a longhauler to test whether anti-histamines are helpful?
DSMC didn't stop the trial at the safety review at 120 patients. Everyone needs to be prepared for the DSMC deciding not to stop the trial at the interim review of 195 patients and to continue the trial to completion of 390 patients. I hope that's not true but it is still a real possibility.
Clamshorter - you are comparing only day 14. Why don't you compare day 3 Leronlimab to placebo? Tamiflu reduces the flu symptoms by only 2 days and that is an FDA approved drug. Leronlimab was 11 days shorter.
Interesting story at CNN about long haulers and test results coming back similar to aids. Maybe a job for Leronlimab? Here's the quote:
But a breakthrough came when he finally visited an immunologist who performed tests that indicated abnormally low function of immune cells, including T cells and B cells.
"Have you been tested for HIV?" the immunologist asked Coopersmith, he recalled. "Your blood work looks like someone about to get AIDS."
From the Yahoo Board: After further research, it seems Bioworld’s been publishing this date for several months now, so nothing to see here. Sorry for the confusion.
I've come to the opinion that the UK and the FDA won't approve Leronlimab until they see the results of the Serious/Critical Phase 3 results. Those results will be unblinded in two weeks and we will probably get results three weeks thereafter. If there is a substantial reduction in deaths, they can justifiably approve it from mild to critical patients without much criticism.
In the US we started with 4 new cases a day and now we have about 30,000 new cases a day. As long as people are afraid of the virus the economy won't go back to normal. So ignoring it won't work (just ask Sweden).
The Forbes article caused the stock price to go up since that happened on Sunday and the BP statement about OWS was on the previous Thursday.
Yes I agree on that $5.95 stock price. If someone had an extra $5.95, I would suggest they invest it in CYDY.
I'm not sure you can get them Leronlimab since the FDA has stopped all EIN use of the drug. Why don't you look into RLF-100 which is allowing emergency use. Here's a story about it and appears to be perfect for your friend's situation.
Link
Do we know for sure the FDA has already peeked at the S/C trial data? I thought they wouldn't do that until we hit the halfway point at 195 patients and we were only at 160 patients as of last week. Plus isn't the S/C end point deaths after 14 days so wouldn't we have to wait another 14 days from the last patient?
Do the trial results require peer review before FDA approval?
Posted on ABC News website. Sounds like they are talking about Leronlimab?
The World Health Organization said it expects interim results on a potential coronavirus treatment drug -- not a vaccine -- within two weeks.
"The group reviewed data from the solidarity trial and agreed on the need for more trials to test different classes of therapeutics at different stages of the disease," WHO Director General Dr. Tedros Adhanom Ghebreyesus said at a news conference Friday, adding that nearly 5,500 patients in 39 countries have been recruited for what's been dubbed the "solidarity trial."
"We expect interim result within the next two weeks," Ghebreyesus added.
The solidarity trial began as a study of five drug candidates, including the Trump-touted hydroxychloroquine, on which testing was halted after no significant coronavirus-related benefited were discovered.
The head of the WHO's Emergencies Program, Dr. Mike Ryan, said it would be "unwise at this point to predict when a vaccine could be rolled out."
Won't there be a lot of resistance at $4.50. If I recall correctly isn't there convertible debt at a share price of $4.50 and once the share price exceeds that price, it will be in the money and the debt will assume to be converted and included in the fully diluted earnings per share calculation.
I am sorry to report that Sarah Gray (UK breast cancer patient) passed away yesterday before she could start the trials.
No news on Sarah Wright from the UK
Yes Dr. Yo has talked to Sarah's husband Adam and has been trying to help them.
They couldn't get Sarah Gray into the Leronlimab trial because her oncologist in the UK refused to sign off on giving her chemo along with Leronlimab (per the study requirements) because he said it would kill her even though they told her previously there was nothing left they could do for her. Her husband is looking for another oncologist or other options. They are still in the UK.
Yea, I've emailed with a few Dr's including at Quest and it doesn't look good on getting treatment in the US for Sarah. It sounds like she has to be on chemo therapy while taking Leronlimab which I guess is a requirement of the trial. I believe Adam is looking for another oncologist among other options.
Also, I emailed Dr. Yo who texts with Dr. Jay everyday and he said he will try to help them if he can.
Thank you. I sent him and Dr. Jay emails.
She has previously received chemo and they have told her there is nothing they can do for her. So I don't know if it is a UK national medical insurance issue that they can't treat you twice with chemo.
Here's her original story in the UK press https://www.bbc.com/news/uk-england-kent-52431390
Well I'm not sure they can quickly find a doctor in the US to agree to start treating her. Don't forget they were coming to the US on Saturday. She doesn't have much time
The issue is that they won't accept her in the trial unless her oncologist will continue to give her chemo treatment and he has refused. I sent an email to Dr. Jay in SF to see if they could give it to her on a EIN basis. Any doctors on this site that have advice?
Someone suggested that they give her chemo in the US and that wouldn't be covered by the trial or the UK govt.
That's not the same couple This is their FB page https://www.facebook.com/savesarahgray
They don't have medical insurance in the US and they couldn't afford to pay for it in the US.
Need Help for UK woman with breast cancer. I just got this email from her husband Adam. Does anyone have connections that can help them.
Hi Mike,
I'm hoping you may be able to help me, tonight we received and email from Quest Clinical declining Sarah access to Leronlimab because she isn't currently receiving chemotherapy and her oncologist isn't willing to prescribe any new treatment alongside Leronlimab.
I have reached out to Nader for advice, as there anything you may be able to do?
We were due to fly out this Saturday but our plans may have just been ruined.....
We are great believers in the ability of leronlimab and it could be the only chance Sarah has for any form of recovery.
Hope to hear from you soon.
Adam
I meant to say that he was replying about the S-3 filing. If you recall, several people were pointing to that and saying he sold stock.
He said it was a lie that he sold stock which is correct. He exercised options and paid for them but didn't sell the stock. Now he will have to pay taxes on his paper gain (difference between the option price and the market price). I would say that is pretty selfless.
It's not Madonna. She posted that she tested positive for the antibodies so she already recovered from it. It has to be someone in the hospital now.
Cytodyn is showing the S-3 on their website being filed on April 30th but not the Form 144. That's because the Form 144 is bogus.
I think the stock sale was bogus and the explanation for the bogus stock sale was bogus too. Until Cytodyn reports the sale of the stock, there is no truth to it.