This is exactly the type of person I'd expect NP to hire.This is supposedly the new communications director for CYDY. It'd be nice and give me a little more confidence if she didn't have a mistake on the front page of her website.![]()
Speaking of mistakes...Pot to kettle->This is supposedly the new communications director for CYDY. It'd be nice and give me a little more confidence if she didn't have a mistake on the front page of her website.![]()
Her website is down. Is she correcting the mistakes?This is supposedly the new communications director for CYDY. It'd be nice and give me a little more confidence if she didn't have a mistake on the front page of her website.![]()
What are you talking about?Speaking of mistakes...Pot to kettle->
I assume she’ll be on StockXXXplode!!! tomorrow to explain what happened.Her website is down. Is she correcting the mistakes?
This seems to have nothing to with COVID or any of the other 456,396 indications CYDY will heal.http://investorsmedia.mesoblast.com/static-files/6c142520-541f-445e-80d0-d7570337e255
https://www.google.com/amp/s/www.wsj.com/amp/articles/the-treatment-that-could-crush-covid-11597360709
I’m no rocket surgeon, but this could be bad for our stock, but good for the country.
What reasons would a company have to halt their stock trading? If it’s bad news, delaying over the weekend won’t matter. If it’s good news, the stock would skyrocket?
maybe a buyout? There’s guys in here with a lot more experience at this than I, so I’m interested in your thoughts.
At .30?“And in the end it turned out CHET was short selling the whole time!!”
Huh? It has COVID in the title and the trials were for treating COVID.This seems to have nothing to with COVID or any of the other 456,396 indications CYDY will heal.
I did more research. I got my answer. Will delete my post as I don’t want to cause alarm.This seems to have nothing to with COVID or any of the other 456,396 indications CYDY will heal.
Trading was halted due to a meeting today, but it was for a different drug they ended up getting approved.Huh? It has COVID in the title and the trials were for treating COVID.
I'm not a subscriber so I couldn't see the whole article. The part that was free mentioned a 12 person study and a 13 person study. Is that all it has so far or is there a larger study mentioned behind the paywall?
As many uses for leronlimab as there are ways to eat shrimp, it fits.The hope for CytoDyn is to become the Forrest Gump of bio-tech.
This is a company that needs attention to the details. And that's a big mistake for your front page.This is supposedly the new communications director for CYDY. It'd be nice and give me a little more confidence if she didn't have a mistake on the front page of her website.![]()
THAT makes you drool???Does know how to take a photo and make you drool.
Yea if they can’t get to the nasdaq the people who didn’t get in ChetCheap may be screwed.Looks like a new trend...now we just cut to the chase and drop 7% out of the gate. Adios Nasdaq.
A Field Guide to Covid-19 Vaccines and Antivirals -- Barrons.com
By Al Root
Wednesday evening, Canadiansmall-cap biotech company CytoDyn announced it had asked the U.S. Food and Drug Administration to grant the company's drug, Leronlimab, an emergency-use authorization to treat mild to moderate Covid-19 cases.
The request was made after the company announced promising data from a Phase 2 Leronlimab drug trial.
That's good news. But following the ins and outs of therapy development can be difficult in any environment. Investors typically aren't doctors. Covid-19 doesn't make it any easier. Investors these days are tracking many antiviral drugs -- some of which were designed for other viruses -- as well as several vaccine candidates.
Vaccines, of course, prevent people from contracting the virus. Antivirals treat the disease. Both are important to defeating Covid.
Antivirals
Leronlimab is an antiviral medication that was originally developed for HIV treatment. It's a "humanized IgG4 monoclonal antibody" that inhibits the ability for a virus to enter a cell. CytoDyn (ticker: CYDY) started testing Leronlimb on Covid-19 patients earlier in 2020.
What the company said Wednesday is that patients given shots of Leronlimb improved more than patients given placebos. The results were statistically significant.
CytoDyn is a $2.1 billion development-stage biotech without sales. Gilead Sciences (GILD) is an $85 billion biotech generating more than $22 billion in annual sales. Gilead's Remdesivir is another antiviral medication that showed promise in clinical trials. The FDA granted Remdesivir emergency-use authorization to treat severe cases in May. Antiviral therapies are also in the works at Eli Lilly (LLY), GlaxoSmithKline (GSK), and Vir Biotechnology (VIR).
Regeneron Pharmaceuticals (REGN) is developing a "cocktail of antibodies" for Covid-19 treatment. Earlier this week, Canaccord Genuity analyst John Newman wrote that Phase 3 data for the cocktail could be ready later this year.
Vaccines
Later this year is also the time frame for data from important Phase 3 vaccine trials. Phase 3 is typically the last phase of clinical testing and is designed to demonstrate efficacy.
Russia made headlines earlier in the week announcing their vaccine was ready. But, in U.S. terms, their vaccine has just exited Phase 1 and 2 trials.
GlaxoSmithKline, Pfizer (PFE), Oxford University, Moderna (MRNA) and Novavax (NVAX) all have vaccine candidates in Phase 3 testing. It has been a while since those entities updated investors, but enrollment should be wrapped up soon. Each of those companies -- and the university -- is recruiting about 30,000 patients in the final trial.
The Stocks
Covid-19 health-care stocks have had a wild 2020. CytoDyn stock actually dropped 8.5% following the conference call. The stock is down 15% for the week, despite positive data. Still, shares have gained more than 300% year to date, far better than the comparable gains of the S&P 500 and Dow Jones Industrial Average over the same span.
The stocks mentioned above are up 465% year to date on average. Novovax is up the most at more than 3,200%. Glaxo is the weakest of the bunch, falling 12.3% year to date.
Write to Al Root at allen.root@dowjones.com
I am buying back some of what I sold in the upper 4'sAnyone buying?
Nah. Have too much at this point (not selling) and it’s less certain than ever for me. That price drop after good covid results was alarming.Anyone buying?
I bought at 3.60, time to start fighting back on this day.Anyone buying?
What changed is they had good results and nobody cared. Good science doesn’t mean anything unless you can get people to know about it.I bought at 3.60, time to start fighting back on this day.
What has changed. Good data for mild to moderate and a severe critical trial that I still believe will have good results.
Yah, I think the Risk to Reward right now is very good. Feels like 2.86 is a solid support. Of course there is risk, but unless a Phase 3 is denied for M-M I dont see below 2.86 in short term.Ahhh, who am I kidding. Bought 2.5k more at 3.72.
I'm a believer. Or an idiot. Or both.
FDA caring is what matters because frankly I don't think the investment community doesnt care, its that they cant decipher whats bull#### and whats not, relying on FDAWhat changed is they had good results and nobody cared. Good science doesn’t mean anything unless you can get people to know about it.
What are the odds of the EAU? I’d put it at around 20% and honestly I’m being generous. A phase 3 is fine but will take longer and they could be passed by another drug.FDA caring is what matters because frankly I don't think the investment community doesnt care, its that they cant decipher whats bull#### and whats not, relying on FDA
Approval = huge bump.
P3 = Potentially a price hit in short term but I'd guess stays in the 2.80 - 4.50 range until S-C gets closer.
Stop trials = We're in the 1's
Personally I was never counting on the mild to moderate trial to be the winner. I think the results are good enough to get them a phase 3 but was happy that it just showed efficacy because I do think this is going to bode well in current and future trials.What changed is they had good results and nobody cared. Good science doesn’t mean anything unless you can get people to know about it.
Yeah, don’t think we hit 3.5 million until after 11 pst yesterdayA lot of volume already in the first hour