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Centivax
Just saw an interview with the CEO of Centivax on Bloomberg TV. Making an injectable MAB for COVID. Phase 1 and they're getting this kind of PR. Also Defense Dept. funding.
Come on CYDY
Thanks for the link newrunner.
I'm wondering if there is a reason posters here look at the Stuttgart exchange rather than Berlin or Munich. Is it a higher volume exchange?
When I click the link I get a graph and a table that shows total volume and short volume.
Here's a link for the OTC short report that's been posted here before. It updates daily.
https://www.otcshortreport.com/company/cydy
The data is from FINRA.
From the chart:
CYDY
- Short Volume Report (REGSHO)
All RegSho Dated reported by: FINRA
Yes the Form D says $1 mil. I don't see a number of shares or share price. Disclosure of this is not required?
Just an FYI.
I've been with Fidelity for 40 years and have never been approached about lending shares until last week. The stock they were looking for? CYDY at 13% interest.
I declined their offer.
Last year NP promised revenue. Now he's talking about how big the dividend is going to be although still no revenue. We still have not even submitting a BLA successfully.
I was starting to feel more hopeful until I watched his performance on Proactive. It literally sickened me to hear him touting dividends for a zero revenue company. No wonder the shorts are all over us. He needs to go or at the very least keep his mouth shut until there is actual news.
I'm all for it at this point. Maybe NP woke up and realizes we don't have the resources to compete.
Just gallows humor. Still long but sweating it.
Worried about how we make it to next year without dilution.
GLTU
"This stock continues to flush out impatient investors who do not understand the process."
So NP sold more shares?
Um, because they have honor and understand the requirements of their job?
NP does not know the results. I did not hear him say they were paying the p statistic penalty to receive the results (which he clearly stated earlier that they would not do).
IMO there was no new information on the video (which is OK. It was for spreading the word not preaching to the converted). He already said they should receive the DSMB statement by Mid October so next Friday fits that.
Don't know if you've noticed but NP is not what you would call accurate in his terminology most of the time. Listen again and tell me he couldn't just mean that if the DSMB calls for stopping the trial because of the efficacy of LL, then FDA should "approve" it (probably EUA) and that MHRA would follow.
Someone previously posted when the DSMB meeting occurred for the earlier safety check and we heard the result (continue the trial) 3 days later. Anyone know where to find their schedule?
Agreed. Even Kelly would be better.
BOD also spend lots of time and effort on their own compensation. Hiring consultant and working the phones to get the vote at the shareholders meeting. You would think that a million plus bonus plus millions of shares that will soon be worth triple digits would allow NP to focus on getting LL approved but apparently not. (Notice how fast the Form 4's were filed and compare to BLA submission timeline)
The BLA needs to be resubmitted before it can be approved! Only timeline given for resubmission by NP was "by the end of the year" which I hope means 2020 (this time).
It is NP making things up. Said today that we're almost ready to enroll in UK.
Used another excuse for why enrollment slowed in the US.
He got a share reward for SUBMITTING the BLA. Didn't matter that it got a refusal to file. That's a great milestone.
Not to mention $1,000,000 salary 100% target bonus and $10,000,000 total comp.
Amazing we continue to work with these sleazeball companies.
LMAO
I think we're united on the fact that CYDY don't know how to write effectively.
AND that LL works.
Why are the advisory board members still not listed on CYDY's website? I've heard about it on at least 3 calls in the last few months but not even one word about the existence of a scientific advisory board on their website since March 29, 2018. That's right 2018! Richard Pestell was the highlight.
I'd be happy to be wrong if someone can find it.
The problem is the FW's that were running this place and that still control the stock. They just repriced their warrants to reflect the lower value of the exchange offer. This should be illegal.
They ran the company into the ground. They took out an extortionist's loan. CGC calls them on their BS and offers less in the exchange. They threaten to vote no on the amended agreement unless they reprice the warrants. Who cares! Let them eat shit like every other investor who bought this company and has lost and is still losing while the rest of the pot world starts rising.
Don't know why the new CEO agreed to repricing
It sounds to me that they are punting on CD-10. The real opportunity is in CD 12. Should have top line results on CD-10 next week as well as the result of the safety review for CD 12.
Dr. L sounded like he said he was suprised the CD 10 results weren't obviously better. Sounded like he wished they would have used the SAE's as the end point measurement but they did not.
I finally got in after 3 browser tries. Meeting was suspended but now restarted. 33 minutes to get into meeting. Now taking questions.
I went back to cytodyn.com and the link is gone and the meeting is listed under Past Events. WTF
Is/was there video? I logged in at 12:15 and only see spinning circles on a blue background in the corner. No audio or video.
There's nothing here that contradicts BP's statements. He's measured many cytokines and chemokines over several weeks of disease treatment and found that RANTES is the main culprit. Other markers go up and down and vary between patients but RANTES was found to be 100's of times elevated. RANTES is not mentioned in the article. Apparently the writers have not seen BP's work.
We are 100% committed and confident we can provide the necessary information to the FDA as soon as possible.
ASAP - I guess you can't miss with that timeline!
Yes. Dr. Been July 4 at about 54 minutes he said "130 or 127"
You are correct. I thought he said that in the Proactive a week ago but it was 120. Still sure I heard 131 before though. Dr. Been?
NP has been saying 131 in CD 12 for at least a week. We shot up in the week prior but now appear stalled again.
You don't think a PDUFA date or complete response letter is material?
It started right on time but NP wasn't ready. Took him 2 minutes to go full page with the presentation (13:32 EDT)
NOBODY knows how many placebo deaths occurred because the study has not been unblinded. NP doesn't. BP doesn't.
That's what I believe. That's why the FDA acceptance letter said July 10 for PDUFA date.
IMO They made the BLA "announcement" to distract us from the possible increase in authorized shares.
Worked for about 2 minutes before price started dropping.
They have to be vague because the FDA may not accept the BLA at all. They could send them a CRL instead.
July 10 is 60 days after the BLA submission was completed. 60 days is standard for FDA acceptance or rejection of BLA.
Nope. He's making a personal loan to the company of $20MM. If he keeps running it into the ground, he'll end up owning the IP according to the link.
Warrants priced at $4.93.
https://www.globenewswire.com/news-release/2020/02/07/1981856/0/en/Acreage-Announces-Comprehensive-Financing-Transactions.html
Not sure why it would be halted for this?
Yes. CGC down hard too. Cancelling the purchase option? Is there a penalty involved at this point or is all ACRGF going to get is the previous payment?