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Positive data from NWBO will get approval, regardless of the FUD. No matter when they release it, it will be contested, but overcome. To your statement, that's because the government and BP were both dishonest and not transparent and lost public trust. It is not a vaccine as it does not prevent getting the disease or prevent you from spreading the disease. If they were honest from the start and said its a protective shot like a flu shot, more would have gotten it. If they were honest from the start and said this impacts the elderly (80% of deaths) and immune compromised mostly and all others should get the shots to help those people, this would have remained a medical science effort rather than political science.
"UK and Germany endpoints are already met by the data that is known to the public. I mean the 2018 JTM blended blinded data."
There is no final data known to the public. Blinded data does not meet endpoints or allow for approvals.
You cannot invalidate meaningful, positive data. Short-term, maybe...like days or weeks. Fear is a horrible strategy. Offense is the best defense.
Beyond Tiring. I am truly concerned there will be a class-action suit demanding information. Based on the company's own PR's, statements and predictions in 2020 and 2021, it would have merit. All they have to do is tell us where in the process they are. Ridiculous notion that someone will get pissed, shorts will use it against us, bla , bla, bla.
18 months next week. SILENCE.
No Powder, taxes due. Added 20,000 last week. Done for now.
LOL, up to something? Every time I see a positive, I expect the opposite with this stock. MM's will try to squash any potential upward move. So when there is a cross like this, I expect a bear raid.
She owns 3 shares. Frivolous lawsuit like the 800 other ones she has filed. No monetary damages requested? Oh, only payment of her legal fees? Which, BTW she is a partner in the firm requesting legal fees to be paid. Total joke and distraction.
The bad news technically, IMO, is the 100DMA crossing below the 50DMA. Minor Death cross. Probably will be some selling into that.
I don't think March disappointment will be any different than February disappointment. With the silence, all we have is a technical view and unfortunately that is currently negative.
Although it was years ago now, I think about the Kite and Juno acquisitions. 10+ Billion each for far less that what this should be valued at. I think $20/share soon after unequivocal, positive topline is in play. That would be 25-26 Billion....
I have been invested for over 7 years to see the results of the first ever successful GBM trial. Still waiting. The production, Sawston, Cognate...all noise IMO. This is a buyout. LP and crew would take another 13 years to get this to patients.
Just a realist. Fact: NWBO has zero commercially-approved products to produce.
To which I replied commercial scale for what? We have nothing to produce. I know there are those who believe the UK specials will result in large revenues. I do not believe that. dribs and drabs, maybe a couple per month, IMO. No one is standing in line as very few people know of DcVAX. Cart before the horse from my perspective. Since we have zero communication from the company, we can HOPE they are spending time and money concurrently on production capabilities since they know the results are approvable. Hope is not a great strategy, it is time to see the data.
Commercial scale for what? Investing time and money into something they are hiding. They may believe they will get approval but until TLD no one knows. We cannot produce anything but specials until TLD and RA approvals.
Who did DI say that to? And, despite your insistence that NWBO is deep into RA discussions for approval, there is no evidence of that. No PR of BLA, no NICE updates, MHRA told a poster via email they have no new info from the company? Pure speculation. They either have a plan (18 months now) for TLD and Journal OR they are backed into a corner. Unfortunately, we have no idea which is true.
Aaah yes, I remember my first ASCO hopes. 2014 or 2015 I think. Getting ridiculous.
We just need it to close over .78 to possibly signal a short-term trend change. What is looming is the potential 50DMA crossing the 100DMA on the downside. That would not be good. Over .80 would be really good.
Ugh, you are correct. I saw the 2020 14A, not 2021. Still, 90 days until ASM, maximum.
14A Proxy statement was filed on March 27, 2021 for ASM on April 22, 2021.
They are running out of time for quiet period, IMO. I believe legally, they have until May 22nd to hold an ASM? So, we are 4 weeks away from notification, at most. We either get TLD/Journal prior to ASM or they have to say something substantive.
No way in hell they can have an ASM and say nothing, stock would be a nickel if they keep the same talking points.
Sorry, where did that rumor come from?
Who's going to pick what time we go red today? JD? Scotty?
What don't you understand? When you finish a clinical trial, you release the trial data as required. Every single completed trial releases the data. There are regulatory obligations to do so and in this case, fiduciary responsibilities as a public company. Especially in this case of a single trick pony whose existence is directly related to these results.
NWBO has been allowed to produce the vaccine under UK specials for years. Efficacy was not known as trial was still continuing, safety record may have allowed initial approval for Specials. How can they determine efficacy without TLD published or submitted?
Usual lunchtime take down.
There is no indication that they have applied for MHRA approval, or do you have some information that they did?. And, I, like many, believe it would not be possible to apply and submit unblinded TLD data without PR'ing it.
ZERO trades or movement in bid/ask for over 12 minutes?
Who told you we submitted for approval with MHRA? Did DI tell you this? Where would you get such information? This is crazyland....
June 3-7?
I will not in the future either. BTW, it was my opinion, not rumor and there was nothing negative.
Boy, you guys are really reaching today. SP meltdown? LOL. It's been almost 18 months, there have been delays for 18 months, that's news to you? Nothing to do with incompetence. Part of this process is to find willing participants in a relatively new review process (external control arms).
Never said DI communicated that.
Stop. I didn't say anything about not finding a Journal nor did I put anyone's stamp on it. Simply my impression that TLD and Journal are not imminent.
The aggregate of the entire conversation is why I think we are still months away, not one specific statement.
Please stop suggesting things I did not say. These are my opinions of "Things that are out of their control."
He did not give me any info on timing. It is my opinion as I stated. We spoke for almost an hour yesterday.
I hope not but I certainly believe ASCO is a possibility again. I believe the hold up is trying to find peers to review the Journal piece. Getting Doctors to follow the lead of the FDA with new ways to look at trials is a problem. Stuck in outdated methodologies and unwilling to adapt.
It is pretty clear UK will be first, then Canada and EU will follow, then FDA. After my recent conversation with DI, I am not confident we will see TLD or Journal for several months. Could be wrong but did not get the impression that we are days or weeks away, seems like months still. He's still confident in the plan they have and we are producing for a patient in UK specials and hopefully that increases quickly. FWIW.
Don't think it is filed yet either.