Explore small cap ideas before they hit the headlines.
Explore small cap ideas before they hit the headlines.
P L E A S E !!!
Is there anyone out there who can translate/interpret/explain
the twaddle from ILT ?
Look, I do not consider myself being a gigantic idiot, but trying to understand
ILT's gobbledygook, I fear to become one.
TIA
No evidence DCVax-L does NOT cure cancer, if you have
ANY evidence, then pls don't be to shy .TIA
If you write :...'Regulatory approval late 2026', you
mean for Flaskwork and C-Unit, right ?
Because if I recall, approval for DCVax could come earlier
as the MAA is based on artisan-production.
Typical Flipper-response :
"If you don't like me and my posts, you are an idiot, FO ".
Brilliant !
Your posts about timing (in general) have been a disaster all
along.
Why should you be correct now ?
Stop it already and do us - and yourself for your reputation -
a favor !
Could this be the first step of leaving the U.S
and move HQ over to the U.K. ?
Or that the potential acquirer is from the U.K. ? (GSK ?)
Based on the number of posts and the posting-diarrhoe by Superinvestor082
one can easily assume that the statements of LP at the ASM are important and
impactful !
Si tacuisses, philosophus mansisses
Not that I disagree with you, but in the past some very
bright, competent and well respected pumpers argued,
that the delay of approval is mainly - if not only - due the
fact NWBO (and MHRA) are waiting for Flaskworks/Eden.
Now all of a sudden it is only about the manufacturing route ?
What's in the MAA : Artisanal or F/E ?
What then are the real reasons for the delay ?
Pretty bold prediction :
https://www.investorvillage.com/smbd.asp?mb=6543&pt=m
1. The CHM will consider the MAA for DCVax-L tomorrow and Friday at the CHM's December 2025 plenary meeting.
2. The CHM will approve the MAA at that meeting and inform NWBO around 11 a.m. EST on Friday 12/19/2025.
3. NWBO will make a public announcement sometime shortly after it receives the news on Friday.
4. Assuming I am right about #1 through #3, NWBO will be trading for more than $2/share by the end of trading on Friday 12/19/2025.
The quality of your posts explains this low compensation !
Brilliant conclusion from from the chief-fudster :
When the markets are closed like on Thanksgiving today
and there are no trades,then the stock is halted.
OUTSTANDING.!!
(Use every fart to bash)
If there is a screw loose, it is very often mothers responsability !
What else could be PR'ed before approval-PR :
- Advent
- Grade C
- ?
- ?
-Approval
... at least salary-wise !
Well, he, too, didn't prove it.
It just fitted very well into his narrative, most likely for two reasons :
- Divert from the never ending dilution
- Keep the longs happy (and quiet) with the story of a forthcoming MOASS
(Just thoughts from a sceptic long !)
Everything and the whole concept starts with the
2 Bill. synthetic shares.
Are there really 2 Bill. of them (proof ?)
and how can Lou know it ? (Link ?)
That such 'shares' exist is out of question but sceptic longs want to know !
HyGro :Are you one, do you just behave like one or are you only lazy and negative by principle ?
I nowhere and never read it, but we should consider the
Advent-acquisition as a DIVIDEND to longterm shareholders
(and a FO to shorts, bashers ...)
Why only hihglighting investing ?
You can easily extend it to Pharma, Biotech
and NWBO for that matter.
Take all by AI generated posts on this board , run it together
thru AI and you will get EVERYTHING you have been dreaming of.
You most likely will at least be a multi Billionaire.
... must be combined with DCVax before blockbuster potential ..
NWBO-shareholders hope or could you come up with details and hard facts ?
That' an interesting take :
This dog is not a dog because he looks like a dog !
What a gigantic idiot you are.
What a simplistic and childish post.
At the same time arrogant and snooty.
Finally, I start to understand :
Keytruda expires in Dec. 2028 and you label that "right around the corner".
Many posters claimed DCVax-approval is "around the corner" or "imminent".
Taking the timing-guidance from your post does that mean DCVax will be approved
somewhen in 2027 or 2028 ?
(Asking for my wife)
... announced today the expansion of patient access to dendritic ...
https://www.globenewswire.com/news-release/2025/09/09/3147259/0/en/Booking-Health-Expands-Access-to-Dendritic-Cell-Therapy-After-Study-Confirms-Survival-Benefit-in-Glioblastoma-Patients.html
? What really does 'expansion' in this context mean ?
Approval in Germany ?
Compassionate use ?
What ?
It doesn't trade in Frankfurt, but in Stuttgart.
And there it was down 13.7% for Sept. 1 close, see here :
https://www.wallstreet-online.de/aktien/northwest-biotherapeutics-aktie
It typically is down when the US-Markets are closed, so I would not
read to much into it.
Yes, I too think, this was the plan all along.
But another flash crosses my mind : Was this prerequisite for MHRA-approval,
i.e. to be a fully vertically integrated company for such a complex treatment ?
He most likely will blame his basher-friends for
not bashing fast and strong enough
Would you pls have the courtesy to explain what qualifies
you to make such statements?
Have you ever been involved in such exercises ? Where ? When ?
If you can/will not then you simply are a basher, and a rather
simplistic one !
Is anyone aware of the next meeting dateS of MHRA, NICE, CHM ?
Stephen W. Tountas
https://www.kasowitz.com/people/all/stephen-w-tountas/
the new member of NWBO's spoofing-team.
Interesting from his CV :
Steve oversees Kasowitz's portfolio of contingency and alternative fee matters and
spearheads the Firm's outreach to litigation funders.
(Just his face-expression should make the defendants tremble (lol)
Peer reviewed ??
Or does the average, less intelligent and greedy investor
just have to take it ?
If AI is involved - and it is - can you provide the algorithm used ?
Merck (and BP) never done any BOs with OTC-companies is simply
the shorts and bashers narrative (or you prove it !) So, you are a short and basher !
Once a product is duly and correctly approved, there is no reason whatsoever
for a BP-company to make this step.
Your post is BS.
Artisan ?
Can anyone pls describe in simple terms of
which major steps the artisan-production of DCVax-L consists ?
I don't remember having read anything about it.
Then the next questions are :
- Is a DCVax-L price of lets say $200 - 250 K justified with 'manual production' ?
- With 'non-artisan' production the price is predicted to lower significantly,
i.e. to $ 100- 150 (?)
- Is it realistic to assume a price-reduction of i.e. $ 100 - 150 K just by the application
of a automated production-unit ? The R&D, development, maintenance and
handling of such units isn't for free either.
What am I missing here ? NOT asking for a friend, but for my better understanding ! TIA
Your comment is double-edged :
If you are a TRUE long and 110% convinced that DCVax will be approved
one day, then why again and again do the longs on this board repeat ad nauseam
the same positives day in day out ?
Conceptually and psychologically there is no difference between a pumper and a basher,
both want the duvet fully on their respective side.
The shorts, haters and negativists are in full force today !
This could lead to the conclusion that something meaningful positive
is under way.
Every statement about NWBO is interpreted by pumpers and bashers
according the own liking.
Here is mine :
Yes, the application has been sent back with the stamp "APPROVED" on it.
It is therefore now in NWBO's corner and no more longer elsewhere.