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The last group of options expire tomorrow, settle Saturday.
ASM Sunday. Hummmmm Losing on the 5 calls. Guess that was the plan
all along.
Two words..
Hostile Takeover
Wall Street Adage:
Announce bad news on Friday
Announce good news on Monday.
End of year is like 2 weeks of Fridays.
Expect good Press Releases first 15 days of January.
By the way, I just do not understand why Australia has not given some
sort of approval by now.. Just not like those beer drinking, forward
thinking, independent mates..
Best Brain images from Cosmos
https://cosmosmagazine.com/biology/neuroscience-in-pictures-the-best-images-of-the-year
I read the book "Eat right for your blood type" and found that many
foods cause inflammation just because that have bad interactions
with our genetic make up. At first I thought it was mostly BS but found
out after trying this approach that it actually worked. It is not so much about what you do but more about what you should not do..
Maybe the answer is easier. The Rhett and PD trial are relatively shorter than most. If approved then off label prescriptions could
be made for AD patients sooner than waiting for AD approval post P3
in US and Europe.
LL,LP,LG are smart people.
All patients are on DC vac L.
All patients are living longer.
You can not advertise that which you can not sell. (Yet)
Week
Ending.....Wed...Fri
1208........24....27
1201........26....28
1124........25....27
1117........17....22
1110........17....16
1103........17....17
FDA..AA..
Partnership or buyout
It is a platform technology.
JMHO
I think that you are correct and the take down to 0.16 is part of BP's effort to collect shares before the buyout. The people that BP employs most
certainly know of DCs and their importance in the immune system or they would not have been hired in the first place.
Contact The Bill Gates Foundation if you want.. Contact info is at bottom of the web page..
https://www.gatesfoundation.org/
You're right Xena.. Please delete that message.. it was young old difference in time .
This is how Mimedx MDXG takes care of it's share holders.
https://www.mimedx.com/content/short-selling-commentary
Buy out at $375 per share..
Maybe I should put the pipe down now..
I think you are correct. Plus I believe that this last round was to
let someone special in at a low price before the news.
FWIW IMHO Just about to break out above the one hour downtrend line.
or not..
I may be wrong but I was assuming that the first group 2008 was treated
with method A, then the hold and the last group would be treated with
Method B.. Why would nwbo treat the last group with method A when method B was shown to be better?
I would prefer 6. Your 3 each broken down by Method A and Method B
106.25?
Due to the patented technology that NWBO owns and is proving to be successful, I wonder how many buyout offers have been informally discussed. With saleable shares being reduced 400/450 it seems like one of the few paths available. She could cut a really good deal for herself after P3.
What are the chances that the market makers are playing "hot potato" with
their or their client's short positions?
Worth a repeat...
If you can't buy on margin below $3 then you should not be able to
short below $3. Shorting start ups hurts all of the free market enterprises.
Try this for those without Level 2
http://www.otcmarkets.com/stock/NWBO/quote
Depends upon how long marketing authorization takes.. Seems like it is
part of Stage 2
"The medicine will be made available free of charge by the company until the
marketing authorisation is granted, after which it would be expected to be subject to
standard NICE technology appraisal."
I agree but would take it one step further.
Since the trial began the method of DCVax has changed dramatically
over the 10 years of the trial.
First is was just dendritic cells
then it was "teen-age" dendritic cells
then it was method A versus method B
then it was with PDL 1 inhibitors.
Who knows how the injection protocol will eventually turn out except
for the better. (I think they will evolve it to chronic remission (cure))
All in all the therapy has gotten much better so I think a straight
comparison of all 331 is incorrect.
UK info from Sep 2014 Phase 3 dependent.
from Evaluate
Tuesday, 09/16/14 11:42:23 PM
Re: None
Post 18995 of 125128
Early Access to Medicines Scheme (EAMS)
"7 April 2014 Applications now welcome"
see post 125069.. It seems that UK can give separate approval.
I do not remember a follow up approval from the UK on the following
press release, In the release they mention that they would be waiting
for positive results. I was considering that it may be the Phase 3
results that they may be waiting for. If the UK has already given
it's innovative medicine approval then I stand corrected.
https://www.nwbio.com/first-uk-promising-innovative-medicine-designation-awarded/
Just as a guess, I am thinking that UK approval is on a separate timeline
from the FDA,s and IF the top line data is released before the conference and if it is sufficiently good then UK may approve before FDA. This may
press FDA to give AA.
From Flipper's calendar..
Sept 27 -- LP speaks at SMI Cancer Vaccine conference (Due Diligence Courtesy of John1045)
I think it will be announced before Sept 27 because Linda will want
something to talk about..
Crossing the blood / brain barrier..
https://cosmosmagazine.com/biology/how-ultrasound-can-get-drugs-across-the-blood-brain-barrier
However, since LP owns a great share of Cognat, she should be able to
afford nwbo's delays towards success.
I hope you are correct.
DCVax is an effective treatment that is getting better with adjunctives
and has few if any side effects.
If the Phase III results are as positive as we longs expect
then will there be separate approvals by the UK and Germany
while we wait for FDA approval? Maybe hiring is related to
quicker non FDA approvals.
Interesting read about antibiotics..
https://cosmosmagazine.com/biology/the-next-generation-of-weapons-against-antibiotic-resistant-superbugs
As for nwbo and the shorts.
"They rob banks because that is where the money is at"
If DCVax-L was not working as advertised then the trial would have
ended last year.
flipper,
Thank you for your calendar.
I know you can not add these dates to your calendar posting but I was
wondering if you could guess the following dates given a July 30 date
of releasing the top line data.
UK approval.
German approval.
FDA approval.
Thanks,
monarch.