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I hope I wrong because I am trying to buy more
I hope I am wrong
But late Friday run looked like capitulation
From the shorts..
Normally a fri afternoon option expire rolls down to lower strike..5
The. rolls down a little more monday..
Monday midday picks up for fear of teus pr..
The upswing fri felt odd
I have no doubt .. zero
Agreed Ba.. ridiculous to have placebo arm when so many failed trials with ample placebo documentation have already occurred
It is early Alzheimers
The progression of the disease varies greatly at the early stage.
It is very possible that some patients will not have deteriorated after 48 months..
In the placebo arm whatever that number is.. simply deduct that number from the
responders in the 30mg cohort and the 50mg cohort..
So if 5 out of 170 placebo consort are. Close to baseline..
And 85 from the 30 Mg cohort are at baseline or above.. reduce that number to 80..
And when 170 of theb50 Mg are at baseline of above you reduce that to 165..
Making the number 245 out of 330 are at or above baseline due to Blarcamesine..
Why argue minutiae? The meat of the data will leave zero doubt only adulation and joy and
will make these arguments pointless for the shorts.
We will blow this away
Blow. It. Away
Normally 4 point drop over year for placebo.. but it is early Alzheimers..
outliers in placebo should have been removed.. I don’t think it’s impossible
that a couple of early Ad patients have fone better( there can be a placebo effect)
The placebo effect is real especially for early ad..
What is about to get even realer..
Is called the Blarcamesine EFFECT!
When Blarcamesine so agonizes the human chaperone Sigma One Receptor
that the Sigma One Expression throughout
the human body explodes!!!!!
The Blarcamesine Effect will be revealed
Soon
Nothing ever like it ever.. in the history of human medicine.. strap yourselves in..
Put in your oxygen masks.. the air is about to get thin..
Mine is at baseline or above
Anavex May delay tlr now to confirm and prepare for scrutiny.. that is it.
They have TLD.. it’s been analyzed and shared.. they have a short window to confirm and prepare the pr.. they might be able to argue to wait until 8k. ..
but no more really…
Dr mcfarlane will still get to be hero..
All eyes will be upon him..
Nope.. read pr.. they will release tlr prior to CTAD.. they will release and let CTAD explain the full human glory
170 50 Mg super supers
85 30 Mg super supers
255 super supers at baseline or better out of 340 dosed participants!
All 340 dosed participants perform significantly better than SOC or Palexo cohort average..
I think they took down my response to thiS!
I expect all 180 high dosage to be super responders as DrM said high dosage is the common denominator.. didn’t say common denominator of what. But what else could it be other than success..
Than I expect 1/2 of all 30 Mg to be at baseline or higher because this is Early Alzheimers sufferers and their S1 r signaling should be strong enough to catch on at 30 Mg..
So about 270 of the 340 dosed should be tremendous responders and all of the dosed patients should be better than average of placebo..
Maybe I said something about the horrific recent fda decisions regarding children and ineffective , evemn dangerous medicines..sometimes those notes just sneak in my posts trying to save children
Ba is that you? So positive Paula..
Nice
I could see him print topline and then having 8k to flesh out.. or vice Versa..
I don’t know if we will have Conf call before CTAD .. but if k comes out he almost has to do Conf call
Well.. so that would be when to look for tlr..
Is there K filing scheduled before 12/1?
Maybe they got the phone call..
We’re screwed
Worst short post ever
They must really be afraid
The cabal says .. don’t hurt us too bad
and live in fear!
Haha up yours cabal..
Praying for your souls..
I think He will Pr when Poster released to CTAD..
Especially now that we know the shorts will have access prior to CTAD through media release
Clue..
Anasveix is hiring National Sales Director
Anavex late breaking at CTAD
Peer reviewed
Hiring spree
Macfarlane gliding’s presentation
And the. Number one blue of all..
Dr M. Paraphrase
The common denominator isn’t S1r wi TLD type the greatest common denominator is high dosage
Those aren’t clues those are statements
Dr m will pr tlr priorr to CTAD..
It will happen when he sends in
Peter’s two CTAD because we now know
The Shorts will have access to the data as well. At that point.
Dr M knows this as well
Dr McFarland shoulda charter a jet and brinG all of the patients that so desire, two CTAD.
Or just bring Em Heaven.. that is one funny Son of a Gun
MAybe chatter jet ands and have Dr Mac Farland shepherd rhee into. CTAD..’
I figure
250 out of 350 still at Baselsine ag tier high dosage OLE
Bring tihe them all
Probably PR same day
Anavex v relgiaters Poster with CTAD
Also means. We will sure PR of TLR before
CTAD..
Pro ab ally same day CTAD sends out potatoes to. Media
Also means
Anavex results are no secret
Biopharma does not go on hiring sprees
unless they KNOw they have the goods..
They have zero income
DrM has counted every single expense aince the beginning.
There is zero way he risks the future
By increasing overhead if he has ANY doubt about immediate success.
He would not do that to the company
He would not do that to the new hires
He would not do that to the investors.
He would not do a late breaking session
if the data wasn’t off the chart
Forget what anybody else has done or would do.. DRM would not..
I don’t understand how we are not over $25 a share but am trying to raise capital to buy more..
High Dosage is the common denominator because phase 2b/3 patients were early Ad..there were still enough S1r signaling cells to resonate throughout the body.
Again.. our drug is not an AD or PDD nor Rett Syndrome drug..
Blarcamesine is a Human Health Revolution
This is why Anavex on hiring spree
I think you are very low
You are not giving the S1r enough credit
These were early AD patients so S1r signal was still relatively strong.
Understanding that the S1r is able to increase its signaling over time when Blarcamesine is taken at high dosage means almost all high dosage stayed level or got better..165.. and more than likely
Of the 170 at medium dosage half stayed at the level they were 85..so numerically
I think you are looking at 250 Early Ad patients after 1 year being at baseline or better..
This is why Anavex has been on a hiring spree
Until you are the. Big dog
You are not
TGD stated that
High Dosage was the number 1
factor which determined outcome..
I don’t know what else everyone needs to
Know
Exactly
A week ago the complaint was
Everything moving too slow..
Now we have late breaking in 5 weeks at CTAD.. and the complaint is?
Honestly sometimes I think you get what you deserve..
Patience..we are saving hundreds of lives
Improving hundreds of lives.. soon it will be millions
Anavex has been on hiring spree the last 6 months..
Including National Sales Director
You figure it out
Improvement from baseline
No Reduction
100% of High Dosage 50mg
For 150 Trial participants
150 participants very little reduction in score..
150 patients. Typical 4 point drop over 48 weeks
No doc..
we wouldn’t have been approved
That BS..
Nothing was getting approved until
The AD data was discovered at the end of the this trial..
To say otherwise is BS
Man I don’t want another ignore
When your posts look like AF wrote them
Maybe you should stop selling calls..
Is that what you are saying Hoskuld?