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Atilla.. yes more positive..
Will it be enough to bust the door down?
For me.. if it’s not.. the price of the stock isn’t what I will lose..
I will lose my mind, my memories my health and all that I love..
I don’t have another 5 years.
Millions are just like me..
Either we bust the door down now..
Or we are forgotten
It’s a leadership move
that is etched in time
Look at this another way..
If results were not fantastic
Would Dr M really put Dr MacFarlane
at the podium to squirm?
Would he do a late breaking session at all?
Would he announce the results will be in article which is peer reviewed?
No he would have pr’d and moved onto A3-71
Plex he didnt make many other presentations..
Dr M has always (if memory serves me correctly) been the lead presenter.
Dr M has humbly and graciously allowed Dr Mac Farlane to be lead.
If you know successful people you understand their need
For adulation..They want to be the hero.. This must not have been an
Easy decision for TGD.!
Think about it..TGD found the Drug, Saved the Drug. Marshaled the Investors.
Marshaled the Drug through multiple clinical trials..
And NOW at the very epicenter of Scientific Hero Worship..
He hands the microphone to Dr Mac..
Ladies and gentlemen..if you didnt respect TGD before..
Recognize the brilliance and humility of this great man.
Thank you DR Missling
Dr MacFarlane IS the presenter..
Dr MacFarlane IS the actual Doctor of the patients treated in PHase 2a and many of the patients in phase 2b/3. And as Director of Hammond Care Dementia he had access to all the patients from Hammond Care b=involved with the Clinical Trial..
(Could see negative results plus who got dizzy and who got better)
Believe it or not..a kind of smart guy can put two and two together..like in that awesome Ageing Australia article….The people getting dizzy seemed to get better.
Wonder if that is the same as High Dosage is THE common denominator of result.?
I ignore so many posters I never see the FUD..I mist the interaction but I know its for the best. I think of the little girls with Rhett Syndrome and their families and when I read the FUD it just sends me over the top..
Peace
We don’t know top line reaultS ..
But Dr macrame and Dr Missling have a pretty good idea..
They decided to do a late breaking presentation at CTAD and have the results peer reviewed..and for Dr Mac Farlane to leave Australia to make the presentation.
They appear confident
The long long journey of life will end for most of us within three decades.
We have difficulty seeing beyond next week much less 100 years.
Our drug is the transformation of the human race.
God has taken mercy upon us
Et tu xena?
Long term tsunami of Glory
Well done
? What?
Haha.. good for you..
None of us are ever alone,,
Peace
Here we are..
About to save all future generations of mankind from the ravages of
multiple terrible diseases..
And we talk of fear?
Fear of a nobody who has done nothing for anyone other than destroy?
We can do better
Agreed
Even though high dosage is now the only
Factor that matters since the his was a hypothesis this data should be available as well
Maybe..
the point is either way
Blarcamesine and it’s metabolite
when combined with a muscaric agonist
are empowering our own bodies most effective homeostasis biological mechanism.
We don’t have to worry about
stopping something or overdoing something because
Blarcamesine is not
THE AGENT OF eFFECT
The S1r is..
The more S1r the more the effect..
We have awakened Our Creators Healer
The biological logical question is..
Are our cells creating S1r where there
We’re none before? Is Blarcamesine having an additional effect of not only
Agonizing cells that already express
S1r but showing other cells how to
Creat their own S1r?
Wouldn’t that be lovely..
Also with regen medicine should not we be able to populate a body with more S1r through live birth placental tcells?
I would think those would be able to be isolated and reproduced..
Yes Atilla. With such a condensation of big announcements.. one feels TGD always has one in his back pocket to respond to
Fud
The Golden Key which anavex has already announced is…
Drum roll please..
The Sigma One Receptor when agonized properly and early enough in a relatively healthy human body
Is able to increase the activity of S1r signaling.
We have shown this in testing..
The next door knocker..
Was when DrM said that the wildtype
And non wildtype group showed the same effect at high dosage over time..
So..that means either our drug works for everyone at a high dose.. or for no one..
Place your bets
There is some Lee way on positive news release reTLD.. anavex could say although they have great news they are still re affirming the data.. and they could take that stance all the way to CTAD.
However.. CTAD doesn’t really offer any defense from the short cabal..
the powers and wealth that are there
don’t crush the cabal they are more like lemmings when it comes to financial matters.. it’s good that they have the science but the true battle is now…
Do you believe DrM? Do you believe DR mcFarlane? If so.. then they just told you..
Blarcamesine works
Or he ccpuld make rhis the greatest CTAD ever..
He does plan on being back at CTAD soon with another powerful new Pharma
A3-71..
He could build some great goodwill letting CTAD be the epicenter of the announcement
The stick and the dog
Raising the stick and the dog knows what happens next.
Only this ain’t no regular dog.
This here is an American Hunting Dog
And last time you beat him with that stick
he learned a lesson. Not to cower in fear
But to prepare a shield so that when you bring that stick down.. it breaks in half on the strength of the truth.
Late Breaking presentations must have
Value. Otherwise they are not late breaking. They don’t ask to be late breaking and they are not granted late breaking. If someone found an exception to that rule..than they are most likely well paid by a cabal of hate.
You don’t get your results published
If they are bad because no one would take the time and energy to confirm negative results. Although I am sure some well suited arse will find a ground breaking peer reviewed article of a BioPharm failure.
Let’s just say the twits are able to find another instance of negative results after being a late breaking presentation and having your results peer reviewed and article published.
( they are competent and well paid shorts no doubt)
Remember WHO our CEO is
TGD!
The man who tried to make Blarcamesine fail so he could move on to A3-71!
Do you think there is any way in Heaven
That DrM would compromise our mission
and be like Biogen? Or any other crap BioPharm?
And there you have your answer..
.
I think all high dose will be better than placebo..
but it could be even better than that..
It could be..
All high dose… improved their scores ..
I agree with these numbers
It’s going to be earth shattering
After reading ..
If TLD is not concrete…. Aka more data crunching .. before CTAD..
They can wait and give themselves more time..
I think legally they can wait for CTAD..
Hosklund.. there obviously something of great importance to report that is why we are doing late breaking presentation..
So you are of the opinion they will pr something relational to TLD & endpoints?
CTAD is tough on data release..
But I think you might be right..
I think they have to announce material knowledge
And I want to add..
I don’t agree with that..
I think we should see top line bullet points..
They aren’t going to keep this secret!
If they sent it to CTAD .. the data is already
Compromised..
Ariana has seen something..
The peer reviewed magazine has seen something..
Just don’t think the world is honest enough to keep this secret for 6 weeks
I am thinking they aren’t releasing
Anything until CTAD..
Unless… it leaks
Is this a legit question..
If results are so good
Why aren’t they just releasing them and asking for immediate FDA approval?
Does anyone see this delay as a negative for the results?
The company has multiple clinical milestones
? Complete data ANAVEX®2-73 U.S. adult Rett syndrome (RTT) Phase 2 study
? Complete data ANAVEX®2-73 Parkinson’s disease dementia (PDD) Phase 2 study
? Top-line data Phase 1 ANAVEX®3-71 clinical trial
? Top-line data AVATAR: Potentially pivotal Phase 3 adult RTT ANAVEX®2-73 clinical trial
! Top-line data ANAVEX®2-73-AD-004: Potentially pivotal Phase 2b/3 AD clinical trial – expected fall 2022
! Data of 48-week OLE PDD Phase 2 study – expected by end 2022
! EXCELLENCE completion: Potentially pivotal Phase 2/3 pediatric RTT clinical trial – expected by end 2022
! Initiation of ANAVEX®2-73 imaging-focused Parkinson’s disease clinical trial – expected 2022
! Initiation of potentially pivotal ANAVEX®2-73 Phase 2/3 Fragile X clinical trial – expected 2022
! Initiation of potentially pivotal ANAVEX®2-73 Phase 2/3 clinical trial for the treatment of a new, rare disease indication – expected 2022
! Initiation of ANAVEX®3-71 Phase 2 clinical trial for FTD, schizophrenias and Alzheimer’s disease – expected 2022
George could you please repost upcoming milestones?
Thx George
Do you have list of other milestones?
Do you have poor results peer reviewed?
Do you request “late breaking” status at the penultimate Alzheimers conference if you have poor reaultS?
Are you granted “late breaking” status if you have poor results?
If they can keep this secret for 6 weeks they have security better than the Supreme Court ..
Guess FBI we just can’t find that leaker, but they try so hard.. hunh..
6 weeks .. is the blink of an eye..
Sleep is going to be a rare commodity for awhile
Still have 6 milestones/releases before end of year..
CTAD released program..
AVXL is on it.
We have “late breaking” presentation at CTAD around dec 1..
Agreed!!
Haha..
I just bought some calls
Your posts are costing me money
Interesting..one foot in quicksand and the other on a rocket ship..
Certify this Raj
If the data sucked
Or was even mediocre
We would never ask for
Nor would we be given
CTAD spot as
“Late Breaking”.. fact
And we have unlocked data set ..
Bbbbbbbbbbam
Agreed
Yes.. they had to present to get
Late breaking
The definition of late breaking isn’t that you just got the data..
It’s that you just got the data
And it’s IMPORTANT..
Bad news on AD is NOT important