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No one currently had the need to ship via Amazon.
Alzheimer’s therapies all seem to need infusions for some reason. So even though BP were able to ship it to your house, could the patient REALLY do it themselves?
Now, if it were pills much like those vitamins or Tylenol…….
Then again, we are getting way over our heads with even thinking of what an Amazon partnership would even do for the pps of AVXL.
Sure everyone can say that is unrealistic. Is it though? Only the two CEOs really know.
Continue on with your daily nonsense.
Let’s see what 2026 will be.
Or better yet 2030
2033 even.
Ignore doesn’t work for me. How do I know? Because I have kund on ignore and I still see posts every….single…day from them.
Vanguard looks like they INCREASED their holding from 4,360,648 in Feb to 4,548,219 in Aug. making it a 3% increase.
Let’s see where it is once all reporting is done. What was it at before, 37% tute owned.
I’d think for Rett, they take the liquid form. So off label would be hard for them to use.
No justifying needed.
Already green no matter what you say
It’s all noise really.
Everyone can be their own expert giving 10%, 20% , or whatever that percent is for chance of approval.
They all have an investment in the co one way or the other.
To say they don’t is a lie.
THIS, is a fact:
Anavex has a better chance of EMA approval than the last 2 FDA approved therapies.
Whoa George….Blarcamesine first.
That was obvious though. It’s why Anavex still sits at sub $7. Any pump, and Missling releases some shares.
Chess at its best.
Sounds like CTAD would be a great time to read the OLE out
I’ll take tutes continuously accumulating over an anonymous poster Alex. I’m sure they agree with you
Funny how discontinuation is the topic these days, not the result. Guess there always has to be something from the data to ridicule and try to get investors to think hmmm….maybe I should sell.
Heavy hitters are starting to attach their names to the Co.
A Year from now, this may finally be approved somewhere in the world.WHY? Cause it just works.
Unfortunately, there is no better alternative.
BP tried to force feed plaques to the public for so long, that it hindered ALL other possibly better therapies.
I know Missling mentioned it in one of the quarterlies as well.
Try looking at the Landmark PR.
“These events are manageable by adjusting titration schedule to slower titration and nighttime dosing, as has been positively observed in the blarcamesine compassionate use program.”
No doubt, it plans to be above $31 for whatever that “offer” they had from last year. Or was it $21?
But why…..? Ain’t the MABs doing its work…..?
Yeah. Enough said. These sufferers deserve better then that.
That’s only using the 48 week result for Blarcamesine correct?
Looking forward to what the OLE reveals
Did he ever provide his true credentials? We all know what happened with the self proclaimed Dr. on SA years ago.
Just asking for a friend btw
They’ll pretend not to.
Can’t be upsetting daddy. He can easily take away their allowance.
Why not expect nothing and be suprised if it ends up tomorrow is the day. Everyone, long and short, is guessing when that day is and planning accordingly.
Funny you mention that. It’s exactly how MABs got approved.
Begging the question. Clearing the “hair loss”, does that really treat AD?
What’s the title?
Wait….
You talking about the same FDA that went against all of their advisors not too long ago and approved a therapy that failed in trials? Only to be data mined later to squeeze “ahh, there it is” BS?
Seem worried Kund.
It’d be fun to see the updated view when that peer review finally does get released.
I’m sure the majority of the board could care less what your doom and gloom thoughts are.
There’s still the entire week for them to PR something.
Heck, they may even PR something juicy with “further details” at “name the conference or date”
Just remember….Anything they DO present, the AF of the world will get it before it’s public thanks to his “reporter” status.
O.T. already approved huh.
There HAS to be something better to do than monitor message boards on a Friday night
Traded I could understand. All bought…..meh
There’s a high degree of probability that post won’t age well.
I wouldn’t be surprised, there was a small convo about Amazon being able to distribute and next thing you know, Missling mentions it.
They’d have to no matter what for pediatric Rett.
Pediatric is a totally different adult trials.
Case closed.
You and I have a different opinion on who the media is.
Whom exactly was the “media”?
I’ll entertain Kunds griping about pill labeling for a second.
Comparing recently approved vs not approved AD therapy.
Let’s label everything that we know of as required, for said therapy, with their ticker.
Let’s forget about cost difference for the insurance companies.
Let’s forget about the total opposite side of the spectrum side effects each had.
Let’s even forget about total time wasted, for patients, to be on each therapy and required visits.
That pill is a powerful message for those who know.
When Anavex finally reveals their cards, I’d not be surprised at all that it’ll beat MABs in a line for line comparison.
Que the peer review
Come on guy. It’s a nothingburger.
Can’t wait for the reaction when A-273 is approved and the pill looks completely different.
Oh no……I’ve been duped.
Because Anavex did get their therapy approved, knowing what the marketing name will be as well…..
Everyone is making a big deal from something so minute as 4 letters on a pill graphic……?
Inhale……breathe out…..everything is ok
Monday we go up, we go down, or maybe even be a flat day.
The world moves on from slide…what was that slide again. ….
Must be doing something right for you to still be posting nonsense