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I believe the raise is twofold...
1). We are going RETT alone (most likely approval early 2024), so there will be funds needed to get the ball rolling. In fact, the ball has started to roll (i.e. recent new hires). TGD likes to maintain a hefty cash balance. As expenses increase, so will his appetite to increase the hoard. Remember we are going it alone on rare diseases so once RETT is approved, others will shorty follow, which will require money.
2). I'm slowly leaning toward a P4 (vs. outright approval) for AD and thus the case to raise cash. Most likely will be announced after RETT data in July. Remember a P4 will cost big dollars to monitor everyone prescribed!!!!
There will be another run (as high as 30+) very very soon, so IMO, TGD will raise then. Also keep in mind most here, when calculating share price, anticipate shares increasing. This recent LPC is just one of them.
Now that RETT is over, expect anecdotal news to start appearing more frequently.
All is good!!! We shall see 13 by end of week...Just watch!
Who's to say they will be needing capital any time soon, a shelf placement is more of a contingency. Missling has control of when and if shares will be sold. Since they have 140mm in the bank now I suspect he wouldn't until share price exceeds 50 dollars.
They also said they didn't need dilution...so how does the comment about not yet meeting with the FDA have any truth to it.
They also have seen the data which triggered the silent money grab...guess they don't want to PR about the money...lol
Yep seems like a good move to me.
First off they need feedback from the FDA on whether another P3 is even needed and that meeting hasn't yet happened according to the last call. Missling just yesterday again released that their trial met both its co-primary and key secondary endpoints, showing statistically significant and clinically meaningful improvement in cognition and function as measured by ADAS-Cog, ADCS-ADL, and CDR-SB, respectively.
We're not the only small bio doing this - Annovis Bio Announces Approval For European Union Clinical Trial Sites For Phase 3 Study Of Buntanetap For Treatment Of Parkinson's Disease
Good post on Stocktwits by Trainguy1--and I agree fully !! It’s well known that the people who least need to borrow money are the people offered the best interest rates. Similarly in businesses, a company that demonstrates its readiness to operate independently gets the best partnering offers. Even though we know Anavex wants to partner, they need to demonstrate complete readiness to operate independently. It’s a serious game of chicken. By signing the Lincoln Park agreement, Anavex is saying they’re ready to play. Game on!
There are 2 ways to read your question:
1. Will AVXL be selling Blarcamesine within 6 months, as in will the drug be available on the open market?
2. Will AVXL be selling Blarcamesine within 6 months, as in will the company license or sell the rights?
I think you were referencing #2, but the answer to both is most likely "no." I expect at this point Dr. Missling is confident enough to submit to the FDA without a partner, and if approved maximize the leverage he has entering negotiation. At worst, he'll be told to run another confirmatory P3 trial -- and he has the cash to do so with minimal dilution. More likely, he'll be asked to run a P4 trial -- and with the LPC deal he'll have the cash to continue advancing the rest of the pipeline.
Sold plenty awhile ago...it has to fill that gap in the 8's sometime.
LOL...listen to the call...it is about BS...he has been feeding you lines for years...what does no more dilution mean to you?
Missling recently said...there is absolutely no reason for further dilution...in Missling we trust...yeah...we trust that there will be more lies. He must now be finished going through the data...his lack of enthusiasm, lack of timeline commitment to data, and lack of keeping to his word about dilution means one thing...data isn't good enough for a partner with up front payments. Need lots if money for a large P3.
They have 4 years cash with their currently plans...came from the horses mouth.
Sure do have a basis. A partner brings a fat upfront payment...but they have to scrape together a lousy 150 million...the amount of the voucher...must not be expecting good rett news if they cannot get the pediatric voucher withing the 4 years for which they already have enough funding.
Maybe you should stop being so laughable and but 2 and 2 together. A nice rett voucher or a partner would not require a bunch of money if you are planning on your current funds to get you through 4 years
I even spelled it out for you 2 different ways.
What’s 6 months? They have enough cash for 3 years
Again listen to the conference call.
It is not about the start, it is about a good start, in order to finish strong.
Missling the forest for the trees is very common around here.
We have data from the two largest indications (markets $$$$$) to be broken down and explained (AD P2/P3, PDD OE).
But you want trial announcements? really?
Beats the schhhiiiiet out of me.
He has been promising to start many of these new trials for some years - so he repeats it this year - we have to see which actually he starts
I mean is better than playing with toilets.
But not quite as good as a real brain when it comes to bullshit detection.
I guess you dont own any insurance on anything you do?
Hey investor, did you sell any trading shares or core yesterday after the conference call?
Asking for a friend.
Or perhaps the analysts you speak about were cleaning toilets as well.
Imagine being a share holder and not being able to listen to the call because of toilet cleaning duties.
Powerwalker:
Thank you very much for that post.......what a great article and Steve Forbes is a clear thinker who gets it!
EBZ. I think that is premature emasculation.
To maintain that $140 Million on hand. Does anybody think they will be selling 2-73 within 6 months?
They obviously cannot get a partner for an unproven new science...
LOL...no dilution...hahahaha...they can't get a partner and now have to go at it alone.
Anavex doesn't need the money. But it's sending a clear signal that Dr. Missling getting his ducks in a row in case he doesn't receive any legitimate partnership offers. I don't think he wants to go at it alone but having access to cash is never a bad thing, because the cost of manufacturing and marketing will easily eat up all of the runway needed to get the other trials complete and further advance A371.
The market rose as Powell began speaking of an end in sight with the rampant inflation, and the markets faded just as quickly when it became clear the process was going to take a very long time. Overlay the AVXL chart with the DJIA chart and you can see exactly when the spike and drop occurred across the entire market.
The price action had very little to do with Dr. Missling or the company as whole. If anything, one analyst allegedly lowered his price target from $80 to $58.
Dude has been playing with ChatGPT AI.... here is a sample Q&A.....
Question - How should publicly traded companies communicate with shareholders?
Answer - Publicly traded companies should communicate with shareholders in a transparent, timely, and accurate manner. This can be achieved through various channels such as earnings releases, annual reports, investor presentations, conference calls, and other regulatory filings such as SEC filings. Additionally, companies can also use social media, websites, and email to reach shareholders. The goal of these communications should be to provide shareholders with a clear understanding of the company's financial performance, strategy, and prospects, and to respond to questions and concerns in a prompt and helpful manner.
More verbal diarrhea!
Wow, an ATM agreement. (Yawn)
Good question..
If partnership was in works i don’t think they would need agreement w vulture firm…they could just file for more shares
If no p3 needed for ad, then, 4 years of cash should have been enough..so its curious timing
So that leaves one option imo..
Wow. I think the AGM should start with everyone singing Kumbaya.
The communication you describe would be nice. It is not close to essential.
What is essential is the company delivering on developing and marketing a drug.
You don't know how LPC vulture works, Misleading used them earlier, diluted from 25mil to 70mil shares in 5year, collecting pennies. LPC is his comfort zone, he might be expecting share to drop big time and needed continues ATM.
It takes a lot of money to do trials and commercialize drugs for every human disease known to man.
In over 38 years Big Pharmas or, biotech companies that focused exclusively on the plaque/tau none have been successful in their treatment of the disease of AD. Even our FDA in desperation to find a meaningful approach to this catastrophic disease approved 2 Biogen drugs that do little to alleviate the significant issues of the disease ... plus their drugs are very expensive, must be given I.V. and must be done by medical personnel ... adding more expense for the treatment .... and the treatment can cause the patient's brain to bleed, which could result in the patient's death. Summed up, just more failures with this dangerous approach.
Am awaiting the approval of Anavex's blarcamesine drug/2 - 73, a safe drug, a pill taken by mouth, that has demonstrated significant results with neuro-degenerative and neuro-developmental diseases affecting the CNS.
Missling is back in bed with vulture investor LPC but not because he couldn’t get any real WS banks to take it on. It’s because he doesn’t want to have to answer hard questions from sophisticated institutional investors or be accountable to those investors who might buy in.
Another fudster masquerading as a shareholder. How refreshing.
Haha. My takes from CM’s CC.
1. AD full data. In 2023? Not sure — could be 2024, 2025. But, I assure you asap.
2. Excellence trial endpoint. RIGHT NOW, our plan is delta-RSBQ, but you know us — can’t promise what it will be in 2 months, or when we see the data.
3. PDD OLD. Oops, are you guys still waiting for it?! Give us 6-12 more months. We need a few more months to compute an average of 400 values.
4. AD discussion with FDA. After we get our “hands” on full data (see #1 above), then we’ll talk **aggressively** with the agencies. Just 1-2 more years wait.
5. Other trials: All our previous trials have failed — so we are being extra cautious that these new ones succeed. So, that’s the reason for delay.
6. PDD trial full data: Forget about it!
The obsession with this dead-end approach has been fanatical, almost cultlike.
There's a lot of that going around these days....
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Anavex®Life Sciences Corp. (the “Company”) is a clinical stage biopharmaceutical company engaged in the development of differentiated therapeutics for the treatment of neurodegenerative and neurodevelopmental diseases including drug candidates to treat Alzheimer’s disease, other central nervous system (“CNS”) diseases, pain and various types of cancer. The Company’s lead compound ANAVEX®2-73 is being developed to treat Alzheimer’s disease, Parkinson’s disease and potentially other central nervous system diseases, including rare diseases, such as Rett syndrome.
Anavex®Life Sciences’ lead drug candidate, ANAVEX®2-73, recently completed successfully a Phase 2a clinical trial for Alzheimer’s disease. ANAVEX®2-73 is an orally available drug candidate that restores cellular homeostasis by targeting sigma-1 and muscarinic receptors. Preclinical studies demonstrated its potential to halt and/or reverse the course of Alzheimer’s disease. It has also exhibited anticonvulsant, anti-amnesic, neuroprotective and anti-depressant properties in animal models, indicating its potential to treat additional CNS disorders, including epilepsy and others. The Michael J. Fox Foundation for Parkinson’s Research has awarded Anavex® a research grant to develop ANAVEX®2-73 for the treatment of Parkinson’s disease to fully fund a preclinical study, which could justify moving ANAVEX®2-73 into a Parkinson’s disease clinical trial. ANAVEX®3-71, also targeting sigma-1 and M1 muscarinic receptors, is a promising preclinical drug candidate demonstrating disease modifications against the major Alzheimer’s hallmarks in transgenic (3xTg-AD) mice, including cognitive deficits, amyloid and tau pathologies, and also with beneficial effects on neuroinflammation and mitochondrial dysfunctions.
The Company is in preparation for ANAVEX®2-73 for a Phase 2/3, placebo-controlled trial in Alzheimer’s disease as well as a Phase 2, placebo-controlled trial in Rett syndrome, for which the U.S. Food and Drug Administration (FDA) granted Orphan Drug Designation (ODD) for ANAVEX®2-73 and a Phase 2, placebo-controlled trial in Parkinson’s disease.
Headquartered in New York, Anavex® Life Sciences is an American publicly traded corporation on Nasdaq quoted as AVXL
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