Long for a Longtime or until they make me an offer I cant' Refuse
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Toss a coin tom
Also food for those hungry MMs
Smart $$$ selling $5 calls then bringing PPS down so they can buy them back for pennies... easy to do with such a small float. We punched through the right shoulder at $6.49 then got rejected...Eased the RSI from nose bleed heights back down below 50. Next week should be good for long...hold your shares and ignore the noise..... GLTAL and have a great weekend
100 million shares
RSI over 94 and we have that gap @ 5.39 to fill..we need to chill a bit before next leg up...just IMO..
Since the lawsuit the company has been very stingy with PRs
We are about to break out to the upside of a long term bullish wedge....
Hang on all!!!!!
Could it also be that the Good Doctor is focusing on Rett PH2... our shortest path to commercialization....
I got in...
Can someone provide a link to the conference call announcement
I agree the good doctor nailed it.
The good doctor has partnered with the cutting edge companies to do the numbers. It takes time to build the models.
I feel not much attention has been paid to the "Not Optimized Doses" and the effective range is from 14 to 50+. The PD/PK data will give them the optimum dosage. Phase 2/3 could very well be short lived... GLTAL
I stand corrected ..this patent was issued 9,180,106
Could you supply links to these PRs
As far as I know, this is awaiting payment of the fees...
http://www.anavex.com/?news=anavex-receives-notice-of-allowance-for-u-s-patent-application-related-to-anavex-2-73
The USPTO issues a Notice of Allowance after it determines that a patent should be granted for a claimed invention that is novel in comparison to all known technology in existence. Based on the timing of this Notice of Allowance, Anavex expects the patent to be issued by the end of 2015.
Could be our next PR "submission of an Investigational New Drug application (IND)"
The request for RAT designation must be made either concurrently with submission of an Investigational New Drug application (IND) submission of an Investigational New Drug application (IND)or as an amendment to an existing IND. We will not grant a RAT designation if an IND is on hold or is placed on hold during the RAT designation review.
From an "real expert"
George Perry, PhD, Dean and Professor at the University of Texas at San Antonio and Editor-in Chief of the Journal of Alzheimer’s Disease, commented, “In addition to the very encouraging results, which point to the therapeutic potential of targeting cellular homeostasis in a complex CNS disease like Alzheimer’s, this trial has been intelligently designed as a highly informative study, looking unprejudiced at all potential relationships and hence allowing to learn from all correlations of the now available pool of data, in order to execute subsequent trials with much more relevant information at hand.”
Is it possible that Australia is going to pay for PH 2/3 for a piece of the action... Just a thought!
Chump change when it comes to an AD drug that is much better than the SOC!
We all make mistakes!
I say release the PR on saturday...catch the shorts flat footed..
Just a speculation....FDA next fast approval...Anavex 2-73 for Rett syndrome...then we are off to the races...and if also stops seizures!!!
Jon,
You forgot... the chance to prove 273 works against seizures...that is huge.
Phase 2 Rett trial could prove 2-73's effectiveness on controlling/preventing seizures (epilepsy market much larger than Rett).
Thanks Neiu.... some times peps lose sight of Anavex's objectives.
Could they have been adjusting doses of both drugs... It would be beneficial to Anavex to come up with the plus combination that works better than SOC.... remember the patent
Thanks for the honest reply.
So prove it...what other drug has failed using Anavex's approach?
Prove me wrong!
So far Anavex's approach to treating this disease has a 0% failure rate.
So far Anavex's approach to treating this disease has a 0% failure rate.
ERP's
An event-related potential (ERP) is the measured brain response that is the direct result of a specific sensory, cognitive, or motor event.[1] More formally, it is any stereotyped electrophysiological response to a stimulus. The study of the brain in this way provides a noninvasive means of evaluating brain functioning in patients with cognitive diseases.
ERPs are measured by means of electroencephalography (EEG). The magnetoencephalography (MEG) equivalent of ERP is the ERF, or event-related field.[2]
You all have heard of the perfect storm...Such a bear trap has never been set.... Happy New Year to all
My virus software warned me about this site...be careful
Originally posted by Stockman69..
SIGMACEPTOR™ Discovery Platform
A potent new approach to drug development
At the heart of Anavex’s innovative approach to drug development is its proprietary SIGMACEPTOR™ Discovery Platform. Developed by Dr. Alexandre Vamvakides, our scientific founder, the SIGMACEPTOR™ platform continues to generate promising compounds, steadily producing new drug candidates ready to enter the company’s robust development pipeline.
The compounds emanating from the SIGMACEPTOR™ Discovery Platform act through sigma receptors, a relatively new class of receptors that is able to activate multiple pathways and provide treatment solutions in many types of diseases. We are at an appropriate stage to evaluate the potential of compounds (ligands) that activate these receptors with regards to effective dosing, safety and efficacy.
Why would the Good Doctor need to rush. He as enough $$$ to start PH2/3 and Retts... After six months in PH2/3 and the drug continues to be safe and shows decent not even great numbers, How much are we worth?
There are many catalyst that could be PR'ed at any time. Shorts loses could be endless.... GOFUNDME.COM!!!!
I just hope you are all out short to back your strong convictions.
Good Luck to you...