Saturday, August 03, 2019 5:03:25 PM
Completely agree with that assessment jvmho, the Company’s been in stealth mode for at least 2 years, and I’ll trust that Dr M and the BOD have their (competitive) reasons.
And you’re right, there’ve still been multiple signs and signals of confidence in the moa and efficacy to date: expanding the pdd trial to AU; expanding the RS Avatar trial to AU in May; letting us know in a conf call that the Spain pdd participants had requested an extension; purchasing 1 million worth of 2-73 inventory; putting in place a large 250 million shelf (commercialization needs?); new patents such as https://patentscope.wipo.int/search/en/detail.jsf?docId=US236451262&tab=NATIONALBIBLIO&office=&prevFilter=%26fq%3DICF_M%3A%22A61K%22&sortOption=Pub+Date+Desc&queryString=&recNum=213&maxRec=2035248
And,
http://appft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220180360796%22.PGNR.&OS=DN/20180360796&RS=DN/20180360796
Also telling were the hiring of Dr Walter Kauffman as our CMO this year, and the display of confidence by Dr Missling when explaining Anavex’s moa/efficacy during the March 2019 ROTH conference panel “Alzheimer’s: Beyond the Rise and Fall of Amyloid”.
Stark contrast between our “rapidly advancing” pipeline compared with the BP giants dropping out of the CNS space and “Biogen on the Brink” (credit Jon Jones & nidan) https://www.bizjournals.com/boston/news/2019/08/02/biogen-on-the-brink-one-of-the-states-largest.html?ana=yahoo&yptr=yahoo
The market forces (BP giants and their entrenched tau/amyloid plaque scientists/media/Hedge funds/FUD agents) are by now aware of Anavex and our consortium/Hampel ties and PM leadership & our expanding/extending CNS trials, and I’m convinced that their game plan has been/is to keep Anavex marginalized for as long as possible.
With compounds that are purported to prompt the body to heal itself and self-correct (as well as modulate autophagy) & thereby potentially treat a WIDE range of various CNS afflictions and diseases (reference our pipeline)
https://www.anavex.com/#!/aboutus
it’s not difficult to understand why our small Company would be quite disruptive and thereby threaten the industry leaders & their treatment centers/billions/side-effect-riddled SOC.
https://www.globenewswire.com/news-release/2019/03/04/1745838/0/en/Anavex-Life-Sciences-Reports-Publication-of-New-Data-that-Show-ANAVEX-2-73-Induces-Cellular-Recycling-Process-Linked-to-the-Prevention-and-Treatment-of-Age-Associated-Diseases.html
Godspeed to the researchers and patients and EU/EMA/AU regulators in our trials.
Will be interesting to see if the BP-beholden Congress/FDA will display leadership & respond quickly and favorably (given our excellent safety record and positive RWE reported by our ph2a patients) if our PDD/Rett trials meet or exceed primary endpoints in the coming 3-4 months.
CNS disease-afflicted patients deserve better treatment options and fewer serious side-effects than the current SOC.
GLTAL
[https://www.google.com/amp/s/finance.yahoo.com/amphtml/news/congress-big-pharma-money-123757664.html
“I’m really much more concerned because Congress is supposed to have oversight for the FDA,” Brown said. “If the FDA isn’t going to hold pharma accountable, and Congress is getting paid to not hold pharma accountable, then it really doesn’t matter who the president is because it’s really about Congress.”]
And you’re right, there’ve still been multiple signs and signals of confidence in the moa and efficacy to date: expanding the pdd trial to AU; expanding the RS Avatar trial to AU in May; letting us know in a conf call that the Spain pdd participants had requested an extension; purchasing 1 million worth of 2-73 inventory; putting in place a large 250 million shelf (commercialization needs?); new patents such as https://patentscope.wipo.int/search/en/detail.jsf?docId=US236451262&tab=NATIONALBIBLIO&office=&prevFilter=%26fq%3DICF_M%3A%22A61K%22&sortOption=Pub+Date+Desc&queryString=&recNum=213&maxRec=2035248
And,
http://appft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PG01&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.html&r=1&f=G&l=50&s1=%2220180360796%22.PGNR.&OS=DN/20180360796&RS=DN/20180360796
Also telling were the hiring of Dr Walter Kauffman as our CMO this year, and the display of confidence by Dr Missling when explaining Anavex’s moa/efficacy during the March 2019 ROTH conference panel “Alzheimer’s: Beyond the Rise and Fall of Amyloid”.
Stark contrast between our “rapidly advancing” pipeline compared with the BP giants dropping out of the CNS space and “Biogen on the Brink” (credit Jon Jones & nidan) https://www.bizjournals.com/boston/news/2019/08/02/biogen-on-the-brink-one-of-the-states-largest.html?ana=yahoo&yptr=yahoo
The market forces (BP giants and their entrenched tau/amyloid plaque scientists/media/Hedge funds/FUD agents) are by now aware of Anavex and our consortium/Hampel ties and PM leadership & our expanding/extending CNS trials, and I’m convinced that their game plan has been/is to keep Anavex marginalized for as long as possible.
With compounds that are purported to prompt the body to heal itself and self-correct (as well as modulate autophagy) & thereby potentially treat a WIDE range of various CNS afflictions and diseases (reference our pipeline)
https://www.anavex.com/#!/aboutus
it’s not difficult to understand why our small Company would be quite disruptive and thereby threaten the industry leaders & their treatment centers/billions/side-effect-riddled SOC.
https://www.globenewswire.com/news-release/2019/03/04/1745838/0/en/Anavex-Life-Sciences-Reports-Publication-of-New-Data-that-Show-ANAVEX-2-73-Induces-Cellular-Recycling-Process-Linked-to-the-Prevention-and-Treatment-of-Age-Associated-Diseases.html
Godspeed to the researchers and patients and EU/EMA/AU regulators in our trials.
Will be interesting to see if the BP-beholden Congress/FDA will display leadership & respond quickly and favorably (given our excellent safety record and positive RWE reported by our ph2a patients) if our PDD/Rett trials meet or exceed primary endpoints in the coming 3-4 months.
CNS disease-afflicted patients deserve better treatment options and fewer serious side-effects than the current SOC.
GLTAL
[https://www.google.com/amp/s/finance.yahoo.com/amphtml/news/congress-big-pharma-money-123757664.html
“I’m really much more concerned because Congress is supposed to have oversight for the FDA,” Brown said. “If the FDA isn’t going to hold pharma accountable, and Congress is getting paid to not hold pharma accountable, then it really doesn’t matter who the president is because it’s really about Congress.”]
Recent AVXL News
- Form 8-K - Current report • Edgar (US Regulatory) • 05/22/2026 12:15:26 PM
- Anavex Life Sciences Receives Expected Nasdaq Delinquency Notification • GlobeNewswire Inc. • 05/22/2026 12:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 05/15/2026 08:15:25 PM
- Form 3 - Initial statement of beneficial ownership of securities • Edgar (US Regulatory) • 05/14/2026 08:15:30 PM
- Form NT 10-Q - Notification of inability to timely file Form 10-Q or 10-QSB • Edgar (US Regulatory) • 05/11/2026 08:30:22 PM
- CEO Transition and Delayed SEC Filing Put Anavex (AVXL) Leadership Changes in Focus • IH Market News • 05/06/2026 02:52:36 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 05/06/2026 11:04:59 AM
- Anavex Life Sciences Board of Directors Appoints Former Senior Vice President of Clinical Development Terrie Kellmeyer, PhD, as Interim Chief Executive Officer • GlobeNewswire Inc. • 05/06/2026 11:00:00 AM
- Form 3 - Initial statement of beneficial ownership of securities • Edgar (US Regulatory) • 05/01/2026 11:18:47 PM
- Anavex Life Sciences Highlights New Scientific Findings on Shared Biology Between Autism and Alzheimer’s Disease • GlobeNewswire Inc. • 04/14/2026 11:30:00 AM
- Anavex Life Sciences to Present at the 25th Annual Needham Virtual Healthcare Conference • GlobeNewswire Inc. • 04/07/2026 11:30:00 AM
- Anavex withdraws EU approval filing for Alzheimer’s therapy • IH Market News • 03/30/2026 12:39:26 PM
- Anavex Life Sciences Provides Comprehensive Regulatory Update • GlobeNewswire Inc. • 03/30/2026 11:30:00 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/25/2026 08:06:00 PM
- Anavex withdraws EU marketing application for Alzheimer’s therapy blarcamesine • IH Market News • 03/25/2026 02:06:58 PM
- Anavex Life Sciences Provides Update on Regulatory Review in the EU for Blarcamesine to Treat Early Alzheimer’s Disease • GlobeNewswire Inc. • 03/25/2026 11:30:00 AM
- Anavex Life Sciences Presents New Data from its AD-004 Phase IIb/III Trial at AD/PD 2026 Conference Demonstrating Consistent Correlation Between the Treatment Effect of Oral Blarcamesine and Preservation of Brain Volume in Early Alzheimer’s Disease • GlobeNewswire Inc. • 03/23/2026 11:30:00 AM
- New Scientific Findings Highlight Hypothesis of Autophagy Failure as a Precursor of Amyloid Beta and Tau Pathology in Alzheimer’s Disease • GlobeNewswire Inc. • 03/20/2026 11:30:00 AM
- Anavex Life Sciences Presents Significant Treatment Effects of Blarcamesine in New Advanced Alpha-Synuclein Model of Parkinson’s Disease at AD/PD 2026 Conference • GlobeNewswire Inc. • 03/17/2026 11:30:00 AM
- Anavex Life Sciences to Present at the Citizens Life Sciences Conference • GlobeNewswire Inc. • 03/03/2026 12:30:00 PM
- Anavex Life Sciences to Present at the 46th TD Cowen Annual Health Care Conference • GlobeNewswire Inc. • 02/25/2026 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/25/2026 11:07:01 AM
- Anavex Life Sciences Appoints Seasoned Healthcare Leader to Board of Directors • GlobeNewswire Inc. • 02/23/2026 12:30:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/09/2026 09:40:27 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/09/2026 12:31:17 PM
