Tuesday, September 16, 2025 8:09:06 AM
Big jumps or drops after news usually occur when the news itself (not just that there is a catalyst) is unexpected. So for example SMMT released highly anticipated key data at WCLC last week. The drug was expected to perform the same in European descent as Asian but the data was nuanced (probably almost as good but not quite --- yet survival data was immature and could look better (or worse) next year). The SP dropped 25% as trial news worse than WS expected. I remember when Acadia got trofinetide approval - first in class and A273 at least a year behind - and yet price moved down 5%. Approval was >90% baked into SP but the realization that now they need to market a poorly tolerated drug with limited benefit kicks in.
With a share price of 9-10, AVXL is priced closer to MAA withdrawal with need for an additional trial, not for success. If WS felt conditional approval or full approval was most probable, the SP would likely be at least 20, and if complete approval was most probable, then even higher. WS interest in a stock and its potential for large pop or drop, to an extent, can be gauged by option price IV. IV is now about 100 (vs typical 75) but was briefly >500 before the highly anticipated CTAD 2022. There is still a couple months for IV to climb (and unless MAA withdrawn shortly, I expect it will) as we are probably still 2 months from MAA withdrawal vs regulatory success/failure time. I would expect a very large jump in SP (>$40) if full marketing authorization occurs and the fantasy of a short bonfire might even come to pass as there is no chance for the shorts to fight the influx of new investors. A conditional approval will still cause a price jump as the market is huge and $20-30 (depending on terms) is probable and shorts may even try to fight the pop in SP but it stays higher than now. Failure for approval (which would be due to limited proof of efficacy not because of a safety flaw) will put the price at $4-5 --- only a 50% drop because this outcome is partially priced in. New investors won't enter.
With a share price of 9-10, AVXL is priced closer to MAA withdrawal with need for an additional trial, not for success. If WS felt conditional approval or full approval was most probable, the SP would likely be at least 20, and if complete approval was most probable, then even higher. WS interest in a stock and its potential for large pop or drop, to an extent, can be gauged by option price IV. IV is now about 100 (vs typical 75) but was briefly >500 before the highly anticipated CTAD 2022. There is still a couple months for IV to climb (and unless MAA withdrawn shortly, I expect it will) as we are probably still 2 months from MAA withdrawal vs regulatory success/failure time. I would expect a very large jump in SP (>$40) if full marketing authorization occurs and the fantasy of a short bonfire might even come to pass as there is no chance for the shorts to fight the influx of new investors. A conditional approval will still cause a price jump as the market is huge and $20-30 (depending on terms) is probable and shorts may even try to fight the pop in SP but it stays higher than now. Failure for approval (which would be due to limited proof of efficacy not because of a safety flaw) will put the price at $4-5 --- only a 50% drop because this outcome is partially priced in. New investors won't enter.
Recent AVXL News
- 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
- Anavex Life Sciences Reports Fiscal 2026 First Quarter Financial Results and Provides Business Update • GlobeNewswire Inc. • 02/09/2026 12:30:00 PM
- Anavex Life Sciences to Announce Fiscal 2026 First Quarter Financial Results on Monday, February 9, 2026 • GlobeNewswire Inc. • 02/03/2026 12:30:00 PM
- Anavex Joins ACCESS-AD, a Major Initiative Funded by the European Commission, Through the Clinical Evaluation of Blarcamesine as Part of a Precision Medicine Approach in Alzheimer’s Disease • GlobeNewswire Inc. • 01/13/2026 12:30:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 01/09/2026 10:26:26 PM
- Edelson Lechtzin LLP Announces an Investigation of Anavex Life Sciences Corp. (NASDAQ: AVXL) and Encourages Investors with Substantial Losses Contact the Firm • PR Newswire (US) • 01/09/2026 01:13:00 AM
- Anavex Life Sciences Appoints Senior Vice President Global Head of Neurology • GlobeNewswire Inc. • 01/08/2026 12:30:00 PM
- Anavex Life Sciences Receives FDA Feedback on Alzheimer’s Disease Program • GlobeNewswire Inc. • 01/06/2026 12:30:00 PM
- Anavex Life Sciences Submitted Request for EMA to Re-Examine Its Opinion • GlobeNewswire Inc. • 12/18/2025 12:30:00 PM
- Anavex Life Sciences Provides Update on Regulatory Review in the EU for Blarcamesine to Treat Early Alzheimer’s Disease • GlobeNewswire Inc. • 12/12/2025 09:05:00 PM
