Annovis Announces Two Presentations at the AD/PD™ 2026 International Conference
Rhea-AI Summary
Annovis (NYSE: ANVS) announced two presentations at AD/PD™ 2026 in Copenhagen, March 17-21, 2026, covering clinical data for buntanetap in Parkinson’s disease and an update on the pivotal Phase 3 trial in early Alzheimer’s disease.
Presenters and session IDs: Presentation #3581 on PD cognition/biomarkers and Presentation #3582 on a 6- and 18-month randomized Phase 3 trial in early AD, both presented by Cheng Fang, Ph.D.
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Key Figures
Market Reality Check
Peers on Argus
Only one close peer, RADX, appeared in the momentum scanner, moving -5.249999836087227% without news, while ANVS showed a modest -0.37% move. Broader biotech peers were mixed, suggesting this headline is more company-specific than sector-driven.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Feb 12 | Alzheimer’s DSMB review | Positive | +2.5% | DSMB cleared pivotal Alzheimer’s Phase 3 to continue without safety changes. |
| Dec 18 | PD OLE study launch | Positive | -0.5% | Announced long-term open-label extension in Parkinson’s to expand buntanetap data. |
| Dec 16 | Corporate webinar notice | Neutral | +4.0% | Scheduled January 2026 update webinar on programs and upcoming milestones. |
| Dec 03 | PD biomarker presentation | Positive | +5.4% | Presented Phase 3 PD biomarker and cognition data at Parkinson Study Group meeting. |
| Nov 24 | CTAD 2025 presentations | Positive | +7.9% | Announced CTAD talks on PD amyloid co-pathology and double 6/18‑month AD Phase 3. |
Recent clinically focused and conference-related updates for ANVS often coincided with positive price reactions, though there has been at least one divergence on favorable Parkinson’s development news.
Over the last several months, Annovis has highlighted multiple milestones around buntanetap. A Feb 12, 2026 DSMB review allowed its pivotal Alzheimer’s Phase 3 trial to continue unchanged, while late 2025 news emphasized new Parkinson’s open-label plans and biomarker-driven presentations at CTAD and the Parkinson Study Group. Those events often saw positive price responses, framing today’s AD/PD™ 2026 presentation announcement as part of an ongoing effort to showcase cognition and biomarker data in Alzheimer’s and Parkinson’s.
Market Pulse Summary
This announcement highlights two buntanetap presentations at the AD/PD™ 2026 conference, emphasizing cognition and biomarker data in Parkinson’s disease and an update on the pivotal Phase 3 Alzheimer’s trial. In recent months, Annovis has reported DSMB clearance for its Alzheimer’s study and multiple conference showcases of biomarker and cognition findings. Investors may watch for detailed efficacy and safety readouts, enrollment progress, and how these data integrate with the broader late-stage program.
Key Terms
phase 3 medical
biomarker medical
randomized, placebo-controlled, double-blind medical
pivotal medical
AI-generated analysis. Not financial advice.
MALVERN, Pa., March 03, 2026 (GLOBE NEWSWIRE) -- Annovis Bio, Inc. (NYSE: ANVS) (“Annovis” or the “Company”), a Phase 3 clinical-stage biotechnology company developing the investigational oral therapy, buntanetap, for neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD), today announced two presentations at the 20th International Conference on Alzheimer’s and Parkinson’s Diseases (AD/PD™ 2026), taking place March 17-21, 2026, in Copenhagen, Denmark.
The presentations will highlight clinical data supporting buntanetap's treatment effect in PD with a particular focus on cognition and biomarker findings, and provide an update on the ongoing pivotal Phase 3 trial in early AD.
Details
Presentation #1 (ID:3581)
- Title: Buntanetap Treatment in Parkinson’s Disease Patients with MCI or Mild Dementia
- Presenter: Cheng Fang, Ph.D., Senior VP, Research & Development
- Theme C: α-Synucleinopathies
Presentation #2 (ID:3582)
- Title: A Dual 6-month & 18-month Randomized, Placebo-Controlled, Double-Blind Clinical Trial Investigating Efficacy and Safety of Buntanetap in Early Alzheimer’s Participants
- Presenter: Cheng Fang, Ph.D., Senior VP, Research & Development
- Theme A: β-Amyloid Diseases
“We are proud to present the continued progress in enrollment for our Alzheimer’s disease pivotal study, reflecting strong engagement from both investigators and patients,” commented Cheng Fang, Ph.D., Senior VP, Research & Development at Annovis. “Additionally, we will present the biomarker data from our Parkinson’s disease study that further support buntanetap’s therapeutic efficacy and mechanism of action.”
AD/PD™ 2026 is a leading international conference dedicated to neurodegenerative diseases, convening top medical and scientific experts to present novel findings that advance understanding of disease mechanisms and improve treatment strategies for conditions such as Alzheimer’s and Parkinson’s.
Additional information and presentation updates are available on the conference’s official website.
About Annovis
Headquartered in Malvern, Pennsylvania, Annovis Bio, Inc. (NYSE: ANVS) is a Phase 3 clinical-stage biotechnology company developing treatments for neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD). The Company's lead drug candidate, buntanetap (formerly posiphen), is an investigational once-daily oral therapy that inhibits the translation of multiple neurotoxic proteins, including APP and amyloid beta, tau, alpha-synuclein, and TDP-43, through a specific RNA-targeting mechanism of action. By addressing the underlying causes of neurodegeneration, Annovis aims to halt disease progression and improve cognitive and motor functions in patients. For more information, visit www.annovisbio.com and follow us on LinkedIn, YouTube, and X.
Investor Alerts
Interested investors and shareholders are encouraged to sign up for press releases and industry updates by registering for email alerts at https://www.annovisbio.com/email-alerts.
Forward-Looking Statements
This press release contains forward-looking statements under the Securities Act of 1933 and the Securities Exchange Act of 1934, as amended. Actual results may differ due to various risks and uncertainties, including those outlined in the Company’s SEC filings under “Risk Factors” in its Annual Report on Form 10-K and Quarterly Reports on Form 10-Q. The Company undertakes no obligation to update forward-looking statements except as required by law.
Contact Information:
Annovis Bio Inc.
101 Lindenwood Drive
Suite 225
Malvern, PA 19355
www.annovisbio.com
Investor Contact:
Alexander Morin, Ph.D.
Director, Strategic Communications
Annovis Bio
ir@annovisbio.com