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ANNOVIS BIO PROVIDES DATA ANNOUNCEMENT UPDATE FOR THE PHASE II/III STUDY OF BUNTANETAP IN ALZHEIMER'S DISEASE MALVERN, Pa .

Key Takeaway: Annovis Bio, Inc. announced the successful completion of data cleaning for its phase II/III study of buntanetap in Alzheimer's patients. This study involved over 700 patients with 353 enrolled and 327 completing the trial. Annovis expects to release topline efficacy data in April, highlighting potential advancements in treating neurodegeneration. The company focuses on developing therapies that inhibit multiple neurotoxic proteins associated with Alzheimer's and Parkinson's diseases.

Market Sentiment Analysis

POSITIVE FACTORS

  • Successful completion of data cleaning for phase II/III study.
  • Anticipation of topline efficacy data next month.
  • Potential to reverse neurodegeneration in Alzheimer's disease.

Full Press Release Details

BIO PROVIDES DATA ANNOUNCEMENT UPDATE FOR THE PHASE II/III STUDY OF BUNTANETAP IN ALZHEIMER'S DISEASE
Pa.-March 20, 2024 -- Annovis Bio, Inc. (NYSE: ANVS), a clinical-stage drug platform company developing novel
therapies for neurodegenerative diseases today announced successful completion of data cleaning for its phase II/III study of buntanetap
in patients with mild to moderate Alzheimer's disease (AD). Topline efficacy data is expected in April.
are excited to share that we now move from data cleaning to organization and statistical evaluation of data for our Alzheimer's
study, which was completed in February. To clean data this fast is truly a tremendous achievement," said Cheng Fang, Ph.D, Senior
Vice President of Annovis. "The team has been working hard to provide trustworthy data, and I look forward to the topline results
as we plan to announce them next month."
phase II/III AD study was a randomized, double-blind, placebo-controlled trial investigating the efficacy, safety, and tolerability of
buntanetap in patients with mild to moderate AD. This was a dose ranging study where patients received either one of three doses of buntanetap
- 7.5mg, 15mg, or 30mg - or placebo on top of their standard of care for 12 weeks. Over 700 patients were screened with a total of 353
patients enrolled and 327 patients completed the study.
are grateful to the participants who enrolled and completed the study as well as their caregivers and families, for supporting their
loved one's involvement in this study; we truly couldn't do it without them. We'd also like to thank our study partners
whose teamwork and dedication allowed us to complete the study in a timely fashion," said Melissa Gaines, Senior Vice President,
Buntanetap (formerly known
as Posiphen or ANVS401) attacks neurodegeneration by inhibiting the formation of multiple neurotoxic proteins - amyloid beta, tau, alpha
synuclein, and TDP43 - thereby improving synaptic transmission, axonal transport and neuroinflammation. Dysregulation of these pathways
has been shown to be the cause of nerve cell degeneration and ultimately death. By attacking these pathways, buntanetap has the ability
to reverse neurodegeneration in Alzheimer's disease.
About Annovis Bio, Inc.
Headquartered in Malvern, Pennsylvania, Annovis Bio, Inc. is a clinical-stage, drug platform company addressing neurodegeneration,
such as Alzheimer's Disease (AD), Parkinson's Disease (PD), and other chronic neurodegenerative diseases. It is believed
to be the only company developing a drug for both AD and PD designed to inhibit more than one neurotoxic protein to restore axonal and
synaptic activity. By improving brain function, the company's goal is to treat memory loss and dementia associated with AD as well
as body and brain dysfunction associated with PD. For more information on Annovis Bio, please visit the Company's website www.annovisbio.com
Forward-Looking Statements
This press release contains "forward-looking" statements within the meaning of Section 27A of the Securities Act of
1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All statements other than statements of historical
fact are statements that could be deemed forward-looking statements. The Company advises caution in reliance on forward-looking statements.
Forward-looking statements include, without limitation, the Company's plans related to clinical trials. These statements involve known
and unknown risks, uncertainties and other factors that may cause actual results to differ materially from those implied by forward-looking
statements, including regarding patient enrollment, the effectiveness of Buntanetap and the timing, effectiveness, and anticipated results
of the Company's clinical trials evaluating the efficacy, safety and tolerability of buntanetap. See also additional risk factors set
forth in the Company's periodic filings with the SEC, including, but not limited to, those risks and uncertainties listed in the section
entitled "Risk Factors," in the Company's Annual Report on Form 10-K and Quarterly Reports on Form 10-Q filed with
the SEC. All forward-looking statements in this press release are based on information available to the Company as of the date of this
filing. The Company expressly disclaims any obligation to update or alter its forward-looking statements, whether as a result of new
information, future events or otherwise, except as required by applicable law.
Maria Maccecchini, Ph.D.

Frequently Asked Questions

What was the recent announcement by Annovis Bio?

Annovis Bio announced successful data cleaning for its phase II/III study of buntanetap in Alzheimer's patients.

When are the topline efficacy results expected?

Topline efficacy data from the study is expected to be released in April.

What does buntanetap target in neurodegeneration?

Buntanetap targets the formation of neurotoxic proteins to improve synaptic and axonal health.

How many patients enrolled in the study?

The study enrolled a total of 353 patients, with 327 completing it.

What is unique about Annovis Bio's approach?

Annovis Bio is developing a drug that targets multiple neurotoxic proteins for Alzheimer's and Parkinson's.

Last updated: Mar 20, 2024