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Annovis Bio refines Alzheimer's trial approach after Phase II/III data

EditorNatashya Angelica
Published 05/06/2024, 02:52 PM
ANVS
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MALVERN, Pa. - Annovis Bio, Inc. (NYSE: ANVS), a clinical-stage drug platform company, announced a strategic update following the evaluation of their Alzheimer's disease (AD) study results. Maria Maccecchini, CEO of Annovis, addressed stockholders regarding the recent Phase II/III trial data for their drug candidate buntanetap, and outlined the company's next steps.

The communication follows a period of intense scrutiny from investors and a significant drop in Annovis' share price. The company acknowledged the disappointment and concern from their stakeholders, affirming their commitment to developing treatments for AD and Parkinson’s disease (PD). In response to the feedback, Annovis emphasized their adherence to rigorous scientific standards and transparent communication.

The Phase II/III study aimed to assess the breadth of buntanetap's efficacy and provided the company with crucial insights. Data indicated a notable cognitive response in patients with early and mild Alzheimer’s, specifically those with Mini-Mental State Examination (MMSE) scores between 21-28, as opposed to moderate AD patients where the response was less clear due to a high placebo effect.

Based on these findings, Annovis plans to refine their approach for the upcoming pivotal Phase III trial. The company intends to prescreen patients for plasma AD biomarkers to confirm diagnoses and enroll only those with early and mild Alzheimer’s. The goal is to build upon the positive response observed in this subpopulation, which demonstrated the highest level of improvement with buntanetap treatment.

Buntanetap is designed to inhibit the formation of multiple neurotoxic proteins, which are implicated in neurodegeneration, and to restore brain function by improving synaptic transmission, axonal transport, and neuroinflammation. Annovis believes the FDA will accept buntanetap for symptomatic relief and allow the continuation of the Phase III study for disease-modification.

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Annovis Bio, headquartered in Malvern, Pennsylvania, is focused on addressing neurodegeneration in diseases such as AD and PD. The company is unique in its approach to developing a drug that targets more than one neurotoxic protein to combat neurodegeneration.

The press release also includes forward-looking statements regarding the company's plans and the potential effectiveness of buntanetap. Still, these statements come with the usual caveats of risks and uncertainties that may cause actual results to differ materially from expectations.

This news article is based on a press release statement from Annovis Bio, Inc.

InvestingPro Insights

In light of Annovis Bio's recent strategic update, investors are closely monitoring the company's financial health and stock performance. According to InvestingPro, Annovis holds more cash than debt on its balance sheet, which could provide a cushion as the company navigates the costly process of drug development and clinical trials.

Moreover, analysts predict the company will be profitable this year, a potential indicator of the market's confidence in Annovis' drug candidate buntanetap and its commercial prospects.

InvestingPro Data reveals that Annovis Bio has a market capitalization of approximately $57.04 million. The company's stock has experienced significant volatility, with a 1-week price total return of -28.85% and a 1-month price total return of -53.33%.

Despite these challenges, Annovis Bio's stock is trading near its 52-week low, which could present a buying opportunity for long-term investors who believe in the company's pipeline and market potential.

For readers looking to delve deeper into Annovis Bio's financials and stock performance, InvestingPro offers additional insights. There are currently 12 more InvestingPro Tips available for Annovis Bio, which can be accessed with a subscription. To sweeten the deal, use the coupon code PRONEWS24 to get an additional 10% off a yearly or biyearly Pro and Pro+ subscription.

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This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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