Annovis Bio Announces Full Enrollment of Its Phase II/III Alzheimer’s Disease Trial, Exceeding Original Projections
27 Novembre 2023 - 1:30PM
Annovis Bio, Inc. (NYSE: ANVS), a clinical-stage drug platform
company addressing neurodegenerative diseases such as Alzheimer’s
(AD) and Parkinson’s disease (PD) and developing novel and
transformative therapies, announced that AD phase II/III study of
its lead compound buntanetap has exceeded full enrollment.
Since the initiation of phase II/III study in March 2023, over
700 patients were screened and a total of 353 patients enrolled
across 54 sites in the United States.
The phase II/III study is a randomized, double-blind,
placebo-controlled trial investigating the efficacy, safety, and
tolerability of buntanetap in patients with mild to moderate AD.
This is a dose ranging study where patients receive either one of
three doses of buntanetap (7.5mg, 15mg, or 30mg) or placebo on top
of their standard of care for 12 weeks.
Buntanetap’s mechanism of action, favorable toxicology profile,
and oral mode of administration distinguish it as superior to other
AD drugs. Other drugs attempt to remove just one neurotoxic protein
and, at best, have a minor effect. Buntanetap reduces levels of
multiple neurotoxic proteins - Amyloid Beta, Tau, alpha Synuclein,
and TDP43 – therefore improving synaptic transmission and axonal
transport and reducing inflammation, which has been shown to be the
cause of cell death. By attacking several pathways involved in
neurodegeneration, buntanetap has the ability to reverse the
destructive effects that Alzheimer’s Disease has on thinking and
memory.
Annovis announced on October 12, 2023, the positive efficacy
interim analysis and on October 30, 2023, the safety review by the
Data and Safety Monitoring Board (DSMB). The efficacy and safety
analysis reviewed by the DSMB recommended that Annovis continue the
trial as originally designed. We expect the data from this study to
read out by the end of March 2024.
“We are very pleased to share the news of the successful
completion of enrollment for our phase II/III study of buntanetap
in Alzheimer’s Disease,” said Annovis’ founder, president and CEO,
Maria Maccecchini, Ph.D. "The number of enrolled patients exceeded
our initial projections, revealing the Alzheimer’s community's
strong endorsement of our mission to develop a treatment targeting
multiple neurotoxic proteins. This not only proves their support
but also underscores their willingness to contribute to advancing
this important cause.”
About Annovis Bio, Inc.Headquartered in Berwyn,
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 and follow us on LinkedIn and
Twitter.
Forward-Looking StatementsThis 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.
Investor Contacts:Maria Maccecchini,
Ph.D.maccecchini@annovisbio.com
Annovis Bio (AMEX:ANVS)
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