Annovis Bio Provides Corporate Updates and Announces First Quarter 2024 Financial Results
May 13 2024 - 7:30AM
Annovis Bio, Inc. (NYSE: ANVS) (“Annovis” or the “Company”), a
clinical-stage drug platform company developing novel therapies for
neurodegenerative diseases, provided updates from across the
organization and announced first quarter financial results.
Clinical Updates
AD Phase II/III Study
- On April 29, Annovis announced statistically significant Phase
II/III data in patients with early Alzheimer’s disease (AD).
- Significantly higher rate of improvement in ADAS-Cog 11 scores
in each treatment dose relative to placebo for patients with mild
AD;
- Improvement in cognition measured by ADAS-Cog 11 at three
months was 3.3 points as compared to 0.3 for placebo, consistent
with previous Phase II AD/PD and Discovery studies;
- Plasma Tau protein levels were reduced, consistent with
previous Phase II biomarker data.
- Based on the findings of this short study, Annovis plans to
conduct a pivotal 18-month disease-modifying Phase III trial in
biomarker-positive early AD patients.
PD Phase III Study
- On January 24, Annovis refined the timeline for Parkinson’s
disease (PD) Phase III data announcement, originally set for the
end of January, due to necessary cleaning efforts required to
deliver reliable and accurate results.
- On May 9, Annovis announced unblinding of the Phase III data
and intends to release topline results in June of 2024.
- The Phase III trial was a randomized, double-blind,
placebo-controlled trial investigating the efficacy, safety, and
tolerability of buntanetap for early PD patients, on top of their
existing standard of care. Patients were treated with 10 mg, 20 mg,
or placebo for 6 months. Out of 616 patients screened, 523 were
randomized and 471 completed the study across 67 sites (43 in the
United States and 24 in the European Union).
Patents
- Annovis announced on January 30, 2024 the filing of a patent
application covering the use of buntanetap and its analogues for
the treatment of neuropsychiatric indications.
- This patent follows the U.S. Provisional Application No.
63/440,890, which was filed on January 24, 2023.
- This patent application addresses mental illnesses such as
autism, attention deficit-hyperactivity disorder, bipolar disorder,
major depressive disorder, anxiety and schizophrenia, which have
been shown to share similar pathological abnormalities with certain
neurodegenerative diseases, including disruptions in synthesis of
neurotoxic proteins, impairment of axonal transport, inflammation,
and nerve cell death.
First Quarter 2024 Financial Results
- The Company’s cash and cash equivalents totaled $3.1 million as
of March 31, 2024, compared to $5.8 million as of
December 31, 2023. The Company estimates that active
management of its cash and working capital positions, combined with
the $0.8 million cash received in connection with its previously
announced ELOC Purchase Agreement, will fund its operations into
the fourth quarter of 2024. The Company had 11.0 million shares of
common stock outstanding as of March 31, 2024.
- Total operating expenses for the three months ended March 31,
2024 were $7.8 million, which included research and development
expenses of $6.5 million and general and administrative expenses of
$1.3 million. This compares to total operating expenses for the
three months ended March 31, 2023 of $10.0 million, which included
research and development expenses of $7.8 million and general and
administrative expenses of $2.2 million.
- Other income for the three months ended March 31, 2024 was $6.7
million, which included a $6.7 million non-cash gain from change in
fair value of liability-classified warrants. This compares to other
income for the three months ended March 31, 2023 of $0.2 million,
which included $0.2 million of interest income.
- Annovis reported basic net loss per common share of $0.10 and
diluted net loss per common share of $0.72 for the three months
ended March 31, 2024. This compares to a basic net loss per common
share of $1.19 and diluted net loss of $1.19 for the three months
ended March 31, 2023.
Conferences
- Annovis participated in the International Conference on
Alzheimer’s and Parkinson’s Diseases (AD/PD™ 2024), which took
place in Lisbon, Portugal from March 5-9, 2024.
- On March 7, Maria Maccecchini participated in a forum
discussion titled “New Insights in the Development of Biomarkers,
Imaging, and Therapy of Alpha-Synuclein, LRKK2, and GBA
Pathologies”.
Message from Dr. Maria Maccecchini
“The first quarter proved to be pivotal for our company as we
continued to wind down our two recent clinical trials - Phase III
in Parkinson’s and Phase II/III in Alzheimer’s. For our PD study,
which concluded late last year, diligent efforts are underway to
meticulously prepare the data, with expected delivery of topline
results in June of this year. For the AD study, we successfully
cleaned the data and were proud to announce cognitive improvements
as measured by ADAS-Cog 11 in patients with early AD, showing us a
pathway for continued clinical development of buntanetap. We extend
our heartfelt gratitude to the patients and their families whose
contribution was the driving force of our research aimed to bring
new treatments to the market.”
- Maria L. Maccecchini, Ph.D.,
Annovis Founder, President, and CEO
About Buntanetap Buntanetap
(formerly known as Posiphen or ANVS401) attacks neurodegeneration
by reducing multiple neurotoxic proteins, thereby improving
synaptic transmission and axonal transport, which is the
information highway of the nerve cell. Dysfunction of synaptic
transmission and axonal transport has been shown to be the cause of
nerve cell degeneration and ultimately death. Unlike other drugs in
development which attempt to remove only one toxic protein,
buntanetap inhibits several toxic proteins before they can form,
thereby preventing the formation of all the major neurotoxic
proteins responsible for PD and AD.
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 and
follow us on LinkedIn and X (formerly known as 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 Contact:Maria Maccecchini,
Ph.D.maccecchini@annovisbio.com
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