Anavex Life Sciences Corp. (“Anavex” or the “Company”) (Nasdaq:
AVXL), a clinical-stage biopharmaceutical company developing
differentiated therapeutics for the treatment of Alzheimer's
disease, Parkinson's disease, schizophrenia, neurodevelopmental,
neurodegenerative, and rare diseases, including Rett syndrome, and
other central nervous system (CNS) diseases, today announced
encouraging preliminary electroencephalography (EEG) biomarker
results from the Part A of the ongoing placebo-controlled Phase 2
clinical study of ANAVEX®3-71 for the treatment of schizophrenia.
Part A of the Phase 2 study ANAVEX®3-71-SZ-001
(NCT06245213), was a multiple ascending dose study in 16
participants treated with either oral placebo, oral ANAVEX®3-71 90
mg daily, or oral ANAVEX®3-71 180 mg daily for 10 days.
Preliminary results demonstrated a
dose-dependent effect of ANAVEX®3-71 on two key EEG biomarkers in
patients with schizophrenia. Treatment with ANAVEX®3-71 compared to
placebo resulted in improvements in 40 Hz Auditory Steady-State
Response (ASSR) Inter Trial Coherence (ITC) and Resting State Alpha
Power, both of which were increased. These effects were most
pronounced in the higher dose group demonstrating a dose-dependent
pharmacodynamic effect.
These results provide evidence of CNS target
engagement and potential therapeutic effects of ANAVEX®3-71 in
schizophrenia.
The observed changes reversed known EEG and ERP
biomarker abnormalities associated with schizophrenia1. These EEG
biomarkers correlate with positive, negative, and cognitive
symptoms of schizophrenia. Individuals with schizophrenia typically
have reduced neural synchrony as measured by 40 Hz ASSR ITC.
Improvements in 40 Hz ASSR ITC indicate enhanced neural
synchronization, potentially leading to reduced auditory
hallucinations (positive symptom), improved executive function, and
working memory (cognitive symptoms).2 Individuals with
schizophrenia also typically have decreased resting state alpha
power correlating with sensory and behavioral problems. Increases
in Resting State Alpha Power reflect improvements in
thalamocortical circuits and sensory gating, potentially resulting
in reduced irritability and anxiety (negative symptoms).3
“We are pleased to see an initial effect of
biomarkers changing in people with schizophrenia treated with our
oral M1/SIGMAR1 therapy ANAVEX®3-71, which could eventually help
patients address both positive, negative, and cognitive symptoms of
schizophrenia,” said Christopher U Missling, PhD, President and
Chief Executive Officer of Anavex. “The results are encouraging for
further development of ANAVEX®3-71 for people with
schizophrenia.”
ANAVEX®3-71 was well tolerated, with no serious
adverse events reported.
Oral ANAVEX®3-71 is a dual SIGMAR1 receptor
agonist and M1 positive allosteric modulator with agonistic
effects. This novel mechanism of action offers the potential to
treat all symptom domains of schizophrenia without the side effects
of standard of care antipsychotics. ANAVEX®3-71 has previously
demonstrated long-lasting, pro-cognitive effects and behavioral
improvements in animal models of neurodegenerative diseases4,5, an
ability to prevent cognitive decline in animal models6,7, and has
shown robust safety signals in healthy volunteers at single doses
ranging from 5 to 200 mg once daily.8,9 Recent research into the
genetic underpinnings of schizophrenia has revealed links between
this psychiatric disorder and neurodegenerative disease, suggesting
the disorders may share certain mechanisms.10
Oral ANAVEX®3-71, in addition to the M1
muscarinic receptor activity, the combined SIGMAR1 receptor
activity might offer a novel mechanism of action that may address
multiple symptom domains without the motor side effects associated
with traditional antipsychotics.
The currently ongoing Part B of the
placebo-controlled Phase 2 study, which includes more participants
and a longer treatment duration, will provide more comprehensive
data on the efficacy and safety of ANAVEX®3-71 in schizophrenia.
Anavex expects data from Part B of the placebo-controlled Phase 2
study in the first half of 2025.
About Schizophrenia
Schizophrenia is a persistent and often
disabling mental illness impacting how a person thinks, feels, and
behaves, and affects nearly 24 million people worldwide, including
2.8 million people in the U.S. It is characterized by three symptom
domains: positive symptoms (hallucinations and delusions), negative
symptoms (difficulty enjoying life and withdrawal from others), and
cognitive impairment (deficits in memory, concentration, and
decision-making). In part due to limitations with current
treatments, people living with schizophrenia often struggle to
maintain employment, live independently, and manage relationships.
While current treatments can be effective in managing select
symptoms, approximately 34% of people do not respond to therapy, 11
with an additional 50-60% experiencing only a partial improvement
in symptoms or unacceptable side effects.12
About Anavex Life Sciences Corp.
Anavex Life Sciences Corp. (Nasdaq: AVXL) is a
publicly traded biopharmaceutical company dedicated to the
development of novel therapeutics for the treatment of
neurodegenerative, neurodevelopmental, and neuropsychiatric
disorders, including Alzheimer's disease, Parkinson's disease,
schizophrenia, Rett syndrome, and other central nervous system
(CNS) diseases, pain, and various types of cancer. Anavex's lead
drug candidate, ANAVEX®2-73 (blarcamesine), has successfully
completed a Phase 2a and a Phase 2b/3 clinical trial for
Alzheimer's disease, a Phase 2 proof-of-concept study in
Parkinson's disease dementia, and both a Phase 2 and a Phase 3
study in adult patients and one Phase 2/3 study in pediatric
patients with Rett syndrome. ANAVEX®2-73 is an orally available
drug candidate designed to restore cellular homeostasis by
targeting SIGMAR1 and muscarinic receptors. Preclinical studies
demonstrated its potential to halt and/or reverse the course of
Alzheimer's disease. ANAVEX®2-73 also exhibited anticonvulsant,
anti-amnesic, neuroprotective, and anti-depressant properties in
animal models, indicating its potential to treat additional CNS
disorders, including epilepsy. The Michael J. Fox Foundation for
Parkinson's Research previously awarded Anavex a research grant,
which fully funded a preclinical study to develop ANAVEX®2-73 for
the treatment of Parkinson's disease. We believe that ANAVEX®3-71,
which targets SIGMAR1 and M1 muscarinic receptors, is a promising
clinical stage drug candidate demonstrating disease-modifying
activity against the major hallmarks of Alzheimer's disease in
transgenic (3xTg-AD) mice, including cognitive deficits, amyloid,
and tau pathologies. In preclinical trials, ANAVEX®3-71 has shown
beneficial effects on mitochondrial dysfunction and
neuroinflammation. Further information is available at
www.anavex.com. You can also connect with the Company on Twitter,
Facebook, Instagram, and LinkedIn.
Forward-Looking Statements
Statements in this press release that are not
strictly historical in nature are forward-looking statements. These
statements are only predictions based on current information and
expectations and involve a number of risks and uncertainties.
Actual events or results may differ materially from those projected
in any of such statements due to various factors, including the
risks set forth in the Company’s most recent Annual Report on Form
10-K filed with the SEC. Readers are cautioned not to place undue
reliance on these forward-looking statements, which speak only as
of the date hereof. All forward-looking statements are qualified in
their entirety by this cautionary statement and Anavex Life
Sciences Corp. undertakes no obligation to revise or update this
press release to reflect events or circumstances after the date
hereof.
For Further Information:Anavex
Life Sciences Corp.Research & Business DevelopmentToll-free:
1-844-689-3939Email: info@anavex.com
Investors:Andrew J.
BarwickiInvestor Relations
Tel: 516-662-9461Email: andrew@barwicki.com
1 Cecchi M, Adachi M, Basile A, et al. Validation of a suite of
ERP and QEEG biomarkers in a pre-competitive, industry-led study in
subjects with schizophrenia and healthy volunteers. Schizophr Res.
2023;254:178-189. doi:10.1016/j.schres.2023.02.0182 Parker DA, Hamm
JP, McDowell JE, et al. Auditory steady-state EEG response across
the schizo-bipolar spectrum. Schizophr Res. 2019;209:218-226.
doi:10.1016/j.schres.2019.04.0143 Newson JJ, Thiagarajan TC. EEG
Frequency Bands in Psychiatric Disorders: A Review of Resting State
Studies. Front Hum Neurosci. 2019;12:521. Published 2019 Jan 9.
doi:10.3389/fnhum.2018.005214 Fisher A, Bezprozvanny I, Wu L, et
al. AF710B, a Novel M1/σ1 Agonist with Therapeutic Efficacy in
Animal Models of Alzheimer’s Disease. Neurodegener Dis.
2016;16(1-2):95-110. doi:10.1159/0004408645 Hall H, Iulita MF,
Gubert P, et al. AF710B, an M1/sigma-1 receptor agonist with
long-lasting disease-modifying properties in a transgenic rat model
of Alzheimer's disease. Alzheimers Dement. 2018;14(6):811-823.
doi:10.1016/j.jalz.2017.11.0096
https://www.anavex.com/post/anavex-life-sciences-reports-new-publication-in-scientific-journal-demonstrating-the-potential-of7
Orciani C, Do Carmo S, Foret MK, et al. Early treatment with an M1
and sigma-1 receptor agonist prevents cognitive decline in a
transgenic rat model displaying Alzheimer-like amyloid pathology
[published online ahead of print, 2023 Sep 26]. Neurobiol Aging.
2023;132:220-232. doi:10.1016/j.neurobiolaging.2023.09.0108 Fadiran
EO, Hammond E, Tran J, et al. Concentration-QTc Relationship from a
Single Ascending Dose Study of ANAVEX3-71, a Novel Sigma-1 Receptor
and Allosteric M1 Muscarinic Receptor Agonist in Development for
the Treatment of Frontotemporal Dementia, Schizophrenia, and
Alzheimer's Disease. Clin Pharmacol Drug Dev. 2023;12(9):888-901.
doi:10.1002/cpdd.13039 Fadiran EO, Hammond E, Tran J, Missling CU,
Ette E. Population-Based Characterization of the Pharmacokinetics
and Food Effect of ANAVEX3-71, a Novel Sigma-1 Receptor and
Allosteric M1 Muscarinic Receptor Agonist in Development for
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Disease. Clin Pharmacol Drug Dev. 2024;13(1):21-31.
doi:10.1002/cpdd.132310 Guo P, Meng C, Zhang S, et al.
Network-based analysis on the genes and their interactions reveals
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Neuropharmacology. 2024;244:109802.
doi:10.1016/j.neuropharm.2023.10980211 Potkin SG, Kane JM, Correll
CU, et al. The neurobiology of treatment-resistant schizophrenia:
paths to antipsychotic resistance and a roadmap for future
research. NPJ Schizophr. 2020;6(1):1. Published 2020 Jan 7.
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Cascella N, Sawa A. Treatment resistant schizophrenia: Clinical,
biological, and therapeutic perspectives. Neurobiol Dis.
2019;131:104257. doi:10.1016/j.nbd.2018.08.016
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