Anavex Life Sciences Announces Issuance of U.S. Patent Covering ANAVEX®2-73 (blarcamesine) for Neurodevelopmental Disorders Therapy
Anavex Life Sciences Corp. (Nasdaq: AVXL) announced the issuance of U.S. Patent No. 11,446,275, enhancing its intellectual property for ANAVEX®2-73 (blarcamesine). This patent covers treatment methods for conditions related to methyl-CpG binding protein 2 defects, including Rett syndrome and autism, ensuring protection until at least 2037. Anavex has recently secured multiple patents supporting its drug portfolio, demonstrating commitment to innovation in therapies for neurodegenerative disorders. ANAVEX®2-73 has shown positive results in Phase 2 and Phase 3 trials.
- Issuance of U.S. Patent No. 11,446,275 enhances Anavex's IP portfolio.
- Patent secures therapeutic methods for methyl-CpG binding protein 2 defects, safeguarding innovation until at least 2037.
- Successful completion of multiple clinical trials for ANAVEX®2-73, indicating strong potential for treatment in neurodevelopmental disorders.
- None.
Issuance of Anavex’s Newest U.S. Patent Will Expand Anavex’s Intellectual Property Portfolio Surrounding ANAVEX®2-73
NEW YORK, Sept. 21, 2022 (GLOBE NEWSWIRE) -- Anavex Life Sciences Corp. (“Anavex” or the “Company”) (Nasdaq: AVXL), a clinical-stage biopharmaceutical company developing differentiated therapeutics for the treatment of neurodegenerative and neurodevelopmental disorders including Alzheimer’s disease, Parkinson’s disease, Rett syndrome and other central nervous system (CNS) disorders, today announced that United States Patent and Trademark Office (USPTO) issued U.S. Patent No. 11,446,275 to Anavex, with claims to treatment methods using its leading drug candidate, ANAVEX®2-73 (blarcamesine) and its analogs, for ameliorating biochemical and functional abnormalities associated with methyl-CpG binding protein 2 defects (MeCP2 defects).
Such defects encompass a range of neurodevelopmental and neurological disorders, including but not limited to, Rett syndrome, Angelman syndrome, Williams syndrome, cerebral palsy, autism spectrum disorder, and multiple sclerosis.
Anavex’s newest patent is the latest in a series of patents recently granted to Anavex and is expected to remain in force at least until 2037, not including any patent term extensions. Recent US patent grants to Anavex also include U.S. Patent No. 10,426,754 granted to Anavex in October 2019, U.S. Patent No. 10,507,196 granted to Anavex in December 2019, and U.S. Patent No. 10,888,543 granted to Anavex in January 2021. The new ‘275 patent adds to the comprehensive patent portfolio supporting ANAVEX®2-73 (blarcamesine), and its analogs, such as ANAVEX®1-41 and ANAVEX®19-144, which are all orally available sigma-1 receptor (SIGMAR1) agonists. The ‘275 patent covers the therapeutic use of these compounds, including ANAVEX®2-73 (blarcamesine), in oral, transdermal, and parenteral compositions to treat abnormalities associated with methyl-CpG binding protein 2 defects (MeCP2 defects).
Using precision medicine included SIGMAR1 biomarker of response, ANAVEX®2-73 (blarcamesine) successfully completed a Phase 2 in adult Rett syndrome and a Phase 3 in adult Rett syndrome, respectively. In addition, ANAVEX®2-73 (blarcamesine) successfully completed a Phase 2 in Parkinson’s disease dementia, Phase 2a clinical trial for Alzheimer’s disease and is expected a larger Phase 2b/3 study for Alzheimer’s disease (NCT03790709) reading out in the fall of 2022.
"We are pleased with the continued development of the patent portfolio for ANAVEX®2-73 (blarcamesine). This latest patent will fortify our robust patent portfolio relating to ANAVEX®2-73 (blarcamesine),” said Christopher U. Missling, PhD, President and Chief Executive Officer of Anavex. “Along with other allowances, it demonstrates our strong overall commitment to protecting the innovation and commercial opportunity of our entire product portfolio," said Christopher U. Missling, PhD, President and Chief Executive Officer of Anavex.
ANAVEX®2-73 (blarcamesine) is an orally available, small-molecule activator of the sigma-1 receptor, which, data suggest, is pivotal to restoring neural cell homeostasis and promoting neuroplasticity.1
About and Rett Syndrome and Neurodevelopmental Disorders
Rett syndrome is a devastating, non-inherited genetic post-natal progressive neurodevelopmental disorder that occurs almost exclusively in girls and leads to severe impairments, affecting nearly every aspect of the child’s life: their ability to speak, walk, eat, and control some autonomic functions (e.g., peripheral vasomotor, breathing). The hallmark of Rett syndrome is near constant repetitive hand movements while awake. The disease is characterized by normal early growth and development (6 to 18 months) followed by a slowing of development, loss of purposeful use of the hands and spoken language, repetitive hand movements, gait impairments, autistic features, and, in a high proportion of individuals, seizures and behavioral abnormalities. Although there could be partial recovery of loss functions, most affected individuals showed marked communication and motor impairments and are diagnosed with intellectual disability.
Rett syndrome is caused by mutations in the MECP2 gene and strikes all racial and ethnic groups. The disease occurs worldwide in approximately one in every 10,000 to 15,000 live births. There is currently no cure for Rett syndrome. MECP2 mutations have been also associated with other clinical presentations, including autism spectrum disorder, Angelman-like syndrome, attention-deficit–hyperactivity disorder, nonspecific intellectual disability, bipolar disorder, schizophrenia, and in males severe postnatal encephalopathy. Abnormal MeCP2 expression has also been reported in the brain of individuals with autism spectrum disorder. While rare, health care costs associated with these conditions are long term and can be devastating.
About Multiple Sclerosis and Neurological Disorders
Neurological disorders are diseases of the peripheral and central nervous system (CNS). They include disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. Multiple sclerosis (MS) is a type of neurological disorder, specifically a chronic inflammatory-neurodegenerative disease of the central nervous system (CNS), resulting in the accumulation of irreversible disabilities such as muscle weakness, visual disturbances, and other neurological impairments. MS is the most common autoimmune disorder of the CNS, and worldwide, ~2.3 million people are affected. Most people experience their first symptoms of MS between the ages of 20 and 40. Currently there is no cure for MS and many medications have serious side effects and some carry significant risks. A huge unmet need remains for agents directly interacting with the central nervous system to achieve regeneration, axonal protection, neuronal protection and remyelination.
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 and neurodevelopmental disorders, including Alzheimer's disease, Parkinson's disease, 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 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 with Rett syndrome. ANAVEX®2-73 is an orally available drug candidate that restores cellular homeostasis by targeting sigma-1 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. ANAVEX®3-71, which targets sigma-1 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 Development
Toll-free: 1-844-689-3939
Email: info@anavex.com
Investors:
Andrew J. Barwicki
Investor Relations
Tel: 516-662-9461
Email: andrew@barwicki.com
1 Advances in Experimental Medicine and Biology Volume 964 (2017) Sigma Receptors: Their Role in Disease and as Therapeutic Targets.
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