Aclarion Adds to Strong Patent Portfolio with Notice of Allowance for New U.S. Patent Application Addressing Key Pain Indicator Biomarker
Aclarion, Inc. (Nasdaq: ACON) has received a Notice of Allowance for its US Patent Application 16/224,590, enhancing its patent portfolio to 22 U.S. patents. This patent allows Aclarion to utilize Magnetic Resonance Spectroscopy (MRS) to identify Propionic Acid, a biomarker linked to bacterial infections in intervertebral discs. The Nociscan platform aids physicians in distinguishing between painful and nonpainful discs, potentially reducing unnecessary surgeries. CEO Brent Ness emphasized the importance of this advancement in supporting optimal treatment decisions for chronic low back pain.
- Received Notice of Allowance for US Patent Application 16/224,590, expanding patent portfolio to 22 U.S. patents.
- Nociscan platform aids in identifying the source of chronic low back pain noninvasively.
- Potential to reduce unnecessary surgeries by using antibiotic treatment when infections are identified.
- None.
Strengthens portfolio by addressing the anaerobic bacteria that can seed into the intervertebral disc, proliferate, and accelerate painful disc degeneration.
Successful commercialization of IP holds the promise of giving physicians better data to make the critical decision as to whether antibiotic therapy or surgery is the preferred treatment option.
Broomfield, CO, Dec. 01, 2022 (GLOBE NEWSWIRE) -- via NewMediaWire -- Aclarion, Inc., (“Aclarion” or the “Company”) (Nasdaq: ACON, ACONW), a healthcare technology company that is leveraging biomarkers and proprietary augmented intelligence algorithms to help physicians identify the location of chronic low back pain, announced today that it has received a Notice of Allowance for its US Patent Application 16/224,590 titled “Magnetic Resonance Spectroscopy System and Method for Diagnosing Pain or Infection Associated with Propionic Acid”.
Conventional imaging (lumbar MRI) for Chronic Low Back Pain offers important structural information but struggles to identify the actual source of pain. Aclarion’s Nociscan solution is the first evidence-supported SaaS platform to noninvasively help physicians distinguish between painful and nonpainful discs in the lumbar spine. Nociscan objectively quantifies chemical biomarkers demonstrated to be associated with disc pain. Biomarker data is entered into proprietary algorithms to highlight if a disc may be a source of pain. When used with other diagnostic tools, Nociscan provides critical insights into the location of a patient’s low back pain, giving physicians clarity to optimize treatment strategies.
The patent application 16/224,590 titled “Magnetic Resonance Spectroscopy System and Method for Diagnosing Pain or Infection Associated with Propionic Acid” expands the Aclarion patent portfolio to broadly cover using MRS to identify Propionic Acid (PA), a biomarker that the literature suggests may be indicative of bacterial infection in a disc. This information may prove critical in supporting the optimal treatment of low back pain when infection is the underlying cause of pain. In these cases, effective treatment with antibiotic therapy alone may eliminate the need for surgical intervention.
"The mission of Aclarion is to give physicians better data so they can make better decisions about the care of their patients,” says Brent Ness, CEO. “We are committed to leading with compelling clinical and economic evidence. The foundation of our leadership is our Nociscan product and the patent portfolio on which it is built. Allowance of this patent strengthens our competitive moat and gives us the opportunity to advance our mission by exploring whether Nociscan can help physicians address the critical diagnostic decision of treating a patient with antibiotics or surgical intervention.”
The Aclarion patent portfolio now includes 22 U.S. patents, 17 foreign patents, 5 pending U.S. patent applications, and 7 pending foreign patent applications, including patents and patent applications exclusively licensed from Regents of the University of California.
About Aclarion, Inc.
Aclarion is a healthcare technology company that leverages Magnetic Resonance Spectroscopy (“MRS”), proprietary signal processing techniques, biomarkers, and augmented intelligence algorithms to optimize clinical treatments. The Company is first addressing the chronic low back pain market with Nociscan, the first, evidence-supported, SaaS platform to noninvasively help physicians distinguish between painful and nonpainful discs in the lumbar spine. Through a cloud connection, Nociscan receives magnetic resonance spectroscopy (MRS) data from an MRI machine for each lumbar disc being evaluated. In the cloud, proprietary signal processing techniques extract and quantify chemical biomarkers demonstrated to be associated with disc pain. Biomarker data is entered into proprietary algorithms to indicate if a disc may be a source of pain. When used with other diagnostic tools, Nociscan provides critical insights into the location of a patient’s low back pain, giving physicians clarity to optimize treatment strategies. For more information, please visit www.aclarion.com.
Forward Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 about the Company's current expectations about future results, performance, prospects and opportunities. Statements that are not historical facts, such as "anticipates," "believes" and "expects" or similar expressions, are forward-looking statements. These forward-looking statements are based on the current plans and expectations of management and are subject to a number of uncertainties and risks that could significantly affect the Company's current plans and expectations, as well as future results of operations and financial condition. These and other risks and uncertainties are discussed more fully in our filings with the Securities and Exchange Commission. Readers are encouraged to review the section titled "Risk Factors" in the Company's Prospectus dated April 21, 2022, as filed with the Securities and Exchange Commission on April 25, 2022 under Rule 424(b)(4), as well as other disclosures contained in the Prospectus and subsequent filings made with the Securities and Exchange Commission. Forward-looking statements contained in this announcement are made as of this date and the Company undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.
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