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BrainsWay Announces Positive Results in Late-Life Depression Post-Marketing Analysis

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BrainsWay (BWAY) announces positive results in a post-marketing study for late-life depression treatment using Deep Transcranial Magnetic Stimulation (Deep TMS™). The study showed a 79.4% response rate and a 60.3% remission rate in patients aged 60-91, addressing concerns about efficacy in older adults.
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The publication of BrainsWay's study results in the Journal of Clinical Medicine sheds light on the efficacy of Deep Transcranial Magnetic Stimulation (Deep TMS) in treating late-life depression. This demographic is particularly significant as the global population ages and mental health treatments for older adults become increasingly necessary. The reported response and remission rates are noteworthy, as they suggest a high level of effectiveness for a patient group that has historically been difficult to treat due to brain atrophy and other age-related changes.

From a medical research perspective, the study's design and its post-marketing nature are important. Real-world outcomes are critical in understanding how treatments perform outside the controlled conditions of clinical trials. The use of the proprietary H1 Coil is also of interest, as it may offer a technological advancement capable of addressing the unique challenges of treating depression in older adults. However, it's essential to consider the FDA's current labeling, which does not extend to patients over 68. This indicates that while the study is promising, regulatory hurdles remain before the treatment can be widely marketed to this age group.

From an economic standpoint, the potential expansion of Deep TMS to treat late-life depression represents a significant market opportunity for BrainsWay. As populations in developed countries age, the prevalence of late-life depression is expected to increase, creating a growing demand for effective treatments. The ability to meet this demand can have a substantial impact on healthcare costs, as depression is associated with increased medical expenses, higher rates of hospitalization and a greater burden on long-term care facilities.

Furthermore, if Deep TMS is recognized by the FDA for older patients, it could lead to changes in insurance coverage and reimbursement policies, affecting the affordability and accessibility of the treatment. This, in turn, could influence the stock market performance of BrainsWay, as investors anticipate the potential for increased revenue streams. However, it's important to monitor the FDA's review process, as any setbacks could impact the company's financial outlook and stock market valuation.

Analyzing the market implications of these study results, BrainsWay may be positioned to capture a unique niche in the mental health treatment sector. The high response and remission rates reported for Deep TMS in older adults could differentiate the company's product in a crowded marketplace. Additionally, the positive publication in a reputable journal serves to enhance the credibility and visibility of BrainsWay's technology among healthcare providers and patients.

It's important to note, however, that market adoption hinges not only on regulatory approval but also on clinician acceptance and patient awareness. The company will likely need to invest in educational initiatives and marketing strategies to promote the benefits of Deep TMS to these stakeholders. The stock market often reacts favorably to positive clinical study results, but sustained growth for BrainsWay will depend on the company's ability to translate these results into tangible sales and market share gains.

Data Published in Leading Peer-Reviewed Publication, Journal of Clinical Medicine

JERUSALEM and BURLINGTON, Mass., March 28, 2024 (GLOBE NEWSWIRE) -- BrainsWay Ltd. (NASDAQ & TASE: BWAY) (“BrainsWay” or the “Company”), a global leader in advanced noninvasive neurostimulation treatments for mental health disorders, announced positive results in a recently published post-marketing study of its Deep Transcranial Magnetic Stimulation (Deep TMS™) for the treatment of late-life depression.

The data were highlighted in an article entitled, “Never Too Late: Safety and Efficacy of Deep TMS for Late-Life Depression,” that was published in the Journal of Clinical Medicine, an international, peer-reviewed, open access journal. The post-marketing study demonstrated real-world outcomes for older adults (60-91 years of age) suffering from major depressive disorder (MDD). In the study, data was analyzed from 247 depression patients at 16 clinical sites in this age group who had been treated with BrainsWay’s proprietary H1 Coil. The results showed a 79.4% response rate (≥50% reduction in symptoms) and a 60.3% remission rate for those patients who had received at least 30 treatment sessions, and were based on the rating scale that was most utilized for each individual patient. The outcomes were comparable to those reported in a post-marketing analysis of over 1,350 patients published in 2023.

"As our population is living longer, late-life depression is fast becoming a critical health care concern that affects a significant number of families and care facilities worldwide. While the use of noninvasive neurostimulation with TMS has shown excellent efficacy for depression patients aged 20-65, there has been some concern that older adults may not receive adequate relief due to typical age-related changes in their brains. Specifically, as we get older, the distance from our scalp to our brain tends to expand due to brain atrophy. This can make it challenging for certain non-invasive technologies to reach the brain areas involved in depression,” said Colleen Hanlon, PhD, Vice President of Medical and Clinical Affairs at BrainsWay. “We believe that the deeper and broader stimulation of BrainsWay’s Deep TMS can play a meaningful role in overcoming these age-related challenges.”

BrainsWay’s existing FDA depression labeling does not extend to patients aged over 68, and the results of this study are subject to further review by the FDA.

About BrainsWay 
BrainsWay is a global leader in advanced noninvasive neurostimulation treatments for mental health disorders. The Company is boldly advancing neuroscience with its proprietary Deep Transcranial Magnetic Stimulation (Deep TMS™) platform technology to improve health and transform lives. BrainsWay is the first and only TMS company to obtain three FDA-cleared indications backed by pivotal clinical studies demonstrating clinically proven efficacy. Current indications include major depressive disorder (including reduction of anxiety symptoms, commonly referred to as anxious depression), obsessive-compulsive disorder, and smoking addiction. The Company is dedicated to leading through superior science and building on its unparalleled body of clinical evidence. Additional clinical trials of Deep TMS in various psychiatric, neurological, and addiction disorders are underway. Founded in 2003, with offices in Burlington, MA and Jerusalem, Israel, BrainsWay is committed to increasing global awareness of and broad access to Deep TMS. For the latest news and information about BrainsWay, please visit www.brainsway.com

Forward Looking Statements   
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential” or similar words. These forward-looking statements and their implications are based on the current expectations of the management of the Company only and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. In addition, historical results or conclusions from scientific research and clinical studies do not guarantee that future results would suggest similar conclusions or that historical results referred to herein would be interpreted similarly in light of additional research or otherwise. The following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: inadequacy of financial resources to meet future capital requirements; changes in technology and market requirements; delays or obstacles in launching and/or successfully completing planned studies and clinical trials; failure to obtain approvals by regulatory agencies on the Company’s anticipated timeframe, or at all; inability to retain or attract key employees whose knowledge is essential to the development of Deep TMS products; unforeseen difficulties with Deep TMS products and processes, and/or inability to develop necessary enhancements; unexpected costs related to Deep TMS products; failure to obtain and maintain adequate protection of the Company’s intellectual property, including intellectual property licensed to the Company; the potential for product liability; changes in legislation and applicable rules and regulations; unfavorable market perception and acceptance of Deep TMS technology; inadequate or delays in reimbursement from third-party payers, including insurance companies and Medicare; inability to commercialize Deep TMS, including internationally, by the Company or through third-party distributors; product development by competitors; inability to timely develop and introduce new technologies, products and applications, which could cause the actual results or performance of the Company to differ materially from those contemplated in such forward-looking statements. 

Any forward-looking statement in this press release speaks only as of the date of this press release. The Company undertakes no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws. More detailed information about the risks and uncertainties affecting the Company is contained under the heading “Risk Factors” in the Company’s filings with the U.S. Securities and Exchange Commission. 

Contacts:   

BrainsWay: 
Ido Marom 
Chief Financial Officer 
844-386-7001 ext. 5
Ido.Marom@BrainsWay.com 

Investors: 
Brian Ritchie
LifeSci Advisors
646-889-1200
britchie@lifesciadvisors.com

Media Contact:
Chris Boyer
844-386-7001
Chris.Boyer@BrainsWay.com


FAQ

What study results did BrainsWay announce?

BrainsWay announced positive results in a post-marketing study for late-life depression treatment using Deep Transcranial Magnetic Stimulation (Deep TMS™).

What were the response and remission rates in the study?

The study showed a 79.4% response rate and a 60.3% remission rate in patients aged 60-91.

What is the age group of patients in the study?

Patients in the study were aged 60-91.

What is the FDA status of BrainsWay's depression labeling for patients over 68?

BrainsWay's existing FDA depression labeling does not extend to patients aged over 68.

Where was the study data published?

The study data was published in the Journal of Clinical Medicine, a leading peer-reviewed publication.

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