Nexalin Technology, Inc. (Nasdaq: NXL; NXLIW) (the “Company”
or “Nexalin”) today released a letter to shareholders from its CEO
Mark White:
Dear Shareholders,
I am pleased to provide an update on Nexalin
Technologies’ recent milestones, which underscore our commitment to
advancing our patented Deep Intracranial Frequency Stimulation
(DIFS) technology for the treatment of neurological and mental
health conditions. The past months have brought exciting
developments, particularly in our Alzheimer’s research, showcasing
Nexalin’s dedication to offering non-invasive treatments without
the potential side effects of medication.
Alzheimer’s Research Breakthrough and Key
Patent
Our Alzheimer’s research achieved an important
breakthrough, with two significant studies published this October.
On October 17, we announced the results of a new study using our
DIFS technology, which demonstrated substantial improvements in
memory and cognitive function for Alzheimer’s patients. This study
confirms DIFS’s effectiveness in positively impacting cognitive
outcomes, addressing Alzheimer’s disease through a non-invasive
approach without the adverse effects associated with
pharmaceuticals. The study’s findings support Nexalin’s goal of
pioneering a potentially safer, alternative treatment for
Alzheimer’s patients, thereby providing renewed hope for caregivers
and families.
Furthermore, our October 28 press release
highlighted a second publication in the Journal of Alzheimer’s
Disease, reinforcing our prior study and validating DIFS as a
promising therapy for cognitive decline. These results collectively
position Nexalin as a leader in Alzheimer’s treatment innovation,
bringing us closer to addressing the core challenges of
neurodegenerative disease management.
In addition to these research milestones, we
announced the issuance of a key patent on June 20 for using
frequency-based deep brain stimulation to treat Alzheimer’s and
dementia. This patent is an essential asset that strengthens our
intellectual property and underscores our leadership in
non-invasive neurostimulation. With this protection, Nexalin is
well-positioned to expand its research and clinical applications,
advancing our Alzheimer’s program with greater confidence.
Positive Clinical Data in Major Depressive
Disorder
Nexalin’s DIFS technology has shown promising
results beyond Alzheimer’s, notably in treating Major Depressive
Disorder (MDD). As detailed in our June 26 press release, a study
published in a leading scientific journal demonstrated that DIFS
effectively reduces symptoms in MDD patients, potentially providing
a new, non-invasive option for individuals seeking alternatives to
antidepressant medications. With millions affected by depression
globally, we believe Nexalin’s approach offers a safe and effective
solution that could transform the mental health landscape.
Clinical Trial with UC San Diego and the San
Diego VA
Expanding our clinical reach, we recently
announced a collaboration with the University of California, San
Diego (UCSD) and the San Diego VA to conduct a clinical trial using
Nexalin’s Gen-3 Halo headset, designed to be used in a virtual
clinic model and allowing patients to receive treatment from the
convenience and privacy of their own home. As described in our
October 22 press release, this trial will explore the effectiveness
of DIFS for treating veterans with mild Traumatic Brain Injury
(mTBI). This collaboration is a significant step toward validating
our technology’s broader applications and addressing the unique
challenges faced by veterans who suffer from these conditions.
Strategic Expansion of Regulatory
Approvals
Aligned with our mission to make Nexalin’s
innovative technology widely accessible, we are pursuing regulatory
pathways to expand DIFS’s approved uses, including Alzheimer’s,
MDD, PTSD, mTBI, and more. As we engage with regulatory agencies
around the world, these approvals will be key to making safe and
effective neurostimulation available for more patients
globally.
As an example, we reached a major milestone in
our international expansion with the approval of Nexalin’s Gen-2 15
mA neurostimulation device by the Brazilian Health Regulatory
Agency (ANVISA) on June 13. This regulatory clearance follows
similar approvals in China and Oman, and allows us to introduce our
technology to the Brazilian market, marking Nexalin’s first
approval in Latin America. Entering Brazil represents a critical
step in our global growth strategy and aligns with our commitment
to reaching patients in need of non-invasive alternatives for
mental health and neurological treatments.
Looking Ahead
The recent Alzheimer’s studies, positive MDD
data, UC San Diego and San Diego VA clinical trial, patent award,
and regulatory clearance in Brazil are all significant milestones
in Nexalin’s journey. Together, they reflect our commitment to
providing safe, effective, and non-invasive solutions for those
impacted by cognitive and mental health challenges.
I am deeply grateful to our shareholders,
partners, and team for their unwavering support and confidence in
Nexalin’s mission. We look forward to the journey ahead as we push
the boundaries of DIFS technology, delivering life-changing
solutions for Alzheimer’s, MDD, and beyond.
Warm regards,
Mark White
CEO, Nexalin Technologies
About Nexalin Technology, Inc.
Nexalin designs and develops innovative
neurostimulation products to uniquely help combat the ongoing
global mental health epidemic. All of Nexalin’s products are
believed to be non-invasive and undetectable to the human body and
are developed to provide relief to those afflicted with mental
health issues. Nexalin utilizes bioelectronic medical technology to
treat mental health issues. Nexalin believes its neurostimulation
medical devices can penetrate structures deep in the mid-brain that
are associated with mental health disorders. Nexalin believes the
deeper-penetrating waveform in its next-generation devices will
generate enhanced patient response without any adverse side
effects. The Nexalin Gen-2 15 milliamp neurostimulation device has
been approved in China, Brazil, and Oman.
Additional information about the Company is
available at: https://nexalin.com/.
Disclaimers
This study was conducted on a limited number of participants,
and larger clinical trials are needed to confirm the efficacy and
safety of DIFS for Alzheimer's disease. The information in this
press release is for informational purposes only and does not
constitute medical advice.
Forward-looking statements
This press release contains statements that
constitute “forward-looking statements,” These statements relate to
future events or Nexalin’s future financial performance. Any
statements that refer to expectations, projections or other
characterizations of future events or circumstances or that are not
statements of historical fact (including without limitation
statements to the effect that Nexalin or its management “believes”,
“expects”, “anticipates”, “plans”, “intends” and similar
expressions) should be considered forward looking statements that
involve risks and uncertainties which could cause actual events or
Nexalin’s actual results to differ materially from those indicated
by the forward-looking statements. Forward-looking statements are
subject to numerous conditions, many of which are beyond the
control of the Company, including those set forth in the Risk
Factors section of the Company's Report on Form 10-K for the year
ended December 31, 2023 and other filings as filed with the
Securities and Exchange Commission. Copies of such filings are
available on the SEC’s website, www.sec.gov. Such forward-looking
statements are made as of the date hereof and may become outdated
over time. Such forward-looking statements are made as of the date
hereof and may become outdated over time. The Company undertakes no
obligation to update these statements for revisions or changes
after the date of this release, except as required by law.
Contact:Crescendo Communications, LLCTel: (212)
671-1020Email: NXL@crescendo-ir.com
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