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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities
Exchange Act of 1934
Date of Report (Date of Earliest Event Reported):
November 16, 2023
NeuroOne Medical Technologies Corporation
(Exact name of registrant as specified in its charter)
Delaware |
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000-54716 |
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27-0863354 |
(State or other jurisdiction
of incorporation) |
|
(Commission File Number) |
|
(IRS Employer
Identification No.) |
7599 Anagram Dr., Eden Prairie, MN 55344
(Address of principal executive offices and zip
code)
952-426-1383
(Registrant’s telephone number including
area code)
(Registrant’s former name or former address,
if changed since last report)
Check the appropriate box below if the Form 8-K
filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
☐ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
Title of each class |
|
Trading Symbol(s) |
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Name of each exchange on which registered |
Common Stock, par value $0.001 per share |
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NMTC |
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The Nasdaq Stock Market LLC |
Indicate by check mark whether the registrant
is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the
Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging Growth Company ☐
If an emerging growth company, indicate by check
mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting
standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 8.01 Other Events.
On November 16, 2023, NeuroOne Medical
Technologies Corporation (the “Company”) issued a press release announcing that on August 4, 2023, the United States
Patent and Trademark Office issued a Notice of Allowance for U.S. Patent Application 16/812,702, titled “Agent-Delivering
Neural Probe Devices and Related Systems and Methods,” which covers novel electrodes that can operate as a standard neural
electrode that also delivers a treatment agent to a target area of the patient’s brain. This patent is the third Notice of
Allowance received by the Company in recent months.
A copy of this press release is filed herewith
as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.
Item 9.01 Financial Statements and
Exhibits.
(d) Exhibits
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, as amended, the Registrant has duly caused this report to be signed on its behalf by the undersigned
hereunto duly authorized.
|
NEUROONE MEDICAL TECHNOLOGIES CORPORATION |
|
|
Dated: November 16, 2023 |
By: |
/s/ David Rosa |
|
|
David Rosa |
|
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Chief Executive Officer |
2
Exhibit 99.1
NeuroOne® Announces Patent Allowance for Drug Delivery
Utilizing a Novel Neural Probe
Patent allowance strengthens IP portfolio
and positions company in pursuing drug delivery using its neural probes
EDEN PRAIRIE, Minn., November 16, 2023 (GlobeNewswire)
-- NeuroOne Medical Technologies Corporation (NASDAQ: NMTC) (“NeuroOne” or the “Company”), a medical technology
company focused on improving surgical care options and outcomes for patients suffering from neurological disorders, announced today that,
the United States Patent and Trademark Office (“USPTO”) issued a Notice of Allowance for U.S. Patent Application 16/812,702,
titled “Agent-Delivering Neural Probe Devices and Related Systems and Methods,” which covers novel electrodes that can operate
as a standard neural electrode that also delivers a treatment agent to a target area of the patient’s brain.
A Notice of Allowance is issued by the USPTO after examination of a
patent application and a determination that a patent should be granted from the application. NeuroOne anticipates the issuance of the
patent in the coming months.
In addition to this allowed patent application, NeuroOne’s patent
portfolio includes the two other allowed patent applications, one issued U.S. patent, eight pending U.S. applications, and several foreign
applications covering a wide variety of thin-film electrode technologies, including both neural and spinal cord electrodes with unique
structures that optimize the functionality and minimized profile of those electrodes.
Dave Rosa, CEO of NeuroOne, commented, “The
Company continues to strengthen its existing patent portfolio with this recent notification by the USPTO. These allowances are especially
important as we advance our efforts to partner with existing biopharma companies to offer the next combination device that can provide
both drug delivery and sEEG recording capabilities.”
About NeuroOne
NeuroOne Medical Technologies Corporation is a
developmental stage company committed to providing minimally invasive and hi-definition solutions for EEG recording, brain stimulation
and ablation solutions for patients suffering from epilepsy, Parkinson’s disease, dystonia, essential tremors, chronic pain due to failed
back surgeries, and other related neurological disorders that may improve patient outcomes and reduce procedural costs. The Company may
also pursue applications for other areas such as depression, mood disorders, pain, incontinence, high blood pressure, and artificial intelligence.
For more information, visit nmtc1.com.
Forward Looking Statements
This press release may include forward-looking
statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act
of 1934, as amended. Except for statements of historical fact, any information contained in this presentation may be a forward–looking
statement that reflects NeuroOne’s current views about future events and are subject to known and unknown risks, uncertainties and
other factors that may cause our actual results, levels of activity, performance or achievements to be materially different from the information
expressed or implied by these forward-looking statements. In some cases, you can identify forward–looking statements by the words
or phrases “may,” “might,” “will,” “could,” “would,” “should,” “expect,”
“intend,” “plan,” “objective,” “anticipate,” “believe,” “estimate,” “predict,”
“project,” “potential,” “target,” “seek,” “contemplate,” “continue, “focused
on,” “committed to” and “ongoing,” or the negative of these terms, or other comparable terminology intended to
identify statements about the future. Forward–looking statements may include statements regarding the development of the Company’s
electrode technology program, applications for, or receipt of, regulatory clearance, the receipt and/or timing of additional feedback
from the FDA relating to the Company’s OneRF ablation system, the receipt and/or timing of regulatory approval of the Company’s
OneRF ablation system, the ability of the OneRF ablation system to offer a safer option for patients, the timing and extent of product
launch and commercialization of our technology, clinical and pre-clinical testing, what the future may hold for electrical stimulation
and NeuroOne’s potential role, business strategy, market size, potential growth opportunities, future operations, future efficiencies,
and other financial and operating information. Although NeuroOne believes that we have a reasonable basis for each forward-looking statement,
we caution you that these statements are based on a combination of facts and factors currently known by us and our expectations of the
future, about which we cannot be certain. Our actual future results may be materially different from what we expect due to factors largely
outside our control, including risks that our partnerships may not facilitate the commercialization or market acceptance of our technology;
whether due to supply chain disruptions, labor shortages, risks that our technology will not perform as expected based on results of our
pre-clinical and clinical trials; risks related to uncertainties associated with the Company’s capital requirements to achieve its business
objectives and ability to raise additional funds: the risk that we may not be able to secure or retain coverage or adequate reimbursement
for our technology; uncertainties inherent in the development process of our technology; risks related to changes in regulatory requirements
or decisions of regulatory authorities; that we may not have accurately estimated the size and growth potential of the markets for our
technology; risks relate to clinical trial patient enrollment and the results of clinical trials; that we may be unable to protect our
intellectual property rights; and other risks, uncertainties and assumptions, including those described under the heading “Risk Factors”
in our filings with the Securities and Exchange Commission. These forward–looking statements speak only as of the date of this press
release and NeuroOne undertakes no obligation to revise or update any forward–looking statements for any reason, even if new information
becomes available in the future.
Contact:
800-631-4030
ir@nmtc1.com
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