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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): August 14, 2024

 

NeuroOne Medical Technologies Corporation

(Exact name of registrant as specified in its charter)

 

Delaware   001-40439   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)   Name of each exchange on which registered
Common Stock, par value $0.001 per share   NMTC   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 2.02 Results of Operations and Financial Condition.

 

On August 14, 2024, NeuroOne Medical Technologies Corporation (the “Company”) issued a press release announcing its financial results for the fiscal quarter ended June 30, 2024. A copy of this press release is furnished herewith as Exhibit 99.1 to this Current Report and is incorporated herein by reference.

 

In accordance with General Instruction B.2. of Form 8-K, the information in this Item 2.02, and Exhibit 99.1 hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section, nor shall it be deemed incorporated by reference in any of the Company’s filings under the Securities Act of 1933, as amended, or the Exchange Act, whether made before or after the date hereof, regardless of any incorporation language in such a filing, except as expressly set forth by specific reference in such a filing.

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits

 

Exhibit No.   Description
99.1   Press Release, dated August 14, 2024
104   Cover Page Interactive Data File (embedded with Inline XBRL document).

 

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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: August 14, 2024    
  By: /s/ David Rosa
    David Rosa
    Chief Executive Officer

 

 

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Exhibit 99.1

 

NeuroOne® Reports Third Quarter Fiscal Year 2024 Financial Results and Provides Corporate Update

 

EDEN PRAIRIE, Minn., August 14, 2024 (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, today announces its operating results for the third quarter fiscal year 2024 ended June 30, 2024.

 

Third Quarter Fiscal Year 2024 and Recent Business Updates

 

Financial Highlights:

 

Product revenue of $826,000 in Q3 2024, compared to $630,000 in Q3 2023

 

Reduced operating expenses from $3.8 million in Q3 2023 to $3.1 million in Q3 2024

 

Raised an additional $1.6 million using the ATM Program in Q3 2024

 

Completed $2.65 million private placement and entered into $3.0 million secured credit facility agreement in August 2024

 

Evo® sEEG:

 

Completed manufacturing transition from sEEG diagnostic electrodes to OneRF electrodes

 

OneRF™ Ablation System:

 

Continued limited commercial launch of the OneRF™ Ablation System, including first shipments, implants and ablations with OneRF™ Ablation System

 

Completed OneRF™ Ablation System training for four sites and initiated sales quote process with 12 additional sites

 

Implanted ~200 RF electrodes and performed more than 50 RF ablations on 3 patients

 

Signed a non-binding term sheet with an undisclosed global medical technology company to distribute our OneRF™ Ablation System. The term sheet is non-binding, and the partnership is subject to the negotiation and execution of definitive documentation, due diligence, and other customary closing conditions

 

Exhibited the OneRF™ Ablation System at the Association of Neurological Surgeons (AANS) Annual Scientific Meeting in May and the American Society for Stereotactic and Functional Neurosurgery Biennial Meeting in June

 

The Centers for Medicare and Medicaid Services (CMS) approved and granted a new ICD-10-PCS (International Classification of Diseases, 10th Revision, Procedure Coding System) code for the OneRF™ ablation procedure. The new code will be effective October 1, 2024 and allows hospital reporting of inpatient procedures that are performed using the OneRF™ Ablation System ensuring efficient and accurate documentation, billing, and analysis

 

Presented posters on preclinical evaluation and ex vivo lesion characterization of OneRF™ Ablation System at the AANS Annual Scientific Meeting in May

 

 

 

 

sEEG-Based Drug Delivery Program:

 

Completed feasibility testing in vivo study providing histology data

 

Completed drug compatibility and adsorption testing

 

Presented posters on feasibility bench testing and in vivo studies of sEEG-based drug delivery into the brain at the American Association of Pharmaceutical Scientists (AAPS-NBC) and the American Society of Gene & Cell Therapy (ASGCT) in May

 

Continued discussions with potential targeted strategic partners for use in clinical studies and research

 

Spinal Cord Stimulation (SCS) Percutaneous Paddle Lead Program:

 

Successfully completed acute animal study in large animal model to evaluate stimulation performance of our percutaneous paddle lead for back and neck pain

 

Successfully completed cadaver lab with physician key opinion leaders to further advance the development of a percutaneous implantation technique for our thin-film SCS percutaneous paddle electrodes

 

Finalized NeuroOne paddle lead design, including testing of electrode specifications

 

Filed a provisional patent on a connector that is compatible with our thin-film SCS electrodes

 

Dave Rosa, CEO of NeuroOne, commented, “We accomplished several key milestones this quarter. We are most excited about completing the first RF ablation cases with our first-to-market OneRF™ Ablation System. We also signed a non-binding term sheet with a large strategic partner to serve as our distribution partner and accelerate the launch of the OneRF™ Ablation System. In August, we completed a financing, entered into a credit facility agreement, and are making good progress with our product pipeline, including additional RF ablation applications, sEEG-based drug delivery and a percutaneous paddle lead for spinal cord stimulation. We are looking forward to securing additional strategic partners for these exciting programs leveraging our thin-film electrode platform technology.”

 

Key Upcoming Milestones

 

OneRF™ Ablation System:

 

Finalize strategic partnership for distribution of OneRF™ Ablation System

 

Continue to add new centers for our limited commercial launch

 

Exhibit OneRF™ Ablation System at the 2024 World Congress of Stereotactic and Functional Neurosurgery meeting in September

 

Present posters on OneRF™ Ablation System at the Congress of Neurological Surgeons 2024 annual meeting in September

 

Continue to explore additional ablation applications and strategic partnership opportunities in other attractive markets that could benefit from NeuroOne’s high-resolution, thin-film electrode technology and RF generator

 

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Spinal Cord Stimulation Percutaneous Paddle Lead Program:

 

Initiate discussions with potential strategic partners to license or acquire the NeuroOne Spinal Cord Stimulation percutaneous paddle lead product

 

Third Quarter Fiscal Year 2024 Financial Results

 

Product revenue was $826,000 in the third quarter of fiscal 2024, compared to product revenue of $630,000 in the third quarter of fiscal 2023. For the first nine months of fiscal 2024, product revenue was $3.2 million, compared to $1.2 million for the same period in fiscal 2023. The Company had no collaboration revenue in the first nine months of fiscal 2024, compared to collaboration revenue of $1.46 million in the first nine months of fiscal 2023. Collaboration revenue in 2023 was derived from the Zimmer Development Agreement and represents the portion of the exclusivity and milestone fee payments eligible for revenue recognition during the period.

 

Total operating expenses in the third quarter of fiscal 2024 were $3.1 million, compared with $3.8 million in the same period of the prior fiscal year. Research and Development (R&D) expense in the third quarter of fiscal 2024 was $1.2 million compared with $1.9 million in the third quarter of fiscal 2023. Selling, General and Administrative (SG&A) expenses were $1.9 million during each of the three months ended June 30, 2024 and 2023. For the first nine months of fiscal 2024, total operating expenses were $10.0 million, compared with $10.5 million in the same period of fiscal 2023. R&D expense in the first nine months of fiscal 2024 was $4.0 million compared with $5.2 million in the same period of fiscal 2023. SG&A expense in the first nine months of fiscal 2024 was $6.1 million compared with $5.3 million in the prior year period.

 

Net loss was $2.8 million for the third quarter of fiscal 2024, compared to a net loss of $3.5 million in the third quarter of fiscal 2023. Net loss for the first nine months of fiscal 2024 was $9.0 million compared with $8.7 million in the same period of fiscal 2023.

 

In the third quarter of fiscal 2024, the Company sold common stock under the ATM Program at an average price of $1.19 per share, from which the Company received net proceeds of $1.6 million.

 

As of June 30, 2024, the Company had cash and cash equivalents of $1.6 million, compared to $5.3 million as of September 30, 2023. The Company had working capital of $2.2 million as of June 30, 2024, compared to working capital of $5.5 million as of September 30, 2023.

 

The Company had no debt outstanding as of June 30, 2024.

 

On August 2, 2024, the Company completed a $2.65 million private placement, resulting in $2.55 million in net proceeds, and entered into a $3.0 million secured credit facility agreement. The Company has not borrowed anything under the credit facility agreement at this time.

 

Conference Call and Webcast

 

Wednesday, August 14, 2024, at 4:30 PM Eastern Time

 

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Participants:

 

Toll Free: 877-545-0320
International: 973-528-0002
Participant Access Code: 579769

 

Phone Replay:

 

Toll Free: 877-481-4010
International: 919-882-2331
Replay Passcode: 51065

Available through August 28, 2024

 

Live Webcast: 

 

Join here.

Webcast replay available for 12 months

 

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 press release 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 securing a strategic partnership for distribution of the OneRF™ Ablation System, the addition of new centers for the Company’s limited commercial launch of the OneRF™ Ablation System, potential strategic partnership opportunities, continued development of the Company’s electrode technology program (including our drug delivery program and spinal cord stimulation program), 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 strategic partnerships may not facilitate the commercialization or market acceptance of our technology; whether due to supply chain disruptions, labor shortages or otherwise; 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.

 

Caution: Federal law restricts this device to sale by or on the order of a physician.

 

Contact:

 

800-631-4030

ir@nmtc1.com

 

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NeuroOne Medical Technologies Corporation

Condensed Balance Sheets

 

   As of
June 30,
   As of
September 30,
 
   2024   2023 
   (unaudited)     
Assets        
Current assets:        
Cash and cash equivalents  $1,619,977   $5,322,493 
Accounts receivable   410,551     
Inventory   1,793,432    1,726,686 
Prepaid expenses   261,477    263,746 
Total current assets   4,085,437    7,312,925 
Intangible assets, net   72,841    89,577 
Right-of-use assets   281,833    169,059 
Property and equipment, net   472,486    525,753 
Total assets  $4,912,597   $8,097,314 
           
Liabilities and Stockholders’ Equity          
Current liabilities:          
Accounts payable  $759,260   $685,104 
Accrued expenses and other liabilities   931,700    1,107,522 
Total current liabilities   1,690,960    1,792,626 
Operating lease liability, long term   209,910    55,284 
Total liabilities   1,900,870    1,847,910 
           
Commitments and contingencies (Note 4)          
           
Stockholders’ equity:          
Preferred stock, $0.001 par value; 10,000,000 shares authorized; no shares issued or outstanding.        
Common stock, $0.001 par value; 100,000,000 shares authorized; 27,846,722 and 23,928,945 shares issued and outstanding as of June 30, 2024 and September 30, 2023, respectively.   27,847    23,929 
Additional paid–in capital   74,637,698    68,911,778 
Accumulated deficit   (71,653,818)   (62,686,303)
Total stockholders’ equity   3,011,727    6,249,404 
Total liabilities and stockholders’ equity  $4,912,597   $8,097,314 

 

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NeuroOne Medical Technologies Corporation

Condensed Statements of Operations

(unaudited)

 

   For the
Three Months Ended
   For the
Nine Months Ended
 
   June 30,   June 30, 
   2024   2023   2024   2023 
Product revenue  $825,776   $629,906   $3,180,719   $1,210,661 
Cost of product revenue   543,904    386,240    2,242,114    947,799 
Product gross profit   281,872    243,666    938,605    262,862 
                     
Collaborations revenue               1,455,188 
                     
Operating expenses:                    
Selling, general and administrative   1,881,099    1,862,389    6,057,520    5,347,234 
Research and development   1,194,674    1,891,512    3,951,559    5,161,322 
Total operating expenses   3,075,773    3,753,901    10,009,079    10,508,556 
Loss from operations   (2,793,901)   (3,510,235)   (9,070,474)   (8,790,506)
Other income, net   26,376    41,462    102,959    66,136 
Loss before income taxes   (2,767,525)   (3,468,773)   (8,967,515)   (8,724,370)
Provision for income taxes                
Net loss  $(2,767,525)  $(3,468,773)  $(8,967,515)  $(8,724,370)
                     
Net loss per share:                    
Basic and diluted  $(0.10)  $(0.20)  $(0.35)  $(0.52)
Number of shares used in per share calculations:                    
Basic and diluted   27,352,660    17,578,871    25,746,503    16,740,546 

 

 

 

6

 

 

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