UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
(Mark One)
☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended September 30, 2025
OR
☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from ______
to ______
Commission file number 801-42567
NEONC TECHNOLOGIES HOLDINGS, INC.
(Exact name of registrant as specified in its charter)
Delaware
95-1954864
(State or other jurisdiction of
incorporation or organization)
(I.R.S. Employer
Identification No.)
23975 Park Sorrento Suite 205 Calabasas , CA
91302
(Address of Principal Executive Offices)
(Zip Code)
( 310 ) 663-7831
Registrant’s telephone number, including area code
Securities registered pursuant to Section 12(b) of the Securities Exchange Act of 1934:
Title of each class
Trading Symbol(s)
Name of each exchange on which registered
Common stock, $0.0001 par value per share
NTHI
Nasdaq Global Market
Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports); and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one):
Large accelerated filer
☐
Accelerated filer
☐
Non-accelerated filer
☒
Smaller reporting company
☒
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. ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act). Yes ☐ No ☒
There were 19,474,303 shares of common stock outstanding as of November 14, 2025.
Explanatory Note
In this report, the term “Company”, “we”, “us”, and “our refers to NEONC TECHNOLOGIES HOLDINGS, INC. and its wholly-owned subsidiary.
This quarterly report on Form 10-Q includes forward-looking statements within the meaning of the federal securities laws. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends affecting the operating results and financial condition of our business. Forward-looking statements should not be read as a guarantee of future performance or results and will not necessarily be accurate indications of the times at, or by, which such performance or results will be achieved. Forward-looking statements are based on information available at the time those statements are made and/or management’s good faith belief as of that time with respect to future events and are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in or suggested by the forward-looking statements. Important factors that could cause such differences include, but are not limited to, statements about:
●
estimates of our expenses, future revenues, capital requirements and our needs for additional financing;
●
our estimates of the size of our market opportunities;
●
our ability to effectively manage our growth;
●
our ability to successfully enter new markets, manage our growth expansion and comply with any applicable laws and regulations;
●
the effects of increased competition from our market competitors;
●
significant disruption in, or breach in security of, our information technology systems and resultant interruptions in service and any related impact on our reputation;
●
the attraction and retention of qualified employees and key personnel;
●
the effectiveness of our internal controls;
●
changes in laws and government regulation affecting our business;
●
the impact of adverse economic conditions;
●
the sufficiency of our cash and cash equivalents to meet our liquidity needs and service our indebtedness; and
●
outcomes of legal or administrative proceedings.
In addition, in this report, the words “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “predict,” “potential” and similar expressions, as they relate to our Company, our business and our management, are intended to identify forward-looking statements. In light of these risks and uncertainties, the forward-looking events and circumstances discussed in this report may not occur and actual results could differ materially from those anticipated or implied in the forward-looking statements.
Forward-looking statements speak only as of the date of this report. You should not put undue reliance on any forward-looking statements. We assume no obligation to update forward-looking statements to reflect actual results, changes in assumptions or changes in other factors affecting forward-looking information, except to the extent required by applicable laws. If we update one or more forward-looking statements, no inference should be drawn that we will make additional updates with respect to those or other forward-looking statements.
You should read this report and the documents that we reference in this report and have filed with the Securities and Exchange Commission (“SEC”) as exhibits to this report with the understanding that our actual future results, levels of activity, performance and events and circumstances may be materially different from what we expect.
i
Table of Contents
Page
Part I - Financial Information
1
Item 1. Financial Statements
1
Condensed Consolidated Balance Sheet (Unaudited)
1
Condensed Consolidated Statement of Operations (Unaudited)
2
Condensed Consolidated Statement of Stockholders’ Deficit (Unaudited)
3
Condensed Consolidated Statement of Cash Flows (Unaudited)
5
Notes to Condensed Consolidated Financial Statements (Unaudited)
6
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
22
Item 3. Quantitative and Qualitative Disclosures About Market Risk
33
Item 4. Controls and Procedures
33
Part II - Other Information
35
Item 1. Legal Proceedings
35
Item 1A. Risk Factors
36
Item 2. Unregistered Sales of Equity Securities
36
Item 3. Defaults Upon Senior Securities
37
Item 4. Mine Safety Disclosures
37
Item 5. Other Information
37
Item 6. Exhibit Index
38
Signatures
39
ii
PART I - FINANCIAL INFORMATION
Item 1. Financial Statements
NEONC TECHNOLOGIES HOLDINGS, INC.
Condensed Consolidated Balance Sheets
September 30,
2025
December 31,
2024
(Unaudited)
Assets
Current Assets
Cash and cash equivalents
$
1,513,224
$
64,893
Deferred offering costs current
99,302
1,071,947
Debt issuance costs current
671,804
671,804
Prepaid expenses and other
677,246
410,085
Total Current Assets
2,961,576
2,218,729
Non-Current Assets
Debt issuance costs net of current portion
694,654
1,198,512
Right of use asset operating lease
379,509
-
Other assets
47,177
-
Total Assets
$
4,082,916
$
3,417,241
Liabilities and Shareholders’ Deficit
Current Liabilities
Accounts payable and accrued expenses
$
1,640,833
$
2,917,801
Accounts payable – related parties
499,900
628,277
Accrued advisory fee related party
3,675,569
-
Litigation settlement payable
4,746,250
4,641,250
Convertible promissory notes, net of discount
4,700,794
-
Accrued compensation
255,099
734,874
Lease liability, current
69,877
-
Total Current Liabilities
15,588,322
8,922,202
Long Term Liabilities
Lease liability, net of current portion
308,864
-
Total Liabilities
15,897,186
8,922,202
Commitments and contingencies
Shareholders’ Deficit:
Preferred stock, $ 0.0001 par value, 10,000,000 shares authorized; no shares were issued and outstanding as of September 30, 2025 and December 31, 2024
-
-
Common stock, $ 0.0001 par value, 100,000,000 shares authorized; 19,474,303 and 18,090,526 shares issued and outstanding as of September 30, 2025 and December 31, 2024, respectively
1,948
1,809
Additional paid in capital
85,414,333
45,101,675
Accumulated deficit
( 97,230,551
)
( 50,608,445
)
Total Shareholders’ Deficit
( 11,814,270
)
( 5,504,961
)
Total Liabilities and Shareholders’ Deficit
$
4,082,916
$
3,417,241
See accompanying notes to the condensed consolidated financial statements.
1
NEONC TECHNOLOGIES HOLDINGS, INC.
Condensed Consolidated Statements of Operations (Unaudited)
For the
Three Months Ended
September 30,
For the
Nine Months Ended
September 30,
2025
2024
2025
2024
Revenues:
Revenue
$
-
$
-
$
39,990
$
63,000
Operating Expenses:
Research and development
715,038
956,725
2,390,592
1,965,726
Legal and professional
276,378
496,803
1,754,287
1,652,141
General and administrative
902,985
243,659
2,736,732
973,923
Share based compensation
5,040,246
-
25,964,096
-
Advisory fees
-
500,000
11,737,806
500,000
Total Operating Expenses
6,934,647
2,197,187
44,583,513
5,091,790
Loss From Operations
( 6,934,647
)
( 2,197,187
)
( 44,543,523
)
( 5,028,790
)
Other Income (Expense):
Interest and other income
6,815
12,687
327,377
12,687
Amortization of debt issuance, and deferred offering costs
( 438,111
)
-
( 798,311
)
-
Interest expense - related parties
( 869,815
)
-
( 1,227,487
)
( 2,559,456
)
Loss on extinguishment of Bridge loan - related party
-
-
-
( 2,069,923
)
Loss on change in fair value of derivative liability related to sales of common stock through equity line of credit
( 380,162
)
-
( 380,162
)
-
Net Loss
$
( 8,615,920
)
$
( 2,184,500
)
$
( 46,622,106
)
$
( 9,645,482
)
Loss per share:
Net loss per share - basic and diluted
$
( 0.45
)
$
( 0.12
)
$
( 2.48
)
$
( 0.56
)
Weighted
average number of common stock outstanding during the period - basic and diluted
19,211,745
17,918,330
18,787,603
17,353,327
See accompanying notes to the condensed consolidated financial statements.
2
NEONC TECHNOLOGIES HOLDINGS, INC.
Condensed Consolidated Statements of Changes in Shareholders’ Deficit (Unaudited)
Three and Nine Months Ended September 30, 2024
Common Stock
Additional
Paid In
Accumulated
Total
Shareholders’
Shares
Amount
Capital
Deficit
Deficit
Balance - January 1, 2024
16,560,000
$
1,656
$
24,720,072
$
( 38,709,981
)
$
( 13,988,253
)
Net loss
-
-
-
( 2,938,976
)
( 2,938,976
)
Balance - March 31, 2024
16,560,000
$
1,656
$
24,720,072
$
( 41,648,957
)
$
( 16,927,229
)
Sale of common stock, net of offering costs
141,889
14
1,702,654
-
1,702,668
Common stock issued for bridge loan conversion
979,039
98
11,748,366
-
11,748,464
Common stock issued for settlement of vendor payable
114,758
12
1,377,078
-
1,377,090
Common stock issued for settlement of accrued compensation
34,375
3
412,497
-
412,500
Net loss
-
-
-
( 4,522,006
)
( 4,522,006
)
Balance - June 30, 2024
17,830,061
$
1,783
$
39,960,667
$
( 46,170,963
)
$
( 6,208,513
)
Sale of common stock, net of offering costs
242,757
25
2,913,098
-
2,913,123
Common stock issued for settlement of vendor payable
12,500
1
149,999
-
150,000
Common stock issued for note payable conversion
5,208
-
62,498
-
62,498
Net loss
( 2,184,500
)
( 2,184,500
)
Balance
- September 30, 2024
18,090,526
$
1,809
$
43,086,262
$
( 48,355,463
)
$
( 5,267,392
)
See accompanying notes to the condensed consolidated financial statements.
3
NEONC TECHNOLOGIES HOLDINGS, INC.
Condensed Consolidated Statements of Changes in
Shareholders’ Deficit (Unaudited)
Three and Nine Months Ended September 30, 2025
Common Stock
Additional
Paid In
Accumulated
Total
Shareholders’
Shares
Amount
Capital
Deficit
Deficit
Balance - January 1, 2025
18,090,526
$
1,809
$
45,101,675
$
( 50,608,445
)
$
( 5,504,961
)
Sale of common stock, net of offering costs
727,750
73
10,252,425
-
10,252,498
Common stock issued for advisory services
46,000
5
557,055
-
557,060
Cashless exercise of warrants
162,500
16
( 16
)
-
-
Share based compensation, as
restated
-
-
17,397,774
-
17,397,774
Net loss
( 32,326,016
)
( 32,326,016
)
Balance - March 31, 2025
19,026,776
$
1,903
$
73,308,913
$
( 82,934,461
)
$
( 9,623,645
)
Share based compensation
-
-
3,526,076
-
3,526,076
Other
( 37,755
)
-
( 37,755
)
Net loss
-
-
-
( 5,680,170
)
( 5,680,170
)
Balance - June 30, 2025
19,026,776
$
1,903
$
76,797,234
$
( 88,614,631
)
$
( 11,815,494
)
Share based compensation
-
-
5,040,246
-
5,040,246
Proceeds from sale of common stock pursuant to equity line of credit
447,527
45
3,576,853
-
3,576,898
Net loss
-
-
-
( 8,615,920 )
( 8,615,920 )
Balance - September 30, 2025
19,474,303
$ 1,948
$ 85,414,333
$ ( 97,230,551 )
$ ( 11,814,270 )
See accompanying notes to the condensed consolidated financial statements.
4
NEONC TECHNOLOGIES HOLDINGS, INC.
Condensed Consolidated Statements of Cash Flows (Unaudited)
For the
Nine Months Ended
September 30,
2025
2024
Cash flows from operating activities:
Net loss
$
( 46,622,106
)
$
( 9,645,482
)
Adjustments to reconcile net loss to net cash used in operating activities:
Increase in bridge loan - expenses paid by bridge loan provider on behalf of the Company
-
476,393
Accretion of original issue discount on bridge loans - related party
300,000
2,558,241
Accretion of original issue discount on convertible promissory note
820,794
-
Write off deferred issuance costs
-
703,796
Share based compensation - restricted stock
25,964,096
-
Loss on extinguishment of bridge loan
-
2,069,923
Loss on change in fair value of derivative liability
380,162
-
Amortization of debt issuance costs and deferred offering costs
1,161,311
-
Amortization of right of use asset
36,461
178,869
Changes in operating assets and liabilities:
Prepaid expenses
( 267,160
)
( 335,916
)
Other assets
( 47,177
)
-
Accrued compensation
( 479,775
)
( 58,127
)
Lease liability
( 37,229
)
( 164,371
)
Accrued advisory fee
3,675,569
-
Accounts payable
and accounts payable - related parties and accrued expenses
( 1,657,722
)
957,162
Net cash used in operating activities
( 16,772,777
)
( 3,259,512
)
Cash flows from financing activities:
Proceeds from the sale of common stock
11,324,372
4,615,789
Proceeds from related party loan
300,000
892,028
Repayment of related party loan
( 600,000
)
( 791,077
)
Deferred offering costs
-
( 154,463
)
Proceeds from sale of common stock pursuant to equity purchase agreement
3,196,736
-
Proceeds from convertible notes payable
4,000,000
-
Net cash provided by financing activities
18,221,108
4,562,277
Net increase in cash and cash equivalents
1,448,331
1,302,765
Cash and cash equivalents - beginning of period
64,893
31,862
Cash and cash equivalents - end of period
$
1,513,224
$
1,334,627
Supplemental disclosure of non-cash financing activities:
Original issue discount on bridge loan - related party
$
300,000
$
1,368,421
Right of use asset, at lease commencement
$
-
$
536,605
Share issued in connection with advisory services
$
557,192
-
Reclassified of deferred offering costs to APIC at the completion of the offering
$
1,391,580
$
-
Increase in bridge loan payable - prepaid and deferred offering costs paid directly by bridge loan provider on behalf of the Company
$
-
$
31,346
Conversion of bridge loan to common stock
$
-
$
11,748,464
Conversion of accrued compensation
$
-
$
412,500
Conversion of account payable to common stock
$
-
$
1,527,090
See accompanying notes to the condensed consolidated financial statements.
5
Note 1 – Description of Business and Liquidity
NeOnc Technologies, Inc. (“NTI”) was incorporated on April 13, 2005, as a California corporation. On April 7, 2023, NTI merged into NeOnc Technologies Holdings, Inc. (“NTHI” and the combined entities “NeOnc” or the “Company”). NTHI was incorporated January 5, 2023, as a Delaware Corporation.
NeOnc is the developer of a novel molecular technology that provides enhanced targeted delivery of technologies for treating central nervous system diseases. The Company’s lead product, NEO100 is in clinical trials treating glioblastoma, and has Orphan Drug and Fast Track designation from the United States Food and Drug Administration (“FDA”). The Company licensed the underlying technology from the University of Southern California. (“USC”).
On October 11, 2024, the Company entered into an agreement with a broker dealer to serve as placement agent and provide broker services in connection with the proposed sale of common stock up to $ 10,000,000 . Under this agreement, through December 31, 2024, the Company closed on commitments from investors to purchase 625,000 shares of common stock of the Company at $ 16 .00 per share for total commitments of $ 10,000,000 , which were to be held in escrow until the Company’s registration statement was declared effective. During the three months ended March 31, 2025, prior to the Company having an effective registration statement, the Company closed on an additional commitment to purchase 102,750 shares of common stock of the Company at $ 16 .00 per share, for total commitments of $ 1,644,000 , On March 10, 2025, the Company’s registration statement was declared effective at which time the $ 11,644,000 in escrow was released to the Company. On March 26, the Company was listed (“Listing”) on the NASDAQ global markets.
Liquidity
The accompanying financial statements have been prepared on the basis that the Company is a going concern, which contemplates, among other things, the realization of assets and satisfaction of liabilities in the normal course of business. At September 30, 2025, the Company had cash totaling $ 1,513,224 . For the three and nine months ended September 30, 2025, the Company incurred a net loss of $ 8,615,920 and $ 46,622,106 , respectively, and has an accumulated deficit of $ 97,230,551 at September 30, 2025. The Company has financed its working capital requirements to date primarily through the sale of common stock, shareholder loans and related party bridge loans.
The Company does not have sufficient available capital to fund operations for a period of twelve months from the issuance date of these financial statements. Although the Company has established agreements with several funding potential sources (see Notes 6, 7 and 10), the Company does not know whether additional financing will be available when needed, whether it will be available on favorable terms, or if it will be available at all. These factors raise substantial doubt regarding the Company’s ability to continue as a going concern. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.
Other risks and uncertainties
The Company is subject to risks common to biopharmaceutical companies, including, but not limited to, new technological innovations, dependence on key personnel, protection of proprietary technology, compliance with government regulations, product liability, and the uncertainty of market acceptance of products and the potential need to obtain additional financing. The Company is dependent on third-party suppliers and, in some cases, single-source suppliers. The Company’s products require approval or clearance from the FDA prior to commencing commercial sales in the United States. Approvals or clearances are also required in foreign jurisdictions where the Company may license or sell its products. There can be no assurance that the Company’s products will receive all required approvals or clearances.
There can be no assurance that the Company’s products, if approved, will be accepted in the marketplace, nor can there be any assurance that any future products can be developed or manufactured at an acceptable cost with appropriate performance characteristics or that such products will be successfully marketed, if at all.
6
Note 2 – Basis of Presentation and Summary of Significant Accounting Policies
Basis of presentation
The unaudited condensed consolidated financial statements
contained herein have been prepared by the Company pursuant to the rules and regulations of the Securities and Exchange Commission (the
“SEC”). Certain information and note disclosures normally included in annual financial statements prepared in accordance
with generally accepted accounting principles have been condensed or omitted pursuant to SEC rules and regulations, although the Company
believes that the disclosures made are adequate to make the information not misleading. Accordingly, the condensed consolidated financial
statements reflect all normal recurring adjustments, which are, in the opinion of management, necessary for a fair presentation of the
results of interim periods and may not include all disclosures required by accounting principles generally accepted in the United States
(“GAAP”). The information as of September 30, 2025, and for the three and nine months ended September 30, 2025,
is unaudited, whereas the consolidated balance sheet as of December 31, 2024, is derived from the Company’s audited condensed
consolidated financial statements as of that date. These condensed consolidated financial statements and notes hereto should be read
in conjunction with the consolidated financial statements and notes thereto included in the audited financial statements for the year
ended December 31, 2024, included on Form S-1, filed with the SEC on February 26, 2025.
The results of operations for the interim periods presented are not necessarily indicative of results to be expected for any other interim period or for the year.
Principles of consolidation
The accompanying condensed consolidated financial statements and related notes to the condensed consolidated financial statements include the accounts of the Company and its wholly owned subsidiary. All significant intercompany balances and transactions have been eliminated in consolidation.
Use of estimates
In preparing the Company’s financial statements in conformity with GAAP, management is required to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosures of contingent assets and liabilities at the date of the financial statements, as well as the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates.
Cash and cash equivalents
The Company, from time to time during the period covered by these financial statements, may have had bank account balances in excess of federally insured limits. The Company has not experienced losses in such accounts. For the statements of cash flows, the Company considers all short-term investments purchased with a maturity of three months or less to be cash equivalents. At September 30, 2025 and December 31, 2024, the Company has money market funds in the amount of approximately $ 12,000 and $ 25,000 , respectively.
Deferred offering costs
The Company complies with the requirements of the ASC 340-10-S99-1 and SEC Staff Accounting Bulletin (“SAB”) Topic 5A “ Expenses of Offering ”. Offering costs consist principally of professional and registration fees incurred through the condensed consolidated balance sheet dated December 31, 2024 that are related to the planned public offering of its securities (See Note 3). These costs have been capitalized and were recognized in equity upon the completion of the securities offering. At September 30, 2025, deferred offering costs consist of the fair value of shares issued in conjunction with the issuance of an equity purchase agreement. These costs have been capitalized and are being amortized over the term of the availability of the equity purchase agreement (Note 6). If planned offerings are terminated, the related capitalized deferred offering costs are written off.
7
Debt issuance costs
Debt issuance costs represent costs directly attributable
to warrants issued for a line of credit commitment. Such costs represent the fair value of warrants issued to the debt facility provider
and are amortized to the statement of operations on a straight-line basis which approximates the effective interest rate method, over
the term of the debt instrument. The debt issuance costs, net of accumulated amortization, are classified as a long-term asset until
the Company begins to draw funds from the debt facility, in accordance with ASC 815: “ Derivatives and Hedging ”. At
such time, the pro-rata portion of amounts borrowed as compared to the total debt facility will be reclassified as a contra-debt account.
Warrants
The Company evaluates the terms of warrants issued and determines if the instrument requires liability or equity accounting classification under ASC 815: Derivatives and Hedging and ASC 480: “ Distinguishing Liabilities from Equity ”.
Leases
The Company classifies its leases either as operating or financing lease at inception. The company has an operating lease. This lease is recorded as an operating lease, right of use (ROU) assets and operating lease liabilities on the accompanying consolidated balance sheets.
Operating lease ROU assets and the related lease liabilities are recognized based on the present value of the future minimum lease payments over the lease term at commencement date. The operating lease ROU assets also include lease incentives and initial direct costs incurred. For operating leases, interest on the lease liability and the amortization of ROU asset result in straight-line rent expense over the lease term. Leases may include options to extend or terminate the lease which are included in the ROU operating lease assets and operating lease liability when they are reasonably certain of exercise. Certain leases include lease and non-leased components, which are accounted for as one single lease component. Operating lease expense associated with minimum lease payments is recognized on a straight-line basis over the lease term.
Fair value measurements
FASB ASC Topic 820, “ Fair Value Measurements and Disclosures ” (“ASC 820”), defines fair value, the methods used to measure fair value and the expanded disclosures about fair value measurements. Fair value is the price received to sell an asset or paid to transfer a liability in an orderly transaction between the buyer and the seller at the measurement date. In determining fair value, the valuation techniques consistent with the market approach, income approach and cost approach shall be used to measure fair value. ASC 820 establishes a fair value hierarchy for inputs, representing the assumptions the buyer and seller use in pricing the asset or liability. These inputs are further defined as observable and unobservable inputs. Observable inputs are those that the buyer and seller would use in pricing the asset or liability based on market data obtained from sources independent of the Company. Unobservable inputs reflect the Company’s assumptions about the inputs the buyer and seller would use to price the asset or liability developed based on the best information available in the circumstances.
The
Company’s money market funds are valued at quoted prices in active markets and are classified as Level 1 within the fair value
hierarchy. The carrying value of the Company’s accounts payable approximates its fair value because of the short-term nature
of these financial instruments. The note payable - related party is reported at fair value as the Company elected the fair value
option for such a note (see Note 4).
The fair value hierarchy is categorized into three levels based on the inputs as follows:
●
Level 1 — Valuations based on unadjusted quoted prices in active markets for identical assets or liabilities that the Company has the ability to access. Valuation adjustments and block discounts are not being applied. Since valuations are based on quoted prices that are readily and regularly available in an active market, the valuation of these securities does not entail a significant degree of judgment.
8
●
Level 2 — Valuations based on (i) quoted prices in active markets for similar assets and liabilities, (ii) quoted prices in markets that are not active for identical or similar assets, (iii) inputs other than quoted prices for the assets or liabilities, or (iv) inputs that are derived principally from or corroborated by the market through correlation or other means.
●
Level 3 — Valuations based on unobservable inputs and significant to the overall fair value measurement.
Revenue
The
Company recognized point-in-time revenue of $ 0
and $ 39,990
for the three and nine months ended September 30, 2025, and $ 0
and $ 63,000
for the three and nine months ended September 30, 2024, respectively, for the right to try its technology in compassion use
cases where the Company has no further performance obligations.
Research and development
Research and development costs are expensed as incurred. Research and development expenses include personnel costs associated with research and development activities, including third-party contractors performing research, conducting clinical trials, and manufacturing drug supplies and materials.
Patent costs
All patent-related costs incurred in filing and prosecuting patent applications are expensed as incurred due to the uncertainty about the recovery of the expenditure. Amounts incurred are classified as legal and professional expenses in the accompanying consolidated statements of operations.
Share-based compensation
The Company has granted stock options and common
stock to employees, non-employee consultants and non-employee members of our Board of Directors. The Company measures the compensation
cost associated with all share-based payments based on the grant date fair values. Compensation costs associated with grants of common
stock are measured at fair value at the date of grant, which has historically been the most recent price paid by investors to purchase
shares of the Company’s common stock prior to such grant. The Company recognizes share-based compensation expense over the requisite
service period of each award, which generally equals the vesting period, using the straight-line method for awards that contain only
service conditions. If the stock grant is contingent upon events that have not yet happened, then the grant is not considered issued.
If an award holder leaves the company prior to vesting, and adjustment of the compensation expense will be made to reflect only those
awards that vested.
The Company recognizes the stock-based compensation expense for the restricted stock units (“RSU”) based upon the fair value of the common stock at the date of the grant. The expense is recognized over the service period provided in the RSU awards, however expense will not be recognized until the listing date (“Listing Date”), as prior to such date it was not probable that condition to commence vesting would be met.
When the vesting contingency is met, the Company will commence to recognize expense related to the RSU’s. For time based vested RSU’s, the expense will be recognized on a straight-line basis from the grant date to the last vesting date. The expense recognized will include the expense from the date of the grant over the total vesting period and reflect the portion attributable to the service provided prior to the listing. For performance based RSU’s, the Company will determine the probability of the contingency being met each quarter end based upon an assessment of progress made under such performance criteria.
9
Net loss per share
Basic net loss per share is computed by dividing
net loss available to common stockholders by the weighted average number of common stock outstanding during the period. Diluted net loss
per share is computed by dividing net loss by the sum of the weighted average number of common stock outstanding during the period. For
periods in which the Company reports a net loss, the diluted net loss per share is the same as basic net loss per share.
For the nine months ended September 30, 2025 there are potentially dilutive securities outstanding of 3,010,000 potentially dilutive restricted stock units which are not included in the diluted net loss per share calculation since their effect is anti-dilutive. For the nine months ended September 30, 2024, respectively, there were no potentially dilutive warrants outstanding and no potentially dilutive restricted stock units.
Income taxes
The Company recognizes federal, state, and foreign current tax liabilities or assets based on its estimate of taxes payable to or refundable by tax authorities in the current fiscal year. For the periods ended September 30, 2025 and 2024, there is no current tax provision due to losses generated. The Company also recognizes federal and state deferred tax liabilities or assets based on the Company’s estimate of future tax effects attributable to temporary differences and carry forwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years those temporary differences are expected to be recovered or settled.
Deferred tax assets are reduced by valuation allowances
if, based on the consideration of all available evidence, it is more likely than not that some portion of the deferred tax asset will
not be realized. The Company evaluates deferred income taxes quarterly to determine if valuation allowances are required by considering
available evidence. If the Company is unable to generate sufficient future taxable income in certain tax jurisdictions, or if there is
a material change in the actual effective tax rates or time period within which the underlying temporary differences become taxable or
deductible, the Company could be required to increase its valuation allowance against its deferred tax assets which could result in an
increase in the Company’s effective tax rate and an adverse impact on operating results. The Company will continue to evaluate
the necessity of the valuation allowance based on the remaining deferred tax assets. The difference between the statutory and effective
rates for the three and nine months ended September 30, 2025 and 2024 is a result of the Company applying a full valuation allowance
against any deferred tax assets as a result of net operating losses due to uncertainties surrounding the usability of such net operating
losses. The ability to utilize such net operating loss carry forwards may be limited due to possible changes in ownership as defined
under Internal Revenue Code section 382.
The Company follows the accounting guidance related to financial statement recognition, measurement and disclosure of uncertain tax positions. The Company recognizes the impact of an uncertain income tax position on an income tax return at the largest amount that is more likely than not to be sustained upon audit by the relevant taxing authority. An uncertain income tax position will not be recognized if it is less than 50% likely to be sustained. Uncertain tax positions are recognized in the first subsequent financial reporting period in which that threshold is met or from changes in circumstances such as the expiration of applicable statutes of limitations. The Company will recognize interest and penalties related to tax positions in income tax expense.
Segment Reporting
In November 2023, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2023-07, “ Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures .” The standard expands reportable segment disclosure requirements for public business entities primarily through enhanced disclosures about significant segment expenses that are regularly provided to the chief operating decision maker (“CODM”) and included within each reported measure of segment profit (referred to as the “significant expense principle”). The standard has been adopted for our fiscal year 2024 annual financial statements and interim financial statements thereafter and have applied this standard retrospectively for all prior periods presented in the financial statements.
Reclassifications
Certain reclassifications of previously reported amounts have been
made to conform to the current year presentation. Such reclassifications did not impact net income as previously reported.
10
Note
3 – Related p arty
t ransactions
AFH Holdings and Advisory, LLC advisory agreement
On December 19, 2022, the Company entered into an advisory agreement with AFH Holdings and Advisory, LLC, an affiliate to assist the Company in connection with its intent to affect a public listing. AFH was retained to assist the Company with investor presentations and decks, coordinate the retention of an investment banker for an initial public offering, identify legal and accounting professionals to assist in connection with such public offering, identify investor relations/public relations firms, advise on private capital markets activities prior to the initial public offering and coordinate the closing process for the offering.
On July 12, 2024, the Company amended the AFH advisory agreement section to allow for an upfront payment on the Listing Date of $ 2,500,000 and the remaining amount of the fee to be paid in equal monthly instalments for one year. AFH was paid a fee of $ 500,000 for the amendment.
On March 26, 2025, and as a result of the listing of the Company on Nasdaq, the Company incurred $ 11,328,565 for the fee earned in accordance with the AFH advisory agreement which was recorded as advisory fee expense in the condensed consolidated statement of operations. In accordance with the amendment, the Company paid $ 2,500,000 of such fee on March 26, 2025. The remaining balance of $ 8,828,565 is payable in 12 equal monthly installments commencing in April 2025. As of September 30, 2025, the remaining outstanding accrued advisory fee totaled $ 3,675,569 recorded on the condensed consolidated balance within accrued advisory fee – related party.
In addition, the Company agreed to retain AFH as an exclusive advisor to the Company on all financing and mergers and acquisitions for a period of two (2) years from the closing of the private securities offering.
Transactions with USC
The Company maintains a license agreement with USC, under which the Company will pay USC an annual patent maintenance fee of $ 20,000 and nonrefundable earned royalties of 4 % on Net Sales (as defined in the Amended Agreement) of Licensed Products covered by the licensed patents in all countries in which the manufacture, use, sale, offer for sale, or import of such Licensed Products, as such capitalized terms are defined in the Amended Agreement. To date, no sales have been made using Licensed Products, and no royalties are due to USC. In addition, the Company will assume responsibility for patent-related costs.
The Company also utilizes laboratory and patent maintenance services from USC. The Company incurred $ 382 and $ 184,449 and $ 98,543 and $ 382,858 related to such services for the three and nine months ended September 30, 2025 and 2024, respectively, of which $ 382 , $ 164,449 and $ 98,543 and $ 362,858 are recorded within research and development expenses and $ 0 , $ 20,000 and $ 0 and $ 20,000 are recorded within general administrative expenses on the condensed consolidated statements of operations. At September 30, 2025 and December 31, 2024, the Company has outstanding payables to USC for such services of $ 499,607 and $ 272,328 respectively, which is included in accounts payable - related parties in the accompanying consolidated balance sheets.
Accrued compensation
The amount accrued for the management team, including related payroll taxes, was $ 255,099 and $ 734,874 as September 30, 2025 and December 31, 2024, respectively.
Note 4 – Related Party Loans Payable
Bridge Loan
In April 2023, the Company entered into a non-interest bearing, non-convertible promissory note with HCWG LLC (the “Bridge Loan”). Borrowings under the Bridge Loan carry a 50% (or 1 times cash amounts borrowed) original issue discount (“OID”) on principal and through subsequent amendments the maximum cash borrowing was increased to $ 10,000,000 . The outstanding amounts under this Bridge Loan were payable at the earlier of the date the Company completes an IPO or December 4, 2024 (the “Maturity Date”).
11
On June 14, 2024, the Company reached an
agreement with HCWG LLC to convert the outstanding principal and interest on the Bridge Loan into 979,039 shares of common stock. As
a result of this conversion, the Bridge Loan was terminated and is no longer available to the Company for borrowing. The Company has
a receivable due from HCWG LLC totaling $ 138,247 which is recorded within prepaid expenses and other on the condensed consolidated balance
sheet at September 30, 2025 and December 31, 2024, respectively.
Through
June 30, 2024, the Company had received under the Bridge Loan an aggregate of $ 7,116,335 .
The OID was recognized ratably over the term of each draw-down under the Bridge Loan through the Maturity Date unless settled earlier,
at which point the accretion is accelerated. Accretion of the OID for nine months ended September 30, 2024, amounted to $ 1,387,493 ,
which is included in interest expense in the accompanying condensed consolidated statement of operations.
Schedule of convertible
debt
For the
Year Ended
December 31,
2024
Bridge loan – carrying value
Balance – January 1, 2024
$
9,802,697
Borrowings
1,368,422
OID
1,368,422
Repayments
( 791,077
)
Total principal outstanding before conversion
11,748,464
Conversion to common stock (June, 14, 2024)
( 11,748,464
)
Principal outstanding December 31, 2024
$
-
Advances from Executive Chairman
In February 2025, our Executive Chairman advanced the Company approximately $ 300,000 . The advances carry a 50% (or 1 times amounts borrowed) original issue discount (“OID”) on the principal. On March 10, 2025, the advance and 1x interest was repaid. Interest expense in the amount of $ 300,000 is included in the condensed consolidated statement of operations as interest expense – related parties for the nine months ended September 30, 2025.
NOTE 5 Convertible
Debt
On July 16 and July 18, 2025, the Company entered
into a series of convertible promissory notes with a group of investors for the aggregate purchase price of $ 4,000,000 (the “Notes”).
The Notes are payable three months after origination for a total amount of $ 5 million (20% OID). The Company may extend the payment date
for up to three additional one-month periods with the OID on the Notes increasing to 25%, 30% and 35% with respect to any such monthly
extensions. Further, upon the occurrence of an Event of Default, as that term is defined in the Notes, the Notes shall be convertible
at the option of the holders into shares of the Common stock of the Company at a price equal to 80% of the lowest closing sale price of
the Company’s common stock as reported on the Nasdaq Global Market on any trading day during the five (5) trading days prior to
the respective conversion date. The Company also recorded debt issuance cost of $ 320,000 to be amortized as interest expense over
the term of the loan using the straight-line method.
In accordance with ASU 2020-06, the Company accounts
for the convertible notes as a single liability instrument. The notes are recorded at amortized cost, and interest expense is recognized
using the effective interest method. The effective interest rate on the notes is approximately 7.72% per annum, which reflects the amortization
of issuance costs and original issuance discount.
Through September 30, 2025, interest expense of
$ 1,020,794 was recognized from the accretion of OID and accretion of the debt issuance cost. Subsequent to September 30, 2025, the Company
exercised the first of three available extensions on the convertible promissory notes. The notes are now set to mature on November 16,
2025.
12
The following table summarizes the Company’s
outstanding Notes as of September 30, 2025:
Schedule of convertible
debt
For the
Nine Months Ended
September 30,
2025
Purchase price of convertible promissory notes
$ 5,000,000
Less: unamortized original issuance discount
( 179,206 )
Less: unamortized debt issuance cost
( 120,000 )
Net convertible promissory note
$ 4,700,794
Note 6 – Leases
On February 1, 2024, the Company entered a 24-month lease for office space, which calls for a monthly base rent of $ 25,000 , increasing at 3 % per annum. The Company has only one operating lease and has no financing leases. The Company’s lease does not contain options to renew or extend the lease term or options to terminate leases early, except for insolvency. On November 27, 2024, the Company amended the lease expiration date from January 31, 2026, to January 31, 2025. As of December 31, 2024, the consolidated balance sheet reflects a right-of-use asset of $ 23,526 and a lease liability of $ 24,722 . The lease liability was computed using an interest rate of 13.49 % .
In April 2025, the Company entered into a 63 month lease for office space which calls for a monthly base rent of $ 6,778 , increasing at approximately 3 % per annum. The lease liability was computed using an interest rate of 3.72 % and as of September 30, 2025 the lease has a remaining 58 months. In calculating the present value of future lease payments, the Company utilized its incremental borrowing rate based on the lease term. The Company’s net lease non-lease components (e.g., standard area maintenance, maintenance, consumables, etc.) are paid separately from rent based on actual costs incurred and, therefore, are not included in the right-of-use asset and lease liability and are reflected as an expense in the period incurred. At September 30, 2025 the consolidated balance sheet reflects a right-of-use asset of $ 379,509 and a lease liability of $378,741 .
The Company recorded lease expense of $ 21,781
and $ 102,704
during the three months ended September 30, 2025 and 2024, respectively, and $ 43,743
and $ 214,497 during
the nine months ended September 30, 2025, and 2024, respectively, within general and administrative expenses on the condensed
consolidated statements of operations. Cash paid for amounts included in the measurement of lease liability was $ 20,335
and $ 125,000
and $ 40,670
and $ 200,000 ,
respectively, during the three and nine months ended September 30, 2025, and 2024, respectively.
The following are the expected maturities of lease liabilities for operating leases as of September 30, 2025:
Schedule of lease liabilities for operating leases
Twelve
Months Ended December 31,
2025 (three months)
$
20,335
2026
83,137
2027
85,663
2028
88,231
2029
90,928
Thereafter
44,944
Total
413,238
Less: interest
( 34,497
)
Present value of lease liability
378,741
Less: current portion
( 69,877
)
Noncurrent portion
$
308,864
13
Note 7 – Common and Preferred Stock
NTHI is authorized to issue 100,000,000
shares of common stock, par value $ 0.0001
per share and 10,000,000
shares of preferred stock, par value $ 0.0001
per share. As of September 30, 2025, no
preferred shares have been issued. The board of directors is authorized, subject to any limitations prescribed by law, to provide
for the issuance of shares of Preferred Stock in one or more series, and by filing a certificate pursuant to the applicable law of
the State of Delaware , to establish from time to time the number of shares to be included in each such series, and to fix the
designation, powers, preferences, and rights of the shares of each wholly unissued series and any qualifications, limitations or
restrictions thereof. The number of authorized shares of Preferred Stock may be increased or decreased (but not below the number of
shares thereof then outstanding) by the affirmative vote of the holders of a majority of the Common Stock, without a vote of the
holders of the Preferred Stock, or any series thereof, unless a vote of any such holders is required pursuant to the terms of any
Preferred Stock Designation.
During
the nine months ended September 30, 2025, the Company sold 727,750
shares of common stock at a price of $ 16.00
per share for gross proceeds of $ 11,644,005
pursuant to a private placement of its securities, issued 46,000
shares as part of advisory services related to the listing and as part of the private placement fee for our equity line of credit,
162,500 shares were issued for the cashless exercise of warrants, and issued 447,527 shares from the sale of shares under the equity
line of credit, and the release of 3,310,000
shares for restricted stock units.
Private Placement
On October 11, 2024, the Company entered into an agreement with RBW Capital Partners LLC, a division of Dawson James Securities, Inc. (“Broker”) to serve as placement agent and provide broker services in connection with the possible sale of common stock up to $10 million. If a sale is made between the Company and any institutional or individual third-party funding source introduced by the placement agent, the Company will pay a placement fee of 8% of the gross proceeds. In addition, the company agrees to pay; (a) 1.0% of the gross proceeds for non-accountable expenses; and (b) out of pocket expenses plus the costs associated with the use of a third-party electronic road show service up to $10,000. The agreement expired on January 11, 2025 and was amended and restated on January 29, 2025 to extend the term for another six months through July 29, 2025 and increased the placement fee to 12% from 8% of the gross proceeds, and eliminated the 1% non-accountable expense fee.
Under this agreement, through December 31, 2024, the Company closed on commitments from investors to purchase 625,000 shares of common stock of the Company at $ 16 per share for total commitments of $ 10,000,000 , which were to be held in escrow until the Company’s registration statement was declared effective. During the three months ended March 31, 2025, prior to the Company having an effective registration statement, the Company closed on an additional commitment to purchase 102,750 shares of common stock of the Company at $ 16 per share, for total commitments of $ 1,644,005 , also to be held in escrow until the Company’s registration statement was declared effective. On March 25, 2025, the Company’s registration statement was declared effective at which time the $ 11,644,005 in escrow was released to the Company.
In connection with the agreement, the Company paid $ 300,000 in placement agent fees to Broker for securing $2,500,000 in commitments for the Private Placement. This fee was paid when the funds were released from escrow and recorded as a reduction to additional paid-in capital on the condensed consolidated statement of shareholders’ deficit as of September 30, 2025.
14
Advisory Services
On
October 3, 2024, as amended on January 23, 2025, the Company entered into an agreement with Broker, for financial advisory
and investment banking services in connection with a direct listing of the Company’s common stock on the Nasdaq Global Market
or other major US market. The agreement provides for a one-time fee of $250,000 payable three days after the direct listing and the
issuance of 30,000 shares of common stock (which are restricted until the shares are registered by filing a resale S-1 within 30
days after the effective date of the direct listing). In addition, the Company agreed to pay up to $ 100,000
for fees and expenses of legal counsel and other out-of-pocket expenses plus the costs associated with the use of a third-party
electronic road show service. Such fees were included in accounts payable and deferred offering costs in the accompanying
consolidated balance sheets as of December 31, 2024. The fair value of the 30,000
shares issued in March 2025, amounting to $ 363,300 ,
was determined using the closing day price of $ 12.11 .
This amount was recorded as an advisory fee on the condensed consolidated statement of operations for the nine months ended
September 30, 2025. The agreement expired on January 3, 2025 and was amended and restated on January 23, 2025 to
extend the term for another six months through July 23, 2025. This agreement expired in July 2025.
Deferred
Offering Costs Direct Listing
Deferred offering costs relating to the Private Placement and direct listing at December 31, 2024 totaled $ 1,071,947 . At September 30, 2025, this amount plus $ 0 and $ 319,633 incurred in the three and nine months ended September 30, 2025, respectively was reclassified against the common stock issued in the condensed consolidated statement of changes in shareholder’s deficit.
Equity Purchase Agreement
On October 22, 2024, the Company entered
into an equity purchase agreement (the “Equity Purchase Agreement”) with Mast Hill Fund, LP (“Mast Hill”) pursuant
to which the Company may sell and issue to Mast Hill, and the investor may purchase from the Company, up to $50,000,000 of Company’s
common stock. Under the Equity Purchase Agreement, the Company has the right, but not the obligation, to direct Mast Hill, by its delivery
to the Mast Hill of a Put Notice from time to time, to purchase Put Shares (i) in a minimum amount not less than $50,000 and (ii) in a
maximum amount up to the lesser of (a) $750,000 or (b) 150% of the average trading volume of the Company’s common stock during the
five trading days immediately preceding the Put Date.
The actual amount of proceeds the Company receives
pursuant to each Put Notice (each, the “Put Amount”) is determined by multiplying the Put Amount requested by the applicable
purchase price. The purchase price for each of the Put Shares equals 95% of the Market Price, (as defined below) less the Clearing Costs
(as defined below). Market Price is the lowest volume weighted average prices of the Company’s common stock on its principal market
on any trading day during the Valuation Period (as defined below). The Valuation Period is the five trading days immediately following
the date on which Mast Hill receives the Put Shares in its brokerage account. Clearing Costs are all the fees incurred by Mast Hill with
respect to its brokerage firm, clearing firm, Company transfer agent fees, and attorney fees, with respect to the Put Shares.
The term of the Equity Purchase Agreement
commenced on the effective date of the direct listing and will terminate on the earlier of (i) the date on which the Mast Hill shall
have purchased Put Shares equal to the $50,000,000, (ii) twenty-four (24) months after the date of the Equity Purchase Agreement,
(iii) written notice of termination by the Company to Mast Hill, (iv) this Registration Statement is no longer effective after the
initial effective date of this Registration Statement, or (v) the date that, pursuant to or within the meaning of any Bankruptcy
Law, the Company commences a voluntary case or any Person commences a proceeding against the Company, a receiver, trustee, assignee,
liquidator or similar official is appointed for the Company or for all or substantially all of its property or the Company makes a
general assignment for the benefit of its creditors. For the three and nine months ended September 30, 2025, the Company sold
447,527 shares of common stock at $ 3.73 $ 9.53 per share under the Equity Purchase Agreement, resulting in net proceeds of
$3,198,735. Since the shares were purchased at a discount as a result of the five-day settlement period, the settlement feature is
considered a derivative liability. The fair value of the derivative approximates the loss on the settlement of such shares or
$ 380,162 which was recognized in the condensed consolidated statement of operations for the three and nine months ended September
30, 2025.
15
In connection with this agreement, we issued 16,000 shares of common stock to Mast Hill. The fair value of the shares granted to Mast Hill upon issuance was determined by using the closing day price of $ 12.11 . Such amount net of amortization was recorded as deferred offering cost on the condensed consolidated balance sheet as of March 31, 2025. For the three and nine months ended September 30, 2025, the Company reported $ 24,220 and $ 94,458 , respectively as amortization expense in the condensed consolidated statement of operations, and the remaining deferred offering costs of $ 99,302 at September 30, 2025 are to be amortized over the remaining term of the Equity Purchase Agreement.
Note 8 – Stock-Based Compensation
On April 12, 2023, the Company adopted the 2023 Equity Incentive Plan (the “2023 Plan”), which allows the issuance of up to 3,440,000 shares of the Company’s authorized and unissued common stock in the form of incentive stock options, non-qualified stock options, restricted stock units, performance share units, or other forms of equity as may be added in the future to employees, directors and consultants of the Company and its affiliates. The allowable number of shares that can be issued under the 2023 Plan increased upon the completion of the listing to 4,764,507 which represents 20% of the fully diluted capitalization of the Company on the closing of Company’s initial public price.
In January and February 2024, 2,460,000 and 200,000 , respectively, restricted stock units (“RSUs”) were granted to the executive officers and members of the Board of Directors further to the 2023 Plan as described above. Of the total RSUs granted (tranche 1) 1,686,667 vest 100% seven months from the date that the Company lists on a national exchange, (tranche 2) 466,667 will vest in equal monthly instalments over a one (1) year period commencing on the eighth month from the effective date of the listing on a national exchange and (tranche 3) 486,666 are performance-based, the vesting of which will be predicated on certain financial and operational performance metrics being met after the effective date of the listing on a national exchange as set forth the grant agreements. Since tranche 3 is performance based, it is not yet probable that all of the performance vesting conditions will be met and as such no expense has been recognized for tranche 3 as of September 30, 2025.
On October 23, 2024, 200,000 RSUs were granted to each of the CEO and the Executive Chairman, for a total of 400,000 , and 100,000 granted to two members of the Board of Directors were canceled. These RSUs vest 100% seven months from the date the Company lists on a national exchange.
On March 26, 2025, 150,000 RSUs were granted to the three board members, in the amount of 50,000 each. These RSUs vest 100% seven months from the date the Company lists on a national exchange.
Prior to March 26, 2025, the Company determined that no expense should be recognized for the RSUs since the contingency related to the commencement of vesting (i.e., the listing) of the RSUs had not been met. On March 26, 2025, the listing occurred, satisfying the contingency required for vesting to begin and defining the service period.
On June 1, 2025, 300,000 RSUs were forfeited resulting in a reversal of $ 1,329,062 of shared based compensation during the nine months ended September 30, 2025.
On June 5, 2025, 200,000 RSUs were granted to the one board member. 66,667 RSUs vest 100% seven months from the date of issuance, 66,667 RSUs vest 100% thirty-six months from the date of issuance. The remaining 66,667 RUS’s vest thirty-six months from the date certain performance metrics are achieved.
The Company determined the fair value of all the RSUs at their respective grant dates to be $ 32,495,174 based on the price of the most recent sale of common stock prior to each grant date for those RSU’s granted prior to the Listing
Date or the quoted market value for the RSU’s granted after the Listing Date. For the nine months ended September 30, 2025, the company
recognized $ 25,964,096 . As of September 30, 2025, there was unamortized stock-based compensation of approximately $ 9,270,400 which the Company expects to recognize over approximately 6.75 years.
16
The activity related to RSUs is summarized as follows:
Schedule of restricted stock units activity
Restricted Stock Units
Activity
RSUs Granted
2024
January 1, 2024
-
Granted
3,060,000
Cancelled
( 100,000
)
December 31, 2024
2,960,000
2025
Granted during nine months ended September 30, 2025
350,000
Forfeited
( 300,000
)
Balance at September 30, 2025
3,010,000
Released RSUs for nine months ended September 30, 2025
-
As of September 30, 2025, 1,754,500 RSU’s remain unissued in the 2023 Plan.
Note 9 – Commitments and Contingencies
Line of Credit Commitment – Related Party
On
October 11, 2024, the Company entered into a Line of Credit Agreement (“the Agreement”) with HCWG for borrowings of
up to $ 10.0
million. Borrowings under the Line of Credit Agreement bear interest at 10.0 %
per annum and increases to 14% if the Agreement is extended. Interest payments are due on the first business day of each calendar
month and the unpaid principal is due on October 12, 2027. No amounts have been borrowed under the facility through
September 30, 2025.
In connection with the agreement, the Company issued HCWG five-year warrants to purchase up to 312,500 shares of our common stock at an exercise price of $ 12.00 per share. These warrants expire on October 23, 2029 . As of December 31, 2024, there were 312,500 warrants issued, outstanding and fully vested. In March 2025, 162,500 warrants were exercised in a cashless exercise, resulting in the issuance of 162,500 shares of common stock. At September 30, 2025, there are 150,000 shares of common stock remaining available to be purchased under the warrant.
The fair value of the warrants on the grant date was determined using the Black-Scholes valuation model, with the following key assumptions:
●
Fair value of common stock: $ 12.00
●
Expected volatility: 86 %
●
Risk-free interest rate: 4.82 %
●
Term: 2.5 years
The fair value of warrants at inception was $ 2,015,413 , which was recorded as additional paid-in capital on the condensed consolidated statement of changes stockholders’ deficit for the year ended December 31, 2024, and as debt issuance costs on the balance sheet. The debt issuance costs are being amortized over the term of the line of credit and amounted to $ 167,951 and $ 503,853 for the three and nine months ended September 30, 2025. At September 30, 2025 and December 31, 2024, unamortized debt issuance costs total $ 1,366,458 and $ 1,870,316 , respectively, which will be amortized over the remaining 13 months of the facility.
17
Litigation
From time to time, the Company is involved in various disputes, claims, liens and litigation matters arising out of the normal course of business which could result in a material adverse effect on the Company’s combined financial position, results of operations or cash flows. Liabilities for loss contingencies arising from claims, assessments, litigation, fines and penalties and other sources are recorded when it is probable that liability has been incurred, and the amount of the assessment can be reasonably estimated. As of September 30, 2025 and December 31, 2024, the Company had no liabilities recorded for loss contingencies, except as below.
License Agreement - Orient EuroPharma Co., Ltd.
On November 8, 2013, the Company entered into a collaboration agreement (“Agreement”) with Orient EuroPharma Co., Ltd. (“OEP”), pursuant to which the parties will develop certain licensed products defined in the Agreement. NeOnc will license OEP the right to commercialize the Company’s drug NEO100, a highly purified form of perillyl alcoho l (“Licensed Product”), in the territories specified in the license agreement (“Territory”).
In 2023, the Company sent notice to OEP indicating their intent to terminate the Agreement with OEP, after which OEP threatened litigation. On February 15, 2024, OEP and the Company entered into a settlement agreement whereas the Company and OEP terminated the Agreement in exchange for a payment in the amount of $ 4,000,000 payable by the Company to OEP within ten days of the date the Company completes its initial public offering. The Company has a litigation settlement payable of $ 4,000,000 in the accompanying condensed consolidated balance sheets as of September 30, 2025 and December 31, 2024, respectively. As of the date of this filing, the Company has not paid the litigation settlement amount.
On June 6, 2023, a vendor filed a complaint against the Company for breach of contract in the Central District of California. The vendor alleged that the Company improperly terminated an Intellectual Property License and Supply Agreement (“IPLSA”) and that the Company also defrauded the vendor in connection with IPLSA. This matter was settled on October 16, 2023, and the Company agreed to pay the vendor $ 600,000 within 5 business days of the close of the date that the Company completes an IPO or March 31, 2024, whichever occurs first. The Company has a litigation settlement payable in the accompanying condensed consolidated balance sheet at September 30, 2025 and December 31, 2024. As of the date of this filing, the Company has not paid the litigation settlement amount.
On March 31, 2024, a vendor agreed to extend the payment until May 15, 2024 for payment of an additional $25,000, payable on demand. On July 25, 2024, the arbitrator granted the implementation of interest at the statutory rate on the unpaid balance commencing May 15, 2024 until paid, therefore an additional $ 48,750 and $ 146,250 of interest expense is recognized in the accompanying condensed consolidated statement of operations during the three and nine months ended September 30, 2025, respectively.
At
September 30, 2025 and December 31, 2024, an aggregate of $ 146,250
and $ 41,250
of accrued interest is included in litigation settlement payable in the accompanying condensed consolidated balance
sheet.
In August 2025, the Company was awarded a grant
totaling $ 400,000 in gross proceeds from the National Institutes of Health (NIH). The Company’s portion of the total proceeds made
available from the NIH Grant is approximately $ 160,000 , net of subcontractor costs, as allowable expenses are incurred. For the three
and nine months ended September 30, 2025 no allowable expenses under the NIH grant were incurred by the Company.
In September 2025, the Company was awarded a
grant totaling approximately $ 1,007,000 in gross proceeds from the National Institutes of Health (NIH). The Company’s portion of
the total proceeds made available from the NIH Grant is approximately $ 245,000 , net of subcontractor costs, as allowable expenses are
incurred. For the three and nine months ended September 30, 2025 no allowable expenses under the NIH grant were incurred by the Company.
18
Note 1 0
– Segment Reporting
The Company manages its business activities on a consolidated
basis and operates as a single operating segment: Biotechnology. The accounting policies of the Biotechnology segment are the same as
those described in Note 1 – Summary of Significant Accounting Policies.
Our Chief Operating Decision Maker (“CODM”)
is our Chief Executive Officer, Amir Heshmatpour. The CODM uses net loss, as reported on our condensed consolidated statement of operations,
in evaluating the performance of the biotechnology segment and determining how to allocate resources of the Company as a whole, including
investing in our research and development programs and acquisition/licensing strategy. The CODM does not review assets in evaluating the
results of the biotechnology segment, and therefore, such information is not presented. The following supplemental information breaks
down the research and development costs for the three and nine months ended September 30, 2025 and 2024, respectively.
Schedule of segment reporting
For the
Nine Months Ended
September 30,
2025
2024
Revenues
$
39,990
$
63,000
Less: Significant and other segment expenses:
NEO100
851,664
693,328
NEO100-02
327,373
203,075
NEO212
798,997
549,249
Pediatric
169,663
103,338
Laboratory
192,377
362,858
Other
50,518
53,878
Total research and development expense
2,390,592
1,965,726
Advisory fee
11,737,806
500,000
Legal and accounting
1,754,287
1,374,869
Employee compensation expenses
516,428
331,873
Amortization expense
798,311
178,869
Investor relations
959,431
18,623
Share based compensation
25,964,096
-
Other general and administrative expense
1,260,873
721,831
Interest expense - related parties’
loans
1,227,487
2,559,456
Loss on extinguishment of Bridge loan - related
party
-
2,069,923
Loss on settlement
380,162
-
Interest and other income
( 327,377
)
( 12,687
)
Net loss
$
( 46,622,106
)
$
( 9,645,482
)
19
For the
Three Months Ended
September 30,
2025
2024
Revenues
$
-
$
-
Less: Significant and other segment expenses:
NEO100
163,036
236,607
NEO100-02
125,586
79,644
NEO212
343,368
189,553
Pediatric
70,653
34,350
Laboratory
-
362,858
Other
12,395
53,713
Total research and development expense
715,038
956,725
Advisory fee
-
500,000
Legal and accounting
276,378
219,531
Employee Expenses
182,268
186,149
Amortization expense
438,111
67,076
Investor relations
188,358
11,960
Share based compensation
5,040,246
-
Other general and administrative expense
532,359
253,348
Interest expense - related parties’
loans
869,815
2,400
Loss on extinguishment of bridge loan
-
-
Loss on settlement
380,162
-
Interest and other income
( 6,815
)
( 12,687
)
Net loss
$
( 8,615,920
)
$
( 2,184,500
)
Note 11
– Subsequent Events
On July 24, 2025, the Company entered into an
agreement with Dr. Ishwar K. Puri and Beth R. Levinson for the acquisition of all equity interests in JandB Holdings LLC, a California
limited liability company (“J&B”). J&B was newly formed and held a single patented asset. No other assets, liabilities,
employees or facilities were acquired. The single asset passed the “screen test” to be considered an asset acquisition. Expenses
of the transaction were not significant.
Under the terms of the asset acquisition, the transaction
consideration includes:
(i)
a cash payment of $500,000 and
(ii)
shares of Company common stock equal to (a) 120,000
shares of Company common stock with an attributed value of $25 per share, less (b) an amount of shares equal to (x) the aggregate
transaction fees incurred by the Company in connection with all of the transactions related to the Agreement divided by (y) $25.00, rounded
up to the nearest whole share.
The Company remitted the cash payment for the patent
on October 3, 2025 and received assignment of the patent effective October 8, 2025. As of November 13, 2025, the shares
have yet to be issued.
20
On October 4, 2025, the Company’s wholly
owned subsidiary, NuroMENA, signed a Master Services Agreement (MSA) with Insights Research Organization & Solutions (IROS), a UAE-
based contract research organization (CRO) and part of the M42 group. The MSA has an initial term of three years from the first work order
executed under the agreement. The first work order to be executed under the MSA covers a multi-site, randomized Phase 2b/3 study titled
A Multi-Site, Randomized, Phase 2b/3 Study Evaluating Overall Survival of Intranasal NEO100 in Patients with Progressive or Recurrent
Grade III Astrocytomas and Glioblastoma Multiforme (GBM), Stratified by IDH1 Mutation Status, Compared to Best Standard of Care.
On November 4, 2025, the Company sold 76,665
shares of common stock at $ 9.78 per share for gross proceeds of approximately $ 750,000 pursuant to Equity Purchase Agreement with Mast
Hill Fund, LP.
On November 6, 2025, the Company granted 1,200,000
RSUs to Amir Heshmatpour and 70,000 RSUs to Grace Fisher.
21
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
The following discussion and analysis of our financial condition and results of operations should be read in conjunction with our consolidated financial statements and related notes thereto included elsewhere in this Quarterly Report on Form 10-Q. In addition to historical information, this discussion and analysis contains forward-looking statements that involve risks, uncertainties and assumptions. Our actual results may differ materially from these forward-looking statements as a result of certain factors. For a complete discussion of such risk factors, see the section entitled “Risk Factors”. Capitalized terms used herein, but not otherwise defined, shall have the meaning ascribed to those terms in the “Part I - Financial Information,” including the related notes to the consolidated financial statements contained therein.
Overview
Our company (f/k/a NAS-ONC, Inc.) was formed in 2008, devoted to developing new drugs with new delivery modes. As a clinical-stage biopharmaceutical company, we have focused on establishing superior treatments for intracranial malignancies, i.e., aggressive cancers located in the brain. These cancer types include primary brain cancers, such as glioblastoma, and secondary brain cancers, that have arrived through metastatic spread from other cancers throughout the body, such as melanoma or breast and lung cancer. Brain-localized malignancies are particularly difficult to treat because the blood-brain barrier prevents efficient entry of most pharmacotherapeutic agents into the brain. As a result, these patients are faced with poor prognoses and shortened average life expectancy. NeOnc is developing novel drug delivery methods to be used in combination with novel drug candidates.
NeOnc’s lead product candidate is NEO100. NEO100 is administered to patients via intranasal delivery. We have completed human safety testing in a Phase 1 clinical trial and are currently conducting preliminary efficacy testing in a Phase 2a trial with recurrent malignant glioma (Grade IV IDH1 mutant and Grade III Astrocytoma IDH1 mutant) patients. NeOnc is also developing a second product candidate, NEO212, which has completed preclinical testing, and an investigational new drug (IND) application has been filed and accepted with the United States Food and Drug Administration (FDA). The company has started Phase 1 clinical trials with patients harbouring primary and secondary malignant brain cancer types. Several additional drug candidates are in the pipeline and are undergoing preclinical development.
Since inception, our operations have focused on organizing and staffing our company, business planning, raising capital, acquiring and developing our technology, establishing our intellectual property portfolio, identifying potential product candidates and undertaking preclinical and clinical studies and manufacturing. We do not have any products approved for sale and have not generated any revenue from product sales other than for humanitarian usage.
On October 11, 2024, the Company entered into an agreement with a broker dealer to serve as placement agent and provide broker services in connection with the proposed sale of common stock up to $10,000,000. Under this agreement, through December 31, 2024, the Company closed on commitments from investors to purchase 625,000 shares of common stock of the Company at $16 per share for total commitments of $10,000,000, which were to be held in escrow until the Company’s registration statement was declared effective. During the three months ended March 31, 2025, prior to the Company having an effective registration statement, the Company closed on an additional commitment to purchase 102,750 shares of common stock of the Company at $16.00 per share, for total commitments of $1,644,000. On March 10, 2025, the Company’s registration statement was declared effective at which time the $11,644,000 in escrow was released to the Company. On March 26, the Company was listed (“Listing”) on the NASDAQ global markets.
Investment and Joint Venture
In June 2025, the Company
(through its recently formed subsidiary – Nuromena Holdings Ltd. “NuroMena”) entered into a letter of intent to form
an investment and joint venture agreement with a Middle-East investor (“Investor”), Quazar Investments. At the formation date,
the Company would own 10 million shares of NuroMena and contribute a license to its technology to NuroMena, and the Investor will purchase
2.5 million shares of NuroMena for a subscription price of $400,000 (“Initial Investment”). Following the formation of the
entity and closing of the Initial Investment, the Investor shall source one or more future investors to purchase up to $50.0 million at
$25/share in common stock of the Company, of which 70% of the proceeds will be maintained by the Company and 30% will be transferred to
an operating entity to be formed under NuroMena, to conduct clinical trials in the middle-east markets. As of the date of this filing,
the Initial Investment has not yet occurred.
22
Liquidity
Since its inception, we have
incurred significant operating losses. Our net loss was $8,615,920 and $2,184,500, for the three months ended September 30, 2025
and 2024, respectively, and $46,622,106 and $9,645,482 for the nine months ended September 30, 2025 and 2024, respectively. We had
an accumulated deficit of $97,230,551 at September 30, 2025. We expect to continue to incur significant and increasing expenses and
operating losses for the foreseeable future, as we advance our current and future product candidates through preclinical and clinical
development, manufacture drug product and drug supply, seek regulatory approval for our current and future product candidates, maintain
and expand our intellectual property portfolio, hire additional research and development and business personnel and operate as a public
company.
We will not generate revenue from product sales unless and until we successfully complete clinical development and obtain regulatory approval for our product candidates. In addition, if we obtain regulatory approval for our product candidates and do not enter a third-party commercialization partnership, we expect to incur significant expenses related to developing our commercialization capability to support product sales, marketing, manufacturing, and distribution activities.
As a result, we will need substantial additional funding to support our continuing operations and pursue our growth strategy. Until we can generate significant revenue from product sales, if ever, we expect to finance our operations through a combination of public or private equity offerings and debt financings or other sources, such as potential collaboration agreements, strategic alliances and licensing arrangements. We may be unable to raise additional funds or enter into such other agreements or arrangements when needed on acceptable terms, or at all. Our failure to raise capital or enter into such agreements as, and when needed, could have a material adverse effect on our business, results of operations and financial condition.
The report of our independent registered public accounting firm on our financial statements as of and for the year ended December 31, 2024 included an explanatory paragraph indicating that there was substantial doubt about our ability to continue as a going concern. See Note 1 to our financial statements for additional information on our assessment.
Components of Results of Operations
Revenue
We occasionally receive a fee from a patient for a “right to try” humanitarian program. Such revenues are not part of our core business.
Operating Expenses
Our operating expenses consist of (i) research and development expenses and (ii) legal and professional expenses and (iii) general and administrative expenses.
Research and Development Expenses
Research and development expenses consist primarily of costs incurred for our research and development activities, including our product candidate discovery efforts and preclinical and clinical studies under our research programs, which include:
●
employee-related expenses, including salaries, benefits and stock-based compensation expense for our research and development personnel;
●
costs of funding research performed by third parties that conduct research and development and preclinical and clinical activities on our behalf;
23
●
costs of manufacturing drug products and drug supply related to our current or future product candidates;
●
costs of conducting preclinical studies and clinical trials of our product candidates;
●
consulting and professional fees related to research and development activities, including equity-based compensation to non-employees;
●
costs of maintaining our laboratory, including purchasing laboratory supplies and non-capital equipment used in our preclinical studies;
●
costs related to compliance with clinical regulatory requirements; and
●
facility costs and other allocated expenses, which include expenses for rent and maintenance of facilities, insurance, depreciation and other supplies.
Research and development costs are expensed as incurred. Costs for certain activities are recognized based on an evaluation of the progress to completion of specific tasks using data such as information provided to us by our vendors and analyzing the progress of our preclinical and clinical studies or other services performed.
The successful development of our product candidates is highly uncertain. We cannot reasonably estimate or know the nature, timing, and estimated costs of the efforts that will be necessary to complete development of our current or future product candidates. We are also unable to predict when, if ever, material net cash inflows will commence from the sale of our product candidates, if they are approved. This is due to the numerous risks and uncertainties associated with developing product candidates, including the uncertainty of:
●
the scope, rate of progress, and expenses of our ongoing research activities as well as any preclinical studies and clinical trials and other research and development activities;
●
establishing an appropriate safety profile;
●
successful enrollment in and completion of clinical trials;
●
whether our product candidates show safety and efficacy in our clinical trials;
●
receipt of marketing approvals from applicable regulatory authorities;
●
establishing commercial manufacturing capabilities or making arrangements with third-party manufacturers;
●
obtaining and maintaining patent and trade secret protection and regulatory exclusivity for our product candidates;
●
commercializing product candidates, if and when approved, whether alone or in collaboration with others; and
●
continued acceptable safety of the products following any regulatory approval.
24
A change in the outcome of any of these variables with respect to the development of our current and future product candidates would significantly change the costs and timing associated with the development of those product candidates.
Research and development activities are central to our business model. Product candidates in later stages of clinical development generally have higher development costs than those in earlier stages of clinical development, primarily due to the increased size and duration of later-stage clinical trials. We expect research and development costs to increase significantly for the foreseeable future as we commence clinical trials and continue the development of our current and future product candidates. However, we do not believe that it is possible at this time to accurately project expenses through commercialization. There are numerous factors associated with the successful commercialization of any of our product candidates, including future trial design and various regulatory requirements, many of which cannot be determined with accuracy at this time based on our stage of development. Additionally, future commercial and regulatory factors beyond our control will impact our clinical development programs and plans.
Legal and Professional Expenses
Legal and professional expenses consist of costs related to corporate and intellectual property legal costs and accounting and auditing fees. We also anticipate increased expenses associated with being a public company, including costs for audit, legal, regulatory and tax-related services related to compliance with the rules and regulations of the Securities and Exchange Commission, or the SEC, and listing standards applicable to companies listed on a national securities exchange, director and officer insurance premiums, and investor relations costs.
General and Administrative Expenses
General and administrative expenses include salaries and other compensation-related costs, including stock-based compensation, for personnel in executive, finance and accounting, business development, operations and administrative roles. Other significant costs include insurance costs, travel costs, facility and office-related costs not included in research and development expenses.
We anticipate that our general and administrative expenses will increase in the future as our business expands to support expected growth in research and development activities, including our future clinical programs. These increases will likely include increased costs related to the hiring of additional personnel and fees to outside service providers, among other expenses. In addition, if we obtain regulatory approval for any of our product candidates and do not enter a third-party commercialization collaboration, we expect to incur significant expenses related to building a sales and marketing team to support product sales, marketing and distribution activities.
Share Based Compensation
Share based compensation expense result from the recognition of the fair value of restricted stock units (RSU) recorded on a straight-line basis from the date of grant to the date the RSU becomes fully vested.
Interest Expense
Interest expense primarily results from the bridge loan and a short-term loan both from related parties. Borrowings under these loans carry a 50% (or 1 times amounts borrowed) original issue discount (“OID”) on principal. The OID to be earned under the bridge loan is recognized ratably over the term of each draw-down under the loan through the maturity date.
25
Amortization
Amortization on debt issuance costs resulted from the grant of warrants for a line of credit commitment. The fair value of the warrants was determined using the Black Scholes valuation method and the fair value is being amortized over the term of the line of credit commitment.
Amortization on deferred offering costs resulted from the issuance of common stock in connection with a private equity agreement.
Loss
on Change in Fair Value of Derivative Liability
Loss on change in fair value of derivative liability relates to the
fair value of the discount offered to stockholders who purchased shares under the equity line of credit.
Comparison of the three and nine months
ended September 30, 2025 and 2024:
Results of Operations
The following table summarizes our results of operations for the periods presented:
For the
Three Months Ended
September 30,
2025
2024
Change
Revenues:
Revenue
$ -
$ -
$ -
Cost of Revenues
-
Operating Expenses:
Research and development
715,038
956,725
(241,687 )
Legal and professional
276,378
496,803
(220,425 )
General and administrative
902,985
243,659
659,326
Share based compensation
5,040,246
-
5,040,246
Advisory Fee
-
500,000
(500,000 )
Total Operating Expenses
6,934,647
2,197,187
4,737,460
Loss From Operations
(6,934,647 )
(2,197,187 )
(4,737,460 )
Other Income (Expense):
Interest and other income
6,815
12,687
(5,872 )
Amortization expense
(438,111 )
-
(438,111 )
Interest expense - related parties
(869,815 )
-
(869,815 )
Loss on change in fair value of derivative liability related to sales of common stock through equity line of credit
(380,162 )
-
(380,162 )
Net Loss
$ (8,615,920 )
$ (2,184,500 )
$ (6,431,420 )
Revenue
No revenue was generated for
fees for a “right to try” humanitarian program during the three months ended September 30, 2025 and 2024.
26
Research and Development Expenses
The following table summarizes the components of our research and development expenses for the periods presented:
For the
Three Months Ended
September 30,
2025
2024
Research and development costs by project:
NEO100-01
$ 163,036
$ 236,607
NEO100-02
125,586
79,644
NEO212
343,368
189,553
Pediatric
70,653
34,350
Laboratory
-
362,858
Other
12,395
53,713
Total
$ 715,038
$ 956,725
For the
Three Months Ended
September 30,
2025
2024
Change
Clinical trial expense
$ 702,643
$ 540,154
$ 162,489
Research and laboratory
12,395
416,571
(404,175 )
Total research and development expense
$ 715,038
$ 956,725
$ (241,686 )
Research and development expenses
were $715,038 and $956,725 for the three months ended September 30, 2025 and 2024, respectively. A portion of these expenses amounting
to approximately $12,395 and $416,571 for the three months ended September 30, 2025 and 2024, respectively are from the University
of Southern California (USC), where Dr. Chen is a member of the faculty. The total decrease of $241,686 was primarily due to:
●
Pre-clinical laboratory work in 2024 was completed, such that there were no such costs in 2025.
●
The recruitment for NEO212.
Legal and Professional Expenses
Legal and professional expenses
were $276,378 and $496,803 for the three months ended September 30, 2025 and 2024, respectively. The decrease of $220,425 was primarily
due to the completion of the direct listing process which occurred in the first quarter of 2025.
General and Administrative Expenses
General and administrative
expenses were $902,985 and $243,659 for the three months ended September 30, 2025 and 2024, respectively. The increase of $659,326
was primary due to a marketing campaign, increased employee headcount and resultant compensation and benefits, rent and travel expenses
and expense incurred in pursuit of the Middle East deal.
Share Based Compensation
Share based compensation resulted
from the granting of RSUs and is the recognition of the expense from the grant date (which included a catch up period from the original
date of issuance of the RSU’s through the Listing Date, due to the removal of the contingency which occurred on the Listing Date)
during the three months ended September 30, 2025.
27
Interest Expense
Interest expense was $869,815
and $0 for the three months ended September 30, 2025 and 2024, respectively. The interest for the three months ended September 30,
2025 relates primarily to the accrued interest for a litigation matter and the accretion of the convertible note payable of $820,794.
Interest and other Income
Interest income was $6,815
and $12,687 for the three months ended September 30, 2025 and 2024, respectively. The interest income for the three months ended
September 30, 2025 and 2024, relates primarily interest earned on the money market account.
Loss on Change in Fair
Value of Derivative Liability
Loss
on change in fair value of derivative liability was $380,162 and $0 for the three months ended September 30, 2025 and 2024, respectively.
The loss on settlement is related to the discount offered investors who purchased shares of common stock under the equity line of credit,
which commenced in July 2025.
Amortization of Debt Issuance and Deferred Offering Costs
The amortization of debt issuance
costs was approximately $438,111 and $0 for the three months ended September 30, 2025 and 2024, respectively. This represents the
amortization of the debt issuance costs associated with the warrants issued for the HCWG line of credit, offering costs relating to the
Mast Hill agreement and debt issuance cost associated with the convertible promissory notes.
The following table summarizes our results of operations for the periods presented:
For the
Nine Months Ended
September 30,
2025
2024
Change
Revenues:
Revenue
$ 39,990
$ 63,000
$ (23,010 )
Cost of Revenues
Operating Expenses:
Research and development
2,390,592
1,965,726
424,866
Legal and professional
1,754,287
1,652,141
102,146
General and administrative
2,736,732
973,923
1,762,809
Share based compensation
25,964,096
-
25,964,096
Advisory fees
11,737,806
500,000
11,237,806
Total Operating Expenses
44,583,513
5,091,790
39,491,723
Loss From Operations
(44,543,523 )
(5,028,790 )
(39,514,733 )
Other Income (Expense):
Interest and other income
327,377
12,687
314,690
Amortization expense
(798,311 )
-
(798,311 )
Interest expense
(1,227,487 )
(2,559,456 )
1,331,969
Loss on extinguishment of Bridge loan - related party
-
(2,069,923 )
2,069,923
Loss on settlement of common share purchases
(380,162 )
-
(380,162 )
Net Loss
$ (46,622,106 )
$ (9,645,482 )
$ (36,976,624 )
28
Revenue
Revenue was generated for fees for a “right to try” humanitarian program during 2025 and 2024.
Research and Development Expenses
The following table summarizes the components of our research and development expenses for the periods presented:
For the
Nine Months Ended
September 30,
2025
2024
Research and development costs by project:
NEO100-01
$ 851,664
$ 693,328
NEO100-02
327,373
203,075
NEO212
798,997
549,249
Pediatric
169,663
103,338
Laboratory
192,377
362,858
Other
50,518
53,878
Total
$ 2,390,592
$ 1,965,726
For the
Nine Months Ended
September 30,
2025
2024
Change
Clinical trial expense
$ 2,147,697
$ 1,548,990
$ 598,707
Research and laboratory
242,895
416,736
(173,841 )
Total research and development expense
$ 2,390,592
$ 1,965,726
$ 424,866
Research and development expenses
were $2,390,592 and $1,965,726 for the nine months ended September 30, 2025 and 2024, respectively. A portion of these expenses amounting
to approximately $242,895 and $416,736 for the nine months ended September 30, 2025 and 2024, respectively are from the University
of Southern California (USC), where Dr. Chen is a member of the faculty. The total increase of $424,866 was primarily due to:
●
The addition of clinical trial sites for NEO100’s clinical trial.
●
The recruitment for NEO212.
●
The start of the clinical trial for NEO100-03for a Pediatric Indication
●
Increased patient recruitment efforts.
Legal and Professional
Expenses
Legal and professional expenses
were $1,754,287 and $1,652,141 for the nine months ended September 30, 2025 and 2024, respectively. The increase of $102,146 was
primarily due to completion of the direct listing process.
29
General and Administrative
Expenses
General and administrative
expenses were $2,736,732 and $973,923 for the nine months ended September 30, 2025 and 2024, respectively. The increase of $,762,809
was primary due to amarketing campaign, increased employee headcount and resultant compensation and benefits, rent and travel expenses.
Share Based Compensation
Share based compensation resulted
from the granting of RSUs and is the recognition of the expense from the grant date (which included a catch up period from the original
date of issuance of the RSU’s through the Listing Date, due to the removal of the contingency which occurred on the Listing Date)
through September 30, 2025.
Advisory Fee
The advisory fee was earned on the Listing Date March 26, 2025.
Interest Expense
Interest expense was $1,227,487
and $2,559,456 for the nine months ended September 30, 2025 and 2024, respectively. The interest for the nine months ended September 30,
2025 relates to the short-term loan in March from a related party in the amount of $300,000 and $146,250 interest for a litigation matter,
and the accretion of the convertible note payable of $820,794. The OID interest for the nine months ended September 30, 2024 relates
to the OID for the related party bridge loan that was converted into common stock in June of 2024.
Amortization of Debt Issuance and Deferred Offering Costs
The amortization of debt issuance
costs was $798,311 and $0 for the nine months ended September 30, 2025 and 2024, respectively. This represents the amortization of
the warrants issued for the HCWG line of credit and deferred offering costs relating to the Mast Hill agreement.
Loss on Change in Fair
Value of Derivative Liability
Loss
on change in fair value of derivative liability was $380,162 and $0 for the three months ended September 2025 and 2024, respectively.
The loss on settlement is related to the discount offered investors who purchased shares of common stock under the equity line of credit,
which commenced in July 2025.
Cash Flows
The following table summarizes our cash flow for the periods indicated:
For the
Nine Months Ended
September 30,
2025
2024
Change
Net cash provided by (used in):
Operating activities
$ (16,772,777 )
$ (3,259,512 )
$ (13,513,265 )
Financing activities
18,221,108
4,562,277
13,658,831
Net increase (decrease) in cash
$ 1,448,331
$ 1,302,765
$ 145,566
30
Operating Activities
During the nine months ended
September 30, 2025, net cash used in operating activities was $16,772,777 consisting primarily of our net loss of $46,622,106, offset
by share based compensation of $25,964,096, accretion of original issue discounts of $820,794, amortization of assets of $1,161,331 and
the accrued advisory fee of $3,675,569. These were offset by decreases in accrued compensation in the amount of $479,775 and prepaid expenses
in the amount of $267,161.
During the nine months ended
September 30, 2024, net cash used in operating activities was $3,259,512 consisting primarily of our net loss of $9,645,482 less
the non-cash charge of the accretion of the original issue discount on the bridge loan in the amount $2,558,241, less the non-cash charge
for the loss on extinguishment of convertible debt of $2,069,923 and an increase in accounts payable of $957,162.
Financing Activities
During the nine months ended
September 30, 2025, cash provided by financing activities was $18,221,108 consisting primarily of the sale of common stock of $11,324,522,
proceeds from the issuance of the convertible note of $4,000,000 and proceeds from the sales of common stock under the equity line of
credit of $3,196,736.
During the nine months ended
September 30, 2024, cash used in financing activities was $4,562,277, consisting primarily of proceeds from the sale of common stock
of $4,615,789.
Liquidity and Capital Resources
Sources of Liquidity/Going Concern
Since our inception, we have funded our operations through the sale and issuance of preferred and common stock and debt financing rounds from related and third parties.
During the nine months ended
September 30, 2025, the Company sold 727,750 shares of common stock at a price of $16.00 per share for gross proceeds of $11,644,005
pursuant to a private placement of its securities, issued 46,000 shares as part of advisory services related to the listing and as part
of the private placement fee for our equity line of credit, 162,500 shares were issued for the cashless exercise of warrants and issued
447,527 shares from the sale of shares under the equity line of credit,
The accompanying consolidated
financial statements have been prepared on a going concern basis, which contemplates the realization of assets and the settlement of liabilities
and commitments in the normal course of business. Since our inception, we have not generated any revenue from product sales or any other
sources, except humanitarian use, and we have incurred significant operating losses. We have not yet commercialized any products, and
we do not expect to generate revenue from sales of any product candidates for a number of years, if ever. As reflected in the accompanying
consolidated financial statements, we have incurred recurring net losses since our inception. For the three and nine months ended September 30,
2025, the Company incurred a net loss of $8,615,920 and $46,622,106, respectively, and had an accumulated deficit of $97,230,551 at September 30,
2025. At September 30, 2025, the Company had cash totaling $1,513,224. These factors raise substantial doubt about our ability to
continue as a going concern. Our ability to continue as a going concern is dependent upon our ability to raise additional funds and implement
our strategies, such as executing additional licensing contracts. The consolidated financial statements do not include any adjustments
that might be necessary if we are unable to continue as a going concern.
The ability to continue as a going concern is dependent on us raising additional capital and attaining and maintaining profitable operations in the future to meet our obligations and repay our liabilities arising from normal business operations when they come due. Since inception, we have funded our operations primarily through equity and debt financings and licensing income and we expect to continue to rely on these sources of capital in the future.
No assurance can be given that any future financing will be available or, if available, that it will be on terms that are satisfactory to us. Even if we are able to obtain additional financing, it may contain undue restrictions on our operations, in the case of debt financing, or cause substantial dilution for our shareholders, in the case of equity financing, or grant unfavorable terms in licensing agreements.
31
Funding Requirements
We expect our expenses to increase in connection with our ongoing activities, particularly as we continue our research and development, initiate and conduct preclinical studies and clinical trials, and seek marketing approval for our current and any of our future product candidates. In addition, if we obtain marketing approval for any of our current or our future product candidates, we expect to incur significant commercialization expenses related to product sales, marketing, manufacturing and distribution, which costs we may seek to offset through entry into collaboration agreements with third parties. Furthermore, we expect to incur additional costs associated with operating as a public company. Accordingly, we will need to obtain substantial additional funding in connection with our continuing operations. If we are unable to raise capital when needed or on acceptable terms, we would be forced to delay, reduce or eliminate our research and development programs or future commercialization efforts.
We expect to finance our operations over the next 12 months primarily through existing cash balances and the proceeds from the aforementioned private placements and supplemented as necessary by funds available through our Line of Credit Agreement with HCWG and sales under the Equity Purchase Agreement, each as described below. We have based this estimate on assumptions that may prove to be wrong, and we may use our available capital resources sooner than we currently expect. Our future capital requirements will depend on a number of factors, including:
●
the costs of conducting preclinical studies and clinical trials;
●
the costs of manufacturing;
●
the scope, progress, results and costs of discovery, preclinical development, laboratory testing, and clinical trials for product candidates we may develop, if any;
●
the costs, timing, and outcome of regulatory review of our product candidates;
●
our ability to establish and maintain collaborations on favorable terms, if at all;
●
the
achievement of milestones or the occurrence of other developments that trigger payments under any license or collaboration
agreements we might have at such time;
●
the costs and timing of future commercialization activities, including product sales, marketing, manufacturing and distribution, for any of our product candidates for which we receive marketing approval;
●
the amount of revenue, if any, received from commercial sales of our product candidates, should any of our product candidates receive marketing approval;
●
the costs of preparing, filing and prosecuting patent applications, obtaining, maintaining and enforcing our intellectual property rights, and defending intellectual property-related claims;
●
our headcount growth and associated costs as we expand our business operations and research and development activities; and
●
the costs of operating as a public company.
32
Until such time, if ever, as we can generate substantial product revenues, we expect to finance our cash needs through public or private equity offerings and debt financings or other sources, such as potential collaboration agreements, strategic alliances and licensing arrangements. To the extent that we raise additional capital through the sale of equity or convertible debt securities, your ownership interests may be diluted, and the terms of these securities may include liquidation or other preferences that could adversely affect your rights as a common stockholder. Additional debt financing, if available, may involve agreements that include restrictive covenants that limit our ability to take specific actions, such as incurring additional debt, making capital expenditures or declaring dividends, that could adversely impact our ability to conduct our business.
If we raise funds through potential collaborations, strategic alliances or licensing arrangements with third parties, we may have to relinquish valuable rights to our technologies, future revenue streams, research programs or product candidates, or to grant licenses on terms that may not be favorable to us. If we are unable to raise additional funds when needed, we may be required to delay, limit, reduce or terminate our product development or future commercialization efforts or grant rights to develop and market product candidates that we would otherwise prefer to develop and market ourselves.
Critical Accounting Estimates
We account for stock-based compensation, including restricted stock units (RSUs), in accordance with ASC 718. RSUs are measured at fair value on the grant date based on our common stock price and expense over the vesting period. For awards with performance or market conditions, expense is recognized based on the probability of achievement and may be accelerated. We estimate forfeitures based on historical data and adjust these estimates periodically. Changes in forfeiture rates, stock price, or performance assumptions can materially affect stock-based compensation expenses. Management reviews these assumptions quarterly and updates estimates as necessary. We consider the accounting for RSUs a critical estimate due to the judgment involved and its material impact on our financial results.
Item 3. Quantitative and Qualitative Disclosures About Market Risk
We are not currently exposed to significant market risk related to changes in foreign currency exchange rates. However, we have contracted with and may continue to contract with foreign vendors that are located in Europe and India. Our operations may be subject to fluctuations in foreign currency exchange rates in the future.
Inflation generally affects
us by increasing our cost of labor. We do not believe that inflation had a material effect on our business, financial condition or results
of operations during the three and nine months ended September 30, 2025 or the year ended December 31, 2024.
Item 4. Controls and Procedures
Disclosure Controls and Procedures
Disclosure controls and procedures are controls and other procedures that are designed to ensure that information required to be disclosed in our reports filed or submitted under the Exchange Act is recorded, processed, summarized and reported, within the time periods specified in the SEC’s rules and forms. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed in our reports filed or submitted under the Exchange Act is accumulated and communicated to our management, including our Chief Executive Officer and Chief Financial Officer, as appropriate to allow timely decisions regarding required disclosure.
We do not expect that our disclosure controls and procedures will prevent all errors and all instances of fraud. Disclosure controls and procedures, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the disclosure controls and procedures are met. Further, the design of disclosure controls and procedures must reflect the fact that there are resource constraints, and the benefits must be considered relative to their costs. Because of the inherent limitations in all disclosure controls and procedures, no evaluation of disclosure controls and procedures can provide absolute assurance that we have identified all of the information required to be disclosed, and that we have detected all our control deficiencies and instances of fraud, if any. The design of disclosure controls and procedures also is based partly on certain assumptions about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under all potential future conditions.
33
Evaluation of Disclosure Controls and Procedures
As required by Rules 13a-15
and 15d-15 under the Exchange Act, our Chief Executive Officer and Chief Financial Officer carried out an evaluation of the effectiveness
of the design and operation of our disclosure controls and procedures as of June 30, 2025. Based upon their evaluation, and due to
material weaknesses in our internal control over financial reporting related to; controls over segregation of duties, entity level controls
over the risk assessment, information and communication and monitoring process, financial controls over all significant transaction classes,
controls over authorization and tracking of related party transactions and controls over information technology over user access and provisioning,
our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures (as defined in Rules 13a-15(e)
and 15d-15(e) under the Exchange Act) were not effective as of September 30, 2025.
Changes in Internal Control over Financial Reporting
There were no changes in our
internal control over financial reporting (as defined in Rule 13a-15(f) under the Securities Exchange Act of 1934) during the quarter
ended September 30, 2025, that have materially affected, or are reasonably likely to materially affect, our internal control over
financial reporting.
Management’s Report on Internal Control Over Financial Reporting
Our management is responsible
for establishing and maintaining adequate internal control over financial reporting, as defined in the Exchange Act Rule 13a-15(f).
Our internal control over financial reporting is designed to provide reasonable assurance to our management and board of directors regarding
the preparation and fair presentation of published consolidated financial statements. A control system, no matter how well designed and
operated, can only provide reasonable, not absolute, assurance that the objectives of the control system are met. Because of these inherent
limitations, management does not expect that our internal control over financial reporting will prevent all errors and all fraud. Management
conducted an evaluation of our internal control over financial reporting based on the framework in Internal Control-Integrated Framework
issued in 2013 by the Committee of Sponsoring Organizations of the Treadway Commission (the “2013 Framework”). Based on our
evaluation under the 2013 Framework, management concluded that our internal control over financial reporting was not effective as of September 30,
2025, due to the material weakness in our internal control over duties separation, company-wide risk and communication processes, major
financial transactions, related party dealings, and IT user access management. As a result, we performed additional analysis as deemed
necessary to ensure that our consolidated financial statements were prepared in accordance with U.S. generally accepted accounting principles.
Accordingly, management believes that the consolidated financial statements included in this Form 10-Q present fairly in all material
respects our financial position, results of operations, and cash flows for the period presented.
Management has implemented remediation steps to improve our internal control over financial reporting. Specifically, we expanded and improved our review process for complex securities and related accounting standards. We plan to further improve this process by enhancing access to accounting literature, identification of third-party professionals with whom to consult regarding complex accounting applications and consideration of additional staff with the requisite experience and training to supplement existing accounting professionals. The Company can offer no assurance that these changes will ultimately have the intended effects.
This Quarterly Report on Form 10-Q does not include an attestation report on internal controls from our independent registered public accounting firm due to our status as an emerging growth company under the JOBS Act.
34
PART II - OTHER INFORMATION
Item 1. Legal Proceedings
On June 6, 2023, a vendor
filed a complaint against the Company for breach of contract in the Central District of California. The vendor alleged that the Company
improperly terminated an Intellectual Property License and Supply Agreement (“IPLSA”) and that the Company also defrauded
the vendor in connection with the IPLSA. This matter was settled on October 16, 2023, and the Company agreed to pay the vendor $600,000
within 5 business days of the close of the date that the Company completes an IPO or March 31, 2024, whichever occurs first. The
Company recognized this as a litigation settlement expense in the accompanying consolidated statement of operations for the year ended
December 31, 2023.
On March 31, 2024, the
vendor agreed to extend the payment until May 15, 2024 for payment of an additional $25,000. The Company has not made the payment
as of October 28, 2024, and the settlement is payable on demand. Such an amount is included in litigation settlement payable in the
accompanying consolidated balance sheet at December 31, 2024. On July 25, 2024 the arbitrator granted the implementation of
interest at the statutory rate on the unpaid balance commencing May 15, 2024 until paid. This is still outstanding at September 30,
2025.
On July 1, 2022, NeOnc
Technologies, Inc. and Fox Infused, LLC, a Delaware limited liability company (“Fox Infused”), entered into an Intellectual
Property License and Supply Agreement effective July 1, 2022 (the “Agreement”) whereby NeOnc agreed to supply certain
products to Fox Infused and license certain of our patents. We terminated the Agreement with Fox Infused on April 25, 2023. On June 6,
2023, Fox Infused filed a complaint against NeOnc in the Central District of California alleging that the termination was improper (Civil
Action No. 2:23-04431). Fox Infused also filed an ex parte application for a temporary restraining order and an order to show cause on
a preliminary injunction against us seeking to have the court stop the termination of the contract. Fox Infused’s temporary restraining
order application was denied and the case dismissed without prejudice. Fox Infused refiled the case in arbitration before the American
Arbitration Association (Case No. 01-23-0002-5020). The parties engaged in settlement discussions and agreed to settle the dispute for
a $600,000 payment by us to Fox Infused within 5 business days of the closing date of the Company’s initial public offering or
March 31, 2024. The Company is currently in default under the terms of such a settlement agreement.
In addition to that set forth above, we are, from time to time, party to various claims and legal proceedings arising out of our ordinary course of business, but we do not believe that any of these claims or proceedings will have a material effect on our business, consolidated financial condition or results of operations.
35
Item 1A. Risk Factors
There have been no material changes to the risk factors previously disclosed under Item 1A, “Risk Factors,” of our Quarterly Report on Form 10-Q for the period ended March 31, 2025.
Investing in our common stock involves a high degree of risk. You should carefully consider the following risk factors, as well as the other information in this Quarterly Report on Form 10-Q, before deciding whether to invest in shares of our common stock. If any of the following risks actually occurs, our business, results of operations and financial condition could be materially adversely affected. In this case, the trading price of our common stock would likely decline, and you might lose part or all your investment in our common stock.
Item 2. Unregistered Sales of Equity Securities and Use of Proceeds
Recent Sales of Unregistered Securities
During the nine months ended September 30, 2025, the Company issued the following unregistered securities:
In February 2025, 50,000 restricted stock units were granted to each of Dr. Steven L. Giannotta, Jim Delshad and Dr. Ming-Fu Chiang. The forgoing restricted stock units vest one hundred percent (100%) seven months following March 25, 2025.
In March 2025, we issued 624,999 shares of common stock to various unaffiliated third parties in a private placement at a price of $16.00 per share for gross proceeds of approximately $10,000,000.
In March 2025, we issued to Dawson James Securities, Inc. and Mast Hill Partner LP 30,000 and 16,000 shares of common stock upon the time of our direct listing, respectively.
In March 2025, we issued 102,750 shares of common stock to various unaffiliated third parties in a private placement at a price of $16.00 per share for gross proceeds of approximately $1,644,000.
In June 2025, 200,000 restricted stock units were granted to Josh Newman. The forgoing restricted stock units vest one hundred percent (100%) thirty-six months following issuance.
None of the foregoing transactions involved any underwriters, underwriting discounts or commissions, or any public offering. Unless otherwise specified above, we believe these transactions were exempt from registration under the Securities Act in reliance on Section 4(2) of the Securities Act (and Regulation D or Regulation S promulgated thereunder) or Rule 701 promulgated under Section 3(b) of the Securities Act as transactions by an issuer not involving any public offering or under benefit plans and contracts relating to compensation as provided under Rule 701. The recipients of the securities in each of these transactions represented their intentions to acquire the securities for investment only and not with a view to or for sale in connection with any distribution thereof, and appropriate legends were placed on the share certificates issued in these transactions. All recipients had adequate access, through their relationships with us, to information about us. The sales of these securities were made without any general solicitation or advertising.
Recent Sales of Registered Securities
In July 2025, the
Company sold 132,342 shares of common stock at $3.73 per share for gross proceeds of approximately $489,000 pursuant to Equity Purchase
Agreement with Mast Hill Fund, LP.
In September 2025, the
Company sold 315,185 shares of common stock at $7.60 – 9.53 per share for gross proceeds of approximately $2,710,000 pursuant to
Equity Purchase Agreement with Mast Hill Fund, LP.
36
Use of Proceeds
Not applicable.
Repurchases
None.
Item 3. Defaults Upon Senior Securities
None.
Item 4. Mine Safety Disclosures
Not applicable.
Item 5. Other Information
None .
37
Item 6. Exhibit Index
Exhibit
Number
Description
3.1
Amended and Restated Certificate of Incorporation (incorporated by reference to Exhibit 3.1 filed on Form 8-K filed by the Registrant on March 27, 2025)
3.2
Amended and Restated Bylaws (incorporated by reference to Exhibit 3.2 filed on Form 8-K filed by the Registrant on March 27, 2025)
4.1
Form of Common Stock Certificate (incorporated by reference to Exhibit 4.1 filed with the Registration Statement on Form S-1 filed by the Registrant on January 3, 2025)
4.2
Fourth Amended & Restated Promissory Note, dated December 4, 2023, by NeOnc Technologies Holdings, Inc. and Holders (incorporated by reference to Exhibit 4.2 filed with the Registration Statement on Form S-1 filed by the Registrant on January 3, 2025)
4.3
Promissory Note, dated October 11, 2024, by NeOnc Technologies Holdings, Inc. and HCWG LLC (incorporated by reference to Exhibit 4.3 filed with the Registration Statement on Form S-1 filed by the Registrant on January 3, 2025)
4.4
Common Stock Purchase Warrant, dated October 11, 2024, by NeOnc Technologies Holdings, Inc. and HCWG LLC (incorporated by reference to Exhibit 4.4 filed with the Registration Statement on Form S-1 filed by the Registrant on January 3, 2025)
4.5
Promissory Note, dated February 25, 2025, by NeOnc Technologies Holdings, Inc. and Amir Heshmatpour (incorporated by reference to Exhibit 4.5 filed with the Registration Statement on Form S-1 filed by the Registrant on February 26, 2025)
4.6
Form of Convertible Promissory Note (incorporated by reference to Exhibit 4.1 filed with the Form 8-K filed by the Registrant on July 22, 2025)
10.1
Form of Convertible Promissory Note Purchase Agreement (incorporated by reference to Exhibit 10.1 filed with the Form 8-K filed by the Registrant on July 22, 2025)
10.2
Letter of Intent dated July 24, 2025, between the Company, Dr. Ishwar Puri and Beth Levinson (incorporated by reference to Exhibit 10.1 filed with the Form 8-K filed by the Registrant on July 30, 2025)
10.3
Subscription Agreement dated June 28, 2025, between NuroMENA and Quazar (incorporated by reference to Exhibit 10.1 filed with the Form 8-K filed by the Registrant on August 1, 2025)
10.4
Share Exchange Agreement, dated August 18, 2025 (incorporated by reference to Exhibit 10.1 filed with the Form 8-K filed by the Registrant on August 22, 2025)
10.5
Master Services Agreement, dated October 4, 2025 (incorporated by reference to Exhibit 10.1 filed with the Form 8-K filed by the Registrant on October 9, 2025)
10.6#
Third Amendment to Employment Agreement (incorporated by reference to Exhibit 10.1 filed with the Form 8-K filed by the Registrant on November 6, 2025)
10.7#
Restricted Stock Award Agreement (incorporated by reference to Exhibit 10.2 filed with the Form 8-K filed by the Registrant on November 6, 2025)
31.1*
Certification of Principal Executive Officer Pursuant to Rules 13a-14(a) and 15d-14(a)
31.2*
Certification of Principal Financial Officer Pursuant to Rules 13a-14(a) and 15d-14(a)
32.1**
Certification of Principal Executive Officer Pursuant to 18 U.S.C. Section 1350
32.2**
Certification of Principal Financial Officer Pursuant to 18 U.S.C. Section 1350
101.INS*
Inline XBRL Instance
101.SCH*
Inline XBRL Taxonomy Extension Schema
101.CAL*
Inline XBRL Taxonomy Extension Calculation
101.LAB*
Inline XBRL Taxonomy Extension Labels
101.PRE*
Inline XBRL Taxonomy Extension Presentation
104
Cover Page Interactive Data File (embedded within the Inline XBRL and contained in Exhibit 101)
*
Filed herewith.
**
Furnished herewith.
38
SIGNATURES
Pursuant
to the requirements of the Securities Act of 1933, the registrant has duly caused this Quarterly Report on Form 10-Q to be signed on its
behalf by the undersigned, thereunto duly authorized, in Los Angeles, California, on November 14, 2025.
By:
/s/ Amir Heshmatpour
Name:
Amir Heshmatpour
Title:
Chief Executive Officer and President
As required under the Securities Act of 1933, this Quarterly Report on Form 10-Q has been signed below by the following persons, in the capacities and on the dates indicated:
Signature
Title
Date
/s/ Amir Heshmatpour
Chief Executive Officer
November 14, 2025
Amir Heshmatpour
(Principal Executive Officer)
/s/ Keithly Garnett
Chief Financial Officer
November 14, 2025
Keithly Garnett
(Principal Accounting Officer)
39
Text extracted from the filing as submitted to EDGAR. Formatting, tables and exhibits are simplified for reading; the original document is authoritative for anything you rely on.