CEL-SCI Corporation

05/13/2022 | Press release | Distributed by Public on 05/13/2022 14:33

Quarterly Report (Form 10-Q)

cvm_10q.htm

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 March 31, 2022

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 001-11889

CEL-SCI CORPORATION

Colorado

84-0916344

State or other

jurisdiction incorporation

(IRS) Employer

Identification Number

8229 Boone Boulevard, Suite 802

Vienna, Virginia22182

Address of principal executive offices

(703) 506-9460

Registrant's telephone number, including area code

Securities registered pursuant to Section 12(b) of the Act:

Title of Each Class

Trading

Symbol(s)

Name of Each Exchange

on Which Registered

Common Stock

CVM

NYSE American

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) had been subject to such filing requirements for the past 90 days. Yes ☒ No ☐

Indicate by check mark whether the registrant has submitted electronically 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, a smaller reporting company or an emerging growth company. See the definitions of "large accelerated filer," "accelerated filer", "smaller reporting company" and "emerging growth company" in Rule 12b-2 of the Exchange Act:

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 Exchange Act Rule 12b-2 of the Exchange Act). Yes ☐ No ☒

Class of Stock

No. Shares Outstanding

Date

Common

43,327,008

May 9, 2022

TABLE OF CONTENTS

PART I FINANCIAL INFORMATION

Item 1.

Page

Condensed Balance Sheets at March 31, 2022 (unaudited) and September 30, 2021

3

Condensed Statements of Operations for the six months ended March 31, 2022 and 2021 (unaudited)

4

Condensed Statements of Operations for the three months ended March 31, 2022 and 2021 (unaudited)

5

Condensed Statements of Stockholders' Equity for the six months ended March 31, 2022 and 2021 (unaudited)

6

Condensed Statements of Cash Flows for the six months ended March 31, 2022 and 2021 (unaudited)

7

Notes to Condensed Financial Statements(unaudited)

9

Item 2.

Management's Discussion and Analysis of Financial Condition and Results of Operations

22

Item 3.

Quantitative and Qualitative Disclosures about Market Risks

26

Item 4.

Controls and Procedures

26

PART II

Item 2.

Unregistered Sales of Equity Securities and Use of Proceeds

27

Item 6.

Exhibits

27

Signatures

28

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CEL-SCI CORPORATION

CONDENSED BALANCE SHEETS

MARCH 31,

SEPTEMBER 30,

ASSETS

2022

2021

(UNAUDITED)

Current assets:

Cash and cash equivalents

$ 34,282,872 $ 36,060,148

U.S. Treasury Bills

- 6,151,385

Receivables

- 54,922

Prepaid expenses

986,872 998,482

Supplies used for R&D and manufacturing

2,005,296 2,006,584

Total current assets

37,275,040 45,271,521

Finance lease right of use assets

11,808,291 12,691,921

Operating lease right of use assets

1,971,746 2,056,178

Property and equipment, net

12,870,911 13,663,562

Patent costs, net

234,658 275,866

Deposits

- 1,910,917

Total assets

$ 64,160,646 $ 75,869,965

LIABILITIES AND STOCKHOLDERS' EQUITY

Current liabilities:

Accounts payable

$ 1,316,542 $ 1,675,813

Accrued expenses

1,058,365 859,216

Due to employees

488,105 265,993

Derivative instruments

- 437,380

Lease liabilities, current portion

1,611,273 698,665

Total current liabilities

4,474,285 3,937,067

Finance lease obligations, net of current portion

12,494,026 13,252,364

Operating lease obligations, net of current portion

1,939,787 2,021,308

Other liabilities

125,000 125,000

Total liabilities

19,033,098 19,335,739

Commitments and contingencies

STOCKHOLDERS' EQUITY

Preferred stock, $0.01 par value-200,000 shares authorized; 0- shares issued and outstanding

- -

Common stock, $0.01 par value - 600,000,000 shares authorized; 43,304,602 and 43,207,183 shares issued and outstanding at March 31, 2022 and September 30, 2021, respectively

433,046 432,072

Additional paid-in capital

481,497,012 474,298,566

Accumulated deficit

(436,802,510 ) (418,196,412 )

Total stockholders' equity

45,127,548 56,534,226

TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY

$ 64,160,646 $ 75,869,965

See notes to condensed financial statements.

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CEL-SCI CORPORATION

CONDENSED STATEMENTS OF OPERATIONS

SIX MONTHS ENDED MARCH 31, 2022 and 2021

(UNAUDITED)

2022

2021

Operating expenses:

Research and development

$ 12,606,984 $ 10,636,274

General and administrative

5,788,250 6,627,640

Total operating expenses

18,395,234 17,263,914

Operating loss

(18,395,234 ) (17,263,914 )

Gain (loss) on derivative instruments

366,791 (2,108,181 )

Other non-operating (loss) gain

(30,793 ) 675,236

Interest expense, net

(546,862 ) (521,125 )

Net loss

(18,606,098 ) (19,217,984 )

Modification of warrants

- (85,779 )

Net loss available to common shareholders

$ (18,606,098 ) $ (19,303,763 )

Net loss per common share - basic and diluted

$ (0.43 ) $ (0.49 )

Weighted average common shares outstanding - basic and diluted

43,100,070 39,351,194

See notes to condensed financial statements.

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CEL-SCI CORPORATION

CONDENSED STATEMENTS OF OPERATIONS

THREE MONTHS ENDED MARCH 31, 2022 and 2021

(UNAUDITED)

2022

2021

Operating Expenses:

Research and development

$ 6,523,817 $ 5,221,514

General and administrative

3,028,042 3,311,484

Total operating expenses

9,551,859 8,532,998

Operating loss

(9,551,859 ) (8,532,998 )

Gain (loss) on derivative instruments

2,195 (3,041,017 )

Other non-operating gain

- 553,630

Interest expense, net

(273,828 ) (260,735 )

Net loss

$ (9,823,492 ) $ (11,281,120 )

Net loss per common share - basic and diluted

$ (0.23 ) $ (0.28 )

Weighted average common shares outstanding - basic and diluted

43,122,671 40,047,273

See notes to condensed financial statements.

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CEL-SCI CORPORATION

STATEMENTS OF STOCKHOLDERS' EQUITY

(UNAUDITED)

Additional

Common Stock

Paid-In

Accumulated

Shares

Amount

Capital

Deficit

Total

BALANCES AT OCTOBER 1, 2021

43,207,183 $ 432,072 $ 474,298,566 $ (418,196,412 ) $ 56,534,226

Warrant exercises

19,705 197 157,757 - 157,954

Equity based compensation - employees

- - 3,262,296 - 3,262,296
401(k) contributions paid in common stock 7,605 76 52,479 - 52,555

Stock and options issued to nonemployees for service

18,020 180 142,980 - 143,160

Option exercises

6,500 65 29,770 - 29,835

Share issuance costs

- - (45,965 ) - (45,965 )

Net loss

- - - (8,782,606 ) (8,782,606 )

BALANCES AT DECEMBER 31, 2021

43,259,013 432,590 477,897,883 (426,979,018 ) 51,351,455

Warrant exercises

5,500 55 13,805 - 13,860

Equity based compensation - employees

- - 3,392,706 - 3,392,706
401(k)contributions paid in common stock 14,614 146 57,371 - 57,517

Stock and options issued to nonemployees for service

25,475 255 139,797 - 140,052

Share issuance costs

- - (4,550 ) - (4,550 )

Net loss

- - (9,823,492 ) (9,823,492 )

BALANCES AT MARCH 31, 2022

43,304,602 $ 433,046 $ 481,497,012 $ (436,802,510 ) $ 45,127,548

Common Stock

Paid-In

Accumulated

Shares

Amount

Capital

Deficit

Total

BALANCES AT OCTOBER 1, 2020

38,730,150 $ 387,302 $ 401,174,675 $ (381,835,303 ) $ 19,726,674

Proceeds from the sale of common stock

1,000,000 10,000 13,549,500 - 13,559,500

Warrant exercises

15,000 150 89,100 - 89,250

Equity based compensation - employees

(2,000 ) (20 ) 3,296,329 - 3,296,309

401(k) contributions paid in common stock

3,564 36 41,635 - 41,671

Stock and options issued to nonemployees for service

15,044 150 152,300 - 152,450

Option exercises

5,300 53 23,458 - 23,511

Modification of warrants

- - 192 - 192

Share issuance costs

- - (117,021 ) - (117,021 )

Net loss

- - - (7,936,864 ) (7,936,864 )

BALANCES AT DECEMBER 31, 2020

39,767,058 397,671 418,210,168 (389,772,167 ) 28,835,672

Warrant exercises

991,239 9,912 7,928,929 - 7,938,841

Equity based compensation - employees

- - 3,282,742 - 3,282,742

401(k) contributions paid in common stock

3,347 33 51,387 - 51,420

Stock and options issued to nonemployees for service

13,486 135 379,142 - 379,277

Option exercises

48,845 489 138,299 - 138,788

Share issuance costs

- - (13,828 ) - (13,828 )

Net loss

- - - (11,281,120 ) (11,281,120 )

BALANCES AT MARCH 31, 2021

40,823,975 $ 408,240 $ 429,976,839 $ (401,053,287 ) $ 29,331,792

See notes to condensed financial statements.

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CEL-SCI CORPORATION

CONDENSED STATEMENTS OF CASH FLOWS

SIX MONTHS ENDED MARCH 31, 2022 and 2021

(UNAUDITED)

2022

2021

Net loss

$ (18,606,098 ) $ (19,217,984 )

Adjustments to reconcile net loss to

net cash used in operating activities:

Depreciation and amortization

1,867,192 1,101,477

Share-based payments for services

402,270 552,664

Equity based compensation

6,655,002 6,579,051

Common stock contributed to 401(k) plan

110,072 93,091

Gain on short-term investments

(615 ) (5,728 )

Loss on patent impairment

30,793 -

(Gain)/loss on derivative instruments

(366,791 ) 2,108,181

Modification of warrants

- 192

(Increase)/decrease in assets:

Receivables

54,922 -

Prepaid expenses

2,552 680,490

Supplies used for R&D and manufacturing

1,288 (638,771 )

Deposits

1,910,917 (48,210 )

Increase/(decrease) in liabilities:

Accounts payable

46,033 123,920

Accrued expenses

89,149 (142,744 )

Due to employees

222,112 9,083

Other liabilities

43,594 20,793

Net cash used in operating activities

(7,537,608 ) (8,784,495 )

CASH FLOWS FROM INVESTING ACTIVITIES:

Proceeds from maturity (purchases) of US treasury bills

6,152,000 (11,145,667 )

Purchases of property and equipment

(550,861 ) (6,629,050 )

Expenditures for patent costs

(22,741 ) -

Net cash provided by (used in) investing activities

5,578,398 (17,774,717 )

CASH FLOWS FROM FINANCING ACTIVITIES:

Proceeds from issuance of common stock

- 13,559,500

Payments of stock issuance costs

(45,965 ) (195,295 )

Proceeds from exercises of warrants and options

131,060 4,599,205

Proceeds from landlord funding of leasehold improvements

786,454 -

Payments on obligations under finance lease

(689,615 ) (481,773 )

Net cash provided by financing activities

181,934 17,481,637

NET DECREASE IN CASH AND CASH EQUIVALENTS

(1,777,276 ) (9,077,575 )

CASH AND CASH EQUIVALENTS, BEGINNING OF PERIOD

36,060,148 15,508,909

CASH AND CASH EQUIVALENTS, END OF PERIOD

$ 34,282,872 $ 6,431,334

See notes to condensed financial statements.

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CEL-SCI CORPORATION

CONDENSED STATEMENTS OF CASH FLOWS

SIX MONTHS ENDED MARCH 31, 2022 and 2021

(UNAUDITED)

2022

2021

SUPPLEMENTAL SCHEDULE OF NON-CASH INVESTING AND FINANCING ACTIVITIES:

Property and equipment included in current liabilities

$ 32,549 $ 1,529,284

Capitalizable patent costs included in current liabilities

$ - $ 20,000

Changes to right of use assets and liabilities

$ 16,268 $ (139,862 )

Finance lease obligation included in accounts payable

$ 374 $ 1,304

Prepaid consulting services paid with issuance of common stock

$ 354,853 $ 483,960

Accrued consulting services to be paid with issuance of common stock

$ 165,000 $ 165,000

Exercise of derivative liabilities

$ 70,589 $ 3,591,185

Financing costs included in current liabilities

$ 4,550 $ (13,947 )

Cash paid for interest

$ 578,837 $ 561,445

See notes to condensed financial statements.

8
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CEL-SCI CORPORATION

NOTES TO CONDENSED FINANCIAL STATEMENTS

SIX MONTHS ENDED MARCH 31, 2022 AND 2021 (UNAUDITED)

A.

BASIS OF PRESENTATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of Presentation

The accompanying condensed financial statements of CEL-SCI Corporation (the Company) are unaudited and certain information and footnote disclosures normally included in the annual financial statements prepared in accordance with accounting principles generally accepted in the United States of America (U.S. GAAP) have been omitted pursuant to the rules and regulations of the Securities and Exchange Commission. While management of the Company believes that the disclosures presented are adequate to make the information presented not misleading, these interim condensed financial statements should be read in conjunction with the financial statements and notes included in the Company's annual report on Form 10-K for the year ended September 30, 2021.

In the opinion of management, the accompanying unaudited condensed financial statements contain all adjustments necessary for a fair presentation of the Company's financial position as of March 31, 2022 and the results of its operations for the six and three months then ended. The condensed balance sheet as of September 30, 2021 is derived from the September 30, 2021 audited financial statements. All accounting policies have been consistently applied in the interim financial statements and the annual financial statements. The results of operations for the six and three months ended March 31, 2022 and 2021 are not necessarily indicative of the results to be expected for the entire year.

The financial statements have been prepared assuming that the Company will continue as a going concern, but due to recurring losses from operations and future liquidity needs, there is substantial doubt about 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. Refer to the discussion in Note B.

Summary of Significant Accounting Policies:

Cash and Cash Equivalents - Cash and cash equivalents consist principally of unrestricted cash on deposit and short-term money market funds. The Company considers all highly liquid investments with a maturity when purchased of less than three months as cash equivalents.

Property and Equipment - Property and equipment is recorded at cost and depreciated using the straight-line method over estimated useful lives of five to seven years. Leasehold improvements are depreciated over the shorter of the estimated useful life of the asset or the term of the lease. Repairs and maintenance which do not extend the life of the asset are expensed when incurred. Property and equipment are reviewed on a quarterly basis to determine if any of the assets are impaired.

Patents - Patent expenditures are capitalized and amortized using the straight-line method over the shorter of the expected useful life or the legal life of the patent (17 years). In the event changes in technology or other circumstances impair the value or life of the patent, appropriate adjustment to the asset value and period of amortization is made. An impairment loss is recognized when estimated future undiscounted cash flows expected to result from the use of the asset, and from disposition, are less than the carrying value of the asset. The amount of the impairment loss would be the difference between the estimated fair value of the asset and its carrying value.

Leases - The Company accounts for contracts that convey the right to control the use of identified property, plant or equipment over a period of time in exchange for consideration as leases upon inception. The Company leases certain real estate, machinery, laboratory equipment and office equipment over varying periods. Many of these leases include an option to either renew or terminate the lease. For purposes of calculating lease liabilities, these options are included in the lease term when it is reasonably certain that the Company will exercise such options. The incremental borrowing rate utilized to calculate the lease liabilities is based on the information available at the commencement date, as most of the leases do not provide an implicit borrowing rate. Short-term leases, defined as leases with initial terms of 12 months or less, are not reflected on the balance sheet. Lease expense for such short-term leases is not material.

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Derivative Instruments - The Company has financing arrangements that consist of freestanding derivative instruments that contain embedded derivative features. The Company accounts for these arrangements in accordance with Accounting Standards Codification (ASC) 815, Accounting for Derivative Instruments and Hedging Activities." In accordance with ASC 815, derivative instruments and hybrid instruments are recognized as either assets or liabilities on the balance sheet and are measured at fair value with gains or losses recognized in earnings or other comprehensive income depending on the nature of the derivative or hybrid instruments. The Company determines the fair value of derivative instruments and hybrid instruments based on available market data using appropriate valuation models considering all the rights and obligations of each instrument. The derivative liabilities are re-measured at fair value at the end of each interim period.

The Company adopted Accounting Standards Update (ASU) 2020-06, Debt-Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging-Contracts in Entity's Own Equity (Subtopic 815-40): Accounting for Convertible Instruments and Contracts in an Entity's Own Equity effective October 1, 2021. The amendments in this Update simplify and clarify the guidance in Subtopic 815-40. There was no financial impact upon adoption.

Stock-Based Compensation - Compensation cost for all stock-based awards is measured at fair value as of the grant date in accordance with the provisions of ASC 718 Compensation - Stock Compensation. The fair value of stock options is calculated using the Black-Scholes option pricing model. The Black-Scholes model requires various judgmental assumptions including volatility and expected option life. The stock-based compensation cost is recognized using the straight-line allocation method as expense over the requisite service or vesting period.

The Company has Incentive Stock Option Plans, Non-Qualified Stock Option Plans, Stock Compensation Plans, Stock Bonus Plans and an Incentive Stock Bonus Plan. These Plans are collectively referred to as the "Plans." All Plans have been approved by the Company's stockholders.

The Company's stock options are not transferable, and the actual value of the stock options that an employee may realize, if any, will depend on the excess of the market price on the date of exercise over the exercise price. For options issued with service conditions only, the assumption for stock price volatility is based on the variance of daily closing prices of the Company's stock. The risk-free interest rate assumption is based on the U.S. Treasury rate at the date of grant with the term equal to the expected life of the option. Forfeitures are accounted for when they occur. The expected term of options represents the period that options granted are expected to be outstanding and has been determined based on an analysis of historical exercise behavior. If any of the assumptions used in the Black-Scholes model change significantly, stock-based compensation expense for new awards may differ materially in the future from that recorded in the current period.

Restricted stock granted under the Incentive Stock Bonus Plan and options granted under the 2021 and 2020 Non-Qualified Stock Option Plans are subject to service, performance and market conditions and meet the classification of equity awards. These awards were measured at fair value on the grant-dates using a Monte Carlo simulation for issuances where the attainment of performance criteria is uncertain. The total compensation cost will be expensed over the estimated requisite service period.

Research and Development Costs - Research and development costs are expensed as incurred. Management accrues Clinical Research Organization (CRO) expenses and clinical trial study expenses based on services performed and relies on the CROs to provide estimates of those costs applicable to the completion stage of a study. Estimated accrued CRO costs are subject to revisions as such studies progress to completion. The Company records revisions to estimated expense in the period in which the facts that give rise to the revision become known.

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Net Loss Per Common Share - The Company calculates net loss per common share in accordance with ASC 260 "Earnings Per Share" (ASC 260). Basic and diluted net loss per common share was determined by dividing net loss applicable to common shareholders by the weighted average number of common shares outstanding during the period. The Company's potentially dilutive shares, which include outstanding common stock options, unvested restricted stock and common stock warrants, have not been included in the computation of diluted net loss per share for all periods as the result would be anti-dilutive.

Income Taxes - The Company uses the asset and liability method of accounting for income taxes. Under the asset and liability method, deferred tax assets and liabilities are recognized for future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating and tax loss carryforwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in income in the period that includes the enactment date. The Company records a valuation allowance to reduce the deferred tax assets to the amount that is more likely than not to be recognized. A full valuation allowance was recorded against the deferred tax assets as of March 31, 2022 and September 30, 2021.

The Company adopted ASU No. 2019-12, Income Taxes (Topic 740): Simplifying the Accounting for Income Taxes effective October 1, 2021. The new standard includes several provisions that simplify accounting for income taxes by removing certain exceptions to the general principles in Topic 740 and increasing consistency and clarity for the users of financial statements. The adoption of ASU 2019-12 had no impact on the Company's financial statements.

Use of Estimates - The preparation of financial statements in conformity U.S. GAAP requires management to make estimates and assumptions that affect the amounts reported in the financial statements and the accompanying disclosures. These estimates are based on management's best knowledge of current events and actions the Company may undertake in the future. Estimates are used in accounting for, among other items, inventory obsolescence, accruals, stock options, useful lives for depreciation and amortization of long-lived assets, right of use assets and lease liabilities, deferred tax assets and the related valuation allowance, and the valuation of derivative liabilities. Actual results could differ from estimates, although management does not generally believe such differences would materially affect the financial statements in any given year. However, regarding the valuation of derivative liabilities determined using the Black-Scholes pricing model, significant fluctuations may materially affect the financial statements in a given year. Additionally, in calculating the right of use assets and lease liabilities, estimates and assumptions were used to determine the incremental borrowing rates and the expected lease terms. The Company considers the estimates used in valuing the derivative liabilities, stock options and the lease assets and liabilities to be significant.

New Accounting Pronouncements

The Company has considered all recently issued accounting pronouncements and does not believe the adoption of such pronouncements will have a material impact on its financial statements.

B.

OPERATIONS AND FINANCING

On June 28, 2021, the Company announced results from its 9.5-year pivotal Phase 3 study for its immunotherapy Multikine® (Leukocyte Interleukin, Injection) in the treatment of advanced (stages III and IV) primary (previously untreated) squamous cell carcinoma of the head and neck (SCCHN). The Phase 3 results showed a long-term 5-year overall survival (OS) benefit in the treatment arm that received Multikine treatment followed by surgery and radiation. The survival benefit for these patients increased over time and at 5 years the overall survival benefit reached an absolute 14.1% advantage for the Multikine treated arm over control (n=380, total study patients treated with surgery plus radiation), control arm 48.6%, Multikine arm 62.7% survival.

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Liquidity

The Company has incurred significant costs since its inception for the acquisition of certain proprietary technology and scientific knowledge relating to the human immunological defense system, patent applications, research and development, administrative costs, construction of laboratory facilities and participation in clinical trials. The Company has funded such costs primarily with proceeds from loans and the public and private sale of its securities. The Company will be required to raise additional capital or find additional long-term financing to continue with its efforts to bring Multikine to market. The ability to raise capital may be dependent upon market conditions that are outside the control of the Company. The ability of the Company to obtain approval from the U.S. Food and Drug Administration (FDA) for the sale of products to be developed on a commercial basis is uncertain. Ultimately, the Company must complete the development of its products, obtain the appropriate regulatory approvals and obtain sufficient revenues to support its cost structure. The Company believes there is a high likelihood that it will continue to receive funds from private and public offerings and warrant exercises similarly to the way it has funded operations in the past. However, there can be no assurance that the Company will be able to raise sufficient capital to support its operations.

To finance the Company through marketing approval, the Company plans to raise additional capital in the form of warrant exercises, corporate partnerships, and debt and/or equity financings. The Company believes that it will be able to obtain additional financing because it has done so consistently in the past and because it showed great survival benefit in the Phase 3 study in one of the two treatment arms for advanced primary head and neck cancer. However, there can be no assurance that the Company will be successful in raising additional funds on a timely basis or that the funds will be available to the Company on acceptable terms or at all. If the Company does not raise the necessary amounts of money, it may have to curtail its operations until such time as it is able to raise the required funding.

Primarily because of the losses incurred to date, the expected continued future losses, and the uncertainties associated with obtaining regulatory approval and ultimately commercializing its products, management has identified conditions and events that raise substantial doubt about the Company's ability to continue as a going concern. Management has evaluated the significance of those conditions and has concluded that there is sufficient cash on hand to meet the Company's budgeted cash requirements. As a result, substantial doubt about the Company's ability to continue as a going concern for more than twelve months from the date of these financial statements has been alleviated.

Impact of the COVID-19 Pandemic

In response to the global outbreak of COVID-19 and the World Health Organization's classification of the outbreak as a pandemic, the Company continues to take the necessary precautions to ensure the safety of its employees and to minimize interruptions to its operations. Management follows the Centers for Disease Control and Prevention's ("CDC") guidance and the recommendations and restrictions provided by state and local authorities. The full impact of the COVID-19 outbreak continues to evolve as of the date of this report. As such, it is uncertain as to the full magnitude of impact the pandemic will have on the Company's financial condition, liquidity and future results of operations. Management is actively monitoring the risks to public health and the impact of overall global business activity on its financial condition, liquidity, operations, suppliers, industry, and workforce.

C.

STOCKHOLDERS' EQUITY

Proceeds from the Sale of Common Stock

In December 2020, the Company sold 1,000,000 shares of common stock at a public offering price of $14.65 per share and received aggregate proceeds of approximately $13.6 million.

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Equity Compensation

Underlying share information for equity compensation plans as of March 31, 2022 is as follows:

Name of Plan

Total Shares Reserved

Under Plans

Shares Reserved for Outstanding Options

Shares

Issued

Remaining Options/Shares

Under Plans

Incentive Stock Option Plans

138,400 76,829 N/A 213

Non-Qualified Stock Option Plans

11,787,200 11,198,714 N/A 178,258

Stock Bonus Plans

783,760 N/A 385,305 398,422

Stock Compensation Plans

634,000 N/A 153,195 462,395

Incentive Stock Bonus Plan

640,000 N/A 614,500 25,500

Underlying share information for equity compensation plans as of September 30, 2021 is as follows:

Name of Plan

Total Shares Reserved

Under Plans

Shares Reserved for Outstanding Options

Shares

Issued

Remaining Options/Shares

Under Plans

Incentive Stock Option Plans

138,400 76,829 N/A 213

Non-Qualified Stock Option Plans

11,787,200 10,972,880 N/A 410,592

Stock Bonus Plans

783,760 N/A 363,086 420,641

Stock Compensation Plans

634,000 N/A 153,195 462,395

Incentive Stock Bonus Plan

640,000 N/A 614,500 25,500

Stock option activity:

Six Months Ended March 31,

2022

2021

Options granted

252,500 8,000

Options exercised

6,500 54,145

Options forfeited

20,166 42,165

Options expired

- 67

Three Months Ended March 31,

2022

2021

Options granted

1,500 500

Options exercised

- 48,845

Options forfeited

7,166 -

Options expired

- 12

During the six months ended March 31, 2022, the Company granted 250,000 performance-based stock options from the 2020 Non-Qualified Stock Option Plan to officers. Each option entitles the holder to purchase one share of the Company's common stock at a price of $10.48 per share, the fair value on the date of issuance. The stock options will vest 100% upon approval of the first marketing application for any pharmaceutical based upon the Company's Multikine technology in the USA, Canada, UK, Germany, France, Italy, Spain, Japan, or Australia. None of the options will be exercisable before November 19, 2022. All options which have not vested as of November 18, 2031 will be canceled. On the grant date, the options were valued using a Monte Carlo Simulation approach. A Monte Carlo Simulation is a statistical technique that is used to model probabilistic systems and establish the probabilities for a variety of outcomes. However, because attainment of the performance condition cannot be considered probable, no compensation cost is recognized relating to these options as of March 31, 2022. Management will re-assess the probability of achieving the performance condition at each reporting date.

Stock-Based Compensation Expense

Six months Ended March 31,

2022

2021

Employees

$ 6,655,002 $ 6,579,051

Non-employees

$ 402,270 $ 552,664

Three months Ended March 31,

2022

2021

Employees

$ 3,392,706 $ 3,282,742

Non-employees

$ 183,952 $ 304,004
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Employee compensation expense includes the expense related to options and restricted stock that is expensed over the vesting periods. Non-employee expense includes the expense related to options and stock issued to consultants expensed over the period of the related service contracts.

Warrants and Non-Employee Options

Warrant/Options

Issue Date

Shares Issuable upon Exercise

of Warrants/ Options

Exercise Price

Expiration Date

Reference

Series N

8/18/2008

85,339 $ 3.00

8/18/2022

*

Series UU

6/11/2018

93,603 $ 2.80

6/30/2022

*

Series X

1/13/2016

120,000 $ 9.25

7/13/2022

*

Series Y

2/15/2016

26,000 $ 12.00

8/15/2022

*

Series MM

6/22/2017

333,432 $ 1.86

6/22/2022

*

Series NN

7/24/2017

200,087 $ 2.52

7/24/2022

2

Series RR

10/30/2017

251,761 $ 1.65

10/30/2022

*

Series SS

12/19/2017

200,000 $ 2.09

12/18/2022

*

Series TT

2/5/2018

600 $ 2.24

2/5/2023

*

Consultants

7/28/2017 -11/18/2020

15,000

$2.18 -

$11.61

11/17/2022 -

7/27/2027

*

* No current period changes to these warrants

1.

Warrant Liabilities

The table below presents the fair value of the warrant liabilities as of:

March 31,

2022

September 30,

2021

Series Z warrants

$ - $ 64,787

Series AA warrants

- 276,035

Series CC warrants

- 94,961

Series HH warrants

- 1,597

Total warrant liabilities

$ - $ 437,380

The table below presents the net gains and (losses) on the warrant liabilities for the six months ended March 31:

2022

2021

Series W warrants

$ - $ 73,570

Series Z warrants

64,787 (696,498 )

Series ZZ warrants

- (11,530 )

Series AA warrants

276,035 (661,821 )

Series BB warrants

- (16,201 )

Series CC warrants

24,372 (795,257 )

Series HH warrants

1,597 (444 )

Net gain (loss) on warrant liabilities

$ 366,791 $ (2,108,181 )
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The table below presents the net gains and (losses) on the warrant liabilities for the three months ended March 31:

2022

2021

Series Z warrants

$ - $ (974,861 )

Series ZZ warrants

- (63,397 )

Series AA warrants

1,400 (995,629 )

Series BB warrants

- (46,833 )

Series CC warrants

- (959,602 )

Series HH warrants

795 (695 )

Net gain (loss) on warrant liabilities

$ 2,195 $ (3,041,017 )

The Company reviews all outstanding warrants in accordance with the requirements of ASC 815. This topic provides that an entity should use a two-step approach to evaluate whether an equity-linked financial instrument (or embedded feature) is indexed to its own stock, including evaluating the instrument's contingent exercise and settlement provisions. The warrant agreements provide for adjustments to the exercise price for certain dilutive events. Under the provisions of ASC 815, the warrants are not considered indexed to the Company's stock because future equity offerings or sales of the Company's stock are not an input to the fair value of a "fixed-for-fixed" option on equity shares, and equity classification is therefore precluded.

In accordance with ASC 815, derivative liabilities must be measured at fair value upon issuance and re-valued at the end of each reporting period through expiration. Any change in fair value between the respective reporting dates is recognized as a gain or loss.

During the six and three months ended March 31, 2022, 15,205 Series CC warrants were exercised at an exercise price of $5.00 for gross proceeds of $76,025.

The following warrants recorded as liabilities were exercised during the following periods.

Six Months Ended March 31, 2021

Three Months Ended March 31, 2021

Warrants

Warrants Exercised

Exercise Price

Proceeds

Warrants Exercised

Exercise Price

Proceeds

Series Z

79,200 $ 13.75 $ 1,089,000 79,200 $ 13.75 $ 1,089,000

Series ZZ

800 $ 13.75 11,000 800 $ 13.75 11,000

Series AA

100,000 $ 13.75 1,375,000 100,000 $ 13.75 1,375,000

Series CC

102,298 $ 5.00 511,490 97,298 $ 5.00 486,490
282,298 $ 2,986,490 277,298 $ 2,961,490

In February 2022, 100,000 Series AA warrants with an exercise price of $13.75 and 200 Series HH warrants with an exercise price of $3.13, expired. In December 2021, 640 Series CC warrants, with an exercise price of $5.00, expired. In November 2021, 184,800 Series Z warrants, with an exercise price of $13.75, expired.

On October 28, 2020, 688,930 Series W warrants, with an exercise price of $16.75, expired.

2.

Equity Warrants

During the six and three months ended March 31, 2022, 10,000 and 5,500 Series NN warrants were exercised at an exercise price of $2.52 for gross proceeds of $25,200 and $13,860, respectively.

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The following warrants recorded as equity were exercised during the following periods.

Six Months Ended March 31, 2021

Three Months Ended March 31, 2021

Warrants

Warrants Exercised

Exercise Price

Proceeds

Warrants Exercised

Exercise Price

Proceeds

Series MM

316,272 $ 1.86 $ 588,265 316,272 $ 1.86 $ 588,265

Series NN

21,834 $ 2.52 55,022 21,834 $ 2.52 55,022

Series RR

70,089 $ 1.65 115,647 70,089 $ 1.65 115,647

Series SS

105,264 $ 2.09 220,002 105,264 $ 2.09 220,002

Series TT

210,482 $ 2.24 471,480 200,482 $ 2.24 449,080
723,941 $ 1,450,416 713,941 $ 1,428,016

On December 7, 2020, the expiration date of the Series N warrants was extended six months from February 18, 2021 to August 18, 2021. The incremental cost of this extension was approximately $1,000, which was recorded as a deemed dividend in the financial statements for the six months ended March 31, 2021. The expiration date of the Series N warrants was later extended to August 18, 2022. The Series N warrants are held by the de Clara Trust, of which the Company's CEO, Geert Kersten, is a beneficiary.

On December 7, 2020, the expiration date of the Series X warrants was extended six months from January 13, 2021 to July 13, 2021. The incremental cost of this extension was approximately $85,000, which was recorded as a deemed dividend in the financial statements for the six months ended March 31, 2021. The expiration date of the Series X warrants was later extended to July 13, 2022. The Series X warrants are held by the de Clara Trust.

On December 7, 2020, the expiration date of the Series Y warrants, which were issued in connection with a financing, was extended six months from February 15, 2021 to August 15, 2021. The incremental cost of this extension was approximately $41,000 and was recorded as additional paid-in capital. The expiration date of the Series Y warrants was later extended to August 15, 2022.

On December 7, 2020, the expiration date of Series UU warrants was extended six months from December 31, 2020 to June 30, 2021. These warrants were previously issued as an inducement to convert notes payable into shares of common stock. The incremental cost of this extension was $192 and was recorded as interest expense for the six months ended March 31, 2021. The expiration date of the Series UU warrants was later extended to June 30, 2022. The Series UU warrants are held by Geert Kersten, Patricia Prichep (current Officers of the Company) and the de Clara Trust.

3.

Options and Shares Issued to Consultants

During the six months ended March 31, 2022 and 2021, the Company issued 43,495 and 28,530 shares, respectively, of restricted common stock to consultants for services. The weighted average grant date fair value of the shares issued to consultants was $7.05 and $17.66 during the six months ended March 31, 2022 and 2021, respectively. During the three months ended March 31, 2022 and 2021, the Company issued 25,475 and 13,486 shares, respectively, of restricted common stock to consultants for services. The weighted average grant date fair value of the shares issued to consultants was $5.00 and $23.47, respectively, during the three months ended March 31, 2022 and 2021.The aggregate values of the issuances of restricted common stock and common stock options are recorded as prepaid expenses and are charged to general and administrative expenses over the periods of service.

No options were issued to consultants during the six and three months ended March 31, 2022. During the six months ended March 31, 2021, the Company issued to a consultant 5,000 options to purchase common stock with an exercise price of $11.61, an aggregate fair value of approximately $28,000 and an expiration date of November 17, 2022. As of March 31, 2022 and September 30, 2021, 15,000 options issued to consultants remained outstanding, all of which were issued from the Non-Qualified Stock Option plans and all of which are vested as of the balance sheet dates.

During the six months ended March 31, 2022 and 2021, the Company recorded total expense of approximately $402,000 and $553,000, respectively, relating to the share-based compensation under these consulting agreements. On March 31, 2022 and September 30, 2021, consulting fees of approximately $355,000 and $364,000, respectively, are included in prepaid expenses.

4.

Securities Purchase Agreement

In prior years, the Company was party to a Securities Purchase Agreement (SPA) with Ergomed plc (Ergomed), one of the Company's Clinical Research Organizations responsible for managing the Company's Phase 3 clinical trial, to facilitate payment of amounts due to Ergomed. Under the Agreement, the Company issued Ergomed shares of common stock and the net proceeds from the sales of those shares reduces outstanding amounts due Ergomed. Upon issuance, the Company expensed the full value of the shares as other non-operating gain/loss and subsequently offset the gain or loss as amounts were realized through the sale by Ergomed and reduced accounts payable to Ergomed. Ergomed resold the final balance of shares issued in the quarter ended September 30, 2021. No shares were issued during the periods presented. No sales were made by Ergomed during the six and three months ended March 31, 2022. During the six and three months ended March 31, 2021, respectively, the Company realized approximately $0.7 million and $0.6 million through the sale by Ergomed of 39,500 and 30,500 shares of common stock and the Company reduced the payable to Ergomed and credited other operating gain by those amounts.

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D.

FAIR VALUE MEASUREMENTS

In accordance with ASC 820-10, "Fair Value Measurements," the Company determines fair value as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. The Company generally applies the income approach to determine fair value. This method uses valuation techniques to convert future amounts to a single present amount. The measurement is based on the value indicated by current market expectations with respect to those future amounts.

ASC 820-10 establishes a fair value hierarchy that prioritizes the inputs used to measure fair value. The hierarchy gives the highest priority to active markets for identical assets and liabilities (Level 1 measurement) and the lowest priority to unobservable inputs (Level 3 measurement). The Company classifies fair value balances based on the observability of those inputs. The three levels of the fair value hierarchy are as follows:

·

Level 1 - Observable inputs such as quoted prices in active markets for identical assets or liabilities.

·

Level 2 - Inputs other than quoted prices that are observable for the asset or liability, either directly or indirectly. These include quoted prices for similar assets or liabilities in active markets, quoted prices for identical or similar assets or liabilities in markets that are not active and amounts derived from valuation models where all significant inputs are observable in active markets.

·

Level 3 - Unobservable inputs that reflect management's assumptions. Assumptions from market participants are used when pricing the assets or liabilities, given there is no readily available market information.

For disclosure purposes, assets and liabilities are classified in their entirety in the fair value hierarchy level based on the lowest level of input that is significant to the overall fair value measurement. The Company's assessment of the significance of an input to the fair value measurement requires judgment and may affect the placement within the fair value hierarchy levels.

The Company purchased short-term U.S. Treasury bills during the year ended September 30, 2021 that are classified as trading securities. Quoted market prices were applied to determine the fair value of short-term investments; therefore, they were categorized as Level 1 in the fair value hierarchy. The Treasury bills matured in December 2021 and yielded a weighted average interest rate of 0.10%.

As of March 31, 2022, there were no outstanding derivative instruments. As of September 30, 2021, all the Company's derivative instruments are classified as Level 3 of the fair value hierarchy.

The following sets forth the reconciliation of beginning and ending balances related to fair value measurements using significant unobservable inputs (Level 3) for the six months ended March 31, 2022 and the year ended September 30, 2021:

Six months ended

Twelve months ended

March 31,

2022

September 30, 2021

Beginning balance

$ 437,380 $ 3,765,613

Issuances

- -

Exercises

(70,589 ) (4,023,091 )

Realized and unrealized net (gain) loss

(366,791 ) 694,858

Ending balance

$ - $ 437,380
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The fair values of the Company's derivative instruments disclosed above under Level 3 are primarily derived from valuation models where significant inputs such as historical price and volatility of the Company's stock, as well as U.S. Treasury Bill rates, are observable in active markets. On September 30, 2021, the Company's Level 3 derivative instruments had a weighted average fair value of $1.45 per share and a weighted average exercise price of $13.28 per share. Fair values were determined using a weighted average risk-free interest rate of 0.05% and volatility of 109% and the instruments had a weighted average time to maturity of 0.3 years as of September 30, 2021.

E.

RELATED PARTY TRANSACTIONS

During the six months ended March 31, 2022, the Company issued officers 250,000 options that vest upon FDA approval of the marketing application. See Note C for more information about the options.

On December 7, 2020, the expiration dates of the Series N and Series X warrants held by the de Clara Trust were extended by six months (Note C). The incremental cost of these modifications was approximately $86,000 and was recorded as a deemed dividend in the financial statements for the six months ended March 31, 2021.

On December 7, 2020, the expiration date of 93,603 Series UU warrants was extended from December 31, 2020 to June 30, 2021. The incremental cost of this extension was $192 and was recorded as interest expense for the six months ended March 31, 2021. The Series UU warrants are held by certain officers of the Company and were originally issued with convertible debt.

F.

COMMITMENTS AND CONTINGENCIES

Clinical Research Agreements

Under co-development and revenue sharing agreements with Ergomed, Ergomed agreed to contribute up to $12 million towards the Company's Phase 3 Clinical Trial in the form of discounted clinical services in exchange for a single digit percentage of milestone and royalty payments, up to a specific maximum amount. The Company accounted for the co-development and revenue sharing agreements in accordance with ASC 808 "Collaborative Arrangements." The Company determined the payments to Ergomed are within the scope of ASC 730 "Research and Development." Therefore, the Company records the discount on the clinical services as a credit to research and development expense on its Statements of Operations. Since the inception of the agreement with Ergomed, the Company has incurred research and development expenses of approximately $35.5 million for Ergomed's services. This amount is net of Ergomed's discount of approximately $11.8 million. During the six months ended March 31, 2022 and 2021, the Company recorded, net of Ergomed's discount, approximately $0.4 million and $1.0 million, respectively, of research and development expense related to Ergomed's services. During the three months ended March 31, 2022 and 2021, the Company recorded, net of Ergomed's discount, approximately $0.2 million and $0.4 million, respectively, as research and development expense related to Ergomed's services.

Lease Agreements

The Company leases a manufacturing facility near Baltimore, Maryland (the San Tomas lease). The building was remodeled in accordance with the Company's specifications so that it can be used by the Company to manufacture Multikine for the Company's Phase 3 clinical trial and sales of the drug if approved by the FDA. The lease is for a term of twenty years and requires annual base rent to escalate each year at 3%. The Company is required to pay all real estate and personal property taxes, insurance premiums, maintenance expenses, repair costs and utilities. The lease allows the Company, at its election, to extend the lease for two ten-year periods or to purchase the building at the end of the 20-year lease, which expires in October 2028. The renewal options are not included in the calculation of the right of use asset and lease liability because exercise of those options is not probable.

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On March 31, 2022 and September 30, 2021, the net book value of the finance lease right of use asset is approximately $11.8 million and $12.7 million, respectively, and the balance of the finance lease liability is approximately $14.0 million and $13.8 million, respectively, of which approximately $1.5 million and $0.6 million is current on March 31, 2022 and September 30, 2021, respectively. These amounts include the San Tomas lease as well as several other smaller finance leases for office equipment. The finance right of use assets are being depreciated using the straight-line method over the underlying lease terms. Total cash paid related to finance leases during the six months ended March 31, 2022 and 2021 was approximately $1.3 million and $1.0 million, respectively, of which approximately $0.6 million was for interest in each six-month period. As of March 31, 2022, the weighted average discount rate of the Company's finance leases is 8.45% and the weighted average time to maturity is 6.6 years.

In August 2020, the Company entered an amendment to the San Tomas lease under which the landlord agreed to allow the Company to substantially upgrade the manufacturing facility in preparation for the potential commercial production of Multikine. The project was completed and the improvements were placed in service in October 2021. Total cost was $11.1 million, of which the landlord agreed to finance $2.4 million. The Company received the final $0.8 million of the landlord financing during the quarter ended March 31, 2022. The landlord financing is being repaid through increased lease payments which started in March 2021 and extend over the remaining lease term. The repayment includes a base rent which escalates at 3% each year plus interest that accrues at 13.75% per year. The Company remeasured the lease liability to account for the modified payments using an 8.45% implicit interest rate. The rate was determined using a synthetic credit rating analysis prepared by an outside valuation specialist. The financing is accounted for as a lease incentive from the landlord and is included in the calculation of the lease liability as it was realized. The leasehold improvements are recorded in property and equipment and are being amortized over the remaining lease term.

The Company was required to deposit the equivalent of one year of base rent in accordance with the lease. Under the landlord's $2.4 million financing arrangement, the Company deposited an additional $0.2 million in March 2021. Because the Company met the minimum cash balance required by the lease, the full balance of the deposit was returned to the Company in January 2022. If the Company's cash balance falls below the required balance, the Company will be required to re-deposit these funds with the landlord. The approximate $1.9 million deposit is included in non-current assets on September 30, 2021.

Approximate future minimum lease payments under finance leases as of March 31, 2022 are as follows:

Six months ending September 30, 2022

$ 1,246,000

Year ending September 30,

2023

2,569,000

2024

2,648,000

2025

2,733,000

2026

2,824,000

2027

2,919,000

Thereafter

3,267,000

Total future minimum lease obligation

18,206,000

Less imputed interest on finance lease obligations

(4,259,000 )

Net present value of finance lease obligations

$ 13,947,000
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The Company leases two facilities under operating leases. The lease for the Company's office headquarters will expire on November 30, 2025. The lease for its research and development laboratory was renewed in September 2021 for an additional ten years and will expire on February 29, 2032. The renewal was considered a modification for accounting purposes and the right of use asset and liability were remeasured as of the date of the renewal. This resulted in an increase of approximately $1.1 million to the operating lease right of use asset and liability. The operating leases include escalating rental payments. The Company is recognizing the related rent expense on a straight-line basis over the terms of the leases. As of March 31, 2022 and September 30, 2021, the net book value of the operating lease right of use assets is approximately $2.0 million and $2.1 million, respectively. As of March 31, 2022 and September 30, 2021, the balance of the operating lease liabilities is approximately $2.1 million. of which approximately $0.2 million and $0.1 million is current on March 31, 2022 and September 31, 2021, respectively. The Company incurred lease expense for operating leases of approximately $181,000 and $132,000, respectively, for the six months ended March 31, 2022 and 2021. The Company incurred lease expense for operating leases of approximately $90,000 and $66,000, respectively, for the three months ended March 31, 2022 and 2021. Total cash paid related to operating leases during the six months ended March 31, 2022 and 2021 was approximately $138,000 and $111,000, respectively. The weighted average discount rate of the Company's operating leases is 9.10% and the weighted average time to maturity is 9.3 years.

As of March 31, 2022, future minimum lease payments on operating leases are as follows:

Six months ending September 30, 2022

$ 171,000

Year ending September 30,

2023

348,000

2024

357,000

2025

366,000

2026

287,000

2027

277,000

Thereafter

1,325,000

Total future minimum lease obligation

3,131,000

Less imputed interest on operating lease obligation

(1,033,000 )

Net present value of operating lease obligation

$ 2,098,000

G.

PATENTS

During the six months ended March 31, 2022 and 2021, respectively, patent impairment charges of approximately $31,000 and $0, were recorded. No patent impairment charges were recorded during the three months ended March 31, 2022 and 2021. For the six months ended March 31, 2022 and 2021, amortization of patent costs totaled approximately $27,000 and $26,000, respectively. For the three months ended March 31, 2022 and 2021, amortization of patent costs totaled approximately $13,000 in each period. Approximate estimated future amortization expense is as follows:

Six months ending September 30, 2022

$ 22,000

Year ending September 30,

2023

38,000

2024

30,000

2025

28,000

2026

24,000

2027

21,000

Thereafter

72,000

Total

$ 235,000
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H.

LOSS PER COMMON SHARE

Basic loss per share is computed by dividing net loss available to common shareholders by the weighted average number of common shares outstanding during the period. For the years presented, the gain on warrant liabilities priced lower than the average market price during the period is excluded from the numerator and the incremental shares, determined using the treasury stock method, are added to the denominator in calculating diluted loss per share.

The following tables provide the details of the basic and diluted loss per-share computations:

Six months ended March 31,

Three months ended March 31,

2022

2021

2022

2021

Loss per share - basic and diluted

Net loss available to common shareholders - basic

$ (18,606,098 ) $ (19,303,763 ) $ (9,823,492 ) $ (11,281,120 )

Weighted average shares outstanding - basic

43,100,070 39,351,194 43,122,671 40,047,273

Basic and diluted loss per common share

$ (0.43 ) $ (0.49 ) $ (0.23 ) $ (0.28 )

In accordance with the contingently issuable shares guidance of FASB ASC Topic 260, Earnings Per Share, the calculation of diluted net earnings (loss) per share excludes the following securities because their inclusion would have been anti-dilutive as of March 31:

2022

2021

Options and Warrants

12,586,365 5,945,064

Unvested Restricted Stock

151,250 302,500

Total

12,737,615 6,247,564

J.

SUBSEQUENT EVENTS

The Company has evaluated subsequent events through the date these financial statements were filed and determined there are no subsequent events that require disclosure.

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Item 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

Liquidity and Capital Resources

On June 28, 2021, the Company announced results from its 9.5-year pivotal Phase 3 study for its immunotherapy Multikine® (Leukocyte Interleukin, Injection) in the treatment of advanced (stages III and IV) primary (previously untreated) squamous cell carcinoma of the head and neck (SCCHN). The Phase 3 results showed a long-term 5-year overall survival (OS) benefit in the treatment arm that received Multikine treatment followed by surgery and radiation. This survival benefit was robust and durable, with no safety issues, something not commonly seen with cancer drugs. In fact, the survival benefit increased over time and at 5 years the overall survival benefit reached an absolute 14.1% advantage for the Multikine treated arm over control (n=380, total study patients treated with surgery plus radiation), control arm 48.6%, Multikine arm 62.7% survival.

The study used the standard of care treatment for advanced primary head and neck cancer patients as a comparison. The patients received surgery followed by either radiation or chemoradiation (chemotherapy and radiation at the same time), as determined by the physician. This means that there were 2 treatment arms, 1) surgery plus radiation or 2) surgery plus chemoradiation. The arm that received Multikine treatment followed by surgery and radiation showed great survival benefit, but when chemotherapy was added in the second treatment arm, the immunological effect of Multikine was negated. Therefore, when the two treatment arms were combined the study did not achieve its primary endpoint of a 10% improvement in overall survival.

However, the analysis of the separate treatment arms was prespecified in the protocol and carried out prior to the Company becoming unblinded. The OS benefit of 14.1% at 5 years for this treatment arm exceeded the 10% OS benefit set out for the study population as a whole. The OS results for this treatment arm are significant (two-sided p=0.0236, HR=0.68) and the effect is robust, durable and increasing over time. The results from the Phase 3 cancer study proved that Multikine met all of the protocol required benefits stated in the study protocol in patients in the treatment arm receiving surgery and radiation as their standard therapies. Based on this, the Company aims to file for FDA approval for the use of Multikine in the treatment of advanced primary head and neck cancer in this patient population of about 210,000 patients annually worldwide.

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Multikine (Leukocyte Interleukin, Injection) is the full name of this investigational therapy, which, for simplicity, is referred to in this report as Multikine. Multikine is the trademark that the Company has registered for this investigational therapy, and this proprietary name is subject to FDA review under the Company's future anticipated regulatory submission for approval. Multikine has not been licensed or approved by the FDA or any other regulatory agency, nor has its safety or efficacy been established for any use.

The Company also owns and is developing a pre-clinical technology called LEAPS (Ligand Epitope Antigen Presentation System). The Company has product candidates under development for the potential treatment of rheumatoid arthritis.

All of the Company's projects are under development. Consequently, the Company cannot predict when it will be able to generate any revenue from the sale of any of its products.

Since inception, the Company has financed its operations through the sale of equity securities, convertible notes, loans and certain research grants. The Company's expenses will continue to exceed its revenues as it continues the development of Multikine and brings other drug candidates into clinical trials. Until the Company becomes profitable, any or all of these financing vehicles or others may be utilized to assist in funding the Company's capital requirements.

Capital raised by the Company has been expended primarily for patent applications, research and development, administrative costs, and the construction and upgrade of the Company's manufacturing and laboratory facilities. The Company does not anticipate realizing significant revenues until entering into licensing arrangements for its technology and know-how or until it receives regulatory approval to sell its products (which could take several years). Thus, the Company has been dependent upon the proceeds from the sale of its securities to meet all its liquidity and capital requirements and anticipates having to do so in the future.

The Company will be required to raise additional capital or find additional long-term financing to continue with its research efforts. The ability to raise capital may be dependent upon market conditions that are outside the control of the Company. The ability of the Company to complete the necessary clinical trials and obtain FDA approval for the sale of products to be developed on a commercial basis is uncertain. Ultimately, the Company must complete the development of its products, obtain the appropriate regulatory approvals and obtain sufficient revenues to support its cost structure. However, there can be no assurance that the Company will be able to raise sufficient capital to support its operations.

As of March 31, 2022, the Company has incurred approximately $63 million of direct costs for the Phase 3 clinical trial and the filing of the clinical study report to the FDA since the Company launched its Phase 3 clinical trial for Multikine. The Company estimates it will incur additional expenses of approximately $0.8 million for the remainder of the Phase 3 clinical trial and the filing of the clinical study report to the FDA. It should be noted that this estimate is based only on the information currently available from the CROs responsible for managing the Phase 3 clinical trial and does not include other related costs, e.g., the manufacturing of the drug.

The Company uses two CROs to manage the global Phase 3 study; ICON and Ergomed, who are both international leaders in managing oncology trials.

Under a co-development agreement, Ergomed agreed to contribute up to $12 million towards the study where it will perform clinical services in exchange for a single digit percentage of milestone and royalty payments, up to a specified maximum amount. Approximately $11.8 million of the committed $12 million contribution has been realized as of March 31, 2022.

During the six months ended March 31, 2022, the Company used approximately $7.9 million in cash, after considering the maturity and transfer to cash of the remaining $6.2 million in U.S. Treasury bills (T-bills). Significant components of this decrease include cash used to fund the Company's regular operations, including its Phase 3 clinical trial, of approximately $7.5 million, leasehold improvement costs of approximately $0.6 million and approximately $0.7 million in lease payments. These outflows are offset by approximately $0.8 million in lease incentives received from the landlord to partially offset costs of the manufacturing facility upgrade and approximately $0.1 million in proceeds from the exercise of options and warrants.

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During the six months ended March 31, 2021, the Company's cash decreased by approximately $9.1 million, $11.1 million of which was due to the purchase of U.S. Treasury Bills (T-bills). Net of the purchase of the T-bills, cash increased by approximately $2.1 million. Significant components of the increase include approximately $13.4 million in net proceeds from the sale of common stock through public offerings and approximately $4.6 million in proceeds from the exercise of warrants and options, offset by net cash used to fund the Company's operations, including its Phase 3 clinical trial, of approximately $8.8 million, approximately $6.6 million of equipment and leasehold improvement expenditures and approximately $0.5 million in lease payments.

In October 2021, the Company completed a major upgrade of its leased manufacturing facility to prepare for the potential commercial production of its products. Total costs of this upgrade were approximately $11.1 million, of which the landlord of the property agreed to finance $2.4 million. The final $0.8 million of the landlord financing was received during the quarter ended March 31, 2022. The landlord financing is being repaid through increased lease payments over the remaining term of the lease.

During the six months ended March 31, 2022, 25,205 warrants were exercised at a weighted average exercise price of $4.02 for total proceeds of approximately $0.1 million. These exercises include 5,500 warrants exercised during the three months ended March 31, 2022 at an exercise price of $2.52. During the six months ended March 31, 2021, 1,006,239 warrants were exercised at a weighted average exercise price of $4.41 for total proceeds of approximately $4.4 million. These exercises include 991,239 warrants exercised during the three months ended March 31, 2021 for proceeds of approximately $4.4 million and a weighted average exercise price of $4.43.

Results of Operations and Financial Condition

The Company incurred a net operating loss of approximately $18.4 million for the six months ended March 31, 2022. This net operating loss consists of significant non-cash expenses including approximately $6.7 million in stock-based employee compensation and approximately $1.9 million in depreciation and amortization expense. The Company incurred a net operating loss of approximately $9.6 million for the three months ended March 31, 2022. This net operating loss consists of significant non-cash expenses including approximately $3.4 million in employee stock-based compensation and approximately $1.0 million in depreciation and amortization expense.

During the six months ended March 31, 2022, research and development expenses increased by approximately $2.0 million, or 19%, compared to the six months ended March 31, 2021. Major components of this increase include approximately $1.1 million increase in employee stock compensation expense and approximately $0.8 million increase in depreciation, primarily related to leasehold improvements to the manufacturing facility that were placed in service in October 2021, and an increase of approximately $0.7 million of costs incurred to prepare for the potential commercial sale of Multikine. These increases were offset by a decrease of approximately $0.6 million in costs related to the Phase 3 clinical study. During the three months ended March 31, 2022, research and development expenses increased by approximately $1.3 million, or 25%, compared to the three months ended March 31, 2021. Major components of this increase include approximately $0.2 million of costs incurred to prepare for the potential commercial sale of Multikine, $0.5 million increase in employee stock compensation expense, $0.4 million increase in depreciation, primarily of leasehold improvements to the manufacturing facility that were placed in service in October 2021, and a net increase of approximately $0.2 million in other research and development expenses.

During the six months ended March 31, 2022, general and administrative expenses decreased by approximately $0.8 million, or 13%, compared to the six months ended March 31, 2021. This decrease is primarily due to a decrease in employee stock compensation expense of approximately $1.0 million offset by a $0.2 million increase in other net general and administrative expenses. During the three months ended March 31, 2021, general and administrative expenses decreased by approximately $0.3 million, or 9%, compared to the three months ended March 31, 2021. This decrease is primarily due to a decrease in employee stock compensation expense of approximately $0.4 million offset by a $0.1 million increase in other net general and administrative expenses.

The approximate $0.4 million gain on derivative instruments for the six months ended March 31, 2022 varies significantly from the $2.1 million loss on derivative instruments for the six months ended March 31, 2021. The variance is the result of the change in fair value of the derivative liabilities at the respective period ends which is caused mainly by fluctuation in the share price of the Company's common stock. All derivative warrants have been exercised or have expired as of March 31, 2022, and therefore, unless additional liability classified warrants are issued, there will be no additional gain or loss reported.

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Other non-operating gain primarily relates to the Securities Purchase Agreement (SPA) with Ergomed plc as described in Item 4 under Note C. Under the SPA, the Company issued Ergomed shares of common stock and the net proceeds from the sales of those shares reduces outstanding amounts due Ergomed. Upon issuance, the Company expensed the full value of the shares as other non-operating gain/loss and subsequently offset the gain or loss as amounts were realized through the sale by Ergomed and reduced accounts payable to Ergomed. Ergomed resold the final balance of shares issued in the quarter ended September 30, 2021.

The amount of the gain or loss is a result of the timing of shares issued to Ergomed and the subsequent re-sale of those shares. There was no activity under the agreement during the six and three months ended March 31, 2022. During the six and three months ended March 31, 2021, the Company realized approximately $0.7 million and $0.6 million, respectively, in value upon the resale of shares.

Research and Development Expenses

The Company's research and development efforts involve Multikine and LEAPS. The table below shows the research and development expenses associated with each project.

Six months ended March 31,

Three months ended March 31,

2022

2021

2022

2021

MULTIKINE

$ 11,995,302 $ 9,732,817 $ 6,203,883 $ 4,720,867

LEAPS

611,682 903,457 319,934 500,647

TOTAL

$ 12,606,984 $ 10,636,274 $ 6,523,817 $ 5,221,514

Clinical and other studies necessary to obtain regulatory approval of a new drug involve significant costs and require several years to complete. The extent of the Company's clinical trials and research programs are primarily based upon the amount of capital available to the Company and the extent to which the Company has received regulatory approvals for clinical trials. The inability of the Company to conduct clinical trials or research, whether due to a lack of capital or regulatory approval, will prevent the Company from completing the studies and research required to obtain regulatory approval for any products which the Company is developing. Without regulatory approval, the Company will be unable to sell any of its products. Since all the Company's projects are under development, the Company cannot predict when it will be able to generate any revenue from the sale of any of its products.

Critical Accounting Estimates and Policies

Management's discussion and analysis of the Company's financial condition and results of operations is based on its unaudited condensed financial statements. The preparation of these financial statements is based on the selection of accounting policies and the application of significant accounting estimates, some of which require management to make judgments, estimates and assumptions that affect the amounts reported in the financial statements and notes.

The Company believes some of the more critical estimates and policies that affect its financial condition and results of operations are in the areas of leases and stock-based compensation.

The measurement of the finance and operating lease right-of-use asset and lease liabilities requires the determination of an estimated lease term and an incremental borrowing rate, which involves complex judgment by management. Significant judgment is required by management to develop inputs and assumptions used to determine the incremental borrowing rate for lease contracts. Share-based compensation cost to employees is measured at fair value as of the grant date in accordance with the provisions of ASC 718. The fair value of the stock options is calculated using the Black-Scholes option pricing model which requires various judgmental assumptions including volatility and expected option life. The compensation cost is recognized as expense over the requisite service or vesting period. Performance-based options are valued using a Monte-Carlo simulation model, which requires inputs based on estimates, including the likelihood of the occurrence of performance and market conditions, volatility and expected option life.

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For more information regarding the Company's critical accounting estimates and policies, see Part II, Item 7 of the Company's Annual Report on Form 10-K for the year ended September 30, 2021. The application of these critical accounting policies and estimates has been discussed with the Audit Committee of the Company's Board of Directors.

Item 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISKS

The Company does not believe that it has any significant exposures to market risk.

Item 4. CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures

Under the direction and with the participation of the Company's management, including the Company's Chief Executive and Chief Financial Officer, the Company has conducted an evaluation of the effectiveness of the design and operation of its disclosure controls and procedures as of March 31, 2022. The Company maintains disclosure controls and procedures that are designed to ensure that information required to be disclosed in its periodic reports with the Securities and Exchange Commission is recorded, processed, summarized and reported within the time periods specified in the SEC's rules and regulations, and that such information is accumulated and communicated to the Company's management, including its principal executive officer and principal financial officer, as appropriate, to allow timely decisions regarding required disclosure. The Company's disclosure controls and procedures are designed to provide a reasonable level of assurance of reaching its desired disclosure control objectives. Based on the evaluation, the Chief Executive and Chief Financial Officer concluded that the Company's disclosure controls and procedures were effective as of March 31, 2022.

Changes in Internal Control over Financial Reporting

There were no changes in the Company's internal control over financial reporting that occurred during the quarter ended March 31, 2022 that have materially affected, or are reasonably likely to materially affect, the Company's internal control over financial reporting.

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PART II

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds.

During the six months ended March 31, 2022 the Company issued 43,495 restricted shares of common stock to consultants for investor relations services.

The Company relied upon the exemption provided by Section 4(a)(2) of the Securities Act of 1933 with respect to the issuance of these shares. The individuals who acquired these shares were sophisticated investors and were provided full information regarding the Company's business and operations. There was no general solicitation in connection with the offer or sale of these securities. The individuals who acquired these shares acquired them for their own accounts. The certificates representing these shares bear a restricted legend which provides they cannot be sold except pursuant to an effective registration statement or an exemption from registration. No commission or other form of remuneration was given to any person in connection with the issuance of these shares.

Item 6.Exhibits

Number

Exhibit

31

Rule 13a-14(a) Certifications

32

Section 1350 Certifications

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SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

CEL-SCI CORPORATION

Date: May 13, 2022

By:

/s/ Geert Kersten

Geert Kersten

Principal Executive Officer*

* Also signing in the capacity of the Principal Accounting and Financial Officer.

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