Table of Contents

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 10-Q

 

(Mark One)

 

x     QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the quarterly period ended December 31, 20182019

 

OR

 

o     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 001-37487

 

AETHLON MEDICAL, INC.

(Exact name of registrant as specified in its charter)

 

NEVADA 13-3632859
(State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.)

 

9635 GRANITE RIDGE DRIVE, SUITE 100, SAN DIEGO, CA 92123

(Address of principal executive offices)    (Zip Code)

 

(858) 459-7800

(Registrant's telephone number, including area code)

 

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

Title of each classTrading SymbolName of each exchange on which registered
Common StockAEMDThe Nasdaq Capital 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 every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (ss.232.405(§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit 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. (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 Exchange Act). YES ☐ NO ☒

 

As of February 11, 2019,February7, 2020, the registrant had outstanding 18,960,505outstanding9,256,249 shares of common stock, $0.001 par value.

 

 

   

 

 

TABLE OF CONTENTS

 

PART I.FINANCIAL INFORMATION3
   
ITEM 1.FINANCIAL STATEMENTS3
   
 CONDENSED CONSOLIDATED BALANCE SHEETS AT DECEMBER 31, 20182019 (UNAUDITED) AND MARCH 31, 201820193
   
 CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS FOR THE THREE AND NINE MONTH PERIODS ENDED DECEMBER 31, 20182019 AND 20172018 (UNAUDITED)4
CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY FOR THE THREE AND NINE MONTHS ENDED DECEMBER 31, 2019 AND 2018 (UNAUDITED)5
   
 CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS FOR THE NINE MONTHS ENDED DECEMBER 31, 20182019 AND 20172018 (UNAUDITED)57
   
 NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED)68
   
ITEM 2.MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS1821
   
ITEM 3.QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK2430
   
ITEM 4.CONTROLS AND PROCEDURES2431
   
PART II.OTHER INFORMATION2532
   
ITEM 1.LEGAL PROCEEDINGS2532
   
ITEM 1A.RISK FACTORS2532
   
ITEM 2.UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS2534
   
ITEM 3.DEFAULTS UPON SENIOR SECURITIES2534
   
ITEM 4.MINE SAFETY DISCLOSURES2534
   
ITEM 5.OTHER INFORMATION2534
   
ITEM 6.EXHIBITS2635

 

 

 

 2 

 

 

PART I. FINANCIAL INFORMATION

 

ITEM 1. CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

 

AETHLON MEDICAL, INC. AND SUBSIDIARY

CONDENSED CONSOLIDATED BALANCE SHEETS

 

  December 31,
2018
  March 31,
2018
 
  (Unaudited)     
ASSETS        
Current assets        
Cash $4,824,901  $6,974,070 
Accounts receivable     74,813 
Prepaid expenses and other current assets  35,067   181,367 
Total current assets  4,859,968   7,230,250 
         
Property and equipment, net  9,669   27,552 
Patents, net  68,959   75,832 
Deposits  12,159   18,270 
Total assets $4,950,755  $7,351,904 
         
LIABILITIES AND STOCKHOLDERS’ EQUITY        
         
Current liabilities        
Accounts payable $69,613  $124,450 
Due to related parties  69,750   90,366 
Convertible notes payable, net  932,014    
Other current liabilities  709,348   263,141 
Total current liabilities  1,780,725   477,957 
         
Convertible notes payable, net     841,153 
         
Total liabilities  1,780,725   1,319,110 
         
Commitments and Contingencies (Note 13)        
         
Stockholders’ Equity        
Common stock, par value $0.001 per share; 30,000,000 shares authorized as of December 31, 2018 and March 31, 2018; 18,577,123 and 17,739,511 shares issued and outstanding as of December 31, 2018 and March 31, 2018, respectively  18,577   17,740 
Additional paid-in capital  107,283,829   105,574,014 
Accumulated deficit  (104,010,327)  (99,457,714)
Total Aethlon Medical, Inc. stockholders’ equity before noncontrolling interests  3,292,079   6,134,040 
         
Noncontrolling interests  (122,049)  (101,246)
         
Total stockholders’ equity  3,170,030   6,032,794 
         
Total liabilities and stockholders’ equity $4,950,755  $7,351,904 

  December 31,
2019
  March 31,
2019
 
  (Unaudited)     
ASSETS        
Current assets        
Cash $4,058,653  $3,828,074 
Accounts receivable  206,729    
Prepaid expenses and other current assets  40,351   210,042 
Total current assets  4,305,733   4,038,116 
         
Property and equipment, net  144,966   6,021 
Right-of-use lease asset  159,838    
Patents, net  59,795   66,668 
Deposits  12,159   12,159 
Total assets $4,682,491  $4,122,964 
         
LIABILITIES AND STOCKHOLDERS’ EQUITY        
         
Current liabilities        
Accounts payable $327,408  $131,931 
Due to related parties  111,212   83,654 
Convertible notes payable, net     962,301 
Deferred revenue  100,000    
Lease liability, current portion  96,712    
Other current liabilities  175,282   646,000 
Total current liabilities  810,614   1,823,886 
         
Lease liability, less current portion  67,695    
Total liabilities  878,309   1,823,886 
         
Commitments and Contingencies (Note 13)        
         
Stockholders’ Equity        
Common stock, par value $0.001 per share; 30,000,000 shares authorized; 4,779,614 and 1,266,979 shares issued and outstanding as of December 31, 2019 and March 31, 2019, respectively  4,781   1,267 
Additional paid-in capital  114,172,714   108,076,275 
Accumulated deficit  (110,243,475)  (105,652,433)
Total Aethlon Medical, Inc. stockholders’ equity before noncontrolling interests  3,934,020   2,425,109 
         
Noncontrolling interests  (129,838)  (126,031)
         
Total stockholders’ equity  3,804,182   2,299,078 
         
Total liabilities and stockholders’ equity $4,682,491  $4,122,964 

 

 

See accompanying notes.

 

 

 

 3 

 

 

AETHLON MEDICAL, INC. AND SUBSIDIARY

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

For the Three and Nine Month Periods Ended December 31, 20182019 and 20172018

(Unaudited)

 

 

  Three Months
Ended
December 31,
2018
  Three Months
Ended
December 31,
2017
  Nine Months
Ended
December 31,
2018
  Nine Months
Ended
December 31,
2017
 
             
REVENUES                
                 
Government contract revenue $  $74,813  $149,625  $74,813 
                 
OPERATING EXPENSES                
                 
Professional fees  587,192   439,117   1,449,218   1,165,318 
Payroll and related expenses  1,161,531   663,245   2,426,828   1,911,553 
General and administrative  215,150   136,078   681,678   557,991 
Total operating expenses  1,963,873   1,238,440   4,557,724   3,634,862 
OPERATING LOSS  (1,963,873)  (1,163,627)  (4,408,099)  (3,560,049)
                 
OTHER EXPENSE                
Interest and other debt expenses  55,107   55,912   165,317   306,495 
Loss on share for warrant exchanges           130,214 
Loss on debt extinguishment           376,909 
Total other expense  55,107   55,912   165,317   813,618 
NET LOSS  (2,018,980)  (1,219,539)  (4,573,416)  (4,373,667)
                 
LOSS ATTRIBUTABLE TO NONCONTROLLING INTERESTS  (5,940)  (4,532)  (20,803)  (12,972)
                 
NET LOSS ATTRIBUTABLE TO AETHLON MEDICAL, INC. $(2,013,040) $(1,215,007) $(4,552,613) $(4,360,695)
                 
BASIC AND DILUTED LOSS PER COMMON SHARE $(0.11) $(0.08) $(0.25) $(0.40)
                 
WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING – BASIC AND DILUTED  18,050,165   14,950,701   17,865,176   10,927,106 

  Three Months
Ended
December 31,
2019
  Three Months
Ended
December 31,
2018
  Nine Months
Ended
December 31,
2019
  Nine Months
Ended
December 31,
2018
 
             
REVENUES                
                 
Government contract revenue $413,458  $  $443,458  $149,625 
                 
OPERATING EXPENSES                
                 
Professional fees  609,933   587,192   1,979,848   1,449,218 
Payroll and related expenses  406,421   1,161,531   1,609,942   2,426,828 
General and administrative  273,510   215,150   998,465   681,678 
Total operating expenses  1,289,864   1,963,873   4,588,255   4,557,724 
OPERATING LOSS  (876,406)  (1,963,873)  (4,144,797)  (4,408,099)
                 
OTHER (INCOME) EXPENSE                
Interest and other debt expenses  126   55,107   54,232   165,317 
(Gain) on share for warrant exchanges  (55,593)     (51,190)   
Loss on debt extinguishment        447,011    
Total other (income) expense  (55,467)  55,107   450,053   165,317 
NET LOSS  (820,939)  (2,018,980)  (4,594,850)  (4,573,416)
                 
LOSS ATTRIBUTABLE TO NONCONTROLLING INTERESTS  (1,358)  (5,940)  (3,808)  (20,803)
                 
NET LOSS ATTRIBUTABLE TO AETHLON MEDICAL, INC. $(819,581) $(2,013,040) $(4,591,042) $(4,552,613)
                 
BASIC AND DILUTED LOSS PER COMMON SHARE $(0.28) $(1.67) $(2.52) $(3.82)
                 
WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING – BASIC AND DILUTED  2,887,883   1,203,344   1,821,557   1,191,012 

 

 

See accompanying notes.

 

 

 

 4 

AETHLON MEDICAL, INC. AND SUBSIDIARY

CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

For the Three and Nine Months Ended December 31, 2019 and 2018

(Unaudited)

  ATTRIBUTABLE TO AETHLON MEDICAL, INC.       
  COMMON STOCK  ADDITIONAL PAID IN  ACCUMULATED  NON-
CONTROLLING
  TOTAL 
  SHARES  AMOUNT  CAPITAL  DEFICIT  INTERESTS  EQUITY 
                   
BALANCE - MARCH 31, 2019  1,266,979  $1,267  $108,076,275  $(105,652,433) $(126,031) $2,299,078 
                         
Issuances of common stock for cash under at the market program  3,087   3   36,619         36,622 
                         
Loss on debt extinguishment        447,011         447,011 
                         
Issuance of common shares upon vesting of restricted stock units  3,539   4   (23,775)        (23,771)
                ��        
Stock-based compensation expense        326,536         326,536 
                         
Net loss           (2,066,424)  (860)  (2,067,284)
                         
BALANCE - JUNE 30, 2019  1,273,605  $1,274  $108,862,666  $(107,718,857)  (126,891) $1,018,192 
                         
Issuances of common stock for cash under the market program  59,340   60   386,552         386,612 
                         
Issuance of common shares upon vesting of restricted stock units  3,236   4   (8,448)        (8,444)
                         
Issuances of common stock upon warrant exchanges  1,078   1   4,402         4,403 
                         
Stock-based compensation expense        326,536         326,536 
                         
Net loss           (1,705,037)  (1,589)  (1,706,626)
                         
BALANCE - SEPTEMBER 30, 2019  1,337,259  $1,339  $109,571,708  $(109,423,894) $(128,480) $20,673 
                         
                         
Proceeds from the issuance of common stock, net  3,432,056   3,432   4,560,802         4,564,234 
                         
Issuance of common shares upon vesting of restricted stock units  3,439   3   (6,772)        (6,769)
                         
Issuances of common stock upon warrant exchanges  2,914   3   (55,596)        (55,593)
                         
Par value of DTC roundup of shares following reverse split  3,946   4   (4)         
                         
Stock-based compensation expense        102,576         102,576 
                         
Net loss           (819,581)  (1,358)  (820,939)
                         
BALANCE - DECEMBER 31, 2019  4,779,614  $4,781  $114,172,714  $(110,243,475) $(129,838) $3,804,182 

Continued on following page

5

AETHLON MEDICAL, INC. AND SUBSIDIARY

CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

For the Three and Nine Months Ended December 31, 2019 and 2018, Continued
(Unaudited)

  ATTRIBUTABLE TO AETHLON MEDICAL, INC.       
  COMMON STOCK  ADDITIONAL PAID IN  ACCUMULATED  NON-
CONTROLLING
  TOTAL 
  SHARES  AMOUNT  CAPITAL  DEFICIT  INTERESTS  EQUITY 
                         
BALANCE - MARCH 31, 2018  1,182,634  $1,183  $105,590,571  $(99,457,714) $(101,246) $6,032,794 
                         
Issuance of common shares upon vesting of restricted stock units  1,446   1   (32,738)        (32,737)
                         
Stock-based compensation expense        263,162         263,162 
                         
Net loss           (1,146,228)  (6,148)  (1,152,376)
                         
BALANCE - JUNE 30, 2018  1,184,080  $1,184  $105,820,995  $(100,603,942) $(107,394) $5,110,843 
                         
Issuance of common shares upon vesting of restricted stock units  3,897   4   (53,036)        (53,032)
                         
Common stock issued for services  1,000   1   19,349         19,350 
                         
Stock-based compensation expense        336,496         336,496 
                         
Net loss           (1,393,345)  (8,715)  (1,402,060)
                         
BALANCE - SEPTEMBER 30, 2018  1,188,977  $1,189  $106,123,804  $(101,997,287) $(116,109) $4,011,597 
                         
Proceeds from the issuance of common stock, net  45,622   45   883,452         883,497 
                         
Issuance of common shares upon vesting of restricted stock units  3,889   4   (50,943)        (50,939)
                         
Stock-based compensation expense        344,854         344,854 
                         
Net loss           (2,013,040)  (5,940)  (2,018,980)
                         
BALANCE - DECEMBER 31, 2018  1,238,488  $1,238  $107,301,167  $(104,010,327) $(122,049) $3,170,029 

See accompanying notes.

6

 

 

AETHLON MEDICAL, INC. AND SUBSIDIARY

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

For the Nine Months Ended December 31, 20182019 and 20172018

(Unaudited)

 

 

 Nine Months
Ended
December 31, 2018
 Nine Months
Ended
December 31, 2017
  Nine Months
Ended
December 31, 2019
 Nine Months
Ended
December 31, 2018
 
Cash flows from operating activities:        
     
Cash flows used in operating activities:        
Net loss $(4,573,416) $(4,373,667) $(4,594,850) $(4,573,416)
Adjustments to reconcile net loss to net cash used in operating activities:                
Depreciation and amortization  24,756   27,402   15,992   24,756 
Stock based compensation  944,512   887,607   755,648   944,512 
Loss on debt extinguishment  447,011    
Gain on share for warrant exchanges  (51,190)   
Amortization of debt discount  30,287   90,861 
Common stock issued for services  19,350   33,600      19,350 
Loss on share for warrant exchanges     130,214 
Loss on debt extinguishment     376,909 
Amortization of debt discount  90,861   215,376 
Non-cash rent expense  68,856    
Changes in operating assets and liabilities:                
Accounts receivable  74,813      (206,729)  74,813 
Prepaid expenses and other current assets  152,411   23,014   169,691   152,411 
Accounts payable and other current liabilities  391,369   (219,806)  (271,533)  391,369 
Deferred revenue  100,000    
Lease liability  (67,994)   
Due to related parties  (20,616)  6,600   27,558   (20,616)
Net cash used in operating activities  (2,895,960)  (2,892,751)  (3,577,253)  (2,895,960)
                
Cash flows from investing activities:        
Cash flows used in investing activities:        
Purchases of property and equipment     (23,705)  (148,064)   
Net cash used in investing activities     (23,705)  (148,064)   
                
Cash flows from financing activities:        
Cash flows provided by (used in) financing activities:        
Proceeds from the issuance of common stock, net  883,500   7,166,081   4,987,468   883,500 
Principal payments on convertible notes  (992,591)   
Tax withholding payments or tax equivalent payments for net share settlement of restricted stock units  (136,709)  (198,527)  (38,981)  (136,709)
Net cash provided by financing activities  746,791   6,967,554 
Net provided by financing activities  3,955,896   746,791 
                
Net (decrease) increase in cash  (2,149,169)  4,051,098 
Net increase (decrease) in cash  230,579   (2,149,169)
                
Cash at beginning of period  6,974,070   1,559,701   3,828,074   6,974,070 
                
Cash at end of period $4,824,901  $5,610,799  $4,058,653  $4,824,901 
                
Supplemental disclosures of cash flow information:                
                
Cash paid during the period for:                
                
Interest $95,388  $  $83,332  $95,388 
                
Supplemental disclosures of non-cash investing and financing activities:                
Issuance of shares under conversions of convertible notes payable and related accrued interest $  $362,765 
Issuance of shares from vesting of restricted stock units $138  $120 
Initial recognition of right-of-use lease asset and lease liability $228,694  $ 
Par value of shares issued for vested restricted stock units $10  $138 
Par value of shares issued for round up following reverse split $4  $ 

 

 

See accompanying notes.

 

 

 57 

 

 

AETHLON MEDICAL, INC. AND SUBSIDIARY

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED)

December 31, 20182019

 

 

1. NATURE OF BUSINESS AND BASIS OF PRESENTATION

 

ORGANIZATION

 

Aethlon Medical, Inc. and its subsidiary (collectively, “Aethlon”, the “Company”, “we” or “us”), is a medical device technology company focused on addressing unmet needs in global healthdeveloping products to diagnose and biodefense.treat life and organ threatening diseases. The Aethlon Hemopurifier® is a clinical-stage immunotherapeutic device designed to combat cancer and life-threatening viral infections. In cancer, the Hemopurifier depletesis designed to deplete the presence of circulating tumor-derived exosomes that promote immune suppression, seed the spread of metastasis and inhibit the benefit of leading cancer therapies. The U.S. Food and Drug Administration, (FDA)or FDA, has designated the Hemopurifier as a "Breakthrough Device" related to the following“Breakthrough Device” for two independent indications:

 

·the treatment of individuals with advanced or metastatic cancer who are either unresponsive to or intolerant of standard of care therapy, and with cancer types in which exosomes have been shown to participate in the development or severity of the disease; and

·the treatment of life-threatening viruses that are not addressed with approved therapies.

We believe the Hemopurifier can be a substantial advance in the treatment of life-threatening virusespatients with advanced and metastatic cancer through the clearance of exosomes that promote the growth and spread of tumors through multiple mechanisms. We are not addressedcurrently preparing for the initiation of clinical trials in patients with approved therapies;advanced and

metastatic cancers. We are initially focused on the treatment of individualssolid tumors, including head and neck cancer, gastrointestinal cancers and other cancers.

On October 4, 2019, the FDA approved our Investigational Device Exemption, or IDE, application to initiate an Early Feasibility Study, or EFS, of the Hemopurifier in patients with advanced or metastatichead and neck cancer who are either unresponsive to or intolerant ofin combination with standard of care therapy,pembrolizumab (Keytruda).  The primary endpoint for the EFS, which will enroll 10-12 subjects at a single center, will be safety, with secondary endpoints including measures of exosome clearance and with cancer types in which exosomes have been shown to participate in the development or severity of the disease.

characterization, as well as response and survival rates.

 

We also believe the Hemopurifier can be a part of the broad-spectrum treatment of life-threatening highly glycosylated, or carbohydrate coated, viruses that are not addressed with an already approved treatment countermeasure objective set forth by the U.S. Government to protect citizens from bioterror and pandemic threats.treatment. In small-scale or early feasibility human studies, the Hemopurifier has been administeredused to treat individuals infected with HIV, hepatitis-C, and Ebola. Additionally,in vitro, the Hemopurifier has been validateddemonstrated to capture Zika virus, Lassa virus, MERS-CoV, cytomegalovirus, Epstein-Barr virus, Herpes simplex virus, Chikungunya virus, Dengue virus, West Nile virus, smallpox-related viruses, H1N1 swine flu virus, H5N1 bird flu virus, and the reconstructed Spanish flu virus of 1918. In several cases, these validationsstudies were conducted in collaboration with leading government or non-government research institutes. Domestically, we are focused on the clinical advancement of the Hemopurifier through investigational device exemptions (IDEs) approved by the FDA. We recently concluded a feasibility study to demonstrate the safety of our device in health-compromised individuals infected with a viral pathogen.

 

We are also the majority owner of Exosome Sciences, Inc. (ESI), or ESI, a company focused on the discovery of exosomal biomarkers to diagnose and monitor life-threatening diseases. Included among ESI’s endeavorsactivities is the advancement of a TauSomeTMTauSome™ biomarker candidate to diagnose chronic traumatic encephalopathy, (CTE)or CTE, in the living. ESI previously documented TauSome levels in former NFL players to be nine times higher than same age-group control subjects. Through ESI, we are also developing exosome based biomarkers in patients with, or at risk for, a number of cancers. We consolidate ESI’s activities in our consolidated financial statements.

We also have a cross-licensing and development agreement with SeaStar Medical, Inc., focused on co-development of our Hemopurifier cartridge with SeaStar’s proprietary cartridges and the development of a closed system for the Hemopurifier using the SeaStar pump and cassettes. This collaboration may allow the deployment of the Hemopurifier into settings that lack dialysis infrastructure, such as chemotherapy infusion centers and field operations for life threatening viral epidemics.

8

 

Successful outcomes of human trials will also be required by the regulatory agencies of certain foreign countries where we intendplan to sell the Hemopurifier. Some of our patents may expire before FDA approval or approval in a foreign country, if any, is obtained. However, we believe that certain patent applications and/or other patents issued more recently will help protect the proprietary nature of the Hemopurifier treatment technology.

 

Our executive offices are located at 9635 Granite Ridge Drive, Suite 100, San Diego, California 92123. Our telephone number is (858) 459-7800. Our website address iswww.aethlonmedical.com. www.aethlonmedical.com.

 

Our common stock is listed on the Nasdaq Capital Market under the symbol “AEMD.”

 

REVERSE STOCK SPLIT

On October 14, 2019, the Company completed a 1-for-15 reverse stock split. Accordingly, 15 shares of outstanding common stock then held by stockholders were combined into one share of common stock. Any fractional shares resulting from the reverse split were rounded up to the next whole share. Authorized common stock remained at 30,000,000 shares (see Note 14). The accompanying unaudited condensed consolidated financial statements and accompanying notes have been retroactively revised to reflect such reverse stock split as if it had occurred on April 1, 2018. All shares and per share amounts have been revised accordingly.

SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

During the nine months ended December 31, 2018,2019, there have beenwere no changes to our significant accounting policies as described in our Annual Report on Form 10-K for the fiscal year ended March 31, 2018.2019, except as described below.

 

Leases

 

At lease commencement, the Company records a lease liability based on the present value of lease payments over the expected lease term. The Company calculates the present value of lease payments using the discount rate implicit in the lease, unless that rate cannot be readily determined. In that case, the Company uses its incremental borrowing rate, which is the rate of interest that the Company would have to pay to borrow on a collateralized basis an amount equal to the lease payments over the expected lease term. The Company records a corresponding right-of-use lease asset based on the lease liability, adjusted for any lease incentives received and any initial direct costs paid to the lessor prior to the lease commencement date.

6

 

After lease commencement, the Company measures its leases as follows: (i) the lease liability based on the present value of the remaining lease payments using the discount rate determined at lease commencement; and (ii) the right-of-use lease asset based on the remeasured lease liability, adjusted for any unamortized lease incentives received, any unamortized initial direct costs and the cumulative difference between rent expense and amounts paid under the lease agreement. Rent expense is recorded on a straight-line basis over the expected lease term (See Note 4).

Basis of Presentation and Use of Estimates

 

The accompanying unaudited condensed consolidated financial statements of the Company have been prepared in accordance with U.S. generally accepted accounting principles (GAAP) for interim financial information and with the instructions to Form 10-Q and Article 8 of the Securities and Exchange Commission (SEC) Regulation S-X. Accordingly, they should be read in conjunction with the audited financial statements and notes thereto for the fiscal year ended March 31, 2018,2019, included in the Company's Annual Report on Form 10-K filed with the SEC on June 8, 2018.July 1, 2019. The accompanying unaudited condensed consolidated financial statements include the accounts of Aethlon Medical, Inc. and its majority-owned subsidiary. All significant inter-company transactions and balances have been eliminated in consolidation. The unaudited condensed consolidated financial statements contain all normal recurring accruals and adjustments that, in the opinion of management, are necessary to present fairly the condensed consolidated financial statements as of and for the three and nine months ended December 31, 2018,2019, and the condensed consolidated statement of cash flows for the nine months ended December 31, 2018.2019. Estimates were made relating to useful lives of fixed assets, impairment of assets, share-based compensation expense and accruals for clinical trial and research and development expenses. Actual results could differ materially from those estimates. The accompanying condensed consolidated balance sheet at March 31, 20182019 has been derived from the audited consolidated balance sheet at March 31, 2018,2019, contained in the above referenced 10-K. The results of operations for the three and nine months ended December 31, 20182019 are not necessarily indicative of the results to be expected for the full year or any future interim periods.

 

9

Reclassifications

Certain prior year balances within the unaudited condensed consolidated financial statements have been reclassified to conform to the current year presentation.

LIQUIDITY AND GOING CONCERN

 

Management expects existing cash as of December 31, 20182019, together with cash raised in January 2020 to be sufficient to fund the Company’s operations for at least twelve months from the issuance date of these condensed consolidated financial statements.

  

2. LOSS PER COMMON SHARE

 

Basic loss per share is computed by dividing net loss by the weighted average number of common shares outstanding during the period of computation. The weighted average number of common shares outstanding for the three and nine months ended December 31, 2019 and 2018 included common shares underlying 215 and 2017 included 46,1253,075 vested restricted stock units.units, respectively. Diluted loss per share is computed similar to basic loss per share, except that the denominator is increased to include the number of additional dilutive common shares that would have been outstanding if potential common shares had been issued, if such additional common shares were dilutive. Since we had net losses for all periods presented, basic and diluted loss per share are the same, and additional potential common shares have been excluded, as their effect would be antidilutive.

 

As of December 31, 2019 and 2018, an aggregate of 3,779,301 and 2017, a total of 6,886,020 and 9,143,480459,068 potential common shares, respectively, consisting of shares underlying outstanding stock options, warrants and unvested restricted stock units, and convertible notes payable, were excluded, as their inclusion would be antidilutive.

  

3. RESEARCH AND DEVELOPMENT EXPENSES

 

Our research and development costs are expensed as incurred. We incurred research and development expenses during the three and nine month periods ended December 31, 20182019 and 2017,2018, which are included in various operating expense line items in the accompanying condensed consolidated statements of operations. Our research and development expenses in those periods were as follows:

 

 December 31, December 31,  December 31, December 31, 
 2018 2017  2019 2018 
Three months ended $243,843  $129,207  $218,571  $243,843 
Nine months ended $655,760  $462,640  $692,022  $655,760 

  

4. FUTURE ACCOUNTING PRONOUNCEMENTSRecent Accounting Pronouncements

 

The Company adopted ASU 2016-02, Leases (Topic 842) changesTopic 842 on April 1, 2019 utilizing the existing accounting standardsalternative transition method allowed for under this guidance. As a result, the Company recorded lease accounting, including requiring lessees toliabilities and right-of-use lease assets of $228,694 on its balance sheet as of April 1, 2019. The lease liabilities represent the present value of the remaining lease payments of the Company’s corporate headquarters lease (see Note 13), discounted using the Company’s incremental borrowing rate as of April 1, 2019. The corresponding right-of-use lease assets are recorded based on the lease liabilities and the cumulative difference between rent expense and amounts paid under its corporate headquarters lease. The Company also elected the short-term lease recognition exemption for its laboratory lease. For the laboratory lease that qualified as short-term, the Company did not recognize most leases on their balance sheets and making targeted changes to lessor accounting. ASU 2016-02 is effective for annual periods beginning after December 15, 2018, including interim periods within those fiscal years. EarlyROU assets or lease liabilities at adoption. The adoption of ASU 2016-02 asdid not have a material impact on either the statement of its issuance is permitted. We are evaluatingoperations or statement of cash flows for the impact the adoption of ASU 2016-02 will have on our financial statements and disclosures.nine months ended December 31, 2019.

   

 

 

 710 

 

Topic 842 also allows lessees and lessors to elect certain practical expedients. The Company elected the following practical expedients:

·Transitional practical expedients, which must be elected as a package and applied consistently to all of the Company’s leases:

°The Company need not reassess whether any expired or existing contracts are or contain leases.
°The Company need not reassess the lease classification for any expired or existing leases (that is, all existing leases that were classified as operating leases in accordance with the previous guidance will be classified as operating leases, and all existing leases that were classified as capital leases in accordance with the previous guidance will be classified as finance leases).
°The Company need not reassess initial direct costs for any existing leases.

·Hindsight practical expedient. The Company elected the hindsight practical expedient in determining the lease term (that is, when considering lessee options to extend or terminate the lease and to purchase the underlying asset) and in assessing impairment of the Company’s right-of-use assets.

  

5. CONVERTIBLE NOTES PAYABLE, NET

In July 2019, we paid off our Convertible Notes Payable. We paid the remaining principal balance of $892,591 and accrued interest of $11,352. As a result, we did not incur any interest expense related to the Convertible Notes in the three months ended December 31, 2019.

For the nine months ended December 31, 2019, we recorded interest expense of $23,759 related to the contractual interest rates of our Convertible Notes and interest expense of $30,287 related to the amortization of the note discount for a total interest expense of $54,046 related to our Convertible Notes.

 

Convertible Notes Payable, Net consisted of the following at DecemberMarch 31, 2018:2019:

 

 Principal Unamortized
Discount
 Net
Amount
 Accrued
Interest
  Principal Unamortized
Discount
 Net
Amount
 Accrued
Interest
 
Convertible Notes Payable, Net:                                
November 2014 10% Convertible Notes (due July 1, 2019) $612,811  $(37,399) $575,412  $21,987  $612,811  $(18,701) $594,110  $37,309 
December 2016 10% Convertible Notes (due July 1, 2019)  379,780   (23,178)  356,602   12,771   379,780   (11,589)  368,191   22,264 
Total Convertible Notes Payable, Net $992,591  $(60,577) $932,014  $34,758  $992,591  $(30,290) $962,301  $59,573 

 

During the nine months ended December 31, 2018, we recorded interest expense of $74,445 related to the contractual interest rates of our convertible notesConvertible Notes and interest expense of $90,861 related to the amortization of the note discount for a total interest expense of $165,306 related to our convertible notesConvertible Notes in the nine months ended December 31, 2018. All of the unamortized discount at December 31, 2018 related to the note discount established upon the June 2017 amendment to the November 2014 10% Convertible Notes and to the December 2016 10% Convertible Notes (see below).

Convertible Notes Payable, Net consisted of the following at March 31, 2018:

  Principal  Unamortized
Discount
  Net
Amount
  Accrued
Interest
 
Convertible Notes Payable, Net – Non-Current Portion:                
November 2014 10% Convertible Notes (due July 1, 2019) $612,811  $(93,590) $519,221  $34,386 
December 2016 10% Convertible Notes (due July 1, 2019)  379,780   (57,848)  321,932   21,315 
Total Convertible Notes Payable, Net $992,591  $(151,438) $841,153  $55,701 

During the nine months ended December 31, 2017, we recorded interest expense of $87,641 related to the contractual interest rates of our convertible notes and interest expense of $215,376 related to the amortization of the note discount for a total interest expense of $303,017 related to our convertible notes. All of the unamortized discount at December 31, 2017 related to the note discount established upon the June 2017 amendment to both the November 2014 10% Convertible Notes and the December 2016 10% Convertible Notes (see below).

NOVEMBER 2014 10% CONVERTIBLE NOTES

In November 2014, we entered into a subscription agreement with two accredited investors providing for the issuance and sale of (i) convertible promissory notes in the aggregate principal amount of $527,780 (the “Notes”) and (ii) five year warrants to purchase up to 47,125 shares of common stock at a fixed exercise price of $8.40 per share (the “Warrants”). These Notes bear interest at the annual rate of 10% and originally matured on April 1, 2016.

The aggregate gross cash proceeds to us were $415,000 after subtracting legal fees of $35,000, a $27,780 due diligence fee and an original issuance discount of $50,000. We recorded deferred financing costs of $112,780 to reflect the legal fees, due diligence fee and original issuance discount and will amortize those costs over the life of the Notes using the effective interest method.

These Notes were originally convertible at the option of the holders into shares of our common stock at a fixed price of $5.60 per share, for up to an aggregate of 94,246 shares of common stock. There are no registration requirements with respect to the shares of common stock underlying the Notes or the Warrants.

The estimated relative fair value of the Warrants issued in connection with the Notes was recorded as a debt discount and is amortized as additional interest expense over the term of the underlying debt. We recorded debt discount of $240,133 based on the relative fair value of these Warrants. In addition, as the effective conversion price of the Notes was less than market price of the underlying common stock on the date of issuance, we recorded an additional debt discount of $287,647 related to the beneficial conversion feature.

8

Initial Amendment of the November 2014 10% Convertible Note Terms

On November 12, 2015, we entered into an amendment of terms (“Amendment of Terms”) with the two investors that participated in the November 2014 10% Convertible Notes. The Amendment of Terms modified the terms of the subscription agreement, Notes and Warrants held by those investors to, among other things, extended the maturity date of the Notes from April 1, 2016 to June 1, 2016, temporarily reduced the number of shares that we must reserve with respect to conversion of the Notes, and temporarily suspended the time period during which one of the investors may exercise its Warrants. In exchange for the investors’ agreements in the Amendment of Terms, we paid one of the investors a cash fee of $90,000, which we recorded as deferred financing costs and amortized over the remaining term of the Notes.

Second Amendment and Extension of the November 2014 10% Convertible Notes

On June 27, 2016, we and certain investors entered into further amendments (the “Amendments”) to the Notes and the Warrants. The Amendments provide that the maturity date was extended from June 1, 2016 to July 1, 2017 and that the conversion price per share of the Notes was reduced from $5.60 per share of common stock to $5.00 per share of common stock. In addition, we reduced the exercise price set forth in the Warrants from $8.40 per share to $5.00 per share of common stock. In connection with these modifications, each of the investors signed a Consent and Waiver providing its consent under certain restrictive provisions, and waiving certain rights, including a right to participate in certain offerings made by us, under a Securities Purchase Agreement dated June 23, 2015 (the “2015 SPA”) to which we, the investors and certain other investors are parties, in order to facilitate an at-the-market equity program.

The Amendments also increased the principal amount of the Notes to $692,811 (in the aggregate) to (i) include accrued and unpaid interest through June 15, 2016, and (ii) increase the principal amount by $80,000 (in the aggregate) as an extension fee for the extended maturity date of the Notes. With respect to each Note, we entered into an Allonge to Convertible Promissory Note (each, an “Allonge”) reflecting the changes in the principal amount, maturity date and conversion price of the Note.

We also issued to the investors new warrants (the “New Warrants”) to purchase an aggregate of 30,000 shares of common stock with an exercise price of $5.00 per share of common stock. We issued the New Warrants in substantially the same form as the prior Warrants, and the New Warrants will expire on November 6, 2019, the same date on which the prior Warrants will expire.

The modification of the Notes was evaluated under FASB Accounting Standards Codification (“ASC”) Topic No. 470-50-40, “Debt Modification and Extinguishments” (“ASC 470-50-40”). Therefore, according to the guidance, the instruments were determined to be substantially different, and the transaction qualified for extinguishment accounting. As a result, we recorded a loss on debt extinguishment of $536,889 and recognized an extension fee expense of $80,000, which are included in other (income) expenses in the accompanying condensed consolidated statements of operations. The debt extinguishment is comprised from the fair value of prior warrants issued in connection with the Notes of $287,676, as well as $325,206 related to beneficial conversion feature and offset by debt discount of $75,993. The beneficial conversion feature is a result of the effective conversion price of the new Notes being less than the market price of the underlying common stock on the date of modification.

Third Amendment and Extension of the November 2014 10% Convertible Notes

In connection with the issuance of the December 2016 10% Convertible Notes, the conversion price of the Notes was reduced from $5.00 to $4.00 per share and the maturity date of the Notes was extended from July 1, 2017 to July 1, 2018.

The modification of the Notes was evaluated under ASC 470-50-40 and the instruments were determined to be substantially different, and the transaction qualified for extinguishment accounting. As a result, we recorded a gain on debt extinguishment of $58,691, which is included in other (income) expenses in the accompanying condensed consolidated statements of operations. The recording of the modified Notes resulted in a beneficial conversion of $233,748 which is the result of the effective conversion price of the new Notes being less than the market price of the underlying common stock on the date of modification.

9

June 2017 Amendment to the November 2014 10% Convertible Notes

In June 2017, we agreed with the holders of the Notes to an extension of the maturity dates of the Notes from July 1, 2018 to July 1, 2019 in exchange for the reduction of the conversion price of those Notes from $4.00 per share to $3.00 per share. The modification of the Notes was evaluated under ASC 470-50-40 and the instruments were determined to be substantially different, and the transaction qualified for extinguishment accounting. Under the extinguishment accounting we recorded a loss on debt extinguishment of $178,655 and recalculated a revised debt discount on the notes.

The following table shows the changes to the principal balance of the Notes:

Activity in Notes    
Initial principal balance $527,780 
Increase in principal balance under the second amendment (see above)  165,031 
Conversions during the fiscal year ended March 31, 2017  (80,000)
Balance as of December 31, 2018 and March 31, 2018 $612,811 

DECEMBER 2016 10% CONVERTIBLE NOTES

In December 2016, we entered into a securities purchase agreement (the “Securities Purchase Agreement”) with two accredited investors (collectively, the “Holders”), pursuant to which the Holders purchased an aggregate of $680,400 principal amount of December 2016 10% Convertible Notes (December 2016 Notes) (inclusive of due diligence fee of $30,000 deemed paid as a subscription amount in the form of a note in the principal amount of $32,400) for an aggregate cash subscription amount of $600,000 and (b) warrants to purchase 127,575 shares of common stock (collectively, the “December 2016 Warrants”).

The December 2016 Notes bear interest at the rate of 10% per annum, and the principal amount and all accrued and unpaid interest thereon is convertible into shares of our common stock at a $4.00 per share conversion price, which is subject to customary adjustment provisions for stock splits, dividends, recapitalizations and the like. The December 2016 Notes mature on July 1, 2018 and are subject to customary and usual terms for events of default and the like. Each Holder has contractually agreed to restrict its ability to convert its December 2016 Note such that the number of shares of the common stock held by the Holder and its affiliates after such exercise does not exceed 4.99% of our then issued and outstanding shares of common stock.

The December 2016 Warrants issued to the Holders are exercisable for a period of five years from the date of issuance at an exercise price of $4.50, subject to adjustment. A Holder may exercise a December 2016 Warrant by paying the exercise price in cash or by exercising the December 2016 Warrant on a cashless basis. In the event a Holder exercises a December 2016 Warrant on a cashless basis, we will not receive any proceeds. The exercise price of the December 2016 Warrants is subject to customary adjustments provision for stock splits, stock dividends, recapitalizations and the like. Each Holder has contractually agreed to restrict its ability to exercise its December 2016 Warrant such that the number of shares of the common stock held by the Holder and its affiliates after such exercise does not exceed 4.99% of our then issued and outstanding shares of common stock.

The estimated relative fair value of December 2016 Warrants issued in connection with the December 2016 Notes was recorded as a debt discount and is being amortized as additional interest expense over the term of the underlying debt. We recorded debt discount of $232,718 based on the relative fair value of these December 2016 Warrants. In addition, as the effective conversion price of the December 2016 Notes was less than market price of the underlying common stock on the date of issuance, we recorded an additional debt discount of $262,718 related to the beneficial conversion feature. We also recorded deferred financing costs of $102,940, which was composed of an 8% original issue discount of $50,400, a $30,000 due diligence fee (which was paid in the form of a note), $22,500 in legal fees, and a $40 bank charge. The combination of the above items led to a combined discount against the December 2016 Notes of $598,376.

June 2017 Amendment to the December 2016 10% Convertible Notes

In June 2017, we agreed with the Holders of the December 2016 Notes to an extension of the expiration dates of the December 2016 Notes from July 1, 2018 to July 1, 2019 in exchange for the reduction of the conversion price of the December 2016 Notes from $4.00 per share to $3.00 per share. The modification of the December 2016 Notes was evaluated under ASC 470-50-40 and the instruments were determined to be substantially different, and the transaction qualified for extinguishment accounting. Under the extinguishment accounting we recorded a loss on debt extinguishment of $198,254 and recalculated a revised debt discount on the December 2016 Notes.

10

The following table shows the changes to the principal balance of the December 2016 Notes:

Activity in the December 2016 Notes
Initial principal balance $680,400 
Conversions during the fiscal year ended March 31, 2018  (300,620)
Balance as of December 31, 2018 and March 31, 2018 $379,780 

 

6. EQUITY TRANSACTIONS IN THE NINE MONTHS ENDED DECEMBER 31, 20182019

 

Shares Issued for ServicesDecember 2019 Public Offering

 

DuringOn December 13, 2019, we entered into an underwriting agreement with H.C. Wainwright and Co., as representative of the nine months ended December 31, 2018, we issued 15,000several underwriters named therein, relating to the public offering, issuance and sale of 3,333,334 shares of restrictedcommon stock (which includes pre-funded warrants to purchase shares of common stock in lieu thereof), and common warrants to purchase up to an aggregate of 3,333,334 shares of common stock at a public offering price of $1.29$1.50 per share (the “December 2019 Public Offering”). Each share of common stock (or pre-funded warrant in lieu thereof) was sold together with a common warrant to purchase one share of common stock. The common warrants have an exercise price of $1.50 per share, were immediately exercisable, and will expire five years from the market price at timedate of issuance,issuance. The offering closed on December 17, 2019.

11

The gross proceeds of the December 2019 Public Offering were approximately $5 million, prior to deducting underwriting discounts and commissions and estimated offering expenses and excluding the exercise of any common warrants and the underwriter's option to purchase additional securities. The net proceeds from the December 2019 Public Offering were $4,091,437. We intend to use approximately $700,000 of the net proceeds from this offering for the currently planned clinical trials for the Hemopurifier® over the next 12 months, with the remainder for working capital and other general corporate purposes.

Subsequent to the completion of the December 2019 Public Offering and prior to December 31, 2019, all of the holders of pre-funded warrants exercised their pre-funded warrants in paymentfull.

In the event of a Fundamental Transaction (a transfer of ownership of the Company as defined in the common warrants issued in the December 2019 Public Offering) within our control, the holders of the unexercised common stock warrants exercisable for investor relations consulting services. The aggregate value$1.50 per share, are entitled to receive cash consideration equal to a Black-Scholes valuation, as defined in the warrant. If such Fundamental Transaction is not within our control, the warrant holders would only be entitled to receive the same form of this share issuance was $19,350.consideration (and in the same proportion) as the holders of our common stock, hence these warrants are classified as a component of permanent equity.

 

Common Stock Sales Agreement with H.C. Wainwright

 

On June 28, 2016, we entered into a Common Stock Sales Agreement, (the “Agreement”)or the Agreement, with H.C. Wainwright & Co., LLC, (“or H.C. Wainwright”)Wainwright, which established an at-the-market equity program pursuant to which we may offer and sell shares of our common stock from time to time as set forth in the Agreement. The Agreement provides for the sale of shares, or the Shares, of our common stock having an aggregate offering price of up to $12,500,000 (the “Shares”).$12,500,000.

On August 6, 2019, we executed Amendment No. 1 to the Agreement with H.C. Wainwright, effective as of August 5, 2019. The amendment provides that references in the Agreement to the registration statement shall refer to the registration statement on Form S-3 (File No. 333-231397), originally filed with the Securities and Exchange Commission on May 10, 2019, declared effective by the Securities and Exchange Commission on August 1, 2019. We terminated the ATM Prospectus Supplement and suspended any sales under the Sales Agreement on January 17, 2020, but the Sales Agreement remains in full force and effect.

 

Subject to the terms and conditions set forth in the Agreement, H.C. Wainwright willagreed to use its commercially reasonable efforts consistent with its normal trading and sales practices to sell the Shares from time to time, based upon our instructions. We have provided H.C. Wainwright with customary indemnification rights, and H.C. Wainwright will beis entitled to a commission at a fixed rate equal to three percent (3.0%) of the gross proceeds per Share sold. In addition, we agreed to pay certain expenses incurred by H.C. Wainwright in connection with the Agreement, including up to $50,000 of the fees and disbursements of their counsel. The Agreement will terminate upon the sale of all of the Shares under the Agreement, unless terminated earlier by either party as permitted under the Agreement (see Note 14).Agreement.

  

Sales of the Shares, if any, under the Agreement shallwill be made in transactions that are deemed to be “at the market offerings” as defined in Rule 415 under the Securities Act, including sales made by means of ordinary brokers’ transactions, including on the Nasdaq Capital Market, at market prices or as otherwise agreed with H.C. Wainwright. We have no obligation to sell any of the Shares, and, at any time, we may suspend offers under the Agreement or terminate the Agreement.

  

In the nine months ended December 30, 2018,31, 2019, we raised aggregate net proceeds of $749,803$896,031 (net of $23,289$27,896 in commissions to H.C. Wainwright and $2,395$5,929 in other offering expenses) under this agreementAgreement through the sale of 555,000161,149 shares of common stock at an average price of $1.35$5.56 per share of net proceeds.

 

Warrant ExercisesRestricted Stock Unit Grants

Our Board of Directors established the 2012 Non-Employee Directors Compensation Program, as amended through August 2016, or the Non-Employee Directors Plan, pursuant to which, in addition to cash compensation, directors of the Company who are not also employees may be granted stock-based compensation in the form of restricted stock units, or RSU’s. The RSUs represent the right to be issued on a future date shares of our common stock for RSUs which have then vested.

12

In April 2019, pursuant to the Non-Employee Directors Plan, we issued RSUs with a value of $35,000 to each of our non-employee directors, as the stock-based compensation element of their overall directors’ compensation, for the fiscal year ending March 31, 2020. Those grants were based on the closing price of our common stock on the one business day prior to the grant date, $14.25 per share. Therefore, 2,456 RSUs were issued to each of our five non-employee directors, for a total of 12,280 RSUs. All of the RSUs are subject to vesting in equal quarterly installments on June 30, 2019, September 30, 2019, December 31, 2019 and March 31, 2020.

  

In the nine months ended December 30, 2018, three investors that participated in the October 2017 public offering exercised 129,300 warrants for aggregate cash proceeds to us of $142,230 before expenses.

Restricted Stock Unit Grants to Executive Officers and Directors

During the nine months ended December 31, 2018, 250,676 Restricted Stock Units (“RSUs”)April 2019, 2,859 vested RSUs held by our current and former executive officers were exchanged for the same number of shares of our common stock. As these executives elected to net settle a portion of their vested RSUs in exchange for the Company paying the related withholding taxes of $18,318 on the share issuance, 1,512 of the vested RSUs were cancelled and we issued a net 1,347 shares to the executives and former executive.

In June 2019, 3,075 vested RSUs held by our non-employee directors were exchanged into the same number of shares of our common stock. Four of our five non-employee directors elected to return 40% of their vested RSUs in exchange for cash, in order to pay their withholding taxes on the share issuances, resulting in 984 of the vested RSUs being cancelled in exchange for $5,453 in aggregate cash proceeds to those independent directors.

In July 2019, 2,861 vested RSUs held by our current and former executive officers were exchanged for the same number of shares of our common stock. As ourthese executives elected to net settle a portion of their RSU’svested RSUs in exchange for usthe Company paying the related withholding taxes and our non-employee directors elected to receive a cash equivalent of the value of their shares equal to their estimated income taxes$4,979 on the share issuance, 112,3661,510 of the vested RSUs were cancelled and we issued a net 138,3111,351 shares to the executives and former executive.

In September 2019, 3,075 vested RSUs held by our non-employee directors were exchanged into the same number of shares of our common stock. Four of our five non-employee directors elected to return 40% of their vested RSUs in exchange for cash, in order to pay their withholding taxes on the share issuances, resulting in 984 of the vested RSUs being cancelled in exchange for $3,463 in aggregate cash proceeds to those independent directors.

In October 2019, 2,859 vested RSUs held by current and former executive officers were exchanged for the same number of shares of our common stock. As these executives elected to net settle a portion of their vested RSUs in exchange for the Company paying the related withholding taxes of $5,938 on the share issuance, 1,511 of the vested RSUs were cancelled and we issued a net 1,348 shares to the current and former executives.

In December 2019, 3,075 vested RSUs held by our non-employee directors were exchanged into the same number of shares of our common stock. Four of our five non-employee directors elected to return 40% of their vested RSUs in exchange for cash, in order to pay their withholding taxes on the share issuances, resulting in 984 of the vested RSUs being cancelled in exchange for $3,463 in aggregate cash proceeds to those independent directors.

RSUs outstanding that have vested as of, and are expected to vest subsequent to, December 31, 2019 are as follows:

Number of RSUs
Vested215
Expected to vest3,075
Total3,290

Common Stock for Warrant Cancellation

During the nine months ended December 31, 2019, we agreed with seven accredited investors to issue an aggregate of 3,992 shares of our common stock to these investors in exchange for the cancellation of outstanding warrants then held by the investors to purchase an aggregate of 39,900 shares of our executivescommon stock. We measured the fair value of the shares issued and directors (see Note 9).the fair value of the warrants exchanged for those shares and recorded a gain of $51,190 on those exchanges based on the changes in fair value between the instruments exchanged.

 

On June 14, 2018, our Board of Directors (the “Board”) approved the issuances of additional RSUs to certain officers and directors (see Note 9).

 

 

 1113 

 

 

7. RELATED PARTY TRANSACTIONS

 

During the ninethree months ended December 31, 20182019, we accrued unpaid Board fees of $69,750 owed to our non-employee directors as of December 31, 2018.2019. For the nine months ended December 31, 2019, we recorded $209,250 in fees to our non-employee directors.

 

As a result of entering into a Separation and Consulting Agreement with our former CEO, we paid out accrued vacation of $32,083 to that former executive in December 2018 (see Note 8 and Note 13). That accrued vacation was previously recorded in theAmounts due to related parties account.were comprised of the following items:

  December 31, 2019  March 31, 2019 
Accrued Board fees $69,750  $69,750 
Accrued vacation to all employees  41,462   13,904 
Total due to related parties $111,212  $83,654 

 

8. OTHER CURRENT LIABILITIES

 

Other current liabilities were comprised of the following items:

 

 December 31, March 31,  December 31, March 31, 
 2018 2018  2019 2019 
Accrued interest $34,758  $55,701  $  $59,573 
Accrued separation expenses for former executives (see Note 7 and Note 13)  505,609    
Accrued separation expenses for former executives     355,189 
Accrued professional fees  168,981   207,440   175,282   231,238 
Total other current liabilities $709,348  $263,141  $175,282  $646,000 

  

9. STOCK COMPENSATION

 

The following tables summarize share-based compensation expenses relating to RSUs and stock options granted and the effect on basic and diluted loss per common share during the three and nine month periods ended December 31, 20182019 and 2017:2018:

 

 Three Months
Ended
December 31,
2018
 Three Months
Ended
December 31,
2017
 Nine Months
Ended
December 31,
2018
 Nine Months
Ended
December 31,
2017
  Three Months
Ended
December 31,
2019
 Three Months
Ended
December 31,
2018
 Nine Months
Ended
December 31,
2019
 Nine Months
Ended
December 31,
2018
 
Vesting of stock options and restricted stock units $344,854  $323,162  $944,512  $887,607  $102,576  $344,854  $755,648  $944,512 
Total stock-based compensation expense $344,854  $323,162  $944,512  $887,607  $102,576  $344,854  $755,648  $944,512 
                                
Weighted average number of common shares outstanding – basic and diluted  18,050,165   14,950,701   17,865,176   10,927,106   2,887,883   1,203,344   1,821,557   1,191,012 
                                
Basic and diluted loss per common share attributable to stock-based compensation expense $(0.02) $(0.02) $(0.05) $(0.08) $(0.04) $(0.29) $(0.41) $(0.79)

 

All of the stock-based compensation expense recorded during the nine months ended December 31, 20182019 and 2017,2018, which totaled $944,512$755,648 and $887,607,$944,512, respectively, is included in payroll and related expense in the accompanying condensed consolidated statements of operations.  Stock-based compensation expense recorded during the nine months ended December 31, 20182019 and 20172018 represented an impact on basic and diluted loss per common share of $(0.05)$(0.41) and $(0.08)$(0.79), respectively.

14

 

We review share-based compensation on a quarterly basis for changes to the estimate of expected award forfeitures based on actual forfeiture experience. The cumulative effect of adjusting the forfeiture rate for all expense amortization is recognized in the period the forfeiture estimate is changed. The effect of forfeiture adjustments for the nine months ended December 31, 20182019 was insignificant.

   

Stock Option Activity

 

12

Restricted Stock Unit Grants to Directors and Executive Officers

On August 9, 2016, our Board granted RSUs to certain of our officers and directors. The RSUs representWe did not issue any stock options during the right to be issued on a future date shares of our common stock for vested RSUs. The Board’s Compensation Committee recommended the grants based on a compensation assessment provided by a third-party compensation consulting firm engaged by us that developed a peer group of companies for market assessment and analyzed compensation at such companies.

On June 14, 2018, our Board approved the issuances of additional RSUs of $35,000 in value to each of our independent directors per the 2012 Non-Employee Directors Compensation Program (the “2012 Program”) as the stock-based compensation element of their overall directors’ compensation for the fiscal year ending March 31, 2019. The Board also approved the issuance of $50,000 of RSUs to a prospective director pursuant to the 2012 Program, if he chose to join our Board. Finally, the Board approved the issuance of $30,000 of RSU’s to our Chief Financial Officer. The Board approval called for all of those RSUs to be priced based on the five day trailing averages of our closing stock price leading up to the acceptance of the Board seat by the prospective director, which occurred on June 19, 2018. That average price was $1.31 per share for the RSU calculations. Therefore, a total of 107,196 RSUs were issued to our existing independent directors, 38,285 RSUs were issued to Mr. Guy Cipriani and 22,971 RSUs were issued to our Chief Financial Officer. All of those RSUs vest ratably on September 30, 2018,three or nine months ended December 31, 2018 and March 31, 2019.

 

The above noted RSUs were granted under our Amended 2010 Stock Incentive PlanOptions outstanding that have vested as of December 31, 2019 and we recorded expenseoptions that are expected to vest subsequent to December 31, 2019 are as follows:

  Number of
Shares
  Weighted
Average
Exercise
Price
  Weighted
Average
Remaining
Contractual
Term in
Years
 
Vested  22,894  $75.24   4.99 
Expected to vest  28,230  $18.89   7.99 
Total  51,124         

A summary of $928,762 instock option activity during the nine months ended December 31, 20182019 is presented below:

  Amount  Range of
Exercise Price
  Weighted
Average
Exercise
Price
 
Stock options outstanding at March 31, 2019  59,111  $18.75 - 187.50  $56.85 
Adjustment for reverse split  14   n/a   n/a 
Exercised    $  $ 
Granted    $  $ 
Cancelled/Expired  (8,001) $75.00 - 142.50  $138.75 
Stock options outstanding at December 31, 2019  51,124  $18.75 - 187.50  $44.12 
Stock options exercisable at December 31, 2019  22,894  $25.20 - 187.50  $75.24 

On December 31, 2019, our stock options had no intrinsic value since the closing price on that date of $0.96 per share was below the weighted average exercise price of our outstanding stock options.

At December 31, 2019, there was approximately $1,418,000 of unrecognized compensation cost related to the RSU grants. share-based payments, which is expected to be recognized over a weighted average period of 3.5 years.

   

RSUs outstanding that have vested and are expected to vest as of December 31, 2018 are as follows:

Number of RSUs
Vested46,125
Expected to vest240,650
Total286,775

During the nine months ended December 31, 2018, 250,676 RSUs held by our executives and directors were exchanged into the same number of shares of our common stock. As our executives elected to net settle a portion of their RSU’s in exchange for us paying the related withholding taxes and our non-employee directors elected to receive a cash equivalent of the value of their shares equal to their estimated income taxes on the share issuance, 112,366 of the RSUs were cancelled and we issued a net 138,311 shares of common stock to our executives and directors.

Stock Option Activity10. WARRANTS

 

During the nine months ended December 31, 2018,2019, we issued pre-funded warrants and common warrants as part of our December 2019 Public Offering (see Footnote 6). All of the pre-funded warrants were fully exercised immediately after the offering. We issued 3,333,334 common warrants in the offering with an option to our new CEO to purchase 552,625 shares of common stock at aexercise price of $1.25$1.50 per share,share. Those common warrants carried a term of five years. We also issued 100,000 warrants to the closingplacement agent in the offering. The placement agent warrants have an exercise price on the date of the option grant.

Options outstanding that$1.875 and have vested and are expected to vest asa term of December 31, 2018 are as follows:five years.

  Number of
Shares
  Weighted
Average
Exercise
Price
  Weighted
Average
Remaining
Contractual
Term in
Years
 
          
Vested  356,047  $8.83   3.59 
Expected to vest  570,625  $1.26   9.95 
Total  926,672         

 

 

 

 1315 

 

 

The following outlines the significant weighted average assumptions used to estimate the fair value information presented, with respect to the stock option grantwarrants, utilizing the Binomial Lattice option pricing models, at, andissued during the nine months ended December 31, 2018:2019:

 

Risk free interest rate2.85%1.71%
Average expected life105 years
Expected volatility94.64%229.6% - 233%
Expected dividends None

A summary of stock option activity during the nine months ended December 31, 2018 is presented below:

  Amount  Range of
Exercise Price
  Weighted
Average
Exercise
Price
 
Stock options outstanding at March 31, 2018  409,047   $1.68-$20.50  $9.51 
Exercised       $ 
Granted  552,625  $1.25  $1.25 
Cancelled/Expired  (35,000) $20.50  $20.50 
Stock options outstanding at December 31, 2018  926,672   $1.25 – $12.50  $4.17 
Stock options exercisable at December 31, 2018  356,047   $1.68 – $12.50  $8.83 

On December 31, 2018, our stock options had no intrinsic value since the closing price on that date of $1.66 per share was below the weighted average exercise price of our outstanding stock options.

At December 31, 2018, there was approximately $1,740,025 of unrecognized compensation cost related to share-based payments, which is expected to be recognized over a weighted average period of 1.3 years.

10. WARRANTS

 

During the nine months ended December 31, 2018, and 2017, we did not issue any warrants.

During the nine months ended December 31, 2019, we agreed with seven accredited investors to issue an aggregate of 3,992 shares of our common stock to these investors in exchange for the cancellation of outstanding warrants then held by the investors to purchase an aggregate of 39,900 shares of our common stock. We measured the fair value of the shares issued and the fair value of the warrants exchanged for those shares and recorded a gain of $51,190 on those exchanges based on the changes in fair value between the instruments exchanged.

 

A summary of warrant activity during the nine months ended December 31, 20182019 is presented below:

 

  Amount  Range of
Exercise
Price
  Weighted
Average
Exercise
Price
 
Warrants outstanding at March 31, 2018  5,922,571   $1.10 - $12.05  $1.83 
Exercised  (129,300) $1.10  $1.10 
Issued     n/a   n/a 
Cancelled/Expired  (463,146)  $2.10 – $6.25  $2.61 
Warrants outstanding at December 31, 2018  5,330,125   $1.10 – $12.05  $1.81 
Warrants exercisable at December 31, 2018  5,330,125   $1.10 – $12.05  $1.81 
  Amount  Range of
Exercise
Price
  Weighted
Average
Exercise
Price
 
Warrants outstanding at March 31, 2019  342,992  $16.50 - 180.75  $38.10 
Warrants issued  3,433,334  $1.50 - 1.875  $1.51 
Adjustment for reverse split  73   n/a   n/a 
Cancelled/Expired  (51,287) $64.50 - 180.75  $91.88 
Warrants outstanding at December 31, 2019  3,725,112  $1.50 – 125.25  $3.98 
Warrants exercisable at December 31, 2019  3,725,112  $1.50 – 125.25  $3.98 

  

11. GOVERNMENT CONTRACTS AND RELATED REVENUE RECOGNITION

 

We have entered into the following twothree contracts/grants with the National Cancer Institute, (NCI),or NCI, part of the National Institutes of Health, (NIH)or NIH, over the past two years:

 

Phase 2 Melanoma Cancer Contract

On September 12, 2019, the NCI awarded to us an SBIR Phase II Award Contract, for NIH/NCI Topic 359, entitled “A Device Prototype for Isolation of Melanoma Exosomes for Diagnostics and Treatment Monitoring”, or the Award Contract. The Award Contract amount is $1,860,561 and runs for the period from September 16, 2019 through September 15, 2021.

The work to be performed pursuant to this Award Contract will focus on melanoma exosomes. This work follows from our completion of a Phase I contract for the Topic 359 solicitation that ran from September 2017 through June 2018 (see Phase 1 Melanoma Cancer Contract below). Following on the Phase I work, the deliverables in the Phase II program will involve the design and testing of a pre-commercial prototype of a more advanced version of the exosome isolation platform.

 

 

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Breast Cancer GrantDuring the nine months ended December 31, 2019, we recognized $413,458 in government contract revenue under this contract as a result of the work involved completing the first two milestones in the project as reported in the kick-off presentation to the NCI and first quarterly report. The kick-off presentation covered the Company's organization and project status, recent achievements, the status of the field, the status of commercial and academic competitors, where the proposed project was positioned against the state of the art, the IP landscape, a refresher on the proposed technology, the detailed plan for the first budget period of the contract and technical risks and alternative approaches. The first quarterly report covered a summary of technical objectives, a description of activities accomplished in the quarter, an analysis of experimental data, comments regarding the timeliness of performance, and a brief explanation of activities to be pursued in the following quarter.

 

In September 2018, the NCI awarded us a government grant (number 1R43CA232977-01). The title of this Small Business Innovation Research (SBIR) Phase I grant is “The Hemopurifier Device for Targeted Removal of Breast Cancer Exosomes from the Blood Circulation.”

This NCI Phase I grant period runs from September 14, 2018 through August 31, 2019. The total amount of the firm grant is $298,444. The grant calls for two subcontractors to work with us. Those subcontractors are University of Pittsburgh and Massachusetts General Hospital.

As of December 31, 2018, we have not recognized any revenue under the grant.

1 Melanoma Cancer Contract

 

We entered into a contract with the NCI inNIH on September 15, 2017. This award was under the NIH’s SBIR program.program which is designed to fund early stage small businesses that are seeking to commercialize innovative biomedical technologies. The title of the award is “SBIRwas SBIR Topic 359 Phase 1 Device Strategy for Selective Isolation of Oncosomes and Non-Malignant Exosomes.

The award from NIH was a firm, fixed-price contract with potential total payments to us of $299,250 over the course of nine months.

 

Fixed price contracts require the achievement of multiple, incremental milestones to receive the full award during each period of the contract. The NIH also had the unilateral right to require us to perform additional work under an option period for an additional fixed amount of $49,800.

Under the terms of the contract, we were required to perform certain incremental work towardstoward the achievement of specific milestones against which we would invoiceinvoiced the government for fixed payment amounts.

 

In the nine months ended December 31, 2018, we performed work under the contract covering the remainder of the technical objectives of the contract (AimAim 1: To validate the Hemopurifier as a device for capture and recovery of melanoma exosomes from plasma, and Aim 2: To validate a method of melanoma exosome isolation consisting of the Hemopurifier followed by mab-based immunocapture to select out the tumor-derived exosomes from non-malignant exosomes and Aim 3: To evaluate the functional integrity of melanoma exosomes purified by the Hemopurifier and immunocapture isolation steps).steps. As a result, we invoicedrecognized $149,625 in revenue from NIH for $149,625 during the nine months ended December 31, 2018.

The Phase 1 Melanoma Cancer Contract is now completed.

Breast Cancer Grant

In September 2018, the NCI awarded us a government grant (number 1R43CA232977-01). The title of this SBIR Phase I grant is “The Hemopurifier Device for Targeted Removal of Breast Cancer Exosomes from the Blood Circulation.”

This NCI Phase I grant period originally ran from September 14, 2018 through August 31, 2019. In August 2019, we applied for and received a no cost, twelve month extension on this grant, so the expiration date was extended to August 31, 2020. The total amount of the firm grant is $298,444. The grant calls for two subcontractors to work with us. Those subcontractors are University of Pittsburgh and Massachusetts General Hospital.

During the nine months ended December 31, 2019, we recognized $30,000 in government contract revenue under this grant as a result of the work involved in one of the three technical objectives of the contract (Aim 2. “Elution of a population of breast cancer exosomes from Hemopurifier cartridges that bear the signatures of malignancy based on expression of CSPG4 and HER2, for triple-negative or HER2-overexpressing cancers, respectively”). We also invoiced the NCI an additional $100,000 in the six month period ended September 30, 2019 in order to pay our subcontractors under the contract. As we did not complete any of the technical objectives beyond Aim 2 noted above during the December period, we recorded this $100,000 as deferred revenue as of December 31, 2019.

17

 

12. SEGMENTS

 

We operate our businesses principally through two reportable segments: Aethlon, which represents our therapeutic business activities, and Exosome Sciences, Inc., or ESI, which represents our diagnostic business activities. Our reportable segments have been determined based on the nature of the potential products being developed. We record discrete financial information for ESI and our chief operating decision maker reviews ESI’s operating results in order to make decisions about resources to be allocated to the ESI segment and to assess its performance.

 

Aethlon’s revenue is generated primarily from government contracts to date and ESI does not yet have any revenues. We have not included any allocation of corporate overhead to the ESI segment.

  

15

The following tables set forth certain information regarding our segments:

 

 Nine Months Ended December 31,  Nine Months Ended December 31, 
 2018 2017  2019 2018 
Revenues:          
Aethlon $149,625  $74,813  $443,458  $149,625 
ESI            
Total Revenues $149,625  $74,813  $443,458  $149,625 
                
Operating Losses:                
Aethlon $(4,304,082) $(3,495,189) $(4,125,758) $(4,304,082)
ESI  (104,017)  (64,860)  (19,039)  (104,017)
Total Operating Loss $(4,408,099) $(3,560,049) $(4,144,797) $(4,408,099)
                
Net Losses:                
Aethlon $(4,469,399) $(4,308,807) $(4,575,811) $(4,469,399)
ESI  (104,017)  (64,860)  (19,039)  (104,017)
Net Loss Before Non-Controlling Interests $(4,573,416) $(4,373,667) $(4,594,850) $(4,573,416)
                
Cash:                
Aethlon $4,824,225  $5,610,061  $4,058,456  $4,824,225 
ESI  676   738   197   676 
Total Cash $4,824,901  $5,610,799  $4,058,653  $4,824,901 
                
Total Assets:                
Aethlon $4,950,079  $5,745,031  $4,682,294  $4,950,079 
ESI  676   5,723   197   676 
Total Assets $4,950,755  $5,750,754  $4,682,491  $4,950,755 
                
Capital Expenditures:                
Aethlon $  $23,705  $148,064  $ 
ESI            
Capital Expenditures $  $23,705  $148,064  $ 
                
Depreciation and Amortization:                
Aethlon $24,756  $27,402  $15,992  $24,756 
ESI            
Total Depreciation and Amortization $24,756  $27,402  $15,992  $24,756 
                
Interest Expense:                
Aethlon $(165,317) $(306,495) $(54,232) $(165,317)
ESI            
Total Interest Expense $(165,317) $(306,495) $(54,232) $(165,317)

 

 

 

 1618 

 

 

13. COMMITMENTS AND CONTINGENCIES

 

CONTRACTUAL OBLIGATIONS AND COMMITMENTS

 

There have been no material changes to our contractual obligations and commitments outside the ordinary course of business from those disclosed under the heading “Management’s Discussion and Analysis of Financial Condition and Results of Operations-Contractual Obligations and Commitments” as contained in our Annual Report on Form 10-K for the year ended March 31, 20182019, filed by us with the SEC on June 8, 2018 except:

On December 10, 2018, we entered into a Separation and Consulting Agreement with James A. Joyce, our former CEO. Under this agreement, we have a contractual obligation to pay Mr. Joyce a total of $385,000 and to cover his medical insurance costs over a twelve month period that began on January 10,July 1, 2019. We also paid Mr. Joyce accrued vacation of $32,083 in December 2018. In addition, we entered into a twelve month consulting arrangement with Mr. Joyce with agreed compensation of $5,000 per month over calendar 2019. Mr. Joyce’s existing RSU’s will continue vesting over the term of the consulting arrangement.

The total expense accrued at December 31, 2018 relating to the separation agreements with Mr. Joyce and our former President, Rodney Kenley, was $505,609 (see Note 7 and Note 8).

 

LEASE COMMITMENTS

 

We currently lease approximately 2,600 square feet of executive office space at 9635 Granite Ridge Drive, Suite 100, San Diego,California 92123 under a 39-month gross plus utilities lease that commenced on December 1, 2014 and expires on August 31, 2021.2021 the “Granite Ridge Lease.” The current rental rate under the lease extension is $7,986$8,265 per month. We believe this leased facility will be satisfactory for our office needs over the term of the lease.

 

We also rent approximately 1,700 square feet of laboratory space at 11585 Sorrento Valley Road, Suite 109, San Diego, California 92121 at the rate of $4,700 per month on a one-year lease that expiresoriginally was to expire on November 30, 2019. In October 2019, we entered into a lease extension for an additional twelve months running from December 1, 2019 through November 30, 2020, at the rate of $5,961 per month.

 

Rent expense, which is included in general and administrative expenses, approximated $126,000$44,000 and $100,000$42,000 for the three month periods ended December 31, 2019 and 2018, respectively. For the nine month periods ended December 31, 2019 and 2018, rent expense approximated $130,000 and 2017,$126,000, respectively.

Future minimum lease payments under the Granite Ridge Lease as of December 31, 2019, are as follows:

January 1, 2020 through March 31, 2020 $24,795 
April 1, 2020 through March 31, 2021  102,074 
April 1, 2021 through August 31, 2021  43,670 
Total future minimum lease payments  170,539 
Less: discount  (6,132)
Total lease liability $164,407 

On April 1, 2019, we recorded a lease liability and ROU lease asset for the Granite Ridge Lease based on the present value of lease payments over the expected remaining lease term of 2.2 years, discounted using our estimated incremental borrowing rate of 4%. For the nine months ended December 31, 2019, reduction of the right-of-use lease asset was $68,856 and reduction of the lease liability was $67,994.

  

LEGAL MATTERS

 

From time to time, claims are made against us in the ordinary course of business, which could result in litigation. Claims and associated litigation are subject to inherent uncertainties and unfavorable outcomes could occur, such as monetary damages, fines, penalties or injunctions prohibiting us from selling one or more products or engaging in other activities.

 

The occurrence of an unfavorable outcome in any specific period could have a material adverse effect on our results of operations for that period or future periods. We are not presently a party to any pending or threatened legal proceedings.

 

19

14. SUBSEQUENT EVENTS

 

Management has evaluated events subsequent to December 31, 20182019 through the date that the accompanying condensed consolidated financial statements were filed with the SEC for transactions and other events which may require adjustment of and/or disclosure in such financial statements.

 

Registered Direct Financing and Private Placement –On January 16, 2020, we engaged H.C. Wainwright & Co., LLC (“Wainwright”) to act as our exclusive placement agent in connection with the private placement and a concurrent registered direct offering (together, the “Offering”) of an aggregate of 1,885,378 shares of our common stock at a purchase price per share of $2.00 (the “Shares”), for aggregate gross proceeds to us of approximately $3.77 million, before deducting fees payable to Wainwright and other estimated offering expenses payable by us. We also entered into a securities purchase agreement (the “Purchase Agreement”) with certain institutional investors (the “Purchasers”), pursuant to which we agreed to sell and issue to the Purchasers warrants (the “Purchase Warrants”) to purchase up to an aggregate of 942,689 shares of our common stock (the “Purchase Warrant Shares”). We agreed to pay Wainwright a cash fee of 6.0% of the aggregate gross proceeds in the Offering, excluding the proceeds, if any, from the exercise of the Purchase Warrants. We also agreed to pay Wainwright an additional 1.0% of the aggregate gross proceeds in the Offering as a management fee and to pay Wainwright for certain expenses in connection with the Offering in an aggregate amount not to exceed $82,900. In addition, Wainwright received placement agent warrants on substantially the same terms as the Purchase Warrants in an amount equal to 3.0% of the aggregate number of Shares sold in the offering, or 56,561 shares of Common Stock, at an exercise price of $2.50 per share and a term expiring on January 17, 2025 (the “Placement Agent Warrants,” and the shares of common stock issuable thereunder, the “Placement Agent Warrant Shares”).

On January 22, 2020, the Company closed the Offering and issued the Purchase Warrants to the Purchasers. The Purchase Warrants are exercisable immediately at an exercise price of $2.75 per share and will expire five and one-half years from the issuance date.

Warrant Exercises – Subsequent to December 31, 2019, investors that participated in the December 2019 Public Offering exercised warrants to purchase an aggregate of 2,591,167 shares of common stock for aggregate cash proceeds to us of $3,888,249 before expenses.

Restricted Stock Unit (“RSU”) IssuancesIssuance – In January 2019, 46,1252020, 215 RSUs held by our current and former executivesan executive were exchanged into the same number of shares of our common stock. As our executivesthe executive elected to net settle a portion of theirhis RSU’s in exchange for us paying the related withholding taxes on the share issuance, 27,014125 of the RSUs were cancelled and we issued a net 19,11190 shares of common stock to the executive. This was the final vested amount under the RSU vesting program to our executives.executives (see Footnote 6).

 

ATM SalesOrder of Suspension of Trading-- Subsequent – On February 7, 2020, the Securities and Exchange Commission (the “SEC”) issued an Order of Suspension of Trading (the “SEC Order”), temporarily suspending trading in our stock for a period of ten days. The SEC Order stated that the suspension was due to December 31, 2018, we sold 210,271 sharesconcerns regarding the accuracy and adequacy of our common stock under our Common Stock Sales Agreement with H.C. Wainwright (see Note 6) and from those sales raised net proceeds of $290,954 (after deducting $9,081 in commissions to H.C. Wainwright and $2,654 in other offering expenses), at an average price of $1.38 per share of net proceeds.

Warrant Exercises –Subsequent to December 31, 2018, two investors that participatedinformation in the October 2017 public offering exercised 154,000 warrants for aggregate cash proceedsmarketplace that appeared to usbe disseminated by third party promotors and recent and unusual market activity since at least January 22, 2020. We are unable to predict the outcome of $169,400 before expenses.

NCI Grant – Subsequent to December 31, 2018, NCI disbursed $50,000 to us under our grant with that agency.the SEC Order or any other actions the SEC may take in connection therewith.

 

  

 

 1720 

 

 

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

 

The following discussion of our financial condition and results of operations should be read in conjunction with, and is qualified in its entirety by, the condensed consolidated financial statements and notes thereto included in Item 1 in this Quarterly Report on Form 10-Q. This item contains forward-looking statements that involve risks and uncertainties. Actual results may differ materially from those indicated in such forward-looking statements.

 

FORWARD LOOKING STATEMENTS

 

All statements, other than statements of historical fact, included in this Form 10-Q are, or may be deemed to be, "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended, (the “Securities Act"),or the Securities Act, and Section 21E of the Exchange Act. Such forward-looking statements involve assumptions, known and unknown risks, uncertainties and other factors which may cause theour actual results, performance, or achievements of Aethlon Medical, Inc. ("we" or "us") to be materially different from any future results, performance, or achievements expressed or implied by such forward-looking statements contained in this Form 10-Q. Such potential risks and uncertainties include, without limitation, completion of our capital-raising activities, our ability to maintain our Nasdaq listing, U.S. Food and Drug Administration, (FDA), approval of our products, other regulations, patent protection of our proprietary technology, product liability exposure, uncertainty of market acceptance, competition, technological change, and other risk factors detailed herein and in other of our filings with the Securities and Exchange Commission, (the “Commission”).or the Commission. The forward-looking statements are made as of the date of this Form 10-Q, and we assume no obligation to update the forward-looking statements, or to update the reasons actual results could differ from those projected in such forward-looking statements.

 

Overview

 

Aethlon Medical, Inc. and its subsidiary (collectively, “Aethlon”, the “Company”, “we” or “us”) is a medical device technology company focused on addressing unmet needs in global healthdeveloping products to diagnose and biodefense.treat life and organ threatening diseases. The Aethlon Hemopurifier® is a clinical-stage immunotherapeutic device designed to combat cancer and life-threatening viral infections. In cancer, the Hemopurifier depletesis designed to deplete the presence of circulating tumor-derived exosomes that promote immune suppression, seed the spread of metastasis and inhibit the benefit of leading cancer therapies. The U.S. Food and Drug Administration, or the FDA, has designated the Hemopurifier as a "Breakthrough Device" related to the followingfor two independent indications:

 

·to the treatment of life-threatening viruses that are not addressed with approved therapies, and
·the treatment of individuals with advanced or metastatic cancer who are either unresponsive to or intolerant of standard of care therapy, and with cancer types in which exosomes have been shown to participate in the development or severity of the disease.disease; and

·the treatment of life-threatening viruses that are not addressed with approved therapies.

 

We believe the Hemopurifier can be a substantial advance in the treatment of patients with advanced and metastatic cancer through the clearance of exosomes that promote the growth and spread of tumors through multiple mechanisms. We are currently preparing for the initiation of clinical trials in patients with advanced and metastatic cancers. We are initially focused on the treatment of solid tumors, including head and neck cancer, gastrointestinal cancers and other cancers.

On October 4, 2019, the FDA approved our Investigational Device Exemption, or IDE, application to initiate an Early Feasibility Study, or EFS, of the Hemopurifier in patients with head and neck cancer in combination with standard of care pembrolizumab (Keytruda).  The primary endpoint for the EFS, which will enroll 10-12 subjects at a single center, will be safety, with secondary endpoints including measures of exosome clearance and characterization, as well as response and survival rates. 

 

We also believe the Hemopurifier can be a part of the broad-spectrum treatment of life-threatening highly glycosylated viruses that are not addressed with an already approved treatment countermeasure objective set forth by the U.S. Government to protect citizens from bioterror and pandemic threats.treatment. In small-scale or early feasibility human studies, the Hemopurifier has been administeredused to treat individuals infected with HIV, hepatitis-C, and Ebola. Additionally,in vitro, the Hemopurifier has been validateddemonstrated to capture Zika virus, Lassa virus, MERS-CoV, cytomegalovirus, Epstein-Barr virus, Herpes simplex virus, Chikungunya virus, Dengue virus, West Nile virus, smallpox-related viruses, H1N1 swine flu virus, H5N1 bird flu virus, and the reconstructed Spanish flu virus of 1918. In several cases, these validationsstudies were conducted in collaboration with leading government or non-government research institutes. Domestically, we are focused on the clinical advancement of the Hemopurifier through investigational device exemptions (IDEs) approved by the FDA. We recently concluded a feasibility study to demonstrate the safety of our device in health-compromised individuals infected with a viral pathogen.

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We are also the majority owner of Exosome Sciences, Inc. (ESI), or ESI, a company focused on the discovery of exosomal biomarkers to diagnose and monitor life-threatening diseases. Included among ESI’s endeavorsactivities is the advancement of a TauSomeTMTauSome™ biomarker candidate to diagnose Chronic Traumatic Encephalopathy (CTE)chronic traumatic encephalopathy, or CTE, in the living. ESI previously documented that TauSome levels in former NFL players to be nine times higher than same age-group control subjects. Through ESI we are also developing exosome based biomarkers in patients with, or at risk for, a number of cancers. We consolidate Exosome’sESI’s activities in our consolidated financial statements.

We also have a cross-licensing and development agreement with SeaStar Medical, Inc., focused on co-development of our Hemopurifier cartridge with SeaStar’s proprietary cartridges and the development of a closed system for the Hemopurifier using the SeaStar pump and cassettes. This collaboration may allow the deployment of the Hemopurifier into settings that lack dialysis infrastructure, such as chemotherapy infusion centers and field operations for life threatening viral epidemics.

 

Successful outcomes of human trials will also be required by the regulatory agencies of certain foreign countries where we intendplan to sell this device.the Hemopurifier. Some of our patents may expire before FDA approval or approval in a foreign country, if any, is obtained. However, we believe that certain patent applications and/or other patents issued more recently will help protect the proprietary nature of the Hemopurifier treatment technology.

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Our common stock is listed on the Nasdaq Capital Market under the symbol “AEMD.”

  

WHERE YOU CAN FIND MORE INFORMATION

 

We are subject to the informational requirements of the Securities Exchange Act of 1934, as amended, and must file reports, proxy statements and other information with the Commission. The Commission maintains a web site (http://www.sec.gov) that contains reports, proxy and information statements and other information regarding registrants, like us, which file electronically with the Commission. Our headquarters are located at 9635 Granite Ridge Drive, Suite 100, San Diego, CA 92123. Our phone number at that address is (858) 459-7800. Our Web site ishttp://www.aethlonmedical.com.

    

RESULTS OF OPERATIONS

  

THREE MONTHS ENDED DECEMBER 31, 20182019 COMPARED TO THE THREE MONTHS ENDED DECEMBER 31, 20172018

 

Government Contract Revenues

 

We recorded government contract revenue of $413,458 in the three months ended December 31, 2019.  This revenue resulted from work performed under Phase 2 Melanoma Cancer Contract with the National Institutes of Health, or NIH. We did not record any government contract revenue in the three month period ended December 31, 2018 and we recorded $74,813 of government contract revenue in the three month period ended December 31, 2017.

Operating Expenses

Consolidated operating expenses for the three months ended December 31, 2018 were $1,963,873 in comparison with $1,238,440 for the comparable period a year ago. This increase of $725,433, or 58.6%, was due to increases in payroll and related expenses of $498,286, in professional fees of $148,075 and in general and administrative expenses of $79,072.

The $498,286 increase in payroll and related expenses was primarily due to the combination of a $472,639 accrual for the separation payments over calendar 2019 for our former CEO and President and a $21,692 increase in stock-based compensation.

The $148,075 increase in our professional fees was due to a $34,900 increase in our Board fees due to the recent expansion of our Board, a $7,273 increase in ESI’s professional fees and a $197,426 increase in scientific consulting fees. Those increases were partially offset by a $71,749 decrease in our legal fees, a $9,890 decrease in our marketing costs and a $9,885 decrease in our accounting fees.

The $79,072 increase in general and administrative expenses was primarily due to the combination of a $44,592 accrual for the health insurance payments over calendar 2019 for our former CEO and President, a $26,086 increase in our insurance costs and an $18,791 increase in rent expense under our renewed leases.

Other Expense

Other expense during the three months ended December 31, 2018 and 2017 consisted of interest expense.

Interest Expense

Interest expense was $55,107 for the three months ended December 31, 2018 and was $55,912 for the three months ended December 31, 2017, a decrease of $805. The various components of our interest expense are shown in the following table:

  Three Months
Ended
  Three Months
Ended
    
  12/31/18  12/31/17  Change 
Interest Expense $24,820  $25,625  $(805)
Amortization of Note Discounts  30,287   30,287    
Total Interest Expense $55,107  $55,912  $(805)

As noted in the above table, since the amortization of note discounts was the same in both periods, the $805 decrease in our interest expense was due to a reduction in our contractual interest expense.

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Net Loss

As a result of the changes in revenues and expenses noted above, our net loss increased from approximately $1,215,000 in the three month period ended December 31, 2017 to $2,013,000 in the three month period ended December 31, 2018.

 

Basic and diluted loss attributable to common stockholders were ($0.11) for the three month period ended December 31, 2018 compared to ($0.08) for the period ended December 31, 2017.

NINE MONTHS ENDED DECEMBER 31, 2018 COMPARED TO THE NINE MONTHS ENDED DECEMBER 31, 2017

Government Contract Revenues

We recorded $149,625 in government contract revenue in the nine months ended December 31, 2018 and we recorded $74,813 in government contract revenue in the nine months ended December 31, 2017. This revenue arose from work performed under our government contract with National Cancer Institute, part of the National Institutes of Health (“NIH”) as follows:

  Nine Months
Ended 12/31/18
  Nine Months
Ended 12/31/17
  Change in
Dollars
 
NIH Contract $149,625  $74,813  $74,812 
Total Government Contract Revenue $149,625  $74,813  $74,812 

We have entered into the following twothree contracts/grants with the National Cancer Institute (NCI),NCI, part of the National Institutes of Health (NIH)NIH over the past two years:

 

BreastPhase 2 Melanoma Cancer GrantContract

 

InOn September 2018,12, 2019, the NCI awarded to us a government grant (number 1R43CA232977-01).an SBIR Phase II Award Contract, for NIH/NCI Topic 359, entitled “A Device Prototype for Isolation of Melanoma Exosomes for Diagnostics and Treatment Monitoring”, or the Award Contract. The titleAward Contract amount is $1,860,561 and runs for the period from September 16, 2019 through September 15, 2021.

The work to be performed pursuant to this Award Contract will focus on melanoma exosomes. This work follows from our completion of this Small Business Innovation Research (SBIR)a Phase I grant is “The Hemopurifier Devicecontract for Targeted Removalthe Topic 359 solicitation that ran from September 2017 through June 2018 (see Phase 1 Melanoma Cancer Contract below). Following on the Phase I work, the deliverables in the Phase II program involve the design and testing of Breast Cancer Exosomes froma pre-commercial prototype of a more advanced version of the Blood Circulation.”exosome isolation platform.

 

This NCI Phase I grant period runs from September 14, 2018 through August 31, 2019. The total amount of the firm grant is $298,444. The grant calls for two subcontractors to work with us. Those subcontractors are University of Pittsburgh and Massachusetts General Hospital.

 

As of

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During the three months ended December 31, 2018,2019, we have not recognized any$413,458 in government contract revenue under this grant.contract as a result of the work involved completing the first two milestones in the project as reported in the kick-off presentation to the NCI and first quarterly report. The kick-off presentation covered the Company's organization and project status, recent achievements, the status of the field, the status of commercial and academic competitors, where the proposed project was positioned against the state of the art, the IP landscape, a refresher on the proposed technology, the detailed plan for the first budget period of the contract and technical risks and alternative approaches. The first quarterly report covered a summary of technical objectives, a description of activities accomplished in the quarter, an analysis of experimental data, comments regarding the timeliness of performance, and a brief explanation of activities to be pursued in the following quarter.

 

Phase 1 Melanoma Cancer Contract

 

We entered into a contract with the NCI in September 2017. This award was under the NIH’s SBIR program. The title of the award iswas “SBIR Topic 359 Phase 1 Device Strategy for Selective Isolation of Oncosomes and Non-Malignant Exosomes.”

The award from NIH was a firm, fixed-price contract with potential total payments to us of $299,250 over the course of nine months.

 

Fixed price contracts require the achievement of multiple, incremental milestones to receive the full award during each period of the contract. The NIH also had the unilateral right to require us to perform additional work under an option period for an additional fixed amount of $49,800.

 

Under the terms of the contract, we were required to perform certain incremental work towards the achievement of specific milestones against which we will invoice the government for fixed payment amounts. The Phase 1 Melanoma Cancer Contract was completed in June 2018. 

Breast Cancer Grant

In September 2018, the NCI awarded us a government grant (number 1R43CA232977-01). The title of this SBIR Phase I grant is “The Hemopurifier Device for Targeted Removal of Breast Cancer Exosomes from the Blood Circulation.”

This NCI Phase I grant period originally ran from September 14, 2018 through August 31, 2019. In August 2019, we applied for and received a no cost, twelve month extension on this grant, so the expiration date was extended to August 31, 2020. The total amount of the firm grant is $298,444. The grant calls for two subcontractors to work with us. Those subcontractors are University of Pittsburgh and Massachusetts General Hospital. We did not recognize any revenue from this contract in the three months ended December 31, 2019 and 2018.

Operating Expenses

Consolidated operating expenses for the three months ended December 31, 2019 were $1,289,864, in comparison with $1,963,873 for the three months ended December 31, 2018. This decrease of $674,009, or 34%, in 2019 was due to a decrease in payroll and related expenses of $755,110, which was partially offset by increases in professional fees of $22,741 and in general and administrative expenses of $58,360.

The $755,110 decrease in payroll and related expenses was due to the combination of a $512,832 reduction in our cash-based compensation expense and a $242,278 decrease in stock-based compensation. The reduction in cash-based compensation expense was due to recording a $505,609 accrual in the December 2018 period related to contractually agreed severance payments to our former CEO and president with no comparable expense in the December 2019 period.

The $22,741 increase in our professional fees in 2019 was primarily due to a $100,577 increase in our legal fees and a $26,927 increase in our accounting fees, which were partially offset by a $103,924 decrease in scientific consulting expenses. The increase in legal and accounting fees related to increased activity in our registration statement filings and in intellectual property actions, among other matters.

 

 

 

 2023 

 

The $58,360 increase in general and administrative expenses in 2019 was primarily due to the combination of a $29,065 increase in our clinical trial expenses and a $18,323 increase in licenses and permitting costs.

Other Income (Expense)

Other income (expense) during the three months ended December 31, 2019 consisted of interest expense and a gain on share for warrant exchanges and during the three months ended December 31, 2018, consisted of interest expense only. Other income for the three months ended December 31, 2019 was $55,467, in comparison with other expense of $55,107 for the three months ended December 31, 2018.

The following table breaks out the various components of our other expense for both periods:

  Three Months
Ended
  Three Months
Ended
    
  12/31/19  12/31/18  Change 
Gain on Share for Warrant Exchanges $55,593  $  $55,593 
Interest Expense  (126)  (55,107)  54,981 
Total Other Income (Expense) $55,467  $(55,107) $110,574 

Gain on Common Stock for Warrant Cancellation

During the three months ended December 31, 2019, we agreed with two accredited investors to issue 2,914 shares of our common stock to these investors in exchange for the cancellation of outstanding warrants then held by the investors to purchase an aggregate of 29,141 shares of our common stock. We measured the fair value of the shares issued and the fair value of the warrants exchanged for those shares and recorded a gain of $55,593 on those exchanges based on the changes in fair value between the instruments exchanged.

Interest Expense

Interest expense was $126 for the three months ended December 31, 2019, and $55,107 for the three months ended December 31, 2018, a decrease of $54,981 in 2019. The various components of our interest expense are shown in the following table:

  Three Months
Ended
  Three Months
Ended
    
  12/31/19  12/31/18  Change 
Interest Expense $126  $24,820  $(24,694)
Amortization of Note Discounts     30,287   (30,287)
Total Interest Expense $126  $55,107  $(54,981)

The $54,981 decrease in our interest expense was due to the payoff of our convertible notes in July 2019.

Net Loss

As a result of the changes in revenues and expenses noted above, our net loss decreased from approximately $2,019,000 in the three month period ended December 31, 2018 to $820,000 in the three month period ended December 31, 2019.

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Basic and diluted loss attributable to common stockholders were ($0.28) for the three month period ended December 31, 2019, compared to ($1.67) for the three month period ended December 31, 2018.

RESULTS OF OPERATIONS

NINE MONTHS ENDED DECEMBER 31, 2019 COMPARED TO THE NINE MONTHS ENDED DECEMBER 31, 2018

Government Contract Revenues

We recorded government contract revenue in the nine months ended December 31, 2019 and 2018. This revenue resulted from work performed under our government contracts with the NIH as follows:

  Nine Months
Ended 12/31/19
  Nine Months
Ended 12/31/18
  Change in
Dollars
 
Phase 2 Melanoma Cancer Contract $413,458  $  $413,458 
Phase 1 Melanoma Cancer Contract     149,625   (149,625)
Breast Cancer Grant  30,000      30,000 
Total Government Contract and Grant Revenue $443,458  $149,625  $293,833 

We have entered into the following three contracts/grants with the NCI, part of the NIH over the past two years:

Phase 2 Melanoma Cancer Contract

On September 12, 2019, the NCI awarded to us an SBIR Phase II Award Contract, for NIH/NCI Topic 359, entitled “A Device Prototype for Isolation of Melanoma Exosomes for Diagnostics and Treatment Monitoring”, or the Award Contract. The Award Contract amount is $1,860,561 and runs for the period from September 16, 2019 through September 15, 2021.

The work to be performed pursuant to this Award Contract will focus on melanoma exosomes. This work follows from our completion of a Phase I contract for the Topic 359 solicitation that ran from September 2017 through June 2018 (see Phase 1 Melanoma Cancer Contract below). Following on the Phase I work, the deliverables in the Phase II program involve the design and testing of a pre-commercial prototype of a more advanced version of the exosome isolation platform.

During the nine months ended December 31, 2019, we recognized $413,458 in government contract revenue under this contract as a result of the work involved completing the first two milestones in the project as reported in the kick-off presentation to the NCI and first quarterly report. The kick-off presentation covered the Company's organization and project status, recent achievements, the status of the field, the status of commercial and academic competitors, where the proposed project was positioned against the state of the art, the IP landscape, a refresher on the proposed technology, the detailed plan for the first budget period of the contract and technical risks and alternative approaches. The first quarterly report covered a summary of technical objectives, a description of activities accomplished in the quarter, an analysis of experimental data, comments regarding the timeliness of performance, and a brief explanation of activities to be pursued in the following quarter.

Phase 1 Melanoma Cancer Contract

We entered into a contract with the NIH on September 15, 2017. This award was under the NIH’s SBIR program which is designed to fund early stage small businesses that are seeking to commercialize innovative biomedical technologies. The title of the award was SBIR Topic 359 Phase 1 Device Strategy for Selective Isolation of Oncosomes and Non-Malignant Exosomes. The award from NIH was a firm, fixed-price contract with potential total payments to us of $299,250 over the course of nine months.

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Fixed price contracts require the achievement of multiple, incremental milestones to receive the full award during each period of the contract. The NIH also had the unilateral right to require us to perform additional work under an option period for an additional fixed amount of $49,800. Under the terms of the contract, we were required to perform certain incremental work toward the achievement of specific milestones against which we invoiced the government for fixed payment amounts.

 

In the nine months ended December 31, 2018, we performed work under the contract covering the remainder of the technical objectives of the contract (Aim 1: To validate the Hemopurifier as a device for capture and recovery of melanoma exosomes from plasma and Aim 2: To validate a method of melanoma exosome isolation consisting of the Hemopurifier followed by mab-based immunocapture to select out the tumor-derived exosomes from non-malignant exosomes and Aim 3: To evaluate the functional integrity of melanoma exosomes purified by the Hemopurifier and immunocapture isolation steps). As a result, we invoiced NIH for $149,625 during the nine months ended December 31, 2018.

All of the revenue noted above related to the The Phase 1 Melanoma Cancer Contract which is now completed.

Breast Cancer Grant

In September 2018, the NCI awarded us a government grant (number 1R43CA232977-01). The title of this Small Business Innovation Research (SBIR) Phase I grant is “The Hemopurifier Device for Targeted Removal of Breast Cancer Exosomes from the Blood Circulation.”

This NCI Phase I grant period originally ran from September 14, 2018 through August 31, 2019. In August 2019, we applied for and received a no cost, twelve month extension on this grant, so the expiration date was extended to August 31, 2020. The total amount of the firm grant is $298,444. The grant calls for two subcontractors to work with us. Those subcontractors are University of Pittsburgh and Massachusetts General Hospital.

During the nine months ended December 31, 2019, we recognized $30,000 in government contract revenue under this grant as a result of the work involved in one of the three technical objectives of the contract (Aim 2. “Elution of a population of breast cancer exosomes from Hemopurifier cartridges that bear the signatures of malignancy based on expression of CSPG4 and HER2, for triple-negative or HER2-overexpressing cancers, respectively”). We also invoiced the NCI for an additional $100,000 during the nine month period ended December 31, 2019 in order to pay our subcontractors under the contract. As we did not complete any additional technical objectives beyond Aim 2 noted above during the period, we recorded this $100,000 as deferred revenue as of December 31, 2019.

Operating Expenses

 

Consolidated operating expenses for the nine months ended December 31, 20182019 were $4,557,724$4,588,255, in comparison with $3,634,862$4,557,724 for the comparable period a year ago.nine months ended December 31, 2018. This increase of $922,862,$30,531, or 25.4%0.7%, in 2019 was due to increases in in payroll and related expenses of $515,275, professional fees of $283,900$530,630 and in general and administrative expenses of $123,687.$316,787, which were partially offset by a reduction in and payroll and related expenses of $816,886.

 

The $515,275$530,630 increase in payrollour professional fees in 2019 was primarily due to a $512,174 increase in our legal fees, a $152,731 increase in our accounting fees and a $65,000 payment to the University of Pittsburgh, a subcontractor on our Breast Cancer grant related to their work on that grant, which were partially offset by a reduction in our scientific consulting expenses of $153,660. The increase in legal and accounting fees related to increased activity in our registration statement filings and in intellectual property actions, among other matters.

The $316,787 increase in general and administrative expenses in 2019 was primarily due to the combination of a $472,639 accrual$189,857 increase in our clinical trial expense, primarily costs associated with the manufacturing of Hemopurifiers for an expected clinical trial in the separation payments over calendar 2019 forcancer space, a $61,354 increase in our former CEOlab supplies expense, primarily related to our breast cancer grant and Presidentlab work related to our IDE application and a $56,905$57,271 increase in stock-based compensation.travel expense.

 

The $283,900 increase in our professional fees was due to a $126,400 increase in our Board fees due to the recent expansion of our Board, a $253,262 increase in scientific consulting fees, a $53,494 increase in our marketing and investor relations fees and a $40,290 increase in ESI’s professional fees. Those increases were partially offset by a $149,235$816,886 decrease in our legal fees, a $29,529 decrease in our accounting feespayroll and a $10,782 decrease in website service fees.

The $123,687 increase in general and administrativerelated expenses was primarily due to the combination of a $44,592$628,022 reduction in our cash-based compensation expense and a $188,864 decrease in stock-based compensation. The reduction in cash-based compensation expense was partially due to recording a $505,609 accrual forin the health insuranceDecember 2018 period related to contractually agreed severance payments over calendar 2019 forto our former CEO and President and $79,484 of clinical trial expenses associatedpresident with no comparable expense in the exosome trial at University of California Irvine, which was partially offset by reductions in a number of additional expenses.December 2019 period.

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Other Expense

 

Other expense during the nine months ended December 31, 20182019 consisted of interest expense, a gain on share for warrant exchanges and a loss on debt extinguishment and during the nine months ended December 31, 20172018, consisted of losses on debt extinguishment, losses on share for warrant exchanges and interest expense.expense only. Other expense for the nine months ended December 31, 20182019 was $165,317$450,053, in comparison with other expense of $813,618$165,317 for the nine months ended December 31, 2017.2018.

 

The following table breaks out the various components of our other expense for both periods:

 

  Nine Months
Ended
  Nine Months
Ended
    
  12/31/18  12/30/17  Change 
Loss on Debt Extinguishment $  $376,909  $(376,909)
Loss on Share for Warrant Exchanges     130,214   (130,214)
Interest Expense  165,317   306,495   (141,178)
Total Other Expense $165,317  $813,618  $(648,301)

  Nine Months
Ended
  Nine Months
Ended
    
  12/31/19  12/31/18  Change 
Loss on Debt Extinguishment $447,011  $  $447,011 
Gain on Share for Warrant Exchanges  (51,190     (51,190
Interest Expense  54,232   165,317   (111,085)
Total Other Expense $450,053  $165,317  $284,736 

  

Loss on Debt Extinguishment

 

Our loss on debt extinguishment forDuring the nine months ended December 31, 2017 resulted from a $376,909 loss associated with the June 2017 amendments to our convertible notes. There was no loss on debt extinguishment for the nine months ended December 31, 2018 - see below for additional information.

June 2017 Amendments – The $376,909 loss on debt extinguishment in the nine months ended December 31, 2017 resulted from an Exchange Agreement with two institutional investors under which2019, we issued 57,844 restricted shares of common stock in exchange for the cancellation of 77,125 warrants held by those investors (see Loss on Share for Warrant Exchanges below). Additionally, the investors agreed to extend the expiration dates of the convertible notes held by them from July 1, 2018 to July 1, 2019 in exchange for the reduction ofreduced the conversion price of thoseon our outstanding convertible notes from $4.00$45.00 per share to $3.00$10.20 per share. The modification of the convertible notes was evaluated under FASB Accounting Standards Codification (“ASC”) Topic No.ASC 470-50-40 “Debt Modification and Extinguishments”. Therefore, according to the guidance, the instruments were determined to be substantially different, and the transaction qualified for extinguishment accounting. Under the extinguishment accounting we recorded a loss on debt extinguishment of $447,011.

 

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This modification of the notes was also evaluated under ASC Topic No. 470-50-40, “Debt Modification and Extinguishments”. Therefore, according to the guidance, the instruments were determined to be substantially different, and the transaction qualified for extinguishment accounting.

LossGain on ShareCommon Stock for Warrant ExchangesCancellation

 

During the nine months ended December 31, 2017,2019, we agreed with two individualseven accredited investors to exchange 11,497 restricted shares for the cancellationissue an aggregate of 22,993 warrants. Additionally, during the period, we entered into an Exchange Agreement with two institutional investors under which we issued 57,844 restricted3,992 shares of our common stock to these investors in exchange for the cancellation of 77,125outstanding warrants then held by those investors.the investors to purchase an aggregate of 39,900 shares of our common stock. We measured the fair value of the shares issued and the fair value of the warrants exchanged for those shares and recorded losses for eacha gain of $51,190 on those exchanges based on the changes in fair value between the instruments exchanged. There was no loss on share for warrant exchanges for the nine months ended December 31, 2018.

 

Interest Expense

 

Interest expense was $54,232 for the nine months ended December 31, 2019, and $165,317 for the nine months ended December 31, 2018, and was $306,495 for the nine months ended December 31, 2017, a decrease of $141,178.$111,085 in 2019. The various components of our interest expense are shown in the following table:

 

 Nine Months
Ended
 Nine Months
Ended
    Nine Months
Ended
 Nine Months
Ended
   
 12/31/18 12/31/17 Change  12/31/19 12/31/18 Change 
Interest Expense $74,456  $91,119  $(16,663) $23,945  $74,456  $(50,511)
Amortization of Note Discounts  90,861   215,376   (124,515)  30,287  90,861  (60,574)
Total Interest Expense $165,317  $306,495  $(141,178) $54,232 $165,317 $(111,085)

 

As noted in the above table, the most significant factor in the $141,178The $111,085 decrease in our interest expense was the $124,515 decrease in the amortization of note discounts, which relateddue to the amortization against the discount onpayoff of our convertible notes. An additional factornotes in the change in our total interest was a $16,663 decrease in our contractual interest expense.July 2019.

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Net Loss

 

As a result of the changes in revenues and expenses noted above, our net loss increaseddecreased from approximately $4,361,000$4,573,000 in the nine month period ended December 31, 20172018 to $4,553,000$4,595,000 in the nine month period ended December 31, 2018.2019.

 

Basic and diluted loss attributable to common stockholders were ($0.25)2.52) for the nine month period ended December 31, 20182019, compared to ($0.40)3.82) for the nine month period ended December 31, 2017.2018.

  

LIQUIDITY AND CAPITAL RESOURCES

 

AtAs of December 31, 2018,2019, we had a cash balance of $4,824,901$4,058,653 and working capital of $3,079,243.$3,495,119. This compares to a cash balance of $6,974,070$3,828,074 and working capital of $6,752,293$2,214,230 at March 31, 2018. While we2019. We expect our currentexisting cash levelsas of December 31, 2019, together with cash raised in January 2020 (see Subsequent Events Footnote), to support ourbe sufficient to fund the Company’s operations for at least twelve months from the issuance date of these interim financial statements, beyond that timeframe, significant additional financing must be obtained in order to provide a sufficient source of operating capital and to allow us to continue to operate as a going concern. In addition, we will need to raise capital to complete anticipated future human clinical trials in the U.S. We anticipate the primary sources of this additional financing will be from proceeds of our at-the-market offering program, debt financing and other forms of equity placements. If we are unable to raise sufficient capital through the above noted sources of financing, we may elect to reduce our expenditures in order preserve cash. Those expenditure reductions may include stopping or slowing any clinical trials and/or reducing our headcount.months.

 

Our primary sources of capital during the nine months ended December 31, 20182019 were the December 2019 Public Offering and our Common Stock Sales Agreement with H.C. Wainwright & Co., LLC, (“or H.C. Wainwright”) and exercises of certain of the warrants from our October 2017 Public Offering for cash.Wainwright. The cash raised from those activities is noted below:

 

December 2019 Public Offering

On December 13, 2019, we entered into an underwriting agreement with H.C. Wainwright and Co., as representative of the several underwriters named therein, relating to the public offering, issuance and sale of 3,333,334 shares of common stock (which includes pre-funded warrants to purchase shares of common stock in lieu thereof), and common warrants to purchase up to an aggregate of 3,333,334 shares of common stock at a public offering price of $1.50 per share (the “December 2019 Public Offering”). Each share of common stock (or pre-funded warrant in lieu thereof) was sold together with a common warrant to purchase one share of common stock. The common warrants have an exercise price of $1.50 per share, were immediately exercisable, and will expire five years from the date of issuance. The offering closed on December 17, 2019.

The gross proceeds of the December 2019 Public Offering were approximately $5 million, prior to deducting underwriting discounts and commissions and estimated offering expenses and excluding the exercise of any common warrants and the underwriter's option to purchase additional securities. The net proceeds from the December 2019 Public Offering were approximately $4,091,437. We intend to use approximately $700,000 of the net proceeds from this offering for the currently planned clinical trials for the Hemopurifier® over the next 12 months, with the remainder for working capital and other general corporate purposes.

Subsequent to the completion of the December 2019 Public Offering and prior to December 31, 2019, all of the holders of pre-funded warrants exercised their pre-funded warrants in full.

In the event of a Fundamental Transaction (a transfer of ownership of the Company as defined in the common warrants issued in the December 2019 Public Offering) within our control, the holders of the unexercised common stock warrants exercisable for $1.50 per share, are entitled to receive cash consideration equal to a Black-Scholes valuation, as defined in the warrant. If such Fundamental Transaction is not within our control, the warrant holders would only be entitled to receive the same form of consideration (and in the same proportion) as the holders of our common stock, hence these warrants are classified as a component of permanent equity.

 

 

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Common Stock Sales Agreement with H.C. Wainwright

 

On June 28, 2016, we entered into a Common Stock Sales Agreement, (the “Agreement”)or the Agreement, with H.C. Wainwright, which established an at-the-market equity program pursuant to which we may offer and sell shares of our common stock from time to time as set forth in the Agreement. The Agreement provides for the sale of shares of our common stock having an aggregate offering price of up to $12,500,000, (the “Shares”).or the Shares.

On August 6, 2019, we executed Amendment No. 1 to the Agreement with H.C. Wainwright, effective as of August 5, 2019. The amendment provides that references in the Agreement to the registration statement shall refer to the registration statement on Form S-3 (File No. 333-231397), originally filed with the Securities and Exchange Commission on May 10, 2019, declared effective by the Securities and Exchange Commission on August 1, 2019. We terminated the ATM Prospectus Supplement and suspended any sales under the Sales Agreement on January 17, 2020, but the Sales Agreement remains in full force and effect.

 

Subject to the terms and conditions set forth in the Agreement, H.C. Wainwright willagreed to use its commercially reasonable efforts consistent with its normal trading and sales practices to sell the Shares from time to time, based upon our instructions. We have provided H.C. Wainwright with customary indemnification rights, and H.C. Wainwright will beis entitled to a commission at a fixed rate equal to three percent (3.0%) of the gross proceeds per Share sold. In addition, we have agreed to pay certain expenses incurred by H.C. Wainwright in connection with the Agreement, including up to $50,000 of the fees and disbursements of their counsel. The Agreement will terminate upon the sale of all of the Shares under the Agreement, unless terminated earlier by either party as permitted under the Agreement.

  

Sales of the Shares, if any, under the Agreement shallwill be made in transactions that are deemed to be “at the market offerings” as defined in Rule 415 under the Securities Act, of 1933, as amended, including sales made by means of ordinary brokers’ transactions, including on the Nasdaq Capital Market, at market prices or as otherwise agreed with H.C. Wainwright. We have no obligation to sell any of the Shares, and, at any time, we may suspend offers under the Agreement or terminate the Agreement.

  

In the nine months ended December 31, 2018,2019, we raised aggregate net proceeds of $749,804$896,031 (net of $23,289$27,896 in commissions to H.C. Wainwright and $2,395$5,929 in other offering expenses) under thethis Agreement through the sale of 555,000161,149 shares at an average price of $1.35$5.56 per share of net proceeds. As of the date of the filing of this Form 10-Q, we had approximately $8.3 million available under the Agreement.

Warrant Exercises

In the nine months ended December 31, 2018, investors that participated in the October 2017 public offering exercised 129,300 warrants for aggregate cash proceeds to us of $142,230 before expenses.

 

Future capital requirements will depend upon many factors, including progress with pre-clinical testing and clinical trials, the number and breadth of our clinical programs, the time and costs involved in preparing, filing, prosecuting, maintaining and enforcing patent claims and other proprietary rights, the time and costs involved in obtaining regulatory approvals, competing technological and market developments, as well as our ability to establish collaborative arrangements, effective commercialization, marketing activities and other arrangements. We expect to continue to incur increasing negative cash flows and net losses for the foreseeable future.

 

Cash Flows

 

Cash flows from operating, investing and financing activities, as reflected in the accompanying Condensed Consolidated Statements of Cash Flows, are summarized as follows:

 

 (In thousands)
For the nine months ended
  (In thousands)
For the nine months ended
 
 December 31,
2018
 December 31,
2017
  December 31,
2019
 December 31,
2018
 
Cash provided by (used in):        
Cash used in:        
Operating activities $(2,896) $(2,893) $(3,577) $(2,896)
Investing activities     (24)  (148)   
Financing activities  747   6,968   3,956   747 
Net (decrease) increase in cash $(2,149) $4,051 
Net increase (decrease) in cash $231  $(2,149)

   

 

 

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NET CASH USED IN OPERATING ACTIVITIES. We used cash in our operating activities due to our losses from operations. Net cash used in operating activities was approximately $2,896,000$3,577,000 in both of the nine month periodsperiod ended December 31, 2018 and 2017.2019, compared to approximately $2,896,000 in the nine month period ended December 31, 2018.

 

NET CASH USED IN INVESTING ACTIVITIES. We used approximately $24,000$148,000 of cash to purchase laboratory and office equipment in the nine months ended December 31, 2017.2019. We had no investing activities in the nine months ended December 31, 2018.

 

NET CASH PROVIDED BY (USED IN)USED IN FINANCING ACTIVITIES. InDuring the nine months ended December 31, 2019, we raised approximately $3,956,000 from the issuance of common stock. That source of cash from our financing activities was partially offset by the use of approximately $993,000 to partially pay down our convertible notes and the use of approximately $39,000 to pay for the tax withholding on restricted stock units, for an aggregate increase of cash provided by financing activities of approximately $3,956,000. During the nine months ended December 31, 2018, we raised approximately $884,000 from the saleissuance of common stock, which was partially offset by the paymentuse of approximately $137,000 to pay for the tax withholding on vested rights while in the nine months ended December 31, 2017 we raised approximately $7,166,000 from the sale of commonrestricted stock which was partially offset by the payment of approximately $199,000 for tax withholding on vested rights.units.

 

As of the date of this filing, we plan to invest significantly into purchases of our raw materials and into our contract manufacturing arrangement, subject to successfully raising additional capital.

  

CRITICAL ACCOUNTING POLICIES

 

Use of Estimates

The preparation of condensed consolidated financial statements in conformity with accounting principles generally accepted in the United States of America, or GAAP, requires us to make a number of estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements. SuchThese estimates and assumptions affect the reported amounts of expenses during the reporting period. On an ongoing basis, we evaluate estimates and assumptions based upon historical experience and various other factors and circumstances. We believe our estimates and assumptions are reasonable in the circumstances; however, actual results may differ from these estimates under different future conditions.

 

We believe that the estimates and assumptions that are most important to the portrayal of our financial condition and results of operations, in that they require the most difficult, subjective or complex judgments, form the basis for the accounting policies deemed to be most critical to us. These critical accounting policiesestimates relate to revenue recognition, measurement of stock purchase warrants issued with notes payable, beneficial conversion feature of convertible notes payable, impairment of intangible assets and long lived assets, stock compensation, deferred tax asset valuation allowance, and the classification of warrant obligations, and evaluation of contingencies. We believe estimates and assumptions related to these critical accounting policies are appropriate under the circumstances; however, should future events or occurrences result in unanticipated consequences, there could be a material impact on our future financial condition or results of operations.

 

There have been no changes to our critical accounting policies as disclosed in our Form 10-K for the year ended March 31, 2018.2019, except for the leases policy disclosed in Note 4 to the accompanying unaudited condensed consolidated financial statements included in Item 1 of this Quarterly Report on Form 10-Q.

  

OFF-BALANCE SHEET ARRANGEMENTS

 

We have no obligations required to be disclosed herein as off-balance sheet arrangements.

   

ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.

 

As a smaller reporting company as defined by Rule 12b-2 of the Exchange Act and in Item 10(f)(1) of Regulation S-K, we are electing scaled disclosure reporting obligations and therefore are not required to provide the information requested by this item.

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ITEM 4. CONTROLS AND PROCEDURES.

 

DISCLOSURE CONTROLS AND PROCEDURES

 

Under the supervision and with the participation of our management, including our Chief Executive Officer and our Chief Financial Officer, we evaluated the effectiveness of the design and operation of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) of the Exchange Act) as of the end of the period covered by this Quarterly Report.

 

Based on such evaluation, our Chief Executive Officer and Chief Financial Officer concluded that, as of the end of such period, our disclosure controls and procedures are effective in recording, processing, summarizing and reporting, on a timely basis, information required to be disclosed by us in the reports that we file or submit under the Securities Exchange Act of 1934, as amended, and are effective in ensuring that information required to be disclosed by us in the reports that we file or submit under the Securities Exchange Act of 1934, as amended, 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.

 

CHANGES IN INTERNAL CONTROL OVER FINANCIAL REPORTING

 

There have been no changes in our internal control over financial reporting during the last fiscal quarter that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

 

 

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PART II. OTHER INFORMATION

 

ITEM 1. LEGAL PROCEEDINGS.

 

From time to time, claims are made against us in the ordinary course of business, which could result in litigation. Claims and associated litigation are subject to inherent uncertainties and unfavorable outcomes could occur, such as monetary damages, fines, penalties or injunctions prohibiting us from selling one or more products or engaging in other activities.

 

The occurrence of an unfavorable outcome in any specific period could have a material adverse effect on our results of operations for that period or future periods. We are not presently a party to any pending or threatened legal proceedings.

 

ITEM 1A. RISK FACTORS.

 

As a smaller reporting company as defined by Rule 12b-2 of the Exchange Act and in Item 10(f)(1) of Regulation S-K, we are electing scaled disclosure reporting obligations and therefore are not required to provide the information requested by this item. For a discussion of our potential risks and uncertainties, please see the information listed in the item captioned “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended March 31, 2018.2019. Except as provided below, there have been no material changes to the risk factors as disclosed in the Form 10-K. You should carefully consider the risk factors discussed below and in our Annual Report on Form 10-K for the year ended March 31, 2018,2019, which could materially affect our business, financial position and results of operations.

 

*Our successproducts are manufactured with raw materials that are sourced from specialty suppliers with limited competitors and we may therefore be unable to access the materials we need to manufacture our products.

Specifically, the Hemopurifier contains three critical components with limited supplier numbers. The base cartridge on which the Hemopurifier is constructed is sourced from Medica S.p.A and we are dependent in part on the continued availability of these cartridges. We currently purchase the diatomaceous earth from Janus Scientific Inc., our distributor; however, the product is manufactured by Imerys Minerals Ltd., which is the only supplier of this product. The Galanthus nivalis lectin, or GNA Lectin, is sourced from Vector Laboratories, Inc. and also is available from other suppliers; however, Sigma Aldrich is the only approved back up supplier at this time. A business interruption at any of these sources could have a few key executive officers.material impact on our ability to manufacture the Hemopurifier.

*Even though we have received breakthrough device designation for the Hemopurifier for two independent indications, this designation may not expedite the development or review of the Hemopurifier and does not provide assurance ultimately of PMA submission or approval by the FDA.

The Breakthrough Devices Program is a voluntary program intended to expedite the review, development, assessment and review of certain medical devices that provide for more effective treatment or diagnosis of life-threatening or irreversibly debilitating human diseases or conditions for which no approved or cleared treatment exists or that offer significant advantages over existing approved or cleared alternatives. All submissions for devices designated as Breakthrough Devices will receive priority review, meaning that the review of the submission is placed at the top of the appropriate review queue and receives additional review resources, as needed.

32

Although breakthrough designation or access to any other expedited program may expedite the development or approval process, it does not change the standards for approval. Although we obtained breakthrough device designation for the Hemopurifier for two indications, we may not experience faster development timelines or achieve faster review or approval compared to conventional FDA procedures. For example, the time required to identify and resolve issues relating to manufacturing and controls, the acquisition of a sufficient supply of our product for clinical trial purposes or the need to conduct additional nonclinical or clinical studies may delay approval by the FDA, even if the product qualifies for breakthrough designation or access to any other expedited program. Access to an expedited program may also be withdrawn by the FDA if it believes that the designation is no longer supported by data from our clinical development program. Additionally, qualification for any expedited review procedure does not ensure that we will ultimately obtain regulatory approval for the product.

*Compliance with laws, regulations, and related interpretations and related legal claims or other regulatory enforcement actions could impact our business, and we face additional risks and uncertainties related to any potential actions resulting from the Securities and Exchange Commission’s (the “SEC”) ongoing investigation, or any other investigation or action.

 

Our success dependsOn February 7, 2020, the SEC issued an Order of Suspension of Trading (the “SEC Order”), temporarily suspending trading in our stock for a period of ten days. The SEC Order stated that the suspension was due to a critical extent onconcerns regarding the continued servicesaccuracy and adequacy of our Chief Executive Officer, Timothy Rodell, MD, and our Chief Financial Officer, James B. Frakes. If one or both of these key executive officers were to leave us, we would be forced to expend significant time and moneyinformation in the pursuitmarketplace that appeared to be disseminated by third party promotors and recent and unusual market activity since at least January 22, 2020. We are unable to predict the outcome of the SEC Order or any other actions the SEC may take in connection therewith. Furthermore, the Company’s reputation may be negatively impacted. As a replacement,result, the potential impact to the Company’s business, if any, cannot be determined.

*Our bylaws designate the Eighth Judicial District Court of Clark County, Nevada, as the sole and exclusive forum for certain types of actions and proceedings that may be initiated by our stockholders, which could limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us or our directors, officers, employees or agents.

Our bylaws require that, to the fullest extent permitted by law, and unless the Company consents in writing to the selection of an alternative forum, the Eighth Judicial District Court of Clark County, Nevada, will, to the fullest extent permitted by law, be the sole and exclusive forum for each of the following:

·any derivative action or proceeding brought in the name or right of the Company or on its behalf,
·any action asserting a claim for breach of any fiduciary duty owed by any director, officer, employee or agent of the Company to the Company or the Company’s stockholders,
·any action arising or asserting a claim arising pursuant to any provision of NRS Chapters 78 or 92A or any provision of our articles of incorporation or bylaws, or
·any action asserting a claim governed by the internal affairs doctrine, including, without limitation, any action to interpret, apply, enforce or determine the validity of our articles of incorporation or bylaws.

However, our bylaws provide that the exclusive forum provisions do not apply to suits brought to enforce any liability or duty created by the Securities Exchange Act of 1934, as amended, or any other claim for which the federal courts have exclusive jurisdiction. We note that there is uncertainty as to whether a court would result in both a delayenforce the provision and that investors cannot waive compliance with the federal securities laws and the rules and regulations thereunder. Although we believe this provision benefits us by providing increased consistency in the implementationapplication of our business plan and the diversion of limited working capital. The unique knowledge and expertise of these individuals would be difficult to replace within the biotechnology field. We can give you no assurances that we can find satisfactory replacements for these key executive officers at all, or on terms that are not unduly expensive or burdensome to us. We do not currently carry key man life insurance policies on any of our key executive officers which would assist us in recouping our costsNevada law in the eventtypes of lawsuits to which it applies, the lossprovision may have the effect of thosediscouraging lawsuits against our directors and officers. If either of our key officers were to leave us, it could make it impossible, if not cause substantial delays and costs, to implement our long-term business objectives and growth.

 

Our failure to meet the continued listing requirements of The Nasdaq Capital Market could result in a de-listing of our common stock.

If we fail to satisfy the continued listing requirements of The Nasdaq Capital Market, such as the minimum stockholders’ equity requirement, Nasdaq may take steps to de-list our common stock. Such a de-listing would likely have a negative effect on the price of our common stock and would impair your ability to sell or purchase our common stock when you wish to do so. In the event of a de-listing, we would take actions to restore our compliance with Nasdaq’s listing requirements, but we can provide no assurance that any such action taken by us would allow our common stock to become listed again, stabilize the market price or improve the liquidity of our common stock, or prevent future non-compliance with Nasdaq’s listing requirements.

33

 

ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS.

 

We did not issue or sell any unregistered securities duringIn the three months ended, December 31, 2018.  2019, an aggregate of 851 shares of our common stock were issued to two accredited investors in exchange for the cancellation of outstanding warrants previously held by these investors to purchase an aggregate of 8,505 shares of our common stock.

The offers, sales and issuances of the securities described above were deemed to be exempt from registration under the Securities Act in reliance on Section 4(a)(2) in that the issuance of securities to the accredited investors did not involve a public offering. The recipients of securities in each of these transactions acquired the securities for investment only and not with a view to or for sale in connection with any distribution thereof and appropriate legends were affixed to the securities issued in these transactions. No underwriters were involved in these transactions.

 

ITEM 3. DEFAULTS UPON SENIOR SECURITIES.

 

We have no disclosure applicable to this item.

 

ITEM 4. MINE SAFETY DISCLOSURES.

 

We have no disclosure applicable to this item.

 

ITEM 5. OTHER INFORMATION.

 

We have no disclosure applicable to this item.

 

 

 

 

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ITEM 6. EXHIBITS.

 

(a) Exhibits. The following documents are filed as part of this report:

      Incorporated by Reference
Exhibit
Number
 Exhibit Description Form SEC File No. Exhibit
Number
 Date Filed
Herewith
             
 3.1 Articles of Incorporation. S-3 333-211151 3.1 May 5, 2016  
              
 3.2 Amended and Restated Bylaws of the Company. 8-K 001-37487 3.1 September 12, 2019  
              
 4.1 Form of Common Stock Certificate. S-1 333-201334 4.1 December 31, 2014  
              
 4.2 Form of Common Stock Purchase Warrant dated August 29, 2012. 8-K 000-21846 4.1 September 6, 2012  
              
 4.3 Form of Common Stock Purchase Warrant dated October, November and December 2012. 10-Q 000-21846 4.1 February 12, 2013  
              
 4.4 Form of Common Stock Purchase Warrant dated June 14, 2013. 10-Q 000-21846 4.1 August 13, 2013  
              
 4.5 Form of Common Stock Purchase Warrant dated June 24, 2014. 8-K 000-21846 4.1 June 30, 2014  
              
 4.6 Form of Common Stock Purchase Warrant dated July 24, 2014. 8-K 000-21846 4.1 July 28, 2014  
              
 4.7 Form of Common Stock Purchase Warrant dated August and September 2014. 10-Q 000-21846 4.3 November 10, 2014  
              
 4.8 Form of Warrant to Purchase Common Stock dated June 25, 2015. 8-K 000-21846 4.1 June 24, 2015  
              
 4.9 Form of Purchase Agent Warrant dated June 25, 2015. 8-K 000-21846 4.1 June 26, 2015  
              
 4.10 Form of Warrant Agreement dated March 27, 2017. 8-K 001-37487 4.1 March 22, 2017  
              
 4.11 Form of Warrant dated _______, 2017. S-1/A 333-219589 4.29 September 18, 2017  
              
 4.12 Form of Placement Agent Warrant dated _______, 2017. S-1/A 333-219589 4.30 September 22, 2017  

 

10.1Separation and Consulting Agreement by and between Aethlon Medical, Inc. and James Joyce dated December 10, 2018.
10.2Employment Agreement by and between Aethlon Medical, Inc. and Timothy C. Rodell dated December 10, 2018.
10.3Employment Agreement by and between Aethlon Medical, Inc. and James Frakes dated December 12, 2018.
10.4Form of Indemnification Agreement for Officers and Directors
10.5Form of Option Grant Agreement for Officers and Directors
10.6Form of Restricted Stock Unit Grant Notice and Restricted Stock Unit Agreement for Directors
10.7Form of Restricted Stock Unit Grant Notice and Restricted Stock Unit Agreement for Executives
31.1Certification of Principal Executive Officer pursuant to Securities Exchange Act rules 13a- 14(a) and 15d-14(a) as adopted pursuant to section 302 of the Sarbanes-Oxley Act of 2002
31.2Certification of Principal Financial Officer pursuant to Securities Exchange Act rules 13a- 14(a) and 15d-14(a) as adopted pursuant to section 302 of the Sarbanes-Oxley Act of 2002
32.1Certification of Principal Executive Officer pursuant to 18 U.S.C. section 1350, as adopted pursuant to section 906 of the Sarbanes-Oxley Act of 2002
32.2Certification of Principal Financial Officer pursuant to 18 U.S.C. section 1350, as adopted pursuant to section 906 of the Sarbanes-Oxley Act of 2002
101Interactive Data Files
101.INSXBRL Instance Document
101.SCHXBRL Schema Document
101.CALXBRL Calculation Linkbase Document
101.DEFXBRL Definition Linkbase Document
101.LABXBRL Label Linkbase Document
101.PREXBRL Presentation Linkbase Document

 

 

 

 2635 

 4.14 Form of Warrant to Purchase Common Stock. S-1/A 333-234712 4.14 December 11, 2019  
              
 4.15 Form of Underwriter Warrant. S-1/A 333-234712 4.15 December 11, 2019  
              
 4.16  Form of Common Stock Purchase Warrant.  8-K  001-37487  4.1 January 17, 2020  
              
 10.1 Assignment Agreement, by and between Aethlon Medical, Inc. and London Health Sciences Center Research Inc., dated November 7, 2006. S-1 333-234712 10.27 November 15, 2019  
              
 10.2 Form of Securities Purchase Agreement, by and between Aethlon Medical, Inc. and the Purchaser’s thereto, dated January 17, 2020.  8-K  001-37487 10.1 January 17, 2020   
              
 31.1 Certification of Principal Executive Officer pursuant to Securities Exchange Act rules 13a- 14(a) and 15d-14(a) as adopted pursuant to section 302 of the Sarbanes-Oxley Act of 2002.         X
              
 31.2 Certification of Principal Financial Officer pursuant to Securities Exchange Act rules 13a- 14(a) and 15d-14(a) as adopted pursuant to section 302 of the Sarbanes-Oxley Act of 2002.         X
              
 32.1 Certification of Principal Executive Officer pursuant to 18 U.S.C. section 1350, as adopted pursuant to section 906 of the Sarbanes-Oxley Act of 2002.         X
              
 32.2 Certification of Principal Financial Officer pursuant to 18 U.S.C. section 1350, as adopted pursuant to section 906 of the Sarbanes-Oxley Act of 2002.         X
              
 101 Interactive Data Files          
 101.INS XBRL Instance Document          
 101.SCH XBRL Schema Document          
 101.CAL XBRL Calculation Linkbase Document          
 101.DEF XBRL Definition Linkbase Document          
 101.LAB XBRL Label Linkbase Document          
 101.PRE XBRL Presentation Linkbase Document          

36

 

 

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.

 

 AETHLON MEDICAL, INC. 
    
Date: February 11, 201910, 2020By:/s/ JAMES B. FRAKES 
  JAMES B. FRAKES 
  CHIEF FINANCIAL OFFICER 
  CHIEF ACCOUNTING OFFICER 

 

 

 

 

 

 

 

 

 

 

 

 

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