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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported):
February 14, 2024
AETHLON
MEDICAL, INC.
(Exact name of Registrant as Specified in Its
Charter)
Nevada |
001-37487 |
13-3632859 |
(State or Other Jurisdiction of
Incorporation) |
(Commission File Number) |
(IRS Employer Identification No.) |
|
|
11555
Sorrento Valley Road, Suite
203
San Diego, California |
92121 |
(Address of Principal Executive Offices) |
(Zip Code) |
Registrant’s Telephone Number, Including
Area Code: (619) 941-0360
N/A
(Former Name or Former Address, if Changed Since
Last Report)
Check the appropriate box below if the Form 8-K filing is intended
to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
☐ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
☐ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
☐ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
☐ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
Title of each class |
Trading Symbol(s) |
Name of each exchange on which registered |
Common Stock, $0.001 par value per share |
AEMD |
The Nasdaq Capital Market |
Indicate by check mark whether the registrant is an emerging growth
company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange
Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant
has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant
to Section 13(a) of the Exchange Act. ☐
Item 2.02 |
Results of Operations and Financial Condition. |
On February 14, 2024, Aethlon Medical, Inc. issued
a press release announcing its financial results for the quarter ended December 31, 2023. A copy of this press release is attached hereto
as Exhibit 99.1.
The information in this Item 2.02 and the exhibit
hereto are being furnished and shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act
of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section, nor shall they be deemed
incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth
by specific reference in such a filing.
Item 9.01 |
Financial Statements and Exhibits. |
(d) Exhibits.
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 hereunto duly authorized.
Date: February 14, 2024 |
Aethlon Medical, Inc. |
|
|
|
|
|
|
|
By: |
/s/ James B. Frakes |
|
Name:
|
James B. Frakes
Interim Chief Executive Officer and Chief Financial Officer |
Exhibit 99.1

Aethlon Medical
Announces Fiscal Third Quarter Financial Results and Provides Corporate Update
Conference Call to be Held Today at 4:30
p.m. ET
SAN DIEGO, February 14, 2024 -- Aethlon Medical,
Inc. (Nasdaq: AEMD), a medical therapeutic company focused on developing products to treat cancer and life-threatening infectious diseases,
today reported financial results for its fiscal third quarter ended December 31, 2023 and provided an update on recent developments.
Company Updates
Aethlon Medical is continuing the research and
clinical development of its Hemopurifier®, a therapeutic blood filtration system designed to bind and remove harmful exosomes
and life-threatening viruses from blood and other biological fluids. These qualities of the Hemopurifier have potential applications in
oncology, where cancer associated exosomes may promote immune suppression and metastasis, and in life-threatening infectious diseases.
Aethlon is also investigating the use of the Hemopurifier in the organ transplant setting, initially focusing on the potential removal
of viruses and exosomes with harmful cargo from recovered kidneys.
In October 2023, Aethlon received clearance from
the Drug Controller General of India (DCGI), the country’s central drug authority, to conduct a phase 1 safety, feasibility and
dose-finding trial of the Hemopurifier in patients with solid tumors who have stable or progressive disease during anti-PD-1 monotherapy
treatment, such as Keytruda® or Opdivo®. The trial is expected to begin following completion of an in vitro binding study of relevant
targets, and subsequent approval by the respective Ethics Boards of interested sites in India.
“In addition to an interested initial site
in India, we have two interested sites in Australia that are also awaiting the data from our in vitro binding study,” stated James
Frakes, Interim Chief Executive Officer and Chief Financial Officer. “Our in vitro binding study of relevant oncology targets is
complex and stands on the cutting edge of extracellular vesicle science. Our goal is to quantify the potential impact of our Hemopurifier
on plasma from cancer patients that have been treated with anti-PD-1 monotherapy treatment in order to provide pre-clinical evidence to
support our trial design.
“While our research and development team
has started to quantify our internal data, the results, to date, are inconclusive. Therefore, while our internal team continues
to finetune their work, in parallel we have engaged several third-party laboratories to independently perform assays on the samples.
“We are also maintaining a position in the
use of our Hemopurifier as a treatment against life-threatening viral infections through our COVID-19 trial in India. We have two participating
sites for this trial -- the Medanta Medicity Hospital and Maulana Azad Medical College, or MAMC. One patient has been treated thus far,
however, we have been informed by our contract research organization that a new COVID-19 subvariant was recently detected in India. Our
COVID-19 trial in India remains open in the event that there are COVID-19 admissions to the intensive care units at our two participating
sites.
“Finally, since being named interim Chief
Executive Officer three months ago, I have focused our efforts on our oncology program, as well as on reducing our expenses. As previously
reported, we disclosed some interesting pre-clinical proof of concept data on the Hemopurifier in organ transplantation. As a result,
we plan to submit one or more articles for publication on our pre-clinical data,” concluded Mr. Frakes.
Financial Results for the Third Quarter Ended
December 31, 2023
As of December 31, 2023, Aethlon Medical had a
cash balance of approximately $8.0 million.
Consolidated operating expenses for the three
months ended December 31, 2023 were approximately $3.6 million, compared to $2.8 million for the three months ended December 31, 2022.
This increase of approximately $717,000, or 25.2%, in the 2023 period was due to increase in payroll and related expenses of approximately
$871,000, offset by decreases in general and administrative expenses of approximately $92,000 and in professional fees of approximately
$61,000.
The $871,000 increase in payroll and related expenses
was primarily due to separation expenses for our former chief executive officer of $873,000 and an increase in salary expense of $81,000
associated with an increase in average headcount, offset by a decrease in stock-based compensation of $83,000.
The $92,000 decrease in general and
administrative expenses was primarily due to a decrease in clinical trial expense of approximately $399,000 and a $33,000 decrease in
travel and conferences expenses. Decreases were offset by a $284,000 increase in supplies for manufacturing and research and
development expense, a $31,000 increase in insurance expense, a $13,000 increase in depreciation expense and a $12,000 increase in
outside services and repairs. The increase in insurance expense included $16,000 of health insurance related to the separation
agreement with our former chief executive officer.
The $61,000 decrease in professional fees was
due to a $54,000 decrease in scientific consulting, a $22,000 decrease in marketing, a $21,000 decrease in recruiting and a net $33,000
decrease in contract labor related to general research and development. These decreases were offset by an increase of $44,000 in legal
expenses relating to the reverse stock split, an $11,000 increase in director fees associated with the addition of a new director and
a $14,000 increase in investor relations and accounting fees.
As a result of the changes in expenses noted above,
the company’s net loss increased to $3.6 million for the three months ended December 31, 2023, from $2.8 million in the three months
ended December 31, 2022.
The condensed consolidated balance sheet for December
31, 2023, and the condensed consolidated statements of operations for the three- and nine-month periods ended December 31, 2023 and 2022
follow at the end of this release.
Conference Call
Aethlon
Medical will hold a conference call today, Wednesday, February 14, 2023, at 4:30 p.m. ET to review its financial results for its fiscal
third quarter ended December 31, 2023 and recent corporate developments. Interested parties can register for the conference by
navigating to https://dpregister.com/sreg/10186345/fb902976dd. Please note that registered participants will receive their dial-in
number upon registration.
Interested parties without internet access or
who are unable to pre-register, may dial in as follows:
Participant Dial In (Toll Free): 1-844-836-8741
Participant International Dial In: 1-412-317-5442
All callers should ask for the Aethlon Medical,
Inc. conference call.
A replay of the call will be available approximately
one hour after the end of the call through March 14, 2024. The replay can be accessed via Aethlon Medical's website or by dialing 1-877-344-7529
(domestic) or 1-412-317-0088 (international) or Canada toll free at 1-855-669-9658. The replay conference ID number is 7691190.
About Aethlon and the Hemopurifier®
Aethlon Medical is a medical therapeutic company
focused on developing the Hemopurifier, a clinical stage immunotherapeutic device which is designed to combat cancer and life-threatening
viral infections and for use in organ transplantation. In human studies, the Hemopurifier has demonstrated the removal of life-threatening
viruses and in pre-clinical studies, the Hemopurifier has demonstrated the removal of harmful exosomes from biological fluids, utilizing
its proprietary lectin-based technology. This action has potential applications in cancer, where exosomes may promote immune suppression
and metastasis, and in life-threatening infectious diseases. The Hemopurifier is a U.S. Food and Drug Administration (FDA) designated
Breakthrough Device indicated for 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. The Hemopurifier also holds an FDA Breakthrough Device designation and an open Investigational Device Exemption (IDE) application
related to the treatment of life-threatening viruses that are not addressed with approved therapies.
Additional information can be found at www.AethlonMedical.com.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 that
involve risks and uncertainties. Statements containing words such as "may," "believe," "anticipate," "expect,"
"intend," "plan," "project," "will," "projections," "estimate," "potentially"
or similar expressions constitute forward-looking statements. Such forward-looking statements are subject to significant risks and uncertainties
and actual results may differ materially from the results anticipated in the forward-looking statements. These forward-looking statements
are based upon Aethlon's current expectations and involve assumptions that may never materialize or may prove to be incorrect. Factors
that may contribute to such differences include, without limitation, the Company's ability to raise additional capital and to successfully
complete development of the Hemopurifier; the Company’s ability to successfully demonstrate the utility of the Hemopurifier in cancer
and infectious diseases and in the transplant setting; the Company’s ability to initiate its oncology clinical trials in India and
Australia; the Company’s ability to manage and successfully complete its clinical trials, if initiated; the Company’s ability
to maintain its Nasdaq listing; the Company’s ability to successfully manufacture the Hemopurifier in sufficient quantities for
its clinical trials, and other potential risks. The foregoing list of risks and uncertainties is illustrative, but is not exhaustive.
Additional factors that could cause results to differ materially from those anticipated in forward-looking statements can be found under
the caption "Risk Factors" in the Company's Annual Report on Form 10-K for the year ended March 31, 2023, and in the Company's
other filings with the Securities and Exchange Commission, including its quarterly Reports on Form 10-Q. All forward-looking statements
contained in this press release speak only as of the date on which they were made. Except as may be required by law, the Company does
not intend, nor does it undertake any duty, to update this information to reflect future events or circumstances.
Company Contact:
Jim Frakes
Interim Chief Executive Officer and Chief Financial Officer
Aethlon Medical, Inc.
Jfrakes@aethlonmedical.com
Investor Contact:
Susan Noonan
S.A. Noonan Communications, LLC
susan@sanoonan.com
917-513-5303
AETHLON MEDICAL, INC. AND SUBSIDIARY
Condensed Consolidated Balance Sheets
ASSETS |
|
|
|
|
|
|
|
|
| |
December 31, 2023 | | |
March 31, 2023 | |
| |
(unaudited) | | |
| |
CURRENT ASSETS | |
| | | |
| | |
Cash | |
$ | 7,972,012 | | |
$ | 14,532,943 | |
Prepaid expenses | |
| 277,321 | | |
| 557,623 | |
| |
| | | |
| | |
TOTAL CURRENT ASSETS | |
| 8,249,333 | | |
| 15,090,566 | |
| |
| | | |
| | |
Property and equipment, net | |
| 1,113,880 | | |
| 1,144,004 | |
Right-of-use lease asset | |
| 951,466 | | |
| 1,151,909 | |
Patents, net | |
| 1,238 | | |
| 1,650 | |
Restricted cash | |
| 87,506 | | |
| 87,506 | |
Deposits | |
| 33,305 | | |
| 33,305 | |
| |
| | | |
| | |
TOTAL ASSETS | |
$ | 10,436,728 | | |
$ | 17,508,940 | |
| |
| | | |
| | |
| |
| | | |
| | |
LIABILITIES AND STOCKHOLDERS' EQUITY | |
| | | |
| | |
| |
| | | |
| | |
CURRENT LIABILITIES | |
| | | |
| | |
Accounts payable | |
$ | 693,154 | | |
$ | 432,890 | |
Due to related parties | |
| 656,045 | | |
| 214,221 | |
Lease liability, current portion | |
| 285,095 | | |
| 269,386 | |
Other current liabilities | |
| 466,329 | | |
| 588,592 | |
| |
| | | |
| | |
TOTAL CURRENT LIABILITIES | |
| 2,100,623 | | |
| 1,505,089 | |
| |
| | | |
| | |
Lease liability, less current portion | |
| 724,848 | | |
| 939,642 | |
| |
| | | |
| | |
TOTAL LIABILITIES | |
| 2,825,471 | | |
| 2,444,731 | |
| |
| | | |
| | |
COMMITMENTS AND CONTINGENCIES | |
| | | |
| | |
| |
| | | |
| | |
EQUITY | |
| | | |
| | |
| |
| | | |
| | |
| |
| | | |
| | |
Common stock, par value of $0.001, 60,000,000 shares authorized;
2,492,908 and 2,299,259 issued and outstanding | |
| 2,596 | | |
| 2,299 | |
Additional paid-in-capital | |
| 159,751,591 | | |
| 157,426,606 | |
Accumulated other comprehensive loss | |
| (1,619 | ) | |
| (6,141 | ) |
Accumulated deficit | |
| (152,141,311 | ) | |
| (142,358,555 | ) |
| |
| | | |
| | |
TOTAL STOCKHOLDERS' EQUITY | |
| 7,611,257 | | |
| 15,064,209 | |
| |
| | | |
| | |
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY | |
$ | 10,436,728 | | |
$ | 17,508,940 | |
AETHLON MEDICAL, INC. AND SUBSIDIARY
Consolidated Statements of Operations
For the three and six month periods ended September 30, 2023 and 2022
| |
Three Months | | |
Three Months | | |
Nine Months | | |
Nine Months | |
| |
Ended 12/30/23 | | |
Ended 12/30/22 | | |
Ended 12/30/23 | | |
Ended 12/30/22 | |
| |
| | |
| | |
| | |
| |
Government contract revenue | |
$ | – | | |
$ | – | | |
$ | – | | |
$ | – | |
| |
| | | |
| | | |
| | | |
| | |
OPERATING COSTS AND EXPENSES | |
| | | |
| | | |
| | | |
| | |
Professional fees | |
| 668,586 | | |
| 729,665 | | |
| 2,778,335 | | |
| 2,575,496 | |
Payroll and related | |
| 1,919,305 | | |
| 1,048,761 | | |
| 4,233,970 | | |
| 3,191,402 | |
General and administrative | |
| 979,197 | | |
| 1,071,327 | | |
| 3,138,289 | | |
| 3,653,832 | |
Total operating expenses | |
| 3,567,088 | | |
| 2,849,753 | | |
| 10,150,594 | | |
| 9,420,730 | |
| |
| | | |
| | | |
| | | |
| | |
OPERATING LOSS | |
| (3,567,088 | ) | |
| (2,849,753 | ) | |
| (10,150,594 | ) | |
| (9,420,730 | ) |
| |
| | | |
| | | |
| | | |
| | |
OTHER EXPENSE (INCOME) | |
| | | |
| | | |
| | | |
| | |
Loss on dissolution of subsidiary | |
| | | |
| – | | |
| – | | |
| 142,121 | |
Interest and Other Income | |
| (100,967 | ) | |
| – | | |
| (367,838 | ) | |
| – | |
| |
| | | |
| | | |
| | | |
| | |
NET LOSS | |
$ | (3,466,121 | ) | |
$ | (2,849,753 | ) | |
$ | (9,782,756 | ) | |
$ | (9,562,851 | ) |
| |
| | | |
| | | |
| | | |
| | |
OTHER COMPREHENSIVE LOSS | |
| 7,951 | | |
| – | | |
| 4,522 | | |
| – | |
| |
| | | |
| | | |
| | | |
| | |
COMPREHENSIVE LOSS | |
$ | (3,458,170 | ) | |
$ | (2,849,753 | ) | |
$ | (9,778,234 | ) | |
$ | (9,562,851 | ) |
| |
| | | |
| | | |
| | | |
| | |
Basic and diluted net loss available to common stockholders per share | |
$ | (1.37 | ) | |
$ | (1.24 | ) | |
$ | (3.95 | ) | |
$ | (4.84 | ) |
| |
| | | |
| | | |
| | | |
| | |
Basic and diluted weighted average number of common shares outstanding | |
| 2,516,511 | | |
| 2,294,649 | | |
| 2,477,282 | | |
| 1,974,146 | |
v3.24.0.1
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