Table of Contents
Filed Pursuant
to Rule 424(b)(5)
Registration
No. 333-237269
PROSPECTUS SUPPLEMENT
(To Prospectus dated March 30, 2020)
Aethlon Medical, Inc.
1,380,555 shares of Common Stock
Aethlon Medical, Inc. is offering 1,380,555 shares of our common stock
pursuant to this prospectus supplement and accompanying prospectus to certain institutional investors.
The last reported sale price of our common stock on The Nasdaq Capital
Market on June 9, 2021 was $10.79 per share.
______________________________
This investment involves risk. See “Risk Factors” beginning on page S-4 of this prospectus supplement.
_____________________________
We have engaged Maxim Group LLC to act as our sole placement
agent in connection with this offering. The placement agent has agreed to use its reasonable best efforts to place the securities offered
by this prospectus supplement. We have agreed to pay the placement agent the fees set forth in the table below.
|
|
Per Share
|
|
|
Total
|
|
Offering price
|
|
$
|
9.00
|
|
|
$
|
12,424,995.00
|
|
Placement agent fees (1)
|
|
$
|
0.4275
|
|
|
$
|
590,187.26
|
|
Proceeds, before expenses, to us
|
|
$
|
8.5725
|
|
|
$
|
11,834,807.74
|
|
|
(1)
|
In addition, we have agreed to reimburse the placement agent for certain offering-related expenses. See “Plan of Distribution” beginning on page S-30 of this prospectus supplement.
|
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved of these securities or determined if this prospectus supplement or accompanying prospectus
is truthful or complete. Any representation to the contrary is a criminal offense.
Delivery of our shares of common stock is expected to be made
on or about June 14, 2021, subject to the satisfaction of certain closing conditions.
Sole Placement Agent
Maxim Group LLC
The date of this prospectus supplement
is June 10, 2021.
TABLE
OF CONTENTS
PROSPECTUS SUPPLEMENT
PROSPECTUS
ABOUT THIS PROSPECTUS SUPPLEMENT
This document is in two parts.
The first part is the prospectus supplement, including the documents incorporated by reference, which describes the specific terms
of this offering. The second part, the accompanying prospectus, including the documents incorporated by reference, provides more
general information. Generally, when we refer to this prospectus, we are referring to both parts of this document combined. Before
you invest, you should carefully read this prospectus supplement, the accompanying prospectus, all information incorporated by
reference herein and therein, as well as the additional information described under “Where You Can Find More
Information” and “Incorporation of Certain Information by Reference” on page S-31
and S-32 of this prospectus supplement. These documents contain information you should consider when making your investment
decision. This prospectus supplement may add, update or change information contained in the accompanying prospectus. To the extent
that any statement that we make in this prospectus supplement is inconsistent with statements made in the accompanying prospectus or
any documents incorporated by reference, the statements made in this prospectus supplement will be deemed to modify or supersede
those made in the accompanying prospectus and such documents incorporated by reference.
You should rely only on the information contained or incorporated
by reference in this prospectus supplement, the accompanying prospectus and in any free writing prospectuses we may provide to you in
connection with this offering. Neither we nor the placement agent have authorized any other person to provide you with any information
that is different. If anyone provides you with different or inconsistent information, you should not rely on it. We are offering to sell,
and seeking offers to buy, the securities offered hereby only in jurisdictions where offers and sales are permitted. The distribution
of this prospectus supplement and the offering of the securities offered hereby in certain jurisdictions may be restricted by law. Persons
outside the United States who come into possession of this prospectus supplement must inform themselves about, and observe any restrictions
relating to, the offering of the securities offered hereby and the distribution of this prospectus supplement outside the United States.
This prospectus supplement does not constitute, and may not be used in connection with, an offer to sell, or a solicitation of an offer
to buy, any securities offered by this prospectus supplement by any person in any jurisdiction in which it is unlawful for such person
to make such an offer or solicitation.
Unless otherwise indicated, information contained in this
prospectus supplement, the accompanying prospectus or the documents incorporated by reference, concerning our industry and the markets
in which we operate, including our general expectations and market position, market opportunity and market share, is based on information
from our own management estimates and research, as well as from industry and general publications and research, surveys and studies conducted
by third parties. Management estimates are derived from publicly available information, our knowledge of our industry and assumptions
based on such information and knowledge, which we believe to be reasonable. In addition, assumptions and estimates of our and our industry’s
future performance are necessarily subject to a high degree of uncertainty and risk due to a variety of factors, including those described
in “Risk Factors” in this prospectus supplement and under similar headings in the other
documents that are incorporated by reference into this prospectus. These and other important factors could cause our future performance
to differ materially from our assumptions and estimates. See “Special Note Regarding Forward-Looking Statements.”
When we refer to “Aethlon Medical,” “we,”
“our,” “us” and the “Company” in this prospectus supplement, we mean Aethlon Medical, Inc. and its
consolidated subsidiaries, unless otherwise specified.
This prospectus supplement, the accompanying prospectus
and the information incorporated herein and therein by reference may include trademarks, service marks and trade names owned by us or
other companies. All trademarks, service marks and trade names included or incorporated by reference into this prospectus supplement or
the accompanying prospectus are the property of their respective owners.
SPECIAL NOTE REGARDING FORWARD-LOOKING
STATEMENTS
This prospectus supplement, the accompanying prospectus,
and the documents incorporated by reference herein and therein contain forward-looking statements within the meaning of Section 27A of
the Securities Act of 1933, as amended, or the Securities Act, Section 21E of the Securities Exchange Act of 1934, as amended, or the
Exchange Act, and the Private Securities Litigation Reform Act of 1995, as amended, that involve substantial risks and uncertainties.
These statements relate to future events or to our future financial performance and involve known and unknown risks, uncertainties and
other factors which may cause our actual results, performance or achievements to be materially different from any future results, performance
or achievements expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited to, statements
about:
|
·
|
the initiation, progress, timing, costs and results of preclinical studies and any clinical trials for our Hemopurifier® and any
other product candidates;
|
|
·
|
our estimates regarding expenses, future revenue, capital requirements and needs for additional financing;
|
|
·
|
our ability to further improve our process development capabilities;
|
|
·
|
the timing or likelihood of regulatory filings and approvals;
|
|
·
|
our plans to explore potential applications of our device platform in other indications in oncology and rare diseases;
|
|
·
|
our expectations regarding the clinical effectiveness and safety and tolerability of our product candidates;
|
|
·
|
our commercialization, marketing and manufacturing capabilities and strategy;
|
|
·
|
the pricing and reimbursement of our product candidates, if approved;
|
|
·
|
our expectation regarding the potential market sizes for our product candidates;
|
|
·
|
our intellectual property position;
|
|
·
|
the potential benefits of our strategic collaborations, our plans with respect to our strategic collaborations and our plans with
respect to and our ability to enter into strategic arrangements;
|
|
·
|
developments and projections relating to our competitors and our industry; and
|
|
·
|
the safety, efficacy and projected development timeline and commercial potential of any product candidates.
|
In some cases, you can identify forward-looking statements
by terms such as “anticipates,” “believes,” “could,” “estimates,” “expects,”
“goal,” “intends,” “may,” “plans,” “potential,” “predicts,” “projects,”
“should,” “will,” “would,” the negative of these words and words or similar expressions intended to
identify forward-looking statements. These statements reflect our views as of the date on which they were made with respect to future
events and are based on assumptions and subject to risks and uncertainties. The underlying information and expectations are likely to
change over time. Given these uncertainties, you should not place undue reliance on these forward-looking statements as actual events
or results may differ materially from those projected in the forward-looking statements due to various factors, including, but not limited
to, those set forth under the heading “Risk Factors” in this prospectus supplement, in the accompanying prospectus, and in
our filings with the SEC. These forward-looking statements represent our estimates and assumptions only as of the date of the document
containing the applicable statement.
You should understand that our actual future results may
be materially different from what we expect. In addition, statements that “we believe” and similar statements reflect our
beliefs and opinions on the relevant subject. These statements are based upon information available to us as of the date the statements
were made, and while we believe such information forms a reasonable basis for such statements, such information may be limited or incomplete,
and our statements should not be read to indicate that we have conducted an exhaustive inquiry into, or review of, all potentially available
relevant information. These statements are inherently uncertain and you are cautioned not to unduly rely upon these statements. We qualify
all of the forward-looking statements in the foregoing documents by these cautionary statements. Unless required by law, we undertake
no obligation to update or revise any forward-looking statements to reflect new information or future events or developments. Thus, you
should not assume that our silence over time means that actual events are bearing out as expressed or implied in such forward-looking
statements. Before deciding to purchase shares of our common stock, you should carefully consider the risk factors discussed or incorporated
by reference herein, in addition to the other information set forth in this prospectus supplement, the accompanying prospectus and in
the documents incorporated by reference herein or therein.
PROSPECTUS SUPPLEMENT SUMMARY
This summary highlights selected information about us, this offering
and information appearing elsewhere in this prospectus supplement, in the accompanying prospectus and in the documents we incorporate
by reference. This summary is not complete and does not contain all of the information you should consider before investing in our securities.
Before making an investment decision, to fully understand this offering and its consequences to you, you should carefully read this entire
prospectus supplement and the accompanying prospectus, including “Risk Factors” beginning
on page S-4 of this prospectus supplement and the financial statements and related notes and the other information that we incorporate
by reference into this prospectus supplement.
Company Overview
We are a medical technology company focused on developing products
to diagnose and treat life and organ threatening diseases. The Aethlon Hemopurifier®, or Hemopurifier, is a clinical-stage immunotherapeutic
device designed to combat cancer and life-threatening viral infections. In cancer, the Hemopurifier is 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 FDA, has designated the Hemopurifier as a “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 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.
As we advance our clinical trials, we are in close contact with our clinical sites to navigate and assess the impact of the global COVID-19
pandemic on our clinical trials and current timelines.
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) (NCT # 04453046). The primary endpoint for the EFS, which is designed to 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. This study, which will be conducted at the UPMC Hillman Cancer Center in Pittsburgh, PA, has been approved
by the Institutional Review Board, or IRB, and is now open for patient enrollment.
We also believe the Hemopurifier can be part of the broad-spectrum
treatment of life-threatening highly glycosylated, or carbohydrate coated, viruses that are not addressed with an already approved treatment.
In small-scale or early feasibility human studies, the Hemopurifier has been used to treat individuals infected with human immunodeficiency
virus, or HIV, Hepatitis-C, and Ebola.
Additionally, in-vitro, the Hemopurifier has been demonstrated 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 validations were conducted in collaboration with leading government or non-government research institutes.
On June 17, 2020, the FDA approved a supplement to the Company’s
open IDE for the Company’s Hemopurifier in viral disease to allow for the testing of the Hemopurifier in patients with SARS-CoV-2/COVID-19
in a New Feasibility Study. That study’s plan is to enroll up to 40 subjects at up to 20 centers in the U.S. Subjects will have
established laboratory diagnosis of COVID-19, be admitted to an intensive care unit, or ICU and will have acute lung injury and/or severe
or life threatening disease among other criteria. Endpoints for this study, in addition to safety, will include reduction in circulating
virus as well as clinical outcomes (NCT # 04595903). The first sites for this trial, Hoag Memorial Hospital Presbyterian in Newport Beach,
CA and Hoag Hospital – Irvine in Irvine, CA now have IRB approval and are preparing to open for patient enrollment. Under Single
Patient Emergency Use regulations, the Company has also recently treated a patient with COVID-19, who successfully completed eight daily
treatments with the Hemopurifier.
We are also the majority owner of Exosome Sciences, Inc., or ESI, a
company focused on the discovery of exosomal biomarkers to diagnose and monitor life-threatening diseases. Included among ESI’s
activities is the advancement of a TauSome™ biomarker candidate to diagnose chronic traumatic encephalopathy, 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.
Successful outcomes of human trials will also be required by the regulatory
agencies of certain foreign countries where we plan 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.
Stock Issuances
On June 9, 2021, we sold 626,000 shares of our common stock in the
open market under our At the Market Offering Agreement with H.C. Wainwright & Co., LLC, or ATM Facility. Additionally, pursuant to
the exercise of outstanding warrants on June 9, 2021, we will issue approximately 1.17 million shares of our common stock to the warrant
holders.
Corporate Information
On March 10, 1999, Aethlon, Inc., a California corporation, Hemex,
Inc., a Delaware corporation and the accounting predecessor to Aethlon, Inc., and Bishop Equities, Inc., a publicly traded Nevada corporation,
completed an Agreement and Plan of Reorganization structured to result in Bishop Equities, Inc.'s acquisition of all of the outstanding
common stock of Aethlon, Inc. and Hemex, Inc. Under the plan's terms, Bishop Equities, Inc. issued shares of its common stock to the stockholders
of Aethlon, Inc. and Hemex, Inc. such that Bishop Equities, Inc. then owned 100% of each company. Upon completion of the transaction,
Bishop Equities, Inc. was renamed Aethlon Medical, Inc. In 2009, we formed ESI, which today is a majority-owned subsidiary of the Company
focused on identifying and monitoring neurological conditions and cancer. We commenced operations of ESI in 2013.
Our Contact Information
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 is www.aethlonmedical.com. The information
on our website is not incorporated by reference into this prospectus supplement and should not be considered to be a part of this prospectus
supplement. Our internet address is included in this prospectus supplement as an inactive textual reference only.
THE OFFERING
Common stock offered by us
|
|
1,380,555 shares
|
|
|
|
Offering price per share
|
|
$9.00
|
|
|
|
Common Stock outstanding immediately before this offering
|
|
12,749,524 shares
|
Common Stock outstanding immediately after this offering
|
|
14,130,079 shares
|
|
|
|
Use of proceeds
|
|
We estimate that our net proceeds from this offering
will be approximately $11.6 million after deducting placement agent fees and other estimated offering expenses payable by us.
We intend to use the net proceeds from this offering
for working capital and general corporate purposes, which may include research and development expenses, general and administrative expenses.
Please see “Use of Proceeds” on page S-28 of this prospectus supplement.
|
|
|
|
Risk factors
|
|
Investing in our securities is highly speculative and involves a high degree of risk. See “Risk Factors” beginning on page S-4 of this prospectus supplement and in the documents incorporated by reference into this prospectus supplement for a discussion of factors that you should read and consider before investing in our securities.
|
|
|
|
Nasdaq Capital Market symbol for Common Stock
|
|
AEMD
|
The number of shares of our common stock to be outstanding immediately
after this offering is based on 12,749,524 shares of common stock outstanding as of December 31, 2020, after giving effect to the issuance
and sale of 626,000 shares of common stock in June 2021 under the ATM Facility, and excludes:
|
·
|
602,323 shares of common stock issuable upon exercise of outstanding stock options under our stock incentive plans as of December
31, 2020 at a weighted average exercise price of $3.29 per share;
|
|
·
|
1,991,973 shares of common stock reserved for issuance under outstanding warrants as of December 31, 2020 with a weighted average
exercise price of $5.93 per share; and
|
|
·
|
1,118,292 additional shares of common stock reserved for future issuance under our stock incentive plans as of December 31, 2020.
|
Unless otherwise indicated, all information in this prospectus supplement
assumes no exercise of the outstanding options or warrants described above.
RISK FACTORS
Investing in our shares of common stock involves a high
degree of risk. Before investing in our shares of common stock, you should consider carefully the risks described below, together with
the other information contained in this prospectus supplement, the accompanying prospectus or incorporated by reference herein or therein.
If any of the risks incorporated by reference or set forth below occur, our business, financial condition, results of operations and future
growth prospects could be materially and adversely affected. In these circumstances, the market price of our securities could decline,
and you may lose all or part of your investment.
Purchasers of shares of our common stock in this offering
will experience immediate and substantial dilution in the book value of their investment.
The offering price per share of common stock in this offering
is substantially higher than the net tangible book value per share of our common stock before giving effect to this offering. Accordingly,
if you purchase shares of common stock in this offering, you will incur immediate substantial dilution of approximately $7.02 per share,
representing the difference between the offering price per share, and our as adjusted net tangible book value as of December 31, 2020.
Furthermore, if outstanding options or warrants are exercised, you could experience further dilution. For a further description of the
dilution that you will experience immediately after this offering, see the section in this prospectus supplement entitled “Dilution.”
A substantial number of shares of common stock may
be sold in the market following this offering, which may depress the market price for our common stock.
Sales of a substantial number of shares of our common stock
in the public market following this offering could cause the market price of our common stock to decline. A substantial majority of the
outstanding shares of our common stock are, and the shares of our common stock offered hereby will be, freely tradable without restriction
or further registration under the Securities Act.
We have broad discretion to determine how to use the
funds raised in this offering, and may use them in ways that may not enhance our operating results or the price of our common stock.
Our management will have broad discretion over the use of
proceeds from this offering, and we could spend the proceeds from this offering in ways our stockholders may not agree with or that do
not yield a favorable return, if at all. We intend to use the net proceeds of this offering for working capital and general corporate
purposes, which may include research and development expenses, general and administrative expenses.
However, our use of these proceeds may differ substantially
from our current plans. If we do not invest or apply the proceeds of this offering in ways that improve our operating results, we may
fail to achieve expected financial results, which could cause our common stock price to decline.
You may experience future dilution
as a result of future equity offerings and other issuances of our common stock or other securities. In addition, this offering and future
equity offerings and other issuances of our common stock or other securities may adversely affect our common stock.
In order to raise additional capital, we may in the future
offer additional shares of our common stock or other securities convertible into or exchangeable for shares of our common stock at prices
that may not be the same as the price per share in this offering. We cannot assure you that we will be able to sell shares or other securities
in any other offering at a price per share that is equal to or greater than the price per share paid by investors in this offering, and
investors purchasing shares or other securities in the future could have rights superior to existing stockholders. The price per share
at which we sell additional shares of our common stock or securities convertible into shares of our common stock in future transactions
may be higher or lower than the price per share in this offering.
In addition, the sale of shares of our common stock in this
offering and any future sales of a substantial number of shares of our common stock in the public market, or the perception that such
sales may occur, could adversely affect the price of our common stock. We cannot predict the effect, if any, that market sales of those
shares of our common stock or the availability of those shares of our common stock for sale will have on the market price of our common
stock.
Risks Relating to Our Financial Position and Need for Additional
Capital
We have incurred significant losses and expect to continue to
incur losses for the foreseeable future.
We have never been profitable. We have generated
revenues during the fiscal years ended March 31, 2021 and March 31, 2020, in the amounts of $659,104, and $650,187, respectively, primarily
from our contracts with the NIH. Our revenues, from research grants, continue to be insufficient to cover our cost of operations. It is
possible that we may not be able to enter into future government contracts beyond our current contract with the NIH. Future profitability,
if any, will require the successful commercialization of our Hemopurifier technology, other products that may emerge from our potential
diagnostic products or from additional government contract or grant income. We may not be able to successfully commercialize the Hemopurifier
or any other products, and even if commercialization is successful, we may never be profitable.
We will require additional financing to sustain our operations.
We will require significant additional financing
for our operations and for expected additional future clinical trials in the U.S., as well as to fund all of our continued research and
development activities for the Hemopurifier and other future products. In addition, as we expand our activities, our overhead costs to
support personnel, laboratory materials and infrastructure will increase. If the financing we may require to sustain our working capital
needs is unavailable to us on reasonable terms, or at all, we may be unable to support our research and FDA development activities, including
our planned clinical trials. The failure to implement our research and clearance activities would have a material adverse effect on our
ability to commercialize our products or continue our business.
We also will need to raise additional funds
through debt or equity financings to achieve our business objectives and to satisfy our cash obligations, which may dilute the ownership
of our existing stockholders.
We will need to raise additional funds through
debt and/or equity financings in order to complete our ultimate business objectives, including funding working capital to support development
and regulatory clearance of our potential products. We also may choose to raise additional funds in debt or equity financings if they
are available to us on reasonable terms to increase our working capital and to strengthen our financial position. Any sales of additional
equity or convertible debt securities could result in dilution of the equity interests of our existing stockholders, which could be substantial.
Also, new investors may require that we and certain of our stockholders enter into voting arrangements that give them additional voting
control or representation on our Board of Directors.
Risks Related to Our Business Operations
We face intense competition in the medical device industry.
We compete with numerous U.S. and foreign companies
in the medical device industry, and many of our competitors have greater financial, personnel, operational and research and development
resources than we do. We believe that because the field of exosome research is burgeoning, multiple competitors are or will be developing
competing technologies to address exosomes in cancer. Progress is constant in the treatment and prevention of viral diseases, so the opportunities
for the Hemopurifier may be reduced there as well. Diagnostic technology may be developed that can supplant diagnostics we are developing
for neurodegenerative diseases and cancer. Our commercial opportunities will be reduced or eliminated if our competitors develop and market
products for any of the diseases we target that:
|
·
|
are more effective;
|
|
·
|
have fewer or less severe adverse side effects;
|
|
·
|
are better tolerated;
|
|
·
|
are more adaptable to various modes of dosing;
|
|
·
|
are easier to administer; or
|
|
·
|
are less expensive than the products or product candidates we are developing.
|
Even if we are successful in developing the Hemopurifier
and potential diagnostic products, and obtain FDA and other regulatory approvals necessary for commercializing them, our products may
not compete effectively with other successful products. Researchers are continually learning more about diseases, which may lead to new
technologies for treatment. Our competitors may succeed in developing and marketing products that are either more effective than those
that we may develop, alone or with our collaborators, or that are marketed before any products we develop are marketed. Our competitors
include fully integrated pharmaceutical companies and biotechnology companies, as well as universities and public and private research
institutions. Many of the organizations competing with us have substantially greater capital resources, larger research and development
staffs and facilities, greater experience in product development and in obtaining regulatory approvals, and greater marketing capabilities
than we do. If our competitors develop more effective pharmaceutical treatments for infectious disease or cancer, or bring those treatments
to market before we can commercialize the Hemopurifier for such uses, we may be unable to obtain any market traction for our products,
or the diseases we seek to treat may be substantially addressed by competing treatments. If we are unable to successfully compete against
larger companies in the pharmaceutical industry, we may never generate significant revenue or be profitable.
We have limited experience in identifying
and working with large-scale contracts with medical device manufacturers; manufacture of our devices must comply with good manufacturing
practices in the U.S.
To achieve the levels of production necessary
to commercialize our Hemopurifier and any other future products, we will need to secure large-scale manufacturing agreements with contract
manufacturers which comply with good manufacturing practice standards and other standards prescribed by various federal, state and local
regulatory agencies in the U.S. and any other country of use. We have limited experience coordinating and overseeing the manufacture of
medical device products on a large-scale. It is possible that manufacturing and control problems will arise as we attempt to commercialize
our products and that manufacturing may not be completed in a timely manner or at a commercially reasonable cost. In addition, we may
not be able to adequately finance the manufacture and distribution of our products on terms acceptable to us, if at all. If we cannot
successfully oversee and finance the manufacture of our products if they obtain regulatory clearances, we may never generate revenue from
product sales and we may never be profitable.
Our Hemopurifier technology may become obsolete.
Our Hemopurifier product may be made unmarketable
prior to commercialization by us by new scientific or technological developments by others with new treatment modalities that are more
efficacious and/or more economical than our products. The homeland security industry is growing rapidly with many competitors that are
trying to develop products or vaccines to protect against infectious disease. Any one of our competitors could develop a more effective
product which would render our technology obsolete. Further, our ability to achieve significant and sustained penetration of our key target
markets will depend upon our success in developing or acquiring technologies developed by other companies, either independently, through
joint ventures or through acquisitions. If we fail to develop or acquire, and manufacture and sell, products that satisfy our customers’
demands, or we fail to respond effectively to new product announcements by our competitors by quickly introducing competitive products,
then market acceptance of our products could be reduced and our business could be adversely affected. Our products may not remain competitive
with products based on new technologies.
Our success is dependent in part on our
executive officers.
Our success depends to a critical extent on the
continued services of our Chief Executive Officer, Charles J. Fisher, Jr., M.D., our Chief Financial Officer, James B. Frakes, our Chief
Medical Officer, Steven LaRosa, M.D., and our Chief Business Officer, Guy Cipriani. If any of these key executive officers were to leave
us, we would be forced to expend significant time and money in the pursuit of a replacement, which would result in both a delay in the
implementation 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 do not currently carry key man life insurance policies on any of our
key executive officers which would assist us in recouping our costs in the event of the loss of those 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 inability to attract and retain qualified
personnel could impede our ability to achieve our business objectives.
We have eleven full-time employees, consisting
of our Chief Executive Officer, our Chief Financial Officer, a Chief Medical Officer, a Chief Business Officer, a Vice President, Manufacturing
and Product Development, a Vice President, Clinical Operations, a Project Manager, a Director of Manufacturing and Product Development
and three research scientists. We utilize, whenever appropriate, consultants in order to conserve cash and resources.
Although we believe that these employees and consultants
will be able to handle most of our additional administrative, research and development and business development in the near term, we will
nevertheless be required over the longer-term to hire highly skilled managerial, scientific and administrative personnel to fully implement
our business plan and growth strategies, including to mitigate the material weakness in our internal control over financial reporting
described above. Due to the specialized scientific nature of our business, we are highly dependent upon our ability to attract and retain
qualified scientific, technical and managerial personnel. Competition for these individuals, especially in San Diego, California, where
many biotechnology companies are located, is intense and we may not be able to attract, assimilate or retain additional highly qualified
personnel in the future. We may not be able to engage the services of qualified personnel at competitive prices or at all, particularly
given the risks of employment attributable to our limited financial resources and lack of an established track record. Also, if we are
required to attract personnel from other parts of the U.S. or abroad, we may have significant difficulty doing so due to the high cost
of living in the Southern California area and due to the costs incurred with transferring personnel to the area. If we cannot attract
and retain qualified staff and executives, we will be unable to develop our products and achieve regulatory clearance, and our business
could fail.
We plan to expand our operations, which
may strain our resources; our inability to manage our growth could delay or derail implementation of our business objectives.
We will need to significantly expand our operations
to implement our longer-term business plan and growth strategies. We will also be required to manage multiple relationships with various
strategic partners, technology licensors, customers, manufacturers and suppliers, consultants and other third parties. This expansion
and these expanded relationships will require us to significantly improve or replace our existing managerial, operational and financial
systems, procedures and controls; to improve the coordination between our various corporate functions; and to manage, train, motivate
and maintain a growing employee base. The time and costs to effectuate these steps may place a significant strain on our management personnel,
systems and resources, particularly given the limited amount of financial resources and skilled employees that may be available at the
time. We cannot assure you that we will institute, in a timely manner or at all, the improvements to our managerial, operational and financial
systems, procedures and controls necessary to support our anticipated increased levels of operations and to coordinate our various corporate
functions, or that we will be able to properly manage, train, motivate and retain our anticipated increased employee base. If we cannot
manage our growth initiatives, we will be unable to commercialize our products on a large-scale in a timely manner, if at all, and our
business could fail.
As a public company with limited financial resources undertaking
the launch of new medical technologies, we may have difficulty attracting and retaining executive management and directors.
The directors and management of publicly traded
corporations are increasingly concerned with the extent of their personal exposure to lawsuits and stockholder claims, as well as governmental
and creditor claims which may be made against them, particularly in view of recent changes in securities laws imposing additional duties,
obligations and liabilities on management and directors. Due to these perceived risks, directors and management are also becoming increasingly
concerned with the availability of directors’ and officers’ liability insurance to pay on a timely basis the costs incurred
in defending such claims. While we currently carry directors’ and officers’ liability insurance, such insurance is expensive
and difficult to obtain. If we are unable to continue or provide directors’ and officers’ liability insurance at affordable
rates or at all, it may become increasingly more difficult to attract and retain qualified outside directors to serve on our Board of
Directors. We may lose potential independent board members and management candidates to other companies in the biotechnology field that
have greater directors’ and officers’ liability insurance to insure them from liability or to biotechnology companies that
have revenues or have received greater funding to date which can offer greater compensation packages. The fees of directors are also rising
in response to their increased duties, obligations and liabilities. In addition, our products could potentially be harmful to users, and
we are exposed to claims of product liability including for injury or death. We have limited insurance and may not be able to afford robust
coverage even as our products are introduced into the market. As a company with limited resources and potential exposures to management,
we will have a more difficult time attracting and retaining management and outside independent directors than a more established public
or private company due to these enhanced duties, obligations and potential liabilities.
If we fail to comply with extensive regulations
of U.S. and foreign regulatory agencies, the commercialization of our products could be delayed or prevented entirely.
Our Hemopurifier product is subject to extensive
government regulations related to development, testing, manufacturing and commercialization in the U.S. and other countries. The determination
of when and whether a product is ready for large-scale purchase and potential use will be made by the U.S. Government through consultation
with a number of governmental agencies, including the FDA, the National Institutes of Health, the Centers for Disease Control and Prevention
and the Department of Homeland Security. Our Hemopurifier has not received required regulatory approval from the FDA, or any foreign regulatory
agencies, to be commercially marketed and sold. The process of obtaining and complying with FDA and other governmental regulatory approvals
and regulations in the U.S. and in foreign countries is costly, time consuming, uncertain and subject to unanticipated delays. Obtaining
such regulatory approvals, if any, can take several years. Despite the time and expense exerted, regulatory approval is never guaranteed.
We also are subject to the following risks and obligations, among others:
|
·
|
the FDA may refuse to approve an application if it believes that applicable regulatory criteria are not satisfied;
|
|
·
|
the FDA may require additional testing for safety and effectiveness;
|
|
·
|
the FDA may interpret data from pre-clinical testing and clinical trials in different ways than we interpret them;
|
|
·
|
if regulatory approval of a product is granted, the approval may be limited to specific indications or limited with respect to its distribution; and
|
|
·
|
the FDA may change its approval policies and/or adopt new regulations.
|
Failure to comply with these or other regulatory
requirements of the FDA may subject us to administrative or judicially imposed sanctions, including:
|
·
|
warning letters;
|
|
·
|
civil penalties;
|
|
·
|
criminal penalties;
|
|
·
|
injunctions;
|
|
·
|
product seizure or detention;
|
|
·
|
product recalls; and
|
|
·
|
total or partial suspension of productions.
|
Delays in successfully completing our planned
clinical trials could jeopardize our ability to obtain regulatory approval.
Our business prospects will depend on our ability
to complete studies, clinical trials, including our ongoing Early Feasibility trial in 10 to 12 patients in head and neck cancer and our
study in Covid-19 patients, obtain satisfactory results, obtain required regulatory approvals and successfully commercialize our Hemopurifier
product candidate. Completion of our clinical trials, announcement of results of the trials and our ability to obtain regulatory approvals
could be delayed for a variety of reasons, including:
|
·
|
slow patient enrollment;
|
|
·
|
serious adverse events related to our medical device candidates;
|
|
·
|
unsatisfactory results of any clinical trial;
|
|
·
|
the failure of our principal third-party investigators to perform our clinical trials on our anticipated schedules;
|
|
·
|
different interpretations of our pre-clinical and clinical data, which could initially lead to inconclusive results; and
|
|
·
|
delays resulting from the coronavirus pandemic.
|
Our development costs will increase if we have
material delays in any clinical trial or if we need to perform more or larger clinical trials than planned. If the delays are significant,
or if any of our product candidates do not prove to be safe or effective or do not receive required regulatory approvals, our financial
results and the commercial prospects for our product candidates will be harmed. Furthermore, our inability to complete our clinical trials
in a timely manner could jeopardize our ability to obtain regulatory approval.
If we or our suppliers fail to comply with
ongoing FDA or foreign regulatory authority requirements, or if we experience unanticipated problems with our products, these products
could be subject to restrictions or withdrawal from the market.
Any product for which we obtain clearance or approval,
and the manufacturing processes, reporting requirements, post-approval clinical data and promotional activities for such product, will
be subject to continued regulatory review, oversight and periodic inspections by the FDA and other domestic and foreign regulatory bodies.
In particular, we and our third-party suppliers may be required to comply with the FDA’s Quality System Regulation, or QSR. These
FDA regulations cover the methods and documentation of the design, testing, production, control, quality assurance, labeling, packaging,
sterilization, storage and shipping of our products. Compliance with applicable regulatory requirements is subject to continual review
and is monitored rigorously through periodic inspections by the FDA. If we, or our manufacturers, fail to adhere to QSR requirements in
the U.S., this could delay production of our products and lead to fines, difficulties in obtaining regulatory clearances, recalls, enforcement
actions, including injunctive relief or consent decrees, or other consequences, which could, in turn, have a material adverse effect on
our financial condition or results of operations.
In addition, the FDA assesses compliance with
the QSR through periodic announced and unannounced inspections of manufacturing and other facilities. The failure by us or one of our
suppliers to comply with applicable statutes and regulations administered by the FDA, or the failure to timely and adequately respond
to any adverse inspectional observations or product safety issues, could result in any of the following enforcement actions:
|
·
|
untitled letters, warning letters, fines, injunctions, consent decrees and civil penalties;
|
|
·
|
unanticipated expenditures to address or defend such actions;
|
|
·
|
customer notifications or repair, replacement, refunds, recall, detention or seizure of our products;
|
|
·
|
operating restrictions or partial suspension or total shutdown of production;
|
|
·
|
refusing or delaying our requests for 510(k) clearance or premarket approval of new products or modified products;
|
|
·
|
withdrawing 510(k) clearances or premarket approvals that have already been granted;
|
|
·
|
refusal to grant export approval for our products; or
|
|
·
|
criminal prosecution.
|
Moreover, the FDA strictly regulates the promotional
claims that may be made about approved products. In particular, a product may not be promoted for uses that are not approved by the FDA
as reflected in the product’s approved labeling. However, companies may share truthful and not misleading information that is otherwise
consistent with a product’s FDA approved labeling. The FDA and other agencies actively enforce the laws and regulations prohibiting
the promotion of off-label uses, and a company that is found to have improperly promoted off-label uses may be subject to significant
civil, criminal and administrative penalties. The COVID-19 pandemic could also potentially affect the business of the FDA and comparable
authorities in other countries, which could result in delays in meetings related to planned clinical trials and ultimately of reviews
and approvals of our product candidates.
Any of these sanctions could have a material adverse
effect on our reputation, business, results of operations and financial condition. Furthermore, our key component suppliers may not currently
be or may not continue to be in compliance with all applicable regulatory requirements, which could result in our failure to produce our
products on a timely basis and in the required quantities, if at all.
Delays, interruptions or the cessation of
production by our third-party suppliers of important materials or delays in qualifying new materials, may prevent or delay our ability
to manufacture or process our Hemopurifier.
Most of the raw materials
used in the process for manufacturing our Hemopurifier are available from more than one supplier. However, there are materials within
the manufacturing and production process that come from single suppliers. We do not have written contracts with all of our single source
suppliers, and at any time they could stop supplying our orders. FDA review of a new supplier may be required if these materials become
unavailable from our current suppliers. Although there may be other suppliers that have equivalent materials that would be available to
us, FDA review of any alternate suppliers, if required, could take several months or more to obtain, if able to be obtained at all. Any
delay, interruption or cessation of production by our third-party suppliers of important materials, or any delay in qualifying new materials,
if necessary, would prevent or delay our ability to manufacture our Hemopurifiers. In addition, an uncorrected impurity, a supplier’s
variation in a raw material or testing, either unknown to us or incompatible with its manufacturing process, or any other problem with
our materials, testing or components, would prevent or delay the release of our Hemopurifiers for use in our clinical trials.
For example, in late 2020, we identified during
our device quality review procedures prior to product release that one of our critical suppliers had produced a Hemopurifier component
that was not produced to our specifications. Although no affected Hemopurifiers were released to us or to any trial sites, we are working
to resolve the issue, and concurrently are working to identify alternative suppliers for this component. We believe that our current Hemopurifier
inventory is sufficient for the conduct of our current ongoing clinical trials, but it is possible that the need for our Hemopurifiers
could increase or the resolution of the issue with one of our current suppliers and identification of an alternative supplier could take
longer than expected. Although we intend to procure alternative supply sources for our component and our current supplier intends to correct
their issue, we can provide no assurance that we will do so in a timely manner. Any such delays could limit our ability to meet demand
for the Hemopurifier and delay our ongoing clinical trials, which would have a material adverse impact on our business, results of operations
and financial condition.
Difficulties in manufacturing our Hemopurifier
could have an adverse effect upon our expenses and our product revenues.
We currently outsource most of the manufacturing
of our Hemopurifier. The manufacturing of our Hemopurifier is difficult and complex. To support our current clinical trial needs, we comply
with and intend to continue to comply with cGMP in the manufacture of our product. Our ability to adequately manufacture and supply our
Hemopurifier in a timely matter is dependent on the uninterrupted and efficient operation of our facilities and those of third-parties
producing raw materials and supplies upon which we rely in our manufacturing. The manufacture of our products may be impacted by:
|
·
|
availability or contamination of raw materials and components used in the manufacturing process, particularly
those for which we have no other source or supplier;
|
|
·
|
our ability to comply with new regulatory requirements, including our ability to comply with cGMP;
|
|
·
|
inclement weather and natural disasters;
|
|
·
|
changes in forecasts of future demand for product components;
|
|
·
|
potential facility contamination by microorganisms or viruses;
|
|
·
|
updating of manufacturing specifications;
|
|
·
|
product quality success rates and yields; and
|
|
·
|
global viruses and pandemics, including the current COVID-19 pandemic.
|
If efficient manufacture and supply of our Hemopurifier
is interrupted, we may experience delayed shipments or supply constraints. If we are at any time unable to provide an uninterrupted supply
of our products for our clinical trials, our ongoing clinical trials may be delayed, which could materially and adversely affect our business,
results of operations and financial conditions.
If our products, or malfunction of our products,
cause or contribute to a death or a serious injury, we will be subject to medical device reporting regulations, which can result in voluntary
corrective actions or agency enforcement actions.
Under the FDA medical device reporting regulations,
medical device manufacturers are required to report to the FDA information that a device has or may have caused or contributed to a death
or serious injury or has malfunctioned in a way that would likely cause or contribute to death or serious injury if the malfunction of
the device or one of our similar devices were to recur. If we fail to report these events to the FDA within the required timeframes, or
at all, FDA could take enforcement action against us. Any such adverse event involving our products also could result in future voluntary
corrective actions, such as recalls or customer notifications, or agency action, such as inspection or enforcement action. Any corrective
action, whether voluntary or involuntary, as well as defending ourselves in a lawsuit, will require the dedication of our time and capital,
distract management from operating our business, and may harm our reputation and financial results.
We outsource many of our operational and
development activities, and if any party to which we have outsourced certain essential functions fails to perform its obligations under
agreements with us, the development and commercialization of our lead product candidate and any future product candidates that we may
develop could be delayed or terminated.
We rely on third-party consultants or other vendors
to manage and implement the much of the day-to-day conduct of conducting clinical trials and manufacturing our current product candidates.
Accordingly, we are and will continue to be dependent on the timeliness and effectiveness of the efforts of these third parties. Our dependence
on third parties includes key suppliers and third-party service providers supporting the development, manufacture and regulatory approval
of our Hemopurifier, as well as support for our information technology systems and other infrastructure. While our management team oversees
these vendors, failure of any of these third parties to meet their contractual, regulatory and other obligations or the development of
factors that materially disrupt the performance of these third parties could have a material adverse effect on our business. For example,
all of the key oversight responsibilities for the development and manufacture of our Hemopurifier are conducted by our management team,
but all other activities are the responsibility of third-party vendors. It is possible that the current COVID-19 epidemic might constrain
the ability of needed third-party vendors to provide services that we require.
If a clinical research organization that we utilize
is unable to allocate sufficient qualified personnel to our studies in a timely manner or if the work performed by it does not fully satisfy
the requirements of the FDA or other regulatory agencies, we may encounter substantial delays and increased costs in completing our development
efforts. Any manufacturer that we select may encounter difficulties in the manufacture of new products in commercial quantities, including
problems involving product yields, product stability or shelf life, quality control, adequacy of control procedures and policies, compliance
with FDA regulations and the need for further FDA approval of any new manufacturing processes and facilities. If any of these occur, the
development and commercialization of our product candidates could be delayed, curtailed or terminated because we may not have sufficient
financial resources or capabilities to continue such development and commercialization on our own.
If we or our contractors or service providers
fail to comply with regulatory laws and regulations, we or they could be subject to regulatory actions, which could affect our ability
to develop, market and sell our product candidates and any other or future product candidates that we may develop and may harm our reputation.
If we or our manufacturers or other third-party
contractors fail to comply with applicable federal, state or foreign laws or regulations, we could be subject to regulatory actions, which
could affect our ability to successfully develop, market and sell our Hemopurifier product candidate or any future product candidates
under development and could harm our reputation and lead to reduced or non-acceptance of our proposed product candidates by the market.
Even technical recommendations or evidence by the FDA through letters, site visits, and overall recommendations to academia or biotechnology
companies may make the manufacturing of a clinical product extremely labor intensive or expensive, making the product candidate no longer
viable to manufacture in a cost-efficient manner. The mode of administration may make the product candidate not commercially viable. The
required testing of the product candidate may make that candidate no longer commercially viable. The conduct of clinical trials may be
critiqued by the FDA, or a clinical trial site’s Institutional Review Board or Institutional Biosafety Committee, which may delay
or make impossible clinical testing of a product candidate. The Institutional Review Board for a clinical trial may stop a trial or deem
a product candidate unsafe to continue testing. This would have a material adverse effect on the value of the product candidate and our
business prospects.
We will need to outsource and rely on third
parties for the clinical development and manufacture, sales and marketing of Hemopurifier or any future product candidates that we may
develop, and our future success will be dependent on the timeliness and effectiveness of the efforts of these third parties.
We do not have the required financial and human
resources to carry out on our own all the pre-clinical and clinical development for our Hemopurifier product candidate or any other or
future product candidates that we may develop, and do not have the capability and resources to manufacture, market or sell our Hemopurifier
product candidate or any future product candidates that we may develop. Our business model calls for the partial or full outsourcing of
the clinical and other development and manufacturing, sales and marketing of our product candidates in order to reduce our capital and
infrastructure costs as a means of potentially improving our financial position. Our success will depend on the performance of these outsourced
providers. If these providers fail to perform adequately, our development of product candidates may be delayed and any delay in the development
of our product candidates would have a material and adverse effect on our business prospects.
We are and will be exposed to product liability risks, and clinical
and preclinical liability risks, which could place a substantial financial burden upon us should we be sued.
Our business exposes us to potential product liability
and other liability risks that are inherent in the testing, manufacturing and marketing of medical devices. Claims may be asserted against
us. A successful liability claim or series of claims brought against us could have a material adverse effect on our business, financial
condition and results of operations. We may not be able to continue to obtain or maintain adequate product liability insurance on acceptable
terms, if at all, and such insurance may not provide adequate coverage against potential liabilities. Claims or losses in excess of any
product liability insurance coverage that we may obtain could have a material adverse effect on our business, financial condition and
results of operations.
Our Hemopurifier product candidate may be used
in connection with medical procedures in which it is important that those products function with precision and accuracy. If our product
candidates, including our Hemopurifier, do not function as designed, or are designed improperly, we may be forced by regulatory agencies
to withdraw such products from the market. In addition, if medical personnel or their patients suffer injury as a result of any failure
of our products to function as designed, or our products are designed inappropriately, we may be subject to lawsuits seeking significant
compensatory and punitive damages. The risk of product liability claims, product recalls and associated adverse publicity is inherent
in the testing, manufacturing, marketing and sale of medical products. We have recently obtained general clinical trial liability insurance
coverage. However, our insurance coverage may not be adequate or available. We may not be able to secure product liability insurance coverage
on acceptable terms or at reasonable costs when needed. Any product recall or lawsuit seeking significant monetary damages may have a
material effect on our business and financial condition. Any liability for mandatory damages could exceed the amount of our coverage.
Moreover, a product recall could generate substantial negative publicity about our products and business and inhibit or prevent commercialization
of other future product candidates.
We have not received, and may never receive,
approval from the FDA to market a medical device in the United States.
Before a new medical device can be marketed in
the U.S., it must first receive a PMA or 510(k) clearance from the FDA, unless an exemption applies. A PMA submission, which is a higher
standard than a 510(k) clearance, is used to demonstrate to the FDA that a new or modified device is safe and effective. The 510(k) is
used to demonstrate that a device is “substantially equivalent” to a predicate device (one that has been cleared by the FDA).
We expect that any product we seek regulatory approval for, including the Hemopurifier, will require a PMA. The FDA approval process involves,
among other things, successfully completing clinical trials and filing for and obtaining a PMA. The PMA process requires us to prove the
safety and effectiveness of our products to the FDA’s satisfaction. This process, which includes preclinical studies and clinical
trials, can take many years and requires the expenditure of substantial resources and may include post-marketing surveillance to establish
the safety and efficacy of the product. Notwithstanding the effort and expense incurred, the process may never result in the FDA granting
a PMA. Data obtained from preclinical studies and clinical trials are subject to varying interpretations that could delay, limit or prevent
regulatory approval. Delays or rejections may also be encountered based upon changes in governmental policies for medical devices during
the period of product development. The FDA can delay, limit or deny approval of a PMA application for many reasons, including:
|
·
|
our inability to demonstrate safety or effectiveness of the Hemopurifier or any other product we develop to the FDA’s satisfaction;
|
|
·
|
insufficient data from our preclinical studies and clinical trials, including for our Hemopurifier, to support approval;
|
|
·
|
failure of the facilities of our third-party manufacturer or suppliers to meet applicable requirements;
|
|
·
|
inadequate compliance with preclinical, clinical or other regulations;
|
|
·
|
our failure to meet the FDA’s statistical requirements for approval; and
|
|
·
|
changes in the FDA’s approval policies, or the adoption of new regulations that require additional data or additional clinical studies.
|
Modifications to products that are approved through
a PMA application generally need FDA approval. Similarly, some modifications made to products cleared through a 510(k) may require a new
510(k). The FDA’s 510(k) clearance process usually takes from three to 12 months, but may last longer. The process of obtaining
a PMA is much costlier and more uncertain than the 510(k) clearance process and generally takes from one to three years, or even longer,
from the time the application is submitted to the FDA until an approval is obtained. Any of our products considered to be a class III
device, which are considered to pose the greatest risk and the approval of which is governed by the strictest guidelines, will require
the submission and approval of a PMA in order for us to market it in the U.S. We also may design new products in the future that could
require the clearance of a 510(k).
Although we have received approval to proceed
with clinical trials of the Hemopurifier in the U.S. under the investigational device exemption, the current approval from the FDA to
proceed could be revoked, the study could be unsuccessful, or the FDA PMA approval may not be obtained or could be revoked. Even if we
obtain approval, the FDA or other regulatory authorities may require expensive or burdensome post-market testing or controls. Any delay
in, or failure to receive or maintain, clearance or approval for our future products could prevent us from generating revenue from these
products or achieving profitability. Additionally, the FDA and other regulatory authorities have broad enforcement powers. Regulatory
enforcement or inquiries, or other increased scrutiny on us, could dissuade some physicians from using our products and adversely affect
our reputation and the perceived safety and efficacy of our products.
The approval requirements for medical products used to fight
bioterrorism and pandemics are still evolving, and any products we develop for such uses may not meet these requirements.
We are advancing product candidates under governmental
policies that regulate the development and commercialization of medical treatment countermeasures against bioterror and pandemic threats.
While we intend to pursue FDA market clearance to treat infectious bioterror and pandemic threats, it is often not feasible to conduct
human studies against these deadly high threat pathogens. For example, the Hemopurifier is an investigational device that has not yet
received FDA approval for any indication. We continue to investigate the potential for the use of the Hemopurifier in viral diseases under
an open IDE and our FDA Breakthrough Designation for “…the treatment of life-threatening glycosylated viruses that are not
addressed with an approved therapy.” We currently have an open FDA approved Expanded Access Protocol for the treatment of Ebola
infected patients in the U.S. and a corresponding HealthCanada approval in Canada. Based on our studies to date, the Hemopurifier can
potentially clear many viruses that are pathogenic in humans, including HCV, HIV and Ebola. We do have preclinical data suggesting that
it could clear a closely related coronavirus (MERS).
On June 17, 2020, the FDA approved a supplement
to our open IDE for the Hemopurifier in viral disease to allow for the testing of the Hemopurifier in patients with SARS-CoV-2/COVID-19
in a New Feasibility Study. That study’s plan is to enroll up to 40 subjects at up to 20 centers
in the U.S. Subjects will have established laboratory diagnosis of COVID-19, be admitted to an intensive care unit, or ICU, and will have
acute lung injury and/or severe or life threatening disease, among other criteria. Endpoints for this study, in addition to safety, will
include reduction in circulating virus as well as clinical outcomes (NCT # 04595903). The initial sites for this trial, Hoag Memorial
Hospital Presbyterian in Newport Beach, CA and Hoag Hospital – Irvine in Irvine, CA and Loma Linda Hospital in Loma Linda, CA, have
completed clinical trial agreements, and have received IRB approval in the case of the Hoag hospitals, and are preparing to open for patient
enrollment. Under Single Patient Emergency Use regulations, the Company has also treated two patients with COVID-19 with the Hemopurifier.
Additionally, we have a very limited supply of
Hemopurifiers and therefore any use in this pandemic will be only investigational in a very small number of patients, even if it appears
that the device can help those patients.
Thus, we may not be able to demonstrate the effectiveness
of our treatment countermeasures through controlled human efficacy studies. Additionally, a change in government policies could impair
our ability to obtain regulatory approval and the FDA may not approve any of our product candidates.
The results of our clinical trials may not
support our product candidate claims or may result in the discovery of adverse side effects.
Any research and development, pre-clinical testing
and clinical trial activities involving our Hemopurifier and any additional products that we may develop are subject to extensive regulation
and review by numerous governmental authorities both in the U.S. and abroad. Clinical studies must be conducted in compliance with FDA
regulations or the FDA may take enforcement action. The data collected from these clinical studies may ultimately be used to support market
clearance for these products. Even if our clinical trials are completed as planned, the results of these trials may not support our product
candidate claims and the FDA may not agree with our conclusions regarding the trial results. Success in pre-clinical studies and early
clinical trials does not ensure that later clinical trials will be successful, and the later trials may not replicate the results of prior
trials and pre-clinical studies. The clinical trial process may fail to demonstrate that our product candidates are safe and effective
for the proposed indicated uses, which could cause us to abandon a product candidate and may delay development of others. Any delay or
termination of our clinical trials will delay the filing of our product submissions and, ultimately, our ability to commercialize our
product candidates and generate revenues. It is also possible that patients enrolled in clinical trials will experience adverse side effects
that are not currently part of the product candidate’s profile.
U.S. legislative or FDA regulatory reforms
may make it more difficult and costly for us to obtain regulatory approval of our product candidates and to manufacture, market and distribute
our products after approval is obtained.
From time to time, legislation is drafted and
introduced in Congress that could significantly change the statutory provisions governing the regulatory approval, manufacture and marketing
of regulated products or the reimbursement thereof. In addition, FDA regulations and guidance are often revised or reinterpreted by the
FDA in ways that may significantly affect our business and our products. Any new regulations or revisions or reinterpretations of existing
regulations may impose additional costs or lengthen review times of future products. It is impossible to predict whether legislative changes
will be enacted or FDA regulations, guidance or interpretations changed, and what the impact of such changes, if any, may be or new product
development efforts.
Our current and future business activities
are subject to applicable anti-kickback, fraud and abuse, false claims, physician payment transparency, health information privacy and
security and other healthcare laws and regulations, which could expose us to significant penalties.
We are currently and will in the future be subject
to healthcare regulation and enforcement by the U.S. federal government and the states in which we will conduct our business once our
product candidates are approved by the FDA and commercialized in the United States. In addition to the FDA’s restrictions on marketing
of approved products, the U.S. healthcare laws and regulations that may affect our ability to operate include: the federal fraud and abuse
laws, including the federal anti-kickback and false claims laws; federal data privacy and security laws; and federal transparency laws
related to payments and/or other transfers of value made to physicians (defined to include doctors, dentists, optometrists, podiatrists
and chiropractors) and other healthcare professionals (beginning January 1, 2022) and teaching hospitals. Many states have similar laws
and regulations that may differ from each other and federal law in significant ways, thus complicating compliance efforts. These laws
may adversely affect our sales, marketing and other activities with respect to any product candidate for which we receive approval to
market in the United States by imposing administrative and compliance burdens on us.
Because of the breadth of these laws and the narrowness
of available statutory exceptions and regulatory safe harbors, it is possible that some of our business activities, particularly any sales
and marketing activities after a product candidate has been approved for marketing in the United States, could be subject to legal challenge
and enforcement actions. If our operations are found to be in violation of any of the federal and state laws described above or any other
governmental regulations that apply to us, we may be subject to significant civil, criminal, and administrative penalties, including,
without limitation, damages, fines, imprisonment, exclusion from participation in government healthcare programs, additional reporting
obligations and oversight if we become subject to a corporate integrity agreement or other agreement to resolve allegations of non-compliance
with these laws, and the curtailment or restructuring of our operations, any of which could adversely affect our ability to operate our
business and our results of operations.
We are subject to stringent and changing
privacy laws, regulations and standards as well as policies, contracts and other obligations related to data privacy and security. Our
actual or perceived failure to comply with such obligations could lead to government enforcement actions (that could include fines and
penalties), a disruption of our clinical trials or commercialization of our products, private litigation, harm to our reputation, or other
adverse effects on our business or prospects.
We collect, receive, store,
process, use, generate, transfer, disclose, make accessible, protect and share personal information and other information, including information
we collect in connection with clinical trials, or “Process” or “Processing”, as necessary to operate our business,
for legal and marketing purposes, and for other business-related purposes.
There are numerous federal,
state, local and international laws, regulations and guidance regarding privacy, information security and Processing, the number and scope
of which is changing, subject to differing applications and interpretations, and which may be inconsistent. We are, or may become, subject
to these laws, regulations, and guidance, and we are also subject to the terms of our external and internal privacy and security policies,
representations, certifications, standards, publications, frameworks, and contractual obligations to third parties related to privacy,
information security and Processing, or Data Protection Obligations.
If we fail, or are perceived
to have failed, to address or comply with Data Protection Obligations, it could: increase our compliance and operational costs; expose
us to regulatory scrutiny, actions, fines and penalties; result in reputational harm; interrupt or stop our clinical trials; result in
litigation and liability; result in an inability to process personal data or to operate in certain jurisdictions; harm our business operations
or financial results or otherwise result in a material harm to our business, or each, a Material Adverse Impact. Additionally, given that
Data Protection Obligations impose complex and burdensome obligations and that there is substantial uncertainty over the interpretation
and application of these obligations, we may be required to incur material costs, divert management attention, and change our business
operations, including our clinical trials, in an effort to comply, which could materially adversely affect our business operations and
financial results.
The California Consumer Privacy
Act of 2018, CCPA, is an example of the increasingly stringent data protection legislation in the United States. The CCPA gives California
residents expanded rights to access and require deletion of their personal information, opt-out of certain personal information sharing,
and receive detailed information about how their personal information is used. The CCPA provides for civil penalties for violations, as
well as a private right of action for data breaches and statutory damages ranging from $100 to $750 per violation, which is expected to
increase data breach class action litigation and result in significant exposure to costly legal judgements and settlements. Although there
are limited exemptions for clinical trial data under the CCPA, the CCPA and other similar laws could impact our business activities depending
on how they are interpreted.
The European Union’s
General Data Protection Regulation, or GDPR, is an example of the type of data protection legislation being passed in international jurisdictions.
The GDPR requires covered businesses to, among other requirements, provide detailed disclosures, contractually commit to data protection
measures in our contracts, maintain adequate data security measures, notify regulators and affected individuals of certain data breaches
and meet extensive privacy governance and documentation requirements. Companies that violate the GDPR can face private litigation, restrictions
on data processing, and fines of up to the greater of 20 million Euros or 4% of their worldwide annual revenue. In addition, the GDPR
includes restrictions on cross-border data transfers. A Recent decision by the Court of Justice of the European Union, or the “Schrems
II” ruling, however, has created substantial uncertainty regarding how to legally transfer personal data from Europe to the United
States. There are few, if any, viable options for us or our vendors to legally transfer personal data from Europe to the United States,
which could materially impact our business.
If our security measures, or those maintained
on our behalf, are compromised, or the security, confidentiality, integrity or availability of our information technology, software, services,
networks, communications or data is compromised, limited or fails, this could result in a Material Adverse Impact.
In the ordinary course of our business, we Process
proprietary, confidential and sensitive information, including personal data, intellectual property, trade secrets, and proprietary business
information owned or controlled by ourselves or other third parties, or collectively, Sensitive Information. We may use and share Sensitive
Information with service providers and subprocessors and other third parties upon whom we rely to help us operate our business. If we,
our service providers, partners, or other relevant third parties have experienced, or in the future experience, any security incident(s)
that result in any data loss; deletion or destruction; unauthorized access to; loss, unauthorized acquisition, disclosure, or exposure
of, Sensitive Information, or compromise related to the security, confidentiality, integrity of our (or their) information technology,
software, services, communications or data (any, a “Security Breach”), it may result in a Material Adverse Impact (as defined
above), including the diversion of funds to address the breach, and interruptions, delays, or outages in our operations and development
programs.
Cyberattacks, malicious internet-based
activity and online and offline fraud are prevalent and continue to increase. In addition to threats from traditional computer “hackers,”
threat actors, software bugs, malicious code (such as viruses and worms), employee theft or misuse, denial-of-service attacks (such as
credential stuffing) and ransomware attacks, sophisticated nation-state and nation-state supported actors now engage in attacks (including
advanced persistent threat intrusions). We may also be the subject of phishing attacks, viruses, malware installation, server malfunction,
software or hardware failures, loss of data or other computer assets, or other similar issues.
We may be required to expend
significant resources, fundamentally change our business activities and practices, or modify our operations, including clinical trial
activities, or information technology in an effort to protect against Security Breaches and to mitigate, detect and remediate actual and
potential vulnerabilities. Applicable Data Protection Obligations (as defined above) may require us to implement specific security measures
or use industry-standard or reasonable measures to protect against Security Breaches. There can be no assurances that our security measures
or those of third parties upon whom we rely will be effective in protecting against Security Incidents.
Applicable Data Protection
Obligations (as defined above) may require us to notify relevant stakeholders of Security Breaches, including affected individuals, partners,
collaborators, regulators, law enforcement agencies and others. Such disclosures are costly, and the disclosures or the failure to comply
with such requirements could lead to Material Adverse Impacts. There can be no assurances that any limitations or exclusions of liability
in our contracts would be adequate or would otherwise protect us from liabilities or damages if we fail to comply with Data Protection
Obligations related to information security or Security Breaches.
We cannot be sure that our
insurance coverage, if any, will be adequate or otherwise protect us from or adequately mitigate liabilities or damages with respect to
claims, costs, expenses, litigation, fines, penalties, business loss, data loss, regulatory actions or Material Adverse Impacts arising
out of our Processing operations, privacy and security practices, or Security Breaches that we may experience. The successful assertion
of one or more large claims against us that exceeds our available insurance coverage, or results in changes to our insurance policies
(including premium increases or the imposition of large excess or deductible or co-insurance requirements), could have a Material Adverse
Impact.
Should our products be approved for commercialization,
lack of third-party coverage and reimbursement for our devices could delay or limit their adoption.
In both the U.S. and international markets, the
use of medical devices is dependent in part on the availability of reimbursement from third-party payors, such as government and private
insurance plans. Healthcare providers that use medical devices generally rely on third-party payors to pay for all or part of the costs
and fees associated with the medical procedures being performed or to compensate them for their patient care services. Should our products
under development be approved for commercialization by the FDA, any such products may not be considered cost-effective, reimbursement
may not be available in the U.S. or other countries, if approved, and reimbursement may not be sufficient to allow sales of our future
products, including the Hemopurifier, on a profitable basis. The coverage decisions of third-party payors will be significantly influenced
by the assessment of our future products by health technology assessment bodies. These assessments are outside our control and any such
evaluations may not be conducted or have a favorable outcome.
If approved for use in the U.S., we expect that
any products that we develop, including the Hemopurifier, will be purchased primarily by medical institutions, which will in turn bill
various third-party payors for the health care services provided to patients at their facility. Payors may include the Centers for Medicare
& Medicaid Services, or CMS, which administers the Medicare program and works in partnership with state governments to administer
Medicaid, other government programs and private insurance plans. The process involved in applying for coverage and incremental reimbursement
from CMS is lengthy and expensive. Further, Medicare coverage is based on our ability to demonstrate that the treatment is “reasonable
and necessary” for Medicare beneficiaries. Even if products utilizing our Aethlon Hemopurifier technology receive FDA and other
regulatory clearance or approval, they may not be granted coverage and reimbursement by any payor, including by CMS. For some governmental
programs, such as Medicaid, coverage and adequate reimbursement differ from state to state and some state Medicaid programs may not pay
adequate amounts for the procedure necessary to utilize products utilizing our technology system, or any payment at all. Moreover, many
private payors use coverage decisions and payment amounts determined by CMS as guidelines in setting their coverage and reimbursement
policies and amounts. However, no uniform policy requirement for coverage and reimbursement for medical devices exists among third-party
payors in the United States. Therefore, coverage and reimbursement can differ significantly from payor to payor. If CMS or other agencies
limit coverage or decrease or limit reimbursement payments for doctors and hospitals, this may affect coverage and reimbursement determinations
by many private payors for any products that we develop.
Should any of our potential products, including
the Hemopurifier, be approved for commercialization, adverse changes in reimbursement policies and procedures by payors may impact our
ability to market and sell our products.
Healthcare costs have risen significantly over
the past decade, and there have been and continue to be proposals by legislators, regulators and third-party payors to decrease costs.
Third-party payors are increasingly challenging the prices charged for medical products and services and instituting cost containment
measures to control or significantly influence the purchase of medical products and services.
For example, in the U.S., the Patient Protection
and Affordable Care Act, as amended by the Health Care and Education Reconciliation Act of 2010, or collectively, PPACA, among other things,
reduced and/or limited Medicare reimbursement to certain providers. However, on December 14, 2018, a Texas U.S. District Court Judge ruled
that the Affordable Care Act is unconstitutional in its entirety because the “individual mandate” was repealed by Congress
as part of the Tax Cuts and Jobs Act of 2017. Additionally, on December 18, 2019, the U.S. Court of Appeals for the 5th Circuit upheld
the District Court ruling that the individual mandate was unconstitutional and remanded the case back to the District Court to determine
whether the remaining provisions of the PPACA are invalid as well. The U.S. Supreme Court is currently reviewing the case, although it
is unclear when a decision will be made or how the Supreme Court will rule. The Budget Control Act of 2011, as amended by subsequent legislation,
further reduces Medicare’s payments to providers by two percent through fiscal year 2030. However, COVID-19 relief legislation suspended
the two percent Medicare sequester from May 1, 2020 through December 31, 2021. These reductions may reduce providers’ revenues or
profits, which could affect their ability to purchase new technologies. Furthermore, the healthcare industry in the U.S. has experienced
a trend toward cost containment as government and private insurers seek to control healthcare costs by imposing lower payment rates and
negotiating reduced contract rates with service providers. Legislation could be adopted in the future that limits payments for our products
from governmental payors. It is possible that additional governmental action is taken to address the COVID-19 pandemic. In addition, commercial
payors such as insurance companies, could adopt similar policies that limit reimbursement for medical device manufacturers’ products.
Therefore, it is possible that our product or the procedures or patient care performed using our product will not be reimbursed at a cost-effective
level. We face similar risks relating to adverse changes in reimbursement procedures and policies in other countries where we may market
our products. Reimbursement and healthcare payment systems vary significantly among international markets. Our inability to obtain international
reimbursement approval, or any adverse changes in the reimbursement policies of foreign payors, could negatively affect our ability to
sell our products and have a material adverse effect on our business and financial condition.
Our ability to use net operating loss carryforwards
and certain other tax attributes to offset future taxable income or taxes may be limited.
Under the Tax Cuts and Jobs Act of 2017, as modified
by the CARES Act, federal net operating losses incurred in tax years beginning after December 31, 2017, may be carried forward indefinitely,
but the deductibility of such federal net operating losses in tax years beginning after December 31, 2020, is limited to 80% of taxable
income. It is uncertain if and to what extent various states will conform to the Tax Cuts and Jobs Act of 2017 or the CARES Act. In addition,
under Sections 382 and 383 of the Internal Revenue Code of 1986, as amended, and corresponding provisions of state law, if a corporation
undergoes an “ownership change,” which is generally defined as a greater than 50% change in its equity ownership value over
a three-year period, the corporation’s ability to use its pre-change net operating loss carryforwards and other pre-change tax attributes
to offset its post-change income or taxes may be limited. We believe we have not experienced an ownership change in the past three years,
however, we could experience ownership changes in the future as a result of subsequent shifts in our stock ownership, some of which may
be outside of our control. If we achieve profitability and an ownership change occurs and our ability to use our net operating loss carryforwards
is materially limited, it would harm our future operating results by effectively increasing our future tax obligations. In addition, at
the state level, there may be periods during which the use of net operating loss carryforwards is suspended or otherwise limited, which
could accelerate or permanently increase state taxes owed. For example, California imposed limits on the usability of California state
net operating losses to offset taxable income in tax years beginning after 2019 and before 2023.
Our use of hazardous materials, chemicals
and viruses exposes us to potential liabilities for which we may not have adequate insurance.
Our research and development involves the controlled
use of hazardous materials, chemicals and viruses. The primary hazardous materials include chemicals needed to construct the Hemopurifier
cartridges and the infected plasma samples used in preclinical testing of the Hemopurifier. All other chemicals are fully inventoried
and reported to the appropriate authorities, such as the fire department, which inspects the facility on a regular basis. We are subject
to federal, state, local and foreign laws governing the use, manufacture, storage, handling and disposal of such materials. Although we
believe that our safety procedures for the use, manufacture, storage, handling and disposal of such materials comply with the standards
prescribed by federal, state, local and foreign regulations, we cannot completely eliminate the risk of accidental contamination or injury
from these materials. We have had no incidents or problems involving hazardous chemicals or biological samples. In the event of such an
accident, we could be held liable for significant damages or fines.
We currently carry a limited amount of insurance
to protect us from damages arising from hazardous materials. Our product liability policy has a $5,000,000 limit of liability that would
cover certain releases of hazardous substances away from our facilities. For our facilities, our property policy provides $25,000 in coverage
for contaminant clean-up or removal and $50,000 in coverage for damages to the premises resulting from contamination. Should we violate
any regulations concerning the handling or use of hazardous materials, or should any injuries or death result from our use or handling
of hazardous materials, we could be the subject of substantial lawsuits by governmental agencies or individuals. We may not have adequate
insurance to cover all or any of such claims, if any. If we were responsible to pay significant damages for violations or injuries, if
any, we might be forced to cease operations since such payments could deplete our available resources.
Our products may in the future be subject
to product recalls. A recall of our products, either voluntarily or at the direction of the FDA or another governmental authority, including
a third-country authority, or the discovery of serious safety issues with our products, could have a significant adverse impact on us.
The FDA and similar foreign governmental authorities
have the authority to require the recall of commercialized products in the event of material deficiencies or defects in design or manufacture.
For the FDA, the authority to require a recall must be based on a finding that there is reasonable probability that the device would cause
serious injury or death. In addition, foreign governmental bodies have the authority to require the recall of our products in the event
of material deficiencies or defects in design or manufacture. Manufacturers may, under their own initiative, recall a product if any material
deficiency in a device is found. The FDA requires that certain classifications of recalls be reported to the FDA within 10 working days
after the recall is initiated. A government-mandated or voluntary recall by us or one of our international distributors could occur as
a result of an unacceptable risk to health, component failures, malfunctions, manufacturing errors, design or labeling defects or other
deficiencies and issues. Recalls of any of our products would divert managerial and financial resources and have an adverse effect on
our reputation, results of operations and financial condition, which could impair our ability to produce our products in a cost-effective
and timely manner in order to meet our customers’ demands. We may also be subject to liability claims, be required to bear other
costs, or take other actions that may have a negative impact on our future sales and our ability to generate profits. Companies are required
to maintain certain records of recalls, even if they are not reportable to the FDA or another third-country competent authority. We may
initiate voluntary recalls involving our products in the future that we determine do not require notification of the FDA or another third-country
competent authority. If the FDA disagrees with our determinations, they could require us to report those actions as recalls. A future
recall announcement could harm our reputation with customers and negatively affect our sales. In addition, the FDA could take enforcement
action for failing to report recalls. We are also required to follow detailed recordkeeping requirements for all firm-initiated medical
device corrections and removals.
Our business is subject to risks arising
from the recent COVID-19 pandemic.
The current COVID-19 worldwide pandemic has presented
substantial public health and economic challenges and is affecting our employees, patients, communities and business operations, as well
as the U.S. and global economy and financial markets.
International and U.S. governmental authorities
in impacted regions are taking actions in an effort to slow the spread of COVID-19, including issuing varying forms of “stay-at-home”
orders, and restricting business functions outside of one’s home. In response, we have implemented a work from home policy for all
non-laboratory employees, following the guidelines or directives issued by federal, state and local government agencies in the U.S.
To date, we do not currently anticipate any interruptions
in supply. In addition, while we are continuing the process of getting our clinical trial underway, we expect that COVID-19 precautions
may directly or indirectly impact the timeline for the trial. As the COVID-19 pandemic continues to spread around the globe, we may experience
disruptions that could severely impact our business, clinical trials and manufacturing and supply chains, including:
|
·
|
further delays or difficulties in enrolling patients in our clinical trials;
|
|
·
|
delays or difficulties in clinical site initiation, including difficulties in recruiting clinical site investigators and clinical site staff;
|
|
·
|
diversion of healthcare resources away from the conduct of clinical trials, including the diversion of hospitals serving as our clinical trial sites and hospital staff supporting the conduct of our clinical trials;
|
|
·
|
interruption of key clinical trial activities, such as clinical trial site monitoring, due to limitations on travel imposed or recommended by federal or state governments, employers and others or interruption of clinical trial subject visits and study procedures, which may impact the integrity of subject data and clinical study endpoints;
|
|
·
|
interruption of, or delays in receiving, supplies of our product candidates from our contract manufacturing organizations due to staffing shortages, production slowdowns or stoppages and disruptions in delivery systems;
|
|
·
|
delays in clinical sites receiving the supplies and materials needed to conduct our clinical trials and interruption in global shipping that may affect the transport of clinical trial materials;
|
|
·
|
limitations on employee resources that would otherwise be focused on the conduct of our clinical trials, including because of sickness of employees or their families or the desire of employees to avoid contact with large groups of people;
|
|
·
|
delays in receiving feedback or approvals from the FDA or other regulatory authorities with respect to future clinical trials or regulatory submissions;
|
|
·
|
changes in local regulations as part of a response to COVID-19 which may require us to change the ways in which our clinical trials are conducted, which may result in unexpected costs, or to discontinue the clinical trials altogether;
|
|
·
|
delays in necessary interactions with local regulators, ethics committees and other important agencies and contractors due to limitations in employee resources or forced furlough of government employees;
|
|
·
|
refusal of the FDA to accept data from clinical trials in affected geographies; and
|
|
·
|
difficulties launching or commercializing products, including due to reduced access to doctors as a result of social distancing protocols.
|
In addition, the spread of COVID-19 has had and
may continue to impact the trading price of shares of our common stock and could further negatively impact our ability to raise additional
capital on a timely basis or at all.
The COVID-19 pandemic continues to rapidly evolve.
The extent to which COVID-19 may impact our business, including our clinical trials, manufacturing and supply chains and financial condition
will depend on future developments, which are highly uncertain and cannot be predicted with confidence, such as the continued geographic
spread of the disease, the duration of the pandemic, travel restrictions and social distancing in the United States and other countries,
continued business closures or business disruptions and the effectiveness of actions taken in the United States and other countries to
contain and treat the disease.
Our products 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 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 agglutinin, or GNA, 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, including interruption
resulting from the coronavirus pandemic, could have a 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.
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, or the SEC, ongoing
investigation, or any other investigation or action.
On February 7, 2020, the SEC issued an Order of
Suspension of Trading, or SEC Order, temporarily suspending trading in our stock for a period of ten days. The SEC Order stated that the
suspension was due to concerns regarding the accuracy and adequacy of information in the marketplace that appeared to be disseminated
by third party promotors and recent and unusual market activity since at least January 22, 2020. Although our stock resumed trading upon
expiration of the SEC Order, we are unable to predict the outcome of the SEC investigation or any other actions the SEC may take in connection
therewith. Furthermore, the Company’s reputation may be negatively impacted. As a 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 Exchange Act, or any other claim for which
the federal courts have exclusive jurisdiction. We note that there is uncertainty as to whether a court would enforce 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 application of Nevada law in the types of lawsuits to which it applies,
the provision may have the effect of discouraging lawsuits against our directors and officers.
Risks Related to Our Intellectual Property and Related Litigation
We rely upon licenses and patent rights from third parties which
are subject to termination or expiration.
We rely in part upon third-party licenses and
ownership rights assigned from third parties for the development of specific uses for our Hemopurifier devices. For example, we are researching,
developing and testing cancer-related applications for our devices under patents assigned from the London Health Science Center Research,
Inc. Should any of our licenses be prematurely terminated for any reason, or if the patents and intellectual property assigned to us or
owned by such entities that we have licensed are challenged or defeated by third parties, our research efforts could be materially and
adversely affected. Our licenses and patents assigned to us may not continue in force for as long as we require for our research, development
and testing of cancer treatments. It is possible that, if our licenses terminate or the underlying patents and intellectual property is
challenged or defeated or the patents and intellectual property assigned to us is challenged or defeated, suitable replacements may not
be obtained or developed on terms acceptable to us, if at all. There is also the related risk that we may not be able to make the required
payments under any patent license or assignment agreement, in which case we may lose to ability to use one or more of the licensed or
assigned patents.
We could become subject to intellectual
property litigation that could be costly, result in the diversion of management’s time and efforts, require us to pay damages, prevent
us from selling our commercially available products and/or reduce the margins we may realize from our products.
The medical devices industry is characterized
by extensive litigation and administrative proceedings over patent and other intellectual property rights. Whether a product infringes
a patent involves complex legal and factual issues, and the determination is often uncertain. There may be existing patents of which we
are unaware that our products under development may inadvertently infringe. The likelihood that patent infringement claims may be brought
against us increases as the number of participants in the infectious market increases and as we achieve more visibility in the market
place and introduce products to market.
Any infringement claim against us, even if without
merit, may cause us to incur substantial costs, and would place a significant strain on our financial resources, divert the attention
of management from our core business, and harm our reputation. In some cases, litigation may be threatened or brought by a patent holding
company or other adverse patent owner who has no relevant product revenues and against whom our patents may provide little or no deterrence.
If we are found to infringe any patents, we could be required to pay substantial damages, including triple damages if an infringement
is found to be willful. We also could be required to pay royalties and could be prevented from selling our products unless we obtain a
license or are able to redesign our products to avoid infringement. We may not be able to obtain a license enabling us to sell our products
on reasonable terms, or at all. If we fail to obtain any required licenses or make any necessary changes to our technologies or the products,
we may be unable to commercialize one or more of our products or may have to withdraw products from the market, all of which would have
a material adverse effect on our business, financial condition and results of operations.
If the combination of patents, trade secrets
and contractual provisions upon which we rely to protect our intellectual property is inadequate, our ability to commercialize our products
successfully will be harmed.
Our success depends significantly on our ability
to protect our proprietary rights to the technologies incorporated in our products. We currently have five issued U.S. patents and five
pending U.S. patent applications. We also have 33 issued foreign patents and have applied for six additional international patents. Our
issued patents begin to expire in 2024, with the last of these patents expiring in 2036, although terminal disclaimers, patent term extension
or patent term adjustment can shorten or lengthen the patent term. We rely on a combination of patent protection, trade secret laws and
nondisclosure, confidentiality and other contractual restrictions to protect our proprietary technology. However, these may not adequately
protect our rights or permit us to gain or keep any competitive advantage.
The issuance of a patent is not conclusive as
to its scope, validity or enforceability. The scope, validity or enforceability of our issued patents can be challenged in litigation
or proceedings before the U.S. Patent and Trademark Office or foreign patent offices where our applications are pending. The U.S. Patent
and Trademark Office or foreign offices may deny or require significant narrowing of claims in our pending patent applications. Patents
issued as a result of the pending patent applications, if any, may not provide us with significant commercial protection or be issued
in a form that is advantageous to us. Proceedings before the U.S. Patent and Trademark Office or foreign offices could result in adverse
decisions as to the priority of our inventions and the narrowing or invalidation of claims in issued patents. The laws of some foreign
countries may not protect our intellectual property rights to the same extent as the laws of the U.S., if at all. Some of our patents
may expire before we receive FDA approval to market our products in the U.S. or we receive approval to market our products in a foreign
country. Although we believe that certain patent applications and/or other patents issued more recently will help protect the proprietary
nature of the Hemopurifier treatment technology, this protection may not be sufficient to protect us during the development of that technology.
Our competitors may successfully challenge and
invalidate or render unenforceable our issued patents, including any patents that may issue in the future, which could prevent or limit
our ability to market our products and could limit our ability to stop competitors from marketing products that are substantially equivalent
to ours. In addition, competitors may be able to design around our patents or develop products that provide outcomes that are comparable
to our products but that are not covered by our patents.
We have also entered into confidentiality and
assignment of intellectual property agreements with all of our employees, consultants and advisors directly involved in the development
of our technology as one of the ways we seek to protect our intellectual property and other proprietary technology. However, these agreements
may not be enforceable or may not provide meaningful protection for our trade secrets or other proprietary information in the event of
unauthorized use or disclosure or other breaches of the agreements.
In the event a competitor infringes upon any of
our patents or other intellectual property rights, enforcing our rights may be difficult, time consuming and expensive, and would divert
management’s attention from managing our business. We may not be successful on the merits in any enforcement effort. In addition,
we may not have sufficient resources to litigate, enforce or defend our intellectual property rights.
We may rely on licenses for new technology,
which may affect our continued operations with respect thereto.
As we develop our technology, we may need to license
additional technologies to optimize the performance of our products. We may not be able to license these technologies on commercially
reasonable terms or at all. In addition, we may fail to successfully integrate any licensed technology into our proposed products. Our
inability to obtain any necessary licenses could delay our product development and testing until alternative technologies can be identified,
licensed and integrated. The inability to obtain any necessary third-party licenses could cause us to abandon a particular development
path, which could seriously harm our business, financial position and results of our operations.
New technology may lead to our competitors
developing superior products which would reduce demand for our products.
Research into technologies similar to ours is
proceeding at a rapid pace, and many private and public companies and research institutions are actively engaged in the development of
products similar to ours. These new technologies may, if successfully developed, offer significant performance or price advantages when
compared with our technologies. Our existing patents or our pending and proposed patent applications may not offer meaningful protection
if a competitor develops a novel product based on a new technology.
If we are unable to protect our proprietary
technology and preserve our trade secrets, we will increase our vulnerability to competitors which could materially adversely impact our
ability to remain in business.
Our ability to successfully commercialize our
products will depend on our ability to protect those products and our technology with domestic and foreign patents. We will also need
to continue to preserve our trade secrets. The issuance of a patent is not conclusive as to its validity or as to the enforceable scope
of the claims of the patent. The patent positions of technology companies, including us, are uncertain and involve complex legal and factual
issues. Our patents may not prevent other companies from developing similar products or products which produce benefits substantially
the same as our products, and other companies may be issued patents that may prevent the sale of our products or require us to pay significant
licensing fees in order to market our products.
From time to time, we may need to obtain licenses
to patents and other proprietary rights held by third parties in order to develop, manufacture and market our products. If we are unable
to timely obtain these licenses on commercially reasonable terms, our ability to commercially exploit such products may be inhibited or
prevented. Our pending patent applications may not result in issued patents, patent protection may not be secured for any particular technology,
and our issued patents may not be valid or enforceable or provide us with meaningful protection.
If we are required to engage in expensive
and lengthy litigation to enforce our intellectual property rights, such litigation could be very costly and the results of such litigation
may not be satisfactory.
Although we have entered into invention assignment
agreements with our employees and with certain advisors, and we routinely enter into confidentiality agreements with our contract partners,
if those employees, advisors or contract partners develop inventions or processes independently that may relate to products or technology
under development by us, disputes may arise about the ownership of those inventions or processes. Time-consuming and costly litigation
could be necessary to enforce and determine the scope of our rights under these agreements. In addition, we may be required to commence
litigation to enforce such agreements if they are violated, and it is certainly possible that we will not have adequate remedies for breaches
of our confidentiality agreements as monetary damages may not be sufficient to compensate us. We may be unable to fund the costs of any
such litigation to a satisfactory conclusion, which could leave us without recourse to enforce contracts that protect our intellectual
property rights.
Other companies may claim that our technology
infringes on their intellectual property or proprietary rights and commence legal proceedings against us which could be time-consuming
and expensive and could result in our being prohibited from developing, marketing, selling or distributing our products.
Because of the complex and difficult legal and
factual questions that relate to patent positions in our industry, it is possible that our products or technology could be found to infringe
upon the intellectual property or proprietary rights of others. Third parties may claim that our products or technology infringe on their
patents, copyrights, trademarks or other proprietary rights and demand that we cease development or marketing of those products or technology
or pay license fees. We may not be able to avoid costly patent infringement litigation, which will divert the attention of management
away from the development of new products and the operation of our business. We may not prevail in any such litigation. If we are found
to have infringed on a third-party’s intellectual property rights, we may be liable for money damages, encounter significant delays
in bringing products to market or be precluded from manufacturing particular products or using particular technology.
Other parties may challenge certain of our foreign
patent applications. If any such parties are successful in opposing our foreign patent applications, we may not gain the protection afforded
by those patent applications in particular jurisdictions and may face additional proceedings with respect to similar patents in other
jurisdictions, as well as related patents. The loss of patent protection in one jurisdiction may influence our ability to maintain patent
protection for the same technology in other jurisdictions.
Risks Related to U.S. Government Contracts
We may not obtain additional U.S. Government
contracts to further develop our technology.
We may not be successful in obtaining additional
government grants or contracts. The process of obtaining government contracts is lengthy with the uncertainty that we will be successful
in obtaining announced grants or contracts for therapeutics as a medical device technology. Accordingly, although we have obtained government
contracts in the past, we may not be awarded any additional U.S. Government grants or contracts utilizing our Hemopurifier platform technology.
U.S. Government agencies have special contracting
requirements, including a right to audit us which create additional risks; a negative audit would be detrimental to
us.
Our business plan to utilize the Aethlon Hemopurifier
technology is likely to continue to involve contracts with the U.S. Government. Many government contracts typically contain unfavorable
termination provisions and are subject to audit and modification by the government at its sole discretion, which subjects us to additional
risks. These risks include the ability of the U.S. Government to unilaterally:
|
·
|
suspend or prevent us for a period of time from receiving new contracts or extending existing contracts based on violations or suspected violations of laws or regulations;
|
|
·
|
audit and object to our contract-related costs and fees, including allocated indirect costs;
|
|
·
|
control and potentially prohibit the export of our products; and
|
|
·
|
change certain terms and conditions in our contracts.
|
As a U.S. Government contractor, we are required
to comply with applicable laws, regulations and standards relating to our accounting practices and would be subject to periodic audits
and reviews. As part of any such audit or review, the U.S. Government may review the adequacy of, and our compliance with, our internal
control systems and policies, including those relating to our purchasing, property, estimating, compensation and management information
systems. Based on the results of its audits, the U.S. Government may adjust our contract-related costs and fees, including allocated indirect
costs. In addition, if an audit or review uncovers any improper or illegal activity, we would possibly be subject to civil and criminal
penalties and administrative sanctions, including termination of our contracts, forfeiture of profits, suspension of payments, fines and
suspension or prohibition from doing business with the U.S. Government. We could also suffer serious harm to our reputation if allegations
of impropriety were made against us. Although we have not had any government audits and reviews to date, future audits and reviews could
cause adverse effects. In addition, under U.S. Government purchasing regulations, some of our costs, including most financing costs, amortization
of intangible assets, portions of our research and development costs, and some marketing expenses, would possibly not be reimbursable
or allowed under such contracts. Further, as a U.S. Government contractor, we would be subject to an increased risk of investigations,
criminal prosecution, civil fraud, whistleblower lawsuits and other legal actions and liabilities.
As a U.S. Government contractor, we are subject to a number of
procurement rules and regulations.
Government contractors must comply with specific
procurement regulations and other requirements. These requirements, although customary in government contracts, impact our performance
and compliance costs. In addition, current U.S. Government budgetary constraints could lead to changes in the procurement environment,
including the Department of Defense’s recent initiative focused on efficiencies, affordability and cost growth and other changes
to its procurement practices. If and to the extent such changes occur, they could impact our results of operations and liquidity, and
could affect whether and, if so, how we pursue certain opportunities and the terms under which we are able to do so.
In addition, failure to comply with these regulations
and requirements could result in reductions of the value of contracts, contract modifications or termination, and the assessment of penalties
and fines, which could negatively impact our results of operations and financial condition. Our failure to comply with these regulations
and requirements could also lead to suspension or debarment, for cause, from government contracting or subcontracting for a period of
time. Among the causes for debarment are violations of various statutes, including those related to procurement integrity, export control,
government security regulations, employment practices, protection of the environment, accuracy of records and the recording of costs,
and foreign corruption. The termination of our government contract as a result of any of these acts could have a negative impact on our
results of operations and financial condition and could have a negative impact on our reputation and ability to procure other government
contracts in the future.
Risks Relating to Our Common Stock and Our Corporate Governance
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, or Nasdaq, such as the minimum stockholders’ equity requirement or the minimum closing bid price requirement,
Nasdaq may take steps to de-list our common stock. For example, in May 2019 we received a letter from Nasdaq indicating that Nasdaq had
determined that we had failed to comply with the minimum bid price requirement of Nasdaq Listing Rule 5550(a)(2). Nasdaq Listing Rule
5550(a)(2) requires that companies listed on the Nasdaq Capital Market maintain a minimum closing bid price of at least $1.00 per share. In
July 2019, we received another letter from Nasdaq indicating that Nasdaq has determined that we have failed to comply with the minimum
stockholder’s equity requirement of Nasdaq Listing Rule 5550(b)(1). Nasdaq Listing Rule 5550(b)(1) requires that companies listed
on the Nasdaq Capital Market maintain a minimum of $2,500,000 in stockholder’s equity. If we fail to maintain compliance with these,
or any other of the continued listing requirements of The Nasdaq Capital Market, 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 any such action taken by us may not be successful.
Historically we have not paid dividends
on our common stock, and we do not anticipate paying any cash dividends in the foreseeable future.
We have never paid cash dividends on our common
stock. We intend to retain our future earnings, if any, to fund operational and capital expenditure needs of our business, and do not
anticipate paying any cash dividends in the foreseeable future. As a result, capital appreciation, if any, of our common stock will be
the sole source of gain for our common stockholders in the foreseeable future.
Our stock price is speculative, and there
is a risk of litigation.
The trading price of our common stock has in the
past and may in the future be subject to wide fluctuations in response to factors such as the following:
|
·
|
failure to raise additional funds when needed;
|
|
·
|
announcements regarding our ongoing development of the Hemopurifier;
|
|
·
|
results from our clinical trials with the Hemopurifier;
|
|
·
|
failure to meet the continued listing requirements of and maintain our listing on
Nasdaq;
|
|
·
|
results of operations or revenue in any quarter failing to meet the expectations, published or otherwise, of the investment community;
|
|
·
|
reduced investor confidence in equity markets;
|
|
·
|
speculation in the press or analyst community;
|
|
·
|
wide fluctuations in stock prices, particularly with respect to the stock prices for other medical device companies;
|
|
·
|
announcements of technological innovations by us or our competitors;
|
|
·
|
new products or the acquisition of significant customers by us or our competitors;
|
|
·
|
changes in interest rates;
|
|
·
|
changes in investors’ beliefs as to the appropriate price-earnings ratios for us and our competitors;
|
|
·
|
changes in recommendations or financial estimates by securities analysts who track our common stock or the stock of other medical device companies;
|
|
·
|
changes in management;
|
|
·
|
sales of common stock by directors and executive officers;
|
|
·
|
rumors or dissemination of false or misleading information, particularly through Internet chat rooms, instant messaging, and other rapid-dissemination methods;
|
|
·
|
conditions and trends in the medical device industry generally;
|
|
·
|
the announcement of acquisitions or other significant transactions by us or our competitors;
|
|
·
|
adoption of new accounting standards affecting our industry;
|
|
·
|
changes in the structure of healthcare payment systems;
|
|
·
|
general market conditions;
|
|
·
|
domestic or international terrorism and other factors, including the effects of the ongoing pandemic; and
|
|
·
|
the other factors described in this section.
|
Fluctuations in the price of our common stock
may expose us to the risk of securities class action lawsuits. Although no such lawsuits are currently pending against us and we are not
aware that any such lawsuit is threatened to be filed in the future, future lawsuits are possible as a result of fluctuations in the price
of our common stock. Defending against any such suits could result in substantial cost and divert management’s attention and resources.
In addition, any settlement or adverse determination of such lawsuits could subject us to significant liability.
If at any time our common stock is subject
to the SEC’s penny stock rules, broker-dealers may experience difficulty in completing customer transactions and trading activity
in our securities may be adversely affected.
If at any time our common stock is not listed
on a national securities exchange or we have net tangible assets of $2,000,000 or less, or we have an average revenue of less than $6,000,000
for the last three years, and our common stock has a market price per share of less than $5.00, transactions in our common stock will
be subject to the SEC’s “penny stock” rules. If our common stock is subject to the “penny stock” rules promulgated
under the Exchange Act, broker-dealers may find it difficult to effectuate customer transactions and trading activity in our securities
may be adversely affected. For any transaction involving a penny stock, unless exempt, the rules require:
|
·
|
that a broker or dealer approve a person’s account for transactions in penny stocks;
|
|
·
|
furnish the investor a disclosure document describing the risks of investing in penny stocks;
|
|
·
|
disclose to the investor the current market quotation, if any, for the penny stock;
|
|
·
|
disclose to the investor the amount of compensation the firm and its broker will receive for the trade; and
|
|
·
|
The broker or dealer receive from the investor a written agreement to the transaction, setting forth the identity and quantity of the penny stock to be purchased.
|
In order to approve a person’s account for
transactions in penny stocks, the broker or dealer must:
|
·
|
obtain financial information and investment experience objectives of the person; and
|
|
·
|
make a reasonable determination that the transactions in penny stocks are suitable for that person and the person has sufficient knowledge and experience in financial matters to be capable of evaluating the risks of transactions in penny stocks.
|
The broker or dealer must also deliver, prior
to any transaction in a penny stock, a disclosure schedule prescribed by the SEC relating to the penny stock market, which, in highlight
form:
|
·
|
sets forth the basis on which the broker or dealer made the suitability determination; and
|
|
·
|
that the broker or dealer received a signed, written agreement from the investor prior to the transaction.
|
Generally, brokers may be less willing to execute
transactions in securities subject to the “penny stock” rules. This may make it more difficult for investors to dispose of
our common stock and cause a decline in the market value of our stock.
Disclosure also has to be made about the risks
of investing in penny stocks in both public offerings and in secondary trading and about the commissions payable to both the broker-dealer
and the registered representative, current quotations for the securities and the rights and remedies available to an investor in cases
of fraud in penny stock transactions. Finally, monthly statements have to be sent disclosing recent price information for the penny stock
held in the account and information on the limited market in penny stocks.
Our common stock has had an unpredictable
trading volume which means you may not be able to sell our shares at or near trading prices or at all.
Trading in our common shares historically has
been volatile and often has been thin, meaning that the number of persons interested in purchasing our common shares at or near trading
prices at any given time may be relatively small or non-existent. This situation is attributable to a number of factors, including the
fact that we are a small company which is relatively unknown to stock analysts, stock brokers, institutional investors and others in the
investment community that generate or influence sales volume, and that even if we came to the attention of such persons, they tend to
be risk-averse and would be reluctant to follow an unproven company such as ours or purchase or recommend the purchase of our shares until
such time as we became more seasoned and viable. As a consequence, there may be periods of several days or more when trading activity
in our shares is minimal, as compared to a seasoned issuer which has a large and steady volume of trading activity that will generally
support continuous sales without an adverse effect on share price. A broader or more active public trading market for our common shares
may not develop or be sustained, and current trading levels may decrease.
The market price for our common stock is
volatile; you may not be able to sell our common stock at or above the price you have paid for it, which may result in losses to you.
The market for our common stock is characterized
by significant price volatility when compared to seasoned issuers, and we expect that our share price will continue to be more volatile
than a seasoned issuer for the indefinite future. During the 52-week period ended June 10, 2021, the high and low closing sale prices
for a share of our common stock were $10.79 and $1.29, respectively. The volatility in our share price is attributable to a number of factors.
First, as noted above, trading in our common stock often has been thin. As a consequence of this lack of liquidity, the trading of relatively
small quantities of shares by our stockholders may disproportionately influence the price of those shares in either direction. The price
for our shares could, for example, decline precipitously in the event that a large number of our common shares are sold on the market
without commensurate demand, as compared to a seasoned issuer which could better absorb those sales without adverse impact on its share
price. Secondly, we are a speculative investment due to our limited operating history, limited amount of cash and revenue, lack of profit
to date, and the uncertainty of future market acceptance for our potential products. As a consequence of this enhanced risk, more risk-adverse
investors may, under the fear of losing all or most of their investment in the event of negative news or lack of progress, be more inclined
to sell their shares on the market more quickly and at greater discounts than would be the case with the stock of a seasoned issuer.
The following factors also may add to the volatility
in the price of our common stock: actual or anticipated variations in our quarterly or annual operating results; announcements regarding
our clinical trials and the development of the Hemopurifier; acceptance of our proprietary technology as a viable method of augmenting
the immune response of clearing viruses and toxins from human blood; government regulations, announcements of significant acquisitions,
strategic partnerships or joint ventures; our capital commitments and additions or departures of our key personnel. Many of these factors
are beyond our control and may decrease the market price of our common shares regardless of our operating performance. We cannot make
any predictions or projections as to what the prevailing market price for our common shares will be at any time, including as to whether
our common shares will sustain their current market prices, or as to what effect the sale of shares or the availability of common shares
for sale at any time will have on the prevailing market price.
Our issuance of additional shares of common
stock or convertible securities, could be dilutive.
We are entitled under our articles of incorporation
to issue up to 30,000,000 shares of common stock. We have reserved for issuance 2,536,062 of those shares of common stock for outstanding
restricted stock units, stock options and warrants. As of March 31, 2021, we had issued and outstanding 12,150,597 shares of common stock.
As a result, as of March 31, 2021 we had 15,313,341 shares of common stock available for issuance to new investors or for use to satisfy
indebtedness or pay service providers.
Our Board of Directors may generally issue shares
of common stock, restricted stock units or stock options or warrants to purchase those shares, without further approval by our stockholders,
based upon such factors as our Board of Directors may deem relevant at that time. It is likely that we will be required to issue a large
amount of additional securities to raise capital to further our development. It is also likely that we will be required to issue a large
amount of additional securities to directors, officers, employees and consultants as compensatory grants in connection with their services,
both in the form of stand-alone grants or under our stock plans.
Our officers and directors are entitled to indemnification from
us for liabilities under our articles of incorporation, which could be costly to us and may discourage the exercise of stockholder rights.
Our articles of incorporation provide that we
possess and may exercise all powers of indemnification of our officers, directors, employees, agents and other persons and our bylaws
also require us to indemnify our officers and directors as permitted under the provisions of the Nevada Revised Statutes, or NRS. We may
also have contractual indemnification obligations under our agreements with our directors, officers and employees. The foregoing indemnification
obligations could result in our company incurring substantial expenditures to cover the cost of settlement or damage awards against directors
and officers. These provisions and resultant costs may also discourage our company from bringing a lawsuit against directors, officers
and employees for breaches of their fiduciary duties, and may similarly discourage the filing of derivative litigation by our stockholders
against our directors, officers and employees even though such actions, if successful, might otherwise benefit our company and stockholders.
Our bylaws and Nevada law may discourage,
delay or prevent a change of control of our company or changes in our management, would have the result of depressing the trading price
of our common stock.
Certain anti-takeover provisions of Nevada law
could have the effect of delaying or preventing a third-party from acquiring us, even if the acquisition arguably could benefit our stockholders.
Nevada’s “combinations with interested
stockholders” statutes (NRS 78.411 through 78.444, inclusive) prohibit specified types of business “combinations” between
certain Nevada corporations and any person deemed to be an “interested stockholder” for two years after such person first
becomes an “interested stockholder” unless the corporation’s board of directors approves the combination (or the transaction
by which such person becomes an “interested stockholder”) in advance, or unless the combination is approved by the board of
directors and sixty percent of the corporation’s voting power not beneficially owned by the interested stockholder, its affiliates
and associates. Further, in the absence of prior approval certain restrictions may apply even after such two year period. However, these
statutes do not apply to any combination of a corporation and an interested stockholder after the expiration of four years after the person
first became an interested stockholder. For purposes of these statutes, an “interested stockholder” is any person who is (1)
the beneficial owner, directly or indirectly, of ten percent or more of the voting power of the outstanding voting shares of the corporation,
or (2) an affiliate or associate of the corporation and at any time within the two previous years was the beneficial owner, directly or
indirectly, of ten percent or more of the voting power of the then outstanding shares of the corporation. The definition of the term “combination”
is sufficiently broad to cover most significant transactions between a corporation and an “interested stockholder.” A Nevada
corporation may elect in its articles of incorporation not to be governed by these particular laws, but if such election is not made in
the corporation’s original articles of incorporation, the amendment (1) must be approved by the affirmative vote of the holders
of stock representing a majority of the outstanding voting power of the corporation not beneficially owned by interested stockholders
or their affiliates and associates, and (2) is not effective until 18 months after the vote approving the amendment and does not apply
to any combination with a person who first became an interested stockholder on or before the effective date of the amendment. We did not
make such an election in our original articles of incorporation and have not amended our articles of incorporation to so elect.
Nevada’s “acquisition of controlling
interest” statutes (NRS 78.378 through 78.3793, inclusive) contain provisions governing the acquisition of a controlling interest
in certain Nevada corporations. These “control share” laws provide generally that any person that acquires a “controlling
interest” in certain Nevada corporations may be denied voting rights, unless a majority of the disinterested stockholders of the
corporation elects to restore such voting rights. These laws would apply to us if we were to have 200 or more stockholders of record (at
least 100 of whom have addresses in Nevada appearing on our stock ledger) and do business in the State of Nevada directly or through an
affiliated corporation, unless our articles of incorporation or bylaws in effect on the tenth day after the acquisition of a controlling
interest provide otherwise. These laws provide that a person acquires a “controlling interest” whenever a person acquires
shares of a subject corporation that, but for the application of these provisions of the NRS, would enable that person to exercise (1)
one fifth or more, but less than one third, (2) one third or more, but less than a majority or (3) a majority or more, of all of the voting
power of the corporation in the election of directors. Once an acquirer crosses one of these thresholds, shares which it acquired in the
transaction taking it over the threshold and within the 90 days immediately preceding the date when the acquiring person acquired or offered
to acquire a controlling interest become “control shares” to which the voting restrictions described above apply. These laws
may have a chilling effect on certain transactions if our articles of incorporation or bylaws are not amended to provide that these provisions
do not apply to us or to an acquisition of a controlling interest, or if our disinterested stockholders do not confer voting rights in
the control shares.
Various provisions of our bylaws may delay, defer
or prevent a tender offer or takeover attempt of us that a stockholder might consider in his or her best interest. Our bylaws may be adopted,
amended or repealed by the affirmative vote of the holders of at least a majority of our outstanding shares of capital stock entitled
to vote for the election of directors, and except as provided by Nevada law, our Board of Directors shall have the power to adopt, amend
or repeal the bylaws by a vote of not less than a majority of our directors. The interests of these stockholders and directors may not
be consistent with your interests, and they may make changes to the bylaws that are not in line with your concerns.
Nevada law also provides that directors may resist
a change or potential change in control if the directors determine that the change is opposed to, or not in the best interests of, the
corporation. The existence of the foregoing provisions and other potential anti-takeover measures could limit the price that investors
might be willing to pay in the future for shares of our common stock. They could also deter potential acquirers of our company, thereby
reducing the likelihood that you could receive a premium for your common stock in an acquisition.
We incur substantial costs as a result of
being a public company and our management expects to devote substantial time to public company compliance programs.
As a public company, we incur significant legal,
insurance, accounting and other expenses, including costs associated with public company reporting. We intend to invest resources to comply
with evolving laws, regulations and standards, and this investment will result in increased general and administrative expenses and may
divert management’s time and attention from product development and commercialization activities. If our efforts to comply with
new laws, regulations and standards differ from the activities intended by regulatory or governing bodies due to ambiguities related to
practice, regulatory authorities may initiate legal proceedings against us, and our business may be harmed. These laws and regulations
could make it more difficult and costly for us to obtain director and officer liability insurance for our directors and officers, and
we may be required to accept reduced coverage or incur substantially higher costs to obtain coverage. These factors could also make it
more difficult for us to attract and retain qualified executive officers and qualified members of our Board of Directors, particularly
to serve on our audit and compensation committees. In addition, if we are unable to continue to meet the legal, regulatory and other requirements
related to being a public company, we may not be able to maintain the quotation of our common stock on the Nasdaq Capital Market or on
any other senior market to which we may apply for listing, which would likely have a material adverse effect on the trading price of our
common stock.
If securities or industry analysts do not
publish research or reports about our business, or if they change their recommendations regarding our stock adversely, our stock price
and trading volume could decline.
The trading market for our common stock will be
influenced by the research and reports that industry or securities analysts publish about us or our business. Our research coverage by
industry and financial analysts is currently limited. Even if our analyst coverage increases, if one or more of the analysts who cover
us downgrade our stock, our stock price would likely decline. If one or more of these analysts cease coverage of our company or fail to
regularly publish reports on us, we could lose visibility in the financial markets, which in turn could cause our stock price or trading
volume to decline.
USE OF PROCEEDS
We estimate that the net proceeds from this offering, after deducting
placement agent fees and estimated offering expenses payable by us, will be approximately $11.6 million.
We intend to use the net proceeds from this offering for working capital
and general corporate purposes, which may include research and development expenses, general and administrative expenses.
The amounts and timing of our actual expenditures will depend on numerous
factors, including the progress of our clinical trials and other development efforts and other factors described under “Risk Factors” in this prospectus supplement, the accompanying prospectus and the documents incorporated by reference herein and
therein, as well as the amount of cash used in our operations. We may find it necessary or advisable to use the net proceeds for other
purposes, and we will have broad discretion in the application of the net proceeds. Pending the uses described above, we plan to invest
the net proceeds from this offering in bank demand deposit accounts or interest bearing bank accounts.
DILUTION
If you invest in our common stock in this offering, your ownership
interest will be immediately diluted to the extent of the difference between the offering price per share of our common stock and the
as adjusted net tangible book value per share of our common stock immediately after this offering.
Our net tangible book value as of December 31, 2020 was approximately
$16.4 million (including $4.9 million in net proceeds from the sales under our ATM Facility in June 2021), or approximately $1.28 per
share. Net tangible book value per share represents our total tangible assets less total tangible liabilities as of December 31, 2020,
divided by the number of shares of common stock outstanding as of December 31, 2020.
Net tangible book value dilution per share to new investors represents
the difference between the amount per share paid by purchasers of shares of common stock in this offering and the as adjusted net tangible
book value per share of common stock immediately after completion of this offering. After giving further effect to the sale of 1,380,555
shares at a price of $9.00 per share, and after deducting placement agent fees and estimated offering expenses payable by us, our as adjusted
net tangible book value as of December 31, 2020 would have been approximately $28.0 million, or approximately $1.98 per share. This amount
represents an immediate increase in net tangible book value of $0.70 per share to our existing stockholders and an immediate dilution
in as adjusted net tangible book value of approximately $7.02 per share to new investors purchasing shares of common stock in this offering.
We determine dilution per share to investors participating in this offering by subtracting as adjusted net tangible book value per share
after this offering from the offering price per share paid by investors participating in this offering. The following table illustrates
this dilution on a per share basis:
Offering price per share
|
|
|
|
|
$
|
9.00
|
|
Historical net tangible book value per share at December 31, 2020, before giving effect to this offering
|
|
$
|
1.28
|
|
|
|
|
|
|
|
|
|
|
|
|
Increase in net tangible book value per share attributable to new investors participating in this offering
|
|
$
|
0.70
|
|
|
|
|
|
|
|
|
|
|
|
|
As adjusted net tangible book value per share after this offering
|
|
|
|
|
$
|
1.98
|
|
|
|
|
|
|
|
|
|
Dilution per share to new investors participating in this offering
|
|
|
|
|
$
|
7.02
|
|
In addition, we may choose to raise additional capital due to market
conditions or strategic considerations even if we believe we have sufficient funds for our current or future operating plans. To the extent
that we raise additional capital through the sale of equity or convertible debt securities, the issuance of these securities could result
in further dilution to our stockholders.
The discussion of dilution, and the table quantifying it, assume the
sale of all shares covered by this prospectus supplement and, except as set forth below, no exercise of any outstanding options or warrants
or other potentially dilutive securities. The exercise of potentially dilutive securities having an exercise price less than the offering
price would increase the dilutive effect to new investors.
The number of shares of our common stock to be outstanding immediately
after this offering is based on 12,749,524 shares of common stock outstanding as of December 31, 2020, after giving effect to the issuance
and sale of 626,000 shares of common stock in June 2021 under the ATM Facility, and excludes:
|
·
|
602,323 shares of common stock issuable upon exercise of outstanding stock options under our stock incentive plans as of December
31, 2020 at a weighted average exercise price of $3.29 per share;
|
|
·
|
1,991,973 shares of common stock reserved for issuance under outstanding warrants as of December 31, 2020 with a weighted average
exercise price of $5.93 per share; and
|
|
·
|
1,118,292 additional shares of common stock reserved for future issuance under our stock incentive plans as of December 31, 2020.
|
Unless otherwise indicated, all information in this prospectus supplement
assumes no exercise of the outstanding options or warrants described above.
PLAN OF DISTRIBUTION
Maxim Group LLC, which we
refer to as the Placement Agent, has agreed to act as the exclusive placement agent in connection with this offering. The Placement Agent
is not purchasing or selling shares of common stock by this prospectus supplement, nor is the Placement Agent required to arrange the
purchase or sale of any specific number of shares of common stock, but has agreed to use its reasonable best efforts to arrange for the
sale of all of the common stock offered hereby. We have entered into a securities purchase agreement with the investors pursuant to which
we will sell to the investors 1,380,555 shares of our common stock in this takedown from our shelf registration statement. We negotiated
the price for the securities offered in this offering with the investors. The factors considered in determining the price included the
recent market price of our common stock, the general condition of the securities market at the time of this offering, the history of,
and the prospects, for the industry in which we compete, our past and present operations, and our prospects for future revenues.
We entered into securities
purchase agreements directly with investors on June 10, 2021, and we will only sell to investors who have entered into a securities purchase
agreement.
We expect to deliver the shares
of common stock being offered pursuant to this prospectus supplement on or about June 14, 2021, subject to customary closing conditions.
We have agreed to pay the
Placement Agent a fee equal to the sum of 4.75% of the aggregate purchase price paid by the investors placed by the Placement Agent. We
have also agreed to reimburse the Placement Agent in the amount not to exceed $50,000 for the reasonable out of pocket accountable fees
and expenses including legal fees.
The following table shows
per share price of common stock and total cash Placement Agent’s fees we will pay to the Placement Agent in connection with the
sale of the common stock pursuant to this prospectus supplement and the accompanying prospectus assuming the purchase of all of the common
stock offered hereby:
|
|
Per Share of Common Stock
|
|
|
Total
|
|
Offering Price
|
|
$
|
9.00
|
|
|
$
|
12,424,995.00
|
|
Placement Agent’s Fees
|
|
$
|
0.4275
|
|
|
$
|
590,187.26
|
|
Proceeds, before expenses, to us
|
|
$
|
8.5725
|
|
|
$
|
11,834,807.74
|
|
After deducting certain fees
and expenses due to the Placement Agent and our estimated offering expenses, we expect the net proceeds from this offering to be approximately
$11,640,000.
Our directors and officers
have agreed, subject to certain exceptions, not to sell any equity securities or securities convertible into equity securities within
30 days following the closing of this offering.
Indemnification
We have agreed to indemnify
the Placement Agent and specified other persons against certain civil liabilities, including liabilities under the Exchange Act, and to
contribute to payments that the placement agent may be required to make in respect of such liabilities.
The Placement Agent may be
deemed to be an underwriter within the meaning of Section 2(a)(11) of the Securities Act, and any commissions received by it, and any
profit realized on the resale of the common stock sold by it while acting as principal, might be deemed to be underwriting discounts or
commissions under the Securities Act. As an underwriter, the placement agent would be required to comply with the Securities Act and the
Exchange Act, including without limitation, Rule 10b-5 and Regulation M under the Exchange Act. These rules and regulations may limit
the timing of purchases and sales of the common stock by the Placement Agent acting as principal. Under these rules and regulations, the
Placement Agent:
|
·
|
may not engage in any stabilization activity in connection with our securities; and
|
|
·
|
may not bid for or purchase any of our securities, or attempt to induce any person to purchase any of our securities, other than as
permitted under the Exchange Act, until it has completed its participation in the distribution in the securities offered by this prospectus
supplement.
|
Relationships
The Placement Agent and its
affiliates may have provided us and our affiliates in the past and may provide from time to time in the future certain commercial banking,
financial advisory, investment banking and other services for us and such affiliates in the ordinary course of their business, for which
they have received and may continue to receive customary fees and commissions. In addition, from time to time, the placement agent and
its affiliates may effect transactions for their own account or the account of customers, and hold on behalf of themselves or their customers,
long or short positions in our debt or equity securities or loans, and may do so in the future. However, except as disclosed in this prospectus
supplement, we have no present arrangements with the placement agent for any further services.
Nasdaq Capital Market Listing
Our common stock is listed on the Nasdaq Capital Market
under the symbol “AEMD”.
Transfer Agent and Registrar
The transfer agent and registrar for our common stock is
Computershare Investor Services. The transfer agent’s address is P.O. Box 30170, College Station, TX 77842.
LEGAL MATTERS
We are being represented by Cooley LLP, San Diego, California. The
validity of the shares of common stock offered pursuant to this prospectus supplement and the accompanying prospectus will be passed upon
for us by Brownstein Hyatt Farber Schreck, LLP. Loeb & Loeb LLP, New York, New York is acting as counsel for the placement agent.
EXPERTS
The consolidated financial statements of Aethlon Medical, Inc. as of
March 31, 2020 and 2019 and for each of the years in the two-year period ended March 31, 2020 incorporated in this prospectus supplement
by reference from the Aethlon Medical, Inc. Annual Report on Form 10-K for the year ended March 31, 2020 have been audited by Squar Milner
LLP (which effective as of November 1, 2020, merged with Baker Tilly US, LLP), an independent registered public accounting firm, as stated
in their report thereon, incorporated herein by reference, and have been incorporated in this prospectus in reliance upon such report
and upon the authority of such firm as experts in accounting and auditing.
WHERE YOU CAN FIND MORE INFORMATION
This prospectus supplement and the accompanying prospectus are part
of the registration statement on Form S-3 we filed with the SEC under the Securities Act and do not contain all the information set forth
in the registration statement. Whenever a reference is made in this prospectus supplement or the accompanying prospectus to any of our
contracts, agreements or other documents, the reference may not be complete and you should refer to the exhibits that are a part of the
registration statement or the exhibits to the reports or other documents incorporated by reference in this prospectus supplement and the
accompanying prospectus for a copy of such contract, agreement or other document. Because we are subject to the information and reporting
requirements of the Exchange Act, we file annual, quarterly and current reports, proxy statements and other information with the SEC.
Our SEC filings are available to the public over the Internet at the SEC’s website at http://www.sec.gov.
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
The SEC allows us to incorporate by reference the information we file
with it, which means that we can disclose important information to you by referring you to another document that we have filed separately
with the SEC. You should read the information incorporated by reference because it is an important part of this prospectus supplement
and the accompanying prospectus. Information in this prospectus supplement supersedes information incorporated by reference that we filed
with the SEC prior to the date of this prospectus supplement, while information that we file later with the SEC will automatically update
and supersede the information in this prospectus supplement and the accompanying prospectus. We incorporate by reference into this prospectus
supplement and the accompanying prospectus the information or documents listed below that we have filed with the SEC (Commission File
No. 001-37487):
|
·
|
Our Annual Report on Form 10-K for the fiscal year ended March 31, 2020, filed with the SEC on June 25, 2020;
|
|
·
|
Our Quarterly Reports on Form 10-Q for the quarters ended June 30, 2020, September
30, 2020, and December 31, 2020, filed with the SEC on August 11, 2020, October 28, 2020, and
February 10, 2021, respectively;
|
|
·
|
The description of our common stock contained in our registration statement on Form 8-A filed
with the SEC on July 8, 2015, including any amendments or reports filed for the purpose of updating such description.
|
We also incorporate by reference any future filings (other than current
reports furnished under Item 2.02 or Item 7.01 of Form 8-K and exhibits filed on such form that are related to such items unless such
Form 8-K expressly provides to the contrary) made with the SEC pursuant to Sections 13(a), 13(c), 14 or 15(d) of the Exchange Act after
the date of this prospectus supplement and prior to the termination of the offering of the securities covered by this prospectus supplement
and the accompanying prospectus. Information in such future filings updates and supplements the information provided in this prospectus
supplement and the accompanying prospectus. Any statements in any such future filings will automatically be deemed to modify and supersede
any information in any document we previously filed with the SEC that is incorporated or deemed to be incorporated herein by reference
to the extent that statements in the later filed document modify or replace such earlier statements.
We will furnish without charge to you, upon written or oral request,
a copy of any or all of the documents incorporated by reference, including exhibits to these documents. You should direct any requests
for documents by writing us at Aethlon Medical, Inc., 9635 Granite Ridge Drive, Suite 100, San Diego, California 92123, (858) 459-7800.
$25,000,000
Common Stock
Debt Securities
Warrants
From time to time, we may offer up to $25,000,000 of any combination
of the securities described in this prospectus in one or more offerings. We may also offer securities as may be issuable upon conversion,
redemption, repurchase, exchange or exercise of any securities registered hereunder, including any applicable anti-dilution provisions.
This prospectus provides a general description of the securities
we may offer. Each time we sell securities, we will provide specific terms of the securities offered in a supplement to this prospectus.
We may also authorize one or more free writing prospectuses to be provided to you in connection with these offerings. The prospectus
supplement and any related free writing prospectus may also add, update or change information contained in this prospectus. You
should carefully read this prospectus, the applicable prospectus supplement and any related free writing prospectus, as well as
any documents incorporated by reference herein and therein, before you invest in any securities.
Our common stock is listed on the Nasdaq Capital Market under
the symbol "AEMD." On March 16, 2020, the last reported sale price for our common stock was $1.23 per share. The applicable
prospectus supplement will contain information, where applicable, as to any other listing on the Nasdaq Capital Market or any securities
market or other exchange of the securities, if any, covered by the prospectus supplement.
As of March 16, 2020, the aggregate market value of our outstanding
common stock held by non-affiliates was approximately $40.5 million, based on 9,364,784 shares of outstanding common stock, of
which approximately 9.3 million shares were held by non-affiliates, and a price of $4.34 per share, which was the last reported
sale price of our common stock on The Nasdaq Capital Market on January 31, 2020. Pursuant to General Instruction I.B.6 of Form
S-3, in no event will we sell securities registered on the registration statement of which this prospectus is a part with a value
of more than one-third of the aggregate market value of our Common Stock held by non-affiliates in any 12-month period, so long
as the aggregate market value of our Common Stock held by non-affiliates is less than $75 million. As of the date of this prospectus,
we have offered an aggregate market value of $4,696,031 of securities pursuant to General Instruction I.B.6. of Form S-3 during
the prior 12 calendar month period that ends on, and includes, the date of this prospectus.
INVESTING IN OUR SECURITIES INVOLVES RISKS. YOU SHOULD REVIEW
CAREFULLY THE RISKS AND UNCERTAINTIES DESCRIBED UNDER THE HEADING "RISK FACTORS" ON PAGE 4 AND CONTAINED IN THE APPLICABLE
PROSPECTUS SUPPLEMENT AND ANY RELATED FREE WRITING PROSPECTUS AND UNDER SIMILAR HEADINGS IN THE OTHER DOCUMENTS THAT ARE INCORPORATED
BY REFERENCE INTO THIS PROSPECTUS.
THIS PROSPECTUS MAY NOT BE USED TO CONSUMMATE
A SALE OF SECURITIES UNLESS ACCOMPANIED BY A PROSPECTUS SUPPLEMENT.
We will sell these securities directly to investors, through
agents designated from time to time or to or through underwriters or dealers, on a continuous or delayed basis. For additional
information on the methods of sale, you should refer to the section entitled "Plan of Distribution" in this prospectus.
If any agents or underwriters are involved in the sale of any securities with respect to which this prospectus is being delivered,
the names of such agents or underwriters and any applicable fees, commissions, discounts or over-allotment options will be set
forth in a prospectus supplement. The price to the public of such securities and the net proceeds we expect to receive from such
sale will also be set forth in a prospectus supplement.
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved of these securities or determined if this prospectus is truthful or complete.
Any representation to the contrary is a criminal offense.
The date of this prospectus is
March 30, 2020.
TABLE OF CONTENTS
ABOUT THIS PROSPECTUS
This prospectus is a part of a registration statement on Form
S-3 that we filed with the SEC utilizing a “shelf” registration process. Under this shelf registration process, we
may sell any combination of the securities described in this prospectus in one or more offerings up to a total aggregate offering
price of $25,000,000. This prospectus provides you with a general description of the securities we may offer.
Each time we sell securities under this prospectus, we will
provide a prospectus supplement that will contain specific information about the terms of that offering. We may also authorize
one or more free writing prospectuses to be provided to you that may contain material information relating to these offerings.
The prospectus supplement and any related free writing prospectus that we may authorize to be provided to you may also add, update
or change information contained in this prospectus or in any documents that we have incorporated by reference into this prospectus.
You should read this prospectus, any applicable prospectus supplement and any related free writing prospectus, together with the
information incorporated herein by reference as described under the heading “Incorporation of Certain Information by Reference,”
before investing in any of the securities offered.
THIS PROSPECTUS MAY NOT BE USED TO CONSUMMATE A SALE OF SECURITIES
UNLESS IT IS ACCOMPANIED BY A PROSPECTUS SUPPLEMENT.
Neither we, nor any agent, underwriter, or dealer has authorized
any person to give any information or to make any representation other than those contained or incorporated by reference in this
prospectus and any applicable prospectus supplement, along with the information contained in any free writing prospectus we have
authorized for use in connection with a specific offering. We have not authorized anyone to provide you with different or additional
information. We are not making an offer to sell or seeking an offer to buy securities under this prospectus or any applicable prospectus
supplement and any related free writing prospectus in any jurisdiction where the offer or sale is not permitted.
The information appearing in this prospectus, any applicable
prospectus supplement or any related free writing prospectus, and the documents incorporated by reference herein and therein, is
accurate only as of the date on the front of the document and any information we have incorporated by reference is accurate only
as of their respective dates, regardless of the time of delivery of this prospectus, any applicable prospectus supplement or any
related free writing prospectus, or any sale of a security. Our business, financial condition, results of operations and prospects
may have changed since those dates.
For investors outside the United States, we have not done
anything that would permit this offering or possession or distribution of this prospectus in any jurisdiction where action for
that purpose is required, other than in the United States. You are required to inform yourselves about and to observe any restrictions
relating to this offering and the distribution of this prospectus outside of the United States.
This prospectus and the information incorporated herein by reference
contains summaries of certain provisions contained in some of the documents described herein, but reference is made to the actual
documents for complete information. All of the summaries are qualified in their entirety by the actual documents. Copies of some
of the documents referred to herein have been filed, will be filed or will be incorporated by reference as exhibits to the registration
statement of which this prospectus is a part, and you may obtain copies of those documents as described below under the heading
“Where You Can Find More Information.”
This prospectus incorporates by reference, and any prospectus
supplement or free writing prospectus may contain and incorporate by reference, industry, statistical and market data from our
own internal estimates and research as well as from industry and general publications and research, surveys and studies conducted
by third parties. Industry publications, studies and surveys generally state that they have been obtained from sources believed
to be reliable, although they do not guarantee the accuracy or completeness of such information. While we believe that each of
these studies and publications is reliable, we have not independently verified statistical, market and industry data from third-party
sources. While we believe our internal company research is reliable and the market definitions are appropriate, neither such research
nor these definitions have been verified by any independent source.
Unless the context requires otherwise or unless otherwise noted,
all references to "Aethlon" are to Aethlon Medical, Inc., a Nevada corporation, and all references to "we,"
"us" or "our" are to Aethlon Medical, Inc. and its subsidiaries.
Trademarks, service marks or trade names of any other companies
appearing in this prospectus are the property of their respective owners. Use or display by us of trademarks, service marks or
trade names owned by others is not intended to and does not imply a relationship between us and, or endorsement or sponsorship
by, the owners of the trademarks, service marks or trade names.
SPECIAL NOTE REGARDING FORWARD-LOOKING
STATEMENTS
This prospectus supplement, the accompanying prospectus,
and the documents incorporated by reference herein and therein contain forward-looking statements within the meaning of Section
27A of the Securities Act, Section 21E of the Securities Exchange Act of 1934, as amended, or the Exchange Act, and the Private
Securities Litigation Reform Act of 1995, as amended, that involve substantial risks and uncertainties. These statements relate
to future events or to our future financial performance and involve known and unknown risks, uncertainties and other factors which
may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements
expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited to, statements
about:
|
•
|
the
initiation, progress, timing, costs and results of preclinical studies and any clinical trials for our Hemopurifier® and any
other product candidates;
|
|
•
|
our
estimates regarding expenses, future revenue, capital requirements and needs for additional financing;
|
|
•
|
our
ability to further improve our process development capabilities;
|
|
•
|
the
timing or likelihood of regulatory filings and approvals;
|
|
•
|
our
plans to explore potential applications of our device platform in other indications in oncology and rare diseases;
|
|
•
|
our
expectations regarding the clinical effectiveness and safety and tolerability of our product candidates;
|
|
•
|
our
commercialization, marketing and manufacturing capabilities and strategy;
|
|
•
|
the
pricing and reimbursement of our product candidates, if approved;
|
|
•
|
our
expectation regarding the potential market sizes for our product candidates;
|
|
•
|
our
intellectual property position;
|
|
•
|
the
potential benefits of our strategic collaborations, our plans with respect to our strategic collaborations and our plans with
respect to and our ability to enter into strategic arrangements;
|
|
•
|
developments
and projections relating to our competitors and our industry; and
|
|
•
|
the
safety, efficacy and projected development timeline and commercial potential of any product candidates.
|
In some cases, you can identify forward-looking
statements by terms such as “anticipates,” “believes,” “could,” “estimates,” “expects,”
“goal,” “intends,” “may,” “plans,” “potential,” “predicts,”
“projects,” “should,” “will,” “would,” the negative of these words and words or
similar expressions intended to identify forward-looking statements. These statements reflect our views as of the date on which
they were made with respect to future events and are based on assumptions and subject to risks and uncertainties. The underlying
information and expectations are likely to change over time. Given these uncertainties, you should not place undue reliance on
these forward-looking statements as actual events or results may differ materially from those projected in the forward-looking
statements due to various factors, including, but not limited to, those set forth under the heading “Risk Factors”
in this prospectus supplement, in the accompanying prospectus, and in our filings with the SEC. These forward-looking statements
represent our estimates and assumptions only as of the date of the document containing the applicable statement.
You should understand that our actual
future results may be materially different from what we expect. In addition, statements that “we believe” and similar
statements reflect our beliefs and opinions on the relevant subject. These statements are based upon information available to us
as of the date the statements were made, and while we believe such information forms a reasonable basis for such statements, such
information may be limited or incomplete, and our statements should not be read to indicate that we have conducted an exhaustive
inquiry into, or review of, all potentially available relevant information. These statements are inherently uncertain and you are
cautioned not to unduly rely upon these statements. We qualify all of the forward-looking statements in the foregoing documents
by these cautionary statements. Unless required by law, we undertake no obligation to update or revise any forward-looking statements
to reflect new information or future events or developments. Thus, you should not assume that our silence over time means that
actual events are bearing out as expressed or implied in such forward-looking statements. Before deciding to purchase shares of
our common stock, you should carefully consider the risk factors discussed or incorporated by reference herein, in addition to
the other information set forth in this prospectus supplement, the accompanying prospectus and in the documents incorporated by
reference.
PROSPECTUS SUMMARY
The following summary highlights selected information contained
elsewhere in this prospectus or incorporated by reference in this prospectus and does not contain all of the information that you
should consider in making your investment decision. Before investing in securities, you should carefully read the entire prospectus,
the applicable prospectus supplement and any related free writing prospectus, including the risks of investing in our securities
discussed under the heading “Risk Factors” contained in this prospectus, the applicable prospectus supplement and any
related free writing prospectus, and under similar headings in the other documents that are incorporated by reference into this
prospectus. You should also carefully read the information incorporated by reference into this prospectus, including our financial
statements, and the exhibits to the registration statement of which this prospectus is a part.
Company Overview
Aethlon Medical, Inc. and its subsidiary is a medical device
technology company focused on developing products to diagnose and treat life and organ threatening diseases. The Aethlon Hemopurifier®
is a clinical-stage device designed to combat cancer and life-threatening viral infections. In cancer, the Hemopurifier is 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 FDA, has designated the Hemopurifier
as a “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 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, or carbohydrate coated, viruses that are not addressed with an already approved
treatment. In small-scale or early feasibility human studies, the Hemopurifier has been used to treat individuals infected with
HIV, hepatitis-C, and Ebola. Additionally, in vitro, the Hemopurifier has been demonstrated 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 studies were conducted in collaboration with leading government or non-government research institutes.
We are also the majority owner of Exosome Sciences, Inc., or
ESI, a company focused on the discovery of exosomal biomarkers to diagnose and monitor life-threatening diseases. Included among
ESI’s activities is the advancement of a TauSome™ biomarker candidate to diagnose chronic traumatic encephalopathy,
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.
Successful outcomes of human trials will also be required by
the regulatory agencies of certain foreign countries where we plan 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.
Corporate Information
On March 10, 1999, Aethlon, Inc., a California corporation,
Hemex, Inc., a Delaware corporation and the accounting predecessor to Aethlon, Inc., and Bishop Equities, Inc., a publicly traded
Nevada corporation, completed an Agreement and Plan of Reorganization structured to result in Bishop Equities, Inc.'s acquisition
of all of the outstanding common stock of Aethlon, Inc. and Hemex, Inc. Under the plan's terms, Bishop Equities, Inc. issued shares
of its common stock to the stockholders of Aethlon, Inc. and Hemex, Inc. such that Bishop Equities, Inc. then owned 100% of each
company. Upon completion of the transaction, Bishop Equities, Inc. was renamed Aethlon Medical, Inc. In 2009, we formed ESI, which
today is a majority-owned subsidiary of the Company focused on identifying and monitoring neurological conditions and cancer. We
commenced operations of ESI in 2013.
Our Contact Information
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 is www.aethlonmedical.com.
The information on our website is not incorporated by reference into this prospectus and should not be considered to be a part
of this prospectus. Our internet address is included in this prospectus as an inactive textual reference only.
The Securities We May Offer
With this prospectus, together with any applicable prospectus
supplement and related free writing prospectus, we may offer common stock, debt securities and warrants, or any combination of
the foregoing. The aggregate initial offering price of all securities we sell in the primary offering under this prospectus will
not exceed $25,000,000. If we issue debt securities at a discount from their original stated principal amount, then, for purposes
of calculating the total dollar amount of all securities issued under this prospectus, we will treat the initial offering price
of the debt securities as the total original principal amount of the debt securities. Each time we offer securities with this prospectus,
we will provide offerees with a prospectus supplement that will contain the specific terms of the securities being offered. The
following is a summary of the securities we may offer with this prospectus.
We may sell the securities to or through underwriters, dealers
or agents or directly to purchasers. We, as well as any agents acting on our behalf, reserve the sole right to accept and to reject
in whole or in part any proposed purchase of securities. Each prospectus supplement will set forth the names of any underwriters,
dealers or agents involved in the sale of securities described in that prospectus supplement and any applicable fee, commission
or discount arrangements with them.
The prospectus supplement and any related free writing prospectus
that we may authorize to be provided to you may also add, update or change information contained in this prospectus or in documents
we have incorporated by reference. However, no prospectus supplement or free writing prospectus will offer a security that is not
registered and described in this prospectus at the time of the effectiveness of the registration statement of which this prospectus
is a part.
This prospectus may not be used to consummate a sale of securities
unless it is accompanied by a prospectus supplement.
Common Stock. We may offer shares of our
common stock, par value $0.001 per share, either alone or underlying other registered securities convertible into or exercisable
for our common stock. Holders of our common stock are entitled to receive ratably such dividends as our Board of Directors may
declare from time to time out of legally available funds. Currently, we do not pay any dividends. Each holder of our common stock
is entitled to one vote per share on all matters to be voted on by the stockholders. In this prospectus, we provide a general description
of, among other things, our dividend policy and the rights and restrictions that apply to holders of our common stock. If we liquidate,
dissolve or wind up, holders of common stock are entitled to share ratably in all assets remaining after payment of all debts and
other liabilities. Holders of common stock have no preemptive, conversion or subscription rights. There are no redemption or sinking
fund provisions applicable to the common stock. All outstanding shares of common stock are, and all shares of common stock to be
outstanding upon completion of this offering will be, validly issued, fully paid and nonassessable.
Debt Securities. We may offer general debt
obligations, which may be secured or unsecured, senior or subordinated and convertible into shares of our common stock. In this
prospectus, we refer to the senior debt securities and the subordinated debt securities together as the "debt securities."
We may issue debt securities under a note purchase agreement or under an indenture to be entered between us and a trustee named
in the indenture. If we issue debt securities under an indenture, a form of the indenture will be filed as an exhibit to the registration
statement of which this prospectus is a part, or will be incorporated by reference from a current report on Form 8-K that we file
with the Commission. The senior debt securities will have the same rank as all of our other indebtedness that is not subordinated.
The subordinated debt securities will be subordinated to our senior debt on terms set forth in the applicable prospectus supplement.
In addition, the subordinated debt securities will be effectively subordinated to creditors of our subsidiaries. Our Board of Directors
will determine the terms of each series of debt securities being offered.
This prospectus contains only general terms and provisions of
the debt securities. The applicable prospectus supplement will describe the particular terms of the debt securities offered thereby.
We urge you to read the prospectus supplements and any free writing prospectus that we may authorize to be provided to you related
to the debt securities being offered, as well as the complete indentures that contain the terms of the debt securities. Although
the forms of indentures may be filed as exhibits to the registration statement to which this prospectus is a part, supplemental
indentures and forms of debt securities containing the terms of debt securities being offered will be incorporated by reference
into the registration statement of which this prospectus is a part in reports we file with the Commission.
Warrants. We may offer warrants for the
purchase of debt securities or shares of common stock. We may issue the warrants by themselves or together with debt securities
or common stock, and the warrants may be attached to or separate from any offered securities. Each series of securities warrants
will be issued under a separate warrant agreement to be entered into between us and the investors or a warrant agent. Our Board
of Directors will determine the terms of the warrants. This prospectus contains only general terms and provisions of the warrants.
The applicable prospectus supplement will describe the particular terms of the warrants being offered thereby. We urge you to read
the prospectus supplements and any free writing prospectus that we may authorize to be provided to you related to the warrants
being offered, as well as the complete warrant agreements and warrant certificates that contain the terms of the warrants.
RISK FACTORS
Selected Risks Associated with an Investment in Our Securities
An investment in our securities involves a high degree of risk.
You should carefully consider the risks described below as well as the other information in this prospectus before deciding to
invest in or maintain your investment in our company. The risks described below are not intended to be an all-inclusive list of
all of the potential risks relating to an investment in our securities. Any of the risk factors described below could significantly
and adversely affect our business, prospects, financial condition and results of operations. Additional risks and uncertainties
not currently known or that are currently considered to be immaterial may also materially and adversely affect our business. As
a result, the trading price or value of our securities could be materially adversely affected and you may lose all or part of your
investment.
Risks Relating to Our Financial Position and Need for Additional
Capital
We have incurred significant losses and expect to continue
to incur losses for the foreseeable future.
We have never been profitable. We have generated revenues during
the fiscal years ended March 31, 2019 and March 31, 2018, in the amounts of $229,625, and $149,625, respectively, from our contracts
and grants with the NIH. Our revenues, from research grants, continue to be insufficient to cover our cost of operations. We cannot
be assured when, if at all, we will be able to enter into future government contracts beyond our current contract with the NIH.
Future profitability, if any, will require the successful commercialization of our Hemopurifier technology, other products that
may emerge from our potential diagnostic products or from additional government contract or grant income. We may not be able to
successfully commercialize one or more of our products, and even if commercialization is successful, we may never be profitable.
Even if this offering is successful, we will require additional
financing to sustain our operations.
We will require significant additional financing for our operations
and for expected additional future clinical trials in the U.S., as well as to fund all of our continued research and development
activities for the Hemopurifier® and other future potential products. In addition, as we expand our activities, our overhead
costs to support personnel, laboratory materials and infrastructure will increase. If the financing we may require to sustain our
working capital needs be unavailable to us on reasonable terms, or at all, we may be unable to support our research and FDA clearance
activities, including our planned clinical trials. The failure to implement our research and clearance activities would have a
material adverse effect on our ability to commercialize our products or continue our business.
Even if this offering is successful, we also will need
to raise additional funds through debt or equity financings to achieve our business objectives and to satisfy our cash obligations,
which may dilute the ownership of our existing stockholders.
We will need to raise additional funds through debt and/or equity
financings in order to complete our ultimate business objectives, including funding working capital to support development and
regulatory clearance of our products. We also may choose to raise additional funds in debt or equity financings if they are available
to us on reasonable terms to increase our working capital and to strengthen our financial position. Any sales of additional equity
or convertible debt securities could result in dilution of the equity interests of our existing stockholders, which could be substantial.
Also, new investors may require that we and certain of our stockholders enter into voting arrangements that give them additional
voting control or representation on our Board of Directors.
We will require additional financing to sustain our operations.
We will require significant additional financing for our operations
and for expected additional future clinical trials in the U.S., as well as to fund all of our continued research and development
activities for the Hemopurifier and other future products. In addition, as we expand our activities, our overhead costs to support
personnel, laboratory materials and infrastructure will increase. If the financing we may require to sustain our working capital
needs be unavailable to us on reasonable terms, or at all, we may be unable to support our research and FDA development activities,
including our planned clinical trials. The failure to implement our research and clearance activities would have a material adverse
effect on our ability to commercialize our products or continue our business.
Risks Related to Our Business Operations
We face intense competition in the medical device industry.
We compete with numerous U.S. and foreign companies in the medical
device industry, and many of our competitors have greater financial, personnel, operational and research and development resources
than we do. Our competitors are developing vaccine candidates, which could compete with the Hemopurifier medical device we are
developing. Our commercial opportunities will be reduced or eliminated if our competitors develop and market products for any of
the diseases we target that:
|
☐
|
have fewer or less severe adverse side effects;
|
|
☐
|
are more adaptable to various modes of dosing;
|
|
☐
|
are easier to administer; or
|
|
☐
|
are less expensive than the products or product candidates we are developing.
|
Even if we are successful in developing the Hemopurifier and
potential diagnostic products, and obtain FDA and other regulatory approvals necessary for commercializing them, our products may
not compete effectively with other successful products. Researchers are continually learning more about diseases, which may lead
to new technologies for treatment. Our competitors may succeed in developing and marketing products that are either more effective
than those that we may develop, alone or with our collaborators, or that are marketed before any products we develop are marketed.
Our competitors include fully integrated pharmaceutical companies and biotechnology companies as well as universities and public
and private research institutions. Many of the organizations competing with us have substantially greater capital resources, larger
research and development staffs and facilities, greater experience in product development and in obtaining regulatory approvals,
and greater marketing capabilities than we do. If our competitors develop more effective pharmaceutical treatments for infectious
disease or cancer, or bring those treatments to market before we can commercialize the Hemopurifier for such uses, we may be unable
to obtain any market traction for our products, or the diseases we seek to treat may be substantially addressed by competing treatments.
If we are unable to successfully compete against larger companies in the pharmaceutical industry, we may never generate significant
revenue or be profitable.
We have limited experience in identifying and working
with large-scale contracts with medical device manufacturers; manufacture of our devices must comply with good manufacturing practices
in the U.S.
To achieve the levels of production necessary to commercialize
our Hemopurifier and other future products, we will need to secure large-scale manufacturing agreements with contract manufacturers
which comply with good manufacturing practice standards and other standards prescribed by various federal, state and local regulatory
agencies in the U.S. and any other country of use. We have limited experience coordinating and overseeing the manufacture of medical
device products on a large-scale. It is possible that manufacturing and control problems will arise as we attempt to commercialize
our products and that manufacturing may not be completed in a timely manner or at a commercially reasonable cost. In addition,
we may not be able to adequately finance the manufacture and distribution of our products on terms acceptable to us, if at all.
If we cannot successfully oversee and finance the manufacture of our products if they obtain regulatory clearances, we may never
generate revenue from product sales and we may never be profitable.
Our Aethlon Hemopurifier technology may become obsolete.
Our Hemopurifier product may be made unmarketable prior to commercialization
by us by new scientific or technological developments by others with new treatment modalities that are more efficacious and/or
more economical than our products. The homeland security industry is growing rapidly with many competitors that are trying to develop
products or vaccines to protect against infectious disease. Any one of our competitors could develop a more effective product which
would render our technology obsolete. Further, our ability to achieve significant and sustained penetration of our key target markets
will depend upon our success in developing or acquiring technologies developed by other companies, either independently, through
joint ventures or through acquisitions. If we fail to develop or acquire, and manufacture and sell, products that satisfy our customers’
demands, or we fail to respond effectively to new product announcements by our competitors by quickly introducing competitive products,
then market acceptance of our products could be reduced and our business could be adversely affected. Our products may not remain
competitive with products based on new technologies.
Our success is dependent in part on our executive officers.
Our success depends to a critical extent on the continued services
of our Chief Executive Officer, Timothy C. 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 money in the pursuit of a replacement,
which would result in both a delay in the implementation 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 do not currently
carry key man life insurance policies on any of our key executive officers which would assist us in recouping our costs in the
event of the loss of those 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 inability to attract and retain qualified personnel
could impede our ability to achieve our business objectives.
We have six full-time employees, consisting of our Chief Executive
Officer, our Chief Financial Officer, three research scientists, and an executive assistant. We utilize, whenever appropriate,
consultants in order to conserve cash and resources.
Although we believe that these employees and consultants will
be able to handle most of our additional administrative, research and development and business development in the near term, we
will nevertheless be required over the longer-term to hire highly skilled managerial, scientific and administrative personnel to
fully implement our business plan and growth strategies, including to mitigate the material weakness in our internal control over
financial reporting described above. Due to the specialized scientific nature of our business, we are highly dependent upon our
ability to attract and retain qualified scientific, technical and managerial personnel. Competition for these individuals, especially
in San Diego, California, where many biotechnology companies are located, is intense and we may not be able to attract, assimilate
or retain additional highly qualified personnel in the future. We may not be able to engage the services of qualified personnel
at competitive prices or at all, particularly given the risks of employment attributable to our limited financial resources and
lack of an established track record. Also, if we are required to attract personnel from other parts of the U.S. or abroad, we may
have significant difficulty doing so due to the high cost of living in the Southern California area and due to the costs incurred
with transferring personnel to the area. If we cannot attract and retain qualified staff and executives, we will be unable to develop
our products and achieve regulatory clearance, and our business could fail.
We plan to grow rapidly which will strain our resources;
our inability to manage our growth could delay or derail implementation of our business objectives.
We will need to significantly expand our operations to implement
our longer-term business plan and growth strategies. We will also be required to manage multiple relationships with various strategic
partners, technology licensors, customers, manufacturers and suppliers, consultants and other third parties. This expansion and
these expanded relationships will require us to significantly improve or replace our existing managerial, operational and financial
systems, procedures and controls; to improve the coordination between our various corporate functions; and to manage, train, motivate
and maintain a growing employee base. The time and costs to effectuate these steps may place a significant strain on our management
personnel, systems and resources, particularly given the limited amount of financial resources and skilled employees that may be
available at the time. We cannot assure you that we will institute, in a timely manner or at all, the improvements to our managerial,
operational and financial systems, procedures and controls necessary to support our anticipated increased levels of operations
and to coordinate our various corporate functions, or that we will be able to properly manage, train, motivate and retain our anticipated
increased employee base. If we cannot manage our growth initiatives, we will be unable to commercialize our products on a large-scale
in a timely manner, if at all, and our business could fail.
As a public company with limited financial resources undertaking
the launch of new medical technologies, we may have difficulty attracting and retaining executive management and directors.
The directors and management of publicly traded corporations
are increasingly concerned with the extent of their personal exposure to lawsuits and stockholder claims, as well as governmental
and creditor claims which may be made against them, particularly in view of recent changes in securities laws imposing additional
duties, obligations and liabilities on management and directors. Due to these perceived risks, directors and management are also
becoming increasingly concerned with the availability of directors’ and officers’ liability insurance to pay on a timely
basis the costs incurred in defending such claims. While we currently carry directors’ and officers’ liability insurance,
such insurance is expensive and difficult to obtain. If we are unable to continue or provide directors’ and officers’
liability insurance at affordable rates or at all, it may become increasingly more difficult to attract and retain qualified outside
directors to serve on our Board of Directors. We may lose potential independent board members and management candidates to other
companies in the biotechnology field that have greater directors’ and officers’ liability insurance to insure them
from liability or to biotechnology companies that have revenues or have received greater funding to date which can offer greater
compensation packages. The fees of directors are also rising in response to their increased duties, obligations and liabilities.
In addition, our products could potentially be harmful to users, and we are exposed to claims of product liability including for
injury or death. We have limited insurance and may not be able to afford robust coverage even as our products are introduced into
the market. As a company with limited resources and potential exposures to management, we will have a more difficult time attracting
and retaining management and outside independent directors than a more established public or private company due to these enhanced
duties, obligations and potential liabilities.
If we fail to comply with extensive regulations of U.S.
and foreign regulatory agencies, the commercialization of our products could be delayed or prevented entirely.
Our Hemopurifier product is subject to extensive government
regulations related to development, testing, manufacturing and commercialization in the U.S. and other countries. The determination
of when and whether a product is ready for large-scale purchase and potential use will be made by the U.S. Government through consultation
with a number of governmental agencies, including the FDA, the National Institutes of Health, the Centers for Disease Control and
Prevention and the Department of Homeland Security. Our product candidates are in the pre-clinical and clinical stages of development
and have not received required regulatory approval from the FDA, or any foreign regulatory agencies, to be commercially marketed
and sold. The process of obtaining and complying with FDA and other governmental regulatory approvals and regulations in the U.S.
and in foreign countries is costly, time consuming, uncertain and subject to unanticipated delays. Obtaining such regulatory approvals,
if any, can take several years. Despite the time and expense exerted, regulatory approval is never guaranteed. We also are subject
to the following risks and obligations, among others:
|
☐
|
the FDA may refuse to approve an application if they believe that applicable regulatory criteria are not satisfied;
|
|
☐
|
the FDA may require additional testing for safety and effectiveness;
|
|
☐
|
the FDA may interpret data from pre-clinical testing and clinical trials in different ways than we interpret them;
|
|
☐
|
if regulatory approval of a product is granted, the approval may be limited to specific indications or limited with respect to its distribution; and
|
|
☐
|
the FDA may change their approval policies and/or adopt new regulations.
|
Failure to comply with these or other regulatory requirements
of the FDA may subject us to administrative or judicially imposed sanctions, including:
|
☐
|
product seizure or detention;
|
|
☐
|
total or partial suspension of productions.
|
Delays in successfully completing our planned clinical
trials could jeopardize our ability to obtain regulatory approval.
Our business prospects will depend on our ability to complete
studies, clinical trials, obtain satisfactory results, obtain required regulatory approvals and successfully commercialize our
Hemopurifier product candidate. Completion of our clinical trials, announcement of results of the trials and our ability to obtain
regulatory approvals could be delayed for a variety of reasons, including:
|
☐
|
slow patient enrollment;
|
|
☐
|
serious adverse events related to our medical device candidates;
|
|
☐
|
unsatisfactory results of any clinical trial;
|
|
☐
|
the failure of our principal third-party investigators to perform our clinical trials on our anticipated schedules;
|
|
☐
|
different interpretations of our pre-clinical and clinical data, which could initially lead to inconclusive results; and
|
|
|
|
|
☐
|
delays resulting from the coronavirus pandemic.
|
Our development costs will increase if we have material delays
in any clinical trial or if we need to perform more or larger clinical trials than planned. If the delays are significant, or if
any of our product candidates do not prove to be safe or effective or do not receive required regulatory approvals, our financial
results and the commercial prospects for our product candidates will be harmed. Furthermore, our inability to complete our clinical
trials in a timely manner could jeopardize our ability to obtain regulatory approval.
If we or our suppliers fail to comply with ongoing FDA
or foreign regulatory authority requirements, or if we experience unanticipated problems with our products, these products could
be subject to restrictions or withdrawal from the market.
Any product for which we obtain clearance or approval, and the
manufacturing processes, reporting requirements, post-approval clinical data and promotional activities for such product, will
be subject to continued regulatory review, oversight and periodic inspections by the FDA and other domestic and foreign regulatory
bodies. In particular, we and our third-party suppliers may be required to comply with the FDA’s Quality System Regulation,
or QSR. These FDA regulations cover the methods and documentation of the design, testing, production, control, quality assurance,
labeling, packaging, sterilization, storage and shipping of our products. Compliance with applicable regulatory requirements is
subject to continual review and is monitored rigorously through periodic inspections by the FDA. If we, or our manufacturers, fail
to adhere to QSR requirements in the U.S., this could delay production of our products and lead to fines, difficulties in obtaining
regulatory clearances, recalls, enforcement actions, including injunctive relief or consent decrees, or other consequences, which
could, in turn, have a material adverse effect on our financial condition or results of operations.
In addition, the FDA assesses compliance with the QSR through
periodic announced and unannounced inspections of manufacturing and other facilities. The failure by us or one of our suppliers
to comply with applicable statutes and regulations administered by the FDA, or the failure to timely and adequately respond to
any adverse inspectional observations or product safety issues, could result in any of the following enforcement actions:
|
☐
|
untitled letters, warning letters, fines, injunctions, consent decrees and civil penalties;
|
|
☐
|
unanticipated expenditures to address or defend such actions;
|
|
☐
|
customer notifications or repair, replacement, refunds, recall, detention or seizure of our products;
|
|
☐
|
operating restrictions or partial suspension or total shutdown of production;
|
|
☐
|
refusing or delaying our requests for 510(k) clearance or premarket approval of new products or modified products;
|
|
☐
|
withdrawing 510(k) clearances or premarket approvals that have already been granted;
|
|
☐
|
refusal to grant export approval for our products; or
|
|
☐
|
criminal prosecution.
|
Moreover, the FDA strictly regulates the promotional claims
that may be made about approved products. In particular, a product may not be promoted for uses that are not approved by the FDA
as reflected in the product’s approved labeling. However, companies may share truthful and not misleading information that
is otherwise consistent with a product’s FDA approved labeling. The FDA and other agencies actively enforce the laws and
regulations prohibiting the promotion of off-label uses, and a company that is found to have improperly promoted off-label uses
may be subject to significant civil, criminal and administrative penalties.
Any of these sanctions could have a material adverse effect
on our reputation, business, results of operations and financial condition. Furthermore, our key component suppliers may not currently
be or may not continue to be in compliance with all applicable regulatory requirements, which could result in our failure to produce
our products on a timely basis and in the required quantities, if at all.
If our products, or malfunction of our products, cause
or contribute to a death or a serious injury, we will be subject to medical device reporting regulations, which can result in voluntary
corrective actions or agency enforcement actions.
Under the FDA medical device reporting regulations, medical
device manufacturers are required to report to the FDA information that a device has or may have caused or contributed to a death
or serious injury or has malfunctioned in a way that would likely cause or contribute to death or serious injury if the malfunction
of the device or one of our similar devices were to recur. If we fail to report these events to the FDA within the required timeframes,
or at all, FDA could take enforcement action against us. Any such adverse event involving our products also could result in future
voluntary corrective actions, such as recalls or customer notifications, or agency action, such as inspection or enforcement action.
Any corrective action, whether voluntary or involuntary, as well as defending ourselves in a lawsuit, will require the dedication
of our time and capital, distract management from operating our business, and may harm our reputation and financial results.
We outsource almost all of our operational and development
activities, and if any party to which we have outsourced certain essential functions fails to perform its obligations under agreements
with us, the development and commercialization of our lead product candidate and any future product candidates that we may develop
could be delayed or terminated.
We generally rely on third-party consultants or other vendors
to manage and implement the day-to-day conduct of our operations, including conducting clinical trials and manufacturing our current
product candidates and any future product candidates that we may develop. Accordingly, we are and will continue to be dependent
on the timeliness and effectiveness of their efforts. Our dependence on third parties includes key suppliers and third-party service
providers supporting the development, manufacture and regulatory approval of our products as well as support for our information
technology systems and other infrastructure. While our management team oversees these vendors, failure of any of these third parties
to meet their contractual, regulatory and other obligations or the development of factors that materially disrupt the performance
of these third parties could have a material adverse effect on our business. For example, all of the key oversight responsibilities
for the development and manufacture of our lead product candidate are conducted by our management team, but all other activities
are the responsibility of third-party vendors.
If a clinical research organization that we utilize is unable
to allocate sufficient qualified personnel to our studies in a timely manner or if the work performed by it does not fully satisfy
the requirements of the FDA or other regulatory agencies, we may encounter substantial delays and increased costs in completing
our development efforts. Any manufacturer that we select may encounter difficulties in the manufacture of new products in commercial
quantities, including problems involving product yields, product stability or shelf life, quality control, adequacy of control
procedures and policies, compliance with FDA regulations and the need for further FDA approval of any new manufacturing processes
and facilities. If any of these occur, the development and commercialization of our product candidates could be delayed, curtailed
or terminated because we may not have sufficient financial resources or capabilities to continue such development and commercialization
on our own. If we rely on only one source for the manufacture of the clinical or commercial supplies of any of our product candidates
or products, any production problems or supply constraints with that manufacturer could adversely impact the development or commercialization
of that product candidate or product.
If we or our contractors or service providers fail to
comply with regulatory laws and regulations, we or they could be subject to regulatory actions, which could affect our ability
to develop, market and sell our product candidates and any other or future product candidates that we may develop and may harm
our reputation.
If we or our manufacturers or other third-party contractors
fail to comply with applicable federal, state or foreign laws or regulations, we could be subject to regulatory actions, which
could affect our ability to develop, market and sell our current product candidates or any future product candidates under development
successfully and could harm our reputation and lead to reduced or non-acceptance of our proposed product candidates by the market.
Even technical recommendations or evidence by the FDA through letters, site visits, and overall recommendations to academia or
biotechnology companies may make the manufacturing of a clinical product extremely labor intensive or expensive, making the product
candidate no longer viable to manufacture in a cost-efficient manner. The mode of administration may make the product candidate
not commercially viable. The required testing of the product candidate may make that candidate no longer commercially viable. The
conduct of clinical trials may be critiqued by the FDA, or a clinical trial site’s Institutional Review Board or Institutional
Biosafety Committee, which may delay or make impossible clinical testing of a product candidate. The Institutional Review Board
for a clinical trial may stop a trial or deem a product candidate unsafe to continue testing. This would have a material adverse
effect on the value of the product candidate and our business prospects.
We will need to outsource and rely on third parties for
the clinical development and manufacture, sales and marketing of our current product candidates or any future product candidates
that we may develop, and our future success will be dependent on the timeliness and effectiveness of the efforts of these third
parties.
We do not have the required financial and human resources to
carry out on our own all the pre-clinical and clinical development for our current product candidates or any other or future product
candidates that we may develop, and do not have the capability and resources to manufacture, market or sell our current product
candidates or any future product candidates that we may develop. Our business model calls for the partial or full outsourcing of
the clinical and other development and manufacturing, sales and marketing of our product candidates in order to reduce our capital
and infrastructure costs as a means of potentially improving our financial position. Our success will depend on the performance
of these outsourced providers. If these providers fail to perform adequately, our development of product candidates may be delayed
and any delay in the development of our product candidates would have a material and adverse effect on our business prospects.
We are and will be exposed to product liability risks,
and clinical and preclinical liability risks, which could place a substantial financial burden upon us should we be sued.
Our business exposes us to potential product liability and other
liability risks that are inherent in the testing, manufacturing and marketing of medical devices. Claims may be asserted against
us. A successful liability claim or series of claims brought against us could have a material adverse effect on our business, financial
condition and results of operations. We may not be able to continue to obtain or maintain adequate product liability insurance
on acceptable terms, if at all, and such insurance may not provide adequate coverage against potential liabilities. Claims or losses
in excess of any product liability insurance coverage that we may obtain could have a material adverse effect on our business,
financial condition and results of operations.
Our Hemopurifier product may be used in connection with medical
procedures in which it is important that those products function with precision and accuracy. If our products do not function as
designed, or are designed improperly, we may be forced by regulatory agencies to withdraw such products from the market. In addition,
if medical personnel or their patients suffer injury as a result of any failure of our products to function as designed, or our
products are designed inappropriately, we may be subject to lawsuits seeking significant compensatory and punitive damages. The
risk of product liability claims, product recalls and associated adverse publicity is inherent in the testing, manufacturing, marketing
and sale of medical products. We have recently obtained general clinical trial liability insurance coverage. However, our insurance
coverage may not be adequate or available. We may not be able to secure product liability insurance coverage on acceptable terms
or at reasonable costs when needed. Any product recall or lawsuit seeking significant monetary damages may have a material effect
on our business and financial condition. Any liability for mandatory damages could exceed the amount of our coverage. Moreover,
a product recall could generate substantial negative publicity about our products and business and inhibit or prevent commercialization
of other future product candidates.
We have not received, and may never receive, approval
from the FDA to market a medical device in the United States.
Before a new medical device can be marketed in the U.S., it
must first receive either premarket approval, or a PMA, or 510(k) clearance from the FDA, unless an exemption applies. A PMA submission,
which is a higher standard than a 510(k) clearance, is used to demonstrate to the FDA that a new or modified device is safe and
effective. The 510(k) is used to demonstrate that a device is “substantially equivalent” to a predicate device (one
that has been cleared by the FDA). We expect that any product we seek regulatory approval for will require a PMA. The FDA approval
process involves, among other things, successfully completing clinical trials and filing for and obtaining a PMA. The PMA process
requires us to prove the safety and effectiveness of our products to the FDA’s satisfaction. This process, which includes
preclinical studies and clinical trials, can take many years and requires the expenditure of substantial resources and may include
post-marketing surveillance to establish the safety and efficacy of the product. Notwithstanding the effort and expense incurred,
the process may never result in the FDA granting a PMA. Data obtained from preclinical studies and clinical trials are subject
to varying interpretations that could delay, limit or prevent regulatory approval. Delays or rejections may also be encountered
based upon changes in governmental policies for medical devices during the period of product development. The FDA can delay, limit
or deny approval of a PMA application for many reasons, including:
|
☐
|
our inability to demonstrate safety or effectiveness to the FDA’s satisfaction;
|
|
☐
|
insufficient data from our preclinical studies and clinical trials to support approval;
|
|
☐
|
failure of the facilities of our third-party manufacturer or suppliers to meet applicable requirements;
|
|
☐
|
inadequate compliance with preclinical, clinical or other regulations;
|
|
☐
|
our failure to meet the FDA’s statistical requirements for approval; and
|
|
☐
|
changes in the FDA’s approval policies, or the adoption of new regulations that require additional data or additional clinical studies.
|
Modifications to products that are approved through a PMA application
generally need FDA approval. Similarly, some modifications made to products cleared through a 510(k) may require a new 510(k).
The FDA’s 510(k) clearance process usually takes from three to 12 months, but may last longer. The process of obtaining a
PMA is much costlier and more uncertain than the 510(k) clearance process and generally takes from one to three years, or even
longer, from the time the application is submitted to the FDA until an approval is obtained. Any of our products considered to
be a class III device, which are considered to pose the greatest risk and the approval of which is governed by the strictest guidelines,
will require the submission and approval of a PMA in order for us to market it in the U.S. We also may design new products in the
future that could require the clearance of a 510(k).
Although we have received approval to proceed with clinical
trials in the U.S. under the investigational device exemption, the current approval from the FDA to proceed could be revoked, the
study could be unsuccessful, or the FDA PMA approval may not be obtained or could be revoked. Even if we obtain approval, the FDA
or other regulatory authorities may require expensive or burdensome post-market testing or controls. Any delay in, or failure to
receive or maintain, clearance or approval for our future products could prevent us from generating revenue from these products
or achieving profitability. Additionally, the FDA and other regulatory authorities have broad enforcement powers. Regulatory enforcement
or inquiries, or other increased scrutiny on us, could dissuade some physicians from using our products and adversely affect our
reputation and the perceived safety and efficacy of our products.
The approval requirements for medical products used to
fight bioterrorism are still evolving, and any products we develop for such uses may not meet these requirements.
We are advancing product candidates under governmental policies
that regulate the development and commercialization of medical treatment countermeasures against bioterror and pandemic threats.
While we intend to pursue FDA market clearance to treat infectious bioterror and pandemic threats, it is often not feasible
to conduct human studies against these deadly high threat pathogens. For example, the Hemopurifier is an investigational device
that has not yet received FDA approval for any indication and Aethlon continues to investigate the potential for the use of the
Hemopurifier in viral diseases under an open Investigational Device Exemption (IDE) and our FDA Breakthrough Designation for “…the
treatment of life-threatening glycosylated viruses that are not addressed with an approved therapy.” Based on our studies
to date, the Hemopurifier can potentially clear many viruses that are pathogenic in humans, including HCV, HIV and Ebola. However,
we do not yet have access to materials from SARS-CoV-2 (the causative agent in COVID-19) for testing. Furthermore, we also do not
know whether clearing SARS-CoV-2 from the blood, which is what the Hemopurifier is designed to do, would have a positive effect
on this disease, which primarily targets the lung; and even if effective, the Hemopurifier would only potentially be indicated
in those patients with the most severe and life-threatening manifestations.
Thus, we may not be able to demonstrate the effectiveness of
our treatment countermeasures through controlled human efficacy studies. Additionally, a change in government policies could impair
our ability to obtain regulatory approval and the FDA may not approve any of our product candidates.
The results of our clinical trials may not support our
product candidate claims or may result in the discovery of adverse side effects.
Any research and development, pre-clinical testing and clinical
trial activities involving any products that we are developing or may develop will be subject to extensive regulation and review
by numerous governmental authorities both in the U.S. and abroad. In the future, we may conduct clinical trials to support approval
of new products. Clinical studies must be conducted in compliance with FDA regulations or the FDA may take enforcement action.
The data collected from these clinical studies may ultimately be used to support market clearance for these products. Even if our
clinical trials are completed as planned, the results of these trials may not support our product candidate claims and the FDA
may not agree with our conclusions regarding the trial results. Success in pre-clinical studies and early clinical trials does
not ensure that later clinical trials will be successful, and the later trials may not replicate the results of prior trials and
pre-clinical studies. The clinical trial process may fail to demonstrate that our product candidates are safe and effective for
the proposed indicated uses, which could cause us to abandon a product candidate and may delay development of others. Any delay
or termination of our clinical trials will delay the filing of our product submissions and, ultimately, our ability to commercialize
our product candidates and generate revenues. It is also possible that patients enrolled in clinical trials will experience adverse
side effects that are not currently part of the product candidate’s profile.
U.S. legislative or FDA regulatory reforms may make it
more difficult and costly for us to obtain regulatory approval of our product candidates and to manufacture, market and distribute
our products after approval is obtained.
From time to time, legislation is drafted and introduced in
Congress that could significantly change the statutory provisions governing the regulatory approval, manufacture and marketing
of regulated products or the reimbursement thereof. In addition, FDA regulations and guidance are often revised or reinterpreted
by the FDA in ways that may significantly affect our business and our products. Any new regulations or revisions or reinterpretations
of existing regulations may impose additional costs or lengthen review times of future products. It is impossible to predict whether
legislative changes will be enacted or FDA regulations, guidance or interpretations changed, and what the impact of such changes,
if any, may be or new product development efforts.
Our current and future business activities may be subject,
directly or indirectly, to applicable anti-kickback, fraud and abuse, false claims, physician payment transparency, health information
privacy and security and other healthcare laws and regulations, which could expose us to significant penalties.
We are currently or will in the future be subject to healthcare
regulation and enforcement by the U.S. federal government and the states in which we will conduct our business once our product
candidates are approved by the FDA and commercialized in the United States. In addition to the FDA’s restrictions on marketing
of approved products, the U.S. healthcare laws and regulations that may affect our ability to operate include: the federal fraud
and abuse laws, including the federal anti-kickback and false claims laws; federal data privacy and security laws; and federal
transparency laws related to payments and/or other transfers of value made to physicians and other healthcare professionals and
teaching hospitals. Many states have similar laws and regulations that may differ from each other and federal law in significant
ways, thus complicating compliance efforts. These laws may adversely affect our sales, marketing and other activities with respect
to any product candidate for which we receive approval to market in the United States by imposing administrative and compliance
burdens on us.
Because of the breadth of these laws and the narrowness of available
statutory exceptions and regulatory safe harbors, it is possible that some of our business activities, particularly any sales and
marketing activities after a product candidate has been approved for marketing in the United States, could be subject to legal
challenge and enforcement actions. If our operations are found to be in violation of any of the federal and state laws described
above or any other governmental regulations that apply to us, we may be subject to significant civil, criminal, and administrative
penalties, including, without limitation, damages, fines, imprisonment, exclusion from participation in government healthcare programs,
additional reporting obligations and oversight if we become subject to a corporate integrity agreement or other agreement to resolve
allegations of non-compliance with these laws, and the curtailment or restructuring of our operations, any of which could adversely
affect our ability to operate our business and our results of operations.
Should our products be approved for commercialization,
lack of third-party coverage and reimbursement for our devices could delay or limit their adoption.
In both the U.S. and international markets, the use of medical
devices is dependent in part on the availability of reimbursement from third-party payors, such as government and private insurance
plans. Healthcare providers that use medical devices generally rely on third-party payors to pay for all or part of the costs and
fees associated with the medical procedures being performed or to compensate them for their patient care services. Should our products
under development be approved for commercialization by the FDA, any such products may not be considered cost-effective, reimbursement
may not be available in the U.S. or other countries, if approved, and reimbursement may not be sufficient to allow sales of our
future products on a profitable basis. The coverage decisions of third-party payors will be significantly influenced by the assessment
of our future products by health technology assessment bodies. These assessments are outside our control and any such evaluations
may not be conducted or have a favorable outcome.
If approved for use in the U.S., we expect that any products
that we develop will be purchased primarily by medical institutions, which will in turn bill various third-party payors for the
health care services provided to patients at their facility. Payors may include the Centers for Medicare & Medicaid Services,
or CMS, which administers the Medicare program and works in partnership with state governments to administer Medicaid, other government
programs and private insurance plans. The process involved in applying for coverage and incremental reimbursement from CMS is lengthy
and expensive. Further, Medicare coverage is based on our ability to demonstrate that the treatment is “reasonable and necessary”
for Medicare beneficiaries. Even if products utilizing our Aethlon Hemopurifier technology receive FDA and other regulatory clearance
or approval, they may not be granted coverage and reimbursement by any payor, including by CMS. For some governmental programs,
such as Medicaid, coverage and adequate reimbursement differ from state to state and some state Medicaid programs may not pay adequate
amounts for the procedure necessary to utilize products utilizing our technology system, or any payment at all. Moreover, many
private payors use coverage decisions and payment amounts determined by CMS as guidelines in setting their coverage and reimbursement
policies and amounts. However, no uniform policy requirement for coverage and reimbursement for drug products exists among third-party
payors in the United States. Therefore, coverage and reimbursement can differ significantly from payor to payor. If CMS or other
agencies limit coverage or decrease or limit reimbursement payments for doctors and hospitals, this may affect coverage and reimbursement
determinations by many private payors for any products that we develop.
Should our products be approved for commercialization,
adverse changes in reimbursement policies and procedures by payors may impact our ability to market and sell our products.
Healthcare costs have risen significantly over the past decade,
and there have been and continue to be proposals by legislators, regulators and third-party payors to decrease costs. Third-party
payors are increasingly challenging the prices charged for medical products and services and instituting cost containment measures
to control or significantly influence the purchase of medical products and services.
For example, in the U.S., the Patient Protection and Affordable
Care Act, as amended by the Health Care and Education Reconciliation Act of 2010, or collectively, PPACA, among other things, reduced
and/or limited Medicare reimbursement to certain providers. However, on December 14, 2018, a Texas U.S. District Court Judge ruled
that the Affordable Care Act is unconstitutional in its entirety because the “individual mandate” was repealed by Congress
as part of the Tax Cuts and Jobs Act of 2017. While the Texas U.S. District Court Judge, as well as the Trump administration and
CMS, have stated that the ruling will have no immediate effect pending appeal of the decision, it is unclear how this decision,
subsequent appeals, and other efforts to repeal and replace the Affordable Care Act will impact the Affordable Care Act. The Budget
Control Act of 2011, as amended by subsequent legislation, further reduces Medicare’s payments to providers by two percent
through fiscal year 2027. These reductions may reduce providers’ revenues or profits, which could affect their ability to
purchase new technologies. Furthermore, the healthcare industry in the U.S. has experienced a trend toward cost containment as
government and private insurers seek to control healthcare costs by imposing lower payment rates and negotiating reduced contract
rates with service providers. Legislation could be adopted in the future that limits payments for our products from governmental
payors. In addition, commercial payors such as insurance companies, could adopt similar policies that limit reimbursement for medical
device manufacturers’ products. Therefore, it is possible that our product or the procedures or patient care performed using
our product will not be reimbursed at a cost-effective level. We face similar risks relating to adverse changes in reimbursement
procedures and policies in other countries where we may market our products. Reimbursement and healthcare payment systems vary
significantly among international markets. Our inability to obtain international reimbursement approval, or any adverse changes
in the reimbursement policies of foreign payors, could negatively affect our ability to sell our products and have a material adverse
effect on our business and financial condition.
Should our products be approved for commercialization,
our financial performance may be adversely affected by medical device tax provisions in the healthcare reform laws.
PPACA currently imposes, among other things, an excise tax of
2.3% on any entity that manufactures or imports medical devices offered for sale in the U.S. Under these provisions, the Congressional
Research Service predicts that the total cost to the medical device industry may be up to $20 billion over the next decade. The
Internal Revenue Service issued final regulations implementing the tax in December 2012, which requires, among other things, bi-monthly
payments and quarterly reporting.
The Consolidated Appropriations Act, 2016 (Pub. L. 114-113),
signed into law on Dec. 18, 2015, included a two-year moratorium on the medical device excise tax imposed by Internal Revenue Code
section 4191. This moratorium was then extended by an additional two years in January 2018. Currently, the medical device excise
tax does not apply to the sale of a taxable medical device by the manufacturer, producer, or importer of the device until January
1, 2020, unless the moratorium is further extended.
Once we market products, if this regulation is not repealed,
we will be subject to this or any future excise tax on our sales of certain medical devices in the U.S. We anticipate that primarily
all of our sales, once commenced, of medical devices in the U.S. will be subject to this 2.3% excise tax.
Our use of hazardous materials, chemicals and viruses
exposes us to potential liabilities for which we may not have adequate insurance.
Our research and development involves the controlled use of
hazardous materials, chemicals and viruses. The primary hazardous materials include chemicals needed to construct the Hemopurifier
cartridges and the infected plasma samples used in preclinical testing of the Hemopurifier. All other chemicals are fully inventoried
and reported to the appropriate authorities, such as the fire department, who inspect the facility on a regular basis. We are subject
to federal, state, local and foreign laws governing the use, manufacture, storage, handling and disposal of such materials. Although
we believe that our safety procedures for the use, manufacture, storage, handling and disposal of such materials comply with the
standards prescribed by federal, state, local and foreign regulations, we cannot completely eliminate the risk of accidental contamination
or injury from these materials. We have had no incidents or problems involving hazardous chemicals or biological samples. In the
event of such an accident, we could be held liable for significant damages or fines.
We currently carry a limited amount of insurance to protect
us from damages arising from hazardous materials. Our product liability policy has a $3,000,000 limit of liability that would cover
certain releases of hazardous substances away from our facilities. For our facilities, our property policy provides $25,000 in
coverage for contaminant clean-up or removal and $50,000 in coverage for damages to the premises resulting from contamination.
Should we violate any regulations concerning the handling or use of hazardous materials, or should any injuries or death result
from our use or handling of hazardous materials, we could be the subject of substantial lawsuits by governmental agencies or individuals.
We may not have adequate insurance to cover all or any of such claims, if any. If we were responsible to pay significant damages
for violations or injuries, if any, we might be forced to cease operations since such payments could deplete our available resources.
Our products may in the future be subject to product recalls.
A recall of our products, either voluntarily or at the direction of the FDA or another governmental authority, including a third-country
authority, or the discovery of serious safety issues with our products, could have a significant adverse impact on us.
The FDA and similar foreign governmental authorities have the
authority to require the recall of commercialized products in the event of material deficiencies or defects in design or manufacture.
For the FDA, the authority to require a recall must be based on a finding that there is reasonable probability that the device
would cause serious injury or death. In addition, foreign governmental bodies have the authority to require the recall of our products
in the event of material deficiencies or defects in design or manufacture. Manufacturers may, under their own initiative, recall
a product if any material deficiency in a device is found. The FDA requires that certain classifications of recalls be reported
to the FDA within 10 working days after the recall is initiated. A government-mandated or voluntary recall by us or one of our
international distributors could occur as a result of an unacceptable risk to health, component failures, malfunctions, manufacturing
errors, design or labeling defects or other deficiencies and issues. Recalls of any of our products would divert managerial and
financial resources and have an adverse effect on our reputation, results of operations and financial condition, which could impair
our ability to produce our products in a cost-effective and timely manner in order to meet our customers’ demands. We may
also be subject to liability claims, be required to bear other costs, or take other actions that may have a negative impact on
our future sales and our ability to generate profits. Companies are required to maintain certain records of recalls, even if they
are not reportable to the FDA or another third-country competent authority. We may initiate voluntary recalls involving our products
in the future that we determine do not require notification of the FDA or another third-country competent authority. If the FDA
disagrees with our determinations, they could require us to report those actions as recalls. A future recall announcement could
harm our reputation with customers and negatively affect our sales. In addition, the FDA could take enforcement action for failing
to report recalls. We are also required to follow detailed recordkeeping requirements for all firm-initiated medical device corrections
and removals.
Our business operations may be adversely
affected by the coronavirus outbreak and face risks that could impact our business.
A novel strain of coronavirus, COVID-19, originated in Wuhan,
China, in December 2019 and has spread globally. Business disruptions in the world could negatively affect our operations,
including the sources and availability of components and raw materials that are essential to the operation of our business. Extended
periods of interruption to our operations due to the coronavirus outbreak could adversely impact the timeline for our clinical
trials, the growth of our business and potentially could cause us to cease or delay operations.
The extent to which the coronavirus impacts our business and
results of operations will depend on future developments, which are highly uncertain and cannot be predicted at this time. This
includes new information that is emerging daily concerning the severity of the coronavirus, the spread and proliferation of the
coronavirus around the world, and the actions taken to contain the coronavirus or treat its impact, among others.
Our products 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 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 agglutinin, or GNA, 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, including
interruption resulting from the coronavirus pandemic, could have a 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.
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.
On 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 concerns regarding the accuracy and adequacy of information in the marketplace that appeared
to be disseminated by third party promotors and recent and unusual market activity since at least January 22, 2020. Although our
stock resumed trading upon expiration of the SEC Order, we are unable to predict the outcome of the SEC investigation or any other
actions the SEC may take in connection therewith. Furthermore, the Company’s reputation may be negatively impacted. As a
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
enforce 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 application of Nevada law
in the types of lawsuits to which it applies, the provision may have the effect of discouraging lawsuits against our directors
and officers.
Risks Related to Our Intellectual Property and Related Litigation
We rely upon licenses and patent rights from third parties
which are subject to termination or expiration.
We rely upon third-party licenses and ownership rights assigned
from third parties for the development of specific uses for our Hemopurifier devices. For example, we are researching, developing
and testing cancer-related applications for our devices under patents assigned from the London Health Science Center Research,
Inc. Should any of our licenses be prematurely terminated for any reason, or if the patents and intellectual property assigned
to us or owned by such entities that we have licensed are challenged or defeated by third parties, our research efforts could be
materially and adversely affected. Our licenses and patents assigned to us may not continue in force for as long as we require
for our research, development and testing of cancer treatments. It is possible that, if our licenses terminate or the underlying
patents and intellectual property is challenged or defeated or the patents and intellectual property assigned to us is challenged
or defeated, suitable replacements may not be obtained or developed on terms acceptable to us, if at all. There is also the related
risk that we may not be able to make the required payments under any patent license or assignment agreement, in which case we may
lose to ability to use one or more of the licensed or assigned patents.
We could become subject to intellectual property litigation
that could be costly, result in the diversion of management’s time and efforts, require us to pay damages, prevent us from
selling our commercially available products and/or reduce the margins we may realize from our products.
The medical devices industry is characterized by extensive litigation
and administrative proceedings over patent and other intellectual property rights. Whether a product infringes a patent involves
complex legal and factual issues, and the determination is often uncertain. There may be existing patents of which we are unaware
that our products under development may inadvertently infringe. The likelihood that patent infringement claims may be brought against
us increases as the number of participants in the infectious market increases and as we achieve more visibility in the market place
and introduce products to market.
Any infringement claim against us, even if without merit, may
cause us to incur substantial costs, and would place a significant strain on our financial resources, divert the attention of management
from our core business, and harm our reputation. In some cases, litigation may be threatened or brought by a patent holding company
or other adverse patent owner who has no relevant product revenues and against whom our patents may provide little or no deterrence.
If we are found to infringe any patents, we could be required to pay substantial damages, including triple damages if an infringement
is found to be willful. We also could be required to pay royalties and could be prevented from selling our products unless we obtain
a license or are able to redesign our products to avoid infringement. We may not be able to obtain a license enabling us to sell
our products on reasonable terms, or at all. If we fail to obtain any required licenses or make any necessary changes to our technologies
or the products, we may be unable to commercialize one or more of our products or may have to withdraw products from the market,
all of which would have a material adverse effect on our business, financial condition and results of operations.
If the combination of patents, trade secrets and contractual
provisions upon which we rely to protect our intellectual property is inadequate, our ability to commercialize our products successfully
will be harmed.
Our success depends significantly on our ability to protect
our proprietary rights to the technologies incorporated in our products. We currently have five issued U.S. patents and seven pending
U.S. patent applications. We also have 26 issued foreign patents and have applied for nine additional international patents. Our
issued patents begin to expire in 2019, with the last of these patents expiring in 2029, although terminal disclaimers, patent
term extension or patent term adjustment can shorten or lengthen the patent term. We rely on a combination of patent protection,
trade secret laws and nondisclosure, confidentiality and other contractual restrictions to protect our proprietary technology.
However, these may not adequately protect our rights or permit us to gain or keep any competitive advantage.
The issuance of a patent is not conclusive as to its scope,
validity or enforceability. The scope, validity or enforceability of our issued patents can be challenged in litigation or proceedings
before the U.S. Patent and Trademark Office or foreign patent offices where our applications are pending. The U.S. Patent and Trademark
Office or foreign offices may deny or require significant narrowing of claims in our pending patent applications. Patents issued
as a result of the pending patent applications, if any, may not provide us with significant commercial protection or be issued
in a form that is advantageous to us. Proceedings before the U.S. Patent and Trademark Office or foreign offices could result in
adverse decisions as to the priority of our inventions and the narrowing or invalidation of claims in issued patents. The laws
of some foreign countries may not protect our intellectual property rights to the same extent as the laws of the U.S., if at all.
Some of our patents may expire before we receive FDA approval to market our products in the U.S. or we receive approval to market
our products in a foreign country. Although we believe that certain patent applications and/or other patents issued more recently
will help protect the proprietary nature of the Hemopurifier treatment technology, this protection may not be sufficient to protect
us during the development of that technology.
Our competitors may successfully challenge and invalidate or
render unenforceable our issued patents, including any patents that may issue in the future, which could prevent or limit our ability
to market our products and could limit our ability to stop competitors from marketing products that are substantially equivalent
to ours. In addition, competitors may be able to design around our patents or develop products that provide outcomes that are comparable
to our products but that are not covered by our patents.
We have also entered into confidentiality and assignment of
intellectual property agreements with all of our employees, consultants and advisors directly involved in the development of our
technology as one of the ways we seek to protect our intellectual property and other proprietary technology. However, these agreements
may not be enforceable or may not provide meaningful protection for our trade secrets or other proprietary information in the event
of unauthorized use or disclosure or other breaches of the agreements.
In the event a competitor infringes upon any of our patents
or other intellectual property rights, enforcing our rights may be difficult, time consuming and expensive, and would divert management’s
attention from managing our business. We may not be successful on the merits in any enforcement effort. In addition, we may not
have sufficient resources to litigate, enforce or defend our intellectual property rights.
We may rely on licenses for new technology, which may
affect our continued operations with respect thereto.
As we develop our technology, we may need to license additional
technologies to optimize the performance of our products. We may not be able to license these technologies on commercially reasonable
terms or at all. In addition, we may fail to successfully integrate any licensed technology into our proposed products. Our inability
to obtain any necessary licenses could delay our product development and testing until alternative technologies can be identified,
licensed and integrated. The inability to obtain any necessary third-party licenses could cause us to abandon a particular development
path, which could seriously harm our business, financial position and results of our operations.
New technology may lead to our competitors developing
superior products which would reduce demand for our products.
Research into technologies similar to ours is proceeding at
a rapid pace, and many private and public companies and research institutions are actively engaged in the development of products
similar to ours. These new technologies may, if successfully developed, offer significant performance or price advantages when
compared with our technologies. Our existing patents or our pending and proposed patent applications may not offer meaningful protection
if a competitor develops a novel product based on a new technology.
If we are unable to protect our proprietary technology
and preserve our trade secrets, we will increase our vulnerability to competitors which could materially adversely impact our ability
to remain in business.
Our ability to successfully commercialize our products will
depend on our ability to protect those products and our technology with domestic and foreign patents. We will also need to continue
to preserve our trade secrets. The issuance of a patent is not conclusive as to its validity or as to the enforceable scope of
the claims of the patent. The patent positions of technology companies, including us, are uncertain and involve complex legal and
factual issues. Our patents may not prevent other companies from developing similar products or products which produce benefits
substantially the same as our products, and other companies may be issued patents that may prevent the sale of our products or
require us to pay significant licensing fees in order to market our products.
From time to time, we may need to obtain licenses to patents
and other proprietary rights held by third parties in order to develop, manufacture and market our products. If we are unable to
timely obtain these licenses on commercially reasonable terms, our ability to commercially exploit such products may be inhibited
or prevented. Our pending patent applications may not result in issued patents, patent protection may not be secured for any particular
technology, and our issued patents may not be valid or enforceable or provide us with meaningful protection.
If we are required to engage in expensive and lengthy
litigation to enforce our intellectual property rights, such litigation could be very costly and the results of such litigation
may not be satisfactory.
Although we have entered into invention assignment agreements
with our employees and with certain advisors, and we routinely enter into confidentiality agreements with our contract partners,
if those employees, advisors or contract partners develop inventions or processes independently that may relate to products or
technology under development by us, disputes may arise about the ownership of those inventions or processes. Time-consuming and
costly litigation could be necessary to enforce and determine the scope of our rights under these agreements. In addition, we may
be required to commence litigation to enforce such agreements if they are violated, and it is certainly possible that we will not
have adequate remedies for breaches of our confidentiality agreements as monetary damages may not be sufficient to compensate us.
We may be unable to fund the costs of any such litigation to a satisfactory conclusion, which could leave us without recourse to
enforce contracts that protect our intellectual property rights.
Other companies may claim that our technology infringes
on their intellectual property or proprietary rights and commence legal proceedings against us which could be time-consuming and
expensive and could result in our being prohibited from developing, marketing, selling or distributing our products.
Because of the complex and difficult legal and factual questions
that relate to patent positions in our industry, it is possible that our products or technology could be found to infringe upon
the intellectual property or proprietary rights of others. Third parties may claim that our products or technology infringe on
their patents, copyrights, trademarks or other proprietary rights and demand that we cease development or marketing of those products
or technology or pay license fees. We may not be able to avoid costly patent infringement litigation, which will divert the attention
of management away from the development of new products and the operation of our business. We may not prevail in any such litigation.
If we are found to have infringed on a third-party’s intellectual property rights, we may be liable for money damages, encounter
significant delays in bringing products to market or be precluded from manufacturing particular products or using particular technology.
Other parties may challenge certain of our foreign patent applications.
If any such parties are successful in opposing our foreign patent applications, we may not gain the protection afforded by those
patent applications in particular jurisdictions and may face additional proceedings with respect to similar patents in other jurisdictions,
as well as related patents. The loss of patent protection in one jurisdiction may influence our ability to maintain patent protection
for the same technology in other jurisdictions.
Risks Related to U.S. Government Contracts
We may not obtain additional U.S. Government contracts
to further develop our technology.
We may not be successful in obtaining additional government
grants or contracts. The process of obtaining government contracts is lengthy with the uncertainty that we will be successful in
obtaining announced grants or contracts for therapeutics as a medical device technology. Accordingly, we may not be awarded any
additional U.S. Government grants or contracts utilizing our Hemopurifier platform technology.
U.S. Government agencies have special contracting requirements,
including a right to audit us which create additional risks; a negative audit would be detrimental to us.
Our business plan to utilize the Aethlon Hemopurifier technology
is likely to continue to involve contracts with the U.S. Government. Such contracts typically contain unfavorable termination provisions
and are subject to audit and modification by the government at its sole discretion, which subjects us to additional risks. These
risks include the ability of the U.S. Government to unilaterally:
|
☐
|
suspend or prevent us for a period of time from receiving new contracts or extending existing contracts based on violations or suspected violations of laws or regulations;
|
|
☐
|
audit and object to our contract-related costs and fees, including allocated indirect costs;
|
|
☐
|
control and potentially prohibit the export of our products; and
|
|
☐
|
change certain terms and conditions in our contracts.
|
As a U.S. Government contractor, we are required to comply with
applicable laws, regulations and standards relating to our accounting practices and would be subject to periodic audits and reviews.
As part of any such audit or review, the U.S. Government may review the adequacy of, and our compliance with, our internal control
systems and policies, including those relating to our purchasing, property, estimating, compensation and management information
systems. Based on the results of its audits, the U.S. Government may adjust our contract-related costs and fees, including allocated
indirect costs. In addition, if an audit or review uncovers any improper or illegal activity, we would possibly be subject to civil
and criminal penalties and administrative sanctions, including termination of our contracts, forfeiture of profits, suspension
of payments, fines and suspension or prohibition from doing business with the U.S. Government. We could also suffer serious harm
to our reputation if allegations of impropriety were made against us. Although we have not had any government audits and reviews
to date, future audits and reviews could cause adverse effects. In addition, under U.S. Government purchasing regulations, some
of our costs, including most financing costs, amortization of intangible assets, portions of our research and development costs,
and some marketing expenses, would possibly not be reimbursable or allowed under such contracts. Further, as a U.S. Government
contractor, we would be subject to an increased risk of investigations, criminal prosecution, civil fraud, whistleblower lawsuits
and other legal actions and liabilities.
As a U.S. Government contractor, we are subject to a number
of procurement rules and regulations.
Government contractors must comply with specific procurement
regulations and other requirements. These requirements, although customary in government contracts, impact our performance and
compliance costs. In addition, current U.S. Government budgetary constraints could lead to changes in the procurement environment,
including the Department of Defense’s recent initiative focused on efficiencies, affordability and cost growth and other
changes to its procurement practices. If and to the extent such changes occur, they could impact our results of operations and
liquidity, and could affect whether and, if so, how we pursue certain opportunities and the terms under which we are able to do
so.
In addition, failure to comply with these regulations and requirements
could result in reductions of the value of contracts, contract modifications or termination, and the assessment of penalties and
fines, which could negatively impact our results of operations and financial condition. Our failure to comply with these regulations
and requirements could also lead to suspension or debarment, for cause, from government contracting or subcontracting for a period
of time. Among the causes for debarment are violations of various statutes, including those related to procurement integrity, export
control, government security regulations, employment practices, protection of the environment, accuracy of records and the recording
of costs, and foreign corruption. The termination of our government contract as a result of any of these acts could have a negative
impact on our results of operations and financial condition and could have a negative impact on our reputation and ability to procure
other government contracts in the future.
Risks Relating to Our Common Stock and Our Corporate Governance
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, or Nasdaq, such as the minimum stockholders’ equity requirement or the minimum closing bid price
requirement, Nasdaq may take steps to de-list our common stock. In May 2019, we received a letter from Nasdaq indicating that Nasdaq
has determined that we have failed to comply with the minimum bid price requirement of Nasdaq Listing Rule 5550(a)(2). Nasdaq Listing
Rule 5550(a)(2) requires that companies listed on the Nasdaq Capital Market maintain a minimum closing bid price of at least $1.00
per share. In July 2019, we received another letter from Nasdaq indicating that Nasdaq has determined that we have failed to comply
with the minimum stockholder’s equity requirement of Nasdaq Listing Rule 5550(b)(1). Nasdaq Listing Rule 5550(b)(1) requires
that companies listed on the Nasdaq Capital Market maintain a minimum of $2,500,000 in stockholder’s equity. If we
fail to regain and maintain compliance with these, or any other of the continued listing requirements of The Nasdaq Capital Market,
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 any such action taken by us may not
be successful.
Historically we have not paid dividends
on our common stock, and we do not anticipate paying any cash dividends in the foreseeable future.
We have never paid cash dividends on our common stock. We intend
to retain our future earnings, if any, to fund operational and capital expenditure needs of our business, and do not anticipate
paying any cash dividends in the foreseeable future. As a result, capital appreciation, if any, of our common stock will be the
sole source of gain for our common stockholders in the foreseeable future.
Our stock price is speculative,
and there is a risk of litigation.
The trading price of our common stock
has in the past and may in the future be subject to wide fluctuations in response to factors such as the following:
|
☐
|
failure to raise additional funds when needed;
|
|
☐
|
failure to maintain our listing on Nasdaq;
|
|
☐
|
results of operations or revenue in any quarter failing to meet the expectations, published or otherwise, of the investment community;
|
|
☐
|
reduced investor confidence in equity markets;
|
|
☐
|
speculation in the press or analyst community;
|
|
☐
|
wide fluctuations in stock prices, particularly with respect to the stock prices for other medical device companies;
|
|
☐
|
announcements of technological innovations by us or our competitors;
|
|
☐
|
new products or the acquisition of significant customers by us or our competitors;
|
|
☐
|
changes in interest rates;
|
|
☐
|
changes in investors’ beliefs as to the appropriate price-earnings ratios for us and our competitors;
|
|
☐
|
changes in recommendations or financial estimates by securities analysts who track our common stock or the stock of other medical device companies;
|
|
☐
|
sales of common stock by directors and executive officers;
|
|
☐
|
rumors or dissemination of false or misleading information, particularly through Internet chat rooms, instant messaging, and other rapid-dissemination methods;
|
|
☐
|
conditions and trends in the medical device industry generally;
|
|
☐
|
the announcement of acquisitions or other significant transactions by us or our competitors;
|
|
☐
|
adoption of new accounting standards affecting our industry;
|
|
☐
|
general market conditions;
|
|
☐
|
domestic or international terrorism and other factors;
|
|
☐
|
the ongoing coronavirus pandemic; and
|
|
|
|
|
☐
|
the other factors described in this section.
|
Fluctuations in the price of our common stock may expose us
to the risk of securities class action lawsuits. Although no such lawsuits are currently pending against us and we are not aware
that any such lawsuit is threatened to be filed in the future, future lawsuits are possible as a result of fluctuations in the
price of our common stock. Defending against any such suits could result in substantial cost and divert management’s attention
and resources. In addition, any settlement or adverse determination of such lawsuits could subject us to significant liability.
If at any time our common stock is subject to the Securities
and Exchange Commission’s penny stock rules, broker-dealers may experience difficulty in completing customer transactions
and trading activity in our securities may be adversely affected.
If at any time our common stock is not listed on a national
securities exchange or we have net tangible assets of $2,000,000 or less, or we have an average revenue of less than $6,000,000
for the last three years, and our common stock has a market price per share of less than $5.00, transactions in our common stock
will be subject to the Securities and Exchange Commission’s, or SEC’s, “penny stock” rules. If our common
stock is subject to the “penny stock” rules promulgated under the Exchange Act, broker-dealers may find it difficult
to effectuate customer transactions and trading activity in our securities may be adversely affected. For any transaction involving
a penny stock, unless exempt, the rules require:
|
☐
|
that a broker or dealer approve a person’s account for transactions in penny stocks;
|
|
☐
|
furnish the investor a disclosure document describing the risks of investing in penny stocks;
|
|
☐
|
disclose to the investor the current market quotation, if any, for the penny stock;
|
|
☐
|
disclose to the investor the amount of compensation the firm and its broker will receive for the trade; and
|
|
☐
|
The broker or dealer receive from the investor a written agreement to the transaction, setting forth the identity and quantity of the penny stock to be purchased.
|
In order to approve a person’s account for transactions
in penny stocks, the broker or dealer must:
|
☐
|
obtain financial information and investment experience objectives of the person; and
|
|
☐
|
make a reasonable determination that the transactions in penny stocks are suitable for that person and the person has sufficient knowledge and experience in financial matters to be capable of evaluating the risks of transactions in penny stocks.
|
The broker or dealer must also deliver, prior to any transaction
in a penny stock, a disclosure schedule prescribed by the Securities and Exchange Commission relating to the penny stock market,
which, in highlight form:
|
☐
|
sets forth the basis on which the broker or dealer made the suitability determination; and
|
|
☐
|
that the broker or dealer received a signed, written agreement from the investor prior to the transaction.
|
Generally, brokers may be less willing to execute transactions
in securities subject to the “penny stock” rules. This may make it more difficult for investors to dispose of our common
stock and cause a decline in the market value of our stock.
Disclosure also has to be made about the risks of investing
in penny stocks in both public offerings and in secondary trading and about the commissions payable to both the broker-dealer and
the registered representative, current quotations for the securities and the rights and remedies available to an investor in cases
of fraud in penny stock transactions. Finally, monthly statements have to be sent disclosing recent price information for the penny
stock held in the account and information on the limited market in penny stocks.
Our common stock has had an unpredictable trading volume
which means you may not be able to sell our shares at or near trading prices or at all.
Trading in our common shares historically has been volatile
and often has been thin, meaning that the number of persons interested in purchasing our common shares at or near trading prices
at any given time may be relatively small or non-existent. This situation is attributable to a number of factors, including the
fact that we are a small company which is relatively unknown to stock analysts, stock brokers, institutional investors and others
in the investment community that generate or influence sales volume, and that even if we came to the attention of such persons,
they tend to be risk-averse and would be reluctant to follow an unproven company such as ours or purchase or recommend the purchase
of our shares until such time as we became more seasoned and viable. As a consequence, there may be periods of several days or
more when trading activity in our shares is minimal, as compared to a seasoned issuer which has a large and steady volume of trading
activity that will generally support continuous sales without an adverse effect on share price. A broader or more active public
trading market for our common shares may not develop or be sustained, and current trading levels may decrease.
The market price for our common stock is volatile; you
may not be able to sell our common stock at or above the price you have paid for them, which may result in losses to you.
The market for our common shares is characterized by significant
price volatility when compared to seasoned issuers, and we expect that our share price will continue to be more volatile than a
seasoned issuer for the indefinite future. During the 52-week period ended March 16, 2020, the high and low closing sale prices
of a share of our common stock were $15.45 and $0.84, respectively. The volatility in our share price is attributable to a number
of factors. First, as noted above, trading in our common shares often has been thin. As a consequence of this lack of liquidity,
the trading of relatively small quantities of shares by our stockholders may disproportionately influence the price of those shares
in either direction. The price for our shares could, for example, decline precipitously in the event that a large number of our
common shares are sold on the market without commensurate demand, as compared to a seasoned issuer which could better absorb those
sales without adverse impact on its share price. Secondly, we are a speculative investment due to our limited operating history,
limited amount of cash and revenue, lack of profit to date, and the uncertainty of future market acceptance for our potential products.
As a consequence of this enhanced risk, more risk-adverse investors may, under the fear of losing all or most of their investment
in the event of negative news or lack of progress, be more inclined to sell their shares on the market more quickly and at greater
discounts than would be the case with the stock of a seasoned issuer.
The following factors also may add to the volatility in the
price of our common shares: actual or anticipated variations in our quarterly or annual operating results; acceptance of our proprietary
technology as a viable method of augmenting the immune response of clearing viruses and toxins from human blood; government regulations,
announcements of significant acquisitions, strategic partnerships or joint ventures; our capital commitments and additions or departures
of our key personnel. Many of these factors are beyond our control and may decrease the market price of our common shares regardless
of our operating performance. We cannot make any predictions or projections as to what the prevailing market price for our common
shares will be at any time, including as to whether our common shares will sustain their current market prices, or as to what effect
the sale of shares or the availability of common shares for sale at any time will have on the prevailing market price.
Our directors and officers own or control approximately
1% of our outstanding common shares, which may limit your ability to propose new management or influence the overall direction
of the business; this concentration of control may also discourage potential takeovers that could otherwise provide a premium to
you.
As of March 16, 2020 our officers and directors beneficially
owned or controlled approximately 1% of our outstanding common stock, assuming the exercise of all outstanding options, restricted
stock units and warrants held by our officers and directors. These persons will have the ability to substantially influence all
matters submitted to our stockholders for approval and to control our management and affairs, including extraordinary transactions
such as mergers and other changes of corporate control, and going private transactions.
A large number of our common shares are issuable upon
exercise of outstanding convertible securities, which, if exercised or converted, would be dilutive to your holdings.
As of March 16, 2020, there were outstanding options and warrants
entitling the holders to purchase 2,072,492 shares of our common stock at a weighted average exercise price of $6.17 per share.
Additionally, as of March 16, 2020, we had reserved 118,637 shares of common stock for issuance under our equity compensation plans.
The exercise price for all of our outstanding options and warrants,
or the conversion price of our convertible notes, may be less than your cost to acquire our common shares. In the event of the
exercise or conversion of these securities, you could suffer substantial dilution of your investment in terms of your percentage
ownership in us as well as the book value of your common shares. In addition, the holders of the convertible notes, common share
purchase options or warrants may sell common shares in tandem with their exercise or conversion of those securities to finance
that exercise or conversion, or may resell the shares purchased in order to cover any income tax liabilities that may arise from
their exercise of the options or warrants or conversion of the notes.
Our issuance of additional common shares, or convertible
securities, would be dilutive to your holdings.
We are entitled under our articles of incorporation to issue
up to 30,000,000 shares of common stock. We have reserved for issuance 2,075,567 of those shares of common stock for outstanding
restricted stock units, stocks, options, and warrants. As of March 16, 2020, we had issued and outstanding 9,364,784 shares of
common stock. As a result, as of March 16, 2020 we had 18,559,669 shares of common stock available for issuance to new investors
or for use to satisfy indebtedness or pay service providers.
Our Board of Directors may generally issue shares of common
stock, restricted stock units or options or warrants to purchase those shares, without further approval by our stockholders based
upon such factors as our Board of Directors may deem relevant at that time. It is likely that we will be required to issue a large
amount of additional securities to raise capital to further our development. It is also likely that we will be required to issue
a large amount of additional securities to directors, officers, employees and consultants as compensatory grants in connection
with their services, both in the form of stand-alone grants or under our stock plans.
Our issuance of additional shares of common stock in satisfaction
of services, or to repay indebtedness, would be dilutive to your holdings.
Subject to compliance with Nasdaq rules, our Board of Directors
may generally issue shares of common stock to pay for debt or services, without further approval by our stockholders based upon
such factors that our Board of Directors may deem relevant at that time.
Our officers and directors are entitled to indemnification
from us for liabilities under our articles of incorporation, which could be costly to us and may discourage the exercise of stockholder
rights.
Our articles of incorporation provide that we possess and may
exercise all powers of indemnification of our officers, directors, employees, agents and other persons and our bylaws also require
us to indemnify our officers and directors as permitted under the provisions of the Nevada Revised Statutes (“NRS”).
We may also have contractual indemnification obligations under our agreements with our directors, officers and employees. The foregoing
indemnification obligations could result in our company incurring substantial expenditures to cover the cost of settlement or damage
awards against directors and officers. These provisions and resultant costs may also discourage our company from bringing a lawsuit
against directors, officers and employees for breaches of their fiduciary duties, and may similarly discourage the filing of derivative
litigation by our stockholders against our directors, officers and employees even though such actions, if successful, might otherwise
benefit our company and stockholders.
Our bylaws and Nevada law may discourage, delay or prevent
a change of control of our company or changes in our management, would have the result of depressing the trading price of our common
stock.
Certain anti-takeover provisions of Nevada law could have the
effect of delaying or preventing a third-party from acquiring us, even if the acquisition arguably could benefit our stockholders.
Nevada’s “combinations with interested stockholders”
statutes (NRS 78.411 through 78.444, inclusive) prohibit specified types of business “combinations” between certain
Nevada corporations and any person deemed to be an “interested stockholder” for two years after such person first becomes
an “interested stockholder” unless the corporation’s board of directors approves the combination (or the transaction
by which such person becomes an “interested stockholder”) in advance, or unless the combination is approved by the
board of directors and sixty percent of the corporation’s voting power not beneficially owned by the interested stockholder,
its affiliates and associates. Further, in the absence of prior approval certain restrictions may apply even after such two year
period. However, these statutes do not apply to any combination of a corporation and an interested stockholder after the expiration
of four years after the person first became an interested stockholder. For purposes of these statutes, an “interested stockholder”
is any person who is (1) the beneficial owner, directly or indirectly, of ten percent or more of the voting power of the outstanding
voting shares of the corporation, or (2) an affiliate or associate of the corporation and at any time within the two previous years
was the beneficial owner, directly or indirectly, of ten percent or more of the voting power of the then outstanding shares of
the corporation. The definition of the term “combination” is sufficiently broad to cover most significant transactions
between a corporation and an “interested stockholder.” A Nevada corporation may elect in its articles of incorporation
not to be governed by these particular laws, but if such election is not made in the corporation’s original articles of incorporation,
the amendment (1) must be approved by the affirmative vote of the holders of stock representing a majority of the outstanding voting
power of the corporation not beneficially owned by interested stockholders or their affiliates and associates, and (2) is not effective
until 18 months after the vote approving the amendment and does not apply to any combination with a person who first became an
interested stockholder on or before the effective date of the amendment. We did not make such an election in our original articles
of incorporation and have not amended our articles of incorporation to so elect.
Nevada’s “acquisition of controlling interest”
statutes (NRS 78.378 through 78.3793, inclusive) contain provisions governing the acquisition of a controlling interest in certain
Nevada corporations. These “control share” laws provide generally that any person that acquires a “controlling
interest” in certain Nevada corporations may be denied voting rights, unless a majority of the disinterested stockholders
of the corporation elects to restore such voting rights. These laws would apply to us if we were to have 200 or more stockholders
of record (at least 100 of whom have addresses in Nevada appearing on our stock ledger) and do business in the State of Nevada
directly or through an affiliated corporation, unless our articles of incorporation or bylaws in effect on the tenth day after
the acquisition of a controlling interest provide otherwise. These laws provide that a person acquires a “controlling interest”
whenever a person acquires shares of a subject corporation that, but for the application of these provisions of the NRS, would
enable that person to exercise (1) one fifth or more, but less than one third, (2) one third or more, but less than a majority
or (3) a majority or more, of all of the voting power of the corporation in the election of directors. Once an acquirer crosses
one of these thresholds, shares which it acquired in the transaction taking it over the threshold and within the 90 days immediately
preceding the date when the acquiring person acquired or offered to acquire a controlling interest become “control shares”
to which the voting restrictions described above apply. These laws may have a chilling effect on certain transactions if our articles
of incorporation or bylaws are not amended to provide that these provisions do not apply to us or to an acquisition of a controlling
interest, or if our disinterested stockholders do not confer voting rights in the control shares.
Various provisions of our bylaws may delay, defer or prevent
a tender offer or takeover attempt of us that a stockholder might consider in his or her best interest. Our bylaws may be adopted,
amended or repealed by the affirmative vote of the holders of at least a majority of our outstanding shares of capital stock entitled
to vote for the election of directors, and except as provided by Nevada law, our Board of Directors shall have the power to adopt,
amend or repeal the bylaws by a vote of not less than a majority of our directors. The interests of these stockholders and directors
may not be consistent with your interests, and they may make changes to the bylaws that are not in line with your concerns.
Nevada law also provides that directors may resist a change
or potential change in control if the directors determine that the change is opposed to, or not in the best interests of, the corporation.
The existence of the foregoing provisions and other potential anti-takeover measures could limit the price that investors might
be willing to pay in the future for shares of our common stock. They could also deter potential acquirers of our company, thereby
reducing the likelihood that you could receive a premium for your common stock in an acquisition.
We incur substantial costs as a result of being a public
company and our management expects to devote substantial time to public company compliance programs.
As a public company, we incur significant legal, insurance,
accounting and other expenses, including costs associated with public company reporting. We intend to invest resources to comply
with evolving laws, regulations and standards, and this investment will result in increased general and administrative expenses
and may divert management’s time and attention from product development and commercialization activities. If our efforts
to comply with new laws, regulations and standards differ from the activities intended by regulatory or governing bodies due to
ambiguities related to practice, regulatory authorities may initiate legal proceedings against us, and our business may be harmed.
These laws and regulations could make it more difficult and costly for us to obtain director and officer liability insurance for
our directors and officers, and we may be required to accept reduced coverage or incur substantially higher costs to obtain coverage.
These factors could also make it more difficult for us to attract and retain qualified executive officers and qualified members
of our Board of Directors, particularly to serve on our audit and compensation committees. In addition, if we are unable to continue
to meet the legal, regulatory and other requirements related to being a public company, we may not be able to maintain the quotation
of our common stock on the Nasdaq Capital Market or on any other senior market to which we may apply for listing, which would likely
have a material adverse effect on the trading price of our common stock.
If securities or industry analysts do not publish research
or reports about our business, or if they change their recommendations regarding our stock adversely, our stock price and trading
volume could decline.
The trading market for our common stock will be influenced by
the research and reports that industry or securities analysts publish about us or our business. Our research coverage by industry
and financial analysts is currently limited. Even if our analyst coverage increases, if one or more of the analysts who cover us
downgrade our stock, our stock price would likely decline. If one or more of these analysts cease coverage of our company or fail
to regularly publish reports on us, we could lose visibility in the financial markets, which in turn could cause our stock price
or trading volume to decline.
Risks Related to This Offering
We may experience volatility in our stock price, which
could negatively affect your investment, and you may not be able to resell your shares at or above the offering price.
The offering price of our common stock may vary from the market
price of our common stock after the offering. If you purchase shares of common stock, you may not be able to resell those shares
at or above your purchase price. The market price of our common stock may fluctuate significantly in response to a number of factors,
some of which are beyond our control, including: a quarterly variations in operating results; changes in financial estimates by
securities analysts; changes in market valuations of other similar companies; announcements by us or our competitors of new products
or of significant technical innovations, contracts, acquisitions, strategic partnerships or joint ventures; additions or departures
of key personnel; any deviations in net sales or in losses from levels expected by securities analysts; and future sales of common
stock. In addition, the stock market has recently experienced extreme volatility that has often been unrelated to the performance
of particular companies. These market fluctuations may cause our stock price to fall regardless of our performance.
USE OF PROCEEDS
Except as described in
any applicable prospectus supplement, we currently intend to use the net proceeds from the sale of the securities for general corporate
purposes, including for research and development, sales and marketing initiatives and general administrative expenses, working
capital and capital expenditures. In addition, our use of proceeds may include the repayment of debt or refinancing of indebtedness,
should any be incurred, or the acquisition of complementary products or companies. However, we have no current commitments or obligations
to do so. We may set forth additional information on the use of proceeds from the sale of our securities we offer under this prospectus
in a prospectus supplement relating to the specific offering.
We have not determined
the amount of net proceeds to be used specifically for the foregoing purposes. As a result, our management will have broad discretion
in the allocation of the net proceeds and investors will be relying on the judgment of our management regarding the application
of the proceeds of any sale of the securities. Pending use of the net proceeds, we intend to invest the proceeds in a variety of
capital preservation instruments, including short-term, investment-grade, interest-bearing instruments.
DESCRIPTION OF CAPITAL
STOCK
The following description of our capital stock is intended as
a summary only and therefore is not a complete description of our capital stock. This description is based upon, and is qualified
in its entirety by reference to, our articles of incorporation, our bylaws and applicable provisions of Nevada corporate law. You
should read our articles of incorporation and bylaws, which have been publicly filed with the SEC, for the provisions that are
important to you.
Authorized Capital Stock
Our authorized capital consists of 30,000,000 shares of common
stock, par value $0.001 per share. As of March 16, 2020, there were 9,364,784 shares of common stock issued and outstanding. Following
approval by our stockholders at the Annual Meeting on October 14, 2019, our Board of Directors unanimously approved a reverse stock
split of all issued and outstanding shares of our common stock, at a ratio of 1-for-15, pursuant to Nevada Revised Statutes, or
NRS, 78.2055. The reverse stock split was implemented on October 14, 2019. Pursuant to the reverse stock split, every 15 shares
of the Company’s issued and outstanding common stock were automatically combined into one issued and outstanding share of
common stock, without any change in par value per share. The number of shares reserved for issuance under the Company’s equity
compensation plans immediately prior to the effective time of the reverse split were reduced proportionately.
No fractional shares were issued in connection with the reverse
stock split and, in accordance with NRS 78.205, any stockholder that otherwise would have held a fractional share of common stock
as a result of the reverse stock split was issued such additional fraction of a share as was necessary to increase the fractional
share to a full share. The reverse stock split affected all stockholders proportionately and did not affect any stockholder’s
percentage ownership of the Company’s common stock, except to the extent that the reverse stock split results in any stockholder
owning an additional fraction of a share as described above. All shares and per share amounts have been revised accordingly to
reflect the reverse stock split.
Common Stock
The holders of our common stock are entitled to one vote per
share on all matters to be voted on by the stockholders. Holders of common stock are entitled to receive ratably such dividends
as may be declared by the Board of Directors out of funds legally available therefor. If we liquidate, dissolve or wind up, holders
of common stock are entitled to share ratably in all assets remaining after payment of all debts and other liabilities. Holders
of common stock have no preemptive, conversion or subscription rights. There are no redemption or sinking fund provisions applicable
to the common stock. All outstanding shares of common stock are, and all shares of common stock to be outstanding upon completion
of this offering will be, validly issued, fully paid and nonassessable.
Our bylaws provide that stockholders representing a majority
of the voting power of our capital stock, represented in person or by proxy (regardless of whether the proxy has authority to vote
on all matters), are necessary to constitute a quorum for the transaction of business at any meeting, but at any time during which
shares of our capital stock are listed for trading on Nasdaq, stockholders representing not less than 33 1/3% of the voting power
of our capital stock, represented in person or by proxy (regardless of whether the proxy has authority to vote on all matters),
are necessary to constitute a quorum for the transaction of business at any meeting of stockholders. Except as otherwise required
or permitted by Nevada law or our articles of incorporation or bylaws, action by the stockholders entitled to vote on a matter,
other than the election of directors, is approved by and is the act of the stockholders if the number of votes cast in favor of
the action exceeds the number of votes cast in opposition to the action. If a quorum is present, directors are elected by a plurality
of the votes cast.
Options and Warrants Convertible into Common Stock
As of March 16, 2020, there were outstanding
stock options entitling the holders to purchase 51,124 shares of our common stock at a weighted average exercise price of $44.12
per share.
As of March 16, 2020, there were outstanding
warrants entitling the holders to purchase 2,021,368 shares of our common stock at a weighted average exercise price of $5.21 per
share.
Anti-Takeover Effects of Certain Provisions of Nevada Law
and Our Articles of Incorporation and Bylaws
Nevada’s “combinations with interested stockholders”
statutes, NRS 78.411 through 78.444, inclusive, prohibit specified types of business “combinations” between certain
Nevada corporations and any person deemed to be an “interested stockholder” for two years after such person first becomes
an “interested stockholder” unless the corporation’s board of directors approves the combination (or the transaction
by which such person becomes an “interested stockholder”) in advance, or unless the combination is approved by the
board of directors and sixty percent of the corporation’s voting power not beneficially owned by the interested stockholder,
its affiliates and associates. Further, in the absence of prior approval certain restrictions may apply even after such two year
period. However, these statutes do not apply to any combination of a corporation and an interested stockholder after the expiration
of four years after the person first became an interested stockholder. For purposes of these statutes, an “interested stockholder”
is any person who is (1) the beneficial owner, directly or indirectly, of ten percent or more of the voting power of the outstanding
voting shares of the corporation, or (2) an affiliate or associate of the corporation and at any time within the two previous years
was the beneficial owner, directly or indirectly, of ten percent or more of the voting power of the then outstanding shares of
the corporation. The definition of the term “combination” is sufficiently broad to cover most significant transactions
between a corporation and an “interested stockholder.” These statutes generally apply to Nevada corporations with 200
or more stockholders of record. However, a Nevada corporation may elect in its articles of incorporation not to be governed by
these particular laws, but if such election is not made in the corporation’s original articles of incorporation, the amendment
(1) must be approved by the affirmative vote of the holders of stock representing a majority of the outstanding voting power of
the corporation not beneficially owned by interested stockholders or their affiliates and associates, and (2) is not effective
until 18 months after the vote approving the amendment and does not apply to any combination with a person who first became an
interested stockholder on or before the effective date of the amendment. We did not make such an election in our original articles
of incorporation and have not amended our articles of incorporation to so elect.
Nevada’s “acquisition of controlling interest”
statutes (NRS 78.378 through 78.3793, inclusive) contain provisions governing the acquisition of a controlling interest in certain
Nevada corporations. These “control share” laws provide generally that any person that acquires a “controlling
interest” in certain Nevada corporations may be denied voting rights, unless a majority of the disinterested stockholders
of the corporation elects to restore such voting rights. Our bylaws provide that these statutes do not apply to us or any acquisition
of our common stock. Absent such provision in our bylaws, these laws would apply to us as of a particular date if we were to have
200 or more stockholders of record (at least 100 of whom have addresses in Nevada appearing on our stock ledger at all times during
the 90 days immediately preceding that date) and do business in the State of Nevada directly or through an affiliated corporation,
unless our articles of incorporation or bylaws in effect on the tenth day after the acquisition of a controlling interest provide
otherwise. These laws provide that a person acquires a “controlling interest” whenever a person acquires shares of
a subject corporation that, but for the application of these provisions of the NRS, would enable that person to exercise (1) one
fifth or more, but less than one third, (2) one third or more, but less than a majority or (3) a majority or more, of all of the
voting power of the corporation in the election of directors. Once an acquirer crosses one of these thresholds, shares which it
acquired in the transaction taking it over the threshold and within the 90 days immediately preceding the date when the acquiring
person acquired or offered to acquire a controlling interest become “control shares” to which the voting restrictions
described above apply.
NRS 78.139 also provides that directors may resist a change
or potential change in control of the corporation if the board of directors determines that the change or potential change is opposed
to or not in the best interest of the corporation upon consideration of any relevant facts, circumstances, contingencies or constituencies
pursuant to NRS 78.138(4).
In addition, our authorized but unissued shares of common stock
are available for our Board of Directors to issue without stockholder approval. We may use these additional shares for a variety
of corporate purposes, including future public or private offerings to raise additional capital, corporate acquisitions and employee
benefit plans. The existence of our authorized but unissued shares of common stock could render more difficult or discourage an
attempt to obtain control of our company by means of a proxy contest, tender offer, merger or other transaction. Our authorized
but unissued shares may be used to delay, defer or prevent a tender offer or takeover attempt that a stockholder might consider
in its best interest, including those attempts that might result in a premium over the market price for the shares held by our
stockholders. The Board of Directors is also authorized to adopt, amend or repeal our Bylaws, which could delay, defer or prevent
a change in control.
Registration Rights
Certain holders of our outstanding warrants to purchase up
to 52,139 shares of our common stock are entitled to require us to register pursuant to a registration statement for filing with
the SEC their respective shares of common stock issuable upon exercise of such warrants. These warrants have exercise prices ranging
from $20.63 to $135.00 per share of common stock issuable upon exercise of the warrants and expiration dates ranging from July
1, 2020 through September 29, 2022. The registration of these shares of our common stock pursuant to the exercise of the registration
rights would enable the holders to trade these shares without restriction under the Securities Act. In addition, the Company currently
has shares of common stock issuable upon exercise of outstanding warrants registered on registration statements on Form S-1 (333-219589,
333-234712 and 333-205832) on file with the Commission.
Nasdaq Capital Market Listing
Our common stock is listed on the Nasdaq Capital Market under
the symbol “AEMD”.
Transfer Agent and Registrar
The transfer agent and registrar for our common stock is Computershare
Investor Services. The transfer agent’s address is P.O. Box 30170, College Station, TX 77842.
DESCRIPTION OF DEBT SECURITIES
We may issue debt securities from time to time, in one or more
series, as either senior or subordinated debt or as senior or subordinated convertible debt. While the terms we have summarized
below will apply generally to any debt securities that we may offer under this prospectus, we will describe the particular terms
of any debt securities that we may offer in more detail in the applicable prospectus supplement. The terms of any debt securities
offered under a prospectus supplement may differ from the terms described below. Unless the context requires otherwise, whenever
we refer to the indenture, we also are referring to any supplemental indentures that specify the terms of a particular series of
debt securities.
We will issue the debt securities under the indenture that we
will enter into with the trustee named in the indenture. The indenture will be qualified under the Trust Indenture Act of 1939,
as amended, or the Trust Indenture Act. We have filed the form of indenture as an exhibit to the registration statement of which
this prospectus is a part, and supplemental indentures and forms of debt securities containing the terms of the debt securities
being offered will be filed as exhibits to the registration statement of which this prospectus is a part or will be incorporated
by reference from reports that we file with the SEC.
The following summary of material provisions of the debt securities
and the indenture is subject to, and qualified in its entirety by reference to, all of the provisions of the indenture applicable
to a particular series of debt securities. We urge you to read the applicable prospectus supplements and any related free writing
prospectuses related to the debt securities that we may offer under this prospectus, as well as the complete indenture that contains
the terms of the debt securities.
General
The indenture does not limit the amount of debt securities that
we may issue. It provides that we may issue debt securities up to the principal amount that we may authorize and may be in any
currency or currency unit that we may designate. Except for the limitations on consolidation, merger and sale of all or substantially
all of our assets contained in the indenture, the terms of the indenture do not contain any covenants or other provisions designed
to give holders of any debt securities protection against changes in our operations, financial condition or transactions involving
us.
We may issue the debt securities issued under the indenture
as “discount securities,” which means they may be sold at a discount below their stated principal amount. These debt
securities, as well as other debt securities that are not issued at a discount, may be issued with “original issue discount,”
or OID, for U.S. federal income tax purposes because of interest payment and other characteristics or terms of the debt securities.
Material U.S. federal income tax considerations applicable to debt securities issued with OID will be described in more detail
in any applicable prospectus supplement.
We will describe in the applicable prospectus supplement the
terms of the series of debt securities being offered, including:
|
☐
|
the title of the series of debt securities;
|
|
☐
|
any limit upon the aggregate principal amount that may be issued;
|
|
☐
|
the maturity date or dates;
|
|
☐
|
the form of the debt securities of the series;
|
|
☐
|
the applicability of any guarantees;
|
|
☐
|
whether or not the debt securities will be secured or unsecured, and the terms of any secured debt;
|
|
☐
|
whether the debt securities rank as senior debt, senior subordinated debt, subordinated debt or any combination thereof, and the terms of any subordination;
|
|
☐
|
if the price (expressed as a percentage of the aggregate principal amount thereof) at which such debt securities will be issued is a price other than the principal amount thereof, the portion of the principal amount thereof payable upon declaration of acceleration of the maturity thereof, or if applicable, the portion of the principal amount of such debt securities that is convertible into another security or the method by which any such portion shall be determined;
|
|
☐
|
the interest rate or rates, which may be fixed or variable, or the method for determining the rate and the date interest will begin to accrue, the dates interest will be payable and the regular record dates for interest payment dates or the method for determining such dates;
|
|
☐
|
our right, if any, to defer payment of interest and the maximum length of any such deferral period;
|
|
☐
|
if applicable, the date or dates after which, or the period or periods during which, and the price or prices at which, we may, at our option, redeem the series of debt securities pursuant to any optional or provisional redemption provisions and the terms of those redemption provisions;
|
|
☐
|
the date or dates, if any, on which, and the price or prices at which we are obligated, pursuant to any mandatory sinking fund or analogous fund provisions or otherwise, to redeem, or at the holder’s option to purchase, the series of debt securities and the currency or currency unit in which the debt securities are payable;
|
|
☐
|
the denominations in which we will issue the series of debt securities, if other than denominations of $1,000 and any integral multiple thereof;
|
|
☐
|
any and all terms, if applicable, relating to any auction or remarketing of the debt securities of that series and any security for our obligations with respect to such debt securities and any other terms which may be advisable in connection with the marketing of debt securities of that series;
|
|
☐
|
whether the debt securities of the series shall be issued in whole or in part in the form of a global security or securities; the terms and conditions, if any, upon which such global security or securities may be exchanged in whole or in part for other individual securities; and the depositary for such global security or securities;
|
|
|
|
|
☐
|
if applicable, the provisions relating to conversion or exchange of any debt securities of the series and the terms and conditions upon which such debt securities will be so convertible or exchangeable, including the conversion or exchange price, as applicable, or how it will be calculated and may be adjusted, any mandatory or optional (at our option or the holders’ option) conversion or exchange features, the applicable conversion or exchange period and the manner of settlement for any conversion or exchange;
|
|
☐
|
if other than the full principal amount thereof, the portion of the principal amount of debt securities of the series which shall be payable upon declaration of acceleration of the maturity thereof;
|
|
☐
|
additions to or changes in the covenants applicable to the particular debt securities being issued, including, among others, the consolidation, merger or sale covenant;
|
|
☐
|
additions to or changes in the events of default with respect to the securities and any change in the right of the trustee or the holders to declare the principal, premium, if any, and interest, if any, with respect to such securities to be due and payable;
|
|
☐
|
additions to or changes in or deletions of the provisions relating to covenant defeasance and legal defeasance;
|
|
☐
|
additions to or changes in the provisions relating to satisfaction and discharge of the indenture;
|
|
☐
|
additions to or changes in the provisions relating to the modification of the indenture both with and without the consent of holders of debt securities issued under the indenture;
|
|
☐
|
the currency of payment of debt securities if other than U.S. dollars and the manner of determining the equivalent amount in U.S. dollars;
|
|
☐
|
whether interest will be payable in cash or additional debt securities at our or the holders’ option and the terms and conditions upon which the election may be made;
|
|
☐
|
the terms and conditions, if any, upon which we will pay amounts in addition to the stated interest, premium, if any and principal amounts of the debt securities of the series to any holder that is not a “United States person” for federal tax purposes;
|
|
☐
|
any restrictions on transfer, sale or assignment of the debt securities of the series; and
|
|
☐
|
any other specific terms, preferences, rights or limitations of, or restrictions on, the debt securities, any other additions or changes in the provisions of the indenture, and any terms that may be required by us or advisable under applicable laws or regulations.
|
Conversion or Exchange Rights
We will set forth in the applicable prospectus supplement the
terms on which a series of debt securities may be convertible into or exchangeable for our common stock or our other securities.
We will include provisions as to settlement upon conversion or exchange and whether conversion or exchange is mandatory, at the
option of the holder or at our option. We may include provisions pursuant to which the number of shares of our common stock or
our other securities that the holders of the series of debt securities receive would be subject to adjustment.
Consolidation, Merger or Sale
Unless we provide otherwise in the prospectus supplement applicable
to a particular series of debt securities, the indenture will not contain any covenant that restricts our ability to merge or consolidate,
or sell, convey, transfer or otherwise dispose of our assets as an entirety or substantially as an entirety. However, any successor
to or acquirer of such assets (other than a subsidiary of ours) must assume all of our obligations under the indenture or the debt
securities, as appropriate.
Events of Default under the Indenture
Unless we provide otherwise in the prospectus supplement applicable
to a particular series of debt securities, the following are events of default under the indenture with respect to any series of
debt securities that we may issue:
|
☐
|
if we fail to pay any installment of interest on any series of debt securities, as and when the same shall become due and payable, and such default continues for a period of 90 days; provided, however, that a valid extension of an interest payment period by us in accordance with the terms of any indenture supplemental thereto shall not constitute a default in the payment of interest for this purpose;
|
|
☐
|
if we fail to pay the principal of, or premium, if any, on any series of debt securities as and when the same shall become due and payable whether at maturity, upon redemption, by declaration or otherwise, or in any payment required by any sinking or analogous fund established with respect to such series; provided, however, that a valid extension of the maturity of such debt securities in accordance with the terms of any indenture supplemental thereto shall not constitute a default in the payment of principal or premium, if any;
|
|
☐
|
if we fail to observe or perform any other covenant or agreement contained in the debt securities or the indenture, other than a covenant specifically relating to another series of debt securities, and our failure continues for 90 days after we receive written notice of such failure, requiring the same to be remedied and stating that such is a notice of default thereunder, from the trustee or holders of at least 25% in aggregate principal amount of the outstanding debt securities of the applicable series; and
|
|
☐
|
if specified events of bankruptcy, insolvency or reorganization occur.
|
If an event of default with respect to debt securities of any
series occurs and is continuing, other than an event of default specified in the last bullet point above, the trustee or the holders
of at least 25% in aggregate principal amount of the outstanding debt securities of that series, by notice to us in writing, and
to the trustee if notice is given by such holders, may declare the unpaid principal of, premium, if any, and accrued interest,
if any, due and payable immediately. If an event of default specified in the last bullet point above occurs with respect to us,
the principal amount of and accrued interest, if any, of each issue of debt securities then outstanding shall be due and payable
without any notice or other action on the part of the trustee or any holder.
The holders of a majority in principal amount of the outstanding
debt securities of an affected series may waive any default or event of default with respect to the series and its consequences,
except defaults or events of default regarding payment of principal, premium, if any, or interest, unless we have cured the default
or event of default in accordance with the indenture. Any waiver shall cure the default or event of default.
Subject to the terms of the indentures, if an event of default
under an indenture shall occur and be continuing, the trustee will be under no obligation to exercise any of its rights or powers
under such indenture at the request or direction of any of the holders of the applicable series of debt securities, unless such
holders have offered the trustee reasonable indemnity. The holders of a majority in principal amount of the outstanding debt securities
of any series will have the right to direct the time, method and place of conducting any proceeding for any remedy available to
the trustee, or exercising any trust or power conferred on the trustee, with respect to the debt securities of that series, provided
that:
|
☐
|
the direction so given by the holder is not in conflict with any law or the applicable indenture; and
|
|
☐
|
subject to its duties under the Trust Indenture Act, the trustee need not take any action that might involve it in personal liability or might be unduly prejudicial to the holders not involved in the proceeding.
|
A holder of the debt securities of any series
will have the right to institute a proceeding under the indenture or to appoint a receiver or trustee, or to seek other remedies
only if:
|
☐
|
the holder has given written notice to the trustee of a continuing event of default with respect to that series;
|
|
☐
|
the holders of at least 25% in aggregate principal amount of the outstanding debt securities of that series have made written request,
|
|
☐
|
such holders have offered to the trustee indemnity satisfactory to it against the costs, expenses and liabilities to be incurred by the trustee in compliance with the request; and
|
|
☐
|
the trustee does not institute the proceeding, and does not receive from the holders of a majority in aggregate principal amount of the outstanding debt securities of that series other conflicting directions within 90 days after the notice, request and offer.
|
These limitations do not apply to a suit instituted by a holder
of debt securities if we default in the payment of the principal, premium, if any, or interest on, the debt securities.
We will periodically file statements with the trustee regarding
our compliance with specified covenants in the indenture.
Modification of Indenture; Waiver
We and the trustee may change an indenture without the consent
of any holders with respect to specific matters:
|
☐
|
to cure any ambiguity, defect or inconsistency in the indenture or in the debt securities of any series;
|
|
☐
|
to comply with the provisions described above under “Description of Debt Securities—Consolidation, Merger or Sale;”
|
|
☐
|
to provide for uncertificated debt securities in addition to or in place of certificated debt securities;
|
|
☐
|
to add to our covenants, restrictions, conditions or provisions such new covenants, restrictions, conditions or provisions for the benefit of the holders of all or any series of debt securities, to make the occurrence, or the occurrence and the continuance, of a default in any such additional covenants, restrictions, conditions or provisions an event of default or to surrender any right or power conferred upon us in the indenture;
|
|
☐
|
to add to, delete from or revise the conditions, limitations, and restrictions on the authorized amount, terms, or purposes of issue, authentication and delivery of debt securities, as set forth in the indenture;
|
|
☐
|
to make any change that does not adversely affect the interests of any holder of debt securities of any series in any material respect;
|
|
☐
|
to provide for the issuance of and establish the form and terms and conditions of the debt securities of any series as provided above under “Description of Debt Securities—General” to establish the form of any certifications required to be furnished pursuant to the terms of the indenture or any series of debt securities, or to add to the rights of the holders of any series of debt securities;
|
|
☐
|
to evidence and provide for the acceptance of appointment under any indenture by a successor trustee; or
|
|
☐
|
to comply with any requirements of the SEC in connection with the qualification of any indenture under the Trust Indenture Act.
|
In addition, under the indenture, the rights of holders of a
series of debt securities may be changed by us and the trustee with the written consent of the holders of at least a majority in
aggregate principal amount of the outstanding debt securities of each series that is affected. However, unless we provide otherwise
in the prospectus supplement applicable to a particular series of debt securities, we and the trustee may make the following changes
only with the consent of each holder of any outstanding debt securities affected:
|
☐
|
extending the fixed maturity of any debt securities of any series;
|
|
☐
|
reducing the principal amount, reducing the rate of or extending the time of payment of interest, or reducing any premium payable upon the redemption of any series of any debt securities; or
|
|
☐
|
reducing the percentage of debt securities, the holders of which are required to consent to any amendment, supplement, modification or waiver.
|
Discharge
Each indenture provides that we can elect to be discharged from
our obligations with respect to one or more series of debt securities, except for specified obligations, including obligations
to:
|
☐
|
provide for payment;
|
|
☐
|
register the transfer or exchange of debt securities of the series;
|
|
☐
|
replace stolen, lost or mutilated debt securities of the series;
|
|
☐
|
pay principal of and premium and interest on any debt securities of the series;
|
|
☐
|
maintain paying agencies;
|
|
☐
|
hold monies for payment in trust;
|
|
☐
|
recover excess money held by the trustee;
|
|
☐
|
compensate and indemnify the trustee; and
|
|
☐
|
appoint any successor trustee.
|
In order to exercise our rights to be discharged, we must deposit
with the trustee money or government obligations sufficient to pay all the principal of, any premium, if any, and interest on,
the debt securities of the series on the dates payments are due.
Form, Exchange and Transfer
We will issue the debt securities of each series only in fully
registered form without coupons and, unless we provide otherwise in the applicable prospectus supplement, in denominations of $1,000
and any integral multiple thereof. The indenture provides that we may issue debt securities of a series in temporary or permanent
global form and as book-entry securities that will be deposited with, or on behalf of, The Depository Trust Company, or DTC, or
another depositary named by us and identified in the applicable prospectus supplement with respect to that series. To the extent
the debt securities of a series are issued in global form and as book-entry, a description of terms relating to any book-entry
securities will be set forth in the applicable prospectus supplement.
At the option of the holder, subject to the terms of the indenture
and the limitations applicable to global securities described in the applicable prospectus supplement, the holder of the debt securities
of any series can exchange the debt securities for other debt securities of the same series, in any authorized denomination and
of like tenor and aggregate principal amount.
Subject to the terms of the indenture and the limitations applicable
to global securities set forth in the applicable prospectus supplement, holders of the debt securities may present the debt securities
for exchange or for registration of transfer, duly endorsed or with the form of transfer endorsed thereon duly executed if so required
by us or the security registrar, at the office of the security registrar or at the office of any transfer agent designated by us
for this purpose. Unless otherwise provided in the debt securities that the holder presents for transfer or exchange, we will impose
no service charge for any registration of transfer or exchange, but we may require payment of any taxes or other governmental charges.
We will name in the applicable prospectus supplement the security
registrar, and any transfer agent in addition to the security registrar, that we initially designate for any debt securities. We
may at any time designate additional transfer agents or rescind the designation of any transfer agent or approve a change in the
office through which any transfer agent acts, except that we will be required to maintain a transfer agent in each place of payment
for the debt securities of each series.
If we elect to redeem the debt securities
of any series, we will not be required to:
|
☐
|
issue, register the transfer of, or exchange any debt securities of that series during a period beginning at the opening of business 15 days before the day of mailing of a notice of redemption of any debt securities that may be selected for redemption and ending at the close of business on the day of the mailing; or
|
|
☐
|
register the transfer of or exchange any debt securities so selected for redemption, in whole or in part, except the unredeemed portion of any debt securities we are redeeming in part.
|
Information Concerning the Trustee
The trustee, other than during the occurrence and continuance
of an event of default under an indenture, undertakes to perform only those duties as are specifically set forth in the applicable
indenture. Upon an event of default under an indenture, the trustee must use the same degree of care as a prudent person would
exercise or use in the conduct of his or her own affairs. Subject to this provision, the trustee is under no obligation to exercise
any of the powers given it by the indenture at the request of any holder of debt securities unless it is offered reasonable security
and indemnity against the costs, expenses and liabilities that it might incur.
Payment and Paying Agents
Unless we otherwise indicate in the applicable prospectus supplement,
we will make payment of the interest on any debt securities on any interest payment date to the person in whose name the debt securities,
or one or more predecessor securities, are registered at the close of business on the regular record date for the interest.
We will pay principal of and any premium and interest on the
debt securities of a particular series at the office of the paying agents designated by us, except that, unless we otherwise indicate
in the applicable prospectus supplement, we will make interest payments by check that we will mail to the holder or by wire transfer
to certain holders. Unless we otherwise indicate in the applicable prospectus supplement, we will designate the corporate trust
office of the trustee as our sole paying agent for payments with respect to debt securities of each series. We will name in the
applicable prospectus supplement any other paying agents that we initially designate for the debt securities of a particular series.
We will maintain a paying agent in each place of payment for the debt securities of a particular series.
All money we pay to a paying agent or the trustee for the payment
of the principal of or any premium or interest on any debt securities that remains unclaimed at the end of two years after such
principal, premium or interest has become due and payable will be repaid to us, and the holder of the debt security thereafter
may look only to us for payment thereof.
Governing Law
The indenture and the debt securities will be governed by and
construed in accordance with the internal laws of the State of New York, except to the extent that the Trust Indenture Act of 1939
is applicable.
DESCRIPTION OF WARRANTS
The following description, together with the additional information
we may include in any applicable prospectus supplements and free writing prospectuses, summarizes the material terms and provisions
of the warrants that we may offer under this prospectus, which may consist of warrants to purchase common stock or debt securities
and may be issued in one or more series. Warrants may be issued independently or together with common stock or debt securities
offered by any prospectus supplement, and may be attached to or separate from those securities. While the terms we have summarized
below will apply generally to any warrants that we may offer under this prospectus, we will describe the particular terms of any
series of warrants that we may offer in more detail in the applicable prospectus supplement and any applicable free writing prospectus.
The terms of any warrants offered under a prospectus supplement may differ from the terms described below. However, no prospectus
supplement will fundamentally change the terms that are set forth in this prospectus or offer a security that is not registered
and described in this prospectus at the time of its effectiveness.
We have filed forms of the warrant agreements as exhibits to
the registration statement of which this prospectus is a part. We will file as exhibits to the registration statement of which
this prospectus is a part, or will incorporate by reference from reports that we file with the SEC, the form of warrant agreement,
if any, including a form of warrant certificate, that describes the terms of the particular series of warrants we are offering.
The following summaries of material provisions of the warrants and the warrant agreements are subject to, and qualified in their
entirety by reference to, all the provisions of the warrant agreement and warrant certificate applicable to the particular series
of warrants that we may offer under this prospectus. We urge you to read the applicable prospectus supplements related to the particular
series of warrants that we may offer under this prospectus, as well as any related free writing prospectuses, and the complete
warrant agreements and warrant certificates that contain the terms of the warrants.
General
We will describe in the applicable prospectus supplement the
terms relating to a series of warrants being offered, including:
|
☐
|
the title of such securities;
|
|
☐
|
the offering price or prices and aggregate number of warrants offered;
|
|
☐
|
the currency or currencies for which the warrants may be purchased;
|
|
☐
|
if applicable, the designation and terms of the securities with which the warrants are issued and the number of warrants issued with each such security or each principal amount of such security;
|
|
☐
|
if applicable, the date on and after which the warrants and the related securities will be separately transferable;
|
|
☐
|
if applicable, the minimum or maximum amount of such warrants which may be exercised at any one time;
|
|
☐
|
in the case of warrants to purchase debt securities, the principal amount of debt securities purchasable upon exercise of one warrant and the price at which, and currency in which, this principal amount of debt securities may be purchased upon such exercise;
|
|
☐
|
in the case of warrants to purchase common stock, the number of shares of common stock, as the case may be, purchasable upon the exercise of one warrant and the price at which, and the currency in which, these shares may be purchased upon such exercise;
|
|
☐
|
the effect of any merger, consolidation, sale or other disposition of our business on the warrant agreements and the warrants;
|
|
☐
|
the terms of any rights to redeem or call the warrants;
|
|
☐
|
the terms of any rights to force the exercise of the warrants;
|
|
☐
|
any provisions for changes to or adjustments in the exercise price or number of securities issuable upon exercise of the warrants;
|
|
☐
|
the dates on which the right to exercise the warrants will commence and expire;
|
|
☐
|
the manner in which the warrant agreements and warrants may be modified;
|
|
☐
|
a discussion of any material or special United States federal income tax consequences of holding or exercising the warrants;
|
|
☐
|
the terms of the securities issuable upon exercise of the warrants; and
|
|
☐
|
any other specific terms, preferences, rights or limitations of or restrictions on the warrants.
|
Before exercising their warrants, holders of warrants will not
have any of the rights of holders of the securities purchasable upon such exercise, including:
|
☐
|
in the case of warrants to purchase debt securities, the right to receive payments of principal of, or premium, if any, or interest on, the debt securities purchasable upon exercise or to enforce covenants in the applicable indenture; or
|
|
☐
|
in the case of warrants to purchase common stock, the right to receive dividends, if any, or, payments upon our liquidation, dissolution or winding up, or to exercise voting rights, if any.
|
Exercise of Warrants
Each warrant will entitle the holder to purchase the securities
that we specify in the applicable prospectus supplement at the exercise price that we describe in the applicable prospectus supplement.
Unless we otherwise specify in the applicable prospectus supplement, holders of the warrants may exercise the warrants at any time
up to the specified time on the expiration date that we set forth in the applicable prospectus supplement. After the close of business
on the expiration date, unexercised warrants will become void.
Unless we otherwise specify in the applicable prospectus supplement,
holders of the warrants may exercise the warrants by delivering the warrant certificate representing the warrants to be exercised
together with specified information, and paying the required amount to the warrant agent in immediately available funds, as provided
in the applicable prospectus supplement. We will set forth on the reverse side of the warrant certificate and in the applicable
prospectus supplement the information that the holder of the warrant will be required to deliver to the warrant agent in connection
with the exercise of the warrant.
Upon receipt of the required payment and the warrant certificate
properly completed and duly executed at the corporate trust office of the warrant agent or any other office indicated in the applicable
prospectus supplement, we will issue and deliver the securities purchasable upon such exercise. If fewer than all of the warrants
represented by the warrant certificate are exercised, then we will issue a new warrant certificate for the remaining amount of
warrants. If we so indicate in the applicable prospectus supplement, holders of the warrants may surrender securities as all or
part of the exercise price for warrants.
Governing Law
Unless we provide otherwise in the applicable prospectus supplement,
the warrants and warrant agreements, and any claim, controversy or dispute arising under or related to the warrants or warrant
agreements, will be governed by and construed in accordance with the laws of the State of New York.
Enforceability of Rights by Holders of Warrants
Each warrant agent will act solely as our agent under the applicable
warrant agreement and will not assume any obligation or relationship of agency or trust with any holder of any warrant. A single
bank or trust company may act as warrant agent for more than one issue of warrants. A warrant agent will have no duty or responsibility
in case of any default by us under the applicable warrant agreement or warrant, including any duty or responsibility to initiate
any proceedings at law or otherwise, or to make any demand upon us. Any holder of a warrant may, without the consent of the related
warrant agent or the holder of any other warrant, enforce by appropriate legal action its right to exercise, and receive the securities
purchasable upon exercise of, its warrants.
LEGAL OWNERSHIP OF SECURITIES
We can issue securities in registered form or in the form of
one or more global securities. We describe global securities in greater detail below. We refer to those persons who have securities
registered in their own names on the books that we or any applicable trustee or depositary maintain for this purpose as the “holders”
of those securities. These persons are the legal holders of the securities. We refer to those persons who, indirectly through others,
own beneficial interests in securities that are not registered in their own names as “indirect holders” of those securities.
As we discuss below, indirect holders are not legal holders and investors in securities issued in book-entry form or in street
name will be indirect holders.
Book-Entry Holders
We may issue securities in book-entry form only, as we will
specify in the applicable prospectus supplement. This means securities may be represented by one or more global securities registered
in the name of a financial institution that holds them as depositary on behalf of other financial institutions that participate
in the depositary’s book-entry system. These participating institutions, which are referred to as participants, in turn,
hold beneficial interests in the securities on behalf of themselves or their customers.
Only the person in whose name a security is registered is recognized
as the holder of that security. Global securities will be registered in the name of the depositary or its participants. Consequently,
for global securities, we will recognize only the depositary as the holder of the securities, and we will make all payments on
the securities to the depositary. The depositary passes along the payments it receives to its participants, which in turn pass
the payments along to their customers who are the beneficial owners. The depositary and its participants do so under agreements
they have made with one another or with their customers; they are not obligated to do so under the terms of the securities.
As a result, investors in a global security will not own securities
directly. Instead, they will own beneficial interests in a global security, through a bank, broker or other financial institution
that participates in the depositary’s book-entry system or holds an interest through a participant. As long as the securities
are issued in global form, investors will be indirect holders, and not legal holders, of the securities.
Street Name Holders
A global security may be terminated in certain situations as
described under “-Special Situations When a Global Security Will Be Terminated,” or issue securities that are not issued
in global form. In these cases, investors may choose to hold their securities in their own names or in “street name.”
Securities held by an investor in street name would be registered in the name of a bank, broker or other financial institution
that the investor chooses, and the investor would hold only a beneficial interest in those securities through an account he
or she maintains at that institution.
For securities held in street name, we or any applicable trustee
or depositary will recognize only the intermediary banks, brokers and other financial institutions in whose names the securities
are registered as the holders of those securities, and we or any such trustee or depositary will make all payments on those securities
to them. These institutions pass along the payments they receive to their customers who are the beneficial owners, but only because
they agree to do so in their customer agreements or because they are legally required to do so. Investors who hold securities in
street name will be indirect holders, not holders, of those securities.
Legal Holders
Our obligations, as well as the obligations of any applicable
trustee or third party employed by us or a trustee, run only to the legal holders of the securities. We do not have obligations
to investors who hold beneficial interests in global securities, in street name or by any other indirect means. This will be the
case whether an investor chooses to be an indirect holder of a security or has no choice because we are issuing the securities
only in global form.
For example, once we make a payment or give a notice to the
legal holder, we have no further responsibility for the payment or notice even if that legal holder is required, under agreements
with its participants or customers or by law, to pass it along to the indirect holders but does not do so. Similarly, we may want
to obtain the approval of the holders to amend an indenture, to relieve us of the consequences of a default or of our obligation
to comply with a particular provision of an indenture, or for other purposes. In such an event, we would seek approval only from
the legal holders, and not the indirect holders, of the securities. Whether and how the legal holders contact the indirect holders
is up to the legal holders.
Special Considerations for Indirect Holders
If you hold securities through a bank, broker or other financial
institution, either in book-entry form because the securities are represented by one or more global securities or in street name,
you should check with your own institution to find out:
|
☐
|
how it handles securities payments and notices;
|
|
☐
|
whether it imposes fees or charges;
|
|
☐
|
how it would handle a request for the holders’ consent, if ever required;
|
|
☐
|
whether and how you can instruct it to send you securities registered in your own name so you can be a holder, if that is permitted in the future;
|
|
☐
|
how it would exercise rights under the securities if there were a default or other event triggering the need for holders to act to protect their interests; and
|
|
☐
|
if the securities are in book-entry form, how the depositary’s rules and procedures will affect these matters.
|
Global Securities
A global security is a security that represents one or any other
number of individual securities held by a depositary. Generally, all securities represented by the same global securities will
have the same terms.
Each security issued in book-entry form will be represented
by a global security that we issue to, deposit with and register in the name of a financial institution or its nominee that we
select. The financial institution that we select for this purpose is called the depositary. Unless we specify otherwise in the
applicable prospectus supplement, the DTC will be the depositary for all securities issued in book-entry form.
A global security may not be transferred to or registered in
the name of anyone other than the depositary, its nominee or a successor depositary, unless special termination situations arise.
We describe those situations below under “-Special Situations When a Global Security Will Be Terminated.” As a result
of these arrangements, the depositary, or its nominee, will be the sole registered owner and legal holder of all securities represented
by a global security, and investors will be permitted to own only beneficial interests in a global security. Beneficial interests
must be held by means of an account with a broker, bank or other financial institution that in turn has an account with the depositary
or with another institution that does. Thus, an investor whose security is represented by a global security will not be a legal
holder of the security, but only an indirect holder of a beneficial interest in the global security.
If the prospectus supplement for a particular security indicates
that the security will be issued as a global security, then the security will be represented by a global security at all times
unless and until the global security is terminated. If termination occurs, we may issue the securities through another book-entry
clearing system or decide that the securities may no longer be held through any book-entry clearing system.
Special Considerations for Global Securities
As an indirect holder, an investor’s rights relating to
a global security will be governed by the account rules of the investor’s financial institution and of the depositary, as
well as general laws relating to securities transfers. We do not recognize an indirect holder as a holder of securities and instead
deal only with the depositary that holds the global security.
If securities are issued only as global securities, an investor
should be aware of the following:
|
☐
|
an investor cannot cause the securities to be registered in his or her name, and cannot obtain non-global certificates for his or her interest in the securities, except in the special situations we describe below;
|
|
☐
|
an investor will be an indirect holder and must look to his or her own bank or broker for payments on the securities and protection of his or her legal rights relating to the securities, as we describe above;
|
|
☐
|
an investor may not be able to sell interests in the securities to some insurance companies and to other institutions that are required by law to own their securities in non-book-entry form;
|
|
☐
|
an investor may not be able to pledge his or her interest in the global security in circumstances where certificates representing the securities must be delivered to the lender or other beneficiary of the pledge in order for the pledge to be effective;
|
|
☐
|
the depositary’s policies, which may change from time to time, will govern payments, transfers, exchanges and other matters relating to an investor’s interest in the global security;
|
|
☐
|
we and any applicable trustee have no responsibility for any aspect of the depositary’s actions or for its records of ownership interests in the global security, nor will we or any applicable trustee supervise the depositary in any way;
|
|
☐
|
the depositary may, and we understand that DTC will, require that those who purchase and sell interests in the global security within its book-entry system use immediately available funds, and your broker or bank may require you to do so as well; and
|
|
☐
|
financial institutions that participate in the depositary’s book-entry system, and through which an investor holds its interest in the global security, may also have their own policies affecting payments, notices and other matters relating to the securities.
|
There may be more than one financial intermediary in the chain
of ownership for an investor. We do not monitor and are not responsible for the actions of any of those intermediaries.
Special Situations When a Global Security Will Be Terminated
In a few special situations described below, a global security
will terminate and interests in it will be exchanged for physical certificates representing those interests. After that exchange,
the choice of whether to hold securities directly or in street name will be up to the investor. Investors must consult their own
banks or brokers to find out how to have their interests in securities transferred to their own names, so that they will be direct
holders. We have described the rights of holders and street name investors above.
A global security will terminate when the following special
situations occur:
|
☐
|
if the depositary notifies us that it is unwilling, unable or no longer qualified to continue as depositary for that global security and we do not appoint another institution to act as depositary within 90 days;
|
|
☐
|
if we notify any applicable trustee that we wish to terminate that global security; or
|
|
☐
|
if an event of default has occurred with regard to securities represented by that global security and has not been cured or waived.
|
The applicable prospectus supplement may also list additional
situations for terminating a global security that would apply only to the particular series of securities covered by the prospectus
supplement. When a global security terminates, the depositary, and neither we nor any applicable trustee, is responsible for deciding
the names of the institutions that will be the initial direct holders.
PLAN OF DISTRIBUTION
We may sell the securities from time to time pursuant to underwritten
public offerings, negotiated transactions, block trades (which may involve crosses) or a combination of these methods. We may sell
the securities to or through underwriters or dealers, through agents, or directly to one or more purchasers. We may distribute
securities from time to time in one or more transactions:
|
•
|
|
at a fixed price or prices, which may be changed;
|
|
•
|
|
at market prices prevailing at the time of sale;
|
|
•
|
|
at prices related to such prevailing market prices; or
|
|
•
|
|
at negotiated prices.
|
We may also sell equity securities covered by this registration
statement in an “at the market offering” as defined in Rule 415(a)(4) under the Securities Act. Such offering may be
made into an existing trading market for such securities in transactions at other than a fixed price, either:
|
•
|
|
on or through the facilities of Nasdaq or any other securities exchange or quotation or trading service on which such securities may be listed, quoted or traded at the time of sale; and/or
|
|
•
|
|
other than on Nasdaq or such other securities exchanges or quotation or trading services.
|
Such at the market offerings, if any, may be conducted by underwriters
acting as principal or agent.
A prospectus supplement or supplements (and any related free
writing prospectus that we may authorize to be provided to you) will describe the terms of the offering of the securities, including,
to the extent applicable:
|
•
|
|
the name or names of any underwriters, dealers or agents, if any;
|
|
•
|
|
the purchase price of the securities and the proceeds we will receive from the sale;
|
|
•
|
|
any over-allotment options under which underwriters may purchase additional securities from us;
|
|
•
|
|
any agency fees or underwriting discounts and other items constituting agents’ or underwriters’ compensation;
|
|
•
|
|
any public offering price;
|
|
•
|
|
any discounts or concessions allowed or reallowed or paid to dealers; and
|
|
•
|
|
any securities exchange or market on which the securities may be listed.
|
Only underwriters named in the prospectus supplement are underwriters
of the securities offered by the prospectus supplement.
If underwriters are used in the sale, they will acquire the
securities for their own account and may resell the securities from time to time in one or more transactions at a fixed public
offering price or at varying prices determined at the time of sale. The obligations of the underwriters to purchase the securities
will be subject to the conditions set forth in the applicable underwriting agreement. We may offer the securities to the public
through underwriting syndicates represented by managing underwriters or by underwriters without a syndicate. Subject to certain
conditions, the underwriters will be obligated to purchase all of the securities offered by the prospectus supplement, other than
securities covered by any over-allotment or other option. Any public offering price and any discounts or concessions allowed or
reallowed or paid to dealers may change from time to time. We may use underwriters with whom we have a material relationship. We
will describe in the prospectus supplement, naming the underwriter, the nature of any such relationship.
We may sell securities directly or through agents we designate
from time to time. We will name any agent involved in the offering and sale of securities, and we will describe any commissions
we will pay the agent in the prospectus supplement. Unless the prospectus supplement states otherwise, our agent will act on a
best-efforts basis for the period of its appointment.
We may authorize agents or underwriters to solicit offers by
certain types of institutional investors to purchase securities from us at the public offering price set forth in the prospectus
supplement pursuant to delayed delivery contracts providing for payment and delivery on a specified date in the future. We will
describe the conditions to these contracts and the commissions we must pay for solicitation of these contracts in the prospectus
supplement.
We may provide agents and underwriters with indemnification
against civil liabilities related to this offering, including liabilities under the Securities Act, or contribution with respect
to payments that the agents or underwriters may make with respect to these liabilities. Agents and underwriters may engage in transactions
with, or perform services for, us in the ordinary course of business.
All securities we may offer, other than common stock, will be
new issues of securities with no established trading market. Any underwriters may make a market in these securities, but will not
be obligated to do so and may discontinue any market making at any time without notice. We cannot guarantee the liquidity of the
trading markets for any securities.
Any underwriter may engage in over-allotment, stabilizing transactions,
short covering transactions and penalty bids. Over-allotment involves sales in excess of the offering size, which create a short
position. Stabilizing transactions permit bids to purchase the underlying security so long as the stabilizing bids do not exceed
a specified maximum. Short covering transactions involve purchases of the securities in the open market after the distribution
is completed to cover short positions. Penalty bids permit the underwriters to reclaim a selling concession from a dealer when
the securities originally sold by the dealer are purchased in a stabilizing or covering transaction to cover short positions. Those
activities may cause the price of the securities to be higher than it would otherwise be. If commenced, the underwriters may discontinue
any of the activities at any time. These transactions may be effected on any exchange or over-the-counter market or otherwise.
Any underwriters or agents who are qualified market makers on
Nasdaq may engage in passive market making transactions in the securities on Nasdaq in accordance with Rule 103 of Regulation M
under the Exchange Act, during the business day prior to the pricing of the offering, before the commencement of offers or sales
of the securities. Passive market makers must comply with applicable volume and price limitations and must be identified as passive
market makers. In general, a passive market maker must display its bid at a price not in excess of the highest independent bid
for such security; if all independent bids are lowered below the passive market maker’s bid, however, the passive market
maker’s bid must then be lowered when certain purchase limits are exceeded. Passive market making may stabilize the market
price of the securities at a level above that which might otherwise prevail in the open market and, if commenced, may be discontinued
at any time.
In compliance with guidelines of the Financial Industry Regulatory
Authority, or FINRA, the maximum consideration or discount to be received by any FINRA member or independent broker dealer may
not exceed the aggregate amount of the securities offered pursuant to this prospectus and any applicable prospectus supplement.
LEGAL MATTERS
The validity of the shares of Common Stock offered pursuant
to this prospectus will be passed upon for us by Brownstein Hyatt Farber Schreck, LLP. Unless otherwise indicated in the applicable
prospectus supplement, certain legal matters in connection with the offering and the enforceability of debt securities or warrants
offered by this prospectus, and any supplement thereto, will be passed upon by Cooley LLP.
EXPERTS
The consolidated financial statements of
Aethlon Medical, Inc. as of March 31, 2019 and 2018 and for each of the years in the two-year period ended March 31, 2019 incorporated
in this Prospectus by reference from the Aethlon Medical, Inc. Annual Report on Form 10-K for the year ended March 31, 2019 have
been audited by Squar Milner LLP, an independent registered public accounting firm, as stated in their report thereon, incorporated
herein by reference, and have been incorporated in this Prospectus and Registration Statement in reliance upon such report and
upon the authority of such firm as experts in accounting and auditing.
WHERE YOU CAN FIND MORE INFORMATION
This prospectus is part of a registration statement we filed
with the SEC. This prospectus does not contain all of the information set forth in the registration statement and the exhibits
to the registration statement. For further information with respect to us and the securities we are offering under this prospectus,
we refer you to the registration statement and the exhibits and schedules filed as a part of the registration statement. Neither
we nor any agent, underwriter or dealer has authorized any person to provide you with different information. We are not making
an offer of these securities in any state where the offer is not permitted. You should not assume that the information in this
prospectus is accurate as of any date other than the date on the front page of this prospectus, regardless of the time of delivery
of this prospectus or any sale of the securities offered by this prospectus.
We file annual, quarterly and current reports, proxy statements
and other information with the SEC. The SEC maintains a website that contains reports, proxy statements and other information regarding
issuers that file electronically with the SEC, including Aethlon Medical. The address of the SEC website is www.sec.gov.
We maintain a website at www.aethlonmedical.com. Information
contained in or accessible through our website does not constitute a part of this prospectus.
INCORPORATION OF CERTAIN INFORMATION
BY REFERENCE
The SEC allows us to “incorporate
by reference” information that we file with it, which means that we can disclose important information to you by referring
you to those documents. The information incorporated by reference is an important part of this prospectus. Information in this
prospectus supersedes information incorporated by reference that we filed with the SEC prior to the date of this prospectus, while
information that we file later with the SEC will automatically update and supersede the information in this prospectus. We also
incorporate by reference into this prospectus the documents listed below and any future filings made by us with the SEC (other
than Current Reports or portions thereof furnished under Item 2.02 or Item 7.01 of Form 8-K and exhibits
filed on such form that are related to such items and other portions of documents that are furnished, but not filed, pursuant to
applicable rules promulgated by the SEC) that are filed by us with the SEC pursuant to Sections 13(a), 13(c), 14 or 15(d)
of the Exchange Act (i) after the date of the initial filing of the registration statement of which this prospectus is a part
and prior to effectiveness of the registration statement, and (ii) after the effectiveness of the registration statement but
prior to the termination of the offering of the common stock covered by this prospectus:
Our Annual Report on Form 10-K for the fiscal year ended March 31, 2019, filed with the SEC on July 1, 2019;
|
Our Quarterly Reports on Form 10-Q for the quarters ended June 30, 2019, September 30, 2019, and December 31, 2019, filed with the SEC on August 14, 2019, November 1, 2019, and February 10, 2020, respectively;
|
Our Definitive Proxy Statement on Schedule 14A, filed with the SEC on September 20, 2019;
|
Our current Reports on Form 8-K filed with the SEC on April 17, 2019, May 8, 2019, July 11, 2019, August 12, 2019, September 12, 2019, September 16, 2019, September 24, 2019, October 3, 2019, October 15, 2019, December 19, 2019, January 17, 2020, January 22, 2020, and February 21, 2020; and
|
The description of our common stock contained in our registration statement on Form 8-A filed with the SEC on July 8, 2015, including any amendments or reports filed for the purpose of updating such description.
|
We will provide to each person, including any beneficial owner,
to whom a prospectus is delivered, without charge upon written or oral request, a copy of any or all of the documents that are
incorporated by reference into this prospectus but not delivered with the prospectus, including exhibits which are specifically
incorporated by reference into such documents. You should direct any requests for documents by writing us at Aethlon Medical, Inc.,
9635 Granite Ridge Drive, Suite 100, San Diego, California 92123, (858) 459-7800.
You should rely only on the information provided in and incorporated
by reference into this prospectus or any prospectus supplement. We have not authorized anyone else to provide you with different
information. You should not assume that the information in this prospectus or any prospectus supplement is accurate as of any date
other than the date on the front cover of these documents.
Any statement contained herein or in a document incorporated
or deemed to be incorporated by reference into this document will be deemed to be modified or superseded for purposes of the document
to the extent that a statement contained in this document or any other subsequently filed document that is deemed to be incorporated
by reference into this document modifies or supersedes the statement.
Aethlon Medical, Inc.
1,380,555 Shares of
Common Stock
__________________
PROSPECTUS SUPPLEMENT
__________________
Sole Placement
Agent
Maxim Group LLC
_________________
June 10, 2021
Aethlon Medical (NASDAQ:AEMD)
Historical Stock Chart
From Mar 2024 to Apr 2024
Aethlon Medical (NASDAQ:AEMD)
Historical Stock Chart
From Apr 2023 to Apr 2024