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SCHEDULE
14A
Proxy
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Definitive
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Soliciting
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AIM ImmunoTech Inc.
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Registrant)
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AIM
ImmunoTech Board Files Definitive Proxy Statement and Sends Letter
to Shareholders
Highlights
Significant Progress Made in Recent Years – and Especially Over
Past 18 Months – in Repurposing Lead Drug Ampligen in Oncology to
Benefit Patients and All Shareholders
Calls
on Shareholders to Support Continued Positive Momentum by
Re-Electing the AIM Board and Discarding Any Materials Received
from Jorgl Activist Group
OCALA,
Fla., September 19, 2022 — The Board of Directors (“Board”) of AIM
ImmunoTech Inc. (NYSE: American AIM) (“AIM” or the “Company”),
today announced that the Company has filed its Definitive Proxy
Statement in connection with AIM’s upcoming 2022 Annual Meeting of
Stockholders (the “Annual Meeting”), to be held on November 3,
2022, and has mailed this statement, along with a letter, to
shareholders.
The
full text of the letter follows.
September
19, 2022
Dear
fellow shareholders:
Thank
you for your investment and your trust in AIM ImmunoTech (“AIM” or
the “Company”). Now is an exciting time for us as we continue to
strive to bring new life-saving oncology therapies to market to
benefit patients and create value for you, our shareholders. As we
will describe in more detail below, we have made significant
progress in recent years – and especially over the past 18 months –
in repurposing our lead drug, Ampligen, into oncology. We also have
strong momentum building upon the positive interim results in
published data from preeminent cancer centers that we are now
seeing from our clinical trials.
Our
2022 Annual Meeting of Stockholders (the “Annual Meeting”) will be
held on November 3, 2022 and we are writing to ask for your support
of our mission to bring life-saving therapies to market.
This
year your vote is especially important because Jonathan Jorgl, an
AIM shareholder who first purchased 1,000 AIM shares on June 27,
2022, has nominated two director candidates (together with Mr.
Jorgl, the “Jorgl Activist Group”) for election to the Board at the
upcoming Annual Meeting. If these two individuals were elected,
they would control the Board.
Alarmingly,
as they disclosed for the first time only last week, the Jorgl
Activist Group’s proxy campaign is being funded by an individual
whose role and identity the Jorgl Activist Group previously
concealed, most likely because he recently pled guilty to criminal
charges of wire fraud relating to fraudulent securities trading,
material misrepresentations to investors and misuse of funds. As a
result, he was recently sentenced by a federal court to three years
of probation and ordered to pay hundreds of thousands of dollars in
restitution.
Additionally,
the Board believes that the Jorgl Activist Group has an undisclosed
arrangement with another individual who pled guilty to insider
trading criminal charges brought by the Department of Justice, and
settled insider trading civil charges brought by the SEC. More
details about the Jorgl Activist Group are contained in the
enclosed proxy materials.
The
Board has unanimously determined that Mr. Jorgl’s director
nominations did not comply with AIM’s bylaws and are invalid. Mr.
Jorgl is attempting to fight this determination in a case currently
pending before a court, but the critical point is this: we strongly
urge you to ignore any proxy materials you receive from the Jorgl
Activist Group and vote on the Company’s WHITE proxy card
for your current highly qualified directors to protect your
investment.
In
contemplating your vote, we ask that you consider the
following:
The
Current Management Team and Board is Successfully Executing on the
Company’s Business and Capital Allocation Strategy
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The
Company and its management team installed in 2016 has gone from
having little cash, a sustained period of poor share price
performance resulting in the threat of delisting from the New York
Stock Exchange American, inadequate reserves of Ampligen to support
major oncology clinical trials, and no such trials underway, to now
having financial stability after manufacturing an adequate supply
of Ampligen to support clinical trials. This was a vital first step
that the Company was unable to achieve previously and has allowed
us to move forward with our development process. |
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AIM
has sufficient liquid assets (~$41.7 million per the Company’s 10-Q
for the period ended June 30, 2022) to advance our priority
development pipeline and fund operations through the end of
2023.
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Further,
we have also initiated and are helping to fund several ongoing
oncology clinical trials and early access programs in large
potential markets with lethal unmet medical needs such as advanced
pancreatic cancer and advanced recurrent ovarian
cancer. |
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Our
clinical trials have been yielding consistently encouraging,
statistically significant interim results with positive safety
profiles, which also have been published in peer reviewed journals.
We have achieved multiple potentially game-changing clinical and
regulatory milestones this year and expect this positive momentum
to continue throughout the rest of 2022 and into next
year. |
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We
received notification from the U.S. Food and Drug Administration
(“FDA”) that the FDA’s Clinical Hold on AIM’s investigational new
drug (“IND”) application for a Phase 2 study of Ampligen as a
therapy for locally advanced pancreatic cancer (AMP-270) has been
lifted and the Company may proceed with the study. |
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In
April of this year, we announced several positive developments
related to Ampligen, including the following: |
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The
Independent Investigators from preeminent oncology research centers
presented strongly positive data in three different cancer
indications at the prestigious American Association for Cancer
Research Annual Meeting. |
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The
Erasmus Medical Center presented published data (Cancers)
demonstrating Ampligen’s potential to offer beneficial anti-tumor
effects in late-stage pancreatic cancer patients, including
Ampligen treatment’s association with higher progression-free and
overall survival in late-stage pancreatic cancer patients when
compared to well-matched historical controls. |
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We
reported positive data from a Phase 2a study evaluating Ampligen as
a component of a chemokine modulatory (CKM) regimen for the
treatment of colorectal cancer metastatic to the liver. |
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We
reported positive data from a Phase 1 study evaluating Ampligen for
the treatment of stage 4 metastatic triple negative breast
cancer. |
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Further,
on July 28, 2022, we reported positive preliminary pilot study data
from our ongoing Expanded Access Program (AMP-511) evaluating
Ampligen in patients with chronic fatigue symptoms following COVID
infections (a form of “Long COVID”). |
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The
preliminary data from this uncontrolled clinical protocol found
that patients reported significant improvements in fatigue symptoms
after treatment with Ampligen compared to baseline, which the
investigators considered a clinically significant decrease in
fatigue-related measures. Based on these early results, we are
working to move forward with a Phase 2 controlled trial in post
COVID Conditions (also known as “Long COVID”). |
An
Experienced, Well-Qualified Board
Your
Board has the right experience, skill sets and deep knowledge of
the Company and its drug candidates to continue overseeing the
successful execution of our strategy to deliver therapies for
patients and value for our shareholders. More detailed biographies
of our directors are contained in the enclosed proxy
materials.
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Stewart
L. Appelrouth possesses key financial and regulatory expertise
as a certified public accountant with over 40 years of accounting
and audit experience. |
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Thomas
K. Equels, M.S. J.D., Executive Vice Chairman, Chief Executive
Officer and President, has over 25 years of experience as a
practicing attorney specializing in complex business litigation. He
also has extensive experience in clinical trial design and
development, creating intellectual property concepts, and in
financing drug development. |
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Dr.
William M. Mitchell, Chairman, has extensive medical industry
experience, including as a Professor of Pathology at Vanderbilt
University School of Medicine, a board-certified physician and a
former member of the Board of Directors of Chronix Biomedical, a
company involved in next generation DNA sequencing for medical
diagnostics. |
We
encourage you, as an AIM shareholder, to support the Board – and
ensure the Company has the leadership to protect investors – by
voting online, by phone or by mail, using the WHITE proxy
card.
***
WE
URGE YOU TO COMPLETE, DATE, AND SIGN THE ENCLOSED WHITE
PROXY CARD AND MAIL IT PROMPTLY IN THE POSTAGE-PAID ENVELOPE
PROVIDED, OR VOTE BY TELEPHONE OR THE INTERNET AS INSTRUCTED ON THE
WHITE PROXY CARD, WHETHER OR NOT YOU PLAN TO ATTEND THE
ANNUAL MEETING.
THE
BOARD RECOMMENDS A VOTE “FOR ALL” OF OUR BOARD’S
NOMINEES
(STEWART
L. APPELROUTH, THOMAS K. EQUELS AND WILLIAM M.
MITCHELL)
ON
PROPOSAL 1 USING THE ENCLOSED WHITE PROXY
CARD.
Sincerely,
The
AIM ImmunoTech Board of Directors
If you have any questions or need assistance voting, please contact
the Company’s proxy solicitor Morrow Sodali LLC (“Morrow Sodali”)
using the below information.
MORROW
SODALI
509
Madison Avenue
Suite
1206
New
York, NY 10022
Banks
and Brokers Call: (203) 658-9400
Stockholders
Call Toll Free: (800) 662-5200
E-mail:
AIM@investor.morrowsodali.com
About
AIM ImmunoTech Inc.
AIM
ImmunoTech Inc. is an immuno-pharma company focused on the research
and development of therapeutics to treat multiple types of cancers,
immune disorders, and viral diseases, including COVID-19. The
Company’s lead product, Ampligen® (rintatolimod) is an
immuno-modulator with broad spectrum activity being developed for
globally important cancers, viral diseases and disorders of the
immune system.
Ampligen
is currently being used as a monotherapy to treat pancreatic cancer
patients in an Early Access Program (EAP) approved by the
Inspectorate of Healthcare in the Netherlands at Erasmus Medical
Center and AIM plans to initiate a Phase 2 clinical study in 2022.
The Company also has multiple ongoing clinical trials to evaluate
Ampligen as a combinational therapy for the treatment of a variety
of solid tumor types both underway and planned at major cancer
research centers. Additionally, Ampligen is approved in Argentina
for the treatment of severe chronic fatigue syndrome (CFS) and is
currently being evaluated in many aspects of SARS-CoV-2/COVID-19
myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and
Post COVID Conditions.
For
more information, please visit aimimmuno.com and connect with the
Company on Twitter, LinkedIn, and Facebook.
Forward-Looking Statements
This
press release contains certain forward-looking statements that
involve risks, uncertainties and assumptions that are difficult to
predict. Words and expressions reflecting optimism, satisfaction or
disappointment with current prospects, as well as words such as
“believes,” “hopes,” “intends,” “estimates,” “expects,” “projects,”
“plans,” “anticipates” and variations thereof, or the use of future
tense, identify forward-looking statements, but their absence does
not mean that a statement is not forward-looking. The Company’s
forward-looking statements are not guarantees of performance, and
actual results could vary materially from those contained in or
expressed by such statements due to risks, uncertainties and other
factors. The Company urges investors to consider specifically the
various risk factors identified in its most recent Form 10-K, and
any risk factors or cautionary statements included in any
subsequent Form 10-Q or Form 8-K, filed with the Securities and
Exchange Commission. You are cautioned not to place undue reliance
on these forward-looking statements, which speak only as of the
date of this press release. Except as required by law, the Company
does not undertake any responsibility to update any forward-looking
statements to take into account events or circumstances that occur
after the date of this press release.
Important Information
The
Company has filed a definitive proxy statement and associated
WHITE proxy card with the SEC in connection with the
solicitation of proxies for the Company’s Annual Meeting. Details
concerning the nominees of the Company’s Board of Directors for
election at the Annual Meeting are included in the proxy statement.
BEFORE MAKING ANY VOTING DECISION, INVESTORS AND STOCKHOLDERS OF
THE COMPANY ARE URGED TO READ ALL RELEVANT DOCUMENTS FILED WITH OR
FURNISHED TO THE SEC, INCLUDING THE COMPANY’S PROXY STATEMENT AND
ANY AMENDMENTS OR SUPPLEMENTS THERETO, WHEN THEY BECOME AVAILABLE
BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION.
Investors
and stockholders will be able to obtain a copy of the definitive
proxy statement, any amendments or supplements thereto and other
documents filed by the Company free of charge from the SEC’s
website, www.sec.gov. Copies of these materials will also be
available free of charge on AIM’s Investor Relations website at
https://aimimmuno.com/sec-filings/.
Participants in the Solicitation
The
Company, its directors and certain of its executive officers are
participants in the solicitation of proxies from stockholders in
respect of the Annual Meeting. Information regarding the names of
the Company’s directors and executive officers and their respective
interests in the Company by security holdings or otherwise is set
forth in the Company’s Definitive Proxy Statement, filed with the
SEC on September 19, 2022. To the extent holdings of such
participants in the Company’s securities have changed since the
amounts described in the Definitive Proxy Statement, such changes
have been or will be reflected on Initial Statements of Beneficial
Ownership on Form 3 or Statements of Change in Ownership on Form 4
filed with the SEC. These documents can be obtained free of charge
from the sources indicated above.
Investor
Contacts:
JTC
Team, LLC
Jenene
Thomas
833-475-8247
AIM@jtcir.com
OR
Morrow
Sodali
AIM@investor.MorrowSodali.com
Media
Contact:
Longacre
Square Partners
Dan
Zacchei / Joe Germani
dzacchei@longacresquare.com
/ jgermani@longacresquare.com
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