CoverageForm 410-K10-Q8-K13D13G13F

AIM Aim Immunotech Inc. - 8-K

Accession
0001493152-26-027210
7.019.01

Item 7.01 - Regulation FD Disclosure

317 words · Exhibit 99.1 attached

Item
7.01

Regulation
FD Disclosure.

On
June 4, 2026, AIM ImmunoTech Inc. (the “Company”) released an on-demand video presentation detailing previously published
pre-clinical findings relating to the potential role of its lead drug candidate Ampligen® (rintatolimod) as a prophylactic and/or
early-onset antiviral treatment for Ebola virus disease (“EVD”). The Virtual Investor “What This Means” segment
is available for viewing at https://virtualinvestorco.com/aim. A copy of the press release relating to the video presentation is furnished
as Exhibit 99.1 hereto and incorporated herein by reference. Additionally, an Investor Presentation slide deck of information related
to the Company’s research into EVD is available for viewing on the Company’s website at https://aimimmuno.com/presentations,
is furnished as Exhibit 99.2 hereto, and is incorporated herein by reference.

The
information furnished under this Item 7.01, including Exhibits 99.1 and 99.2, shall not be deemed “filed” for purposes of
Section 18 of the Exchange Act or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference
in any filing under the Securities Act or the Exchange Act, except as expressly set forth by specific reference in such a filing.

Cautionary
Note Regarding Forward-Looking Statements

This
Current Report on Form 8-K contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended
(the “Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”),
including statements regarding the potential role of Ampligen® as a prophylactic or early-onset antiviral treatment for EVD. These
statements are subject to risks and uncertainties that could cause actual results to differ materially, including but not limited to
risks related to clinical development, regulatory approval, and other factors described in the Company’s filings with the Securities
and Exchange Commission, including its most recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q. The Company
undertakes no obligation to update any forward-looking statements.

Exhibit 99.1 · 1,253 words

EX-99.1
2
ex99-1.htm
EX-99.1

Exhibit
99.1

AIM
ImmunoTech Releases Virtual Investor ‘What This Means’ Video Segment Discussing Ampligen’s Potential in Ebola Virus
Disease Preparedness

Video
segment examines current Ebola outbreak concerns, unmet need surrounding the Bundibugyo strain and Ampligen’s previously published
antiviral research

Discussion
highlights Ampligen’s immune-modulating mechanism, prior Biosafety Level 4 findings and potential applicability across emerging
viral threats

New
Ebola-focused corporate presentation highlighting Ampligen’s antiviral research and preparedness potential is now accessible here

Access
the ‘What This Means’ video segment here

OCALA,
Fla., June 4, 2026 / AIM ImmunoTech Inc. (NYSE American: AIM) (“AIM” or the “Company”) today announced
the release of a Virtual Investor “What This Means” video segment featuring AIM Chief Executive Officer Thomas Equels,
Consulting Medical Officer Charles Lapp, MD, and Consulting Science Officer Christopher Nicodemus, MD.

As
part of the video segment, management discusses the ongoing Bundibugyo (“BDBV”) Ebola outbreak and the growing concern surrounding
the lack of approved targeted therapies or vaccines specifically addressing this strain. The discussion explores the broader public health
implications of emerging viral outbreaks, including containment challenges, cross-border transmission risks and the importance of preparedness
initiatives designed to support healthcare systems and vulnerable populations.

Equels
stated: “BDBV is a lethal, out-of-control disease. Infected patients can receive aggressive supportive care, but there are no approved
vaccines, therapies or meaningful drugs designed to help mitigate the spread of the outbreak. A prophylactic or early-onset therapeutic
is clearly needed. We believe that Ampligen has the potential to be that therapeutic, based on studies such as one conducted at the US
government USAMRIID facility, which showed that intraperitoneal Ampligen could have a prophylactic and/or early-onset impact on Ebola
disease. Further, intranasal Ampligen might more easily provide preventive protection, especially in regions of the world where infusion
therapy is impractical.”

This
video segment reviews previously published Biosafety Level 4 preclinical findings demonstrating 100% protective survival with early administration
of Ampligen in a lethal Ebola mouse model. Management discusses Ampligen’s mechanism as a PAMP restricted TLR3 agonist designed
to activate innate immune pathways and shares perspective on why the Company believes the approach may potentially have relevance across
multiple Ebola variants and other emerging viral threats.

The
discussion highlights AIM’s previously established regulatory and scientific groundwork supporting the program, including orphan
drug designation from both the U.S. Food and Drug Administration and European Medicines Agency for Ebola virus disease. The video segment
further explores the potential future role of scalable antiviral and immune-modulating approaches in broader biodefense, preparedness
and emerging infectious disease response initiatives.

AIM
has made available an updated Ebola-focused corporate presentation further highlighting Ampligen’s previously published antiviral
research, immune-modulating mechanism and broader preparedness potential in emerging viral threats, as well as intravenous and intranasal
Ampligen human safety studies. The Ebola-focused presentation is available under the Presentations section on the Investors
page of the Company’s website ( aimimmuno.com ).

The
Virtual Investor “What This Means” video segment featuring AIM ImmunoTech is now available here .

About
AIM ImmunoTech Inc.

AIM
ImmunoTech Inc. is an immuno-pharma company focused on the research and development of its lead product, Ampligen ® (rintatolimod),
for the treatment of late-stage pancreatic cancer, a lethal and unmet global health problem. Ampligen is a dsRNA and highly selective
TLR3 agonist immuno-modulator that has shown broad-spectrum activity in clinical trials.

For
more information, please visit aimimmuno.com and connect with the Company on X , LinkedIn , and Facebook .

Forward-Looking
Statements

This
press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section
21E of the Securities Exchange Act of 1934, as amended, that involve a number of risks and uncertainties. The video segment may also
contain forward-looking statements. Any forward-looking statements set forth in this press release speak only as of the date hereof and
any forward-looking statements in the video segment speak only as of the date thereof. Such forward-looking statements may include statements
relating to: Ampligen’s potential efficacy and applicability in the treatment of Ebola virus disease; the potential for prophylactic
or early-onset therapeutic applications; the timing of commencement, enrollment, completion, and results of clinical trials; intellectual
property expansion and regulatory progress; and timing for receiving government approvals, if at all. For all forward-looking statements,
the Company claims the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform
Act of 1995. All statements in this press release and the video segment other than statements of historical fact, including statements
regarding the potential of Ampligen’s mechanism of action, anticipated regulatory milestones, our future results of operations
and financial position, our business strategy and plans, and our objectives for future operations, are forward-looking statements. For
both this press release and the video segment, words such as “believe,” “may,” “might,” “will,”
“could,” “should,” “can,” “estimate,” “continue,” “anticipate,”
“intend,” “expect,” “envision,” “potential” and similar expressions are intended to identify
forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. The Company does not
undertake to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof, except
as required by applicable law. The Company is in various stages of seeking to determine whether Ampligen will be effective in the treatment
of multiple types of viral diseases, cancers, and immune-deficiency disorders, and disclosures in the Company’s reports filed with
the SEC, on its website, and in its press releases set forth its current and anticipated future activities. These activities are subject
to change for a number of reasons. Significant additional testing and trials will be required to determine whether Ampligen® will
be effective in the treatment of these conditions, including Ebola virus disease. Results obtained in preclinical studies do not necessarily
predict results in humans. Human clinical trials will be necessary to prove whether or not Ampligen® will be efficacious in humans.
No assurance can be given as to whether current or planned clinical trials will be successful or yield favorable data, and the trials
are subject to many factors including lack of regulatory approval(s), lack of study drug, lack of adequate funding, or a change in priorities
at the institutions sponsoring other trials. Even if these clinical trials are initiated, the Company cannot assure that the clinical
studies will be successful or yield any useful data. No assurance can be given that the findings in preliminary studies will prove true
or that such studies will yield favorable results, or that future studies will not result in findings that are different from those reported
in the studies referenced in the Company’s reports filed with the SEC, on the Company’s website, and in its press releases.
Operating in foreign countries carries with it a number of risks, including potential difficulties in enforcing intellectual property
rights. The Company cannot assure that its potential foreign operations will not be adversely affected by these risks.

For
a detailed discussion of these and other risk factors, please review the “Risk Factors” section in the Company’s most
recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q filed with the SEC. These filings are available at www.sec.gov
and www.aimimmuno.com. You should not place undue reliance on any forward-looking statements. The information found on the Company’s
website or on other websites referenced or linked to in this press release (including in the video segment) is not incorporated by reference
into this press release and such information is referenced or linked for reference purposes only.

Investor
Contact:

JTC
Team, LLC

Jenene
Thomas

908.824.0775

[email protected]

Item 9.01 - Financial Statements and Exhibits

37 words

Item
9.01

Financial
Statements and Exhibits.

(d)
Exhibits

Exhibit
No.

Description

99.1

Press Release, dated June 4, 2026

99.2

Investor Presentation Slide Deck, June 2026

104

Cover
Page Interactive Data File (embedded within the Inline XBRL document).