AIM ImmunoTech Outlines Recent Progress Across Clinical Development Pipeline and Provides Business Update
29 Fevereiro 2024 - 10:45AM
UK Regulatory
AIM ImmunoTech Outlines Recent Progress Across Clinical Development
Pipeline and Provides Business Update
Company continues progress across
Ampligen® clinical development programs
Growing body of promising data demonstrates
Ampligen’s potential to address multiple high-value
indications
OCALA, Fla., Feb. 29, 2024 (GLOBE NEWSWIRE) -- AIM
ImmunoTech Inc. (NYSE American:
AIM) (“AIM” or the “Company”) today highlighted
recent accomplishments and provided a business outlook. AIM’s dsRNA
product candidate, Ampligen® (rintatolimod), is being
evaluated as a combinational therapy for the treatment of a variety
of solid tumor types in multiple clinical trials – both underway
and planned – at major cancer research centers around the
country.
Recent Highlights
- AMP-518 Clinical Study: Phase 2 study evaluating Ampligen as a
potential therapeutic for people with the Post-COVID condition of
fatigue
- Completed treatment in study
- Reported positive topline results offering preliminary evidence
that Ampligen may reduce fatigue in subjects with Post-COVID
conditions
- Bolstered intellectual property estate with issuance of key
U.S. patent for Ampligen in combination with an anti-PD-L1 antibody
for the treatment of cancer
- DURIPANC Clinical Study: Phase 1b/2 clinical trial combining
AIM’s Ampligen with AstraZeneca’s anti-PD-L1 immune checkpoint
inhibitor Imfinzi® (durvalumab) for the treatment of
pancreatic cancer
- Opened for enrollment and enrolled first subject at Erasmus
Medical Center (“Erasmus MC”)
- First subject dosed at Erasmus MC
“AIM’s emphasis throughout 2024 will be building upon our strong
foundation of scientific success,” said AIM Chief Executive Officer
Thomas K. Equels. “Our drug Ampligen is being evaluated in multiple
indications — including pancreatic cancer, ovarian cancer and
Post-COVID conditions — and we believe that success in any one of
these areas would mean both dramatic improvement in people’s lives
and significant value for our stockholders.”
Upcoming Expected Ampligen
Milestones
Q1 2024
- Advanced Recurrent Ovarian Cancer – Protocol-planned interim
results
Q2 2024
- Post-COVID Conditions (AMP-518) – Final dataset
2024
- Locally Advanced Pancreatic Adenocarcinoma (AMP-270) – First
subject dosed
- Publications of data in scientific journals
Ongoing Business Development
Update
As previously announced, the Company engaged Azenova, LLC
(“Azenova”), a professional business development (BD) consulting
firm, to support efforts to partner AIM’s pipeline programs with a
particular focus on the Company’s lead asset, Ampligen®,
for the treatment of various malignant solid tumors. Discussions
for potential partnership, licensing, and other transactional
activities remain ongoing.
In addition to its ongoing clinical and business development
activities, the Company will continue to engage with the industry
and investment communities by actively participating in meetings,
virtual events and key conferences over the course of the year. To
stay up to date with the Company’s activities
visit aimimmuno.com and connect with the Company
on X, LinkedIn, and Facebook.
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 is a first-in-class investigational drug
called Ampligen® (rintatolimod), a dsRNA and highly
selective TLR3 agonist immuno-modulator with broad spectrum
activity in clinical trials for globally important cancers, viral
diseases and disorders of the immune system.
For more information, please visit aimimmuno.com and
connect with the Company on X, LinkedIn,
and Facebook.
Cautionary Statement
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of 1995
(the “PSLRA”). Words such as “may,” “will,” “expect,” “plan,”
“anticipate,” “continue,” “believe,” “potential,” “upcoming” and
other variations thereon and similar expressions (as well as other
words or expressions referencing future events or circumstances)
are intended to identify forward-looking statements. Many of these
forward-looking statements involve a number of risks and
uncertainties. 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 U.S. Securities
and Exchange Commission (the “SEC”). You are cautioned not to place
undue reliance on these forward-looking statements, which speak
only as of the date of this press release. Among other things, for
those statements, the Company claims the protection of the safe
harbor for forward-looking statements contained in the PSLRA. The
Company does not undertake to update any of these forward-looking
statements to reflect events or circumstances that occur after the
date hereof.
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