AIM ImmunoTech Announces Publication of Positive Findings from a Study Evaluating Ampligen® in the Treatment of Pancreatic Cancer in the Journal Clinical Cancer Research
2024年3月25日 - 10:05PM
RNSを含む英国規制内ニュース (英語)
AIM ImmunoTech Announces Publication of Positive Findings from a
Study Evaluating Ampligen® in the Treatment of Pancreatic Cancer in
the Journal Clinical Cancer Research
Data demonstrate compelling evidence of the
immune-stimulatory properties linked to TLR-3 activation through
Ampligen
OCALA, Fla., March 25, 2024 (GLOBE NEWSWIRE) --
AIM ImmunoTech Inc. (NYSE American:
AIM) (“AIM”) today announced the publication of new
data analysis from a long-term Early Access Program (“EAP”)
studying the company’s drug Ampligen® (rintatolimod) for the
treatment of advanced pancreatic ductal adenocarcinoma (“PDAC”).
The manuscript titled “Rintatolimod in Advanced Pancreatic
Cancer enhances Anti-Tumor Immunity through Dendritic Cell-Mediated
T Cell Responses,” appears in the journal Clinical Cancer
Research, one of oncology’s most prestigious journals.
Ampligen is a dsRNA product candidate that acts
via the TLR-3 receptor present on several immune cells, epithelial
cells and tumors. Researchers at the Erasmus University Medical
Center (“Erasmus MC”) found that Ampligen treatment in pancreatic
cancer patients enhances peripheral immune activity at the
transcriptomic and proteomic levels, particularly involving type 1
conventional dendritic cells (cDC1s) and T cells. Post-Ampligen,
the increased peripheral abundance of BTLA+XCR1+ cDC1s and
CD4+SELL+ T cells correlated with improved clinical outcomes.
Patients with stable disease exhibited pronounced overexpression of
genes related to DC and T cell activation. Notably, the expression
of immune checkpoints PD-L1 and PD-L2 decreased post-Ampligen
across all patients.
AIM Chief Executive Officer Thomas K. Equels
stated: “We have already seen that Ampligen as a single-agent
therapy was associated with improved progression-free survival and
overall survival in these Early Access Program pancreatic cancer
patients. This new data analysis provides us further insight into
exactly why that’s the case, which could give us the ability to
identify cancer patients who might benefit more from Ampligen
treatment than they would from other known cancer treatments.
Additionally, the changes in the tumor microenvironment we see in
pancreatic cancer are similar to those we have seen in
triple-negative breast cancer, ovarian cancer and colorectal cancer
metastatic to the liver. We have hypothesized that Ampligen has the
potential to be efficacious in almost every solid tumor type based
on its direct effect on malignant tumor cells and its effect on the
tumor micro-environment. All these data combined lend further
credence to the broad applicability of Ampligen in solid
tumors.”
Prof. Casper H.J. van Eijck, MD, PhD,
Pancreato-biliary Surgeon at Erasmus MC and co-author of the
published paper, stated, “Based on these results, we believe
Ampligen may break immunological tolerance by enhancing anti-tumor
immunity through DC-mediated T-cell responses. The data suggests
that Ampligen infusions modulate PD-L1 and PD-L2 expression in the
tumor microenvironment, while at the same time they upregulate
Ki67+CD4+ and Ki67+CD8+ T-cells. We therefore believe that
combining Ampligen with an immune checkpoint inhibitor — such as
durvalumab — could synergistically circumvent immune blockade and
potentially mitigate the T-cell exhaustion known to occur with
immune checkpoint therapies. We look forward to further evaluating
Ampligen toward potentially meeting the critical need for more
effective therapies to treat pancreatic cancer, including with the
ongoing DURIPANC trial, which looks at the combination effect of
Ampligen and AstraZeneca’s durvalumab.”
AIM is currently evaluating Ampligen as a
therapy for metastatic pancreatic ductal adenocarcinoma in the
Phase 1b/2 DURIPANC clinical study (NCT05927142) and as a therapy
for locally advanced pancreatic adenocarcinoma in the Phase 2
AMP-270 clinical study (NCT05494697).
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. Publication of this data and clinical success
seen to date does not guarantee that Ampligen will be approved for
the commercial treatment of pancreatic cancer. 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. 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.
A photo accompanying this announcement is available at
https://www.globenewswire.com/NewsRoom/AttachmentNg/3fb0a503-5593-4f78-bc1c-65128796be7a
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