AIM ImmunoTech Announces Presentation of New Data from Roswell Park Comprehensive Cancer Center Evaluating Ampligen® as a Component of a Chemokine-Modulating (CKM) Regimen, with Paclitaxel, for the Treatment of Early-Stage Triple Negative Breast Cancer
14 Novembre 2022 - 1:00PM
AIM ImmunoTech Announces Presentation of New Data from Roswell Park
Comprehensive Cancer Center Evaluating Ampligen® as a Component of
a Chemokine-Modulating (CKM) Regimen, with Paclitaxel, for the
Treatment of Early-Stage Triple Negative Breast Cancer
AIM ImmunoTech Inc. (NYSE American: AIM) (“AIM” or
the “Company”), an immune-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
disease caused by the SARS-CoV-2 virus, today announced the
presentation of positive data from research led by Roswell Park
Comprehensive Cancer Center medical oncologist Shipra Gandhi, MD,
evaluating Ampligen® (rintatolimod) as a component of a CKM regimen
for the treatment of early-stage triple negative breast cancer
(TNBC). The data are being presented by Roswell Park Comprehensive
Cancer Center in a poster presentation at the Society for
Immunotherapy of Cancer (SITC) 37th Annual Meeting being held
virtually and in Boston, MA, November 8-12, 2022.
The research was led by Dr. Gandhi, a physician
scientist who is Assistant Professor of Oncology at Roswell Park,
in collaboration with senior investigator Pawel Kalinski, MD, PhD,
Chair of Immunology and Senior Vice President for Team Science at
Roswell Park.
The poster presentation is available at the following
link: Title:
Safety and efficacy of de-escalated neoadjuvant chemoimmunotherapy
of triple negative breast cancer (TNBC) using chemokine-modulating
regimen (rintatolimod, IFN-α2b, celecoxib)1Presenting
Author: Shipra Gandhi, MDAbstract Number:
547
Guided by the preclinical data Roswell Park
proposed this CKM regimen, which combines AIM ImmunoTech’s Ampligen
(rintatolimod) (TLR3 agonist), interferon (IFN)-α2b and celecoxib
(COX-2 inhibitor), as an approach for selectively inducing
cytotoxic T-lymphocytes (CTL)-attractants but decreasing
Treg-attractants.2 The Roswell Park researchers hypothesized that
the combination of CKM with chemotherapy can promote CTL
infiltration and result in higher pathological complete response
(pCR)
In a Phase 1 study, 9 patients with stage I-III
TNBC, median age 47 (37-55) years, were treated with paclitaxel 80
mg/m2 IV weekly for 12 weeks and CKM for the first 3 weeks, days
1-3 (IV Ampligen 200 mg daily and oral celecoxib 200 mg twice
daily). IFN-α2b was administered in an accelerated dose-escalation
at 0 or 5 million units (MU)/m2 [dose levels (DL) 1,2 respectively]
in the first 2 patients; 10 MU/m2 [DL 3] in 4 patients and 20 MU/
m2 [DL 4] in 3 patients. CKM/paclitaxel was followed by standard
dose-dense doxorubicin and cyclophosphamide (AC) and surgery.
Dose-limiting toxicity (DLT) was defined as grade 3 or higher
toxicities within the first 3 weeks. The primary endpoint was
safety and tolerability. Secondary endpoints included pCR rate.
Tumor and blood biomarkers were analyzed in exploratory
studies.
The results of the study demonstrated that
treatment was well-tolerated with mostly grade 1 or 2
treatment-related adverse events (TRAEs) without DLTs or delayed or
immune-related toxicities. Grade 3 TRAEs included neutropenia (3/9)
attributed to CKM (1/9) or paclitaxel (3/9), pneumonia (1/9) and
anemia (1/9) attributed to AC. Additional pneumonia and skin
squamous cell carcinoma in situ were observed, unrelated to study
treatment. Paclitaxel- or AC-related toxicities were not higher
than expected. 5/9 (56%) of patients attained pCR and 1 more
patient attained ypTmic. CTL marker CD8α was selectively elevated
in post-CKM tumor biopsies (5 patients at DL3 and 4) but decreased
in the post-CKM blood.
For more information about the Phase 1 study,
visit ClinicalTrials.gov: NCT04081389.
“Building off of the previously developed
chemokine modulatory regimen combining interferon-α with TLR3
agonist Ampligen®, and the evaluation Roswell Park presented
earlier this year at AACR, we remain encouraged by Ampligen’s
demonstrated potential to enhance the effectiveness of taxane-based
chemotherapy of breast cancer and potentially other diseases.
Ampligen has continued to demonstrate its potential to deliver
promising clinical activity in an area where there remain
significant immune-related permanent toxicities with the current
standard of care. We are pleased with these additional data and
look forward to continued evaluation of Ampligen’s potential,”
commented Thomas K. Equels, Chief Executive Officer of AIM
ImmunoTech.
About Roswell Park Comprehensive Cancer
Center
Roswell Park Comprehensive Cancer Center is a
community united by the drive to eliminate cancer’s grip on
humanity by unlocking its secrets through personalized approaches
and unleashing the healing power of hope. Founded by Dr. Roswell
Park in 1898, it is the only National Cancer Institute-designated
comprehensive cancer center in Upstate New York. Learn more at
www.roswellpark.org, or contact us at 1-800-ROSWELL
(1-800-767-9355) or ASKRoswell@RoswellPark.org.
About Ampligen
Ampligen is AIM’s dsRNA product candidate being
developed for globally important cancers, viral diseases and
disorders of the immune system. Ampligen has demonstrated in the
clinic the potential for standalone efficacy in a number of solid
tumors. Additionally, Ampligen has shown success in increasing
survival rates and efficacy in the treatment of animal tumors when
used in combination with checkpoint blockade therapies.
Ampligen is currently 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. Ampligen is being
used to treat pancreatic cancer patients in an Early Access Program
approved by the Inspectorate of Healthcare in the Netherlands at
Erasmus Medical Center. Additionally, Ampligen is also approved in
Argentina for the treatment of severe chronic fatigue syndrome and
is currently being evaluated in SARS-CoV-2/COVID-19, myalgic
encephalomyelitis/chronic fatigue syndrome (ME/CFS) and Post COVID
Conditions.
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.
For more information, please visit aimimmuno.com
and connect with the Company on Twitter, 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” 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. Among other things, for those statements, the
Company claims the protection of 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.
1 dx.doi.org/10.1136/jitc-2022-SITC2022.0547
Aim Immunotech (LSE:0A4Y)
Graphique Historique de l'Action
De Jan 2025 à Fév 2025
Aim Immunotech (LSE:0A4Y)
Graphique Historique de l'Action
De Fév 2024 à Fév 2025