COYA 303 is an investigational proprietary biologic combination of
low-dose (LD)-IL-2 and GLP-1 receptor agonist (RA) for subcutaneous
administration with potential for treating inflammation-driven diseases
like Alzheimer's Disease, and other neurodegenerative and autoimmune
diseases
COYA 303 significantly reduced peripheral pro-inflammatory cell
expansion, enhanced Regulatory T Cell function, attenuated CNS
inflammation, and shifted macrophages to an anti-inflammatory phenotype,
compared to controls
COYA-303 may represent a next-generation dual immunomodulatory
GLP-1–based therapy uniting the Nobel Prize–recognized science of
regulatory T cells (Tregs) with the emerging immune benefits of GLP-1
receptor agonists.
Representative Data for Systemic Tregs and Immunomodulation Credit: Coya
Therapeutics, Inc.
HOUSTON--(BUSINESS WIRE)-- Coya
Therapeutics, Inc. (NASDAQ: COYA) (“Coya” or the “Company”), a
clinical-stage biotechnology company developing biologics intended to
enhance regulatory T cell (Treg) function, today announced results of an
in vivo animal study designed to evaluate the effects of COYA 303 (LD
IL-2 and GLP-1RA investigational proprietary biologic combination) in a
well-characterized
in vivo lipopolysaccharide (LPS) preclinical mouse
model of systemic and neurologic inflammation. Results from this completed
study confirmed the interim findings previously reported by the Company.
Dr. Fred Grossman, Coya’s Chief Medical Officer, stated, “This study
strengthens our multi-targeted approach developing new therapies for
diseases of high unmet need. COYA 303 has shown synergistic effects reducing
peripheral and central inflammation in vitro and in vivo. We believe this
supports our combination approach with potential development in
neurodegenerative diseases.”
Dr. Arun Swaminathan, Coya’s CEO, stated, “We believe the data supports the
potential of COYA-303 to improve the efficacy of GLP-1 RA in
neurodegenerative diseases like Alzheimer's Disease in a synergistic manner.
The anticipated readout of the Novo Nordisk EVOKE and EVOKE+ trials studying
semaglutide, a GLP-1 RA in patients with mild Alzheimer’s Disease will
inform our strategy moving forward.”
Study Highlights:
In this animal model, mice received daily injections of LPS for five days to
induce a moderate but sustained inflammatory response representative of
chronic inflammation seen in neurodegenerative disease. Animals were treated
with daily injections of COYA 303 for four days, starting a day after
initiation of LPS injections. The study control groups included the
individual components of COYA 303, vehicle-only, and LPS-only treated
animals.
Coya intends to publish a full dataset which the Company believes
demonstrates that COYA 303 significantly modulates multiple systemic and
central nervous system immune parameters and shifts monocytes from a
pro-inflammatory to an anti-inflammatory phenotype. Moreover, the Company
believes COYA 303 has significant effects on multiple Treg-associated
activation and functional markers, indicating enhanced Treg stability and
suppressive capacity.
About Coya Therapeutics, Inc.
Headquartered in Houston, TX, Coya Therapeutics, Inc. (Nasdaq: COYA) is a
clinical-stage biotechnology company developing proprietary treatments
focused on the biology and potential therapeutic advantages of regulatory T
cells (“Tregs”) to target systemic inflammation and neuroinflammation.
Dysfunctional Tregs underlie numerous conditions, including
neurodegenerative, metabolic, and autoimmune diseases. This cellular
dysfunction may lead to sustained inflammation and oxidative stress
resulting in lack of homeostasis of the immune system.
Coya’s investigational product candidate pipeline leverages multiple
therapeutic modalities aimed at restoring the anti-inflammatory and
immunomodulatory functions of Tregs. Coya’s therapeutic platforms include
Treg-enhancing biologics, Treg-derived exosomes, and autologous Treg cell
therapy.
For more information about Coya, please visit
www.coyatherapeutics.com
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impact of all factors on our business or the extent to which any factor, or
combination of factors, may cause actual results to differ materially from
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Source: Coya Therapeutics, Inc.