Io Therapeutics, Inc., presented data from studies of IRX4204, the company’s phase II clinical development stage, highly selective third generation RXR nuclear receptor agonist compound, supporting its potential use for prevention and treatment of normal
July 09 2024 - 8:00PM
Io Therapeutics, Inc., presented today results from studies done on
the potential for prevention and treatment of normal aging-related
neurodegeneration, Parkinson’s disease (PD), and Alzheimer’s
disease (AD), with its clinical stage experimental therapeutic RXR
nuclear receptor agonist compound IRX4204. IRX4204 is a highly
potent and highly selective, orally available, brain penetrant,
third generation RXR agonist compound which has been tested in
early phase clinical trials in patients with Parkinson’s disease or
cancers. The presentation titled “The highly potent and
selective RXR agonist compound IRX4204 is a potential treatment for
normal aging-related neurodegeneration, Parkinson’s disease (PD),
and Alzheimer’s disease (AD)” was delivered at the Federation of
American Societies for Experimental Biology (FASEB) Seventh
International Conference on Retinoids, being held in St. Paul,
Minnesota, USA. The presentation was authored by Vidyasagar
Vuligonda, Ph.D., Chief Science Officer of the company and inventor
of IRX4204, and Martin E. Sanders, M.D., the company’s Chief
Executive Officer.
Normal aging-related neurodegeneration has been reported to be
substantially related to chronic low-grade inflammation in the
brain, so called neuro-inflammaging. Neuro-inflammaging results in
chronic loss of myelinated nerve fibers, causing disruption of
functional neuroelectrical connections between neurons in various
parts of the brain. Chronic neuro-inflammaging eventually leads to
death of neurons. These neurodegenerative processes produce loss of
memory and cognitive functions, and other functional disabilities
in patients with normal brain aging, and in diverse types of
neurological conditions including PD, and AD.
Neuro-inflammaging is related to imbalance of immunosuppressive
T-regulatory cells (Treg) with pro-inflammatory cytokine
interleukin-17 (IL-17) overproducing T-cells (Th17) in the brain.
Neuro-inflammaging also is related to overactivity of brain
microglia, which produce the pro-inflammatory cytokine
interleukin-6 (IL-6), and other pro-inflammatory factors.
Parkinson’s disease (PD) and Alzheimer’s disease (AD) brains
manifest similar neuro-inflammaging pathologies to those observed
in normal brain aging, but also have distinct pathologies related
to deposition of abnormal misfolded proteins such as alpha
synuclein in PD, and beta amyloid in AD. It is generally accepted
within the neurodegenerative diseases research community that
neuro-inflammaging establishes an at-risk environment within the
brain, that may increase vulnerability for development of PD, AD,
and other neurodegenerative diseases.
The presented studies showed that IRX4204 promotes
differentiation and growth of immunosuppressive human Tregs, and
inhibits differentiation of pro-inflammatory human Th17 cells,
while reducing production of IL-17. IRX4204 also inhibits
production by microglia of IL-6 and other pro-inflammatory factors.
In addition, IRX4204 promotes differentiation and growth of
myelin-producing oligodendrocytes in vitro and promotes myelinated
nerve fiber protection and repair (remyelination) in mouse models
of demyelination. IRX4204 demonstrated direct beneficial effects
alone, and additively in combination with insulin, or thyroid
hormone on cortical neurons in vitro, promoting neurite outgrowth,
a neuro-reparative mechanism by which damaged neurons may
re-establish function-preserving connections with other neurons.
These findings support the potential for IRX4204 protecting against
or even reversing neuro-inflammaging-induced chronic loss of
myelinated nerve fibers and neuronal damage in normal brain aging
and neurodegenerative diseases.
Further demonstration of IRX4204 beneficial effects in
neurodegeneration was provided by in vivo studies in rodent models
of PD, and AD. IRX4204 effectively reduced motor deficits in a rat
PD model while increasing dopaminergic neuron survival in the rat
brains. In a transgenic beta amyloid mouse model of AD, IRX4204
decreased deposition of new beta amyloid in the mouse brains while
preserving memory functions in the mice.
IRX4204 has demonstrated safety and tolerability of oral dosing
in phase I and II clinical trials in 85 patients with various
cancers and 15 patients with PD for up to 20 months of continuous
treatment. In PD patients, IRX4204 demonstrated brain penetrance,
and improvement of motor functions in 13 of 15 patients in open
label assessments. The company is planning to initiate a
placebo-controlled phase II clinical trial of IRX4204 in
Parkinson’s disease patients in Q4 of 2024, to further demonstrate
safety and efficacy in PD patients.
Dr. Vuligonda stated, “Our results identify a new approach to
potentially slowing or reversing the neurodegeneration of normal
aging, as well as treating the pathologic conditions of Parkinson’s
disease and Alzheimer’s disease, which cause seriously disabling
chronic decline of cognitive and other functional
abilities.”
Dr. Sanders stated, “IRX4204 has been safe and well tolerated in
patients and has potential to be an effective monotherapy for
prevention or treatment of debilitating neurologic manifestations
associated with normal aging, Parkinson’s disease, Alzheimer’s
disease and other neurologic conditions. In addition,
IRX4204 provides opportunities for future development of
combination treatments with even greater efficacy for these
conditions, by administering IRX4204 with other generally
well-tolerated and already available agents, such as insulin, GLP-1
agonists, other neurotrophic factors, thyroid hormone, or anti-beta
amyloid monoclonal antibodies. We believe multi-agent combination
treatments including IRX4204 will enable development of well
tolerated, highly effective preventative and therapeutic
interventions for diverse types of neurodegenerative diseases.”
About Io Therapeutics: Io Therapeutics, Inc. is a
privately held company headquartered in Spring, Texas.
More information on Io Therapeutics and its product development
programs is available on the company’s web
site: www.io-therapeutics.com
Forward Looking Statements: This news release contains
"forward-looking statements" within the meaning of the safe harbor
provisions of the United States Private Securities Litigation
Reform Act of 1995.
Contact:
info@io-therapeutics.com