ZyVersa Therapeutics Announces Published Data Supporting the Rationale for Inhibiting Inflammasome ASC with IC 100 to Control Chronic Inflammation
August 07 2024 - 7:50AM
ZyVersa Therapeutics, Inc. (Nasdaq: ZVSA, or “ZyVersa”), a clinical
stage specialty biopharmaceutical company developing first-in-class
drugs for treatment of inflammatory and renal diseases, announces
data published in the peer-reviewed journal, EMBO Molecular
Medicine, demonstrating that extracellular ASC has a crucial role
in aggregation and deposition of amyloid A fibrils leading to
associated chronic inflammatory conditions.
“This research highlighting the role of extracellular ASC
specks, independent of IL-1β, in the pathogenesis of chronic
conditions associated with amyloid A amyloidosis reinforces our
selection of ASC as a target for our inflammasome inhibitor IC
100,” stated Stephen C. Glover, ZyVersa’s Co-founder, Chairman,
CEO, and President. “This paper provides one more piece of evidence
that inhibiting extracellular ASC specks associated with multiple
types of inflammasomes has potential to control damaging
inflammation associated with a broad range of inflammatory
diseases.”
The paper titled, The ASC inflammasome adapter governs
SAA-derived protein aggregation in inflammatory amyloidosis,
summarizes data from in vitro and in vivo research investigating
the role of ASC in inflammation-associated amyloidosis. Following
is a summary of key findings:
- ASC colocalized tightly with SAA in
human AA amyloidosis.
- ASC specks accelerated SAA fibril
formation.
- Splenic amyloid load was decreased
in a Pycard knock-out mouse model of AA Amyloidosis which lacks
ASC.
- Treatment with anti-ASCPYD
antibodies decreased amyloid loads in wild-type mice suffering from
AA amyloidosis.
“Our findings might have therapeutic implications that advance
the fields of protein misfolding disorders (PMDs) and chronic
inflammatory diseases in general as ASC could be a target of
disease-modifying therapies that aim to reduce amyloid deposition
and pathology in various proteinopathies,” concluded the
authors.
About Inflammasome ASC Inhibitor IC 100
IC 100 is a novel humanized IgG4 monoclonal antibody that
inhibits the inflammasome adaptor protein ASC. IC 100 was designed
to attenuate both initiation and perpetuation of the inflammatory
response. It does so by binding to a specific region of the ASC
component of multiple types of inflammasomes, including NLRP1,
NLRP2, NLRP3, NLRC4, AIM2, and Pyrin. Intracellularly, IC 100 binds
to ASC monomers, inhibiting inflammasome formation, thereby
blocking activation of IL-1β early in the inflammatory cascade. IC
100 also binds to ASC in ASC Specks, both intracellularly and
extracellularly, further blocking activation of IL-1β and the
perpetuation of the inflammatory response that is pathogenic in
inflammatory diseases. Because active cytokines amplify adaptive
immunity through various mechanisms, IC 100, by attenuating
cytokine activation, also attenuates the adaptive immune response.
The lead indication for IC 100 is obesity and its associated
metabolic complications. To review a white paper summarizing the
mechanism of action and preclinical data for IC 100, Click
Here.
About ZyVersa Therapeutics, Inc.
ZyVersa (Nasdaq: ZVSA) is a clinical stage specialty
biopharmaceutical company leveraging advanced proprietary
technologies to develop first-in-class drugs for patients with
inflammatory or kidney diseases with high unmet medical needs. We
are well positioned in the rapidly emerging inflammasome space with
a highly differentiated monoclonal antibody, Inflammasome ASC
Inhibitor IC 100, and in kidney disease with phase 2 Cholesterol
Efflux MediatorTM VAR 200. The lead indication for IC 100 is
obesity and its associated metabolic complications, and for VAR
200, focal segmental glomerulosclerosis (FSGS). Each therapeutic
area offers a “pipeline within a product,” with potential for
numerous indications. The total accessible market is over $100
billion. For more information, please visit www.zyversa.com.
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Statements
Certain statements contained in this press release regarding
matters that are not historical facts, are forward-looking
statements within the meaning of Section 21E of the Securities
Exchange Act of 1934, as amended, and the Private Securities
Litigation Reform Act of 1995. These include statements regarding
management’s intentions, plans, beliefs, expectations, or forecasts
for the future, and, therefore, you are cautioned not to place
undue reliance on them. No forward-looking statement can be
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forward-looking statements are based on ZyVersa’s expectations and
involve risks and uncertainties; consequently, actual results may
differ materially from those expressed or implied in the statements
due to a number of factors, including ZyVersa’s plans to develop
and commercialize its product candidates, the timing of initiation
of ZyVersa’s planned preclinical and clinical trials; the timing of
the availability of data from ZyVersa’s preclinical and clinical
trials; the timing of any planned investigational new drug
application or new drug application; ZyVersa’s plans to research,
develop, and commercialize its current and future product
candidates; the clinical utility, potential benefits and market
acceptance of ZyVersa’s product candidates; ZyVersa’s
commercialization, marketing and manufacturing capabilities and
strategy; ZyVersa’s ability to protect its intellectual property
position; and ZyVersa’s estimates regarding future revenue,
expenses, capital requirements and need for additional
financing.
New factors emerge from time-to-time, and it is not possible for
ZyVersa to predict all such factors, nor can ZyVersa assess the
impact of each such factor on the business or the extent to which
any factor, or combination of factors, may cause actual results to
differ materially from those contained in any forward-looking
statements. Forward-looking statements included in this press
release are based on information available to ZyVersa as of the
date of this press release. ZyVersa disclaims any obligation to
update such forward-looking statements to reflect events or
circumstances after the date of this press release, except as
required by applicable law.
This press release does not constitute an offer to sell, or the
solicitation of an offer to buy, any securities.
Corporate, Media, and IR Contact:Karen
CashmereChief Commercial
Officerkcashmere@zyversa.com786-251-9641
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