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ZyVersa Therapeutics Highlights Data from Review Article Published in Nature Reinforcing IC 100’s Rationale for Inhibiting ASC and ASC Specks to Attenuate Damaging Inflammation Associated with Various Conditions, Including Obesity and Its Complications

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ZyVersa Therapeutics, Inc. highlights data published in Nature reinforcing the rationale for their Inflammasome ASC Inhibitor IC 100 to combat damaging inflammation associated with obesity and its complications. The drug aims to inhibit inflammasomes and ASC specks to attenuate systemic release of inflammatory cytokines and cell death, potentially offering a therapeutic option for metabolic disorders and cancers linked to obesity.
Positive
  • ZyVersa Therapeutics, Inc. is developing Inflammasome ASC Inhibitor IC 100 to target damaging inflammation associated with obesity and its complications.
  • The drug aims to inhibit inflammasomes and ASC specks, which trigger systemic release of inflammatory cytokines and cell death.
  • Studies have shown that inflammasome activation in fat tissue leads to metabolic disturbances associated with obesity and promotes a pro-tumorigenic microenvironment in cancers linked to obesity.
  • IC 100 blocks formation of NLRP3 and other types of inflammasomes to prevent initiation of the inflammatory cascade and uniquely inhibits ASC specks to reduce the spread of damaging inflammation.
  • The research published in Nature supports the potential therapeutic benefits of Inflammasome ASC Inhibitor IC 100 in treating metabolic syndromes and obesity-related complications.
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  • None.

The exploration of inflammasome activation in the context of obesity is of significant interest, particularly given the global prevalence of obesity-related metabolic disorders. The data suggesting that IC 100, ZyVersa Therapeutics' inflammasome ASC inhibitor, could mitigate the inflammatory response in obesity is promising. From a medical research perspective, the mechanism of action for IC 100 in blocking both NLRP3 and other types of inflammasomes, as well as inhibiting ASC specks, represents a potentially novel approach to addressing the chronic inflammation that contributes to metabolic syndromes. The systemic impact of inflammatory cytokines and the role of macrophages in perpetuating obesity-related inflammation are critical areas of study, as they offer insight into how therapies like IC 100 could disrupt the cycle of inflammation and cell death that leads to metabolic imbalances.

For investors, the development of IC 100 by ZyVersa Therapeutics is a key point of interest. The company's focus on inflammatory and renal diseases taps into a substantial market, with obesity acting as a driver for numerous health complications. The backing of data published in a reputable journal such as Nature adds credibility to ZyVersa's scientific approach and could positively influence investor sentiment. However, it is important to consider the development stage of IC 100 and the regulatory hurdles it must overcome before reaching the market. The investment potential hinges on the successful progression through clinical trials and eventual FDA approval. Investors should weigh the risks associated with clinical-stage biopharmaceutical investments against the potential for IC 100 to meet a significant unmet medical need in a large patient population.

The healthcare industry is increasingly focused on the intersection of inflammation and metabolic diseases and the implications for treatment strategies. ZyVersa's IC 100, if proven effective, could disrupt the current treatment paradigm for obesity-related complications. The specificity of IC 100 in targeting multiple inflammasomes could position it as a first-in-class drug, differentiating it from other anti-inflammatory agents that may have broader and less targeted effects. The potential to inhibit pro-tumorigenic environments related to obesity is another aspect that could have far-reaching implications for the management of obesity-linked cancers. Understanding the competitive landscape and the potential market share that IC 100 could capture is essential for assessing its impact on the healthcare sector.

  • Obesity, which affects over 1.9 billion people worldwide, is a state of low-grade chronic inflammation that causes an array of different metabolic disorders, including insulin resistance, type 2 Diabetes, hypertension, cardiovascular disease, dyslipidemia, and even cancer.
  • The article summarizes data demonstrating that inflammasome activation in fat tissue triggers cell death, known as pyroptosis. Pyroptosis results in systemic release of inflammatory cytokines, IL-1β and IL-18, and ASC specks, which perpetuates and spreads inflammation to other tissues leading to the metabolic disturbances associated with obesity.
  • ZyVersa is developing Inflammasome ASC Inhibitor IC 100, designed to inhibit formation of multiple types of inflammasomes and their associated ASC specks to attenuate initiation and perpetuation of damaging inflammation.

WESTON, Fla., Feb. 28, 2024 (GLOBE NEWSWIRE) -- 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, highlights data published in Nature reinforcing IC 100’s rationale for inhibiting ASC and ASC Specks to attenuate damaging inflammation associated with various conditions, including obesity and its complications.

Studies dating back to 2011 have implicated a pathogenic role for inflammasome activation in initiation of obesity and its metabolic complications. Authors of the review paper published in Nature titled, “Cell death and inflammation during obesity: Know my methods, WAT(son),” reviewed 111 papers, which demonstrated that the state of low-grade chronic inflammation in obesity combined with activated macrophages in adipose tissue result in a vicious cycle of inflammation, cell death, and metabolic dysbalance that together cause metabolic syndromes. This also promotes a pro-tumorigenic microenvironment that induces or supports tumor growth in cancers linked to obesity such as breast, liver, and colon carcinomas.

The authors concluded, “There is no question that macrophage-inflammasome activation triggers systemic inflammation during obesity and it is one of the main culprits of metabolic syndromes.” To read the article, Click Here.

“Obesity, a well-established risk factor for array of different metabolic disorders, including insulin resistance, type 2 Diabetes, hypertension, cardiovascular disease, and cancer, has reached pandemic proportions, and may affect up to two-thirds of the adult population in developed countries,” stated Stephen C. Glover, ZyVersa’s Co-founder, Chairman, CEO and President. “The research published in Nature demonstrates that inflammasome activation in fat tissue triggers cell death. Cell death results in systemic release of inflammatory cytokines, IL-1β and IL-18, and ASC specks, which can perpetuate and spread inflammation to other tissues leading to the metabolic disturbances associated with obesity. This provides support for Inflammasome ASC Inhibitor IC 100 as a potential therapeutic option. By inhibiting ASC, IC 100 blocks formation of NLRP3 and other types of inflammasomes to block initiation of the inflammatory cascade. Likewise, IC 100 uniquely inhibits ASC specks to attenuate spread and perpetuation of damaging inflammation.” To review a white paper summarizing the mechanism of action and preclinical data for IC 100, Click Here.

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, 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.

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 renal and inflammatory diseases who have significant unmet medical needs. The Company is currently advancing a therapeutic development pipeline with multiple programs built around its two proprietary technologies – Cholesterol Efflux Mediator™ VAR 200 for treatment of kidney diseases, and Inflammasome ASC Inhibitor IC 100, targeting damaging inflammation associated with numerous CNS and other inflammatory diseases. For more information, please visit www.zyversa.com.

Cautionary Statement Regarding Forward-Looking 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 guaranteed, and actual results may differ materially from those projected. ZyVersa Therapeutics, Inc (“ZyVersa”) uses words such as “anticipates,” “believes,” “plans,” “expects,” “projects,” “future,” “intends,” “may,” “will,” “should,” “could,” “estimates,” “predicts,” “potential,” “continue,” “guidance,” and similar expressions to identify these forward-looking statements that are intended to be covered by the safe-harbor provisions. Such 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, IR, and Media Contact:
Karen Cashmere
Chief Commercial Officer
kcashmere@zyversa.com
786-251-9641


ZyVersa Therapeutics, Inc. is developing Inflammasome ASC Inhibitor IC 100.

IC 100 inhibits inflammasomes and ASC specks to attenuate systemic release of inflammatory cytokines and cell death.

Studies demonstrated that inflammasome activation in fat tissue leads to metabolic disturbances associated with obesity and promotes a pro-tumorigenic microenvironment in cancers linked to obesity.

IC 100 blocks formation of NLRP3 and other types of inflammasomes.

IC 100 uniquely inhibits ASC specks to reduce the spread of damaging inflammation.

The research published in Nature supports the potential therapeutic benefits of Inflammasome ASC Inhibitor IC 100 in treating metabolic syndromes and obesity-related complications.
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variant pharmaceuticals is an orphan drug company leveraging advanced proprietary technologies to develop best-in-class drugs for patients with rare diseases. our accomplished leadership team, each with more than 15 years of demonstrated success in the biopharmaceutical and medical industries, focuses on assuring that our development efforts serve the needs of all our stakeholders: patients, health care providers, payors, and our investors. our evolving product pipeline is targeted to the $100+ billion orphan drug market. our lead orphan drug candidate is hydroxypropyl beta cyclodextrin (hpβcd) for chronic treatment of two orphan indications, var 200: focal segmental glomerulosclerosis (fsgs) and var 300: alport syndrome (as). both of these conditions are rare progressive forms of kidney disease associated with accumulation of cholesterol and lipids, contributing to impaired kidney function, ultimately leading to dialysis and/or kidney transplantation. hpβcd entraps and removes lipids