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 a
new SAB to support advancement of Inflammasome ASC Inhibitor IC 100
for obesity with metabolic complications. Based on its mechanism of
action, IC 100, in combination with incretin therapy, is
anticipated to augment weight loss, but more importantly, to
attenuate the chronic systemic inflammation leading to metabolic
complications and other inflammatory comorbidities of obesity.
“We are honored to work with such an accomplished and esteemed
group of experts,” stated Stephen C. Glover, ZyVersa’s Co-founder,
Chairman, CEO, and President. “Our advisors’ combined expertise and
insights in the areas of obesity, metabolic diseases, and
inflammasomes will be invaluable as we design IC 100’s clinical
development program for obesity and metabolic complications.”
Members of ZyVersa’s Obesity, Metabolic and Inflammatory
Diseases SAB are listed below. Full biographies are available on
ZyVersa's Website.
Caroline M. Apovian, MD, FACP, FTOS, DABOM
- Co-Director, Center for Weight
Management and Wellness, Division of Endocrinology, Diabetes, and
Hypertension at Brigham and Women’s Hospital
- Professor of Medicine, Harvard
Medical School
Harold Bays, MD, MFOMA, FTOS, FACC, FACE, FNLA,
FASPC
- Medical Director and President,
Louisville Metabolic and Atherosclerosis Research Center
- Clinical Associate Professor,
Endocrinology, University of Louisville School of Medicine
- Chief Science Officer of the Obesity
Medicine Association
Helen Bramlett, PhD
- Professor, Department of
Neurological Surgery, University of Miami Miller School of
Medicine
- The Miami Project to Cure Paralysis,
University of Miami Miller School of Medicine
Marc-Andre Cornier, MD
- Professor of Medicine, Medical
University of South Carolina
- Director, Division of Endocrinology,
Diabetes and Metabolic Diseases, Medical University of South
Carolina
Juan Pablo de Rivero Vaccari, PhD
- Associate Professor, Department of
Neurological Surgery, University of Miami Miller School of
Medicine
- The Miami Project to Cure Paralysis,
University of Miami Miller School of Medicine
- Distinguished Faculty Member, the
Center for Cognitive Neuroscience and Aging, University of Miami
Miller School of Medicine
W. Dalton Dietrich, III, PhD
- Kinetic Concepts Distinguished Chair
in Neurosurgery, and Scientific Director,
- The Miami Project to Cure Paralysis,
University of Miami Miller School of Medicine
- Senior Associate Dean for Discovery
Science and Co-Director, the Institute for Neural Engineering,
University of Miami Miller School of Medicine
- Professor, Neurological Surgery,
Neurology, Biomedical Engineering, and Cell Biology, University of
Miami Miller School of Medicine
Robert W. Keane, PhD
- Professor, Physiology and
Biophysics, Neurological Surgery and Microbiology, and Immunology,
University of Miami Miller School of Medicine
- The Miami Project to Cure Paralysis.
University of Miami Miller School of Medicine
Samuel Klein, MD
- William H. Danforth Professor of
Medicine, Washington University School of Medicine
- Director, Center for Human
Nutrition, Washington University School of Medicine
- Chief, Division of Nutritional
Science and Obesity Medicine, Washington University School of
Medicine
Suneil Koliwad, MD, PhD
- Chief, Division of Endocrinology and
Metabolism, UCSF Health
- Gerold Grodsky Professor of Diabetes
Research, UCSF
- Mount Zion Health Fund Distinguished
Professor of Endocrinology, UCSF
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 spread of inflammation 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 with 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 Mediator™ VAR 200. The lead indication for IC 100 is
obesity with 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.
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, Media, and IR Contact:Karen
CashmereChief Commercial
Officerkcashmere@zyversa.com786-251-9641
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