Galectin Therapeutics to Present Update on its Belapectin Liver Cirrhosis Program at the 20th Edition of Discovery on Target meeting, in Boston, September 25-28, 2023
26 Settembre 2023 - 2:00PM
Galectin Therapeutics, Inc. (NASDAQ: GALT), the leading
developer of therapeutics that target galectin-3, today announced
it will participate in the 20th edition of the Discovery on Target
meeting, the industry’s preeminent event on Novel Drug Targets and
Technologies. The Company will present an update on its belapectin
liver cirrhosis program during the Fibrosis and Inflammation
session. The presentation, titled “Targeting Activated Macrophages
to Improve Liver Cirrhosis: The Discovery and Clinical Translation
of Belapectin,” will take place Wednesday, September
27, at 2:25 PM EDT and will be delivered by Dr. Pol
F. Boudes, M.D., Chief Medical Officer of Galectin Therapeutics.
Boudes commented: “The role of activated macrophages in the
establishment and progression of liver cirrhosis is predominant1.
These cells, when activated, invade the liver, and produce
galectin-3, a pro-inflammatory and pro-fibrotic molecule.
Belapectin is a galectin-3 inhibitor that, thanks to its unique
molecular structure, is captured by activated macrophages and can
inhibit galectin-3 at its site of production. Liver cirrhosis has
been a field that has been neglected for far too long by drug
developers and the Discovery on Target meeting is an excellent
opportunity to familiarize a large audience to the consequences of
liver cirrhosis and portal hypertension and highlight the
opportunity our belapectin program offers for patients affected by
this severe disease.”
1 Ramachandran, et al. Single-cell technologies in hepatology:
new insights into liver biology and disease pathogenesis. Nature
Reviews Gastroenterology and Hepatology 2020;17:457-472.
About BelapectinBelapectin is a complex
carbohydrate drug that targets galectin-3, a critical protein in
the pathogenesis of NASH/MASH and fibrosis. Galectin-3 plays a
major role in diseases that involve scarring of organs, including
fibrotic disorders of the liver, lung, kidney, heart and vascular
system. Belapectin binds to galectin-3 and disrupts its function.
Preclinical data in animals have shown that belapectin has robust
treatment effects in reversing liver fibrosis and cirrhosis. A
Phase 2 study showed belapectin may prevent the development of
esophageal varices in NASH cirrhosis, and these results provide the
basis for the conduct of the NAVIGATE trial. The NAVIGATE trial
(www.NAVIGATEnash.com), titled, “A Seamless Adaptive Phase 2b/3,
Double-Blind, Randomized, Placebo-controlled Multicenter,
International Study Evaluating the Efficacy and Safety of
Belapectin (GR-MD-02) for the Prevention of Esophageal Varices in
NASH Cirrhosis,” is fully enrolled, and further details are posted
on www.clinicaltrials.gov (NCT04365868). Galectin-3 has a
significant role in cancer, and the Company has supported a Phase
1b study in combined immunotherapy of belapectin and Keytruda in
advanced melanoma and in head and neck cancer. This trial provided
a strong rationale for moving forward into a Company-sponsored
Phase 2 development program, which the company is exploring.
About liver cirrhosis due to NASH/MASH and portal
hypertensionNon-alcoholic steatohepatitis (NASH), also
known as MASH, has become a common disease of the liver with the
rise in obesity and other metabolic diseases. NASH is estimated to
affect up to 28 million people in the U.S. It is characterized by
the presence of excess fat in the liver along with inflammation and
hepatocyte damage (ballooning) in people who consume little or no
alcohol. Over time, patients with NASH can develop excessive
fibrosis, or scarring of the liver, and ultimately liver cirrhosis.
Liver cirrhosis is further complicated by portal hypertension which
is one of the main mechanism leading to decompensated liver
cirrhosis. It is estimated that as many as 1 to 2 million
individuals in the U.S. will develop cirrhosis as a result of
NASH/MASH, for which liver transplantation is the only curative
treatment available. Approximately 9,000 liver transplants are
performed annually in the U.S. There are no drug therapies approved
for the treatment of liver cirrhosis.
About Galectin TherapeuticsGalectin
Therapeutics is dedicated to developing novel therapies to
improve the lives of patients with chronic liver disease and
cancer. Galectin’s lead drug belapectin is a carbohydrate-based
drug that inhibits galectin-3, a protein which is directly involved
in multiple inflammatory, fibrotic, and malignant diseases
processes. Belapectin received a Fast Track designation by the U.S.
Food and Drug Administration. The lead development program is liver
cirrhosis caused by non-alcoholic steatohepatitis (NASH), also
known as Metabolic dysfunction-Associated SteatoHepatitis (MASH),
the most advanced form of NASH/MASH-related fibrosis. An additional
development program of belapectin is in combination with
immunotherapy (checkpoint inhibitors) for advanced head and neck
cancers. Advancement of this additional clinical programs is
largely dependent on additional financing and/or finding a suitable
partner. Galectin seeks to leverage extensive scientific and
development expertise as well as established relationships with
external sources to achieve cost-effective and efficient
development. Additional information is available
at www.galectintherapeutics.com.
Forward Looking StatementsThis press release
contains forward-looking statements within the meaning of the
Private Securities Litigation Reform Act of 1995. These statements
relate to future events or future financial performance, and use
words such as “may,” “estimate,” “could,” “expect” and others. They
are based on management’s current expectations and are subject to
factors and uncertainties that could cause actual results to differ
materially from those described in the statements. These statements
include those regarding the hope that Galectin’s development
program for belapectin will lead to the first therapy for the
treatment of fatty liver disease with cirrhosis and those regarding
the hope that our lead compounds will be successful in cancer
immunotherapy and in other therapeutic indications. Factors that
could cause actual performance to differ materially from those
discussed in the forward-looking statements include, among others,
findings of safety of a drug candidate are not indicative of the
drug candidate’s efficacy; that trial endpoints required by the FDA
may not be achieved; Galectin may not be successful in developing
effective treatments and/or obtaining the requisite approvals for
the use of belapectin or any of its other drugs in development; the
Company may not be successful in scaling up manufacturing and
meeting requirements related to chemistry, manufacturing and
control matters; the Company’s current clinical trial and any
future clinical studies as modified to meet the requirements of the
FDA may not produce positive results in a timely fashion, if at
all, and could require larger and longer trials, which would be
time consuming and costly; plans regarding development, approval
and marketing of any of Galectin’s drugs are subject to change at
any time based on the changing needs of the Company as determined
by management and regulatory agencies; regardless of the results of
any of its development programs, Galectin may be unsuccessful in
developing partnerships with other companies or raising additional
capital that would allow it to further develop and/or fund any
studies or trials. Galectin has incurred operating losses since
inception, and its ability to successfully develop and market drugs
may be impacted by its ability to manage costs and finance
continuing operations. Global factors such as coronavirus may
continue to impact NASH patient populations around the globe and
further slow trial enrollment and prolong the duration of the trial
and significantly impact associated costs. For a discussion of
additional factors impacting Galectin’s business, see the Company’s
Annual Report on Form 10-K for the year ended December 31, 2021,
and subsequent filings with the SEC. You should not place undue
reliance on forward-looking statements. Although subsequent events
may cause its views to change, management disclaims any obligation
to update forward-looking statements.
Company Contact:Jack Callicutt, Chief Financial
Officer(678) 620-3186ir@galectintherapeutics.com
Galectin Therapeutics and its associated logo is a registered
trademark of Galectin Therapeutics Inc. Belapectin is the USAN
assigned name for Galectin Therapeutics’ galectin-3 inhibitor
belapectin (GR-MD-02).
Grafico Azioni Galectin Therapeutics (NASDAQ:GALT)
Storico
Da Dic 2024 a Gen 2025
Grafico Azioni Galectin Therapeutics (NASDAQ:GALT)
Storico
Da Gen 2024 a Gen 2025