CytoSorbents Corporation (NASDAQ: CTSO), a leader in the treatment
of life-threatening conditions in the intensive care unit and
cardiac surgery using blood purification via its proprietary
polymer adsorption technology, announces the regulatory approval of
CytoSorb® in Taiwan by the Taiwan Food and Drug Administration
(TFDA). The approved indications include the extracorporeal removal
of cytokines (e.g. cytokine storm, sepsis), bilirubin (e.g. liver
disease), and myoglobin (e.g. trauma) from a patient’s circulating
blood. The removal of the antithrombotic drugs
Brilinta® (ticagrelor, AstraZeneca) and Xarelto® (rivaroxaban,
Janssen/Bayer) during cardiothoracic surgery is also approved, with
the goal of reducing perioperative bleeding. CytoSorb will be
distributed throughout Taiwan by Hemoscien Corporation.
Ms. Bettina Sabisch, Vice President of
International Distributor Sales at CytoSorbents stated, “We are
thrilled to announce this milestone which underscores the value and
efficacy of our CytoSorb therapy and was achieved after navigating
a long and complex approval process. We look forward to
collaborating with Hemoscien and leveraging their long-standing
customer relationships in Taiwan to bring this innovative
therapy to patients in need.”
Mr. Tom Juan, Managing Director of Hemoscien
Corporation emphasized, “There is an ongoing critical need for more
effective therapies to combat infections and to prevent or treat
organ failure. I firmly believe that advanced blood
purification devices such as CytoSorb® can complement the
limitations of traditional pharmaceuticals by restoring peripheral
blood homeostasis and balance. Given the widespread and successful
application of CytoSorb therapy in numerous countries to treat
life-threatening critical illnesses, we are confident in our
ability to take what has been learned and to market and support
CytoSorb in Taiwan's ICU sectors through our deep critical care
network to help save the lives of severely ill patients.”
In addition to Taiwan, CytoSorb is approved in
the European Union and distributed in 75 countries
worldwide. It is an extracorporeal cytokine adsorber
that reduces “cytokine storm” or “cytokine release syndrome” in
common critical illnesses such as sepsis and septic shock, trauma,
acute respiratory distress syndrome, burn injury, pancreatitis, and
others that can lead to massive inflammation, organ failure and
patient death. CytoSorb is also used as an extracorporeal liver
support therapy in acute liver disease (e.g. acute on chronic liver
failure, alcoholic hepatitis) and removes both liver toxins, such
as bilirubin and bile acids, as well as cytokines. It is also used
to treat rhabdomyolysis (e.g. trauma) and the removal of myoglobin.
In these diseases, the risk of death can be extremely high, and
there are few, if any, effective or practical
treatments. CytoSorb is also used during and after
cardiothoracic surgery to remove antithrombotic drugs and
inflammatory mediators that can lead to postoperative
complications, including severe bleeding and multiple organ
failure. As of March 31, 2024, more than 237,000
CytoSorb devices have been used cumulatively around the world.
Taiwan, with approximately 24 million
inhabitants, offers universal coverage to its citizens through its
National Health Insurance System and serves them through a network
of nearly 400 medical centers and regional hospitals. With rising
medical standards, use of advanced technology to increase
administrative and provider efficiency, and access to high quality
healthcare, Taiwan boasts one of the most progressive
healthcare systems globally. Like many other parts of the
world, critical illness including sepsis is a major problem
in Taiwan. For example, there are 150,000 estimated new cases
of sepsis reported each year in Taiwan with mortality rates as high
as 30%, driven by diseases such as pneumonia, which is the third
leading cause of death in Taiwan.
About Hemoscien Corporation
Hemoscien Corporation, a specialized
hemo-epuration service provider, was established in 2008 as a
spinoff from Smile Group Corp., originally founded in 1980. Since
1998, Hemoscien has maintained a strong partnership with Infomed
S.A., a respected ICU hemo-therapy platform developer, achieving
over 50% market share. The company is dedicated to its mission of
addressing unmet medical needs in ICU care, as well as advancing
regenerative medicine and other immune therapies.
About CytoSorbents Corporation (NASDAQ:
CTSO)
CytoSorbents Corporation is a leader in the
treatment of life-threatening conditions in the intensive care unit
and in cardiac surgery through blood purification. CytoSorb, the
Company’s flagship product, was originally launched in the European
Union under CE mark as the first cytokine adsorber. In addition to
the description in the text above, CytoSorb also received FDA
Emergency Use Authorization in the United States for use in adult
critically ill COVID-19 patients with impending or confirmed
respiratory failure.
CytoSorbents’ purification technologies are
based on biocompatible, highly porous polymer beads that can
actively remove toxic substances from blood and other bodily fluids
by pore capture and surface adsorption. Its
technologies have received non-dilutive grant, contract, and other
funding of approximately $50 million from DARPA, the U.S.
Department of Health and Human Services (HHS), the National
Institutes of Health (NIH), National Heart, Lung, and Blood
Institute (NHLBI), the U.S. Army, the U.S. Air Force, U.S. Special
Operations Command (SOCOM), Air Force Material Command (USAF/AFMC),
and others. The Company has numerous marketed products
and products under development based upon this unique blood
purification technology protected by many issued U.S. and
international patents and registered trademarks, and multiple
patent applications pending, including ECOS-300CY®, CytoSorb-XL™,
HemoDefend-RBC™, HemoDefend-BGA™, VetResQ®, K+ontrol™, DrugSorb™,
ContrastSorb, and others. For more information, please
visit the Company’s websites
at www.cytosorbents.com and www.cytosorb.com or
follow us on Facebook and X.
Forward-Looking Statements
This press release includes forward-looking
statements intended to qualify for the safe harbor from liability
established by the Private Securities Litigation Reform Act of
1995. These forward-looking statements include, but are not limited
to, statements about our plans, objectives, future targets and
outlooks for our business, statements about potential exposures
resulting from our cash positions, representations and contentions,
and are not historical facts and typically are identified by use of
terms such as “may,” “should,” “could,” “expect,” “plan,”
“anticipate,” “believe,” “estimate,” “predict,” “potential,”
“continue” and similar words, although some forward-looking
statements are expressed differently. You should be aware that the
forward-looking statements in this press release represent
management’s current judgment and expectations, but our actual
results, events and performance could differ materially from those
in the forward-looking statements. Factors which could cause or
contribute to such differences include, but are not limited to, the
risks discussed in our Annual Report on Form 10-K, filed with the
SEC on March 14, 2024, as updated by the risks reported in our
Quarterly Reports on Form 10-Q, and in the press releases and other
communications to shareholders issued by us from time to time which
attempt to advise interested parties of the risks and factors which
may affect our business. We caution you not to place undue reliance
upon any such forward-looking statements. We undertake no
obligation to publicly update or revise any forward-looking
statements, whether as a result of new information, future events,
or otherwise, other than as required under the Federal securities
laws.
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U.S. Company Contact:Kathleen
Bloch, CFO305 College Road EastPrinceton, NJ 08540+1 (732)
398-5429kbloch@cytosorbents.com
Investor Relations Contact:Eric RibnerLifeSci
Advisors, LLC250 W 55th St, #3401New York, NY 10019+1 (646)
751-4363ir@cytosorbents.com
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