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CytoSorbents Pre-announces Q4 2016 and Full-Year 2016 Results

Key Takeaway: CytoSorbents Pre-announces Q4 2016 and Full-Year 2016 Results JUNCTION, NJ, January 10, 2017 - CytoSorbents Corporation (NASDAQ: CTSO), a critical care immunotherapy leader commercializing its flagship CytoSorb blood filter to treat deadly inflammation in critically-ill and

Full Press Release Details

CytoSorbents Pre-announces Q4 2016 and
Full-Year 2016 Results
JUNCTION, NJ, January 10, 2017 - CytoSorbents Corporation
(NASDAQ: CTSO), a critical care immunotherapy leader commercializing
its flagship CytoSorb blood filter to treat deadly
inflammation in critically-ill and cardiac surgery patients around the world,
pre-announces unaudited Q4 2016 and Full-year 2016 results ahead of its Form 10-K filing.
2016 Financial Highlights:
Phillip Chan, Chief Executive Officer of CytoSorbents stated, "These results reflect the continued importance and momentum
of our CytoSorb therapy in hospitals around the world. In light of our recent partnership and reimbursement updates, we believe
we are well-positioned for a strong 2017."
About CytoSorbents Corporation (NASDAQ: CTSO)
Corporation is a leader in critical care immunotherapy, specializing in blood purification. Its flagship product, CytoSorb
is approved in the European Union with distribution in 42 countries around the world, as a safe and effective extracorporeal
cytokine adsorber, designed to reduce the "cytokine storm" or "cytokine release syndrome" that could otherwise
cause massive inflammation, organ failure and death in common critical illnesses such as sepsis, burn injury, trauma, lung injury
and pancreatitis, as well as in cancer immunotherapy. These are conditions where the risk of death is extremely high, yet no effective
treatments exist. CytoSorb is also being used during and after cardiac surgery to remove inflammatory mediators,
such as cytokines and free hemoglobin, which can lead to post-operative complications, including multiple organ failure. CytoSorbents
has completed its REFRESH (REduction in FREe Hemoglobin) 1 trial - a multi-center, randomized controlled study that has demonstrated
the safety of intra-operative CytoSorb use in a heart-lung machine during complex cardiac surgery. In 2017, the
company plans to initiate a pivotal REFRESH 2 trial intended to support U.S. FDA approval. CytoSorb has been used
safely in more than 20,000 human treatments to date.
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 in excess of $18 million from DARPA, the U.S. Army, the U.S. Department of Health and Human
Services, the National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI), U.S. Special Operations
Command (SOCOM) and others. The Company has numerous products under development based upon this unique blood purification
technology, protected by 32 issued U.S. patents and multiple applications pending, including CytoSorb-XL, HemoDefend ,
ContrastSorb, DrugSorb, and others. For more information, please visit the Company's websites at www.cytosorbents.com and www.cytosorb.com
Forward-Looking Statements
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, 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 9, 2016, 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.
Cytosorbents Contact:
Public Relations Contact:
Pascale Communications
Last updated: Jan 10, 2017