Full Press Release Details
CytoSorbents Announces Closing of $10.3 Million
Registered Direct Offering
Company insiders participated in the transaction
with $435,000 of investment
PRINCETON, N.J., December 13, 2023 - 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, today announces the closing of its previously announced registered
direct offering for the sale by the Company directly to investors of an aggregate of 7,733,090 shares of registered common stock and warrants
to purchase up to 2,706,561 shares of common stock.
Dr. Phillip Chan, Chief Executive Officer of CytoSorbents
stated, "We are pleased to announce the closing of this equity financing, with participation and support from existing institutional
investors, new long-term fundamental investors, as well as all C-level executives and Board Directors, and other key leaders in the Company.
The fundraise represents a key piece of our overall financing strategy which combines equity with non-dilutive debt. Through the anticipated
addition of further debt capital and ongoing expense reductions, we expect to be well-capitalized to fund the operating needs of the Company
through at least the next 18 months. Meanwhile, we are very excited by the expected completion of initial data analysis from our pivotal
U.S. and Canadian STAR-T randomized, controlled trial before the end of this month."
Net proceeds from the offering, after transaction
fees and expenses, are expected to be approximately $9.83 million, excluding any proceeds that may be received upon the exercise of the
warrants. Each warrant is immediately cash exercisable at an exercise price per share of $2.00 and will expire on the fifth anniversary
of the original issue date. Each share of common stock and accompanying warrant to purchase up to 0.35 shares of common stock, were sold
together for a combined purchase price of $1.33, for an aggregate gross purchase price of $10,285,009.70. The Company's executive
officers, directors, and certain non-executive officer employees of the Company also participated in the financing with a combined investment
The Company intends to use the net proceeds from
this offering for general corporate purposes, including to fund clinical and regulatory efforts to file for DrugSorb -ATR marketing
approval in the United States and Canada, to fund clinical studies in the United States and Canada, to support growth initiatives for
CytoSorb , to invest in clinical studies and the generation of new clinical data, and to fund ongoing R&D initiatives and further
About CytoSorbents Corporation
CytoSorbents Corporation is
a leader in the treatment of life-threatening conditions in the intensive care unit and in cardiac surgery through blood purification.
Its lead product, 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 that can lead to massive inflammation, organ failure and patient
death. In these diseases, the risk of death can be extremely high, and there are few, if any, effective 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. At the end of Q3 2023, more than 221,000 CytoSorb devices had been used cumulatively.
CytoSorb was originally launched in the European Union under CE mark as the first cytokine adsorber. Additional CE mark extensions were
granted for bilirubin and myoglobin removal in clinical conditions such as liver disease and trauma, respectively, and for ticagrelor and rivaroxaban removal
in cardiothoracic surgery procedures. CytoSorb has 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. The DrugSorb -ATR
antithrombotic removal system, based on the same polymer technology as CytoSorb, also received two FDA
Breakthrough Device Designations, one for the removal of ticagrelor and
another for the removal of the direct oral anticoagulants (DOAC) apixaban and rivaroxaban in
a cardiopulmonary bypass circuit during urgent cardiothoracic procedures. The Company has completed the FDA-approved, randomized, controlled
STAR-T (Safe and Timely Antithrombotic Removal-Ticagrelor) study of 140 patients at approximately 30 centers in U.S. and Canada to evaluate
whether intraoperative use of DrugSorb-ATR can reduce the perioperative risk of bleeding in patients receiving ticagrelor and undergoing
cardiothoracic surgery. This pivotal study is intended to support U.S. FDA and Health Canada marketing approval for DrugSorb-ATR in this
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
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 9, 2023, 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.
U.S. Company Contact:
305 College Road East