CytoSorbents will host investor meetings in San Francisco during the J.P. Morgan Healthcare Conference from January 13-15, 2025.
Quiver AI Summary
CytoSorbents Corporation, a leader in blood purification technologies for critical care, announced that it will host in-person investor meetings in San Francisco during the 43rd Annual J.P. Morgan Healthcare Conference from January 13-15, 2025. The meetings are coordinated by ICR Healthcare, and attendees can schedule meetings with CEO Dr. Phillip Chan and CFO Peter J. Mariani by contacting ICR Healthcare. The company specializes in treating severe conditions in intensive care and cardiac surgery with its proprietary product CytoSorb®, which has broad applications including reducing inflammatory agents in critical illnesses and the removal of blood thinners during surgery. CytoSorb® is already approved in the EU and used in multiple countries, while the company is also working on new products for antithrombotic removal in surgical settings.
Potential Positives
- CytoSorbents Corporation is set to engage with investors at a prestigious healthcare conference, providing an opportunity to enhance visibility and attract interest in their innovative blood purification technologies.
- The company’s lead product, CytoSorb®, has been successfully utilized in over 250,000 procedures globally, demonstrating significant market acceptance and potential for future growth.
- The recent acceptance of the De Novo medical device application for DrugSorb™-ATR by the U.S. FDA indicates progress in the regulatory pathway and potential for new revenue streams in the critical care market.
- Obtaining FDA Breakthrough Device Designations for DrugSorb™-ATR reinforces the innovative nature of CytoSorbents' products and may expedite their development and approval process in the U.S. market.
Potential Negatives
- The press release indicates that CytoSorbents' lead product, CytoSorb®, is not yet approved in the United States, which may limit market access and potential revenue in a significant market.
- The Company’s investigational device DrugSorb™-ATR is also not yet granted or approved in the United States and Canada, which reflects ongoing delays and uncertainties in obtaining regulatory approvals.
- The forward-looking statements include significant caveats and warnings that actual results may differ materially from management's expectations, which could create concern among investors about the reliability of the Company's future projections.
FAQ
What is the purpose of CytoSorbents' upcoming investor meetings?
The meetings aim to provide insights into the company's blood purification technologies and investment opportunities.
When are the investor meetings taking place?
The in-person investor meetings will occur during the 43rd Annual J.P. Morgan Healthcare Conference, from January 13-15, 2025.
How can investors schedule a meeting with CytoSorbents' management?
Investors can schedule a meeting by contacting ICR Healthcare at ir@cytosorbents.com.
What is CytoSorb® and its significance?
CytoSorb® is the company's lead product for blood purification, approved in the EU and used in over 76 countries.
What recent regulatory submissions has CytoSorbents made?
The company submitted a De Novo application for DrugSorb-ATR to the U.S. FDA, accepted for review in October 2024.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
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Full Release
PRINCETON, N.J., Dec. 12, 2024 (GLOBE NEWSWIRE) -- CytoSorbents Corporation (NASDAQ: CTSO), a leader in the treatment of life-threatening conditions in the intensive care unit and cardiac surgery using blood purification, announced today that management will host in-person investors meetings in San Francisco alongside the 43rd Annual J.P. Morgan Healthcare Conference being held January 13-15, 2025, in San Francisco, CA.
ICR Healthcare is coordinating meetings on the Company’s behalf. To schedule a meeting with Dr. Phillip Chan, Chief Executive Officer, and Peter J. Mariani, Chief Financial Officer, please send requests to ICR Healthcare at ir@cytosorbents.com.
About CytoSorbents Corporation (NASDAQ: CTSO)
CytoSorbents Corporation is a leader in the treatment of life-threatening conditions in the intensive care unit and cardiac surgery through blood purification. CytoSorbents’ proprietary blood 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. Cartridges filled with these beads can be used with standard blood pumps already in the hospital (e.g. dialysis, ECMO, heart-lung machines). CytoSorbents’ technologies are used in a number of broad applications. Specifically, two important applications are 1) the removal of blood thinners during and after cardiothoracic surgery to reduce the risk of severe bleeding and 2) the removal of inflammatory agents in common critical illnesses such as sepsis, burn injury, trauma, lung injury, liver failure, cytokine release syndrome, and pancreatitis 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.
CytoSorbents’ lead product, CytoSorb ® , is approved in the European Union and distributed in 76 countries worldwide, with more than 250,000 devices used cumulatively to date. 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, to reduce pro-inflammatory cytokine levels. CytoSorb is not yet approved in the United States.
In the U.S. and Canada, CytoSorbents is developing the DrugSorb™-ATR antithrombotic removal system, an investigational device based on an equivalent polymer technology to CytoSorb, to reduce the severity of perioperative bleeding in high-risk surgery due to blood thinning drugs. It has 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. In September 2024, the Company submitted a De Novo medical device application to the U.S. FDA requesting marketing approval to reduce the severity of perioperative bleeding in CABG patients on the antithrombotic drug ticagrelor, which was accepted for substantive review in October 2024. In November 2024, the Company received its Medical Device Single Audit Program (MDSAP) certification and submitted its Medical Device License (MDL) application to Health Canada . DrugSorb-ATR is not yet granted or approved in the United States and Canada, respectively.
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 website at www.cytosorbents.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, representations and contentions, and the outcome of our regulatory submissions, 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.
U.S. Company Contact:
Peter J. Mariani, Chief Financial Officer
305 College Road East
Princeton, NJ 08540
pmariani@cytosorbents.com
Investor Relations Contact:
Aman Patel, CFA
ICR Healthcare
ir@cytosorbents.com