Welcome to our dedicated page for Cytosorbents news (Ticker: CTSO), a resource for investors and traders seeking the latest updates and insights on Cytosorbents stock.
CytoSorbents Corporation (NASDAQ: CTSO) develops life-saving blood purification technologies for critical care and cardiac surgery patients. This dedicated news hub provides investors and medical professionals with essential updates about the company’s clinical advancements, regulatory milestones, and strategic initiatives.
Access timely information on earnings reports, product launch announcements, and partnership developments related to CytoSorb® and other polymer adsorption therapies. Our curated collection includes press releases about clinical trial outcomes, European Union regulatory updates, and innovations in cytokine storm management.
Bookmark this page to monitor CTSO’s progress in advancing critical care solutions while staying informed about financial performance and market positioning. Check regularly for verified updates directly from corporate communications and trusted financial news sources.
CytoSorbents Corporation (NASDAQ: CTSO) announced plans to report its Q1 2023 operating and financial results on May 2, 2023, after market close. Management will host a live presentation and Q&A session at 4:30 PM EDT. CytoSorbents specializes in blood purification treatments for critical care, particularly through its flagship product, CytoSorb, which addresses life-threatening conditions by reducing cytokine storms. The product is already approved in the EU and used in over 75 countries, with more than 195,000 devices utilized by the end of 2022. The company has received significant non-dilutive funding, approximately $48 million, from various U.S. government agencies. Forward-looking statements caution investors about potential risks affecting future performance.
CytoSorbents Corporation (NASDAQ: CTSO) announced the successful enrollment of 80 patients in its pivotal STAR-T trial, which is focused on the use of its DrugSorb-ATR system for reducing perioperative bleeding risks in patients undergoing cardiothoracic surgery and treated with ticagrelor. This achievement meets the second enrollment milestone and initiates a Data and Safety Monitoring Board (DSMB) review. The trial aims to enroll 120 patients across 30 centers in the U.S. and Canada and is expected to complete enrollment by summer 2023. Following this, CytoSorbents plans to file for regulatory approval with the U.S. FDA and Health Canada. The DrugSorb-ATR system has previously received FDA Breakthrough Device Designation due to the significant unmet medical need it addresses.
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