109 0 Kommentare CARMAT Announces Its Participation in Several Scientific and Investor Conferences During the Second Quarter of 2024 - Seite 2

For more information, please go to www.carmatsa.com and follow us on LinkedIn.

Name: CARMAT
ISIN code: FR0010907956
Ticker: ALCAR

Disclaimer

This press release and the information contained herein do not constitute an offer to sell or subscribe, nor a solicitation of an order to buy or subscribe to CARMAT shares in any country. This press release may contain forward-looking statements by the company regarding its objectives and prospects. These forward-looking statements are based on the current estimates and anticipations of the company's management and are subject to risk factors and uncertainties such as the company's ability to implement its strategy, the pace of development of CARMAT's production and sales, the pace and results of ongoing or planned clinical trials, technological evolution and competitive environment, regulatory changes, industrial risks, and all risks associated with the company's growth management. The company's objectives mentioned in this press release may not be achieved due to these elements or other risk factors and uncertainties.

Significant and specific risks of the company are those described in its universal registration document filed with the French Financial Markets Authority (Autorité des marchés financiers - the “AMF”) under number D.23-0323 and in its amendment filed with the AMF on January 17, 2024 under number D.23-0323-A1. Readers' attention is particularly drawn to the fact that the company's current cash runway is limited to mid-May 2024. Readers and investors are also advised that other risks, unknown or not considered significant and specific, may or could exist.

Aeson is an active implantable medical device commercially available in the European Union and other countries recognizing CE marking. The Aeson total artificial heart is intended to replace the ventricles of the native heart and is indicated as a bridge to transplant for patients suffering from end-stage biventricular heart failure (INTERMACS classes 1-4) who cannot benefit from maximal medical therapy or a left ventricular assist device (LVAD) and who are likely to undergo a heart transplant within 180 days of implantation. The decision to implant and the surgical procedure must be carried out by healthcare professionals trained by the manufacturer. The documentation (clinician manual, patient manual, and alarm booklet) should be carefully read to understand the features of Aeson and the information necessary for patient selection and proper use (contraindications, precautions, side effects). In the United States, Aeson is currently exclusively available as part of an Early Feasibility Study approved by the Food & Drug Administration (FDA).