Anteris Technologies Ltd (ASX: $AVR) has completed the 15-patient US FDA approved Early Feasibility Study (EFS) of DurAVRTM THV to treat severe aortic stenosis, reporting outstanding haemodynamic function and successful treatment of patients. The Company raised $41.3 million during the quarter, with a cash balance of $30.8 million at 31 December 2023.
These haemodynamics are unparalleled. This biomimetic valve not only allows us to have this acute improvement in flow from a classic haemodynamic performance but, also, we've seen (on cardiac MRI) normalisation of laminar flow out of the aorta. It's likely to have significant implications as we think about the long-term durability of the valve, stress on the leaflets but, also, aortopathies, potentially inflammation and other things as well.
Anteris Technologies (ASX: $AVR) has successfully completed the US FDA approved Early Feasibility Study for DurAVRTM THV, demonstrating outstanding haemodynamic function and successful treatment of severe aortic stenosis patients. The Company raised $41.3 million during the quarter and had a cash balance of $30.8 million at 31 December 2023. Anteris continues to evaluate a potential dual listing of its securities on NASDAQ and ASX. The Company is set to revolutionize the structural heart market by delivering clinically superior solutions for significant unmet clinical needs.
Sourcehttps://announcements.asx.com.au/asxpdf/20240131/pdf/05zxldt8910c30.pdf