Edwards Lifesciences Corporation announced that it received Investigational Device Exemption (IDE) approval from the U.S. Food and Drug Administration (FDA) to initiate a single-arm, non-randomized clinical trial of the SAPIEN 3 transcatheter aortic heart valve in the treatment of intermediate risk patients with severe symptomatic aortic stenosis. The company also completed enrollment in its U.S. clinical trial studying the SAPIEN 3 valve in the treatment of high-risk or inoperable patients. The SAPIEN 3 valve is the only transcatheter heart valve available to U.S. patients that can be delivered through a low-profile 14-French expandable sheath (eSheath).

It also has an outer skirt - a cuff of fabric surrounding the bottom of the frame - to provide a seal to address paravalvular leak. The SAPIEN 3 valve can be implanted with the transfemoral approach through an incision in the leg, as well as alternative access approaches. It is an investigational device that is not available commercially in any country; CE Mark approval in Europe is anticipated in the near future.

The new U.S. trial of the SAPIEN 3 valve will enroll up to 1,000 patients with a Society of Thoracic Surgeons score of 4% to 8%, which indicates the average predicted risk of operative mortality at 30 days. All enrolled patients can receive a SAPIEN 3 valve.