Study findings point out the device met the primary safety endpoint compared to historical controls but did not demonstrate superiority for the primary hierarchical efficacy endpoint.
Results from the SCOPE II trial were presented at TCT Connect and showed the Acurate Neo failed to demonstrate non-inferiority when compared to Medtronic’s CoreValve Evolut.
The Marlborough, MA-based company received CE mark for the valve in April. Boston Scientific gained access to Acurate when it closed its $435 million acquisition of Symetis.