FDA approves expanded enrolment of study evaluating novel heart failure device

AccuCinch The FDA has approved an expansion of enrolment of the CorCinch HFrEF early feasibility study, which is evaluating the AccuCinch ventricular repair system (Ancora Heart) for the management of patients with reduced ejection fraction heart failure (HFrEF). This expansion allows Ancora Heart to double patient enrolment from 15 to 30 patients and [...]

2020-02-05T12:34:19+00:00February 5th, 2020|Tags: , , |

TCT 2019: Interim analysis indicates favourable safety profile for AccuCinch

AccuCinch Today at the 2019 Transcatheter Cardiovascular Therapeutics (TCT) meeting (25–29 September, San Francisco, USA), data from an interim analysis of heart failure patients treated in the CorCinch FMR study were presented. These data show, a press release reports, that the AccuCinch ventricular repair system (Ancora Heart) is associated with a favourable safety [...]

2019-09-26T02:50:32+00:00September 26th, 2019|Tags: , , |

First patient enrolled in European study of AccuCinch ventricular repair system

AccuCinch The first patient has been enrolled in the CorCinch EU study, which is a European multicentre clinical evaluation of the AccuCinch ventricular repair system (Ancora Heart) as a treatment for patients with reduced ejection fraction systolic heart failure. This is the second recently initiated study evaluating the AccuCinch system that specifically [...]

2019-08-14T14:24:20+00:00August 14th, 2019|Tags: , |
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