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Abiomed Europe GmbH Neuenhofer Weg 3 52074 Aachen, Germany http://www.abiomed.com
Contact Ms Ingrid Goldberg +1 978-646-1590
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Abiomed Europe GmbH

Abiomed Receives FDA IDE Approval for Initiation of Door to Unloading (DTU) Prospective Feasibility Study

Study Evaluates the Safety and Feasibility of Unloading of the Left Ventricle with Impella CP® in STEMI Patients, without Cardiogenic Shock

(PresseBox) (Danvers, Mass., )
Abiomed, Inc. (NASDAQ:ABMD), a leading provider of breakthrough heart support and recovery technologies, announced today the U.S. Food and Drug Administration (FDA) approval of a prospective feasibility study to evaluate the use of the Impella CP heart pump for unloading of the left ventricle prior to primary percutaneous coronary intervention (PCI) in patients presenting with ST segment elevation myocardial infarction (STEMI), without cardiogenic shock. This trial will focus on feasibility and safety, and lay the groundwork for a future trial, designed to measure the impact that unloading may have on infarct size related to reperfusion injury, an acceleration of myocardial eqjprq pn iek niqw os cubtvxnyvjeyoetsp, im RYAZS qcbdhvyy.

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