Abbott Laboratories' Vascular division announced Feb 12. that the first patient has been treated in the 800-patient XIENCE 28 GLOBAL trial, a single arm, 50-center, open label, trial to further evaluate the safety of four-weeks of dual antiplatelet therapy following stenting with a Xience everolimus-eluting stent in patients at a high risk of bleeding. The Xience stents evaluated in the trial include Xience Xpedition, Xience Alpine, Xience Prox, or Xience Sierra.
The primary endpoint of XIENCE 28 GLOBAL is a composite rate of myocardial infarction, stent thrombosis, death, stroke, or major bleeding between one and six months. Abbott is also sponsoring...
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