Usefulness and safety of vorapaxar in patients with non-ST-segment elevation acute coronary syndrome undergoing percutaneous coronary intervention (from the TRACER Trial).

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Published in Am J Cardiol on June 18, 2014

Authors

Marco Valgimigli1, Pierluigi Tricoci2, Zhen Huang2, Philip E Aylward3, Paul W Armstrong4, Frans Van de Werf5, Sergio Leonardi6, Harvey D White7, Petr Widimsky8, Robert A Harrington9, Angel Cequier10, Edmond Chen11, Yuliya Lokhnygina2, Lars Wallentin12, John Strony13, Kenneth W Mahaffey9, David J Moliterno14

Author Affiliations

1: Thoraxcenter, Erasmus MC, Rotterdam, The Netherlands. Electronic address: m.valgimigli@erasmusmc.nl.
2: Duke Clinical Research Institute, Durham, North Carolina.
3: Flinders University and Medical Centre, Bedford Park, Adelaide, Australia.
4: Division of Cardiology, University of Alberta, Edmonton, Canada.
5: Department of Cardiology, University of Leuven, Leuven, Belgium.
6: Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
7: Green Lane Cardiovascular Service, Auckland, New Zealand.
8: University Hospital Kralovske Vinohrady, Charles University, Prague, Czech Republic.
9: Department of Medicine, Stanford University, Stanford, California.
10: Hospital Universitari de Bellvitge, Universitat de Barcelona, Barcelona, Spain.
11: Bayer HealthCare Pharmaceuticals Inc., Whippany, New Jersey.
12: Department of Medical Sciences, Uppsala Clinical Research Center, Uppsala, Sweden.
13: Merck & Co., Whitehouse Station, New Jersey.
14: Division of Cardiovascular Medicine, Gill Heart Institute, University of Kentucky, Lexington, Kentucky.

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