Ticagrelor, or AZD6140, was first described in the literature in 2003. Ticagrelor is an ADP derivative developed for its P2Y receptor antagonism. Unlike clopidogrel, ticagrelor is not a prodrug. It is marketed by Astra Zeneca as Brilinta in the US and Brilique or Possia in the EU,.
Ticagrelor was granted EMA approval on 3 December 2010.
Ticagrelor was granted FDA approval on 20 July 2011.
Ticagrelor is indicated to reduce the risk of cardiovascular death, myocardial infarction, and stroke in patients with acute coronary syndrome or a history of myocardial infarction. Ticagrelor is also indicated to reduce the risk of a first myocardial infarction or stroke in high risk patients with coronary artery disease.
Medstar Washington Hospital Center, Washington, District of Columbia, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Research centre Aalst, 3201, Aalst, Belgium
Research centre Genk, 3205, Genk, Belgium
Research centre Graz, 4305, Graz, Austria
General Hospital of Chinese People's Armed Police Forces, Beijing, China
London Health Sciences Centre, London, Ontario, Canada
Careggi Hospital, Florence, Italy
Fletcher Allen Health Care, Burlington, Vermont, United States
Universitätsklinikum Aachen, Aachen, Germany
Deutsches Herzzentrum München, Munich, Bavaria, Germany
Klinikum Wels-Grieskirchen, Wels, Austria
Research Site, Overland Park, Kansas, United States
Loyola University Medical Center, Maywood, Illinois, United States
The Feinstein Institute for Medical Research, Manhasset, New York, United States
Humber River Hospital, Toronto, Ontario, Canada
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