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.
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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.
Athens Red Cross Hospital, Athens, Attica, Greece
University of Florida, Jacksonville, Florida, United States
Icahn School of Medicine at Mount Sinai, New York, New York, United States
Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, South Yorkshire, United Kingdom
Università Campus Bio-Medico di Roma, Rome, Italy
Aurora Health Care, St. Luke's Medical Center, Milwaukee, Wisconsin, United States
Research Site, London, United Kingdom
General Hospital of Shenyang Military Region, Shenyang, Liaoning, China
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