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.
Seoul National University Hospital, Seoul, Korea, Republic of
Research Site, Beaumont, Texas, United States
Research Site, Linden, New Jersey, United States
Cardiology Department Patras University Hospital, Rio, Achaia, Greece
Agios Andreas General Hospital, Nephrology Department, Patras, Achaia, Greece
Careggi Hospital, Florence, Italy
Research site, Overland Park, Kansas, United States
Cardiology Department Patras University Hospital, Rio, Achaia, Greece
Deutsches Herzzentrum, München, Bavaria, Germany
Klinikum der Ludwig-Maximilians-Universität München, München, Bavaria, Germany
Heart Center Balatonfüred, Dept. of Cardiology, Balatonfüred, Hungary
Vancouver General Hospital, Vancouver, British Columbia, Canada
Cardiology Department Patras University Hospital, Rio, Patras, Greece
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