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.
University Hospital Kralovske Vinohrady, Prague, Please Select, Czechia
St. Anne's University Hospital Brno, Brno, Czechia
Department of Cardiology, University Hospital Brno-Bohunice, Brno, Czechia
Research Site, London, United Kingdom
University of Florida, Jacksonville, Florida, United States
Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom
Department of Cardiology, Wrocław Medical University, Wrocław, Dolnośląskie, Poland
Department of Cardiology, Dr. A. Jurasz University Hospital, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Kujawsko-pomorskie, Poland
University of Florida, Jacksonville, Florida, United States
Pedro Dorado, Salamanca, Spain
Biotrial Inc, Newark, New Jersey, United States
Thromboela-Stogram, Beijing, China
APHM, Marseille, France
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