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.
Kharkiv City Clinical Hospital #8, Kharkiv, Ukraine
Altnagelvin Area Hospital, Londonderry, United Kingdom
Golden Jubilee Hospital, Clydebank, United Kingdom
Faculty Hospital Kralovske Vinohrady, Prague, Czechia
Chinese People's Liberation Army General Hospital, Peking, Beijing, China
Teipei Veterans General Hospital, Taipei, Taiwan
Peking Union Medical College Hospital, Beijing, Beijing, China
The Royal Wolverhampton NHS Trust, Wolverhampton, United Kingdom
Wuhan Asia Heart Hospital, Wuhan, Hubei, China
Kantonsspital Aarau Klinik für Neurologie, Aarau, Switzerland
Ospedale Civile di Mirano, Department of Cardiology, Mirano, Italy
Ghent University Hospital - Dept thoracic and vascular surgery, Ghent, Belgium
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