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.
Ling Tao, Xi'an, Shannxi, China
Dep. Cardiology, Skånes universitetssjukhus, Lund, Sweden
Severance Hospital, Yonsei University Health System, Seoul, Korea, Republic of
Kardiologen, Gothenburg, Sweden
Nova Scotia Health, Halifax, Nova Scotia, Canada
Local Institution - 0001, Edinburgh, United Kingdom
Brigham and Women's Hospital, Boston, Massachusetts, United States
Wroclaw Medical University, Wrocław, Dolnośląskie, Poland
University of Alabama Hospital, Birmingham, Alabama, United States
University of South Alabama University Hospital, Mobile, Alabama, United States
St. Joseph's Hospital and Medical Center, Phoenix, Arizona, United States
The First Affiliated Hospital of Dalian Medical University, Dalian, China
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