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.
University of Calgary, Calgary, Alberta, Canada
Dr. Mark I. Boulos - Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
University of Florida Jacksonville, Jacksonville, Florida, United States
Shulan (Hangzhou) Hospital, Huangzhou, China
National Institute of Cardiovascular Diseases, Karachi, Sindh, Pakistan
Mazandaran province, Sari,Iran, Sari, Mazandaran, Iran, Islamic Republic of
El-sahel teaching hospital, Cairo, Egypt
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
Kafr Elsheikh University Hospital, Kafr Ash Shaykh, Egypt
Beijing Tiantan Hosptial, Capital Medical University, Beijing, China
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