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.
Houston Methodist Hospital, Houston, Texas, United States
Memorial Hermann Hospital, Houston, Texas, United States
Baylor-St. Lukes Medical Center, Houston, Texas, United States
Clinique Pasteur, Toulouse, Haute-Garonne, France
University Hospital, Nîmes, France
Hospices civils de Lyon, Lyon, France
Korea University Anam Hospital, Seoul, Korea, Republic of
UH Cleveland Medical Center, Cleveland, Ohio, United States
University Hospital Aintree, Liverpool, United Kingdom
Research Site, London, United Kingdom
University Hospital Limerick, Dooradoyle, Limerick, Ireland
Hospital Clínico San Carlos, Madrid, Spain
Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain
Hospital Universitari de Bellvitge - IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain
General Hospital of Heraklion Venizeleio-Pananeio, Heraklion, Crete, Greece
VU University Medical Center, Amsterdam, Noord-Holland, Netherlands
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