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.
Sinai Center for Thrombosis Research, Baltimore, Maryland, United States
Research Site, Tianjin, China
University of Florida, Jacksonville, Florida, United States
University of Florida, Jacksonville, Florida, United States
Sheffield Clinical Research Facility, Sheffield, South Yorkshire, United Kingdom
Medstar Washington Hospital Center, Washington, District of Columbia, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Research centre Aalst, 3201, Aalst, Belgium
Research centre Genk, 3205, Genk, Belgium
Research centre Graz, 4305, Graz, Austria
General Hospital of Chinese People's Armed Police Forces, Beijing, China
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