Author(s)
Michelson, Alan D.Keywords
Acute Coronary SyndromeAngioplasty, Transluminal, Percutaneous Coronary
Clinical Trials, Phase III as Topic
Dose-Response Relationship, Drug
Drug Administration Schedule
Drug Resistance
Education, Medical, Continuing
Female
Humans
Male
Maximum Tolerated Dose
Membrane Proteins
Platelet Aggregation
Platelet Aggregation Inhibitors
Prognosis
Randomized Controlled Trials as Topic
Receptors, Purinergic P2
Risk Assessment
Survival Analysis
Ticlopidine
Treatment Outcome
Life Sciences
Medicine and Health Sciences
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Show full item recordOnline Access
http://escholarship.umassmed.edu/oapubs/1994https://dx.doi.org/10.1161/ATVBAHA.107.160689
Abstract
The P2Y12 antagonist clopidogrel has a well-established role as an antithrombotic agent in the settings of percutaneous coronary intervention and acute coronary syndromes. However, several challenges remain, including the relatively slow onset of action of clopidogrel and the phenomenon of clopidogrel response variability or "resistance". Novel P2Y12 antagonists, including prasugrel, AZD6140, and cangrelor, have a faster onset of action, as well as more potent, and less variable, inhibition of platelet function ex vivo. Whether this promise will be translated into clinical benefit for patients will be determined by the results of ongoing phase 3 clinical trials.Date
2008-01-05Type
textIdentifier
oai:escholarship.umassmed.edu:oapubs-2993http://escholarship.umassmed.edu/oapubs/1994
http://dx.doi.org/10.1161/ATVBAHA.107.160689