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elinogrel : ウィキペディア英語版
elinogrel

Elinogrel (INN,〔(International Nonproprietary Names for Pharmaceutical Substances (INN): Proposed INN List 101 ) 〕 USAN) was an experimental antiplatelet drug acting as a P2Y12 inhibitor. Similarly to ticagrelor and in contrast to clopidogrel, elinogrel was a reversible inhibitor that acted fast and short (for about 12 hours), and it was not a prodrug but pharmacologically active itself. The substance was used in form of its potassium salt, intravenously for acute treatment and orally for long-term treatment. Development was terminated in 2012.
== History ==
The substance was originally developed by Portola Pharmaceuticals, with Phase II clinical trials conducted around 2008–2011. In February 2009, Novartis bought worldwide rights to develop it further, intending to conduct Phase III studies and commercialise the drug.〔Insciences: (Novartis gains worldwide rights to elinogrel, a Phase II anti-clotting compound with potential to reduce risk of heart attack )〕 The development of the drug was terminated in January 2012 by Novartis.〔BioPortfolio: (Novartis drops elinogrel outright )〕

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