Suvarna Garge (Editor)

Elinogrel

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Routes of administration
  
By mouth, IV

Legal status
  
Development terminated

Synonyms
  
PRT-060128

ATC code
  
None

Excretion
  
Urine, faeces

Molar mass
  
523.945 g/mol

Elinogrel httpswwwtocriscomimagephpItemId429869

Metabolism
  
Mainly unchanged, ~15% N-demethylation

Routes
  
Oral administration, Intravenous therapy

How to pronounce elinogrel


Elinogrel (INN, 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.

Contents

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. The development of the drug was terminated in January 2012 by Novartis.

References

Elinogrel Wikipedia