Literature DB >> 26104312

Vorapaxar, a Protease-Activated Receptor-1 Antagonist, a Double-Edged Sword!

Bharti Bhandari1, Bharati Mehta.   

Abstract

Acute coronary syndrome (ACS) constitutes a group of pathophysiological entities resulting from reduced blood flow in the coronary arteries leading to decreased or improper functioning or death of heart muscle. Such patients are usually prescribed combination antiplatelet drug therapy, containing acetylsalicylic acid (aspirin) and an adenosine diphosphate receptor inhibitor to prevent recurrence of ischemic events. The combination prophylactic therapy to certain extend has been successful in preventing secondary complications including ischemic/thrombotic events in these patients. However, research is still on for newer advances in anti-thrombotic therapy that can further prevent secondary complications of Acute Coronary Syndrome. Vorapaxar is a newer drug recommended along with aspirin or clopidogril for prevention of recurrence of cardiac events. Vorapaxar, a thrombin receptor antagonist acts by reversible inhibition of the protease-activated receptor-1 (PAR-1). PAR-1 is expressed on platelets, and it inhibits platelet aggregation, both thrombin-induced and thrombin receptor agonist peptide (TRAP)-induced. Various trials world -wide have documented its efficacy as an anti-platelet agent for preventing recurrent cardiovascular ischemic events but at the expense of increased bleeding complications including intracranial haemorrhage (ICH), when compared to standard therapy alone. For the same reason, vorapaxar is contraindicated in patients with prior stroke, transient ischemic attack and ICH. U.S. Food and Drug Administration (FDA) approved vorapaxar in May 2014 as an antiplatelet agent along with standard anti-platelet therapy for the reduction of recurring thrombotic cardiovascular events in patients with a history of myocardial infarction or with peripheral arterial disease. Vorapaxar is developed and marketed by Merck Sharp Dohme and is available by the brand name 'Zontivity' as 2.5 mg oral tablet equivalent to 2.08 mg of vorapaxar sulfate. There are two patents protecting this drug.

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Year:  2014        PMID: 26104312     DOI: 10.2174/1574890110666150624100815

Source DB:  PubMed          Journal:  Recent Adv Cardiovasc Drug Discov        ISSN: 1574-8901


  3 in total

Review 1.  Astroglia as a cellular target for neuroprotection and treatment of neuro-psychiatric disorders.

Authors:  Beihui Liu; Anja G Teschemacher; Sergey Kasparov
Journal:  Glia       Date:  2017-03-16       Impact factor: 7.452

2.  Vorapaxar: The missing link in antiplatelet therapy!

Authors:  Abhijit S Nair
Journal:  J Anaesthesiol Clin Pharmacol       Date:  2017 Apr-Jun

3.  Inhibition of Protease-Activated Receptor 1 Does not Affect Dendritic Homeostasis of Cultured Mouse Dentate Granule Cells.

Authors:  Gerlind Schuldt; Christos Galanis; Andreas Strehl; Meike Hick; Sabine Schiener; Maximilian Lenz; Thomas Deller; Nicola Maggio; Andreas Vlachos
Journal:  Front Neuroanat       Date:  2016-06-13       Impact factor: 3.856

  3 in total

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