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Vorapaxar

Generic Name
Vorapaxar
Brand Names
Zontivity
Drug Type
Small Molecule
Chemical Formula
C29H33FN2O4
CAS Number
618385-01-6
Unique Ingredient Identifier
ZCE93644N2
Background

Vorapaxar is a tricyclic himbacine-derived selective inhibitor of protease activated receptor (PAR-1) indicated for reducing the incidence of thrombotic cardiovascular events in patients with a history of myocardial infarction (MI) or with peripheral arterial disease (PAD). By inhibiting PAR-1, a thrombin receptor expressed on platelets, vorapaxar prevents thrombin-related platelet aggregation.

Indication

Vorapaxar is indicated for the reduction of thrombotic cardiovascular events in patients with a history of myocardial infarction (MI) or peripheral arterial disease (PAD). It is usually co-administered with acetylsalicylic acid (ASA) and/or clopidogrel, and should therefore be administered as an addition to these medications as it has not been studied alone.

Associated Conditions
Cardiovascular Events

Trial to Assess the Ocular Safety of Vorapaxar (SCH 530348) in Participants With Atherosclerosis (Study P05183)

Phase 3
Completed
Conditions
Atherosclerosis
Ischemia
Myocardial Infarction
Cerebrovascular Accident
Interventions
First Posted Date
2008-02-15
Last Posted Date
2018-09-21
Lead Sponsor
Merck Sharp & Dohme LLC
Target Recruit Count
258
Registration Number
NCT00617123

Trial to Assess the Effects of Vorapaxar (SCH 530348; MK-5348) in Preventing Heart Attack and Stroke in Particpants With Acute Coronary Syndrome (TRA•CER) (Study P04736)

Phase 3
Terminated
Conditions
Atherosclerosis
Myocardial Infarction
Myocardial Ischemia
Interventions
Drug: Placebo
First Posted Date
2007-09-11
Last Posted Date
2018-09-21
Lead Sponsor
Merck Sharp & Dohme LLC
Target Recruit Count
12944
Registration Number
NCT00527943

Trial to Assess the Effects of Vorapaxar (SCH 530348; MK-5348) in Preventing Heart Attack and Stroke in Patients With Atherosclerosis (TRA 2°P - TIMI 50) (P04737)

Phase 3
Completed
Conditions
Atherosclerosis
Ischemia
Myocardial Infarction
Cerebrovascular Accident
Peripheral Arterial Disease
Interventions
Drug: Placebo
First Posted Date
2007-09-10
Last Posted Date
2018-09-21
Lead Sponsor
Merck Sharp & Dohme LLC
Target Recruit Count
26449
Registration Number
NCT00526474

Safety of SCH 530348 in Subjects Undergoing Non-Emergent Percutaneous Coronary Intervention (Study P03573)

Phase 2
Completed
Conditions
Arterial Obstructive Diseases
Coronary Disease
First Posted Date
2005-08-22
Last Posted Date
2017-05-25
Lead Sponsor
Merck Sharp & Dohme LLC
Target Recruit Count
1030
Registration Number
NCT00132912
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