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Vorapaxar, Aspirin, and Clopidogrel
This combination therapy inhibits platelet aggregation through multiple pathways: vorapaxar blocks the protease-activated receptor-1 (PAR-1), while aspirin and clopidogrel inhibit different steps in platelet activation and clotting cascade.
This combination therapy inhibits platelet aggregation through multiple pathways: vorapaxar blocks the protease-activated receptor-1 (PAR-1), while aspirin and clopidogrel inhibit different steps in platelet activation and clotting cascade. Used for Acute coronary syndrome, Secondary prevention of cardiovascular events in patients with stable coronary artery disease or peripheral artery disease.
At a glance
| Generic name | Vorapaxar, Aspirin, and Clopidogrel |
|---|---|
| Also known as | Group 4 |
| Sponsor | Inova Health Care Services |
| Drug class | Antiplatelet agent combination |
| Target | PAR-1 (vorapaxar); Cyclooxygenase (aspirin); P2Y12 receptor (clopidogrel) |
| Modality | Small molecule |
| Therapeutic area | Cardiovascular |
| Phase | FDA-approved |
Mechanism of action
Vorapaxar is a PAR-1 antagonist that prevents thrombin-induced platelet activation. Aspirin irreversibly inhibits cyclooxygenase and reduces thromboxane A2 production. Clopidogrel is a P2Y12 receptor antagonist that blocks ADP-induced platelet aggregation. Together, these three agents provide complementary antiplatelet effects to reduce thrombotic events.
Approved indications
- Acute coronary syndrome
- Secondary prevention of cardiovascular events in patients with stable coronary artery disease or peripheral artery disease
Common side effects
- Bleeding
- Dyspepsia
- Bruising
- Headache
Key clinical trials
- Vorapaxar on Thrombin Generation and Coagulability (PHASE4)
- Vorapaxar as an Add-On Antiplatelet Therapy in Patients With and Without Diabetes Mellitus (PHASE4)
- Trial to Assess the Safety and Effects of Vorapaxar in Japanese Subjects With Acute Coronary Syndrome (P04772; MK-5348-016) (PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |