Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Vorapaxar + clopidogrel is a combination of two oral antiplatelet agents used to reduce the risk of atherothrombotic events such as heart attack and stroke in patients with a history of myocardial infarction or peripheral arterial disease. Vorapaxar is a first-in-class protease-activated receptor-1 (PAR-1) antagonist that inhibits thrombin-induced platelet activation by selectively blocking PAR-1 on platelets[1][6][8]. Clopidogrel is an antiplatelet agent that irreversibly inhibits the P2Y12 subtype of adenosine diphosphate (ADP) receptor on platelets, thereby preventing platelet aggregation[4]. The combination may be used in secondary prevention settings for patients at high risk for cardiovascular events. Vorapaxar was developed by Schering-Plough (now Merck & Co.), while clopidogrel was developed by Sanofi and Bristol Myers Squibb[6].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on vorapaxar + clopidogrel.