Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination therapy consisting of three agents: - **Rivaroxaban** is an oral direct factor Xa inhibitor anticoagulant that prevents thrombin generation and thrombus development. - **Ticagrelor** is an oral, reversible P2Y12 adenosine diphosphate (ADP) receptor antagonist that inhibits platelet activation and aggregation. - **Acetylsalicylic acid (aspirin)** is an antiplatelet agent that irreversibly inhibits cyclooxygenase-1 (COX-1), reducing thromboxane A2 production and thereby inhibiting platelet aggregation. The combination of these drugs provides both anticoagulant and dual antiplatelet effects. It has been studied in the context of patients with nonvalvular atrial fibrillation undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome, aiming to reduce the risk of cardiovascular events such as myocardial infarction, stroke, or stent thrombosis. However, this triple therapy significantly increases bleeding risk compared to dual regimens[1][6][7]. The use of all three agents together is generally reserved for select high-risk patients under close clinical supervision.
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 rivaroxaban + ticagrelor + acetylsalicylic acid.