Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cangrelor + ticagrelor is a combination of two antiplatelet agents used to achieve rapid and sustained platelet inhibition in acute settings, such as during percutaneous coronary interventions (PCI), particularly in high-risk patients. **Cangrelor** is a selective, reversible, intravenous P2Y12 receptor antagonist with a nucleotide-mimetic structure, characterized by rapid onset and offset of action, leading to profound platelet inhibition within minutes. **Ticagrelor** is an oral, reversible, allosteric antagonist of the P2Y12 receptor; it binds at a non-ADP site, inducing a conformational change. When combined, cangrelor provides immediate platelet inhibition that bridges the time required for ticagrelor to reach maximal effect. Concomitant administration does not result in a clinically significant drug–drug interaction due to their distinct binding modalities[1][2][3][5][6]. This regimen is particularly relevant in ST-segment elevation myocardial infarction (STEMI) or in clinical scenarios requiring rapid transition from intravenous to oral antiplatelet therapy.
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 cangrelor + ticagrelor.