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BMS-986141 is an orally active, selective small molecule antagonist of the thrombin receptor protease-activated receptor 4 (PAR4). It was developed as an antithrombotic agent to inhibit platelet aggregation and reduce thrombus formation. BMS-986141 has demonstrated potent inhibition of PAR4-mediated platelet activation and aggregation, with additive antithrombotic effects when combined with other antiplatelet therapies such as aspirin or ticagrelor. The drug has been investigated in phase 1 and phase 2 clinical trials for thrombosis, stroke prevention, and coronary artery disease. Its primary developer is Bristol Myers Squibb[1][5][8].
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