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Veliflapon is an investigational small molecule drug that acts as a selective inhibitor of the enzyme 5-lipoxygenase activating protein (FLAP). By inhibiting FLAP, veliflapon blocks the biosynthesis of leukotrienes, which are inflammatory mediators implicated in cardiovascular disease. Veliflapon has been primarily developed for the prevention of acute cardiovascular events such as heart attack and stroke in patients with coronary artery disease. The drug has reached Phase 3 clinical trials, notably being studied for its efficacy in reducing risk among African American patients with a history of unstable angina or myocardial infarction. It was originally developed by deCODE genetics[8][10].
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