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Global).","Inclusion Criteria:\n\n* ≥ 18 years\n* Negative pregnancy test\n* Stable or unstable angina, positive functional test, or stable NSTEMI\n* Life expectancy \\>1 year\n* Willing and able to cooperate with study procedures and required follow up evaluations\n\nExclusion Criteria:\n\n* Known hypersensitivity or contraindication to antiplatelet medications or a sensitivity to contrast media which cannot be adequately pre-medicated\n* History of an allergic reaction or significant sensitivity to paclitaxel or any other analogue or derivative\n* Platelet count \\\u003C 100,000 cells\u002Fmm³ or \\> 700,000 cells\u002Fmm³, or a white blood cell (WBC) count \\\u003C 3,000 cells\u002Fmm³\n* Renal insufficiency (or failure)\n* Acute MI\n* Previous PCI of the target vessel within 6 months prior to the procedure\n* Planned PCI of any vessel within 30 days post-index procedure and\u002For planned PCI of the target vessel within 12 months post-procedure\n* History of a stroke or transient ischemic attack (TIA)\n* Active peptic ulcer or upper gastrointestinal (GI) bleeding\n* History of bleeding diathesis or coagulopathy or will refuse blood transfusions\n* Documented left ventricular ejection fraction (LVEF) \\\u003C30%\n* Planned surgery that would cause interruption in recommended DAPT duration per current guidelines\n* Currently participating in an investigational drug or another device study that has not completed the primary endpoint or that clinically interferes with the current study endpoints; or requires additional coronary angiography, IVUS or other coronary artery imaging procedures","ALL","18 Years",{"count":745,"type":746},1205,"ESTIMATED","INTERVENTIONAL",[749],"NA","The purpose of the study is to evaluate the clinical safety and efficacy of the Prevail DCB.",[752],"Coronary Artery 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