Have had a Unstable Angina/Non-ST-Elevation Myocardial Infarction (UA/NSTEMI) index event within 10 days prior to randomization

Have had a Unstable Angina/Non-ST-Elevation Myocardial Infarction (UA/NSTEMI) index event within 10 days prior to randomization

Had a medical management strategy decision made with reasonable certainty that neither percutaneous coronary intervention (PCI) nor coronary artery bypass graft (CABG) is planned for treatment of the index event

Had a medical management strategy decision made with reasonable certainty that neither percutaneous coronary intervention (PCI) nor coronary artery bypass graft (CABG) is planned for treatment of the index event

Had at least 1 of 4 specified high-risk features at the time of the UA/NSTEMI event

ST-segment elevation myocardial infarction (STEMI) as the index event

Cardiogenic shock

Refractory ventricular arrhythmias

New York Heart Association (NYHA) Class IV congestive heart failure (CHF) within the previous 24 hours

History of ischemic or hemorrhagic stroke

History of transient ischemic attack (TIA)

History of Intracranial neoplasm

arteriovenous malformation

aneurysm

History of spontaneous gastrointestinal (GI) or non-GI bleeding requiring hospitalization for treatment, unless definitive treatment has occurred and there is low likelihood of recurrence

Hemodialysis or peritoneal dialysis