A Phase 3, Multicenter, Double-blind, Randomized, Placebo-controlled, Parallelgroup Study to Investigate the Efficacy and Safety of CSL112 in Subjects with Acute Coronary Syndrome (CSL112-3001)
This is a phase 3, multicenter, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the efficacy and safety of CSL112 on reducing the risk of major adverse CV events [MACE - cardiovascular (CV) death, myocardial infarction (MI), and stroke] in subjects with acute coronary syndrome (ACS) diagnosed with either ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI), including those managed with percutaneous coronary intervention (PCI) or medically managed.
CSL112-3001