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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03473223
Study type Interventional
Source CSL Behring
Contact
Status Completed
Phase Phase 3
Start date March 21, 2018
Completion date November 17, 2023

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