Last updated on April 2019

Study to Investigate CSL112 in Subjects With Acute Coronary Syndrome

Brief description of study

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 Study Identifier: NCT03473223

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8400522 - California Heart Specialists

Huntington Beach, CA United States
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8400371 - Danbury Hospital

Danbury, CT United States
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8400805 - PharmaTex Research

Amarillo, TX United States
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8400631 - North Kansas City Hospital

North Kansas City, MO United States
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8400882 - Reid Health

Richmond, IN United States
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8400752 - Regions Hospital

Saint Paul, MN United States
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8400801 - Wheatley

Nashville, TN United States
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8400896 - Advanced Cardiovascular LLC

Alexander City, AL United States
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8400645 - NEA Baptist Clinic

Jonesboro, AR United States
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8400872 - Chambersburg Hospital

Chambersburg, PA United States
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8400488 - Essentia Health

Duluth, MN United States
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8400678 - The Iowa Clinic, PC

West Des Moines, IA United States
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8400521 - CAET Research

Tyler, TX United States
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8400699 - Suburban Hospital

Bethesda, MD United States
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8400490 - University of Florida

Gainesville, FL United States
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0560028 - AZ Klina

Brasschaat, Belgium
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8400545 - Advanced Heart Care LLC

Bridgewater, NJ United States
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8400515 - Wichita Falls Heart Clinic

Wichita Falls, TX United States
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Recruitment Status: Open

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