18-365 - Study to Investigate CSL112 in Subjects With Acute Coronary SyndromeStatus: open
A Phase 3, Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Efficacy and Safety of CSL112 in Subjects with Acute Coronary Syndrome
Treatment for Heart Failure with Iron deficiency
|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.|
SponsorsThis trial is sponsored by Luitpold Pharmaceuticals.
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Providers Associated With This Trial
- Christopher M. Malozzi, D.O.CardiologistAssistant Professor of Internal Medicine
- Bassam A. Omar, M.D., Ph.D., F.A.C.C.CardiologistFellowship Director of Cardiovascular Diseases; Professor of Internal Medicine
- Michael V. Cohen, M.D.CardiologistProfessor of Physiology and Cell Biology
- Ghulam Mustafa Awan, M.D.Interventional CardiologistDirector of Interventional Cardiology and Endovascular Interventions; Associate Professor of Internal Medicine