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Clinical Trial Summary

The purpose of this study is to determine if treatment with omecamtiv mecarbil when added to standard of care is well tolerated and superior to placebo in reducing the risk of cardiovascular death or heart failure events in adults with chronic heart failure with reduced ejection fraction (HFrEF).


Clinical Trial Description

This study was conducted by Amgen as the IND holder, with Cytokinetics as a collaborator. Due to the termination of the collaboration agreement between Amgen and Cytokinetics in May 2021 and subsequent transfer of the omecamtiv mecarbil IND from Amgen to Cytokinetics, Cytokinetics is now listed as the sponsor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02929329
Study type Interventional
Source Cytokinetics
Contact
Status Completed
Phase Phase 3
Start date January 6, 2017
Completion date September 14, 2020

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