4.7 Article

Acute Treatment With Omecamtiv Mecarbil to Increase Contractility in Acute Heart Failure The ATOMIC-AHF Study

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 67, Issue 12, Pages 1444-1455

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2016.01.031

Keywords

arrhythmia; cardiac myosin activator; dyspnea; inotrope

Funding

  1. Amgen, Inc.
  2. Cytokinetics, Inc.
  3. Amgen
  4. Cytokinetics
  5. Mast Therapeutics
  6. Novartis
  7. Sorbent
  8. Trevena
  9. Roche Diagnostics
  10. Otsuka
  11. National Heart, Lung, and Blood Institute
  12. Singulex
  13. Bayer
  14. Servier
  15. Cardiorentis
  16. Vifor
  17. European Union
  18. Abbott
  19. AstraZeneca
  20. Biotronik
  21. Boston Scientific
  22. Johnson Johnson
  23. Medtronic
  24. Merck
  25. Pfizer
  26. Sanofi
  27. Sorin
  28. St. Jude Medical
  29. University of Bergen
  30. Alere
  31. Philips
  32. StealthPeptides
  33. National Institute for Health Research [NF-SI-0611-10227] Funding Source: researchfish

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BACKGROUND Omecamtiv mecarbil (OM) is a selective cardiac myosin activator that increases myocardial function in healthy volunteers and in patients with chronic heart failure. OBJECTIVES This study evaluated the pharmacokinetics, pharmacodynamics, tolerability, safety, and efficacy of OM in patients with acute heart failure (AHF). METHODS Patients admitted for AHF with left ventricular ejection fraction <= 40%, dyspnea, and elevated plasma concentrations of natriuretic peptides were randomized to receive a double-blind, 48-h intravenous infusion of placebo or OM in 3 sequential, escalating-dose cohorts. RESULTS In 606 patients, OM did not improve the primary endpoint of dyspnea relief (3 OM dose groups and pooled placebo: placebo, 41%; OM cohort 1, 42%; cohort 2, 47%; cohort 3, 51%; p = 0.33) or any of the secondary outcomes studied. In supplemental, pre-specified analyses, OM resulted in greater dyspnea relief at 48 h (placebo, 37% vs. OM, 51%; p = 0.034) and through 5 days (p = 0.038) in the high-dose cohort. OM exerted plasma concentration-related increases in left ventricular systolic ejection time (p < 0.0001) and decreases in end-systolic dimension (p < 0.05). The adverse event profile and tolerability of OM were similar to those of placebo, without increases in ventricular or supraventricular tachyarrhythmias. Plasma troponin concentrations were higher in OM-treated patients compared with placebo (median difference at 48 h, 0.004 ng/ml), but with no obvious relationship with OM concentration (p = 0.95). CONCLUSIONS In patients with AHF, intravenous OM did not meet the primary endpoint of dyspnea improvement, but it was generally well tolerated, it increased systolic ejection time, and it may have improved dyspnea in the high-dose group. (Acute Treatment with Omecamtiv Mecarbil to Increase Contractility in Acute Heart Failure [ATOMIC-AHF]; NCT01300013) (C) 2016 by the American College of Cardiology Foundation.

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