Research
Print page Print page
Switch language
Bispebjerg Hospital - a part of Copenhagen University Hospital
Published

Cardiac Myosin Activation with Omecamtiv Mecarbil in Systolic Heart Failure

Research output: Contribution to journalJournal articleResearchpeer-review

DOI

  1. Lower or Higher Oxygenation Targets for Acute Hypoxemic Respiratory Failure

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Sotagliflozin in Patients with Diabetes and Recent Worsening Heart Failure

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Angiotensin-Neprilysin Inhibition in Heart Failure with Preserved Ejection Fraction

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Ticagrelor in Patients with Stable Coronary Disease and Diabetes

    Research output: Contribution to journalJournal articleResearchpeer-review

  • GALACTIC-HF Investigators
View graph of relations

BACKGROUND: The selective cardiac myosin activator omecamtiv mecarbil has been shown to improve cardiac function in patients with heart failure with a reduced ejection fraction. Its effect on cardiovascular outcomes is unknown.

METHODS: We randomly assigned 8256 patients (inpatients and outpatients) with symptomatic chronic heart failure and an ejection fraction of 35% or less to receive omecamtiv mecarbil (using pharmacokinetic-guided doses of 25 mg, 37.5 mg, or 50 mg twice daily) or placebo, in addition to standard heart-failure therapy. The primary outcome was a composite of a first heart-failure event (hospitalization or urgent visit for heart failure) or death from cardiovascular causes.

RESULTS: During a median of 21.8 months, a primary-outcome event occurred in 1523 of 4120 patients (37.0%) in the omecamtiv mecarbil group and in 1607 of 4112 patients (39.1%) in the placebo group (hazard ratio, 0.92; 95% confidence interval [CI], 0.86 to 0.99; P = 0.03). A total of 808 patients (19.6%) and 798 patients (19.4%), respectively, died from cardiovascular causes (hazard ratio, 1.01; 95% CI, 0.92 to 1.11). There was no significant difference between groups in the change from baseline on the Kansas City Cardiomyopathy Questionnaire total symptom score. At week 24, the change from baseline for the median N-terminal pro-B-type natriuretic peptide level was 10% lower in the omecamtiv mecarbil group than in the placebo group; the median cardiac troponin I level was 4 ng per liter higher. The frequency of cardiac ischemic and ventricular arrhythmia events was similar in the two groups.

CONCLUSIONS: Among patients with heart failure and a reduced ejection, those who received omecamtiv mecarbil had a lower incidence of a composite of a heart-failure event or death from cardiovascular causes than those who received placebo. (Funded by Amgen and others; GALACTIC-HF ClinicalTrials.gov number, NCT02929329; EudraCT number, 2016-002299-28.).

Original languageEnglish
JournalThe New England journal of medicine
Volume384
Issue number2
Pages (from-to)105-116
Number of pages12
ISSN0028-4793
DOIs
Publication statusPublished - 14 Jan 2021

    Research areas

  • Aged, Aged, 80 and over, Cardiac Myosins/drug effects, Cardiotonic Agents/adverse effects, Cardiovascular Diseases/mortality, Female, Heart Failure, Systolic/drug therapy, Humans, Male, Middle Aged, Myocardial Contraction/drug effects, Stroke Volume, Urea/adverse effects

ID: 61894279