The selective cardiac myosin activator did not improve exercise capacity in a phase 3 trial.
Physical activity intolerance is a common symptom of heart failure (HF). Omecamtiv mecarbil, a non–FDA-approved selective cardiac myosin activator, improved cardiac performance and resulted in modest improvements in first HF events in the GALACTIC-HF trial. The current manufacturer-sponsored, randomized, placebo-controlled trial, METEORIC-HF, assessed the impact of omecamtiv on exercise capacity measured by peak VO2 during cardiopulmonary testing.
The patient population comprised 276 individuals (median age, 64 years; 15% women; 11% racial/ethnic minority) with symptomatic HF with reduced ejection fraction (HFrEF), elevated N-terminal pro-B-type natriuretic peptide level, and reduced exercise capacity (≤75% of predicted VO2; median, 14.2 mL/…
Reviewing Author
DisclosuresConsultant/Advisory BoardBristol Myers Squibb; CPC Clinical Research
Grant/Research SupportNational Heart, Lung, and Blood Institute
Editorial BoardsUpToDate; American College of Cardiology Self-Assessment Program (SAP)
Leadership Positions in Professional SocietiesAmerican College of Cardiology (Chair, Innovations Committee)
DisclosuresConsultant/Advisory BoardBristol Myers Squibb; CPC Clinical Research
Grant/Research SupportNational Heart, Lung, and Blood Institute
Editorial BoardsUpToDate; American College of Cardiology Self-Assessment Program (SAP)
Leadership Positions in Professional SocietiesAmerican College of Cardiology (Chair, Innovations Committee)