drugset / Trial / NCT01877915

A Study to Assess the Effectiveness and Safety of Rivaroxaban in Reducing the Risk of Death, Myocardial Infarction or Stroke in Participants With Heart Failure and Coronary Artery Disease Following an Episode of Decompensated Heart Failure

NCT01877915 ↗

Phase 3 Completed 5081 enrolled Janssen Research & Development, LLC Bayer · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the effectiveness and safety of rivaroxaban compared with placebo (inactive medication), in reducing the risk of death, myocardial infarction or stroke in participants with heart failure and significant coronary artery disease following an episode of decompensated heart failure.

Timeline

Start
2013-09-10
Primary completion
2018-04-19
Completion
2018-04-19

Outcome

Missed primary endpoint

registry analysis (superiority test); Rivaroxaban vs Placebo; p = 0.270; Hazard Ratio (HR) 0.94 (95% CI 0.84 to 1.05); Log Rank NCT01877915 ↗

paper Rivaroxaban at a dose of 2.5 mg twice daily was not associated with a significantly lower rate of death, myocardial infarction, or stroke than placebo PMID 30146935 ↗

registry analysis (superiority test); Rivaroxaban vs Placebo; p = 0.951; Hazard Ratio (HR) 1.03 (95% CI 0.41 to 2.59); Log Rank NCT01877915 ↗

release “While the COMMANDER HF study demonstrated that rivaroxaban offers no additional benefit on top of standard of care in this group of patients” bayer.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Rivaroxaban Other / unclassified 2.5 mg Oral