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Updated: Jun 22, 2026

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Published on: February 5, 2021
Efficacy of I(f) inhibition with ivabradine in different subpopulations with stable angina pectoris
Michal Tendera1, Jeffrey S Borer, Jean-Claude Tardif
13rd Division of Cardiology, Medical University of Silesia, Katowice, Poland. michal.tendera@gcm.pl
Insights
Ivabradine effectively reduces angina attacks and nitrate use in stable angina patients. Its benefits are consistent across diverse patient groups, including those with comorbidities, demonstrating broad efficacy.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Ivabradine is a proven antianginal and anti-ischemic agent.
- Previous large-scale trials established its efficacy.
- Subpopulation analyses are crucial for understanding treatment effects in diverse patient groups.
Purpose of the Study:
- To analyze the antianginal efficacy of ivabradine in various patient subpopulations.
- To assess the consistency of ivabradine's effects across different demographic and clinical characteristics.
Main Methods:
- Pooled data from 5 randomized trials involving patients with stable angina pectoris.
- Patients received ivabradine at doses of 5, 7.5, or 10 mg twice daily.
- Subpopulations were defined by age, sex, disease severity, and comorbidities.
Main Results:
- Ivabradine reduced angina attack frequency by 59.4% and nitrate consumption by 53.7% in 2,425 patients.
- Consistent efficacy (51-70% reduction in angina attacks) was observed across all analyzed subpopulations.
- Ivabradine demonstrated a favorable safety and tolerability profile, with a 14.5% heart rate reduction.
Conclusions:
- The antianginal efficacy of ivabradine is consistent across diverse patient subpopulations.
- Ivabradine's effectiveness is maintained regardless of angina severity or the presence of comorbidities.
- The drug exhibits a good safety profile in all assessed patient groups.
Objectives:
The antianginal and anti-ischemic efficacy of ivabradine has been demonstrated in large-scale trials. Pooling trial data allowed for subpopulation analyses of ivabradine's antianginal efficacy.
Methods:
Data on the frequency of angina attacks, short-acting nitrate consumption, and heart rate were pooled from 5 randomized trials in patients with stable angina pectoris receiving 5, 7.5, or 10 mg of ivabradine b.i.d. for 3 or 4 months. The subpopulations were defined according to age, sex, disease characteristics, and comorbidities (severity of angina, history of myocardial infarction, cerebrovascular disease, revascularization status, diabetes, asthma/chronic obstructive pulmonary disease, or peripheral vascular disease).
Results:
Efficacy data were available for 2,425 patients (full analysis set), in whom ivabradine reduced the frequency of diary-based angina attacks by 59.4% and nitrate consumption by 53.7%. All subpopulations experienced 51-70% reductions in the frequency of angina attacks, with similar reductions for the other parameters studied. Ivabradine's efficacy was maintained in the presence of different comorbidities. In the safety set, ivabradine reduced heart rate by 14.5%. Ivabradine had a good safety and tolerability profile in all the subpopulations assessed.
Conclusions:
The antianginal efficacy of ivabradine was consistent across all the subpopulations analyzed, independent of the severity of angina and the presence of a comorbidity.
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