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Updated: Mar 18, 2026

Evaluation of Cardiac Contractility Modulation Therapy in 2D Human Stem Cell-Derived Cardiomyocytes
Published on: December 16, 2022
Cardiac contractility modulation: a novel approach for the treatment of heart failure
Freddy Abi-Samra1, David Gutterman2
1, 1516 Jefferson Hwy, New Orleans, LA, 70121, USA.
Insights
Cardiac Contractility Modulation (CCM) offers a new device therapy for heart failure patients with reduced ejection fraction. This innovative treatment improves quality of life and exercise tolerance, addressing a gap in current therapeutic options.
Area of Science:
- Cardiology
- Biomedical Engineering
- Medical Devices
Background:
- Heart failure (HF) is a growing global health concern with high mortality and significant economic burden.
- Current medical and device therapies, including beta-blockers, ARBs, and CRT, have limitations and few new approvals in recent years.
- A therapeutic gap exists for HF patients with reduced ejection fraction (EF) who do not qualify for cardiac resynchronization therapy (CRT).
Purpose of the Study:
- To review the preclinical and clinical literature on Cardiac Contractility Modulation (CCM) as a novel therapeutic device for heart failure.
- To describe the implantation procedure and mechanism of action of CCM.
- To highlight CCM's potential to improve outcomes in a specific HF patient population.
Main Methods:
- Review of preclinical and clinical studies on CCM technology.
- Description of CCM device implantation and signal delivery to the right ventricular septum.
- Analysis of cellular mechanisms, including calcium handling and gene expression changes.
- Examination of clinical outcomes from European commercial use and ongoing US trials.
Main Results:
- CCM acutely increases global contractility and chronically improves quality of life, exercise tolerance, and HF symptoms.
- The technology is approved in Europe, with nearly 3000 patients implanted worldwide.
- CCM targets HF patients with reduced EF and normal or prolonged QRS duration, addressing a key unmet need.
- Cellular mechanisms involve improved calcium handling, reversal of fetal gene programming, and reverse remodeling.
- Retrospective studies suggest long-term mortality benefits; a pivotal US trial is nearing completion.
Conclusions:
- Cardiac Contractility Modulation (CCM) is a safe and effective device therapy for heart failure with reduced ejection fraction.
- CCM fills a critical therapeutic gap for patients ineligible for CRT.
- Further evidence from ongoing randomized controlled trials is expected to solidify CCM's role in HF management.
Abstract:
Heart failure is a major health problem worldwide and, despite effective therapies, is expected to grow by almost 50 % over the next 15 years. Five-year mortality remains high at 50 % over 5 years. Because of the economic burden and large impact on quality of life, substantial effort has focused on treatments with multiple medical (beta-blockers, angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (ARB), aldosterone antagonists, and combination of ARB/neprilysin blockers, ivabradine) and device therapies (ICD, CRT) which have been implemented to reduce disease burden and mortality. However, in the past decade only two new medical therapies and no devices have been approved by the US FDA for the treatment of heart failure. This review highlights the preclinical and clinical literature, and the implantation procedure, related to a relatively new therapeutic device for heart failure; cardiac contractility modulation (CCM). CCM delivers a biphasic high-voltage bipolar signal to the RV septum during the absolute refractory period, eliciting an acute increase in global contractility, and chronically producing a sustained improvement in quality of life, exercise tolerance, and heart failure symptoms. The technology is used commercially in Europe with nearly 3000 patients implanted worldwide. Indications include patients with reduced EF and normal or slightly prolonged QRS duration, thus filling an important therapeutic gap among the 2/3 of patients with heart failure who do not meet criteria for CRT. The mechanism by which CCM provides benefit can be seen at the cellular level where improved calcium handling (phosphorylation of phospholamban, upregulation of SERCA-2A), reversal of the fetal myocyte gene program associated with heart failure, and reverse remodeling are observed. Recent retrospective studies indicate a long-term mortality benefit. A pivotal randomized controlled study is currently being completed in the USA. CCM appears to be an effective, safe technology for the treatment of heart failure with reduced ejection fraction.
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