
Developer of Novel Interventional Tools for Mitral Regurgitation


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Recently, Cardiac Dimensions announced the completion of$53 million(ContractRMB 383 million) ofOversubscribed Series E Financing,Ally Bridge Group (Huiqiao Capital)Led by [Investor Name], with new investor Claret Capital Partners participating, existing investors also provided significant support.
The company designed the Carillon system, which aims to restore natural mitral valve function without damaging the mitral valve leaflets.The company plans to use the funds to complete the pivotal study of the Carillon system in the United States and support the commercialization of the system.

R&D Background
Pathological Mechanism of FMR:Left ventricular dilation in heart failure patients leads to incomplete closure of the anterior and posterior leaflets of the mitral valve, causing blood to regurgitate or leak through the mitral valve. This reduces the amount of oxygen-rich blood delivered by the heart to other parts of the body, impairing cardiac function and exacerbating heart failure. Data shows that up to 74% of heart failure patients suffer from FMR, which is an urgent clinical issue to address.
Current Treatment Status:Transcatheter Mitral Valve Edge-to-Edge Repair (M-TEER) was approved by the FDA for the clinical treatment of primary MR in 2013 and for FMR in 2019, becoming the focus of FMR treatment.
Cardiac Dimensions, Inc. is dedicated to developing novel interventional tools for the treatment of heart failure (HF) and functional mitral regurgitation (FMR). The company has developedCarillon SystemIs aMinimally Invasive Treatment System, Pioneering the reshaping of the mitral valve and improving FMR symptoms.
Product Information


Short Path: Access via the right heart system from the jugular vein, with a shorter path and an implantation time of approximately 1 hour.
Easy to Operate: The percutaneous catheter implantation technique is simple, easy to perform, and has a short learning curve.
Does Not Affect Subsequent Surgery: As an indirect, non-contact mitral valve repair device, it does not affect subsequent heart failure surgical procedures and can be removed if necessary.
Regulation and Commercialization
Carillon Mitral Contour System received Australian Therapeutic Goods Administration (TGA) approval in 2020 and obtained EU MDR certification on April 26, 2023. Market operations have expanded to Australia and Europe, including Kirkland, Washington, Sydney, Australia, and Frankfurt, Germany. Some European countries have provided medical insurance reimbursement, while the United States remains in the research stage. Globally, more than 1,500 patients have been treated with the Carillon system.


Data shows that after treatment with the Carillon Mitral Contour System,Most patients' MR grading and NYHA classification continued to improve over five years. Of these, 58.4% of patients had trace/MR1+ regurgitation, and 57.1% of patients showed improvement in NYHA classification.

In chronic heart failure patients treated with the Carillon device, the 5-year survival rate reached 56.2%, meaning that more than half of the patients survived at least 5 years after receiving Carillon treatment—a positive treatment outcome for chronic heart failure patients.





