Financial & Business, OEM News

MedTech & Irrus Syndicates Lead Study Funding for CroiValve’s Transcatheter Tricuspid Device

The DUO System is a transcatheter heart valve that works in tandem with the native tricuspid valve to restore its function.

By: Michael Barbella

Managing Editor

CroíValve has collected $16 million in Series B funding to help finance an early feasibility study for its DUO System.

Led by the MedTech & Irrus Syndicates, support also came from the company’s current investor slate: Ascentifi, Furthr, Broadview Ventures, Atlantic Bridge University Fund, Enterprise Ireland, Elkstone & SOSV, as well as a new investor, IAG Capital Partners. In conjunction with the financing, Broadview Ventures Director Daniel Gottlieb will join CroiValve’s Board of Directors. Gottlieb has 20 years of experience with medical device and biotechnology companies in business development, marketing, and strategy, and previously served as a CroíValve board observer. IAG Capital Partners Venture Partner Ehsan Jabbarzadeh will take Gottlieb’s place as a CroíValve board observer.
 
The new financing follows a successful European First in Human study (TANDEM I), which demonstrated sustained reductions in tricuspid regurgitation and marked improvements in quality of life for patients treated with the DUO System:

  • 89% of patients experienced > 15-point improvement in the Kansas City Cardiomyopathy Questionnaire (KCCQ)
  • All patients achieved a New York Heart Association (NYHA) classification of I or II post treatment
  • substantial (+63m average) improvement in the 6-minute walk distance (6MWD) 
Proceeds from the financing will be used to fund the TANDEM II Early Feasibility Study, a U.S. Food and Drug Administration-approved, prospective, multicenter study to evaluate the DUO System’s safety and performance in patients with severe or greater symptomatic tricuspid regurgitation (TR). Tricuspid regurgitation is a severe heart condition that occurs when the tricuspid valve in the right side of the heart fails to close properly. TR affects more than 1.6 million U.S. residents and is associated with significant morbidity and reduced life expectancy.
 
The DUO System is a novel transcatheter heart valve that works in tandem with the native tricuspid valve to restore valve function while leaving the patient’s right heart and native valve apparatus untouched through an anchoring mechanism. Designed to treat a broad patient population, the DUO System accommodates the heterogeneity of patient anatomies while avoiding contact with critical structures in the right heart which could lead to complications. The DUO System is also designed to enable a straightforward procedure and reduce the procedural complexity seen with other devices. The procedure is less reliant on expert intraprocedural imaging, enabling a short learning curve with predictable and stable outcomes.
 
“I believe the DUO system can simplify the treatment of TR patients, with a predictable procedure that can be performed with standard imaging techniques. Additionally, with minimal anatomical exclusions, it can reach a broad population. It has the potential to emerge as a meaningful advancement in the field of TR treatment,” said Martin B. Leon, M.D., CroíValve’s Clinical Advisory Board chair and Mallah Family Professor of Cardiology at the Columbia University Irving Medical Center College of Physicians and Surgeons as well as director of the Columbia Center for Interventional Care (CICC) at New York-Presbyterian Hospital/Columbia University Medical Center.
 
“This financing is a testament to the unmet need for treating tricuspid regurgitation and the potential of the DUO System to treat more patients with a reproducible and intuitive procedure. We are excited to bring this technology to the US, with strong support from our shareholder base who are committed to our mission to transform the lives of patients suffering from tricuspid regurgitation,” CroiValve CEO Lucy O’Keeffe stated.
 
CroíValve is a clinical stage medical device company developing a transcatheter device to treat tricuspid regurgitation, with R&D and operations based in Ireland and clinical and regulatory tasks based in the United States. The DUO System is an investigational device and not for sale in any geography.

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