Mitralign Catheter-based Mitral Valve Repair EU Study Completes Enrollment

Cardiac device company Mitralign Inc., says it has completed enrollment in a European study to investigate its lead device, the Mitralign System, in patients with functional mitral regurgitation (FMR). Pending successful outcomes from the study, the company will seek CE Mark approval in the European Union (EU) as a first step toward commercializing the Mitralign System.

Background

FMR is a condition brought on by a single or series of ischemic events, such as a heart attack or by the onset of cardiomyopathy. Patients with FMR often see a progressive enlargement of the heart, stretching open the mitral valve to allow the backflow of blood within the heart, thereby exacerbating the deterioration of heart function.

The Mitralign System utilizes a system of wires and catheters to implant at least one pair of polyester anchors within the mitral annulus, a ring of tissue surrounding the mitral valve. The anchors are then cinched together, reducing the circumference of the mitral valve towards its normal size with a goal to improve heart function and assist in the alleviation of heart failure symptoms.

Mitralign, Inc., is a privately funded venture, with a couple of noteworthy investors keeping their toes in the water. Medtronic and Johnson and Johnson anyone?

Investigator comments 

“Patients with FMR are very sick and often experience a dilation of the heart and the deterioration of heart function, despite optimal medical therapy,” said Georg Nickenig, M.D., Mitralign’s lead investigator and professor at the Universitätsklinikum Bonn in Germany. “It is our hope that this novel device will provide a therapeutic option for these patients and improve their quality of life.”

Company comments

“This is an important milestone for our company and brings our Mitralign System that much closer to patients who suffer this severe heart disease,” said Rick Geoffrion, chief executive officer of Mitralign. “We have completed the enrollment of 61 FMR patients in Europe, and we are in the process of collecting the necessary follow-up data for submission to our notified body in Europe for CE Mark approval. In the meantime, we will continue to enroll patients within our active clinical studies in order to accrue additional data for the medical community. We expect to report results from this trial before the end of 2014.”

Source: Mitralign, Inc., Business Wire

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