May 19, 2015
Tokyo, Japan, May 19, 2015 -- Terumo Corporation and the French company Arterial Remodeling Technologies S.A. (ART) announced today that ART has received CE (Mark clearance in Europe for its Pure Bioresorbable Scaffold.
Through an agreement concluded between the companies in March 2014, Terumo acquired exclusive acquisition rights for the coronary drug eluting bioresorbable scaffold technology. The Pure Bioresorbable Scaffold developed by ART will serve as the platform for the next generation of coronary drug eluting bioresorbable scaffolds to be developed by Terumo.
The CE marking for the pure bioresorbable scaffold represents a major step forward for both companies' joint development of a drug-eluting bioresorbable scaffold through the application of the technology and is expected to contribute to accelerating this development in the future.
Jean Fajadet, MD, PhD, Co-Director of Interventional Cardiology at the Clinique Pasteur, in Toulouse, France, commented on the CE marking for the bioresorbable scaffold technology: "Bioresorbable scaffolds have the potential to address unmet needs in daily clinical practice in interventional cardiology."
Terumo and ART will be presenting the bioresorbable scaffold technology at EuroPCR, which is one of the best-known and largest interventional cardiology courses in Europe. The presentation is scheduled during the ART symposium that will be held on May 20, 2015.
Bioresorbable scaffolds, which biodegrade and are resorbed inside the body, are currently attracting attention as a next-generation drug eluting stent technology. Since they do not remain inside the body like conventional metal stents, bioresorbable scaffolds are expected to reduce thrombosis and shorten the duration of antiplatelet therapy. Over five million stents are used worldwide each year. Drug-eluting bioresorbable scaffolds are anticipated to steadily replace them in the future.
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