BIOTRONIK Advances Clinical Evaluation of Latest Generation DREAMS, World's First Bioabsorbable Magnesium Scaffold
Vascular Intervention / Last Patient Enrolled Marks Significant Step Forward in the BIOSOLVE-II Study
"Quite similar to a contemporary drug-eluting stent, but with the advantage of uncaging the vessel in the long run, DREAMS is a truly unique product that offers ease of deliverability and vessel adaptability. I look forward to allowing my patients to take advantage of it in my clinical practice."
DREAMS is an absorbable scaffold that combines the superior mechanical advantages of a metallic stent with a reliable bioabsorption profile that keeps the vessels open while avoiding the long-term disadvantages of permanent metal stents. The scaffold is made out of a magnesium alloy, coated with a bioabsorbable polymer matrix and an anti-proliferative Limus drug and is designed to be absorbed over time, leaving an uncaged vessel.
There are currently only two coronary scaffolds with CE mark, both based on polymer technology. Completion of enrollment in the BIOSOLVE-II trial marks a significant step towards the commercial use of DREAMS as the first bioabsorbable magnesium scaffold.
Building on the results of the BIOSOLVE-I study, which demonstrated the safety of the first generation of DREAMS, BIOSOLVE-II is a prospective, multi-center clinical trial evaluating the safety and performance of DREAMS in its improved design. A total of 122 patients were enrolled in the study with a primary endpoint of in-segment late lumen loss (LLL) at 6 months.
"The refined DREAMS technology represents the optimal balance between vessel scaffolding, absorption profile and drug elution characteristics," commented Dr. Daniel Buehler, BIOTRONIK President, Vascular Intervention. "As a global pioneer in bioabsorbable magnesium, we pride ourselves on soon being able to offer the world's first magnesium scaffold. Supported by the promising clinical data of the BIOSOLVE-I study, I feel confident we will demonstrate the efficacy of this groundbreaking treatment."
The BIOSOLVE-II study has enrolled patients in Germany, Belgium, Denmark, the Netherlands, Switzerland, Spain, Brazil and Singapore.
One of the world's leading manufacturers of cardio- and endovascular medical devices, BIOTRONIK is headquartered in Berlin, Germany, and represented in over 100 countries by its global workforce of more than 5,600 employees. Several million patients have received BIOTRONIK implants designed to save and improve the quality of their lives, or have been treated with BIOTRONIK coronary and peripheral vascular intervention products. Since its development of the first German pacemaker in 1963, BIOTRONIK has engineered many innovations, including BIOTRONIK Home Monitoring®; the world's first 4 F-compatible 200 mm peripheral stent; Orsiro, the industry's first hybrid drug-eluting stent; and the world's first implantable cardioverter defibrillators and heart failure therapy devices with ProMRI® technology.
For more information, visit: www.biotronik.com
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