Micell’s drug-eluting stent meets primary endpoint in non-inferiority study
Micell Technologies‘ sirolimus-eluting absorbable polymer coronary stent met the primary endpoint in the Dessolve III clinical trial, according to 12-month data published at EuroPCR. The stent demonstrated non-inferior safety and effectiveness outcomes compared to Xience‘s everolimus-eluting coronary stent system.
The 1,400-patient study evaluated the MiStent in patients with symptomatic coronary artery disease, including chronic stable angina, silent ischemia and acute coronary syndrome. All study participants qualified for percutaneous coronary interventions.
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The post EuroPCR Roundup: Micell’s drug-eluting stent meets primary endpoint in non-inferiority study appeared first on MassDevice.
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