First-in man trial with DREAMS (Drug-Eluting Absorbable Magnesium Scaffold)
- Excellent long-term outcomes at 3 years with a low Target Lesion Failure (TLF) rate and no cardiac death or scaffold thrombosis
- No TLF events were observed after the first year
Target Lesion Failure (TLF) defined as a composite of cardiac death, target-vessel myocardial infarction (TV-MI) and clinically driven Target Lesion Revascularization (cd-TLR) at 6 and 12 months
- Late Lumen Loss (LLL) at 6 and 12 months - Scaffold thrombosis at 1, 24 and 36 months - Cumulative rates of TLF at 1, 24 and 36 months
Reference: Haude M et al. Safety and performance of the drug-eluting absorbable metal scaffold (DREAMS) in patients with de novo coronary lesions: 12-month results of the prospective, multi-centre, first-in-man BIOSOLVE-I trial. Lancet. 2013; 381: 836-44.
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