In what will no doubt be a disappointment to Abbott Laboratories Inc., three-year follow-up data from the ABSORB II trial did not show that Abbott’s Absorb GT1 everolimus-eluting biodegradable poly(L-lactide) scaffold improved vasomotor reactivity or late-lumen loss compared to Abbott’s Xience metallic everolimus eluting stent.
The results, the first long-term data on a randomized trial of a bioresorbable stent, were presented by Patrick Serruys of...
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