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Drug-Eluting Stents: Can the Market Rebound from Recent Setbacks?Published by: Decision Resources Published: Apr. 27, 2007 - 17 Pages The price of this report has been reduced due to its age. The original price was $2,025 for PDF.Table of Contents
AbstractA few years after their introduction in 2002, drug-eluting stents had all but replaced bare-metal stents in the treatment of coronary heart disease, capturing up to 90% of the market. Physicians favored the new stents primarily because of their ability to minimize the risk of restenosis associated with bare-metal stents. Recently, however, new safety concerns have begun to erode the market share of drug-eluting stents. The promise of next-generation drug-eluting stents that are beginning to emerge—including Medtronic’s Endeavor, expected to launch in the United States in late 2007, and Abbott’s Xience, currently in clinical trials in the United States and Japan—is likely to help the drug-eluting stent market rebound from its current low. However, lingering safety concerns and the possibility of competitive pricing may keep the market from achieving its earlier high.Get the Answers You Need to Shape Your Strategy
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