Conor CoStar Cleared For European Launch; Firm Modifies U.S. Trial Design
This article was originally published in The Gray Sheet
Executive Summary
Conor Medsystems will launch its CoStar paclitaxel-eluting, cobalt-chromium coronary stent in Europe, having just received a CE mark, the firm said Feb. 17
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Conor Medsystems is already boosting manufacturing capacity in preparation for the U.S. launch of its CoStar drug-eluting stent, though the product is not slated to hit the market until late next year at the earliest
Conor Ramps Up Production Of CoStar Stent To Prep For U.S. Launch
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Conor Corio
Firm announces initiation of the 150-patient RAPID trial to evaluate its Corio pimecrolius-eluting stent in Brazil and Europe on May 11. The drug - licensed from Novartis in March - prevents inflammation, which is believed to be a primary cause of restenosis, according to Conor Medsystems. Data from the study will be compared to historical controls from the firm's EuroSTAR study, which evaluated its CoStar paclitaxel-eluting stent. The trial also will evaluate a reduced duration of anti-platelet therapy following stent implantation. Conor expects to complete enrollment for the RAPID study in the second half of this year, with initial results available in 2007. The firm also plans to test a drug-eluting stent that combines pimecrolius and paclitaxel (1"The Gray Sheet" Feb. 20, 2006, p. 7)...