Healthcare Industry News: SPIRIT II
News Release - June 1, 2007
Abbott Submits XIENCE(TM) V Everolimus Eluting Coronary Stent System Application for U.S. FDA ApprovalSubmission Includes Clinical Data Demonstrating Superiority Over TAXUS(R) Stent in Primary Endpoint
ABBOTT PARK, Ill., June 1 (HSMN NewsFeed) -- Abbott today announced it has completed its application to the U.S. Food and Drug Administration (FDA) to seek U.S. market approval for its XIENCE(TM) V Everolimus Eluting Coronary Stent System to treat coronary artery disease, with the submission of the final module of its Pre-Market Approval (PMA) application. Abbott's PMA submission includes safety and efficacy data from the XIENCE V SPIRIT family of clinical trials, which demonstrated superior results for XIENCE V over the TAXUS® Paclitaxel-Eluting Coronary Stent System in the primary endpoint of reducing vessel re-narrowing (angiographic late loss).
"This is the first-ever PMA submission to include head-to-head clinical trial results that demonstrated superiority of one drug-eluting stent over another in the primary endpoint," said John M. Capek, Ph.D., senior vice president, Abbott Vascular. "With the filing of our third and final PMA module, we have submitted all the pre-agreed data necessary to complete our application for XIENCE V approval in the United States. We look forward to bringing XIENCE V to U.S. physicians and patients."
Abbott's PMA submission for the XIENCE V Everolimus Eluting Coronary Stent System includes data from the following clinical trials:
-- SPIRIT FIRST, a randomized trial comparing the XIENCE V Everolimus Eluting Coronary Stent System with the MULTI-LINK VISION® metallic stent system. SPIRIT FIRST met its primary endpoint and demonstrated no stent thrombosis out to three years.
-- SPIRIT II, a randomized clinical trial evaluating XIENCE V versus TAXUS in Europe and Asia Pacific. SPIRIT II met its primary endpoint and demonstrated the superiority of XIENCE V to TAXUS on in-stent late loss at six months. In-stent late loss is a measure of vessel re-narrowing along the length of the stent.
-- SPIRIT III, a large-scale, randomized pivotal clinical trial comparing XIENCE V to TAXUS in the United States, with additional registry arms in the United States and Japan. SPIRIT III met its primary endpoint and demonstrated the superiority of XIENCE V to TAXUS on in-segment late loss at eight months. In-segment late loss is a measure of vessel re-narrowing along the length of the stent, plus 5 mm beyond the ends of the stent.
"As history unfolds in drug-eluting stent treatment, it has become apparent that there is a critical need for new, next-generation platforms with the potential to improve patient care," said Gregg W. Stone, M.D., of Columbia University Medical Center and the Cardiovascular Research Foundation, New York, and principal investigator in the SPIRIT II and III trials. "Abbott's XIENCE V stent system was designed with the intent of improving upon existing technology, and holds promise for patients as a next-generation treatment in coronary care."
Abbott expects to launch XIENCE V in the United States in the first half of 2008.
The final PMA module that Abbott submitted also requests FDA approval for the PROMUS(TM) Everolimus Eluting Coronary Stent System, which will be distributed by Boston Scientific and is a private-labeled version of the XIENCE V Everolimus Eluting Coronary Stent System. XIENCE V is designed, studied and manufactured by Abbott.
About XIENCE V
XIENCE V was launched in Europe and Asia Pacific in 2006 and is currently an investigational device in the United States and Japan.
The XIENCE V system utilizes everolimus, which has been shown to reduce tissue proliferation in coronary vessels following stent implantation, and one of the world's most popular metallic platforms -- the MULTI-LINK VISION Coronary Stent System.
About Abbott Vascular
Abbott Vascular, a division of Abbott, is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development, and advancing medicine through training and education. Headquartered in Northern California, Abbott Vascular offers a comprehensive portfolio of vessel closure, endovascular and coronary products that are recognized internationally for their safety and effectiveness in treating patients with vascular disease.
Abbott (NYSE: ABT ) is a global, broad-based health care company devoted to the discovery, development, manufacture and marketing of pharmaceuticals and medical products, including nutritionals, devices and diagnostics. The company employs 65,000 people and markets its products in more than 130 countries. Abbott's news releases and other information are available on the company's Web site at http://www.abbott.com.
XIENCE and VISION are registered trademarks of Abbott. TAXUS and PROMUS are registered trademarks of Boston Scientific.
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