Abbott's Absorb™ Bioresorbable Stent Approved as the First Fully Dissolving Heart Stent in Japan
- Japan approval makes first-of-its-kind medical device available to people in Japan with coronary artery disease who prefer an alternative to a permanent metallic implant
- Japan becomes the latest country to approve Absorb, following recent approvals in the United States and Canada
- More than 150,000(1) people in more than 100 countries have been treated with this novel technology
ABBOTT PARK, Ill., Nov. 7, 2016 /PRNewswire/ -- Abbott (NYSE: ABT) announced today that the Ministry of Health, Labor and Welfare (MHLW) in Japan has approved the company's Absorb bioresorbable heart stent, making the first-of-its-kind medical device commercially available to treat people in Japan with coronary artery disease.
Absorb is the only fully dissolving heart stent approved in Japan for the treatment of heart disease, one of the leading causes of death in Japan and worldwide. An estimated 1.73 million2 people in Japan (population: 127 million) have heart disease, and approximately 71.7 thousand3 people die each year from coronary artery disease, making it the secondary leading cause of death in the country annually. Worldwide, more than 7.4 million people die of heart disease each year.4
"Absorb has the potential to address the unsolved challenges of managing coronary artery disease with conventional drug eluting metallic stents," said Prof. Takeshi Kimura, M.D., Ph.D., director of cardiovascular medicine at Kyoto University Hospital in Japan and the principal investigator of ABSORB JAPAN, the clinical study that led to the MHLW's approval of the device. "Our research, which involved 400 patients at 38 Japanese sites, shows that this fully dissolving stent delivered comparable results to the best-in-class Abbott XIENCE® metallic drug-eluting stent on clinically important measures of safety and efficacy."
Japan ranks as the second-largest single-country market for advanced medical technology behind the United States, where the U.S. Food and Drug Administration (FDA) approved Absorb in July 2016.
While stents are traditionally made of metal, Abbott's Absorb stent is made of a naturally dissolving material, similar to dissolving sutures. Absorb disappears completely5 in approximately three years, once it has done its job of keeping a clogged artery open and promoting healing of the treated artery segment. By contrast, metal stents are permanent implants that may cause future blockages.
"We're very excited to bring the promise of Absorb to patients in Japan," said Deepak Nath, Ph.D., senior vice president, vascular, Abbott. "We believe the Absorb bioresorbable stent can help people live better, healthier lives without the concern of a having a metal implant."
Abbott's Absorb stent, sold commercially as the Absorb GT1 Bioresorbable Vascular Scaffold (BVS) system, has been used to treat more than 150,0001 people in more than 100 countries around the world. Absorb was recently approved in the United States and Canada.
About Abbott:
At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world — in nutrition, diagnostics, medical devices and branded generic pharmaceuticals — that create more possibilities for more people at all stages of life. Today, 74,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
1 Based on worldwide device utilization rate. Data on file at Abbott.
2 Ministry of Health, Labour and Welfare Japan, Patients Survey 2014, http://www.mhlw.go.jp/toukei/saikin/hw/kanja/14/index.html
3 Ministry of Health, Labour and Welfare Japan, Population Survey Report vital statistics 2015: http://www.mhlw.go.jp/toukei/saikin/hw/jinkou/kakutei15/index.html
4 World Health Organization
5 Absorb dissolves except for two pairs of tiny metallic markers that remain in the artery to enable a physician to see where the device was placed.
Logo - http://photos.prnewswire.com/prnh/20150928/271488LOGO
SOURCE Abbott
Related Links
WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM?
Newsrooms &
Influencers
Digital Media
Outlets
Journalists
Opted In
Share this article