Data from Randomized Pilot Study, Real-World Use of OrbusNeich's Genous(TM) Bio-engineered R stent(TM) to be Presented in Symposium at EuroPCR 2008
Other Data Presentations to Focus on Use of Pro-Healing Stent with AMI Patients and Those Who Cannot Tolerate Dual-Antiplatelet Therapy
Posted on Thu, May. 08, 2008
By OrbusNeich
HONG KONG, May 8 --
Twelve-month follow-up data from both a
randomized pilot study and the real-world registry use of OrbusNeich's Genous
Bio-engineered R stent, the world's first pro-healing stent, will be presented
next week in a symposium at EuroPCR 2008 in Barcelona, Spain.
The symposium, titled "Clinical Impact of the Pro-Healing Stent," will
take place at noon on May 15. Germano Di Sciascio, M.D., professor and
chairman of cardiology at Campus Biomedico, University of Rome, Italy, will
serve as the chairperson of the symposium and will present 14 month follow up
data on 78 patients treated with the Genous stent.
Jonathan Hill, M.D., of King's College, London, will discuss the
functional importance of endothelial progenitor cells for accelerated natural
healing. Huay-Cheem Tan, M.D., National University Hospital, Singapore will
present on the use of the Genous Bio-engineered R stent in acute myocardial
infarction patients and Michael Kutryk, M.D., Ph.D. of St. Michael's Hospital,
Toronto will focus on the use of the stent in patients who cannot tolerate
dual-antiplatelet therapy.
Robbert de Winter, M.D., Ph.D., director of the catheterization laboratory
at the Academic Medical Center, Amsterdam, will show the 12 month follow-up
data from a 193-patient, single-center, prospective, single blind study called
TRIAS HR Pilot with the Genous stent randomized with a drug eluting stent. In
addition, de Winter will include interim follow up data from patient subsets
in e-HEALING, a monitored, multi-center, worldwide (outside the United States)
prospective registry with 5,000 enrolled patients. Dr de Winter is the
principal investigator of the TRIAS HR Pilot study and co-principal
investigator of the e-HEALING registry.
"We expect the data to strengthen our conviction that Genous is a very
important and promising alternative to drug-eluting stents," said de Winter.
"EuroPCR is the ideal venue at which we can share our findings and demonstrate
the impact that the Genous technology is having on the interventional
cardiology community."
Unlike drug-eluting stents, Genous, which is coated with an antibody,
captures a patient's endothelial progenitor cells (EPCs) to accelerate the
natural healing process. EPCs circulate in the bloodstream and are involved
in the repair of blood vessels. When attracted to the surface of Genous, EPCs
rapidly form an endothelial layer over the stent that provides protection
against thrombus and minimizes restenosis.
OrbusNeich designs, develops, manufactures and markets innovative medical
devices for the treatment of vascular diseases. The company's product
portfolio includes the Genous Bio-engineered R stent, an antibody-coated
device that is the first-ever stent to capture a patient's endothelial
progenitor cells (EPCs) to accelerate the natural healing process following
placement. Other products are stents, balloons and guiding catheters marketed
under the names of Blazer(TM), R stent(TM), Sapphire(TM), Avita(TM), Avita
HP(TM), SafeCut(TM), Lumina(TM) and Saffron.
A global company, OrbusNeich is headquartered in Hong Kong and has
operations in Fort Lauderdale, Fla.; Hoevelaken, The Netherlands; Tokyo; and
Shenzhen, China. OrbusNeich, which has provided cardiology devices to
physicians through its predecessor companies since 1979, today supplies
products to interventional cardiologists in more than 60 countries. For more
information, visit www.OrbusNeich.com.
Editor's Note: OrbusNeich will display the Genous Bio-engineered R stent
at Booth No. F06 at EuroPCR 2008.
SOURCE OrbusNeich
Global Media, David Schull of Russo Partners LLC, +1-212-845-4271 (office), or +1-858-717-2310 (mobile), david.schull@russopartnersllc.com, for OrbusNeich,
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