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TUSTIN, Calif., March 7, 2017 /PRNewswire/ -- MicroVention, Inc., a wholly owned subsidiary of Terumo Corporation, announced today that the multicenter GREAT study achieved its primary and secondary endpoints. The primary endpoint of the study was met with statistical significance showing lower adverse composite outcomes in the patients treated with 2nd generation HydroCoil® Embolic System coils when compared to bare platinum coils.
The GREAT study (German Randomized Endovascular Aneurysm Trial) was a prospective, randomized, controlled trial that enrolled 513 patients at 22 hospitals in France and Germany. The adverse event primary endpoint was a composite of major aneurysm recurrence at 18 months, retreatment at 18 months, morbidity preventing angiographic follow-up, and all deaths regardless of cause. Investigators treated medium-sized (4-12mm) ruptured and unruptured intracranial aneurysms using at least 50% hydrogel coils by length or all bare platinum coils. Principal Investigator for the trial, Professor Christian Taschner from the University of Freiburg, Germany presented the study data at the 2017 International Stroke Conference in Houston, Texas, USA on February 23rd, 2017.
The GREAT trial results showed significant benefits of hydrogel technology, noted Professor Taschner.
"Aneurysm treatment technology is evolving quickly. It is important to understand the safety and efficacy of new devices through sound scientific methods. I was intrigued by the opportunity to test whether MicroVention's unique hydrogel technology can improve patient outcomes in a wide-range of aneurysms," commented Professor Taschner. "We are pleased that this independent study showed that hydrogel technology reduces a composite of adverse events, retreatments, morbidity and mortality compared to traditional bare platinum coils."
"The results of the GREAT randomized trial demonstrate the efficacy of aneurysm treatment using our hydrogel coils and are aligned with the results of other clinical studies on this technology," added Richard E. Cappetta, President and CEO of MicroVention, Inc.
MicroVention's 2nd generation HydroCoil Embolic System features a non-bioactive, inert hydrogel core that absorbs water from the blood and surrounding tissue, to create a stable, mechanical platform for natural tissue proliferation and long-term aneurysm occlusion. HydroFrame®, HydroFill® and HydroSoft® Embolic Coils can be used exclusively or in conjunction with traditional bare platinum coils to safely and effectively embolize a wide range of aneurysms and neurovascular lesions.
About MicroVention, Inc. MicroVention, Inc. is a U.S. subsidiary of Terumo Corporation with its corporate headquarters in Tustin, California, and manufacturing and administrative facilities in Tustin and Aliso Viejo, California, and San José, Costa Rica. MicroVention is a developer, manufacturer and marketer of innovative neuroendovascular technologies for the treatment of vascular diseases in small vessels. MicroVention products are sold throughout the world in more than 70 countries. For more information, visit www.microvention.com.
About Terumo Corporation Tokyo-based Terumo Corporation is one of the world's leading medical device manufacturers with over $5 billion in sales and operations in more than 160 nations. Founded in 1921, the company develops, manufactures and distributes world-class medical devices including products for use in cardiothoracic surgery, interventional procedures and transfusion medicine; the company also manufactures a broad array of syringe and hypodermic needle products for hospital and physician office use. Terumo contributes to society by providing valued products and services to the health care market and by responding to the needs of health care providers and the people they serve. Terumo Corporation's shares are listed on the first section of the Tokyo Stock Exchange (No. 4543, Reuters symbol <4543.T>, or Bloomberg 4543: JP) and is a component of the Nikkei 225, Japan's leading stock index.
Media Contact:Cathy DemyanovichSr. Director, Corporate CommunicationsMicroVention, Inc.800-990-8361+1-714-247-8000
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The GREAT study (German Randomized Endovascular Aneurysm Trial) was a prospective, randomized, controlled trial that enrolled 513 patients at 22 hospitals in France and Germany. The adverse event primary endpoint was a composite of major aneurysm recurrence at 18 months, retreatment at 18 months, morbidity preventing angiographic follow-up, and all deaths regardless of cause. Investigators treated medium-sized (4-12mm) ruptured and unruptured intracranial aneurysms using at least 50% hydrogel coils by length or all bare platinum coils. Principal Investigator for the trial, Professor Christian Taschner from the University of Freiburg, Germany presented the study data at the 2017 International Stroke Conference in Houston, Texas, USA on February 23rd, 2017.
The GREAT trial results showed significant benefits of hydrogel technology, noted Professor Taschner.
"Aneurysm treatment technology is evolving quickly. It is important to understand the safety and efficacy of new devices through sound scientific methods. I was intrigued by the opportunity to test whether MicroVention's unique hydrogel technology can improve patient outcomes in a wide-range of aneurysms," commented Professor Taschner. "We are pleased that this independent study showed that hydrogel technology reduces a composite of adverse events, retreatments, morbidity and mortality compared to traditional bare platinum coils."
"The results of the GREAT randomized trial demonstrate the efficacy of aneurysm treatment using our hydrogel coils and are aligned with the results of other clinical studies on this technology," added Richard E. Cappetta, President and CEO of MicroVention, Inc.
MicroVention's 2nd generation HydroCoil Embolic System features a non-bioactive, inert hydrogel core that absorbs water from the blood and surrounding tissue, to create a stable, mechanical platform for natural tissue proliferation and long-term aneurysm occlusion. HydroFrame®, HydroFill® and HydroSoft® Embolic Coils can be used exclusively or in conjunction with traditional bare platinum coils to safely and effectively embolize a wide range of aneurysms and neurovascular lesions.
About MicroVention, Inc. MicroVention, Inc. is a U.S. subsidiary of Terumo Corporation with its corporate headquarters in Tustin, California, and manufacturing and administrative facilities in Tustin and Aliso Viejo, California, and San José, Costa Rica. MicroVention is a developer, manufacturer and marketer of innovative neuroendovascular technologies for the treatment of vascular diseases in small vessels. MicroVention products are sold throughout the world in more than 70 countries. For more information, visit www.microvention.com.
About Terumo Corporation Tokyo-based Terumo Corporation is one of the world's leading medical device manufacturers with over $5 billion in sales and operations in more than 160 nations. Founded in 1921, the company develops, manufactures and distributes world-class medical devices including products for use in cardiothoracic surgery, interventional procedures and transfusion medicine; the company also manufactures a broad array of syringe and hypodermic needle products for hospital and physician office use. Terumo contributes to society by providing valued products and services to the health care market and by responding to the needs of health care providers and the people they serve. Terumo Corporation's shares are listed on the first section of the Tokyo Stock Exchange (No. 4543, Reuters symbol <4543.T>, or Bloomberg 4543: JP) and is a component of the Nikkei 225, Japan's leading stock index.
Media Contact:Cathy DemyanovichSr. Director, Corporate CommunicationsMicroVention, Inc.800-990-8361+1-714-247-8000
To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/microvention-and-terumo-corporation-announce-data-from-multicenter-great-study-300419036.html
SOURCE MicroVention, Inc.
