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MARCH 8, 2006
Cardica Receives Milestone Payment From COOK For X-Port REDWOOD CITY, Calif. - March 8, 2006 - Cardica, Inc. (Nasdaq: CRDC) today announced that it has received a $500,000 payment from Cook Incorporated after the successful completion of the first milestone in the development the X-Port™ Vascular Access Closure Device, an innovative automated device intended to be used to close holes in the femoral arteries after interventional vascular procedures. "We believe that Cardica's design and micro-clip miniaturization expertise will lead to a significantly enhanced approach to vascular access closure," said Brian Bates, senior vice president, business development of Cook Incorporated. "We are pleased with the progress we are making on this next-generation closure device." In December 2005, Cardica and Cook entered into an agreement to develop the X-Port device under which Cardica is responsible for design and pre-clinical development, which is being directed by a committee that includes representatives from both parties. Cook is responsible for clinical development and regulatory approval, and will have exclusive commercialization rights to market the X-Port device for medical procedures anywhere in the body. Cardica is eligible to receive additional product development milestone payments of up to $1.5 million upon successful completion, as well as, royalties on future worldwide sales. "We are excited to be working with Cook and believe that this collaboration brings together Cook's innovative leadership and expertise in interventional cardiology with our commitment to provide reliable automated systems to enhance the care of patients with a wide range of cardiovascular and other conditions," said Bernard Hausen, M.D., Ph.D., president and chief executive officer of Cardica, Inc. "Cook's support of this program helps us leverage the versatility of our proprietary technology and has the potential to expand beyond this initial development effort."
The X-Port Advantage for Interventional Procedures The potential advantages of the X-Port device include a simple user interface, the ability to place it through the same introducer sheath used for the interventional procedure for greater convenience and speed, scalability, and lower cost of goods. In addition, X-Port is designed to be less invasive with a minimal amount of foreign material placed in the vessel wall. Cardica is now conducting preclinical studies to assess safety and preliminary efficacy of the X-Port device.
About Cook Incorporated
About Cardica, Inc. The C-Port® system, a distal anastomosis system, is marketed in Europe and received 510(K) clearance from the U.S. Food and Drug Administration in November 2005. The PAS-Port® system, a proximal anastomosis system, is marketed in Europe and Japan. Cardica also is developing additional devices to facilitate vascular and other surgical procedures. Go to www.cardica.com for more information.
Forward Looking Statements
Robert Y. Newell
Daryl Messinger |
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