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Company Interview Excerpt
PAUL MCCORMICK - ENDOLOGIX INC (ELGX)
Full article published: 9/5/2006    


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TWST: Would you give us a brief historical sketch of the company and a picture of the things you are doing at the present time?
Mr. McCormick: Endologix has developed the Powerlink System, a minimally invasive technology to treat abdominal aortic aneurysms. Commonly referred to as AAA, it is a weakening of the wall of the aorta, the largest artery in the body, which results in a balloon-like enlargement. Once a AAA develops, it can continue to enlarge, and it becomes susceptible to rupture, which is life threatening. The clinical literature indicates that if it ruptures, approximately 50% of those persons will die before they reach the hospital, and of those who do survive, half of those will succumb due to complications of surgery. If one is fortunate enough to have their AAA diagnosed prior to rupture, the patient is usually sent for a CT scan to characterize the shape and size of the aneurysm. Conventional treatment is open surgery where surgeons make a midline incision and move your intestines to the side to gain access to the aorta. They then clamp above and below the weakened segment, open up the sac and sew in a surgical graft, and then put everything back together again. This procedure carries a surgical mortality of 3% to 8%. To put that into perspective, open-heart surgery carries slightly less than a 1% mortality rate. In addition, the conventional surgery carries a serious morbidity of 15% to 40%, and long recovery times. The Powerlink is a stent graft to treat AAA. Stent grafts are metal cages or scaffolds covered with a material, and the devices are compressed and loaded into small catheters. The catheters are then inserted into the body through the artery of the leg and passed up into the aorta and then deployed. Many patients can have the treatment performed under a regional or local anesthesia. Once in place, the stent graft acts to shunt blood flow away from the weakened wall, which reduces the pressure and the risk of rupture. The company completed an FDA pivotal trial for the Powerlink System with excellent clinical results and began a focused launch here in the US in early 2005. We are now at the next stage of broader US commercialization.

Tickers included in this excerpt: ELGX


For more information call (212) 952 7433. The Wall Street Transcript does not endorse any of the comments made by interviewees, and does not make stock recommendations.

 

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