Avinger Completes Enrollment in the CONNECT Trial

REDWOOD CITY, Calif.--()--Avinger, Inc., medical device manufacturer of innovative, multi-functional catheters for treating patients with peripheral artery disease (PAD), announced that it has successfully completed enrollment in its CONNECT (Chronic TOtal OcclusioN CrossiNg with thE WildCat CatheTer) clinical trial. The CONNECT trial is a prospective, multi-center, non-randomized study to evaluate Wildcat Catheter’s ability to cross chronic total occlusions in femoropopliteal lesions which is the leading cause of amputations associated with PAD in the US.

Avinger’s Wildcat Catheter received FDA 510(k) clearance in February 2009 for use as a guidewire support device to access discreet areas of the vasculature. Avinger conducted this study to secure FDA clearance for an indication specific to crossing CTOs. Patients with peripheral artery disease may have chronic total occlusions that are sometimes difficult to treat with endovascular therapy resulting in either bypass surgery or amputation.

“This is a great day for Avinger and a huge accomplishment for our entire team,” said Avinger founder and CEO, John B. Simpson, PhD, MD. “We have a lot of work to do but this is a giant step forward for our organization. A lot of people put in a lot of long hours to complete this trial and we can’t thank them enough. We’d like to thank our investigating physicians and their phenomenal staffs and the patients that participated in CONNECT.“

Co-Principal investigator for the trial, Dr. M. Laiq Raja of El Paso Cardiology Associates, commented, “I am confident that Wildcat will make a great impact on approaching and successfully crossing long CTO lesions.”

The CONNECT study evaluated 88 patients with femoropopliteal CTO lesions at 15 centers in the US. Patients were followed for 30 days post procedure and an independent group of physicians is currently reviewing the angiographic results to determine crossing efficacy and safety endpoints.

ABOUT AVINGER

Founded in 2007 by renowned cardiologist and medical device entrepreneur Dr. John B. Simpson, Avinger develops next-generation catheter-based technologies for the treatment of peripheral artery disease (PAD). Leveraging core competencies in medical device catheter engineering and intravascular imaging, Avinger markets Wildcat and Kittycat guidewire support catheters, and is currently developing advanced technologies that guide endovascular therapy and intervention with real-time imaging capability. www.avinger.com.

Contacts

Avinger, Inc.
J.D. Simpson, +1-650-363-2400
Vice President, Commercial Operations
jd@avinger.com
or
Press Inquiries:
Mortar PR
Serene Buckley, +1-415-772-9907 ext. 117
serene@mortarpr.com

Release Summary

Enrollment complete in Avinger's CONNECT Study to evaluate Wildcat Catheter’s ability to cross chronic total occlusions in femoropopliteal lesions-the leading cause of amputations in patients with PAD

Contacts

Avinger, Inc.
J.D. Simpson, +1-650-363-2400
Vice President, Commercial Operations
jd@avinger.com
or
Press Inquiries:
Mortar PR
Serene Buckley, +1-415-772-9907 ext. 117
serene@mortarpr.com