VENITI Receives FDA Approval of IDE for VENITI VICI Venous Stent System
ST. LOUIS, MS: VENITI, provider of innovative technology for the treatment of venous disease, has announced that it has received approval from the United States Food and Drug Administration (FDA) for an Investigational Device Exemption (IDE) to begin the VIRTUS trial of the VENITI VICI Venous Stent System.
Today, a large number of people suffer from lower-extremity venous disease, and until recently, the only treatment options available involved the use of re-purposed vascular stents originally designed for use in the arterial system. The VICI Venous Stent System was designed from inception to be compatible with the unique anatomy and pathophysiology of the venous system.
Co-Principal Investigators for the VIRTUS Trial include William Marston, M.D., Chief, Division of Vascular Surgery, Professor, Department of Surgery, UNC Department of Surgery, Chapel Hill, NC and Mahmood Razavi, M.D., Director for Clinical Trials & Research at the Heart and Vascular Center, St. Joseph Hospital, Orange, CA.
"Obstruction of the iliac veins and vena cava have been identified as a frequent cause of severe venous disease resulting in major disabling symptoms including leg swelling, pain, and ulceration," says Dr. Marston. "The development of stents specifically designed for the unique characteristics of the venous system provides the potential to reduce these debilitating symptoms for patients, while improving the cost effectiveness of interventional treatment for venous obstruction."
The trial was commenced in Europe, with first patients enrolled and treated by Marta Ramirez Ortega, M.D. at Hospital Madrid Monteprincipe in Madrid, Spain. "It is important for my patients to be able to be treated with a stent specifically designed for the venous anatomy and for them to have their data collected so that future patients can benefit from knowing how well venous stenting works,” says Dr. Ramirez.
Dr. Razavi adds, "This is an important landmark for VENITI and patients with deep venous disease. Due to the absence of vein-specific stents, physicians have thus far been using stents that were not designed for veins. We look forward to the completion of this important study and availability of optimal stents to treat our patients with deep vein obstructive lesions."