VenoStent Embarks on Clinical Trial to Improve Success Rate of Vascular Surgery Outcomes

Successful enrollment in initial feasibility trial to support future regulatory submissions and provide better outcomes for patients with end-stage renal disease

VenoStent is a clinical-stage tissue engineering company developing tunable, bioabsorbable, smart polymer wraps to fundamentally transform the efficacy of the five million vascular surgeries performed each year, announces successful enrollment in its initial feasibility clinical trial.

The clinical trial is testing the safety and efficacy of its 3D-printed bioabsorbable wraps in humans, a new methodology to improve surgical outcomes for hemodialysis patients.

“We are very pleased to announce that we have successfully enrolled twenty end-stage renal disease patients in our initial feasibility study taking place in Asuncion, Paraguay,” says Tim Boire, CEO. “After years of development, we are confident that our bioabsorbable wrap technology can have a positive impact on the lives of patients that require hemodialysis to sustain life. This is a major milestone toward our mission to improve the quality and length of life for end-stage renal disease patients, as well as others needing vascular surgery.”

Feasibility Study

Enrollment was completed for the initial VenoStent Feasibility Study in Paraguay involving 20 end-stage renal disease patients that were referred for creation of an arteriovenous fistula—surgical connection of an artery to a vein in the arm—to enable hemodialysis treatments. The participants in the study are followed up for several months and the team has already seen highly encouraging safety and performance signals, which could indicate much greater clinical outcomes and quality of life for kidney disease patients when treated with the VenoStent SelfWrap® Bioabsorbable Perivascular Wrap technology.

Approximately 60% of the blood vessels used for dialysis, and 20% of the blood vessels used for quadruple bypass, fail within 12 months of the vascular surgery, risking the lives of 5 million patients every year. The reason for this 60% failure rate is that the vein is not accustomed to, nor equipped for, the high pressure, high flow arterial environment. The thin-walled vein expands, causing tearing of the protective inner lining of the vein. In response to this expansion and tearing, the cells inside the vein wall begin a repair process and migrate inward. This remodeling and cell growth response (also called neointimal hyperplasia) ultimately leads to reduction in, or complete blockage of, blood flow. VenoStent’s proprietary bioabsorbable scaffold goes around these blood vessels at the time of vascular surgery to aid in their “arterialization” process. To make its implantable smart polymer wraps, VenoStent utilizes advanced stereolithography fabrication with 3D printers supplied by Volumetric, a fellow Houston alum of the California-based accelerator Y Combinator.

 

Hot this week

Recor Medical Supports European Society of Cardiology’s Hypertension Guidelines

Record Medical notes the new guidelines, "2024 ESC Guidelines for the management of elevated blood pressure and hypertension," have been published online and recommend the consideration of renal denervation (RDN) as a safe and effective treatment option for patients who have uncontrolled resistant hypertension or those that have uncontrolled hypertension with a higher risk of cardiovascular disease, who express a preference to undergo RDN.

ConTIPI Medical Selects EVERSANA to Support U.S. Commercialization of Non-Surgical Medical Device ProVate for Women with Pelvic Organ Prolapse

EVERSANA is a leading provider of global commercial services to the life sciences industry, to support commercialization for the ProVate device in the United States to help women experiencing pelvic organ prolapse.

Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

The ACURATE Prime aortic valve system is designed with several features to build upon the clinical performance of the ACURATE neo2™ platform including an additional valve size, which expands the treatment range to patients with a larger anatomy.

Noctrix Health Announces New CMS Reimbursement Codes and Payment for Nidra Tonic Motor Activation Therapy for Restless Legs Syndrome

Nidra TOMAC Tonic Motor Activation Therapy, which was authorized for marketing in the United States last year following its designation as a "Breakthrough Device" by the US Food & Drug Administration (FDA), remains the only clinically validated, non-pharmaceutical treatment available for patients with RLS.

Haemonetics Announces Full Market Release for VASCADE MVP® XL Vascular Closure System

Haemonetics notes the VASCADE MVP XL system is now available to U.S. hospitals as the newest addition to Haemonetics' VASCADE® portfolio of vascular closure systems featuring an innovative collapsible disc technology and a proprietary resorbable collagen patch designed to promote rapid hemostasis.