Xeltis Completes Key Trials for aXess Vascular Innovation

Xeltis Completes Patient Enrollment in Pivotal aXess Trial

Xeltis has successfully completed the patient enrollment phase of its EU Pivotal trial for the aXess device, designed to significantly improve vascular access in adults suffering from end-stage renal disease. This trial, which has enrolled 120 patients across 22 centers, represents a major step forward in providing effective treatment for hemodialysis patients.

Understanding the aXess Technology

The aXess device is a groundbreaking restorative vascular access conduit that emphasizes the natural regeneration of living vessels. This technology uniquely addresses the common challenges faced by dialysis patients, particularly the frequent need for reinterventions and the risks of complications. Early data from previous studies have been promising, showcasing a zero infection rate and exceptional performance compared to existing hemodialysis vascular access solutions.

Clinical Trial Overview

The aXess EU pivotal trial focuses on investigating the patency, safety, and overall performance of this innovative conduit. The incorporation of 120 patients in nine countries highlights the extensive reach of the trial, reflecting the growing demand for improved dialysis access solutions globally.

Insights from Investigators

Professor Loreto Gesualdo, a key Principal Investigator, expressed pride in contributing to this vital study. He emphasized the role of aXess in transforming patient outcomes, particularly by reducing the incidence of non-maturation of fistulas, which is a significant concern in hemodialysis treatment.

The Path Towards Market Approval

With expectations of primary endpoint readouts in the second quarter of the following year and market approval anticipated soon after, Xeltis is moving rapidly towards making aXess available to those in need. The recent appointment of Rob Eyers as Chief Technology Officer reinforces the company’s commitment to innovation and excellence in the medtech field.

Leadership and Vision at Xeltis

Rob Eyers brings over 30 years of experience in the cardiovascular medtech industry, previously holding significant roles at various prestigious organizations. His extensive background equips Xeltis with invaluable insights necessary for navigating regulatory pathways and advancing towards commercialization.

Innovative Potential of aXess

The Endogenous Tissue Restoration (ETR) technology incorporated in the aXess design represents a new benchmark in medical device innovation. It is engineered to regenerate a patient's own tissue, thus addressing the critical issue of treatment complications such as infections. This innovative capability positions Xeltis to lead the market in effective and sustainable hemodialysis solutions.

Future Directions for Xeltis

Xeltis is actively pursuing further patient enrollment in its US pivotal trial, demonstrating its dedication to broadening the reach and impact of the aXess vascular access conduit. The collaboration with distinguished medical professionals worldwide reflects the strength of its clinical support system.

About Xeltis

Xeltis stands at the forefront of medtech innovation, dedicated to developing transformative implants that facilitate the natural formation of lasting vascular structures. The company focuses on addressing the critical need for effective hemodialysis access grafts and cardiovascular replacements, reshaping the landscape for millions of patients in need.

Frequently Asked Questions

What is the aXess device?

The aXess device is a restorative vascular access conduit designed for patients requiring hemodialysis, focusing on the natural creation of living blood vessels.

What makes aXess different from other vascular access solutions?

aXess utilizes innovative ETR technology that allows for tissue regeneration, avoiding complications typically associated with traditional treatment options.

How many patients are involved in the aXess trial?

A total of 120 patients are participating in the EU Pivotal trial across 22 centers in multiple European countries.

What are the anticipated outcomes from the trial?

The primary endpoint readouts from the trial are expected to be revealed in the second quarter of the following year, paving the way for potential market approval soon after.

Who leads the research efforts for aXess?

The trial includes notable investigators like Professor Loreto Gesualdo and is supported by Xeltis' Chief Technology Officer, Rob Eyers, who brings extensive industry experience.

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