First Patient Enrolled in Merit Medical’s WRAPSODY™ Registry (WRAP) Study
Merit Medical Systems (MMSI) has announced the successful enrollment of the first patient in the WRAP Registry Study, aimed at assessing the safety and efficacy of the WRAPSODY Cell-Impermeable Endoprosthesis for hemodialysis patients. This international study will enroll up to 500 patients facing vascular access issues due to stenosis or occlusion. It will monitor clinical outcomes over two years, providing critical real-world evidence that may enhance treatment options for over two million global dialysis patients suffering from vascular complications.
- Successful enrollment of the first patient in the WRAP Registry Study.
- Study aims to gather real-world data on WRAPSODY's effectiveness in improving vascular access for hemodialysis patients.
- Potential to enhance treatment options for over two million global dialysis patients.
- None.
Prospective, international, multicenter, observational study to assess the real-world safety and efficacy of the WRAPSODY Cell-Impermeable Endoprosthesis
SOUTH JORDAN, Utah, July 05, 2022 (GLOBE NEWSWIRE) -- Merit Medical Systems, Inc. (NASDAQ: MMSI), a leading global manufacturer and marketer of healthcare technology, announced today the successful enrollment of the first patient in its WRAP Registry Study. This study will evaluate the clinical benefits associated with the use of the WRAPSODY Cell-Impermeable Endoprosthesis in patients receiving hemodialysis that experience a narrowing (stenosis) or blockage (occlusion) of blood vessels required for dialysis (vascular access).
Globally, over two million patients with advanced kidney disease receive dialysis.1 Hemodialysis, the primary approach used for dialysis, requires long-term vascular access that is typically achieved through the surgical creation of an arteriovenous fistula (AVF) or placement of an arteriovenous graft (AVG). However, complications, such as stenosis and/or occlusion within the dialysis outflow circuit of an AVF or AVG, can impair vascular access which compromises the ability to provide adequate dialysis treatment. The WRAPSODY Cell-Impermeable Endoprosthesis was created to help overcome this challenge by maintaining the integrity of the dialysis outflow circuit.
Dr. Dean Huang, consultant diagnostic and interventional radiologist at King’s College Hospital in London, England, enrolled the first patient in the WRAP Registry. “The patients being treated with the WRAPSODY Cell-Impermeable Endoprosthesis have historically had few clinical options,” Dr. Huang said. “These patients have typically faced frequent reinterventions to maintain vessel patency resulting in multiple procedures and hospitalizations. The WRAP study will add to the growing body of evidence on WRAPSODY’s ability to achieve durable outcomes for this vulnerable patient population. We are excited to enroll the first patient in this important study.”
The WRAP Registry Study will enroll up to 500 patients with outflow circuit stenosis or occlusion who are receiving hemodialysis at medical facilities throughout Europe, South America, Australia, and New Zealand. Clinical outcomes of patients after the initial placement of the WRAPSODY Cell-Impermeable Endoprosthesis will be evaluated over a two-year period in accordance with the instructions for use associated with its CE Mark.
“Enrollment of the first patient in the WRAP Registry Study will expand our clinical portfolio of evidence establishing the therapeutic benefits of the WRAPSODY Cell-Impermeable Endoprosthesis and provide real-world insight that can help improve the care for patients receiving hemodialysis worldwide,” said Fred P. Lampropoulos, Merit Medical’s Chairman and CEO.
The WRAPSODY Cell-Impermeable Endoprosthesis is an expandable nitinol stent frame fully enveloped by an external layer of expanded polytetrafluoroethylene (PTFE) and an internal layer of spun PTFE with an interposed cell-impermeable layer. The WRAPSODY Cell-Impermeable Endoprosthesis system is being studied under an Investigational Device Exemption in the United States. It previously received the CE Mark and complements other vascular access products distributed by Merit Medical Systems, Inc., including the HeROâ Graft, Super HeRO® Adapter and Support Seal system, and CentrosFLOâ Hemodialysis Catheter.
WRAPSODY is not approved, cleared, or available for commercial distribution in the United States and may not be approved, cleared, or available for sale or use in other countries. For additional information on the WRAP Registry Study, including ongoing updates, please visit https://www.clinicaltrials.gov/ct2/show/NCT05062291
ABOUT MERIT MEDICAL
Founded in 1987, Merit Medical Systems, Inc. is engaged in the development, manufacture, and distribution of proprietary disposable medical devices used in interventional, diagnostic, and therapeutic procedures, particularly in cardiology, radiology, oncology, critical care, and endoscopy. Merit serves client hospitals worldwide with a domestic and international sales force and clinical support team totaling more than 600 individuals. Merit employs approximately 6,500 people worldwide.
TRADEMARKS
Unless noted otherwise, trademarks and registered trademarks used in this release are the property of Merit Medical Systems, Inc. and its subsidiaries in the United States and other jurisdictions.
CONTACTS
PR/Media Inquiries
Sarah Comstock
Merit Medical
+1-801-432-2864 | sarah.comstock@merit.com
Investor Inquiries
Mike Piccinino, CFA, IRC
Westwicke - ICR
+1-443-213-0509 | mike.piccinino@westwicke.com
Reference
- Liyanage T, Ninomiya T, Jha V, Neal B, Patrice HM, Okpechi I, et al. Lancet. 2015;385(9981):1975-82.
FAQ
What is the purpose of the WRAP Registry Study by Merit Medical (MMSI)?
How many patients will be enrolled in the WRAP Registry Study?
What complications does the WRAPSODY Endoprosthesis address?
What type of patients is the WRAP Registry Study targeting?
What is the duration for evaluating clinical outcomes in the WRAP Registry Study?
