SALT LAKE CITY–(BUSINESS WIRE)–Alucent Biomedical, a privately held medical technology company founded to transform the way vascular disease is treated, today announced Venita Chandra, M.D., will join the company’s scientific advisory board.
Dr. Chandra is board certified in both general and vascular surgery. She is a clinical associate professor of surgery in the Division of Vascular Surgery at Stanford University Medical Center. She also serves as the co-medical director of the Stanford Advanced Wound Care Center and the program director of the Vascular Surgery Fellowship and Vascular Surgery Residency Programs at the Stanford University School of Medicine.
Alucent is currently developing its Natural Vascular Scaffolding (Alucent NVS) Vessel Restoration System with Photoactivated Linking for the treatment of peripheral artery disease (PAD) of the lower extremities. The company announced today it will also seek to adapt the technology for another use, the maturation and preservation of arteriovenous fistula (AVF) for hemodialysis (HD).
The prevalence of end-stage renal disease continues to rise, and there is a growing need for HD. The National Kidney Foundation Kidney Disease Outcomes Quality Initiative (NKF-KDOQI) guidelines and the Fistula First Breakthrough Initiative recommend AVFs as the preferred type of vascular access for HD, as they have superior patency rates, fewer complications, and lower health care costs.1234
“Early pre-clinical studies involving Alucent NVS therapy for AVF have been encouraging. Applying the treatment at fistula creation has facilitated maturation and the promotion of outward remodeling of the AVF,” Dr. Chandra said. “I’m thrilled to connect with Alucent as the company develops this new promising technology to address the challenge of dialysis access for patients suffering from end-stage renal disease.”
As part of the Alucent scientific advisory board, Dr. Chandra joins a team of leading experts in peripheral and cardiovascular disease, including Dr. Gary Ansel, Dr. Elazer Edelman, Dr. Bill Gray, Dr. Larry Kraiss, Dr. Bill Sessa and Dr. Craig Walker.
“Dr. Chandra is a renowned vascular surgeon and will be integral to informing the company’s direction as we seek to add another treatment protocol to our clinical trial portfolio,” said Myles Greenberg, M.D., chief executive officer of Alucent. “Her appointment will strengthen the team’s capabilities in developing this new use for our technology and underscores the untapped potential for Alucent NVS.”
About Alucent Biomedical
Alucent Biomedical, Inc. is a privately held medical technology company headquartered in Salt Lake City, Utah. Alucent was founded by Avera Health to develop and market products using Alucent Natural Vascular Scaffolding (Alucent NVS) technology. Alucent NVS is a first-of-a-kind combination drug-device therapy designed to help the body naturally open and maintain vessel patency. For more information, visit www.alucentbiomedical.com.
________________________ | ||
1 |
Santoro D, Benedetto F, Mondello P, Pipito N, Barilla D, Spinelli F, et al. Vascular access for hemodialysis: current perspectives. International journal of nephrology and renovascular disease. 2014;7:281–94. |
|
2 |
Systemic barriers to optimal hemodialysis access. Donca IZ, Wish JB Semin Nephrol. 2012 Nov; 32(6):519-29. |
|
3 |
Rayner HC, Pisoni RL, Bommer J, Canaud B, Hecking E, Locatelli F, et al. Mortality and hospitalization in haemodialysis patients in five European countries: results from the Dialysis Outcomes and Practice Patterns Study (DOPPS) Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association – European Renal Association. 2004 Jan;19(1):108–20.[PubMed] [Google Scholar] |
|
4 |
Manns B, Tonelli M, Yilmaz S, Lee H, Laupland K, Klarenbach S, et al. Establishment and maintenance of vascular access in incident hemodialysis patients: a prospective cost analysis. Journal of the American Society of Nephrology: JASN. 2005 Jan;16(1):201–9. |
Contacts
MEDIA CONTACT:
Diana Soltesz
Pazanga Health Communications Inc.
818-618-5634
dsoltesz@pazangahealth.com
At 14-months median follow-up in the pivotal trial, 50% of patients achieved a complete response…
Objective response rate of 69.2% observed in heavily pretreated patient population including patients with BTK…
The study met its primary endpoint of overall survival with a 41% reduction in the…
DENVER, CO / ACCESSWIRE / June 15, 2024 / Each year over 120,000 Coloradans are…
REYKJAVIK, Iceland, June 15, 2024 /PRNewswire/ -- In a recent display of global baking talent,…
– ENERGIZE is the First Study to Demonstrate Efficacy of an Oral Treatment for Non-Transfusion-Dependent Alpha-…