ViviGen Cellular Bone Matrix Outperforms MSC-based Allografts and is Equivalent to Gold Standard Autograft According to Recent Peer-Reviewed Publications

VERITAS Vision System Is Introduced by Johnson & Johnson

The company will offer live demos of the new system in a wet lab at the Johnson & Johnson booth (#2813) this weekend at the 2021 American Society of Cataract and Refractive Surgery and American Society of Ophthalmic Administrators Annual Meeting.

GenesisCare Orders 27 Elekta Flexitron Treatment Devices

"GenesisCare continues to demonstrate its commitment to improving patient outcomes worldwide and Elekta is delighted to play a vital partnering role to achieve this mission," said Gustaf Salford, Elekta's President and CEO.

FoodMarble AIRE Shown to Exceed the Performance of ‘Gold Standard’ SIBO Testing in Clinical Trial

SIBO is a very common disorder where there are excessive bacteria present in the small intestine. The true prevalence of SIBO in the general population is largely unknown, with some studies estimating its occurrence in up to 15% of healthy individuals. It is also largely associated with many other common clinical conditions, including irritable bowel syndrome, where 40-80% of IBS patients have SIBO.

December 29, 2020

ViviGen Cellular Bone Matrix, is the first cellular allograft to recover and protect viable, lineage-committed bone cells, supports outcomes that are comparable to autograft and superior to a conventional mesenchymal stem cell (MSC)-based cellular allograft in even high-risk foot and ankle procedures, according to two recent peer-reviewed publications.

ViviGen retrospective analysis of 135 high-risk foot and ankle procedures published in the journal Foot & Ankle Specialist showed that ViviGen supports fusion even in patients with comorbidities that create higher risk of nonunion, such as diabetes, thyroid disease and alcohol abuse. The overall fusion rate across two high-risk patient groups — 113 undergoing arthrodesis and 22 undergoing open reduction internal fixation (ORIF) — was 86 percent, which is comparable to fusion procedures using autograft while avoiding the challenges associated with autograft recovery. There also was no statistical difference in the fusion rate between primary and revision procedures.

“By providing osteogenic cells in an osteoconductive and osteoinductive matrix, ViviGen helps maximize bone healing, even for revision cases, diabetics, and smokers,” said Joseph Park, MD, one of the authors of the study, which was performed at the University of Virginia Health System in Charlottesville, Va.

A second retrospective study, published in Clinical Research on Foot & Ankle, showed that ViviGen outperformed a leading MSC-based graft in both clinical and patient-reported outcomes following foot and ankle fusions. The study involved 47 consecutive cases, with 31 patients receiving ViviGen and 16 receiving the MSC graft. The ViviGen patients experienced fusion at double the rate of the MSC patients — including among patients with comorbidities such as diabetes and tobacco use — experienced fewer complications and reported lower post-operative pain.

These results reinforce that viable, lineage-committed bone cells, such as those in ViviGen, may better support bone fusion than MSCs and demonstrate that ViviGen can lead to successful clinical and patient-reported outcomes with minimal complications in foot and ankle surgery.

“These studies are an exciting advancement of our knowledge of ViviGen,” said Mark Moore, PhD, Chief Scientific Affairs Officer at LifeNet Health. “We developed ViviGen based on pre-clinical research that showed a cellular graft focused on viable, lineage-committed bone cells could result in a safe, clinically effective bone void filler. These clinical results further support that conclusion, especially in comparison to first generation cellular grafts that focus on undifferentiated MSCs.”



Our Sister Publication: Biotechnology News Magazine

Subscribe to Medical Device News Magazine here.