Tele: 561.316.3330
Breaking Medical Device News

Wednesday, September 22, 2021

HomeEXECUTIVESDr. Peter Meintjes joins Transplant Genomics as CCO

Dr. Peter Meintjes joins Transplant Genomics as CCO

Eurofins -Transplant Genomics, Inc. (“TGI”), announces that Dr. Peter Meintjes will join the company as Chief Commercial Officer to lead the commercialization of TruGraf®, the only blood test approved by CMS for surveillance to rule out “silent” subclinical acute rejection in kidney transplant recipients with stable graft function.

Dr. Meintjes joins TGI after six years at Omixon, a world leader in pre-transplant HLA Typing, where he departs as CEO, having grown the company at a CAGR of >75% since its first full year of operation as a molecular diagnostics company. Dr. Meintjes was attracted to TGI by the unique opportunity of commercializing TruGraf, a non-invasive blood test, with established reimbursement that can confirm the absence of “silent” subclinical acute rejection in kidney transplant recipients with stable renal function. TruGraf is significantly differentiated when compared with existing donor-derived cell-free DNA (ddcfDNA) and creatinine/eGFR post-transplant kidney monitoring tests, which are only capable of confirming active rejection in already injured kidneys, without stable graft function.

Dr. Meintjes joins Founder and CEO Dr. Stan Rose, who has led TGI through receiving a Local Coverage Determination (LCD) for TruGraf in November 2019. TruGraf also benefits from the prospective CTOT-08 study, which demonstrated the prevalent incidence of silent subclinical rejection and the importance of early detection and treatment to longer-term outcomes. The clinical utility and validity of TruGraf were established by using paired non-invasive liquid biopsies (blood samples) and invasive tissue biopsies (current gold standard for ruling out silent rejection) which demonstrated a 94% concordance. This highlights how TruGraf is the only test that can be used for routine surveillance to address two critical unmet clinical needs for kidney transplant recipients:

  1. ~35% of patients with stable graft function over two years are actually “silently” rejecting, and go untreated by waiting for evidence of clinical acute rejection (i.e. elevated creatinine or ddcfDNA), indicating damage already done, and leading to worse outcomes for patients
  2. ~75% of patients undergoing invasive surveillance biopsies were not experiencing any form of rejection, putting patients at unnecessary risks from those invasive procedures

By using TruGraf, nephrologists are empowered to make better treatment decisions for their patients.  At the same time, patients who test negative are comforted by learning that they have adequate immune suppression (i.e. immune quiescence, graft stability, healthy kidneys) without having to be subjected to risky, costly, and painful biopsies.

With the resources of parent company Eurofins, TGI is positioning for strong growth into the post-transplant kidney testing market after excellent adoption among early customers. TGI is hiring additional sales, medical science liaisons and marketing personnel to support commercial expansion.

Medical Device News Magazine
Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Stay Connected


Don't Miss

Kleiner Device Labs Receives FDA Market Clearance for KG2 Surge Flow-Thru Interbody System

The system maximizes total bone graft delivery volume, better distributes graft bilaterally into the intervertebral disc space, and streamlines the implant delivery, positioning, and grafting process for TLIF and PLIF spinal fusion procedures.

Matthew Cranfill New ExtriCARE USA Director Of Clinical Services

"Matt's impressive experience and skillset easily made him our top pick," said Peter Mason, President of ExtriCARE USA.

Shannon Lantzy MedCrypt New VP of Consulting

"I met Shannon at a healthcare-related event several years ago and was immediately impressed with her passion and drive to move healthcare into a digital future," said Mike Kijewski, CEO of MedCrypt.

Mark Foster Joins Xenocor BOD

Foster is a versatile and visionary C-Suite executive who brings 20 years of general management and leadership experience from both venture-backed growth-stage organizations and world-class medical device companies

Hinge Health Acquires the Most Advanced Computer Vision Technology for Tracking Human Motion

CEO Daniel Perez explained, “We won’t stop investing in technology to deliver the most patient-centered digital clinic that improves member experience and outcomes while reducing costs. wrnch allows us to take a giant leap forward in all respects.”

Dale W Wood Congratulates the Huma Team on Raising $130 Million

Major health and technology companies across the world have committed upwards of $130 million to Huma Therapeutics, the health-tech company backed by Dale Ventures.

Rhaeos Awarded $4 Million NIH SBIR Grant

Under the NIH SBIR grant, Rhaeos will leverage their existing wireless sensor hardware to provide additional quantitative flow data to the clinician, giving insight into this currently inaccessible and highly relevant shunt performance metric.

By using this website you agree to accept Medical Device News Magazine Privacy Policy