Editor: What To Know
- Dr Peter 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.
- (“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”.
- 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.
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 Peter 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 Peter 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:
- ~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
- ~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.
