-

Naveris Announces Commercial Payor Coverage for NavDx® Test from Highmark, Inc.

Commercial Coverage from Blue Cross Blue Shield Association Licensee Adds to Growing Coverage from Medicare and Other Carriers

WALTHAM, Mass.--(BUSINESS WIRE)--Naveris, Inc., the leader in precision oncology diagnostics for viral-induced cancers, today announced that Highmark Inc. (Highmark), an independent licensee of the Blue Cross Blue Shield Association, now offers coverage for NavDx®, Naveris’ proprietary flagship blood test for Tumor Tissue Modified Viral (TTMV®)-HPV DNA.

NavDx is the first and only clinically validated circulating TTMV-HPV DNA blood test. It provides a non-invasive and precise method for identifying HPV-driven cancers before there is clinical or radiographical evidence of disease. Data supporting the clinical validity and utility of NavDx have been published in nearly 20 peer-reviewed publications, and the test recently received Medicare coverage through the Molecular Diagnostics Services Program MolDX®.

“We are pleased that Highmark has made NavDx available to the patients who need the valuable insights provided by TTMV-HPV DNA,” said James McNally, Chief Executive Officer of Naveris. “This test helps to optimize the management of HPV-driven cancer from diagnosis to post-treatment monitoring to surveilling for molecular residual disease. Receiving coverage from a payor that serves millions of patients is a meaningful step forward as we work to further expand access to NavDx.”

About Naveris

Naveris is a privately held, commercial stage, precision oncology diagnostics company with facilities in Massachusetts and North Carolina. Since its founding in 2017, Naveris has been committed to improving outcomes for the millions of people at risk of developing viral-induced cancers with novel molecular diagnostics that enable earlier cancer detection. The company operates high-complexity testing clinical laboratories that are accredited by the College of American Pathologists and the New York State Department of Health Wadsworth Center, and are certified under CLIA. For more information on Naveris and the clinical impact of NavDx, please visit www.naveris.com and www.NavDx.com. NavDx has not been cleared or approved by the US Food and Drug Administration (FDA).

Contacts

Megan Kernan
ICR Westwicke Healthcare PR
Tel: 646.677.1870
Megan.Kernan@icrinc.com

Naveris, Inc.


Release Versions

Contacts

Megan Kernan
ICR Westwicke Healthcare PR
Tel: 646.677.1870
Megan.Kernan@icrinc.com

More News From Naveris, Inc.

New Multicenter Study Highlights Use of the NavDx® Test in Resolving Clinically Indeterminate Findings

WALTHAM, Mass.--(BUSINESS WIRE)--Naveris, Inc., the leader in precision oncology diagnostics for viral-induced cancers, in collaboration with eight prominent U.S. institutions, announces the publication of a significant study, "Utility of TTMV-HPV DNA in resolving indeterminate findings during oropharyngeal cancer surveillance", in Oral Oncology. The study highlights the crucial role of Naveris' flagship product, the NavDx test, in enhancing diagnostic precision and clinical decision-making in...

Naveris to Present New Data Highlighting Clinical Utility of the NavDx® Test at the 2024 ASCO Annual Meeting

WALTHAM, Mass.--(BUSINESS WIRE)--Naveris, Inc., the leader in precision oncology diagnostics for viral-induced cancers, today announced new data to be presented at The American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago, IL from May 31 – June 2, 2024. These presentations underscore Naveris' continued innovation with the NavDx test, the first and only clinically validated circulating Tumor Tissue Modified Viral (TTMV®)-HPV DNA blood test aiding in the detection and management...

Naveris Announces Launch of Phase II Clinical Study in MRD+ Head and Neck Cancer

WALTHAM, Mass.--(BUSINESS WIRE)--Naveris, Inc., the leader in precision oncology diagnostics for viral-induced cancers, today announced the launch of a Phase II clinical study in minimal residual disease positive (MRD+) HPV-driven head and neck cancer. The study will be led by Memorial Sloan Kettering Cancer Center (MSKCC), a top cancer treatment and research institution. The primary objective of this multicenter randomized study is to evaluate the efficacy of HB-200, a novel intervention, for...
Back to Newsroom