Syantra Receives CE Mark Approval for their Breast Cancer Test Built on the Syantra DX™ Liquid Biopsy Platform

Apr 18, 2023

CALGARY, A.B. Syantra announced today that it has obtained CE marking for the Syantra DX™ Breast Cancer test. Syantra DX™ Breast Cancer is a minimally invasive blood test for the detection of an active breast cancer signature - in the earliest stages when it is easier to treat.


The test evaluates gene expression patterns of 12 unique biomarkers through a custom qPCR process using proprietary software that includes machine learning-derived algorithms. Securing CE marking allows the company to market the blood test in the European Union and other countries that recognize the designation. 


 "Obtaining CE marking for the Syantra DX™ Breast Cancer test brings us one step closer to helping women across the globe detect breast cancer at earlier stages when it is most treatable," said Dr. Kristina Rinker, Syantra Co-founder and Chief Scientific Officer.


"Syantra's blood-based test may help improve breast cancer detection for women with high-risk of developing breast cancer, particularly young individuals with genetic predisposition and women with dense breasts or diverse ethnic backgrounds. For those women, standard screening mammogram may be inadequate and more sensitive tests are urgently needed," said Dr. Massimo Cristofanilli, Professor of Medicine, Director of Breast Medical Oncology and Associate Director of Precision Medicine in the Sandra and Edward Meyer Cancer Center at Weill Cornell Medicine.  Dr. Cristofanilli also serves as a paid scientific advisory board member for Syantra Inc.


About Syantra 

Syantra is a precision biotechnology company changing the way cancer is detected and treated. Its flagship product, Syantra DX™ Breast Cancer, is a minimally invasive and high-performance blood test for the detection of breast cancer, at the earliest stages.


Contact or media inquiries

1-877-331-0516

info@syantra.com 


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