Breakthrough Genomics Joins Forces with the PRECEDE Consortium to Help Accelerate the Early Detection of Pancreatic Cancer

SAN DIEGO, Nov. 21, 2024 /PRNewswire/ — Breakthrough Genomics, a leader in the clinical analysis of genomic data and early cancer diagnostics, announced today its collaboration with the PRECEDE Consortium to advance the clinical evaluation and adoption of its BT-Reveal™ Early Pancreatic Cancer Test.

This groundbreaking blood test can detect the earliest signs of pancreatic cancer in circulating cell-free DNA, often before symptoms appear. Utilizing patented DNA methylation technology, the test received the FDA’s coveted Breakthrough Device Designation and is currently available for high-risk patients through Breakthrough Genomics which operates a CAP and CLIA-certified clinical lab in Southern California. 

Early detection is critical for pancreatic cancer as most cases are diagnosed at an advanced stage when treatment options are limited. This has made pancreatic cancer one of the most deadly types of cancers with a mortality rate that has remained largely unchanged despite gains in other cancer types.

The partnership with PRECEDE offers Breakthrough Genomics access to a network of the world’s foremost pancreatic cancer researchers, clinicians, and high-risk centers. Led by world-renown surgeon and scientist, Dr. Diane Simeone, the PRECEDE Consortium is conducting the largest longitudinal study of its kind, with over 7,000 patients enrolled across 54 leading institutions.

The technology behind the BT-Reveal™ Early Pancreatic Cancer Test originated from UC San Diego’s bioengineering department and has been further refined and validated by Singlera Genomics. 

At the recent PRECEDE Annual Meeting, Breakthrough Genomics and Singlera presented a scientific talk that highlighted the test’s potential to revolutionize current practices by minimizing unnecessary procedures and enabling the accurate detection of pancreatic cancer in its earliest stages.

The companies also joined consortium members in dedicating themselves to a shared mission: increasing the 5-year survival rate of pancreatic cancer by nearly 400% within the next decade.

November is Pancreatic Cancer Awareness Month and is a time to recognize the incredible efforts of practitioners, scientists, and patient support groups working tirelessly to combat this devastating disease. Breakthrough Genomics is proud to contribute to this mission.

For more information, visit https://btreveal.com

For all inquiries, contact Scott Braman at Scott@BTGenomics.com 

View original content to download multimedia:https://www.prnewswire.com/news-releases/breakthrough-genomics-joins-forces-with-the-precede-consortium-to-help-accelerate-the-early-detection-of-pancreatic-cancer-302312236.html

SOURCE Breakthrough Genomics

Staff

Recent Posts

Matwings Technology Raised Series A Funding of Tens of Millions USD to Redefine Protein Design

'Beyond Structure, Predicting Function' SHANGHAI, Dec. 25, 2024 /PRNewswire/ -- Recently, Shanghai Matwings Technology Co.,…

4 hours ago

Casect Launches AI-Enhanced Case Log Platform for Surgeons

SHERIDAN, Wyo., Dec 25, 2024 /PRNewswire/ -- Casect, LLC, a medical education technology company, announces…

10 hours ago

CorVel Announces Effectiveness of Three-For-One Forward Stock Split

FORT WORTH, Texas, Dec. 24, 2024 (GLOBE NEWSWIRE) -- CorVel Corporation (NASDAQ: CRVL) today announced…

19 hours ago

Achilles Therapeutics Announces Sale of Technology Assets to AstraZeneca

- Proprietary data and samples from TRACERx and Achilles’ Material Acquisition Platform (MAP) will be…

19 hours ago

The Anxiety Clinic Launches Innovative Approach to Transform Anxiety into Positive Energy

Transforming Anxiety into Positive Energy: A New Approach by The Anxiety ClinicBondi Junction, New South…

1 day ago