We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
Sekisui Diagnostics

Download Mobile App




DxS Further Develops Companion Diagnostic for Erbitux

By LabMedica International staff writers
Posted on 04 Sep 2009
DxS (Manchester, UK) has entered into a collaboration agreement with Bristol-Myers Squibb (BMS; New York, NY, USA) and ImClone Systems (New York, NY, USA) to develop further a K-RAS companion diagnostic for Erbitux (cetuximab) in the United States and Canada. More...
Financial terms of the agreement were not disclosed.

Erbitux is licensed to Bristol-Myers Squibb for commercialization in the U.S. and Canada and to Merck KGaA (Darmstadt, Germany), for commercialization outside the U.S. and Canada. In Japan, ImClone Systems, Bristol-Myers Squibb, and Merck KGaA jointly develop and commercialize Erbitux.

In combination with the chemotherapeutic agent irinotecan, Erbitux is indicated for the treatment of EGFR-expressing, metastatic colorectal cancer (mCRC) in irinotecan-refractory patients. As a single agent, Erbitux is indicated for the treatment of mCRC in patients who are intolerant to irinotecan-based chemotherapy. However, it can cause adverse effects and is very expensive. Therefore, only colon patients who might derive benefit from its use should be treated with it.

The use of monoclonal antibody EGFR inhibitors is not recommended for the treatment of metastatic colorectal cancer in patients with mutations in codon 12 or 13 in the K-RAS oncogene. The DxS TheraScreen: K-RAS mutation kit detects K-RAS mutations in these codons. About 40% of patients with mCRC have K-RAS mutations while the majority, 60%, has the wild-type K-RAS gene. The mutation kit, if approved by the U.S. Food and Drug Administration (FDA; Silver Spring, MD, USA), will become a companion diagnostic for use with Erbitux in mCRC to determine which patients have wild-type K-RAS status in the United States.

Dr. Stephen Little, CEO of DxS said: "We are very pleased to be continuing our work with Bristol-Myers Squibb and ImClone Systems to ensure K-RAS testing is available to all patients in need of treatment for metastatic colorectal cancer in the United States.”

DxS, a personalized company, has a portfolio of cancer mutation products for diagnostic assays and research. The TheraScreen range of CE-marked in vitro diagnostic (IVD) kits identifies genetic tumor mutations that affect how patients respond to cancer therapies. DxS currently produces two diagnostic kits, TheraScreen K-RAS and TheraScreen EGFR29. Working in partnership with pharmaceutical companies, DxS supports the development and sales of targeted cancer therapies by providing biomarkers and companion diagnostics.

Related Links:

DxS
Bristol-Myers Squibb
ImClone Systems
Merck KGaA
U.S. Food and Drug Administration



Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
βeta-Hydroxybutyrate Reagent
β-Hydroxybutyrate LiquiColor®
POC Immunoassay Analyzer
Procise DX
Gold Member
Platelet Function Analyzer
PL-12
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Molecular Diagnostics

view channel
Image: The automated multiplex PCR assay runs on the BioFire Spotfire Vaginitis System, bringing molecular vaginitis testing to the point of care (Photo courtesy of bioMérieux)

Molecular Vaginitis Panel Gains FDA Clearance and CLIA Waiver for Point-of-Care Use

Vaginitis affects most women at least once in their lifetime and can cause painful, disruptive symptoms. Common causes include bacterial vaginosis, vulvovaginal candidiasis, and trichomoniasis, reflecting... Read more

Immunology

view channel
Image Credit: iStock

Antibody Profiling Predicts Inflammatory Bowel Disease Years Before Diagnosis

Inflammatory bowel disease (IBD), which includes Crohn’s disease and ulcerative colitis, involves abnormal immune responses that cause persistent inflammation and damage in the digestive system.... Read more

Pathology

view channel
Image: The CE-marked software IVD combines digital histopathology and clinicopathological data to generate a prognostic classification (Image Credit: Shutterstock)

Digital Pathology Test Stratifies Recurrence Risk in Early Breast Cancer

In hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative early breast cancer, accurate recurrence-risk assessment helps guide treatment decisions. However, individual risks... Read more

Technology

view channel
Image: Signals LabGistics uses AI to turn natural-language instructions and SOPs into coordinated scientific workflows, helping connect teams, systems, and processes. (Photo courtesy of Revvity)

New AI-Powered System Aims to Streamline Laboratory and Manufacturing Workflows

Scientific laboratories supporting drug development, biotechnology, and materials research increasingly rely on coordinated digital workflows to move data, samples, and activities across teams.... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.