Medical Device News Magazine

BGI Genomics Partners with Zentya to Launch Fecal DNA Test for Colorectal Cancer in Slovakia

About Medical Device News Magazine

About Medical Device News Magazine. We are a digital publication founded in 2008 located in the United States.

Advertise with Medical Device News Magazine! Join Our #1 Family of Advertisers!

We pride ourselves on being the best-kept secret when it comes to distributing your news! Our unique digital approach enables us to circulate your...

BGI Genomics is pleased to announce the launch of COLOTECTTM 1.0 in Slovakia, in collaboration with its partner, Zentya. Zentya is a Slovak-based company that is passionate about providing patients with the latest technology in genetic screening, aiming to help identify and facilitate timely treatments.

COLOTECTTM 1.0 is one of the first-ever fecal DNA tests for colorectal cancer that is available in Slovakia. It is a non-invasive fecal DNA test for detecting colorectal cancer and precancerous lesions. It uses multiplex methylation-specific PCR technology to trace abnormal colorectal cancer DNA-methylation biomarkers from fecal samples.

A product launch press conference was held in Bratislava, Slovakia. Dr. Martin Huroka (Chief Gastroenterology Specialist, Ministry of Health), Dr. Lucia Starovecká Copák (Medical Geneticist), and Dr. Jozef Dolinský (Clinical Oncologist), were the invited speakers.

Dr. Martin Huroka explained that age and family history are significant factors in the incidence of colorectal cancer. “The risk of colorectal cancer increases dramatically after age 50, or with a positive family history. Colorectal cancer is almost 100% preventable, and people would not have to die from intestinal cancer with regular preventive examinations”, Dr. Huroka stated.

Early detection is the key to the prevention of colorectal cancer and the improvement of survival rate because the progression of colorectal cancer development is generally very slow. It can take 10 to 15 years to develop from normal epithelium to adenomatous polyps and then undergo malignant transformation to become colorectal cancer.

“When diagnosed early – localized stage, the five-year survival rate of patients can be as high as 90%. However, the five-year survival rate drops significantly to only 10 to 15% at the advanced – metastatic stage. Economically, it also costs much less to treat an early-diagnosed disease than advanced cancer”, said Dr. Dolinský.

The availability of COLOTECTTM 1.0 in Slovakia offers an easy and convenient alternative for accurate screening and detection. “Its sensitivity for detecting colorectal cancers is 88%, and specificity for identifying subjects without advanced colorectal neoplasm is 92%. Most importantly, for early detection, its sensitivity for advanced adenoma is 46%”, Dr. Lucia Starovecká Copák noted.

COLOTECTTM 1.0 is CE-marked, available in more than 20 countries across South-East Europe, including Slovakia, Hungary, Poland, Romania, Portugal, and many more.

For its availability in Slovakia, please visit www.colotect.sk.

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Other News

Shoulder Innovations Further Strengthens IP Portfolio in Key Areas with Recent Patent Grants

"These recent grants further strengthen key patent families that are foundational to our technology, and we are pleased the USPTO continues to recognize our meaningful innovation in the shoulder arthroplasty segment," said Rob Ball, CEO of Shoulder Innovations. "This noteworthy expansion of our IP position represents the culmination of over 10 years of research and development, and we are proud of our team for their continued dedication to creating practical solutions for shoulder surgeons and advancing patient outcomes."

Radical Catheter Technologies Presents Analysis of Disruptive, Recently FDA-Cleared Endovascular Technology at the Society of NeuroInterventional Surgery 21st Annual Meeting

This new catheter, the first product commercialized from this novel technology platform, is designed to enable access to the blood vessels in the brain for both femoral and radial access. A multi-center analysis of this disruptive technology is being presented today at Society of NeuroInterventional Surgery 21st annual meeting. In addition, the Company confirmed the closing of a $20 million financing round led by NeuroTechnology Investors, which will be used to scale the company and expand the Radical platform notes Radical Catheter Technologies.

Rapid Medical™ Completes Initial Neurovascular Cases in the USA Following FDA Clearance of Its Active Access Solution

“With DRIVEWIRE, our design goal was to bring new levels of access and control to the interventional suite while improving best-in-class guidewires,” comments Giora Kornblau, Chief Technology Officer at Rapid Medical. “When physicians are looking for technologies that increase the clinical possibilities and safety for the patient, we want Rapid to be the first place they look.”