Biocartis NV Achieves Milestone with Idylla™ EGFR Test Certification
Biocartis Milestone: IVDR Certification for Idylla™ EGFR Test
Biocartis NV, a pioneer in molecular diagnostics, has announced an exciting achievement—the certification of its Idylla™ EGFR Mutation Test under the European In Vitro Diagnostic Medical Device Regulation (IVDR) 2017/746. This achievement signifies a major step forward for Biocartis, setting new standards for diagnostic testing in the field of oncology.
Understanding the Idylla™ EGFR Mutation Test
The Idylla™ EGFR Mutation Test now stands as a prominent Class C Companion Diagnostic IVD Medical Device. It is specifically designed for detecting key biomarkers in lung cancer, focusing on EGFR exon 19 deletions and the L858R mutation. These biomarkers play a crucial role in guiding targeted therapies for patients diagnosed with non-small cell lung cancer (NSCLC).
What Does This Certification Mean?
With the IVDR certification, the Idylla™ EGFR Mutation Test adheres to rigorous European standards, enhancing patient safety, transparency, and data traceability for healthcare providers. This regulation ensures that patients receive reliable and effective diagnostic tools, leading to timely and accurate treatment decisions.
How the Test Works
The Idylla™ test operates on the innovative Idylla™ Platform, enabling laboratories to conduct genetic testing at remarkable speed. The test can qualitatively detect 44 mutations across multiple exons of the EGFR gene using only a single cartridge. Notably, it delivers results in under three hours, significantly streamlining the workflow for medical practitioners and enabling rapid treatment decisions.
Key Benefits of the Idylla™ EGFR Mutation Test
Healthcare professionals utilizing the Idylla™ EGFR Mutation Test can expect exceptional reliability, with a sensitivity rate of 99.2% and a specificity rate of 99.0% for the targeted mutations. This remarkable accuracy empowers healthcare providers with actionable results, crucial for making informed decisions regarding NSCLC treatment.
Future Prospects and Continuous Development
While the Idylla™ EGFR Mutation Test is currently available in European markets, Biocartis is also working tirelessly to expand its availability in other regions, progressively reaching non-US markets. Furthermore, there are plans in motion for the development of the Idylla™ EGFR CDx Test in collaboration with AstraZeneca, which will facilitate the identification of NSCLC patients who may benefit from Tagrisso® (Osimertinib), a groundbreaking treatment option.
Insight from the CEO
Roger Moody, the Chief Executive Officer of Biocartis, shared his pride in this significant milestone, stating, “Achieving IVDR certification for our Idylla™ EGFR Mutation Test exemplifies our commitment to regulatory excellence and quality in diagnostics. As we strive to enhance patient safety and diagnostic accuracy, we are thrilled to lead in this new wave of European diagnostics.”
More About Biocartis
Biocartis aims to enable personalized medicine through its revolutionary Idylla™ Platform, providing accessible and fast molecular testing. The Idylla™ system is designed for optimal laboratory efficiency and patient care, offering real-time PCR-based molecular biomarker testing within a compact timeframe. Their expanding repertoire of tests addresses critical clinical needs across various cancer types including lung, skin, thyroid, and more.
Frequently Asked Questions
What is the Idylla™ EGFR Mutation Test used for?
The Idylla™ EGFR Mutation Test is designed to identify significant mutations in the EGFR gene, aiding in the treatment decisions for patients with non-small cell lung cancer.
How quickly can results be generated using this test?
The test offers rapid results, typically delivering them in less than three hours, which allows oncologists to make timely decisions for patient treatment.
What regulatory standards does the test comply with?
The Idylla™ EGFR Mutation Test complies with the European Union's IVDR standards, ensuring high-quality safety and performance criteria.
Are there future plans for other markets?
Yes, while the test is currently available across Europe, Biocartis is expanding its reach to additional non-US markets progressively.
How does Biocartis enhance patient care through diagnostics?
By providing fast and accurate molecular testing, Biocartis empowers healthcare professionals to make informed treatment decisions, ultimately improving patient outcomes.
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