Daily Newsletter

03 November 2023

Daily Newsletter

03 November 2023

FDA approves Abbott’s HPV screening solution

The Alinity m HR HPV assay will provide data on 14 different potentially cancer-causing virus genotypes.

Archana Rani November 03 2023

The US Food and Drug Administration (FDA) has approved Abbott's molecular human papillomavirus (HPV) screening solution, an addition to the Alinity m diagnostic assay family.

The screening solution tool is designed to detect high-risk HPV infections that are said to be common in most sexually active adults, according to the US Centers for Disease Control.

Abbott said there are several variants of the HPV, distinguished by their distinct genetic signatures or genotypes.

Certain HPV genotypes have the potential to cause cancer, particularly cervical cancer in females.

Traditionally, Pap tests were employed for cervical cancer screening. However, current professional guidelines advocate for primary screening via HPV infection tests as the superior method for detecting cervical cancer over Pap testing.

As per professional medical guidelines, the Alinity m high risk (HR) HPV assay is approved for HPV detection and regular cervical cancer screening.

The assay is also authorised for co-testing, in conjunction with a Pap test, for those patients and physicians who opt for both tests.

The Alinity m HR HPV assay will provide data on five risk categories, encompassing the 14 different potentially cancer-causing genotypes of the virus.

This would assist physicians in not only detecting the presence of an HPV infection but also determining whether the infection stems from one or more of the types that might lead to cancer.

Abbott molecular business vice-president Keith Cienkus said: “HPV testing is a powerful tool for detecting HPV infections that can lead to certain cancers, including cervical cancer and illustrates the power of molecular diagnostics in infectious disease.”

The Abbott Alinity m HR HPV assay is planned to be made available for use on Abbott's Alinity m laboratory instrument.

The assays that will be made available for use on the Alinity m system in the US include Resp-4-Plex, SARS-CoV-2, HCV (Hepatitis C), HIV-1 (Human Immunodeficiency Virus type 1), HBV (Hepatitis B), STI (CT/NG/TV/MG), CMV (Cytomegalovirus) and EBV (Epstein–Barr virus).

Is the healthcare industry ready to fully embrace the benefits of digitalization and AI?

The healthcare, pharma, and medical devices industries are often risk-averse compared to other sectors when adopting new technologies. However, mainly due to COVID-19, these sectors have witnessed an acceleration in digital transformation. AI can revolutionize the drug discovery process and significantly reduce the time and cost to get a drug to market, particularly in areas of unmet need. There is also huge potential for AI in medical diagnostics. However, using healthcare data for AI development raises data privacy concerns, thereby limiting its adoption.

Newsletters by sectors

close

Sign up to the newsletter: In Brief

Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Thank you for subscribing

View all newsletters from across the GlobalData Media network.

close