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BD Onclarity™ HPV Assay Receives FDA Approval for Use with Both BD SurePath™ Liquid-based Pap Test and Hologic ThinPrep® Pap Test BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today announced U.S. Food and Drug Administration (FDA)...

Key Takeaway: BD (Becton, Dickinson and Company) has received FDA approval for its Onclarity HPV Assay, which is now authorized for use alongside the ThinPrep Pap Test. This assay is particularly notable as it can individually identify high-risk HPV31, improving cervical cancer risk assessment compared to other tests that pool results. The approval represents a significant advance in diagnostic solutions for women's health, increasing access to more tailored screening methods. Additionally, it comes backed by a robust real-world evidence study, underscoring its clinical validation in routine clinical practice.

Market Sentiment Analysis

POSITIVE FACTORS

  • FDA approval allows the Onclarity HPV Assay to be used with ThinPrep Pap Test, enhancing cervical cancer detection.
  • The assay uniquely identifies high-risk HPV types, providing more precise risk assessment for cervical cancer.
  • Expands BD’s strategies in molecular diagnostics and women’s health, tapping into a larger market.
  • Real-world evidence from a large study supports the assay's clinical validation.

Full Press Release Details

Expands Access to BD HPV Test that More Precisely Identifies Patients' Risk for Cervical Cancer
FRANKLIN LAKES, N.J. , Feb. 21, 2023 /PRNewswire/ -- BD (Becton, Dickinson and Company) (NYSE: BDX ), a leading global medical technology company, today announced U.S. Food and Drug Administration (FDA) market approval for the BD Onclarity™ HPV Assay to be used with the ThinPrep® Pap Test.
"Most tests report multiple HPV types in a single pooled result, which can mask the true risk of developing cervical cancer," said Brooke Story , worldwide president of Integrated Diagnostics Solutions for BD. "Being able to identify high-risk HPV31 individually is critical to the detection and prevention of cervical cancer. HPV31 poses the second-highest risk for cervical pre-cancer, and the BD Onclarity™ HPV Assay is the only FDA-approved assay that screens for it individually."
This important milestone supports BD's strategy to penetrate the large and growing molecular diagnostics market through its expanded installed base and providing additional testing solutions for women's health.
The BD Onclarity™ HPV Assay detects and identifies 14 high-risk human papillomavirus (HPV) types in a single analysis. The assay reports genotypes beyond HPV types 16, 18, and 45 to include types 31, 51, 52, 33/58, 35/39/68, and 56/59/66, making the BD Onclarity™ HPV Assay the only FDA-approved assay to individually identify and report these genotype results. The BD Onclarity™ HPV Assay has FDA approval for use in vaccinated women. As the previously vaccinated subpopulation ages, the screening population will progressively include women with reduced prevalence of HPV 16 and 18, increasing the value of extended genotype reporting in a mixed population of vaccinated and unvaccinated women.
The evidence generation for the clinical validation of BD Onclarity™ HPV Assay out of PreservCyt® media was achieved by one of the largest real-world evidence studies of its kind, conducted by Dr. Cosette Wheeler , with the New Mexico HPV and Pap Registry, including a random sample of 19,879 women's preserved samples who had undergone opportunistic cervical screening and follow-up in routine clinical practice, with known clinical outcomes.
"Cervical cancer is preventable," said Dr. Jeff Andrews , vice president of medical affairs for BD. "When more people with a cervix are better able to manage their health through more accurate and precise testing, we are taking another step forward toward eliminating cervical cancer in our lifetimes."
The ThinPrep® Pap Test with the BD Onclarity™ HPV Assay can be used on the BD COR™ or BD Viper™ LT instrument platforms without the need to change current cytology equipment. The BD COR™ System offers integrated and automated workflows, designed to free up time in the high-throughput laboratory, and the extended claim for the BD Onclarity™ HPV Assay allows mid- to low-throughput labs to leverage the benchtop BD Viper™ LT instrument to enhance their HPV test offering.
About BD BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. The company supports the heroes on the frontlines of health care by developing innovative technology, services and solutions that help advance both clinical therapy for patients and clinical process for health care providers. BD and its 77,000 employees have a passion and commitment to help enhance the safety and efficiency of clinicians' care delivery process, enable laboratory scientists to accurately detect disease and advance researchers' capabilities to develop the next generation of diagnostics and therapeutics. BD has a presence in virtually every country and partners with organizations around the world to address some of the most challenging global health issues. By working in close collaboration with customers, BD can help enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care. For more information on BD, please visit bd.com or connect with us on LinkedIn at www.linkedin.com/company/bd1/ and Twitter @BDandCo .
Contacts:
Media : Investors :
Troy Kirkpatrick Francesca DeMartino
VP, Public Relations SVP, Head of Investor Relations
858.617.2361 201.847.5743
[email protected] [email protected]
SOURCE BD (Becton, Dickinson and Company)

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Frequently Asked Questions

What does the BD Onclarity™ HPV Assay detect?

The assay detects and identifies 14 high-risk HPV types in a single analysis.

Why is HPV31 significant in cervical cancer risk?

HPV31 has the second-highest risk for cervical pre-cancer and is identified individually.

Is the BD Onclarity™ HPV Assay FDA approved for vaccinated women?

Yes, it has FDA approval for use in vaccinated women as well.

What study validated the BD Onclarity™ HPV Assay?

It was supported by one of the largest real-world evidence studies of its kind.

How does the BD Onclarity™ HPV Assay enhance screening?

It allows for extended genotype reporting, aiding in cervical cancer prevention efforts.

Last updated: Feb 21, 2023