{"id":934046,"date":"2026-02-04T12:38:13","date_gmt":"2026-02-04T17:38:13","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/"},"modified":"2026-02-04T12:38:13","modified_gmt":"2026-02-04T17:38:13","slug":"hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/","title":{"rendered":"Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio"},"content":{"rendered":"

<\/p>\n

Hologic Receives FDA Approval for Aptima<\/b>\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio<\/b><\/p>\n

Expanded FDA approval across multiple cervical cancer screening modalities supports clinical flexibility and provider choice<\/i><\/p>\n

MARLBOROUGH, Mass.–(BUSINESS WIRE<\/a>)–
\nHologic, Inc. (Nasdaq: HOLX) announced today that its Aptima\u00ae<\/sup> HPV Assay received FDA approval for clinician-collected HPV primary screening. Hologic\u2019s human papillomavirus (HPV) test is the only FDA-approved mRNA-based assay, designed specifically to detect infections most likely to lead to cervical cancer.<\/p>\n

This press release features multimedia. View the full release here: https:\/\/www.businesswire.com\/news\/home\/20260126336815\/en\/<\/a><\/p>\n

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\nScreening for cervical cancer is critically important to women\u2019s health. In the United States, it is estimated that in 2026, approximately 13,490 new cases of invasive cervical cancer will be diagnosed, and about 4,200 women will die from the disease.1<\/sup> However, many of these deaths are preventable with regular screening and appropriate follow-up on abnormal results. Timely follow-up is essential for early detection and treatment to reduce cervical cancer cases and deaths.1<\/sup><\/p>\n

\n\u201cHologic has been at the forefront of cervical cancer screening for decades, and the additional indication of the Aptima HPV Assay reflects our ongoing commitment to advancing women\u2019s health through innovative, evidence-based solutions,\u201d said Jennifer Schneiders, Ph.D., President of Diagnostic Solutions at Hologic. \u201cOur commitment to providing comprehensive cervical health solutions that meet provider and patient needs is unwavering, and by offering providers more choice and flexibility, we can help them deliver the most personalized care for each patient.\u201d<\/p>\n

\nThe additional indication for the Aptima HPV Assay expands Hologic\u2019s offerings to now include Pap + HPV (co-testing), Pap testing, and HPV primary testing \u2014 three major FDA-approved and guideline-recommended methods for cervical cancer screening. This additional approval for the Aptima HPV Assay follows the clearance of the Genius\u00ae<\/sup> Digital Diagnostics System with the Genius\u00ae<\/sup> Cervical AI Algorithm, which leverages advanced digital imaging and artificial intelligence to help detect cytologic abnormalities and precancerous lesions.<\/p>\n

\nThe approval comes following the completion of one of the largest real-world evidence HPV screening studies, involving over 650,000 women across multiple U.S. health systems that reflect diverse, real-life patient populations and clinical settings. This innovative study compared the Aptima HPV Assay to an FDA-approved DNA-based HPV test for primary screening and found that the sensitivity of the Aptima HPV Assay is clinically comparable to the comparator test. The Aptima HPV Assay is effective for use in primary screening for the detection of CIN2+ and CIN3+.<\/p>\n

\nWhile co-testing remains the most comprehensive screening modality \u2014 with more than 90% of providers reporting strong confidence for women ages 30 to 65, and data showing that co-testing (Pap + HPV) detected up to 95% of cervical cancers \u2014 Hologic’s range of testing options gives providers greater flexibility in selecting an approach based on a patient\u2019s age, access and risk factors.2-5<\/sup><\/p>\n

About Hologic\u2019s Cervical Health Solutions<\/b><\/p>\n

\nHologic offers a broad portfolio for cervical cancer screening, supporting both cytology and molecular workflows from sample collection to results. The portfolio includes innovations such as the ThinPrep\u00ae<\/sup> Pap Test, the first liquid-based cytology test, the Aptima HPV Assay, the first and only approved mRNA-based HPV tests, and the Genius Digital Diagnostics System, the first and only FDA-cleared digital cytology system. These technologies are designed to support clinicians and laboratory professionals in the detection and prevention of cervical cancer, all backed by Hologic\u2019s support and partnership. To learn more, please visit Hologic.com<\/b><\/a>.<\/p>\n

About Hologic, Inc.<\/b><\/p>\n

\nHologic, Inc. is a global leader in women\u2019s health dedicated to developing innovative medical technologies that effectively detect, diagnose and treat health conditions and raise the standard of care around the world. To learn more, visit www.hologic.com<\/b><\/a> and connect with us on LinkedIn<\/b><\/a>, Facebook<\/b><\/a>, X<\/b><\/a>, Instagram<\/b><\/a> and YouTube<\/b><\/a>.<\/p>\n

Forward-Looking Statements<\/b><\/p>\n

\nThis news release may contain forward-looking information that involves risks and uncertainties, including statements about the use of Hologic\u2019s and its subsidiaries\u2019 products. There can be no assurance these products will achieve the benefits described herein or that such benefits will be replicated in any particular manner with respect to an individual patient, as the actual effect of the use of the products can only be determined on a case-by-case basis. In addition, there can be no assurance that these products will be commercially successful or achieve any expected level of sales. Hologic expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any such statements presented herein to reflect any change in expectations or any change in events, conditions or circumstances on which any such data or statements are based.<\/p>\n

\nHologic, Aptima, ThinPrep, Genius and associated logos are trademarks and\/or registered trademarks of Hologic, Inc. and\/or its subsidiaries in the United States and\/or other countries. All other trademarks are the property of their respective owners.<\/p>\n

References:<\/b>1.<\/b> American Cancer Society. Cancer Statistics Center. Accessed January 2026. https:\/\/cancerstatisticscenter.cancer.org\/types\/cervix<\/a>. 2.<\/b> Austin et al. Enhanced Detection of Cervical Cancer and Precancer Through Use of Imaged Liquid-Based Cytology in Routine Cytology and HPV Cotesting. Am J Clin Patho 2018; 150:385-392 1. 3.<\/b> Blatt AJ, et al. Comparison of cervical cancer screening results among 256,648 women in multiple clinical practices. Cancer Cytopathol. 2015;123(5):282-288. doi:10.1002\/cncy.21544. 4.<\/b> Kaufman H, et al. Contributions of Liquid-Based (Papanicolaou) Cytology and Human Papillomavirus Testing in Cotesting for Detection of Cervical Cancer and Precancer in the United States. Am J Clin Pathol. 2020:XX:0-0 DOI: 10.1093\/AJCP\/AQAA074 (Study included ThinPrep Pap test, ThinPrep imaging, SurePath Pap test, SurePath imaging, Aptima HPV and Hybrid Capture 2). 5. <\/b>Kruse G, et al. Provider beliefs in effectiveness and recommendations for primary HPV testing in 3 health-care systems. JNCI Cancer Spectrum. 2023;7(1).<\/p>\n

SOURCE: Hologic, Inc.<\/b><\/p>\n

\"\"<\/p>\n

View source version on businesswire.com: <\/span>https:\/\/www.businesswire.com\/news\/home\/20260126336815\/en\/<\/a><\/span><\/p>\n

Media Contact:
\n<\/b>
Bridget Perry
\n
Senior Director, Corporate Communications
\n
(+1) 508.263.8654
\n
bridget.perry@hologic.com<\/b><\/a><\/p>\n

Investor Contact:
\n<\/b>
Michael Watts
\n
Corporate Vice President, Investor Relations
\n
(+1) 858.410.8514
\n
michael.watts@hologic.com<\/b><\/a><\/p>\n

KEYWORDS:<\/b> Massachusetts United States North America<\/p>\n

INDUSTRY KEYWORDS:<\/b> Women Biotechnology Pharmaceutical Oncology Health FDA Medical Devices Consumer<\/p>\n

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Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio Expanded FDA approval across multiple cervical cancer screening modalities supports clinical flexibility and provider choice MARLBOROUGH, Mass.–(BUSINESS WIRE)– Hologic, Inc. (Nasdaq: HOLX) announced today that its Aptima\u00ae HPV Assay received FDA approval for clinician-collected HPV primary screening. Hologic\u2019s human papillomavirus (HPV) test is the only FDA-approved mRNA-based assay, designed specifically to detect infections most likely to lead to cervical cancer. This press release features multimedia. View the full release here: https:\/\/www.businesswire.com\/news\/home\/20260126336815\/en\/ Screening for cervical cancer is critically important to women\u2019s health. In the United States, it is estimated that in 2026, approximately 13,490 new cases of invasive cervical cancer will be diagnosed, and about 4,200 … <\/p>\n

Continue reading “Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio”<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-934046","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"\nHologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio Expanded FDA approval across multiple cervical cancer screening modalities supports clinical flexibility and provider choice MARLBOROUGH, Mass.–(BUSINESS WIRE)– Hologic, Inc. (Nasdaq: HOLX) announced today that its Aptima\u00ae HPV Assay received FDA approval for clinician-collected HPV primary screening. Hologic\u2019s human papillomavirus (HPV) test is the only FDA-approved mRNA-based assay, designed specifically to detect infections most likely to lead to cervical cancer. This press release features multimedia. View the full release here: https:\/\/www.businesswire.com\/news\/home\/20260126336815\/en\/ Screening for cervical cancer is critically important to women\u2019s health. 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(Nasdaq: HOLX) announced today that its Aptima\u00ae HPV Assay received FDA approval for clinician-collected HPV primary screening. Hologic\u2019s human papillomavirus (HPV) test is the only FDA-approved mRNA-based assay, designed specifically to detect infections most likely to lead to cervical cancer. This press release features multimedia. View the full release here: https:\/\/www.businesswire.com\/news\/home\/20260126336815\/en\/ Screening for cervical cancer is critically important to women\u2019s health. In the United States, it is estimated that in 2026, approximately 13,490 new cases of invasive cervical cancer will be diagnosed, and about 4,200 … Continue reading \"Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/","og_site_name":"Market Newsdesk","article_published_time":"2026-02-04T17:38:13+00:00","og_image":[{"url":"https:\/\/mms.businesswire.com\/media\/20260126336815\/en\/2704859\/4\/HPV-Primary-Edit.jpg","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"5 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio","datePublished":"2026-02-04T17:38:13+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/"},"wordCount":1005,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/#primaryimage"},"thumbnailUrl":"https:\/\/mms.businesswire.com\/media\/20260126336815\/en\/2704859\/4\/HPV-Primary-Edit.jpg","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/hologic-receives-fda-approval-for-aptima-hpv-assay-primary-screening-option-expanding-cervical-health-portfolio\/","name":"Hologic Receives FDA Approval for Aptima\u00ae HPV Assay Primary Screening Option, Expanding Cervical Health Portfolio - 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