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Myriad Genetics Underscores Commitment to Cancer Care Continuum with New Data Presentations at SGO Annual Meeting

Key Takeaway: Myriad Genetics will present new data at the SGO Annual Meeting, including findings on Precise MRD testing for ovarian cancer. The data suggest that monitoring ctDNA levels can predict recurrence risk. Additionally, three presentations will discuss genetic variant prevalence and hereditary cancer screening, emphasizing the company's commitment to cancer research.
Price reaction · baseline $4.77 (2026-04-08 close) · hit pre-market · 1 other MYGN headline(s) in the window, move may be shared
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POSITIVE FACTORS

  • Myriad Genetics presents significant new data at SGO Annual Meeting.
  • Precise MRD testing shows promise in predicting ovarian cancer recurrence.
  • Research registry data highlights the importance of genetic insights in cancer care.
  • Company demonstrates commitment to advancing cancer care through research.

Full Press Release Details

SALT LAKE CITY, April 09, 2026 (GLOBE NEWSWIRE) --Myriad Genetics, Inc.(NASDAQ: MYGN), a leader in molecular diagnostic testing and precision medicine, today announces that it will share new data at the Society of Gynecologic Oncology (SGO) Annual Meeting, including two oral presentations and two posters.
“Having four abstracts accepted at the prestigious SGO annual meeting underscores the importance of the data we are sharing and our commitment to the cancer care continuum,” said Dale Muzzey, PhD, Chief Scientific Officer, Myriad Genetics. “We are particularly pleased to be presenting the latest Precise MRD™data, showing that Precise MRD testing after adjuvant therapy for ovarian cancer was significantly prognostic of recurrence during the monitoring period. Importantly, recurrence risk tracked with the quantitative ctDNA fraction detected by Precise MRD, with elevated risk observed even at ctDNA levels detectable only by an ultrasensitive assay.”
The remaining three presentations use data from theMyriad Collaborative Research Registry™(MCRR), one of the largest pan-cancer registries accessible for research use, including de-identified data for more than 1.3 million participants. The studies demonstrate Myriad’s commitment to externally driven research that addresses diverse questions with immediate clinical implications:
Germline pathogenic and likely pathogenic variant prevalence is associated with age and ancestry in patients diagnosed with ovarian cancer before age 40;
Ovarian cancer diagnosis varies by Lynch syndrome gene, informing counseling and risk-reducing surgery recommendations;
Universal hereditary cancer screening identifies more individuals at high risk for endometrial cancer compared to age-based screening.
These studies will be presented at theSociety of Gynecologic Oncology Annual Meetingon April 10-13 at the Puerto Rico Convention Center in San Juan. Myriad will exhibit at booth #523. For more information, visit:https://myriad.com/oncology/oncology-conferences/
Myriad Genetics PresentationsPrecise MRDEvaluation of the Relationship of Molecular Residual Disease Testing to Ovarian Cancer RecurrencePoster Board Number: 1590Sun., April 12 at 12:00-1:00 pm ASTPresenter: John Nakayama, MD, Allegheny Health Network
MCRRPrevalence of germline pathogenic variants in patients with endometrial cancer diagnosed before and after 65 years old within a laboratory-based research registryRapid Fire Oral I: Genetics Prevention and SurgerySat., April 11 – 3:05-3:08 pm ASTPresenter: Kieran Seay, MD, University of Pittsburgh Medical Center
Broad landscape of genetic variants and ancestry associated with ovarian cancer before age fortyPoster Board Number: 1450Sun., April 12 – 4:00-4:45 pm ASTPresenter: Eliya K. Shachar, MD, University of California, Los Angeles
Age at ovarian cancer diagnosis varies by lynch syndrome gene: a genetic testing laboratory registry studyFocused Forum X: Genetics - Keeping up with the GenesMon., April 13 – 9:30-10:30 am ASTPresenter: Ying L. Liu, MD, MPH, Memorial Sloan Kettering Cancer Center
About Myriad GeneticsMyriad Genetics is a leading molecular diagnostic and precision medicine company committed to advancing health and well-being for all. Myriad Genetics develops and commercializes molecular tests that help patients and providers uncover genetic insights. Our tests assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where molecular insights can significantly improve patient care, support earlier detection, enable more precise treatment and contribute to lowering healthcare costs. For more information, visitmyriad.com.
Myriad Genetics Safe Harbor StatementThis press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements that the studies demonstrate the company’s commitment to externally driven research that addresses diverse questions with immediate clinical implications. These “forward-looking statements” are management’s expectations of future events as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company’s filings with the U.S. Securities and Exchange Commission, including the company’s Annual Report on Form 10-K filed on February 24, 2026, as well as any updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. Myriad is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise except as required by law.

Investor ContactMatt Scalo(801) 584-3532IR@myriad.com

Media ContactKate Schraml(224) 875-4493PR@myriad.com

Frequently Asked Questions

What data will Myriad Genetics present at the SGO meeting?

Myriad Genetics will present findings on Precise MRD testing and genetic variant prevalence related to ovarian cancer.

When is the SGO Annual Meeting taking place?

The SGO Annual Meeting is scheduled for April 10-13, 2026.

What is the significance of Precise MRD testing?

Precise MRD testing is significant for predicting ovarian cancer recurrence based on ctDNA levels.

How many abstracts were accepted by Myriad at the SGO meeting?

Four abstracts were accepted for presentation at the SGO Annual Meeting.

Last updated: Apr 9, 2026