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Myriad Genetics Expands Access for MyChoice Test to Prostate Cancer Patients in Japan

Key Takeaway: Myriad Genetics has received approval from Japan's Ministry of Health for the MyChoice Test to be used as a companion diagnostic for prostate cancer patients. This allows clinicians to assess homologous recombination deficiency and BRCA1/2 status, broadening access to genomic insights. The approval is expected to enhance treatment options for patients, particularly those with castration-resistant prostate cancer.
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POSITIVE FACTORS

  • Approval expands MyChoice Test access to prostate cancer patients.
  • Clinicians can now utilize the test for better treatment decisions.
  • The initiative reflects Myriad's commitment to precision medicine.
  • Potential to benefit a significant number of prostate cancer patients.

Full Press Release Details

SALT LAKE CITY, April 14, 2026 (GLOBE NEWSWIRE) --Myriad Genetics Inc., (NASDAQ: MYGN), a leader in molecular diagnostic testing and precision medicine, today announced that Japan’s Ministry of Health, Labour and Welfare (MHLW) has approved the use of the MyChoice®Test for prostate cancer patients as a companion diagnostic for Lynparza®(olaparib). With this approval, clinicians can now order the MyChoice Test to determine homologous recombination deficiency (HRD) status for patients with ovarian cancer, and BRCA1/2 status for breast and prostate cancers.
“Expanding the MyChoice test into prostate cancer marks an important milestone for Myriad Genetics in Japan,” said Brian Donnelly, Chief Commercial Officer, Myriad Genetics. “Previously, MyChoice testing was only reimbursed under Japan’s National Health Insurance (NHI) for breast and ovarian cancer patients, so this new approval broadens access to critical genomic insights that help clinicians make informed treatment decisions for their patients. This also reflects Myriad’s continued focus on adding high value precision medicine tests to its Cancer Care Continuum portfolio.”
According to theWorld Cancer Research Fund, more than 100,000 men are newly diagnosed with prostate cancer annually in Japan, and a portion of those patients will be diagnosed with or later progress to metastatic castration-resistant (mCRP).
“The reimbursement approval of MyChoice for prostate cancer provides a new testing option for patients with castration-resistant prostate cancer. In addition to the previously available germline BRCA1/2 testing, the inclusion of tumor-based testing is expected to expand the number of patients who may benefit from treatment with PARP inhibitors,” said Dr. Hiroji Uemura, Project Professor, Department of Urological Oncology, Yokohama City University Graduate School of Medicine.
About the MyChoice TestThe MyChoice Test offers comprehensive homologous recombination deficiency (HRD) testing enabling physicians to identify patients with tumors that have lost the ability to repair double-stranded DNA breaks, resulting in increased susceptibility to DNA-damaging drugs such as platinum drugs or PARP inhibitors. The MyChoice tests comprise tumor sequencing of theBRCA1andBRCA2genes and a composite of three proprietary technologies (loss of heterozygosity, telomeric allelic imbalance and large-scale state transitions). The test is offered for breast, ovarian, and prostate cancer indications in Japan. For more information about Myriad Genetics in Japan, visitmyriadgenetics.jp.
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 inclusion of tumor-based testing is expected to expand the number of patients who may benefit from treatment with PARP inhibitors. 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 is the MyChoice Test?

The MyChoice Test assesses homologous recombination deficiency to guide treatment decisions.

Who can benefit from the MyChoice Test?

Patients with prostate, breast, and ovarian cancers can benefit from the MyChoice Test.

What does the approval mean for prostate cancer patients?

It provides new testing options for patients, particularly those with castration-resistant prostate cancer.

How does the MyChoice Test aid treatment decisions?

It helps identify patients who may respond to DNA-damaging drugs like PARP inhibitors.

Last updated: Apr 14, 2026