YD Bio Limited announces support for commercialization of OkaiDx™, a RUO test for post-treatment breast cancer monitoring.
Quiver AI Summary
YD Bio Limited has announced its support for the commercialization of OkaiDx™, a research-use-only blood test designed for post-treatment breast cancer monitoring, available through its affiliate EG Biomed US Inc. at their certified laboratory in the U.S. The test, which utilizes cfDNA methylation profiling, aims to provide molecular surveillance information for research purposes and has shown promising performance metrics in independent validations. YD Bio's collaboration with EG BioMed enhances the accessibility of this assay for research institutions and industry partners, although it is important to note that OkaiDx™ has not received FDA approval and is not intended for clinical use. The company aims to leverage this test to further the understanding of post-treatment monitoring in breast cancer patients and enhance patient outcomes through its ongoing research and development efforts in biotechnology.
Potential Positives
- YD Bio is supporting the global commercialization of OkaiDx™, a research-use-only blood test for post-treatment breast cancer monitoring, enhancing its product portfolio and market presence.
- The test demonstrates impressive independent validation performance metrics with 95.1% accuracy, 89.4% sensitivity, and 96.5% specificity, potentially increasing trust and interest from research laboratories and partners.
- The collaboration with EG BioMed allows YD Bio to leverage CLIA/CAP-certified laboratory capabilities, which strengthens its position in the biotechnology market and supports its ongoing commitment to scientific innovation and precision medicine.
Potential Negatives
- OkaiDx™ is currently only a research-use-only (RUO) test and has not been cleared or approved by the U.S. Food and Drug Administration, which may limit its market potential and public perception.
- The reliance on independent validation for performance metrics may raise concerns regarding the test's efficacy until more definitive regulatory approvals are obtained.
- The press release includes numerous forward-looking statements that carry inherent risks and uncertainties, which could lead to investor skepticism regarding the company's future prospects.
FAQ
What is OkaiDx™ and its purpose?
OkaiDx™ is a research-use-only blood test designed for post-treatment breast cancer monitoring, utilizing cfDNA methylation profiling.
How does YD Bio Limited support OkaiDx™?
YD Bio supports the commercialization of OkaiDx™ by coordinating researcher engagement, sample logistics, and expanding U.S. laboratory access.
Is OkaiDx™ FDA approved?
No, OkaiDx™ has not been cleared or approved by the U.S. Food and Drug Administration and is for research use only.
What are the performance metrics of OkaiDx™?
OkaiDx™ has reported performance metrics of 95.1% accuracy, 89.4% sensitivity, and 96.5% specificity according to independent validation.
Where can I find more information about YD Bio Limited?
More information about YD Bio Limited can be found on their official website: ir.ydesgroup.com.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$YDES Hedge Fund Activity
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- CERITY PARTNERS LLC added 32,406 shares (+inf%) to their portfolio in Q3 2025, for an estimated $630,944
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Full Release
Taipei, Taiwan, Nov. 05, 2025 (GLOBE NEWSWIRE) -- YD Bio Limited (“YD Bio” or the “Company”) (NasdaqGM: YDES), a biotechnology company advancing DNA methylation-based cancer detection technology and ophthalmologic innovations, today announced its support for the global commercialization of OkaiDx ™ , a research‑use‑only (RUO) blood test for post‑treatment breast cancer monitoring now available through the Company’s affiliate EG Biomed US Inc. (“EG BioMed”)’s CLIA/CAP‑certified laboratory in the United States. YD Bio’s role is to support commercialization efforts for OkaiDx ™ under the authorization granted to the Company, working alongside EG BioMed to make the assay accessible to research laboratories, academic groups and industry partners conducting surveillance and translational studies.
OkaiDx ™ was developed through international scientific collaboration and uses cfDNA methylation profiling to generate molecular surveillance information for research settings. The test has been reported in peer‑reviewed journals such as Clinical Epigenetics and Biomolecules , and presented at major oncology conferences. EG BioMed’s CLIA and CAP accreditation enables U.S. testing and reporting of RUO assays in an accredited laboratory environment, while YD Bio’s support complements EG BioMed’s laboratory capabilities by helping coordinate commercialization, researcher engagement and sample logistics for study use.
YD Bio’s involvement follows its ongoing partnership activities with EG BioMed to expand U.S. laboratory access for cutting‑edge molecular assays, said Dr. Ethan Shen, Founder, Chairman and Chief Executive Officer of YD Bio Limited. “Independent validation already reported performance metrics of 95.1% accuracy, 89.4% sensitivity and 96.5% specificity,” he said.
YD Bio is helping to commercialize OkaiDx ™ for research applications. As of present day, the test is for research use only, and has not been cleared or approved by the U.S. Food and Drug Administration, and is not intended to diagnose, treat, cure or prevent any disease. The Company expects OkaiDx ™ to provide a research‑grade tool that may enable investigators to study post‑treatment monitoring approaches and to generate additional evidence that could inform future clinical development.
About YD Bio Limited
YD Bio Limited is a biotechnology company focused on advancing clinical trials, new drug development, cancer prevention diagnostics, and stem cell and exosome therapies with the potential to transform the treatment of diseases with high unmet medical need. The Company is committed to improving patient outcomes through scientific innovation and precision medicine. In addition to its R&D efforts, YD Bio Limited is a recognized supplier of clinical trial drugs and has expanded into the development and distribution of post-market auxiliary products. For more information, please visit the Company’s website: ir.ydesgroup.com
Forward-Looking Statements
Certain statements in this announcement are forward-looking statements, including, but not limited to, YD Bio’s business plan and outlook. These forward-looking statements involve known and unknown risks and uncertainties and are based on YD Bio’s current expectations and projections about future events that YD Bio believes may affect its financial condition, results of operations, business strategy and financial needs. Investors can identify these forward-looking statements by words or phrases such as “approximates,” “believes,” “hopes,” “expects,” “anticipates,” “estimates,” “projects,” “intends,” “plans,” “will,” “would,” “should,” “could,” “may” or other similar expressions. YD Bio undertakes no obligation to update or revise publicly any forward-looking statements to reflect subsequent occurring events or circumstances, or changes in its expectations, except as may be required by law. Although YD Bio believes that the expectations expressed in these forward-looking statements are reasonable, it cannot assure you that such expectations will turn out to be correct, and YD Bio cautions investors that actual results may differ materially from the anticipated results and encourages investors to review other factors that may affect its future results in YD Bio’s registration statement and other filings with the U.S. Securities and Exchange Commission.
For investor and media inquiries, please contact:
YD Bio Limited
Investor Relations
Email:
[email protected]