Trinity Biotech Announces Positive Results for Enhanced Prostate Cancer Test
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Mar 24 2026
0mins
Should l Buy TRIB?
Source: NASDAQ.COM
- Clinical Study Results: Trinity Biotech's EpiCapture prostate cancer test was evaluated in approximately 750 patient samples, demonstrating a clinical accuracy of 85%, indicating strong clinical utility in oncology diagnostics that can aid physicians in making more precise clinical decisions.
- Significant Market Potential: With U.S. national expenditures for prostate cancer care exceeding $20 billion annually, the launch of EpiCapture positions Trinity Biotech to enter the precision oncology diagnostics market, addressing growing market demand and driving future revenue growth for the company.
- Non-Invasive Testing Advantage: EpiCapture, as a urine liquid biopsy test, offers a simpler and non-invasive method for assessing high-grade prostate cancer risk compared to high-resolution MRI scans and needle biopsies, potentially attracting more patients to opt for this testing.
- Future Commercialization Plans: Trinity plans to commercialize EpiCapture as a proprietary Laboratory Developed Test (LDT) through a New York State Department of Health-certified diagnostic reference laboratory, which will expedite the rollout of precision oncology testing services across the U.S.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy TRIB?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on TRIB
About TRIB
Trinity Biotech plc is a commercial stage biotechnology company focused on diabetes management solutions and human diagnostics, including wearable biosensors. The Company develops, acquires, manufactures and markets diagnostic systems, including both reagents and instrumentation, for the point-of-care and clinical laboratory segments of the diagnostic market. The products are used to detect infectious diseases and to quantify the level of Hemoglobin A1c and other chemical parameters in serum, plasma and whole blood, and the Company intends to develop a range of biosensor devices and related services, starting with a continuous glucose monitoring product. Its TrinScreen Human Immunodeficiency Virus (HIV) rapid point-of-care test is a high-quality, single-use immunoassays to aid in the diagnosis of HIV. The Uni-Gold range of rapid point-of-care test devices consist of high-quality, single-use immunoassays to aid in the diagnosis of HIV.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
Trinity Biotech Reports FY 2025 Financial Results
- Revenue Decline: Trinity Biotech reported FY 2025 revenue of $43.8 million, a 28.9% year-over-year decrease, indicating significant sales challenges amid intensified market competition and weak product demand, which may impact future liquidity.
- Increased Net Loss: The company recorded a net loss of $37.4 million, up from $31.8 million in 2024, which included a one-off IFRS charge of $10 million related to modifications in Perceptive financing arrangements, highlighting financial management pressures.
- Adjusted EBITDA Improvement: The adjusted EBITDA for 2025 was negative $5.9 million, an improvement from negative $11.3 million in 2024, suggesting some progress in cost control despite the overall financial situation remaining challenging.
- Financing Agreement Signed: Trinity Biotech entered into a $25 million standby equity purchase agreement with investors to strengthen its capital structure and provide operational funding, reflecting proactive measures in seeking financial stability.
See More
Trinity Biotech Appoints New Head of North America Operations
- Executive Appointment: Trinity Biotech has appointed Jerry Lydon as Head of North America Commercial Operations, aiming to enhance revenue growth and profitability in its core diagnostics business, reflecting ongoing progress in the company's Comprehensive Transformation Plan.
- Product Upgrade: The Premier HbA1c 9210™ platform has received the prestigious
See More
Trinity Biotech Announces Positive Results for Enhanced Prostate Cancer Test
- Clinical Study Results: Trinity Biotech's EpiCapture prostate cancer test was evaluated in approximately 750 patient samples, demonstrating a clinical accuracy of 85%, indicating strong clinical utility in oncology diagnostics that can aid physicians in making more precise clinical decisions.
- Significant Market Potential: With U.S. national expenditures for prostate cancer care exceeding $20 billion annually, the launch of EpiCapture positions Trinity Biotech to enter the precision oncology diagnostics market, addressing growing market demand and driving future revenue growth for the company.
- Non-Invasive Testing Advantage: EpiCapture, as a urine liquid biopsy test, offers a simpler and non-invasive method for assessing high-grade prostate cancer risk compared to high-resolution MRI scans and needle biopsies, potentially attracting more patients to opt for this testing.
- Future Commercialization Plans: Trinity plans to commercialize EpiCapture as a proprietary Laboratory Developed Test (LDT) through a New York State Department of Health-certified diagnostic reference laboratory, which will expedite the rollout of precision oncology testing services across the U.S.
See More
Trinity Biotech PLC Secures $25 Million SEPA with Yorkville Advisors Global Affiliate
Investment Announcement: Trinity Biotech PLC has entered into a $25 million SEPA with an affiliate of Yorkville Advisors.
Financial Partnership: The agreement involves a financing partnership aimed at supporting Trinity Biotech's growth and operational needs.
See More
Trinity Biotech Receives Regulatory Approval for New Production Model Launch
- Regulatory Milestone: Trinity Biotech has received local regulatory approval, marking the initiation of upstream manufacturing activities for its Uni-Gold™ HIV rapid test under a new outsourced production model, which is a key component of the company's comprehensive transformation plan.
- Cost Efficiency Improvement: The implementation of the offshore and outsourced production model is expected to significantly enhance gross margins and improve working capital efficiency, thereby strengthening the company's long-term competitiveness in the global HIV rapid testing market.
- Market Demand Support: This transition will not only meet the anticipated growth in demand for Uni-Gold™ HIV products but also provide the necessary scalability to ensure the company remains agile and responsive in a rapidly changing market environment.
- Strategic Transformation Plan: This approval complements the WHO authorization obtained in November 2025, demonstrating the company's strong commitment to executing its comprehensive transformation plan, which is expected to lay a solid foundation for future financial performance.
See More
Dow Jones Index Gains Over 100 Points as Durable Goods Orders Decline 2.2%
- Dow Jones Index Rise: The Dow Jones index increased by over 100 points on Tuesday, closing at 48,469.41, indicating a moderate market recovery despite disappointing economic data.
- Durable Goods Orders Decline: U.S. durable goods orders fell by 2.2% month-over-month to $307.4 billion in October, significantly missing market expectations of a 1.5% decline, reflecting weak manufacturing demand that could impact future economic growth.
- Accelerated GDP Growth: The U.S. GDP grew at an annualized rate of 4.3% in the third quarter, up from 3.8% in the previous quarter and exceeding market estimates of 3.3%, indicating potential for economic recovery that may positively influence the stock market.
- Mixed Sector Performance: Communication services rose by 0.5% while consumer staples fell by 0.5%, demonstrating varied market reactions across sectors, prompting investors to monitor industry dynamics for strategic adjustments.
See More
Trinity Biotech Reports FY 2025 Financial Results
- Revenue Decline: Trinity Biotech reported FY 2025 revenue of $43.8 million, a 28.9% year-over-year decrease, indicating significant sales challenges amid intensified market competition and weak product demand, which may impact future liquidity.
- Increased Net Loss: The company recorded a net loss of $37.4 million, up from $31.8 million in 2024, which included a one-off IFRS charge of $10 million related to modifications in Perceptive financing arrangements, highlighting financial management pressures.
- Adjusted EBITDA Improvement: The adjusted EBITDA for 2025 was negative $5.9 million, an improvement from negative $11.3 million in 2024, suggesting some progress in cost control despite the overall financial situation remaining challenging.
- Financing Agreement Signed: Trinity Biotech entered into a $25 million standby equity purchase agreement with investors to strengthen its capital structure and provide operational funding, reflecting proactive measures in seeking financial stability.
See More
Trinity Biotech Appoints New Head of North America Operations
- Executive Appointment: Trinity Biotech has appointed Jerry Lydon as Head of North America Commercial Operations, aiming to enhance revenue growth and profitability in its core diagnostics business, reflecting ongoing progress in the company's Comprehensive Transformation Plan.
- Product Upgrade: The Premier HbA1c 9210™ platform has received the prestigious
See More
Trinity Biotech Announces Positive Results for Enhanced Prostate Cancer Test
- Clinical Study Results: Trinity Biotech's EpiCapture prostate cancer test was evaluated in approximately 750 patient samples, demonstrating a clinical accuracy of 85%, indicating strong clinical utility in oncology diagnostics that can aid physicians in making more precise clinical decisions.
- Significant Market Potential: With U.S. national expenditures for prostate cancer care exceeding $20 billion annually, the launch of EpiCapture positions Trinity Biotech to enter the precision oncology diagnostics market, addressing growing market demand and driving future revenue growth for the company.
- Non-Invasive Testing Advantage: EpiCapture, as a urine liquid biopsy test, offers a simpler and non-invasive method for assessing high-grade prostate cancer risk compared to high-resolution MRI scans and needle biopsies, potentially attracting more patients to opt for this testing.
- Future Commercialization Plans: Trinity plans to commercialize EpiCapture as a proprietary Laboratory Developed Test (LDT) through a New York State Department of Health-certified diagnostic reference laboratory, which will expedite the rollout of precision oncology testing services across the U.S.
See More
Trinity Biotech PLC Secures $25 Million SEPA with Yorkville Advisors Global Affiliate
Investment Announcement: Trinity Biotech PLC has entered into a $25 million SEPA with an affiliate of Yorkville Advisors.
Financial Partnership: The agreement involves a financing partnership aimed at supporting Trinity Biotech's growth and operational needs.
See More
Trinity Biotech Receives Regulatory Approval for New Production Model Launch
- Regulatory Milestone: Trinity Biotech has received local regulatory approval, marking the initiation of upstream manufacturing activities for its Uni-Gold™ HIV rapid test under a new outsourced production model, which is a key component of the company's comprehensive transformation plan.
- Cost Efficiency Improvement: The implementation of the offshore and outsourced production model is expected to significantly enhance gross margins and improve working capital efficiency, thereby strengthening the company's long-term competitiveness in the global HIV rapid testing market.
- Market Demand Support: This transition will not only meet the anticipated growth in demand for Uni-Gold™ HIV products but also provide the necessary scalability to ensure the company remains agile and responsive in a rapidly changing market environment.
- Strategic Transformation Plan: This approval complements the WHO authorization obtained in November 2025, demonstrating the company's strong commitment to executing its comprehensive transformation plan, which is expected to lay a solid foundation for future financial performance.
See More
Dow Jones Index Gains Over 100 Points as Durable Goods Orders Decline 2.2%
- Dow Jones Index Rise: The Dow Jones index increased by over 100 points on Tuesday, closing at 48,469.41, indicating a moderate market recovery despite disappointing economic data.
- Durable Goods Orders Decline: U.S. durable goods orders fell by 2.2% month-over-month to $307.4 billion in October, significantly missing market expectations of a 1.5% decline, reflecting weak manufacturing demand that could impact future economic growth.
- Accelerated GDP Growth: The U.S. GDP grew at an annualized rate of 4.3% in the third quarter, up from 3.8% in the previous quarter and exceeding market estimates of 3.3%, indicating potential for economic recovery that may positively influence the stock market.
- Mixed Sector Performance: Communication services rose by 0.5% while consumer staples fell by 0.5%, demonstrating varied market reactions across sectors, prompting investors to monitor industry dynamics for strategic adjustments.
See More
