Trinity Biotech Reaches Profitability Inflection Point, Marking Major Milestone in Strategic Turnaround
Trinity Biotech (NASDAQ: TRIB), a commercial stage biotechnology company, announced reaching a significant profitability milestone in Q2 2025, projecting to be Adjusted EBITDA-positive going forward. The company expects to achieve meaningful positive Adjusted EBITDA and cash flow from operations starting Q3 2025.
For Q1 2025, Trinity reported revenue of $7.6 million with a gross profit of $1.9 million and an operating loss of $6.5 million. The company projects Q2 2025 revenue to increase significantly to $11-12 million, driven by ramped-up manufacturing under its revised operational structure and normalized demand for rapid HIV tests.
Trinity Biotech continues development of its next-generation continuous glucose monitoring (CGM) solution, targeting the $13 billion global CGM market. The company recently completed a pre-pivotal trial on upgraded sensor technology and plans to unveil key aspects of its innovative design solution soon. Additionally, Trinity is advancing the international rollout of its upgraded diabetes care HbA1c testing product and TrinScreen HIV tests, while progressing on pipeline developments including preeclampsia screening and prostate cancer tests.
Trinity Biotech (NASDAQ: TRIB), un'azienda biotecnologica in fase commerciale, ha annunciato di aver raggiunto un importante traguardo di redditività nel secondo trimestre del 2025, prevedendo di essere Adjusted EBITDA positivo d'ora in avanti. L'azienda prevede di ottenere un significativo EBITDA rettificato positivo e flussi di cassa operativi a partire dal terzo trimestre del 2025.
Per il primo trimestre del 2025, Trinity ha riportato ricavi di 7,6 milioni di dollari con un utile lordo di 1,9 milioni di dollari e una perdita operativa di 6,5 milioni di dollari. L'azienda prevede che i ricavi del secondo trimestre 2025 aumenteranno significativamente, raggiungendo tra 11 e 12 milioni di dollari, grazie all'aumento della produzione sotto la sua struttura operativa rivista e alla domanda normalizzata per i test rapidi HIV.
Trinity Biotech continua lo sviluppo della sua soluzione di monitoraggio continuo del glucosio (CGM) di nuova generazione, mirando al mercato globale CGM da 13 miliardi di dollari. Recentemente ha completato uno studio pre-pivotal sulla tecnologia del sensore aggiornato e prevede di svelare presto gli aspetti chiave del suo design innovativo. Inoltre, Trinity sta avanzando nel lancio internazionale del suo prodotto aggiornato per il test HbA1c per la cura del diabete e dei test TrinScreen per l'HIV, mentre procede con sviluppi in pipeline che includono screening per la preeclampsia e test per il cancro alla prostata.
Trinity Biotech (NASDAQ: TRIB), una empresa biotecnológica en etapa comercial, anunció haber alcanzado un hito significativo de rentabilidad en el segundo trimestre de 2025, proyectando ser Adjusted EBITDA positivo en adelante. La compañía espera lograr un EBITDA ajustado positivo significativo y flujo de caja operativo a partir del tercer trimestre de 2025.
Para el primer trimestre de 2025, Trinity reportó ingresos de 7,6 millones de dólares con una ganancia bruta de 1,9 millones de dólares y una pérdida operativa de 6,5 millones de dólares. La empresa proyecta que los ingresos del segundo trimestre de 2025 aumentarán significativamente a 11-12 millones de dólares, impulsados por una mayor producción bajo su estructura operativa revisada y una demanda normalizada para las pruebas rápidas de VIH.
Trinity Biotech continúa desarrollando su solución de monitoreo continuo de glucosa (CGM) de próxima generación, apuntando al mercado global de CGM de 13 mil millones de dólares. Recientemente completó un ensayo pre-pivotal sobre tecnología de sensores mejorada y planea revelar pronto aspectos clave de su innovador diseño. Además, Trinity avanza en el lanzamiento internacional de su producto mejorado para pruebas de HbA1c en el cuidado de la diabetes y las pruebas TrinScreen para VIH, mientras progresa en desarrollos en su pipeline que incluyen pruebas para preeclampsia y cáncer de próstata.
트리니티 바이오텍 (NASDAQ: TRIB)은 상업 단계에 있는 생명공학 회사로, 2025년 2분기에 중요한 수익성 이정표를 달성했으며 앞으로 조정 EBITDA 흑자를 예상한다고 발표했습니다. 회사는 2025년 3분기부터 의미 있는 긍정적 조정 EBITDA와 영업 현금 흐름을 달성할 것으로 기대하고 있습니다.
2025년 1분기 트리니티는 매출 760만 달러, 총이익 190만 달러, 영업손실 650만 달러를 보고했습니다. 회사는 2025년 2분기 매출이 1100만~1200만 달러로 크게 증가할 것으로 예상하며, 이는 개편된 운영 구조 하에서 제조가 확대되고 신속 HIV 검사에 대한 수요가 정상화된 데 따른 것입니다.
트리니티 바이오텍은 차세대 연속 혈당 모니터링(CGM) 솔루션 개발을 계속 진행 중이며, 130억 달러 규모의 글로벌 CGM 시장을 목표로 하고 있습니다. 최근 업그레이드된 센서 기술에 대한 전임상 시험을 완료했으며, 혁신적인 설계 솔루션의 주요 내용을 곧 공개할 계획입니다. 또한 트리니티는 업그레이드된 당뇨병 관리용 HbA1c 검사 제품과 TrinScreen HIV 테스트의 국제 출시를 추진 중이며, 자간전증 선별 검사와 전립선암 검사 등 파이프라인 개발도 진행하고 있습니다.
Trinity Biotech (NASDAQ : TRIB), une entreprise biotechnologique en phase commerciale, a annoncé avoir atteint un jalon significatif de rentabilité au deuxième trimestre 2025, prévoyant d’être positif en EBITDA ajusté à l’avenir. La société s’attend à générer un EBITDA ajusté positif significatif et un flux de trésorerie opérationnel à partir du troisième trimestre 2025.
Pour le premier trimestre 2025, Trinity a déclaré un chiffre d’affaires de 7,6 millions de dollars, avec un bénéfice brut de 1,9 million de dollars et une perte d’exploitation de 6,5 millions de dollars. La société prévoit une augmentation significative du chiffre d’affaires au deuxième trimestre 2025, atteignant entre 11 et 12 millions de dollars, portée par une production accrue dans le cadre de sa structure opérationnelle révisée et une demande normalisée pour les tests rapides du VIH.
Trinity Biotech poursuit le développement de sa solution de surveillance continue du glucose (CGM) de nouvelle génération, visant le marché mondial du CGM de 13 milliards de dollars. Elle a récemment achevé un essai pré-pivotal sur une technologie de capteur améliorée et prévoit de dévoiler prochainement les aspects clés de son design innovant. De plus, Trinity progresse dans le déploiement international de son produit amélioré de tests HbA1c pour le suivi du diabète et des tests TrinScreen VIH, tout en avançant dans le développement de sa pipeline incluant le dépistage de la prééclampsie et des tests pour le cancer de la prostate.
Trinity Biotech (NASDAQ: TRIB), ein Biotechnologieunternehmen in der kommerziellen Phase, gab bekannt, im zweiten Quartal 2025 einen bedeutenden Profitabilitätsmeilenstein erreicht zu haben und künftig adjustiertes EBITDA-positiv zu sein. Das Unternehmen erwartet, ab dem dritten Quartal 2025 ein deutlich positives Adjusted EBITDA und operativen Cashflow zu erzielen.
Für das erste Quartal 2025 meldete Trinity Umsätze von 7,6 Millionen US-Dollar mit einem Bruttogewinn von 1,9 Millionen US-Dollar und einem operativen Verlust von 6,5 Millionen US-Dollar. Das Unternehmen prognostiziert für das zweite Quartal 2025 einen deutlichen Umsatzanstieg auf 11 bis 12 Millionen US-Dollar, angetrieben durch eine hochgefahrene Produktion im Rahmen der überarbeiteten Betriebsstruktur und eine normalisierte Nachfrage nach schnellen HIV-Tests.
Trinity Biotech setzt die Entwicklung seiner nächsten Generation der kontinuierlichen Glukoseüberwachung (CGM) fort und zielt auf den 13 Milliarden US-Dollar schweren globalen CGM-Markt ab. Kürzlich wurde eine prä-pivotal Studie zur verbesserten Sensortechnologie abgeschlossen, und das Unternehmen plant, bald wichtige Aspekte seines innovativen Designs vorzustellen. Zusätzlich treibt Trinity den internationalen Rollout seines verbesserten HbA1c-Testprodukts zur Diabetesversorgung und der TrinScreen HIV-Tests voran, während es Fortschritte bei Pipeline-Entwicklungen wie Präeklampsie-Screening und Prostatakrebstests macht.
- Achievement of Adjusted EBITDA-positive operations in Q2 2025
- Projected significant revenue growth from $7.6M in Q1 to $11-12M in Q2 2025
- Successfully completed operational restructuring with consolidated and offshored manufacturing
- Recently completed pre-pivotal trial for upgraded CGM sensor technology
- Targeting expansion in $13B global CGM market
- Received World Health Organisation approval for offshored manufacturing of TrinScreen HIV
- Q1 2025 operating loss of $6.5M
- Net financing expense of $2.3M in Q1 2025
- Low Q1 2025 gross profit of $1.9M on $7.6M revenue
Insights
Trinity Biotech reaches EBITDA profitability milestone after restructuring, with projected revenue growth and progress on CGM development.
Trinity Biotech's announcement represents a significant inflection point in its turnaround strategy. After implementing extensive operational restructuring—including consolidating and offshoring manufacturing and corporate services—the company projects it has achieved
The Q1 2025 results show the company is still in transition with
Beyond the immediate financial improvements, Trinity is advancing several potential growth drivers. Near-term opportunities include the international rollout of its upgraded HbA1c testing product and TrinScreen HIV tests. The company is also developing preeclampsia and prostate cancer screening tests. Most notably, Trinity continues progressing its next-generation continuous glucose monitoring (CGM) solution, targeting the
The restructuring appears to be delivering the intended cost benefits, creating a leaner organization with improved operational leverage. While the company has cleared a significant milestone with projected
-Trinity Biotech projects it reached Adjusted EBITDA1 -positive operations during Q2 2025 and expects to be Adjusted EBITDA1 positive going forward, reflecting continued strong execution on its comprehensive transformation plan.-
- The Company now expects to be meaningfully Adjusted EBITDA1 -positive and cashflow positive from ongoing operating activities, starting Q3 2025 and into the foreseeable future.-
DUBLIN, July 01, 2025 (GLOBE NEWSWIRE) -- Trinity Biotech plc (Nasdaq: TRIB), a commercial stage biotechnology company focused on human diagnostics and diabetes management solutions, including wearable biosensors, today provided a business update announcing that the Company believes it has reached a critical profitability inflection point during the latter part of the current financial quarter, a key milestone in its comprehensive transformation strategy. The Company now expects to be meaningfully Adjusted EBITDA1 -positive and to be cash flow positive from its ongoing operating activities starting Q3 2025 and into the foreseeable future. In addition, the Company today also released details regarding its results for the quarter ended March 31, 2025.
Key Highlights and Developments
- This profitability inflection point achievement follows a period of rapid and decisive operational restructuring, during which Trinity Biotech consolidated and offshored its manufacturing and corporate services to significantly reduce its cost base. These strategic moves have laid the groundwork for a leaner, more agile organization capable of delivering sustainable profitability.
- With the major structural changes largely behind it, Trinity Biotech is now concentrating on fine-tuning its global operations, leveraging its new foundation to unlock further efficiencies and EBITDA improvements.
- The Company also continues to focus on near term opportunities for profitable growth, underpinned by its new, leaner and more scalable operating foundation, with the continued international roll out of its most recently launched products including:
- its upgraded diabetes care HbA1c testing product, and
- additional launch countries for its TrinScreen HIV tests.
- The Company is also continuing to progress towards commercialisation on its pipeline of key medium term strategic growth drivers currently under development, including its innovative:
- preeclampsia screening test, and
- prostate cancer test.
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1 Earnings before interest, tax, depreciation, amortisation, and share-based compensation charges – also excludes impairment charges and restructuring costs.
Continuous Glucose Monitoring Update
- The Company continues to progress the development of our next generation continuous glucose monitoring (“CGM”) solution for diabetes management, which we believe is the Company’s largest scale growth opportunity.
- We have recently completed a further pre-pivotal trial on our upgraded sensor technology and expect to issue key findings from this trial shortly.
- We also continue to refine the design of our next-generation, lower-waste and lower-cost CGM solution and are planning to unveil to the public key aspects of this unique and innovative design solution in the near future.
- We remain excited about the opportunities for our innovative CGM solution to deliver a meaningful impact in global diabetes care, a
$13b n and rapidly growing global CGM market, and to deliver very significant growth for Trinity Biotech.
First Quarter Results (Unaudited)
The Company also today released details regarding its results for the quarter ended March 31, 2025:
- Revenue was
$7.6m which was in line with the Company’s previously issued guidance. Gross profit was$1.9m . Operating loss was$6.5m before net financing expense of$2.3m . - The Company expects a significant quarter-on-quarter increase in revenue to a range of approximately
$11 million to approximately$12 million in Q2, 2025 as manufacturing under the Company’s revised operational structure, including outsourced & offshored manufacturing, ramps up and normalised demand for rapid HIV tests returned in the latter part of the quarter. - The Company expects a further significant quarter-on-quarter increase in revenue in Q3, 2025 as the Company resumes manufacture and supply of its flagship rapid HIV test, TrinScreen HIV, underpinned by its recently announced World Health Organisation approval of its offshored and outsourced manufacturing.
The Company has issued a full presentation of its Q1, 2025 results which can be viewed on the Company’s website www.trinitybiotech.com/investor-relations/financial-reports.
Use of Non-IFRS Financial Measures
The Company’s unaudited financial statements were prepared in accordance with International Financial Reporting Standards (IFRS). To supplement the consolidated financial statements presented in accordance with IFRS, the Company presents non-IFRS presentations of EBITDA and Adjusted EBITDA. The adjustments to the Company's IFRS results are made with the intent of providing both management and investors a more complete understanding of the Company's underlying operational results, trends, and performance. Non-IFRS financial measures mainly exclude, if and when applicable, the effect of share-based compensation charges, depreciation, amortization and impairment charges.
EBITDA and Adjusted EBITDA is presented to evaluate the Company's financial and operating results on a consistent basis from period to period. The Company also believes that these measures, when viewed in combination with the Company's financial results prepared in accordance with IFRS, provides useful information to investors to evaluate ongoing operating results and trends. EBITDA and Adjusted EBITDA, however, should not be considered as an alternative to operating income or net income for the period and may not be indicative of the historic operating results of the Company; nor is it meant to be predictive of potential future results. EBITDA and Adjusted EBITDA are not measures of financial performance under IFRS and may not be comparable to other similarly titled measures for other companies. Reconciliation between the Company's operating profit/(loss) and EBITDA and Adjusted EBITDA are presented with the Company’s financial results available on the Company’s website, www.trinitybiotech.com/investor-relations/financial-reports.
Forward-Looking Statements
This release includes statements that constitute “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 (the “Reform Act”), including but not limited to statements related to Trinity Biotech’s cash position, financial resources and potential for future growth, market acceptance and penetration of new or planned product offerings, and future recurring revenues and results of operations. Trinity Biotech claims the protection of the safe harbor for forward-looking statements contained in the Reform Act. These forward-looking statements are often characterised by the terms “may,” “believes,” “projects,” “expects,” “anticipates,” or words of similar import, and do not reflect historical facts. Specific forward-looking statements contained in this presentation may be affected by risks and uncertainties, including, but not limited to, our ability to capitalize on our purchase of the assets of Waveform, our continued listing on the Nasdaq Stock Market, our ability to achieve profitable operations in the future, the impact of the spread of COVID-19 and its variants, potential excess inventory levels and inventory imbalances at the company’s distributors, losses or system failures with respect to Trinity Biotech’s facilities or manufacturing operations, the effect of exchange rate fluctuations on international operations, fluctuations in quarterly operating results, dependence on suppliers, the market acceptance of Trinity Biotech’s products and services, the continuing development of its products, required government approvals, risks associated with manufacturing and distributing its products on a commercial scale free of defects, risks related to the introduction of new instruments manufactured by third parties, risks associated with competing in the human diagnostic market, risks related to the protection of Trinity Biotech’s intellectual property or claims of infringement of intellectual property asserted by third parties and risks related to condition of the United States economy and other risks detailed under “Risk Factors” in Trinity Biotech’s annual report on Form 20-F for the fiscal year ended December 31, 2024 and Trinity Biotech’s other periodic reports filed from time to time with the United States Securities and Exchange Commission. Forward-looking statements speak only as of the date the statements were made. Trinity Biotech does not undertake and specifically disclaims any obligation to update any forward-looking statements.
About Trinity Biotech
Trinity Biotech is a commercial stage biotechnology company focused on diabetes management solutions and human diagnostics, including wearable biosensors. Our current products are used to detect a variety of health conditions including autoimmune, infectious and sexually transmitted diseases, and quantify the level of HbA1c in human blood. In January of 2024, we entered into the biosensor industry, with the acquisition of the biosensor assets of Waveform Technologies Inc. and we are currently developing a range of biosensor devices and related services, starting with a continuous glucose monitoring product. Trinity Biotech sells direct in the United States, Germany, France and the U.K. and through a network of international distributors and strategic partners in over 75 countries worldwide.
For further information, please see the Company's website: www.trinitybiotech.com.
Contact: | Trinity Biotech plc Susan O’Connor (353)-1-2769800 E-mail: investorrelations@trinitybiotech.com | RedChip Companies Inc David Gentry (1)-407-644-4256 E-mail: TRIB@redchip.com |
