TrilliumBiO and Oncobit Launch Advanced Uveal Melanoma Monitoring Solution in the U.S.

12.05.2026

Oncularexpands access to advanced molecular testing to support patient management for a rare eye cancer

ROCKVILLE, Md. and ZURICH, May 12, 2026 /PRNewswire/ -- TrilliumBiO, a leader in biomarker discovery and precision diagnostics, and Oncobit, a Swiss precision oncology company, today announced the launch of Oncular™, bringing Oncobit's uveal melanoma monitoring solution to the U.S. through TrilliumBiO's multi-accredited laboratory. The assay expands access to advanced molecular testing for patients with uveal melanoma, a rare and historically underserved cancer.

Oncular, Oncobit, & TrilliumBiO logos

Oncular™ brings Oncobit's proprietary platform for personalized cancer monitoring to physicians nationwide, enabling real‑time, quantitative assessment of circulating tumor DNA (ctDNA) from a simple blood draw. Designed to complement conventional imaging approaches, the assay provides precise insights into disease dynamics, supporting informed patient management across the care continuum.

Unlike traditional monitoring methods that rely primarily on imaging or nonspecific blood markers, Oncular™ combines personalized digital PCR with standardized, cloud‑based data analysis to deliver sensitive and reproducible molecular results. This approach addresses key limitations of existing monitoring strategies, including limited sensitivity, delayed detection of disease progression, high cost, and invasiveness. The approach is designed to be both time- and cost-efficient while remaining scalable for routine clinical practice.

Oncular™ delivers molecular monitoring insights, including:

  • Molecular residual disease (MRD) status



  • Longitudinal ctDNA trends



  • Early molecular signals of treatment response or disease progression, which may precede

    radiographic findings

Published research has demonstrated that ctDNA dynamics measured using Oncobit's proprietary platform can predict treatment response and disease progression in metastatic uveal melanoma, underscoring the clinical relevance of this testing approach.1,2,3

"Launching Oncular™ in the U.S. reflects our commitment to translating innovative science into high-quality diagnostic solutions for patients with rare diseases," said Laura Vivian, CEO of TrilliumBiO. "By making this assay available through our laboratory, we are helping clinicians access reliable insights to better understand disease behavior and support patient care."

The launch combines TrilliumBiO's expertise in assay implementation and clinical laboratory operations with Oncobit's leadership in precision oncology and ctDNA-based testing. Oncular™ is a laboratory‑developed test (LDT) performed within TrilliumBiO's CLIA‑certified and CAP-accredited laboratory infrastructure, ensuring consistency, quality, and nationwide availability.

"We are thrilled to see our uveal melanoma assay reach clinical practice in the U.S. with TrilliumBiO," said Dr. Claudia Scheckel, CEO of Oncobit. "The launch of Oncular™ represents an important step toward expanding access to advanced molecular testing for this rare cancer and supports continued progress in biomarker development and advancing precision oncology."

Together, TrilliumBiO and Oncobit aim to improve disease understanding and patient management in uveal melanoma by providing clinicians with sensitive, informative molecular testing to support evidence-based care decisions.

For more information on assay availability or how to order Oncular™, visit Oncular™ - TrilliumBiO, contact TrilliumBiO at oncular@trilliumbio.com, or call 1-888-261-2812.  

About TrilliumBiO

TrilliumBiO is a translational diagnostics company transforming how biomarkers are integrated into patient care. The company's unified platform spans discovery, validation, and commercialization to deliver clinically actionable diagnostics. These solutions identify at-risk patients, monitor disease, and guide emerging therapies supporting a more personalized, data-driven model of care.

With a scalable, high-performing laboratory infrastructure, TrilliumBiO offers a portfolio of specialized, clinically tailored assays. Its partnership-driven model enables the rapid development and deployment of diagnostics in complex and underserved disease areas. 

Headquartered in Maryland, just outside Washington, D.C., TrilliumBiO operates within the nation's third-largest biopharma hub. Learn more at www.TrilliumBiO.com.

About Oncobit

Oncobit, a leading Swiss precision oncology company, has developed a scalable, data-driven cancer monitoring platform based on the quantitative and highly sensitive detection of cancer markers in liquid biopsies. By focusing on the most clinically impactful biomarkers and leveraging cutting-edge technology, Oncobit provides cost-effective and time-efficient solutions that enable close monitoring of a patient's cancer and support optimized therapy management. Its cloud-based data analysis and interpretation software, trained on both healthy and patient datasets, ensures robust and standardized result reporting. Oncobit's diagnostic solutions are trusted by a growing number of pharmaceutical companies, clinical laboratories, and hospital institutions. Learn more at www.Oncobit.com.

TrilliumBiO Contact:

Olivia McCann

PR & Marketing Strategy Manager

olivia.mccann@trilliumbio.com

Oncobit Contact:

Dr. Claudia Scheckel

CEO

claudia.scheckel@oncobit.com

1 Kadefors M, et al. Immuno-Oncology and Technology. 2025;28(C):101079. doi:10.1016/j.iotech.2025.101079.

2 Machiraju D, et al. J Exp Clin Cancer Res. 2025;44:213. doi:10.1186/s13046-025-03451-2.

3 Ramelyte E, Koett, J, et al. Clinical Cancer Research. Accepted.

Logo - https://mma.prnewswire.com/media/2977317/TrilliumBiO_Logo.jpg

Cision View original content:https://www.prnewswire.co.uk/news-releases/trilliumbio-and-oncobit-launch-advanced-uveal-melanoma-monitoring-solution-in-the-us-302769574.html

Other news

CAR-Institut: 2,5 Milliarden Euro Zusatzkosten durch Trumps EU-Autozölle

04.05.2026

Die von US-Präsident Donald Trump angekündigten Zölle von 25 Prozent auf Neuwagenimporte aus der Europäischen Union würden nach Einschätzung von Branchenexperten vor allem die deutsche Autoindustrie treffen. Berechnungen des Center Automotive Research (CAR) in Bochum zufolge kämen allein auf die Autoproduktion in Deutschland zusätzliche Belastungen von rund 2,5 Milliarden Euro pro Jahr zu. Hinzu kämen weitere Kosten für US-Exporte deutscher Hersteller aus Werken in anderen EU-Staaten.

Obwohl sich die Maßnahmen formal gegen die gesamte EU richten, sieht CAR-Direktor Ferdinand Dudenhöffer insbesondere Deutschland im Visier Washingtons. Die Exporte anderer ausländischer Autobauer in die USA seien „unwesentlich“, sagte er und sprach mit Blick auf die neuen Zoll-Drohungen vom möglichen Beginn eines „Wirtschaftskriegs gegen Deutschland“. Die Maßnahmen würden die Hersteller jedoch unterschiedlich hart treffen, abhängig von ihrer Produktionsstruktur und Präsenz in den Vereinigten Staaten.

Relativ besser gestellt wären demnach Konzerne wie BMW und Mercedes-Benz, die über umfangreiche Produktionskapazitäten in den USA verfügen. In ihren US-Werken fertigen sie vor allem SUV-Modelle, die den Großteil ihrer Verkäufe auf dem US-Markt ausmachen. Diese lokale Produktion wirkt nach Einschätzung Dudenhöffers wie ein „Zollschutz“, weil in den USA montierte Fahrzeuge nicht unter die geplanten Importzölle auf Neuwagen aus der EU fallen würden.

Deutlich verwundbarer wären dagegen Marken wie Audi und Porsche, die ihre Fahrzeuge bislang weitgehend aus Europa in die USA liefern. Für sie könnten die neuen Einfuhrabgaben ein Anreiz sein, Pläne zum Aufbau eigener Produktionsstätten in den Vereinigten Staaten zu beschleunigen. Vollständig auffangen können die Hersteller die zusätzlichen Kosten nach Einschätzung des CAR-Instituts jedoch nicht. Ein Teil der Belastungen dürfte über Preiserhöhungen an die US-Käufer weitergegeben werden. Dank der starken Markenbindung rechnet Dudenhöffer zwar nicht mit einem abrupten Nachfrageeinbruch, die deutschen Autobauer stünden jedoch vor der Herausforderung, ihre Preissetzung und Standortstrategie zügig an die neue handelspolitische Lage anzupassen.