Get In Touch
Xeraya Capital Sdn Bhd
26.03–26.08, G Tower
#199 Jalan Tun Razak, KL
+603 2381 8700
Submit a Proposal

InterVenn Receives Foundational Patent, CLIA Lab Certification to Develop Clinical Glycoproteomics Solutions

Breakthrough Data on Predicting Immuno-Oncology Treatment Response, Additional Partnerships, and Pending Launch of Ovarian Cancer Test Expand Opportunities in 2021 and Beyond

SOUTH SAN FRANCISCO, Calif.–(BUSINESS WIRE)–InterVenn Biosciences, the leader in glycoproteomics, today announced the accomplishment of multiple milestones in advancing the world’s first glycoproteomics-based LDT(Lab-Developed Test). The company’s first diagnostic product, a noninvasive liquid biopsy test for ovarian cancer, will have final data from its initial clinical trial, V.O.C.A.L.™, in the first half of 2021; and InterVenn’s on-site laboratory has recently received CLIA certification to make its tests available to the medical community. Of note, InterVenn has recently been issued a key patent covering its core foundational technology IP on artificial intelligence and machine learning for the identification and use of glycopeptides as biomarkers for diagnosis and treatment monitoring.

The company is also working to develop a test predicting response to immuno-oncology therapies. Results from three separate studies indicate that the company’s liquid biopsy assay platform is uniquely capable of successfully predicting patient response across the class of checkpoint inhibitors, outperforming all other currently available predictive tests.

“Checkpoint inhibitors are extremely powerful and highly effective cancer drugs, but only 20 to 30 percent of cancer patients ultimately respond to them. Currently, there is no effective way to predict likely responders, which results in many patients suffering from serious side effects while deriving no benefits, and an increasingly unsustainable burden of healthcare expenditures,” said Klaus Lindpaintner, MD, Chief Scientific Officer and Chief Medical Officer of InterVenn. “There is a tremendous need to develop a solution with real clinical utility. We’re highly encouraged by our early results and feel extremely bullish about scaling up these studies, expanding them to explore additional indications and drug molecules, and bringing a clinical test to patients as quickly as possible.”

In the course of planned 2021 studies, InterVenn will continue to engage in a range of partnerships to develop predictive and companion diagnostic claims. InterVenn has established additional collaborations with leading U.S. and international oncology centers, including Omico, a nationwide network of research and treatment centers in Australia, to further explore the predictive power of blood-based glycoproteomic signatures. InterVenn also recently became a member of the Mayo Clinic Innovation Exchange.

“We’ve been engaged in a range of pilot studies with a number of partners across a spectrum of applications, and we continue to see extremely impressive results differentiating clinical phenotypes based on glycoproteomic profiles, giving us the confidence to accept unknown, blinded samples from collaborators — and being able to correctly identify the signatures each and every time,” said Aldo Carrascoso, Chief Executive Officer of InterVenn. “Together with our partners, we continue to be impressed and inspired by how powerfully glycoproteomics recognizes and distinguishes health, disease, drug response, and other phenotypes.”

Bolstered by emerging data, InterVenn is planning a platform challenge to be announced in time for the American Association of Cancer Research (AACR) meeting. Researchers may apply to InterVenn and have their samples analyzed by InterVenn’s glycoproteomics platform. Full details on how applicants may gain access to this program will be announced in the coming weeks leading up to the AACR annual meeting.

To find out more about InterVenn Biosciences and how the company is leveraging artificial intelligence and mass spectrometry to the transformation of medical technology, visit