BioNexus Signs $2M Exclusive License Agreement with Fidelion for VitaGuard in Southeast Asia
BioNexus Gene Lab has executed an Exclusive Intellectual Property License Agreement for Southeast Asia with Fidelion Diagnostics for the VitaGuard minimal residual disease liquid biopsy platform. The license is a key condition precedent to the closing of the previously announced Share Subscription and Shareholders' Agreement among BGLC, Fidelion and Tongshu Gene, under which BGLC will become a strategic shareholder in Fidelion and, in return, Fidelion will hold a minority stake in BGLC. Under the license, Fidelion grants BGLC an exclusive, irrevocable, royalty-free license to use, develop, manufacture, market, distribute and sell VitaGuard-based products and services in Southeast Asia. The agreement grants BGLC comprehensive rights to manufacture, market, and distribute VitaGuard-based tests across Southeast Asia, as well as the authority to hold local regulatory approvals and sublicense to third-party partners. As consideration, BGLC will pay Fidelion a $2 million license fee, in 24 equal monthly instalments and commit to at least $500,000 of VitaGuard reagent and system purchases in the first 24 months. Once the license fee is fully paid, the agreement becomes fully paid-up and royalty-free in the Territory, with no ongoing IP royalties or milestones on VitaGuard-based sales. The term is structured as a perpetual, exclusive license in Southeast Asia, designed to "run with" the VitaGuard IP in the Territory even if ownership of the underlying patents changes hands. The license agreement sits alongside the Share Subscription and Shareholders' Agreement signed on November 12, 2025. Execution of the Southeast Asia license is specifically referenced in that agreement as a condition to completion of the equity transaction.
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BioNexus Launches VitaGuard™ Deployment Phase for Oncology Monitoring
- Technological Breakthrough: BioNexus Gene Lab Corp. has officially commenced the 2026 Deployment Phase for its VitaGuard™ Minimal Residual Disease platform, aiming to replace high-cost monitoring systems in Southeast Asia, which is expected to significantly reduce cancer monitoring costs and enhance market competitiveness.
- Economic Impact: By leveraging proprietary cfDNA recovery and high-frequency sequencing workflows, VitaGuard™ aims to lower testing costs below $3,000, making it more accessible to Southeast Asia's 680 million population, thereby enhancing economic flexibility for regional healthcare systems.
- Data-Driven Approach: The 2026 deployment is viewed as a

BioNexus Gene Lab Corp. Secures $500 Million Equity Purchase Agreement with ARC Group
- Enhanced Financial Flexibility: BioNexus Gene Lab Corp. has entered into a $500 million equity purchase agreement with ARC Group, which is expected to provide long-term capital to support the commercialization of precision oncology diagnostics and CDMO services across Southeast Asia.
- Strengthened Strategic Partnership: The agreement allows BioNexus to issue shares at its discretion over the next 36 months, enhancing its competitive position in the oncology testing and biologics production sectors.
- Technology Platform Expansion: The exclusive licensing agreement with Fidelion Diagnostics to commercialize the VitaGuard™ MRD platform will be supported by ARC's funding, facilitating clinical adoption in Malaysia, Singapore, Indonesia, and Thailand.
- Support for CDMO Transformation: This financing will enable BioNexus to invest in quality system upgrades and manufacturing capacity, aligning its operations with global CDMO standards and enhancing overall business capabilities.









