RenovoRx Presents TIGeR-PaC Clinical Trial Data at Oncology Symposium
RenovoRx announced that a new clinical data abstract from a pharmacokinetic and pharmacodynamic sub-study of its ongoing Phase III TIGeR-PaC clinical trial will be presented at the American Society of Clinical Oncology Gastrointestinal Cancers Symposium 2026, being held today through January 10th in San Francisco, California. The abstract, titled "Intra-arterial Gemcitabine Versus Intravenous Gemcitabine: Pharmacokinetic and Pharmacodynamic Sub-study of the TIGeR-PaC Phase 3 Clinical Trial," was led by Dr. Paula Novelli of the University of Pittsburgh Medical Center. The data presented is from a sub-study of RenovoRx's ongoing Phase III TIGeR-PaC clinical trial, which is evaluating the use of intra-arterial gemcitabine, IAG, a drug-device combination product candidate that uses the Company's patented Trans-Arterial Micro-Perfusion, TAMP, therapy platform, in treating locally advanced pancreatic cancer, LAPC.
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RenovoRx to Present New Research at 2026 SIO Meeting
- Research Presentation: RenovoRx's abstract will be showcased at the 2026 SIO Annual Meeting, focusing on optimizing chemotherapy delivery through a double-balloon catheter, highlighting the company's innovative potential in oncology treatment.
- Clinical Data Sharing: Led by Dr. Christopher Laing from Sutter Health, the study is set for presentation on February 6, 2026, emphasizing the significance of real-time intra-arterial pressure monitoring in drug delivery, potentially paving the way for personalized treatment approaches.
- Market Outlook: As an FDA-cleared drug delivery device, RenovoCath is expected to drive the company's commercialization efforts in the oncology market, having generated approximately $900,000 in sales revenue in the first nine months of 2025, indicating growing market demand.
- Strategic Development: RenovoRx is actively exploring further collaborations with medical device commercial partners to meet the increasing demand for RenovoCath, reflecting the company's focus on future market opportunities and strategic positioning.

Oncolytics Biotech's Breakthroughs in Cancer Treatment
- Market Potential: The global oncology market is projected to reach $668 billion by 2034, positioning companies like Oncolytics Biotech at the forefront of this rapid growth, particularly in innovative treatments for gastrointestinal cancers, indicating strong market demand and investment appeal.
- Clinical Trial Progress: Oncolytics Biotech's pelareorep achieved a 33% response rate in colorectal cancer patients, significantly surpassing the 6-11% typical response rates of conventional chemotherapy, which not only enhances treatment efficacy but also has the potential to redefine treatment standards in this field, bolstering the company's competitive edge.
- Management Team Upgrade: The recent appointments of John McAdory as Executive Vice President of Strategy and Operations and Yujun Wu as Vice President, Head of Biostatistics, both with extensive clinical trial experience, will provide critical support for Oncolytics' execution of complex multi-country registration trials, ensuring rapid and compliant advancement.
- FDA Trial Design Approval: Oncolytics has secured FDA approval for its Phase 3 trial design for pancreatic cancer, marking the imminent launch of the only immunotherapy registration trial planned for this notoriously difficult-to-treat disease, further solidifying its leadership position in oncology innovation.






