Portage Biotech Unveils Promising Preclinical Data for PORT-7 in Mesothelioma, Paving Way for First-In-Human Trial

DENVER, Colo., Apr 28, 2025 (247marketnews.com)- Portage Biotech (NASDAQ:PRTG) released compelling preclinical efficacy data for PORT-7 (TT-4), a selective adenosine A2B receptor inhibitor, supporting its advancement toward a first-in-human clinical trial. The data, to be presented by Dr. Luciano Mutti of the University of L’Aquila, Italy, a globally recognized mesothelioma expert, at today’s American Association for Cancer Research (AACR) Annual Meeting in Chicago, highlight PORT-7’s potential as a novel therapy for mesothelioma, an aggressive cancer with limited treatment options.

PORT-7: Breakthrough Preclinical Results

In a murine mesothelioma model, PORT-7 demonstrated superior single-agent activity compared to anti-PD1 antibody treatment. The combination of PORT-7 and anti-PD1 outperformed either therapy alone, showing enhanced tumor suppression. Immunohistochemistry revealed tertiary lymphoid structures in tumors treated with the combination, indicating a robust immune response, alongside increased immune effector cells. These findings suggest PORT-7 could overcome immune resistance in mesothelioma, a disease with a five-year survival rate of ~10% and ~3,000 annual U.S. diagnoses, per the American Cancer Society.

Synergistic Strategy: Combining PORT-6 and PORT-7

Portage is also advancing PORT-6, a potent A2A adenosine receptor inhibitor, in the dose-escalation phase of its ADPORT-601 trial. The company plans to co-administer PORT-6 and PORT-7, marking the first clinical combination of highly selective A2A and A2B antagonists. This innovative approach aims to fully neutralize adenosine-mediated immune suppression in the tumor microenvironment, enhancing anti-tumor responses across solid tumors. By targeting both adenosine pathways, Portage seeks to broaden immunotherapy’s impact, addressing a critical unmet need in oncology.

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