Ocean Biomedical (NASDAQ: OCEA) Congratulates Joint Venture Partner, Virion Therapeutics, on Positive Immunogenicity Results from Their Lead Checkpoint Modifier-Containing Immunotherapy, VRON-0200, for HBV Functional Cure, at EASL 2024

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Ocean Biomedical, Inc.
Ocean Biomedical, Inc.

Providence, RI, June 05, 2024 (GLOBE NEWSWIRE) -- Ocean Biomedical, Inc. (NASDAQ: OCEA), a biopharma company working to accelerate the development of compelling discoveries from top research scientists, today congratulates its JV partner Virion Therapeutics, LLC, a clinical-stage biotechnology company developing novel T cell-based immunotherapies, on its late breaker presentation highlighting the first-ever human immunogenicity data from its novel checkpoint modifier immunotherapy for HBV functional cure (VRON-0200), at the EASL 2024 Congress (The European Association for the Study of the Liver), taking place in Milan, Italy from June 5 - 8.

The late breaker Phase 1b data presented today, (for more information, go to VirionTx.com), which includes Virion’s first checkpoint modifier, glycoprotein D (gD), demonstrated that VRON-0200 was not only safe and well tolerated, but immunogenic in the majority of chronically HBV-infected patients, following a single intramuscular injection. “Chronic HBV infection severely impairs a patient’s ability to clear the virus. A single low dose injection of VRON-0200 was able to stimulate T cell responses in the majority of patients, most of whom had little, to no, documented HBV immunity prior to treatment” said Virion’s CEO, Dr. Andrew Luber. Luber added,VRON-0200 is our lead clinical program and these clinical safety and immunogenicity data will further support our proprietary platform technologies and other pipeline programs in development, including VRON-0300, which is for patients with advanced solid tumors.”

Unlike monoclonal antibody checkpoint inhibitors which attempt to “rescue” already activated, but exhausted, CD8+ T cells, Virion’s checkpoint modifiers alter T cell activation to amplify and broaden a patient’s own immune response; this may include regions of a tumor or infectious disease that are not normally stimulated during a chronic disease, thereby potentially producing a “new” immune response. Additionally, after it is administered through an intramuscular injection, the checkpoint modifiers act locally, at the injection site, and not throughout the body, thereby limiting the risk for serious adverse events such as those seen following the intravenous administration of monoclonal antibody checkpoint inhibitors.

Ocean Biomedical co-founder and Executive Chairman Dr. Chirinjeev Kathuria, commented: “We congratulate Virion on these exciting data, as they continue to advance VRON-0200, not only as a safe, well tolerated, and easy to administer treatment, but also, now with positive clinical immunogenity data, which is advancing their goal of an interferon-sparing treatment option for the 300 million persons worldwide infected with Chronic HBV. Treatments for chronic HBV are in high demand and could capture an estimated global market of $6.5+ billion by 2032. Ocean is pleased to partner with Virion and we look forward to helping accelerate this, and other programs, in development.”