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      Immorta Bio Reports Reduction of Tumors in Validated Models of Lung, Brain, Pancreatic, and Breast Cancers Using Anti-Aging Vaccine "SenoVax™"

      Immorta Bio Inc.

      News provided by

      Immorta Bio Inc.

      Dec 04, 2025, 11:39 ET

      Share this article

      Share this article


      Scientific Longevity Company Collaborates with Major Academic Institutions to Remove Tumor Defense Mechanisms and Help Defeat Cancer in a Non-Toxic Manner

      MIAMI, Dec. 4, 2025 /PRNewswire/ -- Immorta Bio today announced the publication of a landmark preclinical study in the Journal of Translational Medicine demonstrating that its novel immunotherapy, SenoVax™, dramatically reduces multiple types of solid tumors in murine models. Earlier this year, Immorta Bio filed IND #30745 with the FDA for a first-in-human trial in advanced lung cancer.

      Continue Reading
      Dr. Gilberto Lopes, Chief of Medical Oncology at the University of Miami
      Dr. Gilberto Lopes, Chief of Medical Oncology at the University of Miami

      The paper, titled "Reduction of Solid Tumors by Senescent Cell Immunization," was authored in collaboration with leading researchers from the University of Miami, Cedars-Sinai, UC San Diego, the Institute for Human Optimization, George Washington University, and Translational and Advanced Biosciences.

      Full text: https://link.springer.com/article/10.1186/s12967-025-07393-3 In well-characterized mouse models of aggressive cancers, SenoVax™, a personalized autologous immunotherapy that trains the immune system to attack senescent cells, achieved significant tumor shrinkage across lung, glioblastoma (brain), pancreatic, and breast cancers.

      Senescent cells, which accumulate with age and chronic stress, are increasingly implicated in creating an immunosuppressive, pro-tumor microenvironment. By targeting antigens uniquely expressed on these cells, SenoVax™ appears to reprogram the tumor microenvironment, turning immunologically "cold" tumors "hot" by boosting CD8⁺ T-cell infiltration and reducing immune-suppressive cell populations. Key findings:

      • Statistically significant tumor growth inhibition and prolonged survival in both orthotopic and syngeneic models

      • Robust CD8⁺ T-cell infiltration and depletion of immunosuppressive cells in treated tumors

      • Strong activity as monotherapy and in combination with other treatments

      "These data provide compelling proof-of-concept that immunizing against senescent cells represents an entirely new therapeutic modality in oncology," said Dr. Thomas Ichim, President and Chief Scientific Officer of Immorta Bio and lead author of the study. "We have already filed IND #30745 with the FDA for a first-in-human trial in advanced lung cancer and are completing the GMP manufacturing required to begin the study."

      Dr. Gilberto Lopes, Chief of Thoracic Medical Oncology at the Sylvester Comprehensive Cancer Center (University of Miami) and study co-author, commented: "Many deadly solid tumors remain resistant to current immunotherapies because they are immunologically 'cold.' Converting the tumor microenvironment into a more inflamed, T-cell-friendly state by eliminating senescent cells could dramatically broaden the reach of checkpoint inhibitors and other immune therapies."

      Dr. Boris Reznik, Chairman and CEO of Immorta Bio and senior author, added: "This publication lays a strong translational foundation for bringing senescent-cell-targeted therapies into the clinic, not only for cancer, but potentially for the many age-related diseases driven by pathologic cellular senescence."

      The publication describes preclinical experiments in validated murine models demonstrating that immunization with SenoVax™—a personalized, autologous immunotherapy designed to elicit immune responses against senescent cells—was associated with reduced tumor burden in lung, brain, pancreatic, and breast cancer settings. Senescent cells are increasingly recognized as contributors to tumor progression, immune evasion, and chronic inflammation. The work builds on prior evidence that removing senescent cells can modify the tumor microenvironment and may enhance antitumor immunity.

      "These findings support further investigation of senescent-cell–targeted immunotherapy in oncology," said Dr. Thomas Ichim, President and Chief Scientific Officer of Immorta Bio and first author of the study. "Immorta Bio has submitted IND #30745 to the FDA for a planned first-in-human study in lung cancer and is completing the required GMP manufacturing run to enable initiation."

      "Therapeutic resistance remains a major challenge, particularly in tumors with limited immune infiltration," said Dr. Gilberto Lopes, Chief of Medical Oncology at the University of Miami and second author of the publication. "These preclinical results raise the possibility that targeting senescent cells could improve immune responsiveness and complement existing treatment approaches."

      Dr. Boris Reznik, Chairman and CEO of Immorta Bio and senior author, added: "This study provides foundational evidence for clinical development of senescent-cell–directed therapies in oncology, with potential future application to other aging-related biological processes."

      About Immorta Bio

      Immorta Bio Inc. is a scientific longevity company developing two complementary platforms to reverse aging and treat age-related diseases: SenoVax™, a first-in-class senolytic immunotherapy that eliminates senescent cells, and StemCellRevivify™, a personalized cellular rejuvenation technology based on young organ-specific progenitor and mesenchymal stem cells. Immorta Bio's mission is to restore youthful biology, extend healthy lifespan, and treat the major diseases of aging through the integration of immunotherapy and regenerative medicine.

      Media Contact:
      Immorta Bio Inc.
      +1 (305) 632-2939
      Email: 405946@email4pr.com
      Website: www.ImmortaBio.com

      SOURCE Immorta Bio Inc.

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