Recurrent Glioblastoma Clinical Trial
Official title:
Expanded Access Use Of Tvi-Brain-1 For Treatment Of Recurrent Grade 4 Astrocytoma (Glioblastoma Multiforme; GBM)
NCT number | NCT05936216 |
Other study ID # | TVI-AST-EAU |
Secondary ID | |
Status | Available |
Phase | |
First received | |
Last updated |
TVI-Brain-1 is being offered as a potential treatment option to a Named Patient (Emergency Use Authorization IND) for recurrent glioblastoma as there is no effective systemic treatment available for this disease or patient. TVI-Brain-1 is an experimental treatment that takes advantage of the fact that your body can produce immune cells, called 'killer' white blood cells that have the ability to kill large numbers of the cancer cells that are present in your body. TVI-Brain-1 is designed to generate large numbers of those 'killer' white blood cells and to deliver those cells into your body so that they can kill your cancer cells.
Status | Available |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: Recurrent glioblastoma diagnosis confirmed - Age > 18 - Informed consent - Diagnosis of grade IV glioma with progression following standard treatment. - Must be able to tolerate surgery to provide tumor tissue for vaccine. - Must be able to produce viable vaccine from tumor tissue. - Karnofsky Performance Status must be 70 or greater. - Negative HIV test. - Negative for hepatitis B and C virus. - Respiratory reserve must be reasonable. - Sufficient renal function. - Satisfactory blood counts. - Negative pregnancy test for women of childbearing potential. Exclusion Criteria: - Surgically removed cancer reveals that it is not grade IV glioma. - Concomitant life-threatening disease. - Active autoimmune disease. - Currently receiving chemotherapy or biological therapy for the treatment of cancer. - Currently receiving immunosuppressive drugs for any reason. - Prior treatment with Avastin or other anti-angiogenesis treatment within 6 months. - Prior treatment with Gliadel wafers. - Corticosteroids beyond peri-operative period. - Psychological, familial, sociological or geographical conditions that do not permit adequate medical follow-up and compliance with the study protocol. |
Country | Name | City | State |
---|---|---|---|
United States | Providence St. Vincent Medical Center | Portland | Oregon |
Lead Sponsor | Collaborator |
---|---|
TVAX Biomedical |
United States,
Rosenberg SA, Packard BS, Aebersold PM, Solomon D, Topalian SL, Toy ST, Simon P, Lotze MT, Yang JC, Seipp CA, et al. Use of tumor-infiltrating lymphocytes and interleukin-2 in the immunotherapy of patients with metastatic melanoma. A preliminary report. N Engl J Med. 1988 Dec 22;319(25):1676-80. doi: 10.1056/NEJM198812223192527. — View Citation
Sloan AE, Dansey R, Zamorano L, Barger G, Hamm C, Diaz F, Baynes R, Wood G. Adoptive immunotherapy in patients with recurrent malignant glioma: preliminary results of using autologous whole-tumor vaccine plus granulocyte-macrophage colony-stimulating factor and adoptive transfer of anti-CD3-activated lymphocytes. Neurosurg Focus. 2000 Dec 15;9(6):e9. doi: 10.3171/foc.2000.9.6.10. — View Citation
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