TVI-Brain-1 in Expanded Access Patient

Sponsor
TVAX Biomedical (Industry)
Overall Status
Available
CT.gov ID
NCT05936216
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Biological: TVI-Brain 1

Detailed Description

The TVI-Brain-1 treatment involves several steps. First, the patient's cancer will be surgically removed to provide cells for the vaccine. Second, the patient will be vaccinated with the vaccine formulation. Third, the patient's blood will be filtered for killer T cell precursors which will then be cultured and stimulated to reach a higher (killer) activity level. Fourth, the activated cells will be infused into the patient's bloodstream so that they will be able to attack the cancer.

Study Design

Study Type:
Expanded Access
Official Title:
Expanded Access Use Of Tvi-Brain-1 For Treatment Of Recurrent Grade 4 Astrocytoma (Glioblastoma Multiforme; GBM)

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Providence St. Vincent Medical Center Portland Oregon United States 97225

    Sponsors and Collaborators

    • TVAX Biomedical

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    TVAX Biomedical
    ClinicalTrials.gov Identifier:
    NCT05936216
    Other Study ID Numbers:
    • TVI-AST-EAU
    First Posted:
    Jul 7, 2023
    Last Update Posted:
    Jul 7, 2023
    Last Verified:
    Jun 1, 2023
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 7, 2023