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Tumor RNA Transfected Dendritic Cell Vaccines

US Department of Veterans Affairs (VA) logo

US Department of Veterans Affairs (VA)

Status and phase

Completed
Phase 1

Conditions

Prostate Cancer

Treatments

Biological: Tumor RNA transfected dendritic cells

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT00108264
CLIN-021-02S

Details and patient eligibility

About

The purpose of this study is to use dendritic cells transfected with amplified RNA from autologous tumor cells to develop a vaccine strategy for the treatment of prostate cancer in patients with disseminated disease.

Full description

The specific aims are: 1) to evaluate, in a phase I clinical trial, the safety of vaccinating patients with dendritic cells transfected with RNA from autologous cancer cells; 2) to analyze the T cell responses induced by the treatment; and 3) to improve the efficacy of the treatment by developing methods to increase the induction of CD4+T cell responses.

Sex

Male

Ages

10+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a histologically confirmed diagnosis of metastatic prostate cancer stages D1 - D3 are eligible for this study.
  • They must not have a history of autoimmune disease, serious intercurrent chronic or acute illness, pulmonary disease, active hepatitis, serologic evidence for HIV, or be receiving corticosteroid or immunosuppressive therapy.

Exclusion criteria

  • Patients will be excluded from the study if they have received chemotherapy or other forms of immunotherapy in the 6 weeks prior to study entry.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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