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Phase II Study of Adenovirus/PSA Vaccine in Men With Recurrent Prostate Cancer After Local Therapy APP21

NCT00583752 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2023-05-18

Study results available
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Summary

The purpose of this study is to determine whether vaccination with the Ad/PSA vaccine will induce an anti-PSA immunity that will result in the destruction of the remaining prostate cancer cells.

Conditions

  • Recurrent Prostate Cancer

Interventions

BIOLOGICAL

Adenovirus/PSA Vaccine

1x10E8pfu in Gelfoam subcutaneously on day 0, 30, 60

Sponsors & Collaborators

  • United States Department of Defense

    collaborator FED

  • David M Lubaroff

    lead OTHER

Principal Investigators

  • David M Lubaroff, PhD · University of Iowa

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2020-12-31
Completion
2023-01-31
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00583752 on ClinicalTrials.gov