PROSTVAC-VF is an investigational cancer vaccine. The vaccine is based on the theory that the immune system can be taught to fight cancer by directing the immune system to attack specific targets found on cancer cells. These targets are called Tumor Associated Antigens, or TAA's. This trial will help determine if this vaccine can help fight cancer. This multi-center, double-blind, randomized, empty vector-controlled trial is designed to evaluate the safety and efficacy of PROSTVAC-VF/TRICOM co-administered with GM-CSF versus the empty viral vector co-administered with placebo in the treatment of patients with androgen-independent prostate cancer (AIPC). All patients will be required to sign an informed consent prior to the performance of any on-study procedures. Patients will be screened for eligibility within 14 days prior to vaccine administration. Patients who meet all inclusion and exclusion criteria will be centrally randomized into the study and will receive a unique patient identification number and a blinded treatment assignment. The ratio of active treatment to empty vector control (placebo) is 2:1.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
120
Urology Centers of Alabama
Homewood, Alabama, United States
Alaska Clinical Research Center
Anchorage, Alaska, United States
Urology Associates of Central California
Fresno, California, United States
San Diego Urology Center
La Mesa, California, United States
Loma Linda University
Loma Linda, California, United States
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Atlantic Urology Medical Group
Long Beach, California, United States
Pacific Clinical Research
Santa Monica, California, United States
Western Clinical Research, Inc.
Torrance, California, United States
UCHSC Anschutz Cancer Pavilion
Aurora, Colorado, United States
Connecticut Clinical Research Center
Waterbury, Connecticut, United States
...and 37 more locations