APC8015 and Bevacizumab in Treating Patients With Prostate Cancer
Part of paid clinical trials in San Francisco, California.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT00027599
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- bevacizumab — BIOLOGICAL
- prostatic acid phosphatase-sargramostim fusion protein — BIOLOGICAL
- sipuleucel-T — BIOLOGICAL
- therapeutic autologous dendritic cells — BIOLOGICAL
- in vitro-treated peripheral blood stem cell transplantation — PROCEDURE
Study Details
Phase II trial to study the effectiveness of APC8015 combined with bevacizumab in treating patients who have undergone radiation therapy and/or surgery and who have progressive prostate cancer. Biological therapies such as APC8015 use different ways to stimulate the immune system and stop cancer cells from growing. Monoclonal antibodies such as bevacizumab can locate tumor cells and kill them without harming normal cells. Combining monoclonal antibody therapy with biological therapy may kill more cancer cells.
Key Dates
- First listed
- May 7, 2003
- Start date
- Dec 31, 2001
- Status verified
- Dec 2003
- Primary completion
- Jul 31, 2007
Study Design
- Enrollment
- 25 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm IAutologous dendritic cells (DCs) are harvested and pulsed with prostatic acid phosphatase-sargramostim fusion protein to produce APC8015 (Provenge). Patients receive APC8015 IV over 30 minutes and bevacizumab IV over 30-60 minutes on day 1. Treatment repeats every 14 days for 3 courses. Patients continue to receive bevacizumab alone every 14 days in the absence of disease progression or unacceptable toxicity.
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UCSF Comprehensive Cancer Center | San Francisco | California | 94115 | - |
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