Bevacizumab and Gemcitabine in Treating Patients With Advanced Pancreatic Cancer
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT00028834
- Phase
- PHASE2
- Status
- Completed
Conditions
- Adenocarcinoma of the Pancreas
- Recurrent Pancreatic Cancer
- Stage III Pancreatic Cancer
- Stage IV Pancreatic Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- gemcitabine hydrochloride — DRUGGiven IV
- bevacizumab — BIOLOGICALGiven IV
- laboratory biomarker analysis — OTHERCorrelative studies
Study Details
This phase II trial is to see if combining gemcitabine with bevacizumab works in treating patients who have advanced pancreatic cancer. Drugs used in chemotherapy work in different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them. Combining chemotherapy with a monoclonal antibody may kill more tumor cells
Key Dates
- First listed
- Jan 27, 2003
- Start date
- Feb 28, 2002
- Status verified
- Jan 2013
- Primary completion
- Dec 31, 2004
Study Design
- Enrollment
- 50 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (gemcitabine hydrochloride, bevacizumab)Patients receive gemcitabine IV over 30 minutes on days 1, 8, and 15 and bevacizumab IV over 30-90 minutes on days 1 and 15. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Objective response rate (complete or partial responses) [ Time Frame: Up to 2 years ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago Comprehensive Cancer Center | Chicago | Illinois | 60637-1470 | - |
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