Gemcitabine Hydrochloride With or Without Bevacizumab in Treating Patients Who Are Undergoing Surgery for Pancreatic Cancer
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT00253526
- Phase
- PHASE2
- Status
- Withdrawn
Conditions
- Adenocarcinoma of the Pancreas
- Recurrent Pancreatic Cancer
- Stage I Pancreatic Cancer
- Stage II Pancreatic Cancer
- Stage III Pancreatic Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- bevacizumab — DRUG
- gemcitabine hydrochloride — DRUG
- adjuvant therapy — PROCEDURE
- anti-cytokine therapy — PROCEDURE
- antiangiogenesis therapy — PROCEDURE
- antibody therapy — PROCEDURE
- biological therapy — PROCEDURE
- chemotherapy — PROCEDURE
- conventional surgery — PROCEDURE
- growth factor antagonist therapy — PROCEDURE
- monoclonal antibody therapy — PROCEDURE
- surgery — PROCEDURE
Study Details
RATIONALE: Drugs used in chemotherapy, such as gemcitabine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells an help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of pancreatic cancer by blocking blood flow to the tumor. Giving gemcitabine hydrochloride together with bevacizumab after surgery may kill any remaining tumor cells. PURPOSE: This phase II trial is studying gemcitabine hydrochloride and bevacizumab to see how well they work compared to gemcitabine hydrochloride alone in treating patients who are undergoing surgery for pancreatic cancer.
Key Dates
- First listed
- Nov 15, 2005
- Status verified
- Dec 2006
Study Design
- Enrollment
- 0 participants (actual)
- Primary purpose
- TREATMENT
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