Vandetanib and Bevacizumab in Treating Patients With Advanced Solid Tumors or Lymphoma
Part of paid clinical trials in Bethesda, Maryland.
- Sponsor
- National Institutes of Health Clinical Center (CC)
- Study ID
- NCT00734890
- Phase
- PHASE1
- Status
- Completed
Conditions
- Lung Cancer
- Lymphoma
- Lymphoproliferative Disorder
- Small Intestine Cancer
- Unspecified Adult Solid Tumor, Protocol Specific
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- bevacizumab — BIOLOGICAL
- vandetanib — DRUG
- laboratory biomarker analysis — OTHER
- pharmacological study — OTHER
Study Details
RATIONALE: Vandetanib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. 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 carry cancer-killing substances to them. Bevacizumab and vandetanib may also stop the growth of cancer cells by blocking blood flow to the cancer. Giving vandetanib together with bevacizumab may kill more cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of vandetanib and bevacizumab in treating patients with advanced solid tumors or lymphoma.
Key Dates
- First listed
- Aug 14, 2008
- Start date
- Mar 31, 2008
- Status verified
- Mar 2012
- Primary completion
- Jun 30, 2010
- Completion
- Feb 28, 2011
Study Design
- Enrollment
- 18 participants (estimated)
- Primary purpose
- TREATMENT
Primary Outcome Measure
Maximum tolerated dose
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office | Bethesda | Maryland | 20892-1182 | - |
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