S0108 Bevacizumab in Treating Patients With Non-Hodgkin's Lymphoma
Part of paid clinical trials in San Antonio, Texas.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT00016094
- Phase
- PHASE2
- Status
- Completed
Conditions
- Anaplastic Large Cell Lymphoma
- Recurrent Adult Burkitt Lymphoma
- Recurrent Adult Diffuse Large Cell Lymphoma
- Recurrent Mantle Cell Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 19 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- bevacizumab — BIOLOGICALGiven IV
- laboratory biomarker analysis — OTHERCorrelative studies
Study Details
Phase II trial to study the effectiveness of bevacizumab in treating patients who have non-Hodgkin's lymphoma. Monoclonal antibodies such as bevacizumab may stop the growth of cancer by stopping blood flow to the tumor. Bevacizumab may be an effective treatment for non-Hodgkin's lymphoma
Key Dates
- First listed
- Jan 27, 2003
- Start date
- Apr 30, 2001
- Status verified
- Jan 2013
- Primary completion
- Aug 31, 2005
- Completion
- Sep 30, 2008
Study Design
- Enrollment
- 60 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (bevacizumab)Patients receive bevacizumab IV over 30-90 minutes on days 1 and 15. Treatment repeats every 28 days for a maximum of 24 courses in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Progression-free survival rate in patients treated with single agent bevacizumab [ Time Frame: Date of registration to date of first observation of progressive disease, or death due to any cause, assessed up to 6 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Southwest Oncology Group | San Antonio | Texas | 78245 | - |
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