Clinical Trials Directory

Trials / Completed

CompletedNCT00016094

S0108 Bevacizumab in Treating Patients With Non-Hodgkin's Lymphoma

Bevacizumab (rhuMab VEGF) (NSC-704865) Therapy for Patients With Relapsed Aggressive Non-Hodgkin's Lymphoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

PRIMARY OBJECTIVES: I. To estimate the 6-month progression-free survival rate in patients with relapsed aggressive NHL treated with single agent bevacizumab therapy. II. To evaluate response rate and toxicity in patients with relapsed aggressive NHL treated with this regimen. III. To measure tumor VEGF and VEGF receptor 1 and 2 expression (Flt-1 and Flk-1/KDR) and to explore the correlation between expression level and histology and response. IV. To measure pre-therapy, week 8 and time to progression biologic measures of VEGF activity including plasma VEGF levels, urinary VEGF levels, and circulating number of endothelial cells and explore the correlation with response. OUTLINE: 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. Patients are followed every 6 months for 3 years

Conditions

Interventions

TypeNameDescription
BIOLOGICALbevacizumabGiven IV
OTHERlaboratory biomarker analysisCorrelative studies

Timeline

Start date
2001-04-01
Primary completion
2005-08-01
Completion
2008-09-01
First posted
2003-01-27
Last updated
2013-01-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00016094. Inclusion in this directory is not an endorsement.