Clinical Trials Directory

Trials / Completed

CompletedNCT00143871

Study of Rituximab Plus High-Dose Chemotherapy Non-Hodgkin's Lymphoma

Rituximab Plus High-dose Chemotherapy With Autologous Stem Cell Support for Non-Hodgkin's Lymphoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
35 (planned)
Sponsor
University of Michigan Rogel Cancer Center · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This study is being conducted to determine the safety, side effects, and response to a combination of an established high-dose chemotherapy regimen, plus the addition of Rituximab (which is a form of immunotherapy).

Detailed description

Combination chemotherapy is the standard treatment as initial therapy for advanced stage aggressive Non-Hodgkin's lymphoma (NHL). Standard chemotherapy cures less than 40% of patients. When patients relapse, they may be eligible to receive high-dose chemotherapy with autologous stem cell support. Multiple studies have shown the value of high-dose chemotherapy, with increased disease-free survival and overall survival, when compared with second-line conventional chemotherapy. Unfortunately high-dose chemotherapy is curative in less than half the patients who receive it, and other treatment strategies are needed to improve the cure rate. Another treatment option called immunotherapy is being tested in lymphoma patients. Immunotherapy involves attempts to use the immune system or products of the immune system to fight lymphoma. For example, NHL cells have a protein called CD20 on their surface. Rituximab is an antibody directed against the CD20 protein, which may result in the death of the lymphoma cell. Patients in this study will receive Rituximab to see if it is a safe treatment option for NHL patients.

Conditions

Interventions

TypeNameDescription
DRUGRituximab

Timeline

Start date
2001-04-01
Primary completion
2006-12-01
Completion
2007-01-01
First posted
2005-09-02
Last updated
2012-02-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00143871. Inclusion in this directory is not an endorsement.