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HuMax-CD4 in Non-Cutaneous T-Cell Lymphoma

T Cell Lymphoma Clinical Trial

Official title:
An Open-Label Therapeutic Exploratory Clinical Trial of HuMax-CD4, a Fully Human Monoclonal Anti-CD4 Antibody, in Patients With Refractory or Relapsed Non-Cutaneous CD4+ T-Cell Lymphoma

Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of treatment of non-cutaneous T-cell lymphoma with treatment with CD4.

Clinical Trial Description

The study is closed and all subjects have completed treatment. The study is to evaluate the safety and efficacy of Humax CD4 with CHO vs CHO alone in subjects with non-cutaneous T cell lymphoma. The primary efficacy will be evaluated by time to relapse. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00877656
Study type Interventional
Source Emergent BioSolutions
Contact
Status Completed
Phase Phase 2/Phase 3
Start date August 2005
Completion date December 2008
View Details
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