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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


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

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