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Clinical Trial Summary

The purpose of this trial is to determine the safety and efficacy of HuMax-CD20 as a treatment for Follicular Lymphoma (FL).


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00092274
Study type Interventional
Source GlaxoSmithKline
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date September 2004
Completion date January 2005

See also
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