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Clinical Trial Summary

- Primary : To determine the safety profile of each treatment group.

- Secondary : To determine efficacy in term of overall response, disease free survival and survival at 1 and 2 years.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00271323
Study type Interventional
Source Sanofi
Contact
Status Terminated
Phase Phase 2
Start date May 2005
Completion date February 2007

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