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Clinical Trial Summary

Primary:

- To assess the overall response rate of oxaliplatin in patients with bidimensionally measurable disease at baseline.

Secondary:

- To assess the safety and tolerability of oxaliplatin

- To assess time to progression and overall survival.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00782041
Study type Interventional
Source Sanofi
Contact
Status Terminated
Phase Phase 2
Start date January 2003

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