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Clinical Trial Summary

Primary:

- To evaluate the efficacy of capecitabine in combination with oxaliplatin (XELOX) in terms of overall response rate (based on RECIST criteria) in patients with metastatic NPC without prior chemotherapy for relapse.

Secondary:

- To evaluate the efficacy profile of oxaliplatin (XELOX) in patients with metastatic NPC in terms of time to progression of disease, survival time, duration of response and complete response rate.

- To study the safety and tolerability of the regimen in patients with metastatic NPC.


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 NCT00363831
Study type Interventional
Source The University of Hong Kong
Contact Public Registry GMA
Email PublicRegistryGMA@sanofi-aventis.com
Status Recruiting
Phase Phase 2
Start date July 2006

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