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Clinical Trial Summary

OBJECTIVES OF THE TRIAL Primary objective Evaluation of efficacy in terms of progression-free survival at 9 months of the combination of intensified methotrexate, vinblastine, doxorubicin and cisplatin with or without panitumumab as first-line treatment of advanced urothelial carcinoma in patients without Harvey nor Kirsten rat sarcoma viral oncogene homolog mutations. Secondary objectives - To assess toxicity - To assess response rate - To assess overall survival - To assess time to progression - To study the correlation between response rate, time to progression, overall survival and biological parameters


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02818725
Study type Interventional
Source UNICANCER
Contact
Status Completed
Phase Phase 3
Start date June 2010
Completion date September 2017

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