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Clinical Trial Summary

Primary objective: to increase knowledge about safety, tolerability, quality of life and efficacy under conditions of routine use of SUTENT®. Secondary objectives: treatment response, hypothyroidism prevalence.The efficacy will be assessed using the Objective Response Rate, Time to Progression based on the RECIST criteria and the ECOG performance data.


Clinical Trial Description

180 patients will be enrolled at 20 key oncological centres, the sample size is sufficient for exploratory analysis. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00684645
Study type Observational
Source Pfizer
Contact
Status Completed
Phase N/A
Start date June 2008
Completion date April 2011

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