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Clinical Trial Summary

To assess the efficacy and safety of the regimen in previously untreated, unresectable invasive thymoma or thymic carcinoma


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 NCT00818090
Study type Interventional
Source Korean Cancer Study Group
Contact
Status Terminated
Phase Phase 2
Start date September 2008
Completion date November 2011

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