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Clinical Trial Summary

To evaluate the rate of complete pathological response after 3 cycles of gemcitabine containing chemotherapy.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00191256
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 2
Start date June 2001
Completion date July 2006

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