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Clinical Trial Summary

The purpose of this study is to determine the recommended dose of NC-6004 according to the dose-limiting toxicity (DLT) in combination with Gemcitabine, and to assess the efficacy, safety and tolerability.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00910741
Study type Interventional
Source Nanocarrier Co., Ltd.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date May 2009
Completion date July 2013

See also
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