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Clinical Trial Summary

The purpose of this study is to determine Maximum Tolerated Dose (MTD) or recommended phase II dose of LDE225 when administered orally to two adult patient groups of East Asian (i.e., Japanese and Chinese/Taiwanese) with advanced solid tumors that have progressed despite standard therapy or for which no standard therapy exists.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01208831
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 1
Start date October 2010
Completion date October 2013

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