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Clinical Trial Summary

The purpose of this Phase 1 study is to determine the maximum tolerated dose (MTD) through observation of dose limiting toxicity (DLT), which is in advance defined, in patients with peripheral or cutaneous T-cell lymphoma.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01401530
Study type Interventional
Source Eisai Inc.
Contact
Status Completed
Phase Phase 1
Start date July 2011
Completion date January 2016

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