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Clinical Trial Summary

The purpose of this dose-escalation study is to assess the safety and tolerability of treatment with Chidamide in a range of doses combined with CHOP in fixed dose in patients with newly diagnosed peripheral T-cell lymphoma.


Clinical Trial Description

The purpose of this study is to assess the tolerability and safety include adverse events, vital signs, laboratory tests, etc., of a range of doses of chidamide combined with CHOP in peripheral T-cell lymphoma patients, and to determine the dose limit toxicity and the maximum tolerable dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02809573
Study type Interventional
Source Chipscreen Biosciences, Ltd.
Contact
Status Completed
Phase Phase 1
Start date August 11, 2016
Completion date January 8, 2019

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