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Clinical Trial Summary

The primary objective of this first in human study is to assess the safety and tolerability of increasing intravenous (IV) doses of single agent IPH4102 administered to patients with relapsed/refractory CTCL to characterize the dose limiting toxicities (DLT) and identify a Maximum Tolerated Dose (MTD).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02593045
Study type Interventional
Source Innate Pharma
Contact
Status Completed
Phase Phase 1
Start date October 2015
Completion date April 2020

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