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Clinical Trial Summary

The purpose of this study is to determine the maximum tolerated dose (MTD) of ARGX-110 and/or the recommended Phase II dose (RP2D) in combination with a standard dose of azacytidine (AZA) in Phase 1; and to evaluate efficacy of ARGX-110 when administered at a RP2D level established in Phase I in combination with a standard dose of AZA (proof-of concept) by evaluating overall response rate (ORR) in Phase 2.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03030612
Study type Interventional
Source OncoVerity, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date December 2016
Completion date August 2022

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