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Clinical Trial Summary

This is a multi-center, open-label, dose escalation study that will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of liposomal annamycin as a single agent for the treatment of subjects with AML that is refractory to or relapsed after standard induction therapy


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03315039
Study type Interventional
Source Moleculin Biotech, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 28, 2018
Completion date June 20, 2020

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