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Clinical Trial Summary

This is a first-in-human, open-label, phase 1, sequential dose escalation study. AMG 673 will be evaluated as a short term intravenous (IV) infusion in adult subjects with relapsed/refractory AML. The study will be conducted at approximately 7 sites in the United States, Australia and Germany.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03224819
Study type Interventional
Source Amgen
Contact Amgen Call Center
Phone 866-572-6436
Email medinfo@amgen.com
Status Recruiting
Phase Early Phase 1
Start date September 7, 2017
Completion date March 22, 2020

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