MAX-40279 in Subjects With Acute Myelogenous Leukemia (AML)

Status Recruiting

Clinical Trial Summary

This is a dose-escalation phase I trial to evaluate the safety and tolerability of MAX-40279 in subjects with acute myelogenous leukemia(AML).

Clinical Trial Description

The class III receptor tyrosine kinase FMS-related tyrosine kinase 3 (FLT3), is mutated and activated in about 30% of adult patients with AML. The mutations involve either an internal tandem duplication (ITD) (in about 25% of AML patients) or a point mutation in the tyrosine kinase domain (TKD) (in about 7% of patients). Patients with mutations in FLT3, particularly those with ITD mutations, have a worse prognosis, with lower rate of complete remission, and lower overall survival . Thus, inhibition of activated FLT3 kinase by a pharmacologic agent is an attractive therapeutic strategy in AML. The aberrant of fibroblast growth factor receptor (FGFR) might be a major reason fot resistance to targeted therapies, and FGFR inhibitors significantly suppress leukemia development in vivo. MAX-40279 is a dual inhibitor of FLT3 and FGFR. Our goal is to develpe this uqiue dual inhibitor to be a more effective and wider use for AML treatment than the current known FLT3 inhibitors. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03412292
Study type	Interventional
Source	Maxinovel Pty., Ltd.
Contact	Chun Fong, MD
Phone	+61394965000
Email	chun.fong@austin.org.au
Status	Recruiting
Phase	Phase 1
Start date	August 1, 2018
Completion date	December 1, 2022

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