RecruitingPhase 1Phase 2NCT06235801

A Phase I/II Study of Gilteritinib and Momelotinib for Patients With Relapsed or Refractory FLT3-Mutated Acute Myeloid Leukemia


Sponsor

M.D. Anderson Cancer Center

Enrollment

20 participants

Start Date

May 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To learn the recommended dose of momelotinib that can be given in combination with gilteritinib to participants with AML.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing a combination of two drugs — gilteritinib and momelotinib — for patients with relapsed or treatment-resistant acute myeloid leukemia (AML) that has a mutation in the FLT3 gene. **You may be eligible if...** - You are 18 or older - You have AML that has a FLT3 mutation (either FLT3-ITD or FLT3 D835/D836) - Your AML has come back or stopped responding to previous treatment - Your liver and kidneys are functioning adequately - You are willing to use contraception during and for 4 months after the study **You may NOT be eligible if...** - You have a congenital heart condition called long QT syndrome - Your heart rhythm test (ECG) shows a QTcF greater than 450 ms - Your kidney function is significantly impaired (creatinine clearance below 30 mL/min) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGGilteritinib

Given by PO

DRUGMomelotinib

Given by PO


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT06235801


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