RecruitingPhase 1NCT06034470

Combination Chemotherapy (FLAG-Ida) With Pivekimab Sunirine (PVEK [IMGN632]) for the Treatment of Newly Diagnosed Adverse Risk Acute Myeloid Leukemia and Other High-Grade Myeloid Neoplasms

Phase 1 Study of FLAG-Ida With Pivekimab Sunirine (PVEK [IMGN632]) for Adults With Newly Diagnosed Adverse-Risk Acute Myeloid Leukemia and Other High-Grade Myeloid Neoplasms


Sponsor

Fred Hutchinson Cancer Center

Enrollment

30 participants

Start Date

Dec 18, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This phase I trial finds the best dose of PVEK when given together with fludarabine, cytarabine, granulocyte colony-stimulating factor (G-CSF), and idarubicin, (FLAG-Ida) regimen and studies the effectiveness of this combination therapy in treating patients with newly diagnosed adverse risk acute myeloid leukemia (AML) and other high-grade myeloid neoplasms. PVEK is a monoclonal antibody linked to a chemotherapy drug. PVEK is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as CD123 receptors, and delivers the chemotherapy drug to kill them. Chemotherapy drugs, such as idarubicin, fludarabine, high-dose cytarabine work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. G-CSF helps the bone marrow make more white blood cells in patients with low white blood cell count due to cancer treatment. Giving PVEK with the FLAG-Ida regimen may be a safe and effective treatment for patients with acute myeloid leukemia and other high-grade myeloid neoplasms.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding pivekimab sunirine (a targeted antibody-drug) to standard intensive chemotherapy (FLAG-Ida) improves outcomes for patients newly diagnosed with high-risk acute myeloid leukemia (AML) or related blood cancers. **You may be eligible if...** - You are 18 or older - You have been newly diagnosed with AML (not a specific subtype called APL) or a related high-grade blood cancer - Your disease is classified as high-risk (adverse risk) based on genetic testing - Your cancer cells express the CD123 protein - You are medically fit enough for intensive chemotherapy - You have not received prior treatment for AML (some low-intensity treatments for prior lower-grade conditions may be allowed) **You may NOT be eligible if...** - You have significant liver, kidney, or heart problems - You have an active, uncontrolled infection - You are pregnant or breastfeeding - You have received prior intensive chemotherapy for AML 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

PROCEDUREBiospecimen Collection

Undergo blood sample collection

PROCEDUREBone Marrow Aspiration

Undergo bone marrow aspirate

PROCEDUREBone Marrow Biopsy

Undergo bone marrow biopsy

DRUGCytarabine

Given IV

PROCEDUREEchocardiography

Undergo ECHO

DRUGFludarabine

Given IV

DRUGGranulocyte Colony-Stimulating Factor

Given SC

DRUGIdarubicin

Given IV

PROCEDUREMultigated Acquisition Scan

Undergo MUGA scan

DRUGPivekimab Sunirine

Given IV


Locations(1)

Fred Hutch/University of Washington Cancer Consortium

Seattle, Washington, United States

View Full Details on ClinicalTrials.gov

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NCT06034470


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