RecruitingPhase 2NCT05401097

IDH Targeted/Non- Targeted vs Non-targeted/IDH-targeted Approaches in the Treatment of Newly Diagnosed IDH Mutated AML Patients Not Candidates for Intensive Induction Therapy (I- DATA Study)

Randomized, Sequential, Open-Label Study to Evaluate the Efficacy of IDH Targeted/Non- Targeted Versus Non-targeted/IDH-targeted Approaches in the Treatment of Newly Diagnosed IDH Mutated AML Patients Not Candidates for Intensive Induction Therapy (I- DATA Study)


Sponsor

Alice Mims

Enrollment

125 participants

Start Date

Sep 13, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II study compares the order of treatment with ivosidenib or enasidenib and azacitidine plus venetoclax in treating older patients with acute myeloid leukemia with genetic changes in the IDH1 or IDH2 genes (IDH mutated). Ivosidenib is in a class of medications called isocitrate dehydrogenase-1 (IDH1) inhibitors. It works by slowing or stopping the growth of cancer cells. Enasidenib is in a class of medications called an IDH2 inhibitor. It also works by slowing or stopping the growth of cancer cells. Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival. Azacitidine is in a class of medications called demethylation agents. It works by helping the bone marrow to produce normal blood cells and by killing abnormal cells. This study may help researchers determine which treatment order is best for older patients with IDH mutated acute myeloid leukemia: 1) ivosidenib or enasidenib followed by azacitidine plus venetoclax; or 2) azacitidine plus venetoclax followed by ivosidenib or enasidenib.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two treatment sequences in people with newly diagnosed AML (a type of blood cancer) that has a specific mutation (IDH1 or IDH2), who are not well enough for intensive chemotherapy. The study tests whether starting with a targeted IDH inhibitor or with a gentler standard chemotherapy first leads to better outcomes. **You may be eligible if...** - You have been newly diagnosed with AML with an IDH1 or IDH2 mutation - You are not able to tolerate or have chosen not to have intensive induction chemotherapy - Your kidneys and liver are functioning adequately - Your overall health status is reasonably good (ECOG 0–2) **You may NOT be eligible if...** - You have previously received treatment for AML or a related blood disorder - You have certain serious infections or other active cancers - You have significant heart problems - You are pregnant or breastfeeding 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

DRUGAzacitidine

Given IV or SC

PROCEDUREBiopsy

Undergo biopsy of the bone marrow

DRUGEnasidenib

Given PO

DRUGIvosidenib

Given PO

DRUGVenetoclax

Given PO


Locations(1)

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

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NCT05401097


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