RecruitingPhase 2NCT06236724

Phase II Study Assessing Efficacy and Safety of Asciminib in Patients With Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase.


Sponsor

M.D. Anderson Cancer Center

Enrollment

50 participants

Start Date

Jan 31, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if asciminib can help to control CML. The safety and effects of this drug will also be studied.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing asciminib — a newer type of drug that targets the BCR-ABL1 protein — as a first-line treatment for patients newly diagnosed with chronic myeloid leukemia (CML) in chronic phase (a blood cancer). **You may be eligible if...** - You are 18 or older - You have been newly diagnosed with CML in chronic phase within the last 12 months - Your cancer is positive for the Philadelphia chromosome or BCR::ABL1 gene fusion - Your liver and kidneys are functioning adequately - You are willing to use contraception as required **You may NOT be eligible if...** - Your CML has progressed beyond the chronic phase to an accelerated or blast phase - You have received more than a few days of prior CML treatment (except hydroxyurea or brief courses of TKIs) - Your organ function falls below the required thresholds 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

DRUGAsciminib

Given by PO


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06236724


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