RecruitingPhase 2NCT06629584

Phase II Study of Asciminib for Second-line Treatment of Chronic Phase Chronic Myeloid Leukemia


Sponsor

M.D. Anderson Cancer Center

Enrollment

40 participants

Start Date

Feb 14, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is an open label, phase 2 study investigating asciminib in patients previously treated with one line of TKI therapy.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a drug called asciminib as a second-line treatment for people with chronic myeloid leukemia (CML) — a type of blood cancer — who have already tried one standard targeted therapy (called a TKI) but it stopped working or caused too many side effects. **You may be eligible if...** - You are 18 or older - You have chronic phase CML confirmed by genetic testing - You have had one prior TKI therapy that failed or was not tolerated - Your overall health status is good enough to handle treatment **You may NOT be eligible if...** - Your leukemia has a specific mutation called T315I - You have significant heart problems (severe heart failure, recent heart attack, dangerous heart rhythms) - You have active HIV, hepatitis B or C - You are pregnant or breastfeeding - You have a history of pancreatitis 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

Patients will receive asciminib 80 mg PO once daily continuously for 28-day cycles for 2 years.


Locations(1)

The University of Texas MD Anderson Cancer Center

Houston, Texas, United States

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NCT06629584


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