RecruitingPhase 1Phase 2NCT06308588

Phase I/II Study of the Combination of Blinatumomab and Asciminib in Patients With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia


Sponsor

M.D. Anderson Cancer Center

Enrollment

40 participants

Start Date

Aug 5, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if the combination of blinatumomab and asciminib can help to control Ph+ ALL.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study combines two targeted drugs — blinatumomab and asciminib — to treat Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL), a type of blood cancer driven by a specific genetic abnormality. The trial aims to find out whether this combination can help patients who are newly diagnosed, relapsed, or not responding to existing therapies. **You may be eligible if...** - You are 12 years or older and have been diagnosed with Ph+ ALL (a specific type of leukemia caused by the Philadelphia chromosome) - You are newly diagnosed and not suitable for intensive chemotherapy, OR your leukemia has returned or is not responding to previous treatment - You weigh at least 40 kg - Your liver and kidney function are within acceptable ranges **You may NOT be eligible if...** - You have active, uncontrolled cancer that has spread to the brain or spinal cord - You have serious heart conditions - You are pregnant or breastfeeding - You have an active, uncontrolled infection 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

DRUGBlinatumomab

Given by Infusion

DRUGAsciminib

Given by PO


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06308588


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