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(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06308588
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