RecruitingPhase 1NCT06401603
A Phase I Study of Decitabine, Lisaftoclax, and Olverembatinib in Patients With Advanced Chronic Myeloid Leukemia and Philadelphia Chromosome-Positive Acute Myeloid Leukemia
Sponsor
M.D. Anderson Cancer Center
Enrollment
30 participants
Start Date
Aug 6, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
To find the recommended doses of lisaftoclax and olverembatinib that can be given in combination with decitabine to participants with advanced CML and Ph+ AML.
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is testing a combination of three drugs — decitabine, lisaftoclax, and olverembatinib — in people with advanced chronic myeloid leukemia (CML) or Philadelphia chromosome-positive acute myeloid leukemia (Ph+ AML) that is no longer responding to standard targeted therapies.
**You may be eligible if...**
- You are 18 or older
- You have advanced CML (accelerated or blast phase) or Ph+ AML that has relapsed or is treatment-resistant
- You have tried and failed or could not tolerate at least one standard targeted therapy (BCR-ABL inhibitor)
- Your heart, liver, kidney, and pancreatic function are within acceptable ranges
**You may NOT be eligible if...**
- You have previously received lisaftoclax or olverembatinib
- You have had acute pancreatitis in the past year
- You have serious heart failure or significant cardiovascular disease
- You have active leukemia in the brain or spinal cord
- You are HIV positive (unless well controlled on treatment)
- You have active hepatitis B or C
- You are pregnant or breastfeeding
- You cannot swallow pills
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
DRUGDecitabine
Given by IV
DRUGListaftoclax
Given by PO
DRUGOlverembatinib
Given by PO
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06401603