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)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT06401603