RecruitingPhase 2NCT07163793

Pilot Study of Reduced Venetoclax Exposure

A Pilot Study of Reduced Venetoclax Exposure in Patients With Acute Myeloid Leukemia in Complete Remission


Sponsor

Northwell Health

Enrollment

41 participants

Start Date

Oct 7, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Pilot Study of Reduced Venetoclax Exposure


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether people with acute myeloid leukemia (AML) — a blood cancer — who have responded well to initial treatment can do just as well with a lower dose of a drug called venetoclax during ongoing therapy. The goal is to reduce side effects while keeping the cancer in remission. **You may be eligible if...** - You have been diagnosed with AML - You were treated with a combination of azacitidine or decitabine plus venetoclax - Your AML has gone into remission (less than 5% cancer cells in bone marrow) - You achieved remission within 3 treatment cycles - You are able to take oral medications and follow the study schedule **You may NOT be eligible if...** - You have not yet achieved remission - You are unable to take oral medications - You are not willing to follow the study protocol 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

DRUGAzacitidine

Given Day 1-7 with Venetoclax Day 1-14 every 28 days until off study

DRUGDecitabine

Given Day 1-5 with Venetoclax Day 1-14 every 28 days until off

DRUGVenetoclax

Venetoclax up to 400mg a day on Day 1-14 every 28 days until off in combination with Azacitidine or Decitabine


Locations(1)

Zuckerberg Cancer Center

New Hyde Park, New York, United States

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NCT07163793


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