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Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AML

Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AML

Recruiting
18 years and older
All
Phase N/A

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Overview

The purpose of this research is to see how certain genetic variations relate to side effects and outcomes experienced while receiving treatment with azacitidine and venetoclax.

Description

This is a prospective pilot study of the association of SNPs and venetoclax levels with toxicity and response to azacitidine plus venetoclax (Aza/Ven) as well as pharmacogenomics and venetoclax levels in patients with newly diagnosed AML determined to be unfit for intensive induction. Newly diagnosed AML patients over 18 years old who receive Aza/Ven as standard of care will be eligible for this study. Buccal swabs for SNPs and pharmacogenomic analysis can occur at any point before or after starting treatment during the study period. Venetoclax peak and trough levels will be obtained during SOC Aza/Ven treatments. Participants will be recruited initially at AHWFBCCC locations.

Eligibility

Inclusion Criteria:

  • Written informed consent and HIPAA authorization for release of personal health information.
  • Age ≥ 18 years of age at the time of enrollment
  • Confirmed diagnosis of AML
  • Planned initial treatment with azacitidine and venetoclax
  • Ability to read and understand the English and/or Spanish language
  • As determined by the enrolling investigator, ability of the participant to understand and comply with study procedures for the entire length of the study

Exclusion Criteria:

  • None

Study details
    Leukemia
    Myeloid
    Acute

NCT06580106

Wake Forest University Health Sciences

15 October 2025

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