RecruitingNCT06580106

Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AML

A Prospective Pilot Study of the Genetic Determinants of Toxicity and Response to Azacitidine and Venetoclax in Patients With Newly Diagnosed Acute Myeloid Leukemia Through Evaluation of Polymorphisms in Pharmacokinetic Genes and Venetoclax Levels


Sponsor

Wake Forest University Health Sciences

Enrollment

50 participants

Start Date

Apr 9, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria6

  • 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 Criteria1

  • None

Interventions

OTHERBiospecimen samples

Buccal swabs and Blood samples will be collected throughout study.


Locations(2)

Levine Cancer Institute

Charlotte, North Carolina, United States

Wake Forest Baptist Comprehensive Cancer Center

Winston-Salem, North Carolina, United States

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NCT06580106


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