Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AML

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWake Forest University Health Sciences

About this trial

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 criteria

Qualifiers

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

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Biospecimen samples

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators

Wake Forest University Health Sciences

Lead sponsor

Atrium Health Levine Cancer Institute

Collaborator

Swim Across America

Collaborator