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NCT06580106 · ClinicalTrials.gov registry record

Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AML

A clinical trial of Leukemia, Myeloid, Acute, sponsored by Wake Forest University Health Sciences.

Recruiting
Registry status
50
Enrollment target
2
Study locations

NCT06580106 is a study of Leukemia, Myeloid, Acute that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 50 participants, below the 114-participant average among 30 other Leukemia, Myeloid, Acute trials with a reported enrollment target (56% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT06580106, a study of Leukemia, Myeloid, Acute, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.

RECRUITING
Registry status
50 participants
Enrollment target
2
Study locations

Study 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.

Conditions Studied

Interventions

  • OTHER Biospecimen samples

Study Locations (2)

North Carolina

  • Levine Cancer Institute - Charlotte
  • Wake Forest Baptist Comprehensive Cancer Center - Winston-Salem

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-04-09
Est. Completion 2030-01

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT06580106

The ClinicalTrials.gov registry entry for NCT06580106 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 114-participant average among 30 other Leukemia, Myeloid, Acute trials with a reported enrollment target (56% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Leukemia, Myeloid, Acute appearing as the primary indexed condition, and to 1 intervention - of which Biospecimen samples is the first listed.

NCT06580106 reports 2 study locations spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT06580106 about?

NCT06580106 is a clinical study titled "Toxicity Genetic Determinants and Response to Azacitidine and Venetoclax in AML". 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.

What is the current status of trial NCT06580106?

This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2025-04-09. Estimated completion is 2030-01.

What conditions does trial NCT06580106 study?

This clinical trial studies the following conditions: Leukemia, Myeloid, Acute.

What interventions are being tested in trial NCT06580106?

The interventions under investigation include: Biospecimen samples (OTHER).

Who is sponsoring clinical trial NCT06580106?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06580106 being conducted?

This trial has 2 study locations across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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