OncoMatch

OncoMatch/Clinical Trials/NCT05317403

Venetoclax to Augment Epigenetic Modification and Chemotherapy

Is NCT05317403 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments for acute myeloid leukemia, in relapse.

Phase 1RecruitingMedical College of WisconsinNCT05317403Data as of Jun 2026

Treatment: Venetoclax · Azacitadine · Vorinostat · Cytarabine · Fludarabine · FilgrastimThe investigator is testing the addition of venetoclax to 5-azacitidine and vorinostat followed by standard chemotherapy to enhance treatment response in AML patients.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

VenetoclaxVorinostat

Chemotherapy

CytarabineFludarabine

Other

AzacitadineFilgrastim

Cancer type

Acute Myeloid Leukemia

Demographics

Ages 1–25

Lab requirements

Kidney function

Calculated creatinine clearance or radioisotope GFR ≥ 70ml/min/1.73m2 OR a normal serum creatinine

Liver function

Direct bilirubin < 1.5 x ULN for age or normal, AND ALT < 5 x ULN for age. Hepatic requirements are waived for patients with known or suspected liver involvement by leukemia, with study chair approval.

Cardiac function

Shortening fraction of ≥ 27% OR ejection fraction of ≥ 50%

Adequate renal and hepatic functions as indicated by the following laboratory values: ... Adequate Cardiac Function Defined as: Shortening fraction of ≥ 27% OR ejection fraction of ≥ 50%.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Children's Wisconsin · Milwaukee, Wisconsin

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT05317403 currently recruiting?

Yes, this trial is currently recruiting patients.

Is there an age limit?

Yes. Patients must be 25 years or younger and at least 1 years old.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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