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OncoMatch/Clinical Trials/NCT06284486

A Multi-Site Break Through Cancer Trial: Phase II Study Investigating Dual Inhibition of BCL2 and Menin in AML MRD Using the Combination of Venetoclax and Revumenib

Is NCT06284486 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including Venetoclax and Revumenib for acute myeloid leukemia.

Phase 1/2RecruitingM.D. Anderson Cancer CenterNCT06284486Data as of Jun 2026

Treatment: Venetoclax · RevumenibTo learn if the combination of venetoclax and revumenib can help to control MRD-positive AML.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

VenetoclaxRevumenib

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Required: KMT2A (MLL) rearrangement

Required: NPM1 mutation

Required: NUP98 rearrangement

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

ECOG performance status of ≤ 2 (if aged ≥18 years); Karnofsky Performance Scale of ≥50 (if aged ≥16 years and <18 years); Lansky Performance Score of ≥50 (if aged <16 years)

Demographics

Ages ≥ 12

Prior therapy

Must have received: high intensity chemotherapy — first remission

first remission following high intensity chemotherapy

Must have received: hypomethylating agent — first remission

at least 2 cycles of low intensity therapy (e.g. hypomethylating agent or low-dose cytarabine-based)

Must have received: low-dose cytarabine-based — first remission

at least 2 cycles of low intensity therapy (e.g. hypomethylating agent or low-dose cytarabine-based)

Cannot have received: menin inhibitor

Prior treatment with a menin inhibitor

Lab requirements

Kidney function

estimated glomerular filtration rate ≥ 60 ml/min based on local institutional practice for age-appropriate determination

Liver function

direct bilirubin < 1.5x uln unless increase is due leukemic involvement, and ast and/or alt < 3x uln unless considered due to leukemic involvement, in which case direct bilirubin or ast and/or alt < 5x uln will be considered eligible

Cardiac function

baseline ejection fraction must be > 40%

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

US trial sites

  • Johns Hopkins University · Baltimore, Maryland
  • Dana-Farber Cancer Center · Boston, Massachusetts
  • Memorial Sloan Kettering Cancer Center · New York, New York
  • MD Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06284486 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior menin inhibitor disqualifies patients from enrollment.

Does this trial require KMT2A?

Yes, KMT2A rearrangement is a required biomarker for enrollment.

Does this trial require NPM1?

Yes, NPM1 mutation is a required biomarker for enrollment.

Does this trial require NUP98?

Yes, NUP98 rearrangement is a required biomarker for enrollment.

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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