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OncoMatch/Clinical Trials/NCT06652438

Revumenib in Combination With Azacitidine + Venetoclax in Patients NPM1-mutated or KMT2A-rearranged AML

Is NCT06652438 recruiting? Yes, currently enrolling (Sep 2026). This Phase 3 trial studies Revumenib for acute myeloid leukemia, adult.

Phase 3RecruitingStichting Hemato-Oncologie voor Volwassenen NederlandNCT06652438Data as of Sep 2026Location: International · 18 countries

Treatment: RevumenibTreatment of patients with newly diagnosed AML who are not eligible for intensive chemotherapy has remained an area of high unmet medical need. The combination therapy with two medicines, azacitidine and venetoclax, is the usual plan of action. This has brought significant progress in the treatment, but it nevertheless is not curative and the disease does relapse over time. Revumenib blocks a specific molecule called menin in the cell nucleus. Some types of AML are reliant on menin working properly. These are leukemia cells with a change in the DNA, i.e. a mutation in the NPM1 or KMT2A gene. Revumenib can prevent the production of these types of leukemia cells by disrupting the production of this menin. The current study investigates whether adding revumenib to the combination therapy improves the prognosis for AML patients with a mutation in the NPM1 or KMT2A gene. This is a randomized, double-blind, placebo-controlled clinical study where subjects will be treated until disease progression, or development of side effects or death. From the moment of inclusion of the last patient, there will be a 4-year observational follow-up study in order to register survival duration and follow-up visits. Approximately 448 previously untreated patients with a mutation in the NPM1 or KMT2A gene and with newly diagnosed AML, who are not eligible for intensive chemotherapy. Patients must be ≥18 years of age.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Revumenib

Cancer type

Acute Myeloid Leukemia

Biomarker criteria

Required: NPM1 mutation

newly diagnosed NPM1-mutated AML, consistent with NPM1c

Required: KMT2A (MLL) rearrangement

newly diagnosed KMT2A-rearranged AML

Performance status

ECOG 0–3(Limited self-care)

ECOG performance status 0-2 (≥75 years); ECOG performance status 2 or 3 (18-74 years)

Prior therapy

No prior treatment (treatment-naive required)

Cannot have received: treatment for AML

Exception: hydroxyurea to control WBC counts is allowed

Subject has previously been treated for AML; a treatment period with hydroxyurea to control WBC counts is allowed

Cannot have received: hypomethylating agent for MDS-EB

prior treatment with a hypomethylating agent for MDS-EB is not allowed

Lab requirements

Kidney function

Serum creatinine ≤ 2.0 × ULN or creatinine clearance >30 mL/min (Cockcroft-Gault); creatinine clearance ≥ 30 mL/min to <45 ml/min allowed for ineligibility for intensive chemotherapy.

Liver function

Serum total bilirubin ≤ 3.0 × ULN unless considered due to Gilbert's disease or leukemic involvement with sponsor approval; AST, ALT, ALP ≤ 3.0 × ULN unless considered due to leukemic involvement with sponsor approval; moderate hepatic impairment with total bilirubin > 1.5 to < 3.0 × ULN allowed for ineligibility for intensive chemotherapy.

Adequate renal function as evidenced by serum creatinine ≤ 2.0 × ULN or creatinine clearance >30 mL/min based on the Cockcroft-Gault GFR. Adequate hepatic function as evidenced by: Serum total bilirubin ≤ 3.0 × ULN unless considered due to Gilbert's disease, or leukemic involvement following written approval by the sponsor (Co-)Principal Investigator. AST, ALT, ALP ≤ 3.0 × ULN, unless considered due to leukemic involvement following written approval by the sponsor (Co-)Principal Investigator.

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

US trial sites

  • US-Los Angeles CA-UCLA · Los Angeles, California
  • US-San Francisco CA-UCSF · San Francisco, California
  • US-Jacksonville FL-MAYOFL · Jacksonville, Florida
  • US-Atlanta GA-EMORY · Atlanta, Georgia
  • US-Kansas City KS-KUMC · Kansas City, Kansas

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06652438 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require NPM1?

Yes, NPM1 mutation is a required biomarker for enrollment.

Does this trial require KMT2A?

Yes, KMT2A 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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