OncoMatch/Clinical Trials/NCT06652438
Revumenib in Combination With Azacitidine + Venetoclax in Patients NPM1-mutated or KMT2A-rearranged AML
Is NCT06652438 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies Revumenib for acute myeloid leukemia, adult.
Treatment: Revumenib — Treatment 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 415 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.
Check if I qualifyExtracted eligibility criteria
Cancer type
Acute Myeloid Leukemia
Biomarker criteria
Required: KMT2A (MLL) rearrangement
Required: NPM1 mutation
Performance status
ECOG 0–3(Limited self-care)
Prior therapy
Cannot have received: hypomethylating agent
Exception: for MDS-EB
prior treatment with a hypomethylating agent for MDS-EB is not allowed
Lab requirements
Blood counts
WBC count < 25 x 10^9/L (hydroxyurea allowed to reduce WBC count)
Kidney function
Serum creatinine ≤ 2.0 × ULN or creatinine clearance >30 mL/min based on 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 written approval; AST, ALT, ALP ≤ 3.0 × ULN unless considered due to leukemic involvement with written approval; Moderate hepatic impairment with total bilirubin > 1.5 to < 3.0 x ULN allowed for ineligibility for intensive chemotherapy.
Cardiac function
No significant active cardiac disease within 3 months prior to start of study treatment, including NYHA class III/IV CHF, MI, unstable angina, severe arrhythmias, congenital long QT syndrome, QTcF >450 msec (males), >470 msec (females)
Adequate renal function as evidenced by serum creatinine ≤ 2.0 × ULN or creatinine clearance >30 mL/min based on the Cockcroft-Gault glomerular filtration rate (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 (copy in HO177@erasmusmc.nl). Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) ≤ 3.0 × ULN, unless considered due to leukemic involvement following written approval by the sponsor (Co-)Principal Investigator (copy in HO177@erasmusmc.nl).
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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