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Compound · clinical trials

Revumenib

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 4 trials in our USA, UK and Ireland registers that name Revumenib as an intervention. Synced 24 Sep 2026
4Trials tracked
3Recruiting now
2Lead sponsors
3Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

Revumenib is named as a drug or biological intervention in 4 clinical trials in our USA, UK and Ireland trial registers, 3 of which are recruiting. Lead sponsors include Syndax Pharmaceuticals (3) and Stichting Hemato-Oncologie voor Volwassenen Nederland (1). Registered phases: Phase 3, Phase 1 and Phase 1/2. Conditions studied include Acute Myeloid Leukemias; Acute Myeloid Leukemia, Adult; Acute Myeloid Leukemia.

01

Clinical trials of Revumenib

4 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT06652438 Revumenib in Combination With Azacitidine + Venetoclax in Patients NPM1-mutated or KMT2A-rearranged AML
Acute Myeloid Leukemia, Adult
Phase 3 Recruiting Stichting Hemato-Oncologie voor Volwassenen Nederland Ireland
NCT07211958 Study of Revumenib in Combination With Intensive Chemotherapy in Newly Diagnosed Acute Myeloid Leukemia (AML) With a NPM1 Mutation (ClinicalTrials.gov ↗)
Acute Myeloid Leukemias
Phase 3 Recruiting Syndax Pharmaceuticals UK, USA
NCT04065399 A Study of Revumenib in R/R Leukemias Including Those With an MLL/KMT2A Gene Rearrangement or NPM1 Mutation (ClinicalTrials.gov ↗)
Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Mixed Lineage Acute Leukemia
Phase 1/2 Recruiting Syndax Pharmaceuticals USA
NCT06226571 A Study of Revumenib in Combination With Intensive Chemotherapy in Participants With Acute Myeloid Leukemias (ClinicalTrials.gov ↗)
Acute Myeloid Leukemias
Phase 1 Active, closed Syndax Pharmaceuticals UK, USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied

6 conditions
Condition (as registered)Trials
Acute Myeloid Leukemias2
Acute Myeloid Leukemia, Adult1
Acute Myeloid Leukemia1
Acute Lymphoblastic Leukemia1
Mixed Lineage Acute Leukemia1
Mixed Phenotype Acute Leukemia1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Syndax Pharmaceuticals3
Stichting Hemato-Oncologie voor Volwassenen Nederland1
04

Trials by country register

A trial with sites in more than one country appears in each of those registers.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Revumenib works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Revumenib (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 24 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.