Drug

Revumenib

As of the edition of 20 October 2026, Revumenib is a small molecule: marketed, first approved in 2024 (US); acts on KMT2A and MEN1; US protection ends in 2037.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2024
Kind
Small molecule
Brand name
Revuforj
First approved
15 November 2024 (US)
Approvals on record
3 in 1 region
Holder of the most recent approval
Syndax Pharmaceuticals
Registered trials
27, 3 stopped early
Disease areas
Blood and lymph; Cancer; Immune system; Digestive system; Infections

US protection

US protection ends in 2037.

The last listed US drug-substance patent ends in 2037. The application that gives this date is held by Syndax Pharmaceuticals.

This is the US only, and it is not the date generics or biosimilars can enter.

The exact date and the listings behind it

In the product

15 listings count towards this date. The exact date and each listing are in the product.

See the exact date and the 15 listings behind itRequest access. Nothing is shown until you do.

Companies that need a new molecule because of this drug

1 company-target row on route B because of this drug.

Companies on route B for this drug

In the product

1 company-target row is on route B because of Revumenib.

Targets

GeneProteinUniProt
MEN1MeninO00255
KMT2AHistone-lysine N-methyltransferase 2AQ03164

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated1000
Phase 111272
Phase 2120111
Phase 33030
All trials27

Who has held its approvals

CompanyRoleYears
Syndax PharmaceuticalsOriginator and Lead sponsor of trials2024 to now