Drug

Vorasidenib

As of the edition of 20 October 2026, Vorasidenib is a small molecule: marketed, first approved in 2024 (US); acts on IDH1 and IDH2; US protection ends in 2039.

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

The drug

Status
Marketed; latest approval 2025
Kind
Small molecule
Brand name
Voranigo
First approved
6 August 2024 (US)
Approvals on record
6 in 4 regions
Holder of the most recent approval
Nihon Servier Co., Ltd.; 4 holders in all
Registered trials
24, 0 stopped early
Disease areas
Cancer; Blood and lymph; Immune system; Nervous system

US protection

US protection ends in 2039.

The last listed US drug-substance patent ends in 2039. The application that gives this date is held by Servier.

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

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

See the exact date and the 10 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 Vorasidenib.

Targets

GeneProteinUniProt
IDH1Isocitrate dehydrogenase [NADP] cytoplasmicO75874
IDH2Isocitrate dehydrogenase [NADP], mitochondrialP48735

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated4030
Phase 1141130
Phase 22020
Phase 34040
All trials24

Who has held its approvals

CompanyRoleYears
ServierOriginator, Applicant and Lead sponsor of trials2023 to now