Drug

Fezolinetant

As of the edition of 20 October 2026, Fezolinetant is a small molecule: marketed, first approved in 2023 (US); acts on TACR3; US protection ends in 2034.

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
Veozah
First approved
12 May 2023 (US)
Approvals on record
4 in 4 regions
Holder of the most recent approval
Astellas; 3 holders in all
Registered trials
30, 1 stopped early
Disease areas
Cancer; Urinary and reproductive; Hormones; Inherited and neonatal; Mental health; Nervous system

US protection

US protection ends in 2034.

The last listed US drug-substance patent ends in 2034. The application that gives this date is held by Astellas.

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

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

See the exact date and the 3 listings behind itRequest access. Nothing is shown until you do.

Companies that need a new molecule because of this drug

1 company on route B because of this drug.

Companies on route B for this drug

In the product

1 company is on route B because of Fezolinetant.

Target

GeneProteinUniProt
TACR3Neuromedin-K receptorP29371

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated3210
Phase 17610
Phase 28431
Phase 312840
All trials30

Who has held its approvals

CompanyRoleYears
AstellasOriginator, Applicant and Lead sponsor of trials2017 to now