Drug

Vimseltinib

As of the edition of 20 October 2026, Vimseltinib is a small molecule: marketed, first approved in 2025 (US); acts on CSF1R; US protection ends in 2044.

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
Romvimza
First approved
14 February 2025 (US)
Approvals on record
4 in 2 regions
Holder of the most recent approval
Deciphera Pharmaceuticals; 2 holders in all
Registered trials
9, 0 stopped early
Disease areas
Cancer; Bones, joints and muscles; Digestive system; Immune system; Infections; Lungs and airways

US protection

US protection ends in 2044.

The last listed US drug-substance patent ends in 2044. The application that gives this date is held by Deciphera 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 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 Vimseltinib.

Target

GeneProteinUniProt
CSF1RMacrophage colony-stimulating factor 1 receptorP07333

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase 15320
Phase 23030
Phase 31010
All trials9

Who has held its approvals

CompanyRoleYears
Deciphera PharmaceuticalsOriginator, Applicant and Lead sponsor of trials2017 to now