Drug

Capmatinib

As of the edition of 20 October 2026, Capmatinib is a small molecule: marketed, first approved in 2020 (US); acts on MET; US protection ends in 2032.

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

The drug

Status
Marketed; latest approval 2022
Kind
Small molecule
Brand name
Tabrecta
First approved
6 May 2020 (US)
Approvals on record
7 in 4 regions
Holder of the most recent approval
Novartis; 2 holders in all
Registered trials
53, 18 stopped early
Disease areas
Cancer; Lungs and airways; Skin and connective tissue; Digestive system; Blood and lymph; Pregnancy and women's health

US protection

US protection ends in 2032.

The last listed US drug-substance patent ends in 2032. The application that gives this date is held by Novartis.

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

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

See the exact date and the 8 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 Capmatinib.

Target

GeneProteinUniProt
METHepatocyte growth factor receptorP08581

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated4300
Phase 113913
Phase 23010513
Phase 35122
Phase 41100
All trials53

Who has held its approvals

CompanyRoleYears
NovartisOriginator, Applicant and Lead sponsor of trials2020 to now