Drug

Telisotuzumab vedotin

As of the edition of 20 October 2026, Telisotuzumab vedotin is an antibody drug conjugate: marketed, first approved in 2025 (US); acts on MET, TUBB and TUBB1 and 7 more; US protection ends in 2037.

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

The drug

Status
Marketed; latest approval 2025
Kind
Antibody drug conjugate
Brand name
Emrelis
First approved
14 May 2025 (US)
Approvals on record
2 in 1 region
Holder of the most recent approval
AbbVie
Registered trials
10, 2 stopped early
Disease areas
Cancer; Lungs and airways

US protection

US protection ends in 2037.

US protection ends in 2037, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by AbbVie. The date is computed, not published.

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

1 listing counts towards this date. The exact date and each listing are in the product.

See the exact date and the 1 listing behind itRequest access. Nothing is shown until you do.

Companies that need a new molecule because of this drug

10 company-target rows on route B because of this drug.

Companies on route B for this drug

In the product

10 company-target rows are on route B because of Telisotuzumab vedotin.

Targets

GeneProteinUniProt
TUBB4ATubulin beta-4A chainP04350
TUBBTubulin beta chainP07437
METHepatocyte growth factor receptorP08581
TUBB4BTubulin beta-4B chainP68371
TUBB3Tubulin beta-3 chainQ13509
TUBB2ATubulin beta-2A chainQ13885
TUBB8Tubulin beta-8 chainQ3ZCM7
TUBB6Tubulin beta-6 chainQ9BUF5
TUBB2BTubulin beta-2B chainQ9BVA1
TUBB1Tubulin beta-1 chainQ9H4B7

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated1000
Phase 12110
Phase 25131
Phase 32011
All trials10

Who has held its approvals

CompanyRoleYears
AbbVieOriginator and Lead sponsor of trials2022 to now