Drug

Tralokinumab

As of the edition of 20 October 2026, Tralokinumab is an antibody: marketed, first approved in 2021 (EU); acts on IL13; US protection ends in 2033.

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

The drug

Status
Marketed; latest approval 2022
Kind
Antibody
Brand name
Adbry
First approved
17 June 2021 (EU)
Approvals on record
7 in 4 regions
Holder of the most recent approval
LEO Pharma; 3 holders in all
Registered trials
35, 5 stopped early
Disease areas
Immune system; Inherited and neonatal; Skin and connective tissue; Lungs and airways; Digestive system

US protection

US protection ends in 2033.

US protection ends in 2033, 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 LEO Pharma. 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

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 Tralokinumab.

Target

GeneProteinUniProt
IL13Interleukin-13P35225

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated3030
Phase 16501
Phase 211902
Phase 3131201
Phase 42011
All trials35

Who has held its approvals

CompanyRoleYears
LEO PharmaApplicant and Lead sponsor of trials2017 to now