Drug

Bimekizumab

As of the edition of 20 October 2026, Bimekizumab is an antibody: marketed, first approved in 2021 (EU); acts on IL17A and IL17F; US protection ends in 2035.

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

The drug

Status
Marketed; latest approval 2023
Kind
Antibody
Brand name
Bimzelx
First approved
20 August 2021 (EU)
Approvals on record
9 in 3 regions
Holder of the most recent approval
UCB; 3 holders in all
Registered trials
55, 2 stopped early
Disease areas
Skin and connective tissue; Bones, joints and muscles; Infections; Immune system; Heart and blood vessels; Inherited and neonatal

US protection

US protection ends in 2035.

US protection ends in 2035, 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 UCB. 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.

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Companies that need a new molecule because of this drug

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

Companies on route B for this drug

In the product

2 company-target rows are on route B because of Bimekizumab.

Targets

GeneProteinUniProt
IL17AInterleukin-17AQ16552
IL17FInterleukin-17FQ96PD4

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated1010
Phase 18611
Phase 2161240
Phase 3251960
Phase 45221
All trials55

Who has held its approvals

CompanyRoleYears
UCBApplicant and Lead sponsor of trials2012 to now