Drug

Risankizumab

As of the edition of 20 October 2026, Risankizumab is an antibody: marketed, first approved in 2019 (JP); acts on IL23A; US protection ends in 2031.

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

The drug

Status
Marketed; latest approval 2021
Kind
Antibody
Brand name
Skyrizi
First approved
26 March 2019 (JP)
Approvals on record
25 in 5 regions
Holder of the most recent approval
AbbVie; 2 holders in all
Registered trials
83, 2 stopped early
Disease areas
Skin and connective tissue; Digestive system; Bones, joints and muscles; Immune system; Lungs and airways; Infections

US protection

US protection ends in 2031.

US protection ends in 2031, 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

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

See the exact date and the 2 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 Risankizumab.

Target

GeneProteinUniProt
IL23AInterleukin-23 subunit alphaQ9NPF7

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated6041
Phase 1191711
Phase 2191360
Phase 33120110
Phase 48610
All trials83

Who has held its approvals

CompanyRoleYears
AbbVieOriginator, Later holder and Lead sponsor of trials2017 to now