Friday, July 10, 2026

Drug profile · INN

tildrakizumab-asmn

tildrakizumab-asmn (ILUMYA) is a interleukin-23 inhibitor. Route of administration: injection. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — tildrakizumab-asmn
US status
approved
Class
Route
INJECTION
Patents
0
Programs
0
Data quality
0.84

Quick answer

tildrakizumab-asmn (ILUMYA) is a interleukin-23 inhibitor. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN tildrakizumab-asmn
Brand ILUMYA
Mechanism Interleukin-23 inhibitor
Target Interleukin-23
Route INJECTION
Formulation INJECTABLE

Mechanism of action

Interleukin-23 inhibitor

Primary target: Interleukin-23

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. tildrakizumab Antineoplastic and immunomodulating agents (L04)
  2. guselkumab Antineoplastic and immunomodulating agents (L04)
  3. mirikizumab-mrkz Interleukin-23 inhibitor
  4. risankizumab-rzaa Interleukin-23 inhibitor
  5. mirikizumab Antineoplastic and immunomodulating agents (L04)
  6. risankizumab Antineoplastic and immunomodulating agents (L04)

Frequently asked questions

What is tildrakizumab-asmn?

tildrakizumab-asmn (ILUMYA) is a interleukin-23 inhibitor. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for tildrakizumab-asmn?

ILUMYA is a marketed brand name for tildrakizumab-asmn. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of tildrakizumab-asmn?

tildrakizumab-asmn has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.