Friday, July 10, 2026

Drug profile · INN

tralokinumab

tralokinumab (ADTRALZA) is a interleukin-13 inhibitor. Route of administration: injection. Current US regulatory status: approved.

FDA: approved EMA: approved Dermatologicals (D11) D11
US status approved
Patents linked 0
Pipeline programs 4
News articles 0
Drug details — tralokinumab
US status
approved
Class
Dermatologicals (D11)
Route
INJECTION
Patents
0
Programs
4
Data quality
0.84

Quick answer

tralokinumab (ADTRALZA) is a interleukin-13 inhibitor. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN tralokinumab
Brand ADTRALZA
Mechanism Interleukin-13 inhibitor
Target Interleukin-13
Therapeutic class Dermatologicals (D11)
Route INJECTION
Formulation INJECTABLE
ATC code D11

Mechanism of action

Interleukin-13 inhibitor

Primary target: Interleukin-13

Approval history

Authority Status Date
FDA approved
EMA approved

Pipeline programs

  1. LP0162-1336 Phase 3 · LEO Pharma US · Treatment of moderate-to-severe Atopic dermatitis
  2. Adtralza 150 mg solution for injection in pre-filled syringe Phase 2 · LEO Pharma US · Treatment of moderate-to-severe Atopic dermatitis
  3. Tralokinumab 300 mg, Q2W Phase 2 · MedImmune · Asthma
  4. LP0162-2328 Approved · LEO Pharma US · Atopic dermatitis and moderate-to severe atopic hand eczema

Related & competitor drugs

  1. beremagene geperpavec Dermatologicals (D03)
  2. dupilumab Dermatologicals (D11)
  3. imiquimod Dermatologicals (D06)
  4. lebrikizumab Dermatologicals (D11)
  5. retapamulin Dermatologicals (D06)
  6. tacrolimus Dermatologicals (D11)

Frequently asked questions

What is tralokinumab?

tralokinumab (ADTRALZA) is a interleukin-13 inhibitor. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for tralokinumab?

ADTRALZA is a marketed brand name for tralokinumab. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of tralokinumab?

tralokinumab 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.