Wednesday, July 8, 2026

Drug profile · INN

adalimumab

adalimumab (ABRILADA) is a tnf-alpha inhibitor. Associated with Pfizer Australia Pty Ltd. Current US regulatory status: approved.

FDA: approved EMA: approved TGA: approved PMDA: approved NMPA: clinical trials Antineoplastic and immunomodulating agents (L04) L04AB04
US status approved
Patents linked 20
Pipeline programs 57
News articles 4
Drug details — adalimumab

Quick answer

adalimumab (ABRILADA) is a tnf-alpha inhibitor. Associated with Pfizer Australia Pty Ltd. Current US regulatory status: approved.

Key facts

INN adalimumab
Brand ABRILADA
Mechanism TNF-alpha inhibitor
Target Tumor necrosis factor
Therapeutic class Antineoplastic and immunomodulating agents (L04)
Formulation VIAL
ATC code L04AB04

Mechanism of action

TNF-alpha inhibitor

Primary target: Tumor necrosis factor

Approval history

Authority Status Date
FDA approved
EMA approved
TGA approved
PMDA approved
NMPA clinical trials

Recent coverage

Pipeline programs

  1. 20210184 Phase 3 · Amgen · Chronic Weight Management
  2. 20220196 Phase 3 · Amgen · Atherosclerotic cardiovascular disease (ASCVD) and obesity o
  3. 20230225 Phase 3 · Amgen · "Moderate to severe obstructive sleep apnea (OSA) in adults
  4. 207503 Phase 3 · GSK Glaxo Smith · Multiple Myeloma
  5. AMG 133, Placebo for Maridebart Cafraglutide Phase 3 · Amgen · Chronic Weight Management
  6. AMG 479 Phase 3 · Takeda · Adenocarcinoma of the Pancreas
  7. AMG 706 Phase 3 · Takeda · Non-Small Cell Lung Cancer
  8. Adalimumab Phase 3 · AbbVie · Juvenile Psoriatic Arthritis

Related & competitor drugs

  1. abiraterone acetate Antineoplastic and immunomodulating agents (L02)
  2. adalimumab-aqvh TNF-alpha inhibitor
  3. anagrelide Antineoplastic and immunomodulating agents (L01)
  4. apremilast Antineoplastic and immunomodulating agents (L04)
  5. arsenic trioxide Antineoplastic and immunomodulating agents (L01)
  6. axitinib Antineoplastic and immunomodulating agents (L01)
  1. WO 2026112486

    MÉTHODES DE TRAITEMENT DE L'OBÉSITÉ ET DES AFFECTIONS LIÉES À L'OBÉSITÉ

    Expires Wed May 23 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  2. WO 2026102199

    THÉRAPIE COMBINÉE D'UN INHIBITEUR DE PRMT5 ET DU DARAXONRASIB POUR UTILISATION DANS LE TRAITEMENT DU CANCER MTAP-NUL

    Expires Thu May 10 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  3. WO 2026072909

    PROTÉINES DE LIAISON À FLT1 ET MÉTHODES D'UTILISATION

    Expires Wed Mar 28 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  4. WO 2026055477

    COMPOSÉS MACROCYCLIQUES CONSTITUANT DES MODULATEURS DE KRAS ET LEURS UTILISATIONS

    Expires Wed Mar 07 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  5. WO 2026039538

    MÉTHODES DE TRAITEMENT DE TUMEURS PANCRÉATIQUES EXPRIMANT CERTAINS BIOMARQUEURS

    Expires Wed Feb 14 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  6. WO 2026039321

    MÉTHODES DE TRAITEMENT DU CANCER DE LA PROSTATE

    Expires Wed Feb 14 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  7. WO 2026020076

    MÉTHODE DE TRAITEMENT DU PRURIGO NODULAIRE

    Expires Wed Jan 17 2046 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  8. WO 2026006803

    COMPOSÉS À NOYAU À 5 CHAÎNONS UTILISÉS EN TANT QUE MODULATEURS DE L'HÉLICASE D'ADN RECQ DU SYNDROME DE WERNER ET LEURS UTILISATIONS

    Expires Thu Dec 28 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  9. WO 2026006805

    COMPOSÉS À NOYAU À 6 CHAÎNONS UTILISÉS COMME MODULATEURS DE L'HÉLICASE À ADN RECQ DU SYNDROME DE WERNER ET LEURS UTILISATIONS

    Expires Thu Dec 28 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  10. WO 2026006398

    RÉDUCTASES D'IMINE MODIFIÉES ET LEURS PROCÉDÉS D'UTILISATION

    Expires Thu Dec 28 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  11. WO 2025265110

    COMPOSITIONS PHARMACEUTIQUES ORALES RENFERMANT UN COMPOSÉ DE NAPHTYRIDINE

    Expires Thu Dec 21 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  12. WO 2025259749

    FRAGMENTS VARIABLES À CHAÎNE UNIQUE STABLES

    Expires Wed Dec 13 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  13. WO 2025259515

    POLYTHÉRAPIE

    Expires Wed Dec 13 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  14. WO 2025260042

    CONSTRUCTIONS D'ARNI ET PROCÉDÉS D'INHIBITION DE L'EXPRESSION DE CNR1

    Expires Wed Dec 13 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  15. WO 2025250569

    TRAITEMENTS DU CANCER UTILISANT DES INHIBITEURS DE PRMT5 MTA-COOPÉRATIFS ET DES INHIBITEURS DE MAT2A

    Expires Wed Nov 29 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  16. WO 2025230878

    COMPOSÉS MACROCYCLIQUES UTILISÉS EN TANT QUE MODULATEURS DE KRAS ET LEURS UTILISATIONS

    Expires Wed Nov 01 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  17. WO 2025230862

    COMPOSÉS AMINÉS MACROCYCLIQUES UTILISÉS EN TANT QUE MODULATEURS DE KRAS ET LEURS UTILISATIONS

    Expires Wed Nov 01 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  18. WO 2025230860

    FORMES SOLIDES DE COMPOSÉS MACROCYCLIQUES ET LEURS UTILISATIONS

    Expires Wed Nov 01 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  19. WO 2025230528

    MÉTHODES DE TRAITEMENT DE LA SCLÉROSE LATÉRALE AMYOTROPHIQUE

    Expires Wed Nov 01 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  20. US 2025333381

    SOLID STATE FORMS

    Expires Wed Oct 25 2045 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is adalimumab?

adalimumab (ABRILADA) is a tnf-alpha inhibitor. Associated with Pfizer Australia Pty Ltd. Current US regulatory status: approved.

What is the brand name for adalimumab?

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

What is the US approval status of adalimumab?

adalimumab 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.