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Adalimumab biosimilar - Pfizer

Drug Profile

Adalimumab biosimilar - Pfizer

Alternative Names: ABRILADA; Adalimumab-afzb; Amsparity; PF-06410293

Latest Information Update: 05 Nov 2023

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At a glance

  • Originator Pfizer
  • Class Anti-inflammatories; Anti-TNF monoclonal antibodies; Antineoplastics; Antipsoriatics; Antirheumatics; Eye disorder therapies; Hepatoprotectants; Immunotherapies; Nootropics; Skin disorder therapies
  • Mechanism of Action Antibody-dependent cell cytotoxicity; Immunosuppressants; Tumour necrosis factor alpha inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity No

Highest Development Phases

  • Registered Ankylosing spondylitis; Axial spondyloarthritis; Crohn's disease; Hidradenitis suppurativa; Juvenile rheumatoid arthritis; Plaque psoriasis; Psoriatic arthritis; Rheumatoid arthritis; Ulcerative colitis; Uveitis

Most Recent Events

  • 10 Nov 2022 Efficacy and adverse events data from a phase III trial in Rheumatoid arthritis presented at the ACR Convergence 2022
  • 25 Feb 2022 FDA assigns the Biosimilar User Fee Act (BsUFA) goal date of Q4 2022 for Adalimumab biosimilar for Rheumatoid arthritis
  • 25 Feb 2022 The US FDA accepts for review the Prior Approval Supplement (PAS) to the Biologics License Application (BLA) for ABRILADA™ (adalimumab-afzb) as an interchangeable biosimilar to Humira® (adalimumab)
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