Drug intelligence / Profile preview

adalimumab-afzb

Development stage
Approved
Lead developer
Pfizer
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Subcutaneous
01

Overview

Adalimumab-afzb (PF-06410293) is a recombinant human IgG1 monoclonal antibody developed by Pfizer as a biosimilar to Humira. It functions as a tumor necrosis factor (TNF) blocker by binding specifically to TNF-alpha and neutralizing its biological activity. By blocking the interaction of TNF-alpha with the p55 and p75 cell surface TNF receptors, adalimumab-afzb inhibits the pro-inflammatory signaling cascades that drive various autoimmune and inflammatory conditions. It is administered via subcutaneous injection and is approved for the treatment of multiple indications, including rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, ulcerative colitis, plaque psoriasis, hidradenitis suppurativa, and non-infectious uveitis. In 2023, it received FDA designation as an interchangeable biosimilar.

Brand names
Abrilada
Other names
adalimumab-afzb
02

Targets

TNFA (Tumor necrosis factor alpha (soluble))

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