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Adalimumab: Difference between revisions

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== References ==
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[[Category:TNF inhibitors]]
[[Category:Biologics]]
[[Category:DMARDs]]
[[Category:Immunosuppressants]]
[[Category:Monoclonal antibodies]]

Latest revision as of 10:43, 23 May 2026

Adalimumab
Humira; biosimilars Amjevita, Cyltezo, Hadlima, Hulio, Hyrimoz, Idacio, Yusimry, Abrilada

Experience

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Problems

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Titration strategies

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Effects

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Summary
Common uses
Rheumatoid arthritis0, Psoriatic arthritis0, Ankylosing spondylitis0, Crohn's disease0, Ulcerative colitis0, Moderate-to-severe plaque psoriasis0, Hidradenitis suppurativa0, Non-infectious uveitis0, Juvenile idiopathic arthritis0
Pharmacy
Starting dose
40 mg SC every other week (most adult indications); IBD induction 160 mg week 0, 80 mg week 2, then 40 mg every other week
Preparations
40 mg/0.4 mL or 40 mg/0.8 mL prefilled syringe and autoinjector pen; 10, 20, 80 mg pediatric/induction strengths
US FDA Max
40 mg every week (selected indications); otherwise 40 mg every other week
Pharmacology
Routes
Subcutaneous
Onset
Symptomatic effect within weeks; full response by 12-24 weeks
Duration
2 weeks per dose
Half-life
~14 days[1]
Bioavailability
~64% from SC depot[1]
Pregnancy
Generally continued through pregnancy when needed for disease control; placental transfer is minimal in the first trimester but increases in third trimester, so dose timing around delivery and considerations for live-vaccine schedule in the infant are standard.[citation needed]
Legal status
Rx-only in US. Carries Boxed Warnings for serious infections (TB reactivation, invasive fungal, opportunistic bacterial/viral) and malignancy (lymphoma, including rare hepatosplenic T-cell lymphoma in young patients with IBD on combination immunosuppression)[1]
Purported mechanism
Adalimumab is a fully human recombinant IgG1 monoclonal antibody that binds tumor necrosis factor α (TNF-α), neutralizing its interaction with TNF receptors 1 and 2 and lysing TNF-α-expressing cells via Fc-mediated complement and ADCC; the net effect is broad suppression of TNF-driven inflammatory signaling in immune-mediated diseases.0 Pre-treatment screening for latent TB (PPD or IGRA) and chronic hepatitis B is standard. Anti-drug antibody formation is a recognized cause of secondary loss of response[1].

References

  1. 1.0 1.1 1.2 1.3 FDA Prescribing Information, Humira (adalimumab), AbbVie, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/125057s415lbl.pdf