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. 2014 Feb 15;8:67–81. doi: 10.2147/BTT.S41477

Table 2.

Characteristics, route of administration, dosage, and potential side effects for selected biologic agents

Generic names Trade names Specific target Route Dosage Potential side effects
TNF inhibitors
Infliximab Remicade TNF-α IV 3–5 mg/kg loading at weeks 0, 2, and 6, then maintenance 3–10 mg/kg every 4–8 weeks; maximal dose 20 mg/kg in children aSusceptibility to infections, including: reactivation of tuberculosis, histoplasmosis, hepatitis B, and fungal infection; hypersensitivity reactions; demyelinating disease; lupus-like syndrome; malignancy; thromboembolic events; congestive heart failure
Adalimumab Humira TNF-α SQ 40 mg every 1–2 weeks (if bodyweight <30 kg; 20 mg every 2 weeks); loading doses of 80–160 mg are recommended for CD and PsO
Etanercept Enbrel TNF-α,-β SQ Adults 50 mg weekly (may be given 50 mg twice weekly for first 3 months for PsO); children 0.8 mg/kg/week (max 50 mg/week)
Golimumab Simponi TNF-α SQ 50 mg SQ monthly; except for UC 200 mg at week 0, 100 mg at week 2, then 100 mg every 4 weeks
Certolizumab Cimzia TNF-α SQ 400 mg SQ at weeks 0, 2, and 4, then 200 mg every 2 weeks or 400 mg every 4 weeks
Lymphocyte inhibitors
Daclizumab Zenapax T-cells (IL-2Rα) IV, SQ 1–2 mg/kg every 2 or 4 weeks Hypersensitivity reactions, headache, and gastrointestinal disturbance
Rituximab Rituxan B-cells (CD20) IV 500 or 1,000 mg at week 0 and 2; may repeat at 6–12 months thereafter (different regimen for hematologic malignancies) Susceptibility to infections, infusion reactions, gastrointestinal disturbance, cardiovascular events, muscle spasm, and headache
Abatacept Orencia T-cells (CTLA-4) IV, SQ Adult RA 500–1,000 mg IV loading, then 125 mg SQ weekly; JIA 10 mg/kg, max 1,000 mg IV at weeks 0, 2, and 4, then every 4 weeks Susceptibility to infections, allergic reactions, headache, nausea, and malignancy
Basiliximab Simulect T-cells (IL-2Rα; CD25) IV 40 mg IV at weeks 0, 2, 4, 8, and 12 Gastrointestinal disturbance, headache, susceptibility to infections, and hypersensitivity reactions
Specific receptor antagonists
Anakinra Kineret IL-1 receptor SQ 100 mg SQ daily; children, starting 1–2 mg/kg to max 8 mg/kg daily (dose adjustment for renal insufficiency) Injection-site reaction, infections, headache, gastrointestinal disturbance, and fever
Canakinumab Ilaris IL-1β IV, SQ Systemic JIA: 4 mg/kg (max 300 mg) SQ every 4 weeks; CAPS, 2–3 mg/kg SQ every 8 weeks (see text) Susceptibility to infections, headache, nausea, and abdominal pain
Gevokizumab (XOMA 052) IL-1β IV, SQ In experiment Susceptibility to infections and hypersensitivity reactions
Tocilizumab Actemra IL-6 receptor IV Initial 4 mg/kg IV every 4 weeks, then increase to 8–12 mg/kg every 2–4 weeks Serious infections, hypersensitivity reactions, and gastrointestinal perforation
Alemtuzumab Campath CD52 IV 30 mg IV, 3 days per week for 12 weeks Cytopenias, infusion reactions, infections, gastrointestinal disturbance, and insomnia
Efalizumab Raptiva CD11a SQ 0.7 mg/kg first dose, then 1 mg/kg weekly (max 200 mg/dose) Infections, progressive multifocal leukoencephalopathy, malignancy, arthritis, and thrombocytopenia
Interferons
Interferon α-2a Roferon-A Nonspecific SQ 3–6 million units SQ daily, tapering over 6 months Injection-site reactions, flu-like symptoms, and bone marrow suppression

Notes:

a

Listed side effects apply to all TNF inhibitors shown in this table. Copyright 2012. Adapted with permission from Retina Today. Pasadhika S, Suhler EB, Cunningham ET. Biologic therapy for posterior uveitis and panuveitis. Retina Today. 2012:74–79.49

Abbreviations: CAPS, cryopyrin-associated periodic syndromes; CD, Crohn’s disease; IL, interleukin; IV, intravenously; JIA, juvenile idiopathic arthritis; PsO, plaque psoriasis; RA, rheumatoid arthritis; SQ, subcutaneously; TNF, tumor necrosis factor; UC, ulcerative colitis.