Table 1.
Drug | Anakinra | Canakinumab | Rilonacept |
---|---|---|---|
Mechanism | Recombinant human protein inhibiting IL-1α and IL-1β | Monoclonal IgG antibody inhibiting IL-1β | Dimeric fusion protein inhibiting IL-1α and IL-1β |
Administration | Subcutaneous, intravenous | Subcutaneous | Subcutaneous |
Dosing |
No loading dose 2 mg/kg (up to 100 mg) daily |
No loading dose 4 mg/kg or 150 mg (single dose) every 4–8 weeks |
Loading 320 mg (4.4 mg/kg up to 320 mg in 12–17 year olds) Maintenance 160 mg weekly (2.2 mg/kg up to 160 mg in 12–17 year olds) |
Dose adjustment |
Renal: creatinine clearance < 30 mL/min consider alternate day dosing Hepatic: none necessary |
Renal: none necessary Hepatic: none necessary |
Renal: none necessary Hepatic: none necessary |
Half-life | 4–6 h | 26 days | 7 days |
Adverse events | Injection site reactions, infections, hepatitis | Injection site reactions, infections, neutropenia | Injection site reactions, infections, dyslipidemia, neutropenia |
Monitoring | C-reactive protein, complete blood count, infection, baseline tuberculosis, and hepatitis screening | C-reactive protein, complete blood count, infection, baseline tuberculosis screening | C-reactive protein, complete blood count, lipid profile, infection |