Canakinumab Dosage
Medically reviewed by Drugs.com. Last updated on Aug 16, 2023.
Applies to the following strengths: 150 mg; 150 mg/mL
Usual Adult Dose for:
- Familial Cold Autoinflammatory Syndrome
- Muckle Wells Syndrome
- Cryopyrin-Associated Periodic Syndrome
- Familial Mediterranean Fever
- Hyperimmunoglobulin D Periodic Fever Syndrome
- Tumor Necrosis Factor Receptor Associated Periodic Fever Syndrome
- Still's Disease
Usual Pediatric Dose for:
- Familial Cold Autoinflammatory Syndrome
- Muckle Wells Syndrome
- Cryopyrin-Associated Periodic Syndrome
- Familial Mediterranean Fever
- Hyperimmunoglobulin D Periodic Fever Syndrome
- Tumor Necrosis Factor Receptor Associated Periodic Fever Syndrome
- Juvenile Idiopathic Arthritis
Additional dosage information:
Usual Adult Dose for Familial Cold Autoinflammatory Syndrome
15 kg less than or equal to 40 kg: 2 mg/kg subcutaneously every 8 weeks
Greater than 40 kg: 150 mg subcutaneously every 8 weeks
Use: Cryopyrin-associated periodic syndromes (CAPS) including familial cold autoinflammatory syndrome (FCAS) and muckle-wells syndrome (MWS)
Usual Adult Dose for Muckle Wells Syndrome
15 kg less than or equal to 40 kg: 2 mg/kg subcutaneously every 8 weeks
Greater than 40 kg: 150 mg subcutaneously every 8 weeks
Use: Cryopyrin-associated periodic syndromes (CAPS) including familial cold autoinflammatory syndrome (FCAS) and muckle-wells syndrome (MWS)
Usual Adult Dose for Cryopyrin-Associated Periodic Syndrome
15 kg less than or equal to 40 kg: 2 mg/kg subcutaneously every 8 weeks
Greater than 40 kg: 150 mg subcutaneously every 8 weeks
Use: Cryopyrin-associated periodic syndromes (CAPS) including familial cold autoinflammatory syndrome (FCAS) and muckle-wells syndrome (MWS)
Usual Adult Dose for Familial Mediterranean Fever
Up to 40 kg: 2 mg/kg subcutaneously every 4 weeks; dose can be increased to 4 mg/kg subcutaneously every 4 weeks if response is not adequate
Greater than 40 kg: 150 mg subcutaneously every 4 weeks; dose can be increased to 300 mg subcutaneously every 4 weeks if response is not adequate
Uses: For autoinflammatory periodic fever syndromes including periodic tumor necrosis factor receptor associated periodic syndrome (TRAPS), hyperimmunoglobulin D syndrome/mevalonate kinase deficiency (MKD), and familial Mediterranean fever (FMF)
Usual Adult Dose for Hyperimmunoglobulin D Periodic Fever Syndrome
Up to 40 kg: 2 mg/kg subcutaneously every 4 weeks; dose can be increased to 4 mg/kg subcutaneously every 4 weeks if response is not adequate
Greater than 40 kg: 150 mg subcutaneously every 4 weeks; dose can be increased to 300 mg subcutaneously every 4 weeks if response is not adequate
Uses: For autoinflammatory periodic fever syndromes including periodic tumor necrosis factor receptor associated periodic syndrome (TRAPS), hyperimmunoglobulin D syndrome/mevalonate kinase deficiency (MKD), and familial Mediterranean fever (FMF)
Usual Adult Dose for Tumor Necrosis Factor Receptor Associated Periodic Fever Syndrome
Up to 40 kg: 2 mg/kg subcutaneously every 4 weeks; dose can be increased to 4 mg/kg subcutaneously every 4 weeks if response is not adequate
Greater than 40 kg: 150 mg subcutaneously every 4 weeks; dose can be increased to 300 mg subcutaneously every 4 weeks if response is not adequate
Uses: For autoinflammatory periodic fever syndromes including periodic tumor necrosis factor receptor associated periodic syndrome (TRAPS), hyperimmunoglobulin D syndrome/mevalonate kinase deficiency (MKD), and familial Mediterranean fever (FMF)
Usual Adult Dose for Still's Disease
7.5 kg or greater: 4 mg/kg (maximum 300 mg) subcutaneously every 4 weeks
Use: Still's Disease, including Adult-Onset Still's Disease (AOSD)
Usual Pediatric Dose for Familial Cold Autoinflammatory Syndrome
4 years and older:
- Weight 15 kg to less than or equal to 40 kg: 2 mg/kg subcutaneously every 8 weeks; for children 15 to 40 kg with an inadequate response, the dose can be increased to 3 mg/kg subcutaneously every 8 weeks
- Weight greater than 40 kg: 150 mg subcutaneously every 8 weeks
Use: Cryopyrin-associated periodic syndromes (CAPS) including familial cold autoinflammatory syndrome (FCAS) and muckle-wells syndrome (MWS) in children 4 years and older
Usual Pediatric Dose for Muckle Wells Syndrome
4 years and older:
- Weight 15 kg to less than or equal to 40 kg: 2 mg/kg subcutaneously every 8 weeks; for children 15 to 40 kg with an inadequate response, the dose can be increased to 3 mg/kg subcutaneously every 8 weeks
- Weight greater than 40 kg: 150 mg subcutaneously every 8 weeks
Use: Cryopyrin-associated periodic syndromes (CAPS) including familial cold autoinflammatory syndrome (FCAS) and muckle-wells syndrome (MWS) in children 4 years and older
Usual Pediatric Dose for Cryopyrin-Associated Periodic Syndrome
4 years and older:
- Weight 15 kg to less than or equal to 40 kg: 2 mg/kg subcutaneously every 8 weeks; for children 15 to 40 kg with an inadequate response, the dose can be increased to 3 mg/kg subcutaneously every 8 weeks
- Weight greater than 40 kg: 150 mg subcutaneously every 8 weeks
Use: Cryopyrin-associated periodic syndromes (CAPS) including familial cold autoinflammatory syndrome (FCAS) and muckle-wells syndrome (MWS) in children 4 years and older
Usual Pediatric Dose for Familial Mediterranean Fever
2 years and older:
- Weight 40 kg or less: 2 mg/kg subcutaneously every 4 weeks; can increase to 4 mg/kg subcutaneously every 4 weeks if response is inadequate
- Weight greater than 40 kg: 150 mg subcutaneously every 4 weeks; can increase to 300 mg subcutaneously every 4 weeks if response is inadequate
Use: For the treatment of autoinflammatory periodic fever syndromes including TRAPS, HIDS/MKD, and FMF in pediatric patients 2 years and older
Usual Pediatric Dose for Hyperimmunoglobulin D Periodic Fever Syndrome
2 years and older:
- Weight 40 kg or less: 2 mg/kg subcutaneously every 4 weeks; can increase to 4 mg/kg subcutaneously every 4 weeks if response is inadequate
- Weight greater than 40 kg: 150 mg subcutaneously every 4 weeks; can increase to 300 mg subcutaneously every 4 weeks if response is inadequate
Use: For the treatment of autoinflammatory periodic fever syndromes including TRAPS, HIDS/MKD, and FMF in pediatric patients 2 years and older
Usual Pediatric Dose for Tumor Necrosis Factor Receptor Associated Periodic Fever Syndrome
2 years and older:
- Weight 40 kg or less: 2 mg/kg subcutaneously every 4 weeks; can increase to 4 mg/kg subcutaneously every 4 weeks if response is inadequate
- Weight greater than 40 kg: 150 mg subcutaneously every 4 weeks; can increase to 300 mg subcutaneously every 4 weeks if response is inadequate
Use: For the treatment of autoinflammatory periodic fever syndromes including TRAPS, HIDS/MKD, and FMF in pediatric patients 2 years and older
Usual Pediatric Dose for Juvenile Idiopathic Arthritis
2 years and older:
7.5 kg or greater: 4 mg/kg (maximum 300 mg) subcutaneously every 4 weeks
Use: For the treatment of active systemic juvenile idiopathic arthritis (SJIA) in patients 2 years and older and 7.5 kg or more
Renal Dose Adjustments
Data not available
Liver Dose Adjustments
Data not available
Precautions
CONTRAINDICATIONS:
- Hypersensitivity to the active component or any of the ingredients
Safety and efficacy have not been established in patients younger than 4 years with CAPS.
Safety and efficacy have not been established in patients younger than 2 years with TRAPS, HIDS/MKD, FMF.
Safety and efficacy have not been established in patients younger than 2 years or weighing less than 7.5 kg with SJIA.
Consult WARNINGS section for additional precautions.
Dialysis
Data not available
Other Comments
Administration advice:
- Avoid injection into scar tissue.
- Vials are intended for single use in 1 patient; discard any unused portion.
Storage requirements:
- The unopened vial should be refrigerated 2C to 8C (36F to 46 F). Do not freeze.
- Store in the original carton to protect from light.
- Do not use beyond the date stamped on the label.
- This drug does not contain preservatives.
General:
- Do not use beyond the date stamped on the label.
- This drug does not contain preservatives.
- Discard any unused portion or waste material in accordance with local requirements.
More about canakinumab
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- Drug class: interleukin inhibitors
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