Monograph
L04AC08 - Canakinumab |
Propably not porphyrinogenic |
PNP |
Important Information
Patients on immunosuppressive therapy have an increased risk of infections. Since infections have a potential to trigger acute porphyric attacks vigilance is motivated regarding signs or symptoms of infection and/or possible symptoms of a porphyric attack.
Side effects
Infections are common in patients using immunosuppressants and since infections might trigger an acute porphyric attack, vigilance regarding signs and symptoms of an infection and/ or a porphyric attack is recommended. A common adverse reaction of canakinumab that can be confused with symptoms of an acute porphyric attack is abdominal pain.
Rationale
Antibody preparation with no CYP metabolism. Based on the pharmacokinetics, canakinumab is not expected to have any porphyrinogenic effects.
Chemical description
Canakinumab is a fully human monoclonal antibody against interleukin 1-beta produced in murine cells by recombinant DNA technology
Therapeutic characteristics
Canakinumab is used in the treatment of Cryopyrin-Associated Periodic Syndromes (CAPS). It is administered as a subcutaneous injection.
Metabolism and pharmacokinetics
The metabolism of canakinumab is expected to be similar as for endogenous antibodies, which are metabolised to peptides and amino acids in various body tissues and in plasma by circulating phagocytic cells or by their target antigen-containing cells.
Immunosuppressive treatment can reverse the down regulation of the expression of CYP enzymes (CYP 3A4, 1A2, 2C9 or 2C19) caused by inflammatory cytokines. This effect is not suspected to be porphyrinogenic as the CYP enzyme activity is not induced above a normal level.
References
# | Citation details | PMID |
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* | Scientific articles | |
1. | Keizer, R.J., Huitema, A.D.R., Clinical Pharmacokinetics of Therapeutic Monoclonal Antibodies.
Clin Pharmacokinet. 2010 Aug 1;49(8):493-507 |
20608753 |
* | Drug reference publications | |
2. | Sweetman SC, editor. Martindale: The complete drug reference. Canakinumab. Pharmaceutical Press 2009.
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* | Summary of Product Characteristics | |
3. | Norwegian medicines agency. Summary of Product Characteristics (SPC). Ilaris.
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4. | The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Ilaris.
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Netherlands
Ilaris · Ilaris 150 mg poeder voor oplossing voor injectie · Ilaris 150 mg/ml, oplossing voor injectieBelgium
Ilaris · Ilaris 150 mg sol. inj. (pdr.) s.c. flac. · Ilaris 150 mg/ml sol. inj. s.c. flac.United Kingdom
Ilaris · Ilaris 150mg powder for solution for injection vials · Ilaris 150mg/1ml solution for injection vialsDenmark
IlarisNorway
IlarisPoland
IlarisLuxembourg
IlarisIceland
IlarisFinland
IlarisLatvia
IlarisSerbia
Ilaris · Ilaris®
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