Acute Porphyria Drug Database

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
*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.
*Summary of Product Characteristics
3. Norwegian medicines agency. Summary of Product Characteristics (SPC). Ilaris.
4. The electronic Medicines Compendium (emc). Summary of Product Characteristics (SPC). Ilaris.

Similar drugs
Explore alternative drugs in similar therapeutic classes L04A / L04AC or go back.

Tradenames and packages
From some sources, we get a list of packages (United Kingdom, Ireland, Estonia). Other sources contain more or less "clean" versions of the trade name (Denmark, Finland, Iceland, Lithuania, Norway). What you see here is the raw data we get from each country, so there will appear to be duplicates. The bold names are the searchable terms. The gray names that follow are all mapped to the bolded term.
Note: The cleaning is done automatically by a proprietary algorithm, and it may produce errors. We strive to improve it continuously.
Netherlands
Ilaris · Ilaris 150 mg poeder voor oplossing voor injectie · Ilaris 150 mg/ml, oplossing voor injectie
Belgium
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 vials
Denmark
Ilaris
Norway
Ilaris
Poland
Ilaris
Luxembourg
Ilaris
Iceland
Ilaris
Finland
Ilaris
Latvia
Ilaris
Serbia
Ilaris · Ilaris®
 
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