Canakinumab

Anti-IL-1beta monoclonal antibody

Response rate
~67%
Onset
Days to weeks
Route
SC 150-300 mg every 4 weeks
Line
2nd
IgM effect
Rapid ferritin reduction

Evidence summary

Long-acting anti-IL-1beta monoclonal antibody. The CONSIDER phase II RCT showed 67% response (vs 41% placebo). Received EMA conditional marketing authorization for Still's disease (including AOSD) in 2020. FDA approved canakinumab for sJIA in 2013 but has not granted a separate AOSD indication. Advantage over anakinra is less frequent dosing (monthly vs daily). Effective for both systemic and articular manifestations.

Molecular targets (1)

MoleculeRoleExpressionEvidence
IL-1βCentral pro-inflammatory cytokine driving systemic inflammationElevatedestablished

Sources (2)

DetailsKedor C et al. (2020) Canakinumab for treatment of adult-onset Still's disease to achieve reduction of arthritic manifestation (CONSIDER): phase II, randomised, double-blind, placebo-controlled trial · Ann Rheum DisPubMed
DetailsTomaras S et al. (2021) Adult-onset Still's disease: clinical aspects and therapeutic approach · J Clin MedPubMed