Abstract

Results At baseline, 7 patients were treated with the initial dosage of 2 mg/kg (or 150 mg, if > 40 Kg) every 8 weeks. In 5 patients (2 MWS/CINCA overlap, 5 CINCA) the dosage was 4 mg/kg (or 300 mg) every 8 weeks. During the following 12 months modification of dosage of frequency was performed in 7/12 patients. The 5 patients at higher dosage during the CACZ885D2306 study needed to increase the frequency of administration with a mean frequency of 6 weeks (range 4-8). The mean reason was the presence of mild clinical manifestation and/or persistent elevation of acute phase reactants. In one of these patients the therapy was subsequently discontinued due to persistent disease activity. An increased frequency (6 and 7 weeks) was also performed in 1 MWS and 1 CINCA patient, respectively. In 5 patients the treatment was not modified being effective in the control of the disease.

Highlights

  • No clear information on the optimal dosage of Canakinumab in cryopyrin-associated periodic syndromes (CAPS) is available

  • Aim To analyse the modification of dosage schedule of Canakinumab in CAPS in 12 months of routinely clinical practice

  • Patients were previously enrolled in the CACZ885D2306 trial and studied for the following 12 months

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Summary

Introduction

No clear information on the optimal dosage of Canakinumab in CAPS is available. Canakinumab in the routinary clinical practice in cryopyrin-associated periodic syndromes (CAPS): one year of follow-up R Caorsi1*, L Lepore2, F Zulian3, M Alessio4, A Stabile5, M Finetti1, A Martini1, M Gattorno1 From 18th Pediatric Rheumatology European Society (PReS) Congress Bruges, Belgium.

Results
Conclusion

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