Volume 11 Supplement 1

7th Congress of International Society of Systemic Auto-Inflammatory Diseases (ISSAID)

Open Access

OR10-006 - Canakinumab in patients with TRAPS

  • HJ Lachmann1,
  • L Obici2,
  • A Meini3,
  • V Tormey4,
  • K Abrams5,
  • N Davis5,
  • C Andrews6,
  • SG Bhansali5 and
  • M Gattorno7
Pediatric Rheumatology201311(Suppl 1):A189

https://doi.org/10.1186/1546-0096-11-S1-A189

Published: 8 November 2013

Introduction

TNF-receptor associated periodic syndrome (TRAPS) is a rare, dominantly inherited periodic fever syndrome due to mutations of the TNFRSF1A gene. The IL-1 receptor antagonist anakinra has been reported to be an efficacious daily treatment. Canakinumab (CAN) is a fully human monoclonal selective anti-IL-1β antibody with a T1/2 of ~4 wks. Interim clinical and PK data of CAN treatment in patients with active TRAPS are presented.

Objectives

To assess the efficacy, PK, and safety of canakinumab in patients with active TRAPS.

Methods

14 adults and 6 children (7-78 yrs) with active TRAPS entered a 3-part trial: 4 months open-label 150 mg (or 300 mg) CAN every 4 wks followed by up to 5 months treatment withdrawal, then 24 months open-label CAN. Primary endpoint was complete or almost complete response at Day 15 based on physician assessed absent or minimal TRAPS signs/symptoms and normal or ≥70% reduced CRP and/or SAA. Those without response by Day 8 were eligible for another 150 mg dose and then 300 mg thereafter. Patients were observed after last dose until relapse (5 month max) before restarting CAN. Population PK analysis was performed using NONMEM based on CAN concentrations determined by ELISA from blood samples collected at pre-specified times points during the first month, at each pre-dose of CAN, and at flares thereafter.

Results

At Day 15, 19 (95%) patients achieved complete/almost complete response, including all 4 patients without it at Day 8. Two patients were dose up titrated. Clinical remission was maintained by all from Day 15 onwards except 1 who relapsed at Day 85 (during 4 month treatment period), responding to that visit’s CAN dose. Upon CAN withdrawal, all patients relapsed after a median of 92 days (range 72-122 days). 18 regained response 8-27 days after restarting CAN and 2 relapsed at final visit following last dose administered during treatment period without follow-up at time of this analysis. Population PK analysis showed that serum clearance and volume of distribution of CAN were dependent on bodyweight. The estimated apparent serum clearance (CL/F) was 0.238±0.0139 L/day and the corresponding volume of distribution (Vss/F) was 8.06 L. Following the first dose, mean±SD observed Cmax was 16.4±4.62 μg/mL and the median Tmax was 7.4 days. Apparent weight normalized PK parameters were comparable to the PK observed in other indications. All patients reported at least one adverse event (AE); infections, mostly of the upper respiratory tract, (n=15, 75%), followed by headache (n=9) and abdominal pain (n=7). Two serious AEs, an upper respiratory tract infection and a TRAPS relapse, were reported. All patients are ongoing in the trial.

Conclusion

Canakinumab produced a rapid clinical and serological benefit which was maintained with continued monthly dosing. Relapse occurred at a median of 92 days after last dose and remission achieved upon re-dosing. Weight normalized PK parameters were comparable to PK observed in other indications. Further studies are needed to better define CAN therapy in TRAPS.

Declarations

Authors’ Affiliations

(1)
University College London Medical School
(2)
IRCCS Fondazione Policlinico San Matteo
(3)
Pediatric Immunology and Rheumatology
(4)
Galway University Hospitals
(5)
Novartis Pharmaceuticals Corporation
(6)
Novartis Pharmaceuticals UK Limited
(7)
G Gaslini Institute

Copyright

© Lachmann et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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