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BioMed Central Page 1 of 1 (page number not for citation purposes) Pediatric Rheumatology Open Access Poster presentation Open label multicenter study of once weekly Etanercept 0.8 mg/kg in active polyarticular Juvenile idiopathic arthritis (JIA) G Horneff* 1 , K Minden 2 , I Foeldvari 3 , J Kuemmerle-Deschner 4 , A Thon 5 , H Girschick 6 and HI Huppertz 7 Address: 1 Asklepios Clinic, Sankt Augustin, Germany, 2 Charite, Berlin, Germany, 3 Private office, Hamburg, Germany, 4 University Hospital, Tuebingen, Germany, 5 University Hospital, Hannover, Germany, 6 University Hospital, Wuerzburg, Germany and 7 Prof. Hess Kinderklinik, Bremen, Germany * Corresponding author Background In Europe Etanercept is licensed for the treatment of resist- ant polyarticular JIA at a dosage of 0.4 mg/kg bw. twice weekly in children older than 4 years. Objectives To evaluate the safety and efficacy of Etanercept once weekly 0.8 mg/kg up to 50 mg in a formal trial. Methods At each study site an independent ethics committee approved the protocol, and each patient's parent gave written informed consent (EudraCT No. 2007-000255- 34). 20 patients 4 to 17 years old were included and received 0.8 mg/kg bw. of etanercept subcutaneously once weekly for 12 weeks "Active" polyarticular disease was defined by the presence of five or more active joints. PedACR30/50/70 criteria were calculated. Safety assessments were based on adverse events (AE) reported. Results 15 of 20 JIA patients, 16 girls and 4 boys, mean age 12.9 years, disease duration 4.1 years, already have completed the 12 week study period. The mean dosage was 0.80 +/- 0.04 mg/kg Etanercept. Concomitant treatments were kept stable 3 months before and throughout the study and consisted of NSAID (n = 20), prednisone (n = 4), meth- otrexate (n = 12), leflunomide (n = 2), sulfsalazine (n = 1). A PedACR 30/50/70 response was reached by 73%/ 26%/10% of patients after 4 weeks, 86%/73%/40% after 8 weeks and 92%/92%/79% after 12 weeks of treatment. There were 33 AEs but no SAE: 9 minor infections 12 injection site reactions and 12 other AEs. There was no drop out. Conclusion These data indicate that once weekly application of Etanercept at double dosage of 0.8 mg/kg bodyweight up to 50 mg per injection is safe and efficacious in polyartic- ular JIA patients. from 15 th Paediatric Rheumatology European Society (PreS) Congress London, UK. 14–17 September 2008 Published: 15 September 2008 Pediatric Rheumatology 2008, 6(Suppl 1):P39 doi:10.1186/1546-0096-6-S1-P39 <supplement> <title> <p>15<sup>th </sup>Paediatric Rheumatology European Society (PreS) Congress</p> </title> <editor>Wietse Kuis, Patricia Woo, Angelo Ravelli, Hermann Girschick, Michaël Hofer, Johannes Roth, Rotraud K Saurenmann, Alberto Martini, Pavla Dolezova, Janjaap van der Net, Pierre Quartier, Lucy Wedderburn and Jan Scott</editor> <note>Meeting abstracts – A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/PDF/1546-0096-6-S1-full.pdf">here</a>.</note> </supplement> This abstract is available from: http://www.ped-rheum.com/content/6/S1/P39 © 2008 Horneff et al; licensee BioMed Central Ltd.

Open label multicenter study of once weekly Etanercept 0.8 mg/kg in active polyarticular Juvenile idiopathic arthritis (JIA)

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BioMed Central

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Pediatric Rheumatology

Open AccessPoster presentationOpen label multicenter study of once weekly Etanercept 0.8 mg/kg in active polyarticular Juvenile idiopathic arthritis (JIA)G Horneff*1, K Minden2, I Foeldvari3, J Kuemmerle-Deschner4, A Thon5, H Girschick6 and HI Huppertz7

Address: 1Asklepios Clinic, Sankt Augustin, Germany, 2Charite, Berlin, Germany, 3Private office, Hamburg, Germany, 4University Hospital, Tuebingen, Germany, 5University Hospital, Hannover, Germany, 6University Hospital, Wuerzburg, Germany and 7Prof. Hess Kinderklinik, Bremen, Germany

* Corresponding author

BackgroundIn Europe Etanercept is licensed for the treatment of resist-ant polyarticular JIA at a dosage of 0.4 mg/kg bw. twiceweekly in children older than 4 years.

ObjectivesTo evaluate the safety and efficacy of Etanercept onceweekly 0.8 mg/kg up to 50 mg in a formal trial.

MethodsAt each study site an independent ethics committeeapproved the protocol, and each patient's parent gavewritten informed consent (EudraCT No. 2007-000255-34). 20 patients 4 to 17 years old were included andreceived 0.8 mg/kg bw. of etanercept subcutaneously onceweekly for 12 weeks "Active" polyarticular disease wasdefined by the presence of five or more active joints.PedACR30/50/70 criteria were calculated.

Safety assessments were based on adverse events (AE)reported.

Results15 of 20 JIA patients, 16 girls and 4 boys, mean age 12.9years, disease duration 4.1 years, already have completedthe 12 week study period. The mean dosage was 0.80 +/-0.04 mg/kg Etanercept. Concomitant treatments werekept stable 3 months before and throughout the study andconsisted of NSAID (n = 20), prednisone (n = 4), meth-

otrexate (n = 12), leflunomide (n = 2), sulfsalazine (n =1). A PedACR 30/50/70 response was reached by 73%/26%/10% of patients after 4 weeks, 86%/73%/40% after8 weeks and 92%/92%/79% after 12 weeks of treatment.There were 33 AEs but no SAE: 9 minor infections 12injection site reactions and 12 other AEs. There was nodrop out.

ConclusionThese data indicate that once weekly application ofEtanercept at double dosage of 0.8 mg/kg bodyweight upto 50 mg per injection is safe and efficacious in polyartic-ular JIA patients.

from 15th Paediatric Rheumatology European Society (PreS) CongressLondon, UK. 14–17 September 2008

Published: 15 September 2008

Pediatric Rheumatology 2008, 6(Suppl 1):P39 doi:10.1186/1546-0096-6-S1-P39

<supplement> <title> <p>15<sup>th </sup>Paediatric Rheumatology European Society (PreS) Congress</p> </title> <editor>Wietse Kuis, Patricia Woo, Angelo Ravelli, Hermann Girschick, Michaël Hofer, Johannes Roth, Rotraud K Saurenmann, Alberto Martini, Pavla Dolezova, Janjaap van der Net, Pierre Quartier, Lucy Wedderburn and Jan Scott</editor> <note>Meeting abstracts – A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/PDF/1546-0096-6-S1-full.pdf">here</a>.</note> </supplement>

This abstract is available from: http://www.ped-rheum.com/content/6/S1/P39

© 2008 Horneff et al; licensee BioMed Central Ltd.