Canakinumab (ACZ885, a fully human IgG1 anti-IL-1β mAb) induces sustained remission in pediatric patients with cryopyrin-associated periodic syndrome (CAPS)

Cryopyrin-associated periodic syndrome (CAPS) represents a spectrum of three auto-inflammatory syndromes, familial cold auto-inflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease/chronic infantile neurological cutaneous and articular syndrome...

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Auteurs principaux: Kümmerle-Deschner, Jasmin (Auteur) , Ramos, Eduardo (Auteur) , Blank, Norbert (Auteur) , Roesler, Joachim (Auteur) , Felix, Sandra D. (Auteur) , Jung, Thomas (Auteur) , Stricker, Kirstin (Auteur) , Chakraborty, Abhijit (Auteur) , Tannenbaum, Stacey (Auteur) , Wright, Andrew M. (Auteur) , Rordorf, Christiane (Auteur)
Format: Article (Journal)
Langue:anglais
Publié: 28 February 2011
In: Arthritis Research & Therapy
Year: 2011, Volume: 13, Pages: 1-10
ISSN:1465-9913
DOI:10.1186/ar3266
Accès en ligne:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1186/ar3266
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Notes sur l'auteur:Jasmin B. Kuemmerle-Deschner, Eduardo Ramos, Norbert Blank, Joachim Roesler, Sandra D. Felix, Thomas Jung, Kirstin Stricker, Abhijit Chakraborty, Stacey Tannenbaum, Andrew M. Wright and Christiane Rordorf
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Résumé:Cryopyrin-associated periodic syndrome (CAPS) represents a spectrum of three auto-inflammatory syndromes, familial cold auto-inflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disease/chronic infantile neurological cutaneous and articular syndrome (NOMID/CINCA) with etiology linked to mutations in the NLRP3 gene resulting in elevated interleukin-1β (IL-1β) release. CAPS is a rare hereditary auto-inflammatory disease, which may start early in childhood and requires a life-long treatment. Canakinumab, a fully human anti-IL-1β antibody, produces sustained selective inhibition of IL-1β. This study was conducted to assess the efficacy, safety, and pharmacokinetics of canakinumab in the treatment of pediatric CAPS patients.
Description:Gesehen am 11.07.2022
Description matérielle:Online Resource
ISSN:1465-9913
DOI:10.1186/ar3266