Trial of Satralizumab in Neuromyelitis Optica Spectrum Disorder
Author(s) -
Takashi Yamamura,
Ingo Kleiter,
Kazuo Fujihara,
Jacqueline Palace,
Benjamin Greenberg,
Beata ZakrzewskaPniewska,
Francesco Patti,
ChingPiao Tsai,
Albert Saiz,
Hayato Yamazaki,
Yuichi Kawata,
Pádraig Wright,
de Sèze
Publication year - 2019
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1901747
Subject(s) - medicine , neuromyelitis optica , placebo , clinical endpoint , spectrum disorder , hazard ratio , randomized controlled trial , gastroenterology , confidence interval , multiple sclerosis , immunology , pathology , alternative medicine , psychiatry
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune disease of the central nervous system and is associated with autoantibodies to anti-aquaporin-4 (AQP4-IgG) in approximately two thirds of patients. Interleukin-6 is involved in the pathogenesis of the disorder. Satralizumab is a humanized monoclonal antibody targeting the interleukin-6 receptor. The efficacy of satralizumab added to immunosuppressant treatment in patients with NMOSD is unclear.
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