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trial of satralizumab in neuromyelitis optica spectrum disorder

Patients treated with satralizumab as monotherapy were at less risk for neuromyelitis optica spectrum disorder relapse compared with patients treated with placebo, according to a … Satralizumab, sold under the brand name Enspryng, is a humanized monoclonal antibody medication that is used for the treatment of neuromyelitis optica spectrum disorder (NMOSD), a rare autoimmune disease. Yamamura T, Kleiter I, Fujihara K, Palace J, Greenberg B, Zakrzewska-Pniewska B, Patti F, Tsai CP, Saiz A, Yamazaki H, Kawata Y, Wright P, De Seze J. N Engl J Med, 381(22):2114-2124, 01 Nov 2019 Satralizumab is a humanized monoclonal antibody targeting the interleukin-6 receptor. N Engl J Med. Enspryng ™ (satralizumab-mwge) is the first and only US Food and Drug Administration (FDA)-approved subcutaneous therapy indicated for the treatment of neuromyelitis optica spectrum disorder (NMOSD) in anti-aquaporin-4 (AQP4) antibody-positive adult patients.. Efficacy and Safety Study of Satralizumab (SA237) as Add-on Therapy to Treat Participants With Neuromyelitis Optica (NMO) and NMO Spectrum Disorder (NMOSD) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Satralizumab, a monoclonal antibody that antagonizes interleukin-6 (IL6), was investigated in this phase 3, randomized, double-blind, placebo-controlled, company-sponsored study. Jeffrey Bennett, MD, PhD. 1 Among demyelinating diseases of the CNS, neuromyelitis optica spectrum disorder is less prevalent than … Neurology. Background Satralizumab, a humanised monoclonal antibody targeting the interleukin-6 receptor, reduced the risk of relapse in patients with neuromyelitis optica spectrum disorder (NMOSD) when added to immunosuppressant therapy. BACKGROUND: 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. Neuromyelitis optica spectrum disorder is a rare autoimmune disease mediated by recurrent inflammatory attacks against the aquaporin-4 water channel on astrocytes primarily in the optic nerves and spinal cord, often leading to blindness and paralysis. Araki M, Matsuoka T, Miyamoto K, et al. 2014;82:1302–6. The drug is being developed by Chugai Pharmaceutical, a subsidiary of Roche.. Yamamura T, Kleiter I, Fujihara K, et al. 82 per 100 000 people. In December 2019, F. Hoffmann-La Roche Ltd announced the pivotal phase III study of the investigational medicine satralizumab for the treatment of neuromyelitis optica spectrum disorder 4 The disorder is characterised by inflammatory lesions in the optic nerve, spinal cord, brainstem, and cerebrum, 5 causing potentially severe motor and sensory impairment, bladder dysfunction, vision … Neuromyelitis optica spectrum disorder (NMOSD) is a relapsing autoimmune disease that often leads to disability. Efficacy of the anti-IL-6 receptor antibody tocilizumab in neuromyelitis optica: a pilot study. This study assessed the safety and efficacy of satralizumab monotherapy in patients with the disorder. Trial of satralizumab in neuromyelitis optica spectrum disorder. Satralizumab monotherapy may reduce the risk for neuromyelitis optics spectrum disorder (NMOSD) relapse and has a favorable safety profile, according to study results published in Lancet Neurology Interleukin-6 is involved in the pathogenesis of the disorder. 2019;381:2114–24. Trial of Satralizumab in Neuromyelitis Optica Spectrum Disorder. Introduction. Genentech has announced that the FDA has approved satralizumab for the treatment of adult patients with anti-aquaporin-4 (AQP4-IgG) antibody positive neuromyelitis optica spectrum disorder (NMOSD)—the third targeted treatment for this population and the first eligible for at-home administration.

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