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• W2130136130 abstract "<h3>Objective:</h3> The study was designed to test the efficacy of ATX-MS-1467 in a relevant preclinical model and to assess its safety for the treatment of patients with secondary progressive multiple sclerosis (SPMS). <h3>Methods:</h3> ATX-MS-1467 was tested for its ability to suppress experimental autoimmune encephalomyelitis (EAE) in the (Ob x DR2)F1 mouse both before and after disease onset. Safety was assessed by clinical assessment, MRI analysis, and the measurement of immune responses to self- and nonself-antigens in patients with SPMS. <h3>Results:</h3> ATX-MS-1467 displayed a dose-dependent inhibition of EAE and was more effective than glatiramer acetate in the treatment of ongoing disease in humanized mice. A phase 1 open-label dose-escalating study demonstrated that ATX-MS-1467 was safe and well-tolerated in a group of 6 patients with SPMS, up to a dose of 800 µg. <h3>Conclusions:</h3> The results of this study support further development of ATX-MS-1467 in a clinical trial powered to investigate the immunologic and clinical benefits of treatment in relapsing-remitting MS. <h3>Classification of evidence:</h3> This study provides Class IV evidence that ATX-MS-1467 is safe and tolerated in a group of 6 patients with SPMS." @default.
• W2130136130 created "2016-06-24" @default.
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• W2130136130 date "2015-03-12" @default.
• W2130136130 modified "2023-09-27" @default.
• W2130136130 title "Preclinical development and first-in-human study of ATX-MS-1467 for immunotherapy of MS" @default.
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• W2130136130 doi "https://doi.org/10.1212/nxi.0000000000000093" @default.
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