Ocrelizumab: A Review in Multiple Sclerosis

被引:54
作者
Syed, Yahiya Y. [1 ]
机构
[1] Springer, Private Bag 65901, Auckland 0754, New Zealand
关键词
III DOUBLE-BLIND; PHASE-III; DISABILITY PROGRESSION; INTERFERON BETA-1A; OPERA I; DOUBLE-DUMMY; NO EVIDENCE; ORATORIO; PLACEBO; OUTCOMES;
D O I
10.1007/s40263-018-0568-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Ocrelizumab (Ocrevus (R)) is a humanized anti-CD20 monoclonal antibody approved for the treatment of adults with relapsing multiple sclerosis (RMS) or primary progressive multiple sclerosis (PPMS). In the two identically designed, 96-week OPERA I and II trials in patients with RMS, ocrelizumab significantly reduced annualized relapse rates versus interferon beta-1a. In the >= 120-week ORATORIO trial in patients with PPMS, ocrelizumab significantly reduced the risk of >= 12-week confirmed disability progression relative to placebo. These primary endpoint results were supported by a number of secondary outcomes, including disease activity in the brain assessed by magnetic resonance imaging. Ocrelizumab was generally well tolerated in these studies, with infusion-related reactions and infections being the most common adverse events, which were mostly mild to moderate in severity. In summary, ocrelizumab is a novel high-efficacy disease-modifying therapy for RMS that is more effective than interferon beta-1a and also a valuable new treatment option for delaying progression in early PPMS. It offers a convenient once every 6 months treatment regimen, with no need for routine monitoring.
引用
收藏
页码:883 / 890
页数:8
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