首页> 外文期刊>Expert opinion on pharmacotherapy >Oral fingolimod for relapsing-remitting multiple sclerosis Evaluation of: Kappos L, Radue E-M, O'Connor P, et al. A placebo-controlled trial of oral fingolimod in relapsing multiple sclerosis. N Engl J Med 2010;362:387-401; and Cohen JA, Barkhof F, Comi G, et al. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. N Engl J Med 2010;362:402-15.
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Oral fingolimod for relapsing-remitting multiple sclerosis Evaluation of: Kappos L, Radue E-M, O'Connor P, et al. A placebo-controlled trial of oral fingolimod in relapsing multiple sclerosis. N Engl J Med 2010;362:387-401; and Cohen JA, Barkhof F, Comi G, et al. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. N Engl J Med 2010;362:402-15.

机译:口服芬戈莫德用于复发缓解型多发性硬化症的评估:Kappos L,Radue E-M,O'Connor P等。口服芬戈莫德治疗复发性多发性硬化症的安慰剂对照试验。 N Engl J Med 2010; 362:387-401;和Cohen JA,Barkhof F,Comi G等。口服芬戈莫德或肌内干扰素可复发多发性硬化症。新英格兰医学杂志2010; 362:402-15。

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摘要

Most people with multiple sclerosis (MS) have the relapsing-remitting type. The objective was to evaluate two clinical trials of fingolimod in relapsing MS. FREEDOMS (FTY720 Research Evaluation Effects of Daily Oral therapy in Multiple Sclerosis), a Phase III placebo-controlled trial, showed that fingolimod (0.5 or 1.25 mg) reduced the relapse rate and disability in MS, compared with placebo. Fingolimod (0.5 or 1.25 mg) has been compared to interferon-beta-1a in a Phase III clinical trial (TRANSFORMS; Trial Assessing Injectable Interferon versus FTY720 Oral in Relapsing-Remitting Multiple Sclerosis) and shown to be more efficacious than interferon-beta-1a in reducing relapse rates. However, fingolimod did increase the risk of infections and skin cancers. Only the lower dose of fingolimod (0.5 mg), which possibly has less toxicity, should be considered for prevention of relapses in relapsing-remitting MS.
机译:大多数患有多发性硬化症(MS)的人都患有复发缓解型。目的是评估芬戈莫德在复发性MS中的两项临床试验。 III期安慰剂对照试验FREEDOMS(FTY720对多发性硬化症每日口服疗法的研究评估效果)显示,与安慰剂相比,芬戈莫德(0.5或1.25 mg)降低了MS的复发率和残疾。芬戈莫德(0.5或1.25 mg)在一项III期临床试验中已与干扰素-β-1a进行了比较(TRANSFORMS;复发性多发性硬化症中可注射性干扰素与FTY720口服药物的临床试验),并显示出比干扰素-β-a更有效1a在降低复发率上。但是,芬戈莫德确实增加了感染和皮肤癌的风险。仅应考虑使用较低剂量的芬戈莫德(0.5 mg),该药物可能具有较小的毒性,以防止复发型MS复发。

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