TERIFLUNOMIDE: NEW ORAL IMMUNMODULANT DRUG IN THERAPY OF MULTIPLE SCLEROSIS

被引:0
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作者
Bencsik Krisztina [1 ]
Rozsa Csilla [2 ]
Vecsei Laszlo [1 ,3 ]
机构
[1] Szegedi Tudomanyegyetem, Altalanos Orvostudomanyi Kar, Szent Gyorgyi Albert Klin Kozpont, Neurol Klin, H-6720 Szeged, Hungary
[2] Jahn Ferenc Del Pesti Korhaz, Neurol Osztaly, Budapest, Hungary
[3] MTA SZTE, Idegtudomanyi Kutato Csoport, Szeged, Hungary
来源
关键词
teriflunomide; multiple sclerosis; PHASE-III TRIAL; DOUBLE-BLIND; INTRAMUSCULAR INTERFERON; DISEASE; MULTICENTER; MANAGEMENT; EFFICACY; SAFETY;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple sclerosis (MS) is the autoimmune, demyelinating, neurodegenerative disorder of the central nervous system (CNS). There are nine drugs available in Hungary reimbursed by the National Health Insurance Fund of Hungary (OEP) to reduce the activity of the disease, from which seven can be used as first line therapies. We have approximately 20 years of experience with the interferon beta-1a/1b and glatiramer-acetate products. Though in case of approximately 30% of the patients using one of the first line drugs, the disease remains active, that we call break-through disease. The reasons for break-through disease could be the insufficient adherence and compliance, the appearance of neutralizing antibodies or the high activity of the disease. One of the oral immunomodulating drugs for MS, teriflunomide, was registered in Europe in 2013. Because of the anti-proliferative and anti-inflammatory effect of teriflunomide, it can be used for the reduction of the disease activity in the relapsing-remitting course of MS. The effect of teriflunomide was proved in one Phase II. and four Phase III. (TEMSO, TOWER, TENERE, TOPIC) studies. Teriflunomide 14 mg once daily was able to demonstrate in two consecutive placebo-controlled phase 3 clinical trials that significantly reduces the relapse rate (31.5% and 36.3%) and in both studies significantly reduces the sustained disability progression (29.8% and 31.5%) moreover delays the appearance of the clinically definitive MS in patients with clinically isolated syndrome (CIS). According to the TENERE study there were no significant differences observed between teriflunomide 14 mg and IFN beta-1a s.c. in time to failure and annualized relapse rate but the treatment satisfaction domains of global satisfaction, side-effects and convenience were significantly improved with teriflunomide compared with s.c. IFN beta-1a.
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页码:79 / 87
页数:9
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