作者
Virginia Devonshire, Eva Havrdova, Ernst Wilhelm Radue, Paul O'Connor, Lixin Zhang-Auberson, Catherine Agoropoulou, Dieter Adrian Häring, Gordon Francis, Ludwig Kappos
发表日期
2012/5/1
期刊
The Lancet Neurology
卷号
11
期号
5
页码范围
420-428
出版商
Elsevier
简介
Background
Fingolimod 0·5 mg once daily is approved for treatment of relapsing multiple sclerosis (MS). In the phase 3, 2-year FREEDOMS (FTY720 Research Evaluating Effects of Daily Oral therapy in MS) study, fingolimod significantly reduced annualised relapse rates (ARRs) and the risk of confirmed disability progression compared with placebo. We aimed to investigate whether the beneficial treatment effect reported for the overall population is consistent in subgroups of patients with different baseline characteristics.
Methods
We did subgroup analyses of ARRs (primary outcome) and confirmed disability progression (a secondary outcome) over 24 months in the FREEDOMS study, a randomised, double-blind study that included 1272 patients with relapsing-remitting MS who were assigned 1:1:1 to fingolimod (0·5 mg or 1·25 mg) or placebo once daily for 24 months. Subgroups were predefined, predefined and …
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