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vortioxetín bol v primárnom výslednom kritériu, čase do relapsu mdd, nadradený (p = 0,004) placebu s pomerom rizík 2,0; to znamená, že riziko relapsu bolo v skupine užívajúcej placebo dvakrát vyššie ako v skupine užívajúcej vortioxetín.
vortioxetine was superior (p=0.004) to placebo on the primary outcome measure, the time to relapse of mdd, with a hazard ratio of 2.0; that is, the risk of relapse was two times higher in the placebo group than in the vortioxetine group.
Last Update: 2017-04-26
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