Progressive MS trials: Lessons learned

被引:15
|
作者
Tur, Carmen [1 ,2 ,3 ]
Montalban, Xavier [1 ,2 ]
机构
[1] Univ Autonoma Barcelona, Dept Neurol Neuroimmunol, Hosp Univ Vall dHebron, Passeig Vall dHebron 119-129, Barcelona 08035, Spain
[2] Univ Autonoma Barcelona, Multiple Sclerosis Ctr Catalonia Cemcat, Hosp Univ Vall dHebron, Passeig Vall dHebron 119-129, Barcelona 08035, Spain
[3] UCL, Inst Neurol, Dept Neuroinflammat, Queen Sq Multiple Sclerosis Ctr, London, England
关键词
Multiple sclerosis; MRI; treatment response; outcome measurement; disease modifying therapies; clinical trial; REMITTING MULTIPLE-SCLEROSIS; RANDOMIZED CONTROLLED TRIAL; DOUBLE-BLIND; INTERFERON BETA-1B; CLINICAL-TRIAL; PHASE-III; MENINGEAL INFLAMMATION; BRAIN ATROPHY; PLACEBO; MULTICENTER;
D O I
10.1177/1352458517729460
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Up to very recently, no treatments had proved effective in progressive multiple sclerosis (MS). In 2016, four drugs, two tested in phase 3 and two in phase 2 trials, showed a beneficial effect in primary or secondary progressive MS. Although this could indicate a turning point in progressive MS treatment, most of these successes have been modest and mainly restricted to patients with active inflammation, in the context of trials with powerful anti-inflammatory agents. This paper summarises these reasons, particularly focusing on the main lessons learned for the design of future trials. First, a drug's mechanism of action should tackle the specific pathogenic mechanisms that characterise progressive MS. Second, trial populations where new drugs are to be tested should be carefully chosen, possibly including younger patients with shorter disease durations, which have greater chances of showing active deterioration during the trial, therefore increasing the power to detect treatment effects. Third, outcome measures used in future phase 2 and phase 3 trials should be highly sensitive and be accompanied by smart trial designs.
引用
收藏
页码:1583 / 1592
页数:10
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