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临床试验/JPRN-UMIN000025614
JPRN-UMIN000025614已完成2 期

Perampanel for sporadic amyotrophic lateral sclerosis (ALS): A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase 2 Trial - Perampanel for sporadic amyotrophic lateral sclerosis (ALS)

Department of Neurology, Tokyo Medical University0 个研究点目标入组 66 人开始时间: 2017年2月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
66

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
40years-old 至 78years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • - Patients who underwent tracheostomy. - Patients who experienced non-invasive positive pressure ventilation. - Patients whose percent-predicted forced vital capacity (%FVC) is <80%. - Patients with progressive bulbar palsy type. - Patients with cognitive impairment, severe disease in the renal, cardiovascular, or hematological system. - Patients with hepatic disease. - Patients with malignant tumor. - Pregnant women or women with a possibility of becoming pregnant. - Patients who participated in another clinical study within 12 weeks before starting the observation period. - Patients who has initiated perampanel therapy in the past or at present. - Patients who are judged to be ineligible for study entry by the investigators.

研究者

发起方
Department of Neurology, Tokyo Medical University

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