EUCTR2016-004952-30-Outside-EU/EEA进行中(未招募)1 期
A Placebo-Controlled, Double-Blind Comparative Study of E2080 in Lennox-Gastaut Syndrome Patients
Eisai Co, Ltd.0 个研究点目标入组 58 人开始时间: 2017年2月13日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 58
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Participants who are diagnosed as LSG with tonic/atonic seizures and atypical absence seizures (A history of atypical absence seizures will also be incorporated).
- •2. Participants who had a slow spike-and-wave pattern in an electroencephalogram within 6 months prior to the enrollment for the Observation Period.
- •3. Participants who had at least a total of 90 seizures in the 28 days prior to the enrollment for the Observation Period.
- •4. Participants who have been on 1 - 3 anti-epileptic drugs from 28 days prior to the enrollment for the Observation Period and have not changed the type of the anti-epileptic drugs.
- •5. Participants who have not changed the type nor the dose or administration of the anti-epileptic drugs they are taking in the Observation Period.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 35
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 23
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Participants who had a history of generalized tonic-clonic status epilepticus within baseline.
- •2. Participants who received drug therapy at least 4 times to be rescued from status epilepticus within baseline.
- •3. Participants who had a history of hypoxia which needed emergency resuscitation within 12 months prior to the Treatment Period.
- •4. Participants who were on a ketogenic diet or have received adrenocorticotropic hormone (ACTH) therapy or Vitamin B6 therapy within 6 months prior to the Treatment Period.
- •5. Participants who had a history of suicide attempt within the 1 year prior to the Treatment Period.
- •6. Participants who had a history of or has an allergy to triazole compound.
- •7. Participants who have clinically significant electrocardiogram abnormalities at baseline.
- •8. Participants who are pregnant, who may be pregnant, who are lactating or who wish to be pregnant.
研究者
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