EUCTR2017-002397-39-IT进行中(未招募)1 期
A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy and Safety of Erenumab in Children (6 to < 12 Years) and Adolescents (12 to < 18 Years) With Episodic Migraine (OASIS PEDIATRIC [EM]) - NA
AMGEN INC.0 个研究点目标入组 456 人开始时间: 2020年10月7日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 456
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
- •- Children (6 to < 12 years of age) or adolescent (12 to < 18 years of age) at the time of signing, if developmentally appropriate, the formal assent to
- •participate to the study.
- •- Subject's parent or legal representative has provided written informed consent before initiation of any study-specific activities/procedures.
- •- History of migraine (with or without aura) for > = 12 months before screening according to the IHS Classification ICHD-3 based on medical records
- •and/or subject self-report or parents' or legal representative's report.
- •- History of < 15 headache days per month of which > = 4 headache days were assessed by the subject as migraine days per month in each of the 3 months
- •prior to screening.
- •- Migraine frequency: > = 4 and < 15 migraine days during the baseline phase based on the eDiary calculations.
- •- Headache frequency: < 15 headache days during the baseline phase based on the eDiary calculations.
- •- Demonstrated at least 80% compliance with the eDiary
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- History of cluster headache or hemiplegic migraine headache.
- •- No therapeutic response with > 2 of the following 10 medication categories for prophylactic treatment of migraine after an adequate therapeutic trial
- •- Malignancy within 5 years before screening.
- •- History of suicidal behavior or the subject is at risk of self-harm or harm to others as evidenced by endorsement of items 4 or 5 on the pediatric Columbia-suicide Severity Rating Scale (C-SSRS) assessed at screening
- •- Evidence of drug or alcohol abuse or dependence within 12 months before screening, based on medical records, subject self-report, or positive urine drug test performed during screening
- •*Please, refers to protocol for the full list
研究者
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