EUCTR2016-002452-25-HU进行中(未招募)1 期
A MULTICENTER, OPEN-LABEL STUDY TO EVALUATE THE PHARMACOKINETICS, SAFETY, AND TOLERABILITY OF INTRAVENOUS BRIVARACETAM IN SUBJECTS =1 MONTH TO <16 YEARS OF AGE WITH EPILEPSY
CB BIOPHARMA SPR0 个研究点目标入组 50 人开始时间: 2018年2月27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
- 50
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
- •- Male or female from >= 1 month to < 16 years of age. For subjects who are < 1 year from birth and
- •who were preterm infants, the corrected gestational age should be used for this entry requirement
- •- Weight >= 3 kg (6.6 lbs)
- •- Diagnosis of epilepsy
- •- Acceptable candidate for venipuncture and intravenous (iv) infusion
- •- Treatment with >=1 anti epileptic drug (AED; including BRV) without a change of dose regimen for at
- •least 7 days prior to Screening
- •- No treatment with vagus nerve stimulation (VNS), OR the subject is being treated with VNS and the
- •settings have been constant for >=7 days prior to Screening
- •- For female subjects: not of childbearing potential, OR of childbearing potential and not sexually
- •active/negative pregnancy test, OR of childbearing potential and sexually active/negative pregnancy
- •test/uses medically acceptable contraceptive methods
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 50
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range 0
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •- Subject has previously received iv Brivaracetam (BRV) in this study.
- •- Subject is being treated with BRV at a dose >5mg/kg/day (rounded) or >200mg/day for subjects with
- •body weights >40kg.
- •- Subject requires or is likely to require a change in concomitant antiepileptic drug(s) (AED[s]), dose of
- •concomitant AED(s), or formulation of AED(s) during the 7 days prior to the intravenous (iv)
- •pharmacokinetic (PK) Period.
- •- Subject is likely, in the opinion of the Investigator, to require rescue medication during the Initiating
- •Oral BRV (IOB) Treatment or iv PK Periods.
- •- Subject has experienced generalized convulsive status epilepticus in the 28 days prior to Screening or
- •during the Screening Period.
研究者
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