跳至主要内容
临床试验/JPRN-jRCT2080224540
JPRN-jRCT2080224540已完成2 期

AN OPEN LABEL, MULTICENTER, EXTENSION STUDY TO EVALUATE THE SAFETY AND EFFICACY OF PADSEVONIL AS ADJUNCTIVE TREATMENT OF FOCAL-ONSET SEIZURES IN ADULT SUBJECTS WITH DRUG-RESISTANT EPILEPSY

CB Japan Co., Ltd.0 个研究点目标入组 25 人开始时间: 2019年1月31日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
25

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Subject is an adult (18 years of age or more )
  • - Subject with epilepsy who has completed 1 of the previous Padsevonil (PSL) studies which allow access to the present study
  • - Female subjects of child bearing potential must have a serum negative pregnancy test at the Entry Visit, which is confirmed to be negative by urine testing prior to further dispensing at each study visit thereafter. Subjects will be withdrawn from the study as soon as pregnancy is known. Female subjects will use an efficient form of contraception for the duration of the study and for a period of 3 months after their final dose of PSL.

排除标准

  • - Subject has any severe medical, neurological, or psychiatric condition, or laboratory value which may have an impact on the safety of the subject
  • - Subject has active suicidal ideation as indicated by a positive response ('Yes') to either Question 4 or Question 5 of the 'Since Last Visit' version of the Columbia-Suicide Severity Rating Scale (C-SSRS)
  • - Subject has >2x upper limit of normal (ULN) of any of the following: alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), or >ULN total bilirubin (>= l.5x ULN total bilirubin if known Gilbert's syndrome) at the Entry Visit
  • - Subject has a clinically-significant abnormality on electrocardiogram (ECG) that, in the opinion of the investigator, increases the risks associated with participating in the study
  • - Subject has an abnormality on echocardiogram at last echocardiogram assessment, or foreseen in parent study as assessed by central reader that is accompanied by clinical symptoms or a Grade 2* (or higher)/moderate severity abnormality, or a history of rheumatic heart disease, or other known valvular abnormalities (*according to the ASE Guidelines, 2017; Zoghbi et al 2017)
  • - Female subject who plans to be pregnant or is breastfeeding

研究者

发起方
CB Japan Co., Ltd.

相似试验

进行中(未招募)
1 期
An open-label extension study of UCB0942 in adult patients with highly drug-resistant focal epilepsy.highly drug-resistant focal epilepsyMedDRA version: 21.1Level: LLTClassification code 10065337Term: Focal epilepsySystem Organ Class: 100000004852
EUCTR2015-001268-20-ITCB Biopharma SR30
进行中(未招募)
1 期
An open-label extension study of UCB0942 in adult patients with highly drug-resistant focal epilepsy.
EUCTR2015-001268-20-ESCB Biopharma SPR42
进行中(未招募)
1 期
An open-label (treatment received will be known) follow-up study to evaluate the safety and efficacy of brivaracetam when used treating partial onset seizures for a long period of time in patients with epilepsy (=16 years to 80 years)Epilepsy
EUCTR2010-020345-27-SECB BIOSCIENCES, INC.720
进行中(未招募)
1 期
An open-label (treatment received will be known) follow-up study to evaluate the safety and efficacy of brivaracetam when used treating seizures for a long period of time in patients with epilepsy (aged 16 years or older)Epilepsy
EUCTR2010-020345-27-BGCB BIOSCIENCES, INC.720
进行中(未招募)
1 期
An open-label (treatment received will be known) follow-up study to evaluate the safety and efficacy of brivaracetam when used treating partial onset seizures for a long period of time in patients with epilepsy (=16 years to 80 years)MedDRA version: 14.1 Level: PT Classification code 10015037 Term: Epilepsy System Organ Class: 10029205 - Nervous system disordersEpilepsy
EUCTR2010-020345-27-FICB BIOSCIENCES, INC.720