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临床试验/EUCTR2009-016996-31-HU
EUCTR2009-016996-31-HU进行中(未招募)不适用

A Randomized, Multicenter, Double-Blind, Placebo–Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-Onset Seizures

psher-Smith Laboratories, Inc.0 个研究点目标入组 270 人开始时间: 2011年11月3日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
270

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

  • Subject has a confirmed diagnosis of partial-onset seizures with or without secondary generalization for at least 12 months prior to Visit 1. The diagnosis of partial-onset seizures with or without secondary generalized seizure is defined by the ILAE commission in 1981 (Appendix 1).
  • Currently on a stable dosing regimen of 1 to 3 AEDs for at least 4-weeks prior to Visit 1 (12 weeks for phenobarbital and primidone).
  • oNote: VNS can be counted as one of the AEDs provided the VNS has been in place for at least 6 months and on a stable setting for at least 1 month prior to Visit 1. The VNS settings must not change throughout the course of the study (baseline, titration, and maintenance phases).
  • oNote: Benzodiazepines (BZD) taken more than once per week, for any indication, will be counted as one of the AEDs.
  • Male or female, aged 18 to 75 years, inclusive.
  • Can safely be treated, in the opinion of the investigator, with topiramate
  • Have a minimum of 8 partial-onset seizures and no more than 21 consecutive seizure free days, during the 8-week baseline.
  • oNote: Only simple partial seizures with motor signs, complex partial seizures, and partial seizures with secondary generalization are counted toward this inclusion.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 230
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 40

排除标准

  • Have a predisposing condition or medications that may interfere with the absorption of USL255. For example, Crohn’s disease, ileostomy, short bowel syndrome, chronic diarrhea.
  • Have a history of seizure episodes lasting less than 30 minutes in which several seizures occur with such frequency that the initiation and completion of each individual seizure cannot be distinguished, within 3 months prior to Visit 1.
  • Have a history of pseudoseizures, or status epilepticus, within 3 months prior to Visit 1.
  • Have a history of metabolic acidosis, nephrolithiasis, ureterolithiasis, or narrow angle glaucoma.
  • Have a history of suicidal attempts, suicidal ideation, or uncontrolled psychiatric illness within 2 years of Visit 1.
  • Have taken topiramate within the past 6 months.
  • History of lack of efficacy to topiramate, for epilepsy, despite adequate exposure (200mg/day)
  • History of safety or tolerability issues to topiramate not related to dosage titration
  • Currently taking, or have taken felbamate within the past 18 months, or have taken vigabatrin in the past.

研究者

发起方
psher-Smith Laboratories, Inc.

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