BENITIONSClinical Trial Intelligence

A Study of Soticlestat as an Add-on Therapy in Children and Adults With Dravet Syndrome or Lennox-Gastaut Syndrome

3期 提前终止 NCT05163314

适应症Dravet Syndrome, Lennox Gastaut Syndrome
分期3期
申办方Takeda
状态提前终止
受试者人数352 人
干预(药物)Soticlestat
开始日期2022年3月4日
完成日期2025年9月24日
结果公布日2026年6月9日

摘要

The main aim of the study is to learn if soticlestat, when given as an add-on therapy, reduces the number of seizures in children and adults with Dravet Syndrome (DS) or Lennox-Gastaut Syndrome (LGS). Participants will receive their standard anti-seizure therapy, plus tablets of soticlestat. There will be scheduled visits and follow-up phone calls throughout the study.

Number of Participants With At Least One Treatment Emergent Adverse Event (TEAE)

Up to end of study (approximately 3.6 years) · Participants

Soticlestat293 Participants

Number of Participants in Each Category of the Columbia-Suicide Severity Rating Scale (C-SSRS) Over Time

At first visit post-baseline (Visit 1 [V1], Day 1 of the current study), Week 13 (V4), Week 26 (V5), Week 52 (V7), Week 78 (V9), Week104 (v11), Week 130 (V12) and Week 156 (V13) · Participants

Soticlestat267 Participants
Soticlestat2 Participants
Soticlestat1 Participants
Soticlestat1 Participants
Soticlestat2 Participants
Soticlestat1 Participants

Change From Baseline in Body Weight for All Age Groups

From Baseline to Week 104 · kilogram (kg)

Soticlestat8.63 ± 3.669 kilogram (kg)
Soticlestat4.53 ± 1.559 kilogram (kg)
Soticlestat7.33 ± 5.777 kilogram (kg)
Soticlestat2.94 ± 1.365 kilogram (kg)
Soticlestat4.21 ± 4.091 kilogram (kg)
Soticlestat3.73 ± 3.083 kilogram (kg)

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。