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 |
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| 分期 | 3期 |
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| 申办方 | Takeda |
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| 状态 | 提前终止 |
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| 受试者人数 | 352 人 |
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| 干预(药物) | Soticlestat |
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| 开始日期 | 2022年3月4日 |
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| 完成日期 | 2025年9月24日 |
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| 结果公布日 | 2026年6月9日 |
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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
| Soticlestat | 293 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
| Soticlestat | 267 Participants |
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| Soticlestat | 2 Participants |
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| Soticlestat | 1 Participants |
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| Soticlestat | 1 Participants |
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| Soticlestat | 2 Participants |
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| Soticlestat | 1 Participants |
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Change From Baseline in Body Weight for All Age Groups
From Baseline to Week 104 · kilogram (kg)
| Soticlestat | 8.63 ± 3.669 kilogram (kg) |
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| Soticlestat | 4.53 ± 1.559 kilogram (kg) |
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| Soticlestat | 7.33 ± 5.777 kilogram (kg) |
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| Soticlestat | 2.94 ± 1.365 kilogram (kg) |
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| Soticlestat | 4.21 ± 4.091 kilogram (kg) |
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| Soticlestat | 3.73 ± 3.083 kilogram (kg) |
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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。