NCT00541996已完成1 期
A Randomized, Open-Label, Single-Dose, 4-Period Crossover, Comparative Bioavailability Study of 3 Sustained- Release Formulations and an Immediate- Release Formulation of Vabicaserin (SCA-136) in Healthy Subjects
Wyeth is now a wholly owned subsidiary of Pfizer1 个研究点 分布在 1 个国家开始时间: 2007年8月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 试验地点
- 1
- 主要终点
- Assess the bioavailability of four oral formulations of vabicaserin.
研究概览
简要总结
The purpose of this study is to determine the absorption rate of four oral formulations of vabicaserin.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 是
入选标准
- •Healthy men aged 18-50 years.
排除标准
- •Any significant disease state.
- •History of drug or alcohol abuse within 1 year.
- •Abnormal liver function tests.
结局指标
主要结局
Assess the bioavailability of four oral formulations of vabicaserin.
次要结局
- Obtain additional safety and tolerability data for vabicaserin in healthy male subjects.
研究者
研究点 (1)
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