ACTRN12605000408684已完成1 期
A Randomised, Placebo-Controlled, Double-Blind, Single and Multiple Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneous Doses of ACV1 in Healthy Adult Male Subjects.
Metabolic Pharmaceuticals Ltd.0 个研究点目标入组 60 人开始时间: 2005年9月14日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 49 Years（—）
- 性别
- Male
入选标准
- •Weight <= 100 kg, BMI 19 to 30, generally healthy, adequate venous access, fluent English, have given written informed consent.
排除标准
- •Hypersensitivity, medical conditions, organ dysfunction, drug or alcohol abuse, taking medication.
研究者
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