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临床试验/NCT00689559
NCT00689559已完成1 期

A Single-Centre, Double-Blind, Randomised, Parallel Group Study of Repeated Oral Doses of AZD3480/Placebo and a Single Dose of Aripiprazole to Evaluate the Pharmacokinetic Interaction Between AZD3480 and Aripiprazole in Healthy Subjects (Phase I)

AstraZeneca1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2008年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
AstraZeneca
入组人数
52
试验地点
1
主要终点
PK variables

研究概览

简要总结

The purpose of the study is to evaluate if AZD3480 and warfarin interact with each other or not, i.e. show the same or altered plasma concentration profiles when co-administered compared to administered alone.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Provision of signed written informed consent
  • Clinically normal physical findings and laboratory values

排除标准

  • Clinically significant illness or clinically relevant trauma within three weeks before the first dose
  • History of clinically significant disease
  • Use of prescribed medication during the 2 weeks before administration of the first dose of investigational product

研究组 & 干预措施

1

Experimental

AZD3480 + Aripiprazole

干预措施: AZD3480 (Drug)

1

Experimental

AZD3480 + Aripiprazole

干预措施: Aripiprazole (Drug)

2

Experimental

Placebo + Aripiprazole

干预措施: Placebo (Drug)

2

Experimental

Placebo + Aripiprazole

干预措施: Aripiprazole (Drug)

结局指标

主要结局

PK variables

时间窗: Frequent sampling occasions during

次要结局

  • Safety variables (adverse events, blood pressure, pulse, safety lab)(During the whole treatment period)

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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