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临床试验/NCT00963183
NCT00963183已完成1 期

A Phase I, Single Centre, Double-blind, Randomised, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability and Pharmacokinetics of Inhaled AZD5423 After Single Ascending Doses in Healthy Male Subjects

AstraZeneca1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2009年8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
72
试验地点
1
主要终点
Safety variables (ECG, adverse events, blood pressure, pulse, body temp, safety lab), lung function and physical examination

研究概览

简要总结

The aim of the study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of AZD5423 following single ascending dose administrations in healthy male subjects.

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
Triple (Participant, Care Provider, Investigator)

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 and dated informed consent prior to any study specific procedures
  • Have a body mass index (BMI) between 18 and 30 kg/m2 and weigh at least 50 kg and no more than 100 kg

排除标准

  • Any clinically significant disease or disorder
  • Any clinically significant abnormalities at screening examination
  • Use of any prescribed or non-prescribed medication

研究组 & 干预措施

A

Experimental

Drug: AZD5423

干预措施: AZD5423 (Drug)

B

Placebo Comparator

Drug: Placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Safety variables (ECG, adverse events, blood pressure, pulse, body temp, safety lab), lung function and physical examination

时间窗: Frequent sampling occasions during study days

次要结局

  • Pharmacokinetics - Maximum plasma concentration (Cmax), time to Cmax (tmax), area under the plasma concentration-time curve from zero to the time of the last measurable concentration [AUC(0-t)] and from zero to infinity (AUC)(Frequent sampling occasions during study days)
  • Add'l pharmacokinetics - Terminal rate constant (λz); terminal half-life (t½λz), Apparent plasma clearance (CL/F), apparent volume of distribution during terminal phase (Vz/F), mean residence time (MRT).(Frequent sampling occasions during study days)
  • Pharmacodynamics - Plasma cortisol concentrations(Frequent sampling occasions during study days)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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