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临床试验/NCT01443208
NCT01443208已完成1 期

A Phase 1, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, Parallel-Group, Single and Multiple-Dose Study of Desvenlafaxine in Korean Healthy Subjects

Pfizer1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2011年11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
Pfizer
入组人数
36
试验地点
1
主要终点
For multiple dose: trough concentration (Ctrough)

研究概览

简要总结

To evaluate the pharmacokinetics and safety of single dose and multiple doses of desvenlafaxine in Korean healthy subjects and compare to westerners.

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 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy male and/or female subjects
  • Between the ages of 18 and 55 years, inclusive
  • Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs)

排除标准

  • Elevated risk of suicide, in the opinion of the investigator or expert consultant
  • Pregnant or nursing females
  • Females of childbearing potential who are unwilling or unable to use an acceptable method of contraception

研究组 & 干预措施

100 mg

Experimental

干预措施: desvenlafaxine (Drug)

50 mg

Experimental

干预措施: desvenlafaxine (Drug)

200 mg

Experimental

干预措施: desvenlafaxine (Drug)

结局指标

主要结局

For multiple dose: trough concentration (Ctrough)

时间窗: day 8

For single dose: time to first occurence of Cmax (Tmax)

时间窗: day 1

For single dose: area under curve (0-time for last quantifiable concentration) (AUClast)

时间窗: day 1

For multiple dose: area under curve (0-24hours) (AUC0-24)

时间窗: day 8

For multiple dose: maximum concentration (Cmax)

时间窗: day 8

For single dose: maximum concentration (Cmax)

时间窗: day 1

For multiple dose: time to first occurence of Cmax (Tmax)

时间窗: day 8

次要结局

  • For multiple dose if data permit: accumulation factor (Rac)(day 8)
  • For multiple dose if data permit: terminal elimination half life (t1/2)(day 8)
  • For multiple dose if data permit: apparent volume of distribution (Vz/F)(day 8)
  • For single dose if data permit: terminal elimination half life (t1/2)(day 1)
  • For single dose if data permit: apparent volume of distribution (Vz/F)(day 1)
  • For single dose if data permit: oral clearance (CL/F)(day 1)
  • For multiple dose if data permit: oral clearance (CL/F)(day 8)
  • For single dose if data permit: area under curve (0-infinity) (AUCinf)(day 1)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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