跳至主要内容
临床试验/NCT01557257
NCT01557257已完成1 期

An Open-label, Single-dose and Multiple-dose, Randomized, Crossover Study to Evaluate Pharmacokinetics, Safety and Tolerability After Administration of ALO-02 40 Mg Twice Daily Compared to ALO-02 80 Mg Once Daily and to Oxycontin 40 Mg Twice Daily in Healthy Volunteers

Pfizer1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2012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
Pfizer
入组人数
13
试验地点
1
主要终点
Single-dose administration: Maximum Observed Plasma Concentration (Cmax) of oxycodone

研究概览

简要总结

To characterize the single- and multiple-dose pharmacokinetics of oxycodone following the administration of ALO-02 40 Mg Twice Daily, ALO-02 80 Mg Once Daily or Oxycontin 40 Mg Twice Daily in Healthy Volunteers

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

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.

排除标准

  • Evidence or history of clinically significant diseases.

研究组 & 干预措施

40 mg ALO-02 capsule

Experimental

Single- and multiple-dose of 40 mg ALO-02 capsule under 50 mg naltrexone block

干预措施: ALO-02 (Drug)

40 mg ALO-02 capsule

Experimental

Single- and multiple-dose of 40 mg ALO-02 capsule under 50 mg naltrexone block

干预措施: Naltrexone block (Drug)

80 mg ALO-02 capsule

Experimental

Single- and multiple-dose of 80 mg ALO-02 capsule under 50 mg naltrexone block

干预措施: ALO-02 (Drug)

80 mg ALO-02 capsule

Experimental

Single- and multiple-dose of 80 mg ALO-02 capsule under 50 mg naltrexone block

干预措施: Naltrexone block (Drug)

40 mg OxyContin tablet

Experimental

Single- and multiple-dose of 40 mg OxyContin tablet under 50 mg naltrexone block

干预措施: OxyContin (Drug)

40 mg OxyContin tablet

Experimental

Single- and multiple-dose of 40 mg OxyContin tablet under 50 mg naltrexone block

干预措施: Naltrexone block (Drug)

结局指标

主要结局

Single-dose administration: Maximum Observed Plasma Concentration (Cmax) of oxycodone

时间窗: 0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing

Single-dose administration: Area under the plasma concentration versus time curve from time zero to 24 hours (AUC24) of oxycodone

时间窗: 0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing

Single-dose administration: Time to Reach Maximum Observed Plasma Concentration (Tmax) of oxycodone

时间窗: 0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing

Multiple-dose administration: Area under the plasma concentration versus time curve from time zero to 24 hours (AUC24) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Area under the plasma concentration versus time curve within a dosing interval of τ at steady state (AUCτ) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Maximum plasma concentration at steady state on Day 5 (Cmax,ss) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Minimum plasma concentration at steady state on Day 5 (Cmin,ss) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Average plasma concentration at steady state on Day 5 (Cave,ss) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Time to Reach Maximum Observed Plasma Concentration on Day 5 (Tmax) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Plasma Decay Half-Life (t1/2) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Peak to trough fluctuation at steady state (PTF) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

Multiple-dose administration: Accumulation ratio based on Area Under Curve (AUC) (Rac) of oxycodone, as data permit.

时间窗: 96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing

次要结局

  • Multiple-dose administration: Rac of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Time to Reach Maximum Observed Plasma Concentration (Tmax) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Single-dose administration: Dose normalized Maximum Observed Plasma Concentration (Cmax(dn)) of oxycodone, noroxycodone, and oxymorphone.(0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing)
  • Single-dose administration: Dose-normalized Area under the plasma concentration versus time curve from time zero to 24 hours (AUC24(dn)) of oxycodone, noroxycodone, and oxymorphone.(0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing)
  • Single-dose administration: Maximum Observed Plasma Concentration (Cmax) of noroxycodone and oxymorphone.(0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing)
  • Single-dose administration: Area under the plasma concentration versus time curve from time zero to 24 hours (AUC24) of noroxycodone and oxymorphone.(0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing)
  • Single-dose administration: Time to Reach Maximum Observed Plasma Concentration (Tmax) of noroxycodone and oxymorphone.(0, 1, 2, 4, 6, 8, 12, 14, 16, and 24 hours post Day 1 dosing)
  • Multiple-dose administration: Accumulation ratio (Rac) of oxycodone, as data permit(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Maximum Observed Plasma Concentration (Cmax) of oxycodone, as data permit(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Area under the plasma concentration versus time curve from time zero to 24 hours (AUC24) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Peak to trough fluctuation at steady state (PTF) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Maximum Observed Plasma Concentration (Cmax) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Area under the plasma concentration versus time curve within a dosing interval of τ (AUCτ) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Maximum plasma concentration at steady state (Cmax,ss) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Minimum plasma concentration at steady state (Cmin,ss) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Average plasma concentration at steady state (Cave,ss) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)
  • Multiple-dose administration: Plasma Decay Half-Life (t1/2) of noroxycodone and oxymorphone, as data permit.(96,96.5,97,98,100,102,104,108,108.5,109,110,112,114,116,120,132,144,168 hours post Day 1 dosing)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Pharmacokinetics Study of ALO-02 and OxyContin | 临床试验