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临床试验/NCT02117583
NCT02117583已完成1 期

An Open-Label, Randomized, 2-Cohort, Single-Dose, Crossover Study To Estimate The Effects Of Food On Oxycodone Pharmacokinetics Following Oral Administration Of 40 Mg Doses Of Pf 00345439 Formulation K Taken Whole Or After Chewing In Healthy Volunteers

Pain Therapeutics1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2014年4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
入组人数
34
试验地点
1
主要终点
Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - 8)]

研究概览

简要总结

To estimate the effect of food on the pharmacokinetics and relative bioavailability of oxycodone following oral administration of single 40 mg doses of PF 00345439 Formulation K taken whole or after chewing in healthy volunteers. We have described below the two cohorts each with two arms in this crossover study by listing them as four Arms/Groups in order to capture the differences between the cohorts prior to the crossover and after the crossover. 14 participants are planned for the first cohort and 18 participants are planned for the second cohort.

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 18 and 55 years of age

排除标准

  • Evidence or history of clinically significant disease.
  • Positive urine drug test

研究组 & 干预措施

Treatment A

Experimental

Single dose of 40 mg PF-00345439 under naltrexone block (50 mg of naltrexone administered by mouth 12 hours before, 30 minutes before, and 12 hours after study drug administration).

干预措施: Oxycodone (Drug)

Treatment B

Experimental

Single dose of 40 mg PF-00345439 under naltrexone block (50 mg of naltrexone administered by mouth 12 hours before, 30 minutes before, and 12 hours after study drug administration).

干预措施: Oxycodone (Drug)

Treatment C

Experimental

Single dose of 40 mg PF-00345439 under naltrexone block (50 mg of naltrexone administered by mouth 12 hours before, 30 minutes before, and 12 hours after study drug administration).

干预措施: Oxycodone (Drug)

Treatment D

Experimental

Single dose of 40 mg PF-00345439 under naltrexone block (50 mg of naltrexone administered by mouth 12 hours before, 30 minutes before, and 12 hours after study drug administration).

干预措施: Oxycodone (Drug)

结局指标

主要结局

Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - 8)]

时间窗: 0,0.5,1,2,3,4,5,6,8,10,12,16,24,36,48

AUC (0 - 8)= Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0 - 8). It is obtained from AUC (0 - t) plus AUC (t - 8).

Maximum Observed Plasma Concentration (Cmax)

时间窗: 0,0.5,1,2,3,4,5,6,8,10,12,16,24,36,48

次要结局

  • Plasma Decay Half-Life (t1/2)(0,0.5,1,2,3,4,5,6,8,10,12,16,24,36,48)
  • Time to Reach Maximum Observed Plasma Concentration (Tmax)(0,0.5,1,2,3,4,5,6,8,10,12,16,24,36,48)
  • Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast)(0,0.5,1,2,3,4,5,6,8,10,12,16,24,36,48)
  • Concentration at time 24 hours (C24)(0,0.5,1,2,3,4,5,6,8,10,12,16,24,36,48)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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