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临床试验/NCT01761565
NCT01761565已完成1 期

Single- and Multiple-Dose Pharmacokinetics of Sublingual Sufentanil NanoTab® PCA System (Zalviso™) in Healthy Subjects

Talphera, Inc1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2013年1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
Talphera, Inc
入组人数
40
试验地点
1
主要终点
Cmax

研究概览

简要总结

Determine the plasma concentration profile after single and multiple dosing of Sufentanil NanoTabs

研究设计

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

入排标准

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

入选标准

  • Non smoking
  • Ages 18 to 45 year, inclusive
  • BMI between 18 and 30

排除标准

  • Subjects taking any prescription or OTC medications or vitamins or supplements
  • Pregnant females
  • Subjects with pulmonary disease or sleep apnea

研究组 & 干预措施

Single dose of SUF NT 15 mcg then 40 doses of SUF NT 15 mcg

Experimental

Period 1: Single dose of SUF NT 15 mcg

Period 2: 40 consecutive doses of SUF NT 15 mcg taken every 20 minutes

干预措施: Single dose of SUF NT 15 mcg (Drug)

Single dose of SUF NT 15 mcg then 40 doses of SUF NT 15 mcg

Experimental

Period 1: Single dose of SUF NT 15 mcg

Period 2: 40 consecutive doses of SUF NT 15 mcg taken every 20 minutes

干预措施: 40 consecutive doses of SUF NT 15 mcg taken every 20 minutes (Drug)

结局指标

主要结局

Cmax

时间窗: 24 hours in Treatment A, 37 hours in Treatment B

For Treatment A, serial blood samples were taken at 0 (predose), 5, 10, 15, 20, 30, 40, 50, 60, 70, 80, 90, 120, 180, 240, 360, 480, 600, 720, 800, and 840 minutes, and 24 hours after the Sufentanil NanoTab dose on Day 1. For Treatment B, serial blood samples were collected at 0, 20, 120, 240, 360, 480, 600, 720, 760, 780, 785, 790, 795, 800, 810, 820, 830, 840, 850, 860, 870, 900, 960, 1020, 1140, 1260, 1380, 1500, 1580, and 1620 minutes, and 37 hours after the first Sufentanil NanoTab dose on Day 3

CST½

时间窗: 24

the time for plasma concentrations to decrease from Cmax to 50% of Cmax after discontinuation of drug administration

Time to Steady State

时间窗: 24 hours

Steady state, for the cohort, was assessed using Helmert's method (ratio of the geometric mean concentration of each time point to the geometric mean concentrations pooled over all remaining time points, and achieved at the first not-statistically significant time point (i.e., p \>0.05)

次要结局

未报告次要终点

研究者

发起方
Talphera, Inc
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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