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临床试验/NCT01721070
NCT01721070已完成1 期

IAP104 - Assessment of Pharmacokinetic Changes Following Concurrent Administration of Sufentanil NanoTab and Ketoconazole in Healthy Subjects

Talphera, Inc1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2012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
Talphera, Inc
入组人数
19
试验地点
1
主要终点
AUC (0-inf)

研究概览

简要总结

Evaluate the effect of taking ketoconazole on sufentanil plasma concentrations following sublingual administration of sufentanil NanoTab.

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

SUF NT 15 mcg

Experimental

Period 1: One dose of SUF NT 15 mcg administered sublingually. Subjects also received one dose of oral naltrexone 50 mg in the evening before and the morning of each SUF NT dosing to block the opioid effects of the sufentanil.

干预措施: Sufentanil NanoTab (SUF NT) 15 mcg (Drug)

Ketoconazole 400 mg, SUF NT 15 mcg

Experimental

Ketoconazole 400 mg administered once daily for three days. One dose of SUF NT 15 mcg was co-administered sublingually with the third (last) ketoconazole dose.

Subjects also received one dose of oral naltrexone 50 mg in the evening before and the morning of each SUF NT dosing to block the opioid effects of the sufentanil.

干预措施: Ketoconazole 400 mg, sufentanil NanoTab (SUF NT) 15 mcg (Drug)

结局指标

主要结局

AUC (0-inf)

时间窗: 0 (pre-dose), 10, 20, 30, 40, 50, 60, 70, 80, 90, 120, 180, 240, 360, 480, 600, 720, and 840 minutes, and 24 hours after dosing.24 hours

Total amount of sufentanil absorbed; After each dosing of Sufentanil NanoTab, serial blood samples will be taken at regular time points.

Cmax

时间窗: 0 (pre-dose), 10, 20, 30, 40, 50, 60, 70, 80, 90, 120, 180, 240, 360, 480, 600, 720, and 840 minutes, and 24 hours after dosing.

Maximum plasma concentration; After each dosing of Sufentanil NanoTab, serial blood samples will be taken at regular time points.

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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