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临床试验/NCT01521767
NCT01521767已完成1 期

A Single-Dose Pharmacokinetics And Relative Bioavailability Study Of Tolterodine From Two Microspheres In Powder Blend Extended Release Formulations Compared To The Commercial Extended Release Capsules

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2011年10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
入组人数
16
试验地点
1
主要终点
Maximum Observed Plasma Concentration (Cmax) of tolterodine

研究概览

简要总结

A Single-Dose Pharmacokinetics And Relative Bioavailability Study Of Tolterodine From Two Microspheres In Powder Blend Extended Release Formulations Compared To The Commercial Extended Release Capsules

详细描述

Pharmacokinetics And Relative Bioavailability Study Of Tolterodine From Two Microspheres In Powder Blend Extended Release Formulations Compared To The Commercial Extended Release Capsules

研究设计

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

入排标准

年龄范围
21 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 21 and 55 years, inclusive

排除标准

  • Evidence or history of clinically significant diseases

研究组 & 干预措施

A

Experimental

4 mg tolterodine extended release capsules, administered with water and under fasting condition.

干预措施: tolterodine tartrate (Drug)

B

Experimental

4 mg microspheres in powder blend release rate 2 (MPB-RR2), administered without water and under fasting condition.

干预措施: tolterodine tartrate (Drug)

C

Experimental

4 mg microspheres in powder blend release rate 1 (MPB-RR1), administered without water and under fasting condition.

干预措施: tolterodine tartrate (Drug)

D

Experimental

4 mg MPB-RR1, administered without water and under fed condition.

干预措施: tolterodine tartrate (Drug)

E

Experimental

4 mg MPB-RR1, administered with water and under fasting condition.

干预措施: tolterodine tartrate (Drug)

结局指标

主要结局

Maximum Observed Plasma Concentration (Cmax) of tolterodine

时间窗: 0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose

Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) of tolterodine

时间窗: 0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose

次要结局

  • Plasma Decay Half-Life (t1/2) of tolterodine(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - ∞)] of 5-HMT(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Maximum Observed Plasma Concentration (Cmax) of 5-HMT(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Time to Reach Maximum Observed Plasma Concentration (Tmax) of 5-HMT(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - ∞)] of tolterodine.(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) of 5-HMT(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Time to Reach Maximum Observed Plasma Concentration (Tmax) of tolterodine(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)
  • Plasma Decay Half-Life (t1/2) of 5-HMT(0, 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 16, 24, 30, 36 hours post-dose)

研究者

发起方
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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