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临床试验/NCT01195324
NCT01195324已完成1 期

An Open-Label Drug Interaction Study to Assess the Pharmacokinetics and Pharmacodynamics of Warfarin When Administered Alone and in Combination With Multiple-Dose JNJ-28431754 (Canagliflozin) in Healthy Male and Female Subjects

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.0 个研究点目标入组 14 人开始时间: 2010年9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
14
主要终点
Plasma concentrations of canagliflozin

研究概览

简要总结

The purpose of the study is to assess the effect of multiple oral doses of canagliflozin on a single oral dose of warfarin.

详细描述

This is an open-label (volunteers will know the names of treatments they are assigned) single-center study of canagliflozin (JNJ-28431754) and warfarin in healthy adult volunteers. Canagliflozin is a drug currently under development to lower blood sugar levels in patients with type 2 diabetes mellitus and warfarin is an approved anticoagulant (ie, a drug that stops blood from clotting). After an overnight fast (without eating food) of at least 10 hours, volunteers will receive Sequence 1 (canagliflozin 300 mg, orally, once daily on Days 1-12 with a single, oral 30 mg dose of warfarin on Day 6 [Treatment A] followed 14 days later by a single, oral 30 mg dose of warfarin on Day 1 [Treatment B]) OR Sequence 2 (Treatment B followed 14 days later by Treatment A).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
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 volunteers with a body mass index between 18 and 30 kg/m

排除标准

  • Any blood coagulation disorder determined to be clinically relevant by the Investigator
  • Medications known to affect coagulation taken within 7 to 14 days of study entry

研究组 & 干预措施

001

Experimental

Canagliflozin/Warfarin Treatment A: Tablets oral canagliflozin 300 mg once daily for 12 days and canagliflozin 300 mg + warfarin 30 mg single dose on Day 6 followed 14 days later by Treatment B: Tablets oral warfarin 30 mg single dose on Day 1

干预措施: Canagliflozin/Warfarin (Drug)

002

Experimental

Canagliflozin/Warfarin Treatment B: Tablets oral warfarin 30 mg single dose on Day 1 followed 14 days later by Treatment A: Tablets oral canagliflozin 300 mg once daily for 12 days and canagliflozin 300 mg + warfarin 30 mg single dose on Day 6

干预措施: Canagliflozin/Warfarin (Drug)

结局指标

主要结局

Plasma concentrations of canagliflozin

时间窗: At protocol-specified times during Treatment A on Days 1 through 12.

Plasma concentrations of warfarin

时间窗: At protocol specified times during Treatment B on Days 1 through 8

Measurement of Prothrombin time (PT) to assess the international normalized ratio (INR)

时间窗: At protocol-specified times during Treatment A on Days 6 through 13

Measurement of PT to assess the INR

时间窗: At protocol-specified time points during Treatment B on Days 1 through 8

次要结局

  • The number and type of adverse events reported(Day 1 of Treatment B through 10 days after Day 13 of Treatment A)

研究者

申办方类型
Industry
责任方
Sponsor

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