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临床试验/NCT02272764
NCT02272764已完成1 期

A Phase 1 Study of the Effects of Itraconazole on the Pharmacokinetics of ALKS 5461 in Healthy Volunteers

Alkermes, Inc.1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2014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
入组人数
24
试验地点
1
主要终点
Drug-Drug Interaction - AUC0-t

研究概览

简要总结

This study will evaluate the impact of Itraconazole on the pharmacokinetics of ALKS 5461.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Has a body mass index (BMI) of 18.0 - 30.0 kg/m2
  • Is in good physical health
  • Agrees to use an approved method of contraception for the duration of the study
  • Additional criteria may apply

排除标准

  • Has current evidence, or history of any clinically significant medical or psychiatric condition or observed abnormality
  • Is currently pregnant or breastfeeding
  • Has a history of or current infection with hepatitis B virus, hepatitis C virus, or human immunodeficiency virus (HIV)
  • Has a lifetime history of opioid abuse or dependence
  • Has current abuse or dependence on alcohol or any drugs
  • Has used nicotine within 90 days prior to randomization
  • Additional criteria may apply

研究组 & 干预措施

Itraconazole

Other

Itraconazole or placebo

干预措施: Itraconazole (Drug)

ALKS 5461

Experimental

ALKS 5461 or placebo Sublingual tablet

干预措施: ALKS 5461 (Drug)

结局指标

主要结局

Drug-Drug Interaction - AUC0-t

时间窗: Up to 48 hours

Area under the concentration time curve from time zero to the last measureable time point (AUC0-t) of ALKS 5461 in the presence and absence of itraconazole

Drug-Drug Interaction - AUC0-inf

时间窗: Up to 48 hours

Area under the concentration time curve from time zero to infinity (AUC0-inf) of ALKS 5461 in the presence and absence of itraconazole

Drug-Drug Interaction - Cmax

时间窗: Up to 48 hours

Maximum plasma concentration (Cmax) of ALKS 5461 in the presence and absence of itraconazole

次要结局

  • Safety and tolerability will be measured by incidence of adverse events(Up to 32 Days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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