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临床试验/NCT02218021
NCT02218021已完成1 期

A Randomized, Double-Blind, Placebo- and Positive-Controlled, Crossover Study to Evaluate the Abuse Potential and Safety of Orally Administered Samidorphan in Non-Dependent Recreational Opioid Users

Alkermes, Inc.1 个研究点 分布在 1 个国家目标入组 59 人开始时间: 2014年8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
59
试验地点
1
主要终点
Pharmacodynamics: Abuse potential measured by visual analog scales (VAS)

研究概览

简要总结

The purpose of this study is to evaluate the abuse potential and safety of samidorphan in healthy, non-dependent, adult, recreational opioid users.

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
Double (Participant, Investigator)

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

  • Be in good general physical health
  • Body mass index of 18-34 kg/m2, inclusive with minimum weight of 50 kg
  • Recreational opioid use experience for non-therapeutic purposes (at >/= 10 times in lifetime and >/= 1 in previous 3 months
  • Agree to use an approved method of birth control for the duration of the study
  • Additional criteria may apply

排除标准

  • Currently pregnant or breastfeeding
  • History of or current infection with hepatitis B virus, hepatitis C virus or HIV
  • Current or history of any clinically significant medical or psychiatric condition
  • Current or history of in the last 2 years of dependence on alcohol or any illicit drugs
  • Have used any prescription or over-the-counter medication, including natural health products (with the exception of prescription birth control or hormonal replacements, acetaminophen, ibuprofen, or multivitamins) within 14 days
  • Have a history of intolerance or hypersensitivity to opioid antagonists, opioid agonists or related drugs (eg, naltrexone, naloxone, oxycodone, morphine)
  • Additional criteria may apply

研究组 & 干预措施

Samidorphan Dose 2

Experimental

干预措施: Samidorphan (Drug)

Samidorphan Dose 3

Experimental

干预措施: Samidorphan (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

Oxycodone Dose 1

Active Comparator

干预措施: Oxycodone (Drug)

Oxycodone Dose 2

Active Comparator

干预措施: Oxycodone (Drug)

Samidorphan Dose 1

Experimental

干预措施: Samidorphan (Drug)

结局指标

主要结局

Pharmacodynamics: Abuse potential measured by visual analog scales (VAS)

时间窗: Approximately 4 weeks

次要结局

  • Safety: Incidence of adverse events (AEs)(Approximately 5.5 weeks)
  • Pharmacokinetics: Plasma concentrations of samidorphan and metabolite(Approximately 4 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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