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Effects of Rifampicin on the Pharmacokinetics and Pharmacodynamics of Sublingual and Intravenous Buprenorphine

2014年11月19日 更新者:Mari Fihlman、Turku University Hospital

Effects of Rifampicin on the Pharmacokinetics and Pharmacodynamics of Sublingual and Intravenous Buprenorphine: A Four-phase Cross-over Study in Healthy Subjects.

This study is aimed to examine the possible interactions of sublingual and intravenous buprenorphine with rifampicin.

研究概览

详细说明

Variability in drug response can be due to either pharmacokinetic or pharmacodynamic factors. The reasons why people differ in pharmacokinetics or pharmacodynamics are manifold and include, e.g., genetic factors, diseases, age and concomitantly administered drugs. Oxidation reactions are dominant in the metabolism of drugs and cytochrome P-450 enzymes (CYP) have been recognized as chief contributors. We have previously shown that drug interactions mediated by the inhibition of CYP enzymes may be of major clinical significance.Buprenorphine is a semisynthetic partial µ-opioid receptor agonist. In low doses, it is used in the treatment of moderate acute and chronic pain whereas in high doses, it is used in the management of opioid withdrawal symptoms and opioid addiction. It has high affinity for the µ-opioid receptor and its analgesic efficacy is 20-40 times that of morphine. It acts as an antagonist at the myy-opioid receptor and as an agonist at the myy-opioid receptor and opioid-like receptor (ORL-1).

Buprenorphine undergoes extensive first-pass metabolism and has low oral bioavailability of 15 %. Bioavailability following sublingual administration of buprenorphine is higher, 50-60 %. After high sublingual doses of buprenorphine (8-24 mg), peak plasma concentrations are reached in 1 hour and after low sublingual doses (0.4 mg) they are reached in approximately 3 h. Approximately two-thirds of a buprenorphine dose is excreted unchanged, and the rest is metabolized in the liver and intestinal wall. N-dealkylation of buprenorphine mainly via CYP3A but also CYP2C8 yields norbuprenorphine, and glucuronidation yields buprenorphine-3-glucuronide. Norbuprenorphine is excreted in the urine after subsequent conjugation. 80-90 % of buprenorphine is excreted by the biliary system and enterohepatic circulation.Although few interaction studies of high-dose buprenorphine and antiretrovirals have been conducted, the effect of CYP3A inducers on the pharmacokinetics of low-dose buprenorphine is unknown. Because the use of buprenorphine in pain management is increasing after the introduction of transdermal buprenorphin patches to the market, it is clinically relevant to study and quantify possible interactions of buprenorphine with inducers of its CYP3A-mediated metabolism such as rifampicin.

研究类型

介入性

注册 (实际的)

12

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Turku、芬兰、20500
        • Turku University Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 40年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • non-smoking
  • aged 18-40 years
  • body weights within ±15% of the ideal weight for height

Exclusion Criteria

  • A previous history of intolerance to the study drugs or to related compounds and additives.
  • Concomitant drug therapy of any kind for at least 14 days prior to the study.
  • Subjects younger than 18 years and older than 40 years.
  • Existing or recent significant disease.
  • History of hematological, endocrine, metabolic or gastrointestinal disease, including gut motility disorders.
  • History of asthma or any kind of drug allergy.
  • Previous or present alcoholism, drug abuse, psychological or other emotional problems that are likely to invalidate informed consent, or limit the ability of the subject to comply with the protocol requirements.
  • A positive test result for urine toxicology.
  • A "yes" answer to any one of the Abuse Questions.
  • Pregnancy or nursing.
  • Donation of blood for 4 weeks prior and during the study.
  • Special diet or life style conditions which would compromise the conditions of the study or interpretation of the results.
  • Participation in any other studies involving investigational or marketed drug products concomitantly or within one month prior to the entry into this study.
  • Smoking for one month before the start of the study and during the whole study period.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
有源比较器:Rifampicin
The volunteers will be given oral rifampicin (Rimapen, Orion, Finland) 600 mg as a single daily dose at 20.00 for 7 days
The volunteers will be given oral rifampicin (Rimapen, Orion, Finland) 600 mg as a single daily dose at 20.00 for 7 days
安慰剂比较:Placebo
The volunteers will be given oral placebo at 20.00 for 7 days
The volunteers will be given Oral placebo at 20.00 for 7 days [Phase 1 ]
有源比较器:Buprenorphine
The volunteers will be given single dose of 0,4 mg intra venous buprenorphine or 0,6 mg sublingual buprenorphine on day 5.
The volunteers will be given single dose of 0,4 mg intra venous buprenorphine or 0,6 mg sublingual buprenorphine on day 5.
其他名称:
  • Temgesic 0,2 mg resoriblet
  • Temgesic 0,3 mg/ml

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Concentration of buprenorphine and its metabolites in plasma and urine concebtration of buprenorphine
大体时间:0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12 and 20 hours after administration of buprenorphine
0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12 and 20 hours after administration of buprenorphine

次要结果测量

结果测量
措施说明
大体时间
Pharmacodynamic effects
大体时间:1, 2,3, 4, 5, 6, 8, 10, 12, 20 hours after administration of buprenorphine
The psychomotor effects on bubrenorphine will be assessed with the measurement of pupil size, Maddox wing test and symbol substitution test.
1, 2,3, 4, 5, 6, 8, 10, 12, 20 hours after administration of buprenorphine
Analgesia
大体时间:1, 2, 3, 4, 5, 6, 8, 10, 12 hours after the administration of buprenorphine
The analgesic effect of buprenorphine will be evaluated using the cold pressor test. The cold pain test has been shown to be sensitive to opioid analgesia, and it enables repeated assessments of cold pain threshold, tolerance, intensity and unpleasantness
1, 2, 3, 4, 5, 6, 8, 10, 12 hours after the administration of buprenorphine

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2013年4月1日

初级完成 (实际的)

2014年11月1日

研究完成 (实际的)

2014年11月1日

研究注册日期

首次提交

2013年4月27日

首先提交符合 QC 标准的

2013年5月12日

首次发布 (估计)

2013年5月15日

研究记录更新

最后更新发布 (估计)

2014年11月20日

上次提交的符合 QC 标准的更新

2014年11月19日

最后验证

2014年11月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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