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临床试验/NCT06692933
NCT06692933招募中1 期

Effects of a Hemp Product on the Pharmacokinetics and Pharmacodynamics of Clopidogrel

Washington State University1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2024年6月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
24
试验地点
1
主要终点
AUC ratio of clopidogrel active metabolite

研究概览

简要总结

The goal of this clinical trial is to determine how two different doses of cannabidiol (CBD), given as a hemp product, change the blood concentrations of the drug clopidogrel in the body. Results will be used to help design future studies and to assist healthcare providers in informing their patients about the safe use of CBD.

详细描述

The popularity of cannabis products has grown exponentially over the past decade as several states continue to decriminalize or legalize recreational and/or medicinal use. Cannabis contains >500 phytoconstituents, including >100 cannabinoids. The most well-studied cannabinoids are tetrahydrocannabinol (THC) and cannabidiol (CBD). Although both are psychoactive, THC produces the characteristic "high," while CBD does not. CBD is available as a prescription drug (Epidiolex®) to treat seizure disorders. Hemp, a popular CBD-containing botanical product, is defined as containing <0.3% THC. Hemp was federally legalized in the United States in 2018 following passage of the Farm Bill. Since passage of that bill, hemp and other CBD-containing products have become widely available over the counter. As such, hemp/CBD products have become top-selling botanicals, with sales projected to reach nearly $4.5 billion by 2024. Common uses include self-treatment for pain, anxiety, and sleep disorders.

Despite increasing use of cannabis products, the pharmacokinetic interaction potential with pharmaceutical medications remains understudied. Previous pharmacokinetic studies have yielded convincing evidence that CBD significantly inhibits the activity of the drug metabolizing enzyme cytochrome P450 (CYP) 2C19. Despite the valuable information generated by these and numerous other studies, several unanswered questions about CBD-containing products remain:

  1. Do real-world doses and dosing regimens of CBD (< 300 mg) have similar CYP interaction potential as that of higher doses investigated in previous pharmacokinetic studies?
  2. What are the effects of CBD on high-impact CYP2C19 substrates, such as the anti-platelet drug clopidogrel (Plavix®)?
  3. Does chronic administration of a real-world dose of CBD have similar interaction potential as a very high single dose of CBD?

The primary objective of the proposed study is to evaluate the effects of a well-characterized, widely used hemp product on the pharmacokinetics of the commonly prescribed CYP2C19 substrate clopidogrel (Plavix®) in healthy adult participants who are confirmed to be CYP2C19 normal, rapid, or ultra-rapid metabolizers. Results could be used to inform a future study design involving elderly people, which is a population of interest. Results could also be used to guide healthcare providers in helping their patients make informed decisions about the safe use of hemp

研究设计

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

入排标准

年龄范围
21 Years 至 64 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •21-64 years old and healthy;
  • •Confirmed by genetic test to be a CYP2C19 normal, rapid, or ultra-rapid metabolizer;
  • •Not taking any medications (prescription and non-prescription, including clopidogrel) or dietary supplements/botanical products known to alter the pharmacokinetics of cannabis and/or clopidogrel;
  • •Have taken hemp or cannabis (in any form) before and tolerated it well;
  • •Willing to abstain from consuming dietary supplements/botanical products and citrus juices for the duration of the study;
  • •Willing to abstain from cannabis/marijuana, hemp, THC- and/or CBD-containing products for several weeks;
  • •Willing to abstain from consuming caffeinated beverages or other caffeine-containing products the evening before and morning of any inpatient day;
  • •Willing to abstain from consuming alcoholic beverages for one day prior to any inpatient day;
  • •Willing to use a secondary method of birth control that does not include the introduction or discontinuance of hormonal-based birth control (such as abstinence, copper IUD, or condoms), continuing for 1 week after completing the study;
  • •Have the ability to and are willing to comply with the requirements of the study;
  • •Geographically located within a 40-mile radius of Spokane and have the time to participate and;
  • •Can read and speak English

排除标准

  • •Under the age of 21 or over the age of 64;
  • •Any major illness;
  • •Pregnant or nursing;
  • •History of allergy or intolerance to cannabis or clopidogrel;
  • •Taking concomitant medications, both prescription and non-prescription (including clopidogrel) or dietary supplements/botanical products known to alter the pharmacokinetics of cannabis and/or clopidogrel;
  • •Never taken cannabis (in any form) before;
  • •Presence of a condition or abnormality that, in the opinion of the Investigator, would compromise participant safety or the quality of the data;
  • •Currently using or have recently used drugs or other illicit substances for recreational purposes;
  • •Have used cannabis/marijuana, hemp, THC- and/or CBD-containing products within the last 4 weeks;
  • •Have an out-of-range clinical laboratory value such that the study physician considers participation in the study a health risk, or;
  • •Unable to read and speak English

研究组 & 干预措施

Arm 2: chronic hemp (30 mg CBD) + clopidogrel

Experimental

Participants will self-administer a single low dose of hemp (30 mg CBD) as an oral softgel at home daily for 5 consecutive days. On day 6, participants will return to the research setting, where they will be administered a single low dose of hemp (30 mg CBD) and a single oral dose of clopidogrel (75 mg). Blood will be collected for 72 hours and urine will be collected for 24 hours.

干预措施: Clopidogrel (Drug)

Arm 3: chronic hemp (240 mg CBD) + clopidogrel

Experimental

Participants will repeat the Arm 2 procedures using a higher dose of hemp (240 mg CBD)

干预措施: Clopidogrel (Drug)

Arm 3: chronic hemp (240 mg CBD) + clopidogrel

Experimental

Participants will repeat the Arm 2 procedures using a higher dose of hemp (240 mg CBD)

干预措施: Cannabidiol in the form of hemp (Drug)

Arm 2: chronic hemp (30 mg CBD) + clopidogrel

Experimental

Participants will self-administer a single low dose of hemp (30 mg CBD) as an oral softgel at home daily for 5 consecutive days. On day 6, participants will return to the research setting, where they will be administered a single low dose of hemp (30 mg CBD) and a single oral dose of clopidogrel (75 mg). Blood will be collected for 72 hours and urine will be collected for 24 hours.

干预措施: Cannabidiol in the form of hemp (Drug)

Arm 1: clopidogrel alone

Experimental

Participants will be administered a single oral dose (75 mg) of clopidogrel. Blood and urine will be collected for 24 hours.

干预措施: Clopidogrel (Drug)

结局指标

主要结局

AUC ratio of clopidogrel active metabolite

时间窗: 0-24 hours

Ratio of the area under the plasma concentration vs. time curve of the active metabolite of clopidogrel in the presence to absence of hemp

次要结局

  • Cannabidiol AUC(0-72 hours)
  • AUC of cannabidiol metabolites(0-72 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mary Paine

Professor

Washington State University

研究点 (1)

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