THCV Treatment for Smokers
2026年8月3日 更新者:Lara Ray, PhD、University of California, Los Angeles
Development of Tetrahydrocannabivarin as a Treatment for Smokers
This study will randomize 32 non-treatment-seeking individuals who smoke cigarettes daily into a randomized, crossover, double-blind, placebo-controlled study testing the safety, tolerability, and initial efficacy of Δ9-tetrahydrocannabivarin (Δ9-THCV).
研究概览
地位
尚未招聘
详细说明
The objective of this study is to examine the safety, tolerability, and initial efficacy of Δ9-tetrahydrocannabivarin (Δ9-THCV) in daily smokers.
We will randomize 32 non-treatment-seeking adults who smoke cigarettes daily (50% female) into a randomized, double-blind, placebo-controlled, counter-balanced, within-subject human laboratory study of Δ9-THCV (10 mg oral) and matched placebo.
Specifically, participants will complete two 5-day outpatient medication periods, with a 14-day washout period in between, during which they will receive either Δ9-THCV or placebo in a counter-balanced order, such that all participants will complete both medication conditions across the study.
Following each 5-day medication period, participants will complete a laboratory study visit during which they will undergo the McKee Smoking Lapse Task to assess the ability to resist smoking, cigarette self-administration, craving, withdrawal, and subjective effects of nicotine.
Total study participation will be approximately 4 weeks.
研究类型
介入性
注册 (估计的)
32
阶段
- 阶段2
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。
学习联系方式
- 姓名:Jessica Jenkins, MS
- 电话号码:310-206-6756
- 邮箱:jenkinsj@ucla.edu
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
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Be between the ages of 21 and 65;
- Smoke 10 or more combustible cigarettes per day;
- Have fewer than 3 months of smoking abstinence in the past year;
- Has self-reported ≥10 lifetime uses of cannabis products;
- Have self-reported recent (past 3-month) use of cannabis products;
- Agree to abstain from all other cannabinoid use during the study;
- Agree to abstain from all other medication use during the study, other than methods of birth control as listed in inclusion criteria for female participants;
- Agree to one of the following methods of birth control (if female), unless she or partner are surgically sterile: oral contraceptives, Contraceptive sponge, patch, double barrier, intrauterine contraceptive device, etonogestrel implant, medroxyprogesterone acetate contraceptive injection, hormonal vaginal contraceptive ring, complete abstinence from sexual intercourse.
Exclusion Criteria:
- Have current (last 12 months) DSM-5 diagnosis of substance use disorder for any psychoactive substances other than nicotine;
- Have a lifetime DSM-5 diagnosis of schizophrenia, bipolar disorder, or any other psychotic disorder;
- Have a score of 3 or greater on the Columbia Suicide Severity Rating Scale (C-SSRS) at screening or anytime during study participation;
- Have a positive urine screen for any substances, including cannabis
- Have a breathalyzer reading above 0.000 g/dl;
- Be pregnant, nursing, or planning to become pregnant while taking part in the study;
- Have a medical condition that may interfere with safe study participation;
- Have clinically significant abnormalities on the EKG;
- Have evidence of renal impairment, defined by an eGFR value of <90 ml/min;
- Have evidence of hepatic impairment, defined by a score of ≥5 points on the Child-Pugh assessment of liver function;
- Exceed Grade 2 laboratory or vital sign abnormalities, based on FDA Guidance Document "Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials";
- Have past month use of cannabis or cannabis products;
- Have past month use of electronic nicotine delivery system (ENDS);
- Have use of any medications (other than methods of birth control as listed in inclusion criteria for female participants) within 14 days or 5 half-lives (whichever is longer) prior to study drug administration, and throughout the study, including medication for smoking cessation, any prescription, OTC, dietary supplements, herbal products, or vitamins;
- Have any other circumstances that, in the opinion of the investigators, would not be a good fit for study participation.
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:治疗
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Δ9-THCV first, then placebo.
Participants will first take a 10mg Δ9-THCV gummy once a day for 5 days.
After a 14-day washout period, participants will take a matched placebo gummy (0mg Δ9-THCV) once a day for 5 days.
|
10mg Δ9-Tetrahydrocannabivarin oral gummy
Matched Placebo (oral gummy, 0mg Δ9-Tetrahydrocannabivarin)
|
|
实验性的:Placebo first, then THCV
Participants will take a placebo gummy (0mg Δ9-THCV) once a day for 5 days.
After a 14-day washout period, participants will take a 10mg Δ9-THCV gummy once a day for 5 days.
|
10mg Δ9-Tetrahydrocannabivarin oral gummy
Matched Placebo (oral gummy, 0mg Δ9-Tetrahydrocannabivarin)
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Latency to initiate smoking
大体时间:Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
Participants will complete the McKee Smoking Lapse Task following overnight abstinence to assess the effects of oral Δ9-THCV (10 mg), compared with placebo, on the ability to resist smoking.
The primary outcome is latency to initiate smoking during the 50-minute delay period, defined as the number of minutes participants delay smoking their first cigarette (range: 0-50 minutes).
|
Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
|
Number of cigarettes smoked during self-administration
大体时间:Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
Participants will complete the McKee Smoking Lapse Task following overnight abstinence to assess the effects of oral Δ9-THCV (10 mg), compared with placebo, on cigarette self-administration.
The outcome is the number of cigarettes smoked during the 60-minute self-administration period of the task (no set range).
|
Assessed during each 5-day medication condition, following overnight abstinence on Day 5
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Questionnaire of Smoking Urges-Brief total score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
Participants will complete the 10-item Questionnaire of Smoking Urges-Brief (QSU-Brief) during the McKee Smoking Lapse Task to assess cigarette craving.
The QSU-Brief assesses urges and cravings using a 7-point Likert response scale, with higher scores indicating greater craving (range: 10-70).
Cue-induced cigarette craving in response to cigarette (vs.
neutral) cues will be calculated and compared between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
|
Minnesota Nicotine Withdrawal Scale score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
Participants will complete ratings of nicotine withdrawal following overnight abstinence using the 8-item Minnesota Nicotine Withdrawal Scale (MNWS), with higher values indicating more severe withdrawal (range: 0-32).
Differences in MNWS scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence
|
|
Modified Cigarette Evaluation Questionnaire satisfaction score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess satisfaction associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The satisfaction subscale score is calculated as the sum of Items 1, 2, and 12 (range: 3-21).
Differences in satisfaction scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire psychological reward score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess psychological reward associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The psychological reward subscale score is calculated as the sum of Items 4, 5, 6, 7, 8 (range: 5-35).
Differences in psychological reward scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire nausea/dizziness score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess nausea and dizziness associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The nausea/dizziness subscale score is calculated as the sum of Items 9 and 10 (range: 2-14).
Differences in nausea/dizziness scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire craving relief score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess craving relief associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The craving relief subscale score is based on Item 11 (range: 1-7).
Differences in craving relief scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
|
Modified Cigarette Evaluation Questionnaire enjoyment of airway sensations score
大体时间:Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
Participants will complete the 12-item Modified Cigarette Evaluation Questionnaire (mCEQ) during the cigarette self-administration period of the McKee Smoking Lapse Task to assess the enjoyment of airway sensations associated with smoking.
Items are rated on a 7-point scale, with higher scores indicating greater endorsement.
The enjoyment of airway sensations subscale score is based on Item 3 (range: 1-7).
Differences in enjoyment of airway sensations scores will be evaluated between the Δ9-THCV and placebo conditions.
|
Assessed during each 5-day medication condition during the Day 5 laboratory session following overnight abstinence.
|
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。
调查人员
- 首席研究员:Lara A Ray, PhD、University of California, Los Angeles
- 首席研究员:Erica N Grodin, PhD、University of California, Los Angeles
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 (估计的)
2026年10月1日
初级完成 (估计的)
2028年5月31日
研究完成 (估计的)
2028年5月31日
研究注册日期
首次提交
2026年5月26日
首先提交符合 QC 标准的
2026年6月2日
首次发布 (实际的)
2026年6月9日
研究记录更新
最后更新发布 (实际的)
2026年8月4日
上次提交的符合 QC 标准的更新
2026年8月3日
最后验证
2026年8月1日
更多信息
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