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临床试验/NCT07758231
NCT07758231尚未招募1 期

Impact of GLP-1 Receptor Agonist Therapy on Alcohol Pharmacokinetics

University of Wisconsin, Madison1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2026年10月1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
尚未招募
入组人数
5
试验地点
1
主要终点
Maximum Ethanol Concentration (Cmax)

研究概览

简要总结

This study is to learn how the weight loss drug tirzepatide (Zepbound) changes the way a body handles alcohol. 5 participants aged 21-55 who take Zepbound will be enrolled and can expect to be on study for up to 4 weeks.

详细描述

Participants will:

  • Arrive to study visit in a fasted state
  • Provide blood, breath, and urine samples prior to intervention
  • Complete baseline cognitive assessments
  • Self-administer the intervention (time 0), followed by breakfast (time 30 minutes)
  • Complete subjective and cognitive assessments throughout treatment visit
  • Provide blood, breath, and urine samples throughout treatment visit
  • Consume lunch 260 minutes after dosing
  • Complete study visit at 360 minutes
  • Complete a final study survey

Primary Objective: Characterize the pharmacokinetics of ethanol in participants receiving maintenance Glucagon-like peptide-1 (GLP-1) receptor agonist (RA) therapy (tirzepatide).

Secondary Objectives:

- Determine the effects of GLP-1 RA therapy on alcohol-induced impairment, as measured by

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
21 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • At least 21 years of age, no older than 55 years of age
  • BMI 30-45 kg/m2
  • Taking stable dose of prescribed, branded tirzepatide for at least 28 days
  • Self-reported regular alcohol consumption
  • Good mental health as determined by self-reported responses to the Psychopathology Screener and review by Study Physician as necessary
  • Absence of any major medical, cardiovascular, endocrine, and neurological condition as determined by self-reported responses to the Medical History Screener
  • In possession of a valid drivers' license with at least two years of driving experience
  • English-speaking (able to provide consent and complete questionnaires)
  • Written Informed Consent

排除标准

  • AUDIT score of >8 requires Study Physician review
  • Use of compounded GLP-1 RA
  • History of or current substance use disorder as determined by self-reported responses to the Internalizing, Externalizing, and Substance Use Disorder Screener, Drug Use Disorders Identification Test, Alcohol Use Disorder Identification Test
  • Pregnancy or lactation (pregnancy test, if needed)
  • Use of medications that may impact cognitive ability or potentiate alcohol (e.g., mood stabilizers, sedatives)
  • Use of medications that are known to significantly delay gastric emptying as determined by Study Physician
  • History of pancreatitis, severe gastroparesis, or personal or family history of medullary thyroid or multiple endocrine neoplasia syndrome type 2

研究组 & 干预措施

Healthy adults on Tirzepatide

Experimental

Participants will complete a screening and enrollment visit, one study visit, and a follow-up correspondence over the course of approximately 4 weeks.

干预措施: Acute Ethanol Dose (Drug)

结局指标

主要结局

Maximum Ethanol Concentration (Cmax)

时间窗: prior to dosing (-25 minutes), start of dosing (0 minutes), 15 minutes, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes, 180 minutes, 240 minutes, 300 minutes, 350 minutes

Cmax will be determined from visual inspection of the concentration-time plots.

Time to Maximum Ethanol Concentration (Tmax)

时间窗: prior to dosing (-25 minutes), start of dosing (0 minutes), 15 minutes, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes, 180 minutes, 240 minutes, 300 minutes, 350 minutes

Tmax will be determined from visual inspection of the concentration-time plots.

Ethanol Elimination Rate: Blood samples

时间窗: prior to dosing (-25 minutes), start of dosing (0 minutes), 15 minutes, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes, 180 minutes, 240 minutes, 300 minutes, 350 minutes

Data derived from blood samples.

Ethanol Elimination Rate: Breath tests

时间窗: prior to dosing (-25 minutes), 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes, 180 minutes, 240 minutes, 300 minutes, 350 minutes

Data derived from breath alcohol test.

Ethanol Elimination Rate: Urine samples

时间窗: prior to dosing (-25 minutes), 60 minutes, 120 minutes, 180 minutes, 240 minutes, 300 minutes

Data derived from urine samples.

次要结局

  • Biphasic Alcohol Effects Scale (BAES) Score(5 minutes, 35 minutes, 65 minutes, 95 minutes, 125 minutes, 185 minutes, 245 minutes, 290 minutes, 340 minutes)
  • Risk Perception and Safety Appraisal (RPSA) Score(5 minutes, 35 minutes, 65 minutes, 95 minutes, 125 minutes, 185 minutes, 245 minutes, 290 minutes, 340 minutes)
  • Divided Attention Task (DAT)(prior to dosing (-20 minutes), 10 minutes, 100 minutes, 220 minutes)
  • Digital Symbol Substitution Task (DSST)(prior to dosing (-20 minutes), 10 minutes, 100 minutes, 220 minutes)
  • Paced Serial Addition Task (PSAT)(prior to dosing (-20 minutes), 10 minutes, 100 minutes, 220 minutes)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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