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Semaglutide for Nicotine Addiction
Phase 2
Waitlist Available
Led By Christian Hendershot, PhD
Research Sponsored by University of North Carolina, Chapel Hill
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (week 0) to study endpoint (week 10)
Summary
This trial is testing a medication to help smokers quit by reducing cravings for nicotine. The study will involve smokers who are addicted to nicotine and will measure their smoking behavior after using the medication.
Who is the study for?
This trial is for adults aged 21-65 who smoke at least 5 cigarettes daily over the past year without a break of more than 90 days. Participants must have moderate nicotine dependence, be motivated to quit within the next 3-18 months, and willing to take study medication and attend lab sessions involving smoking. Exclusions include those with diabetes, certain medical conditions or histories (like cancer), uncontrolled blood pressure, extreme BMI values, use of conflicting medications or substances, and women who are pregnant or not using effective contraception.
What is being tested?
The trial tests Semaglutide's effects on nicotine intake among smokers. It's a double-blind study where participants won't know if they're getting Semaglutide or a placebo. The goal is to see if this drug can help reduce cigarette consumption by affecting biological mechanisms related to addiction.
What are the potential side effects?
While specific side effects for this trial aren't listed, common ones for Semaglutide may include nausea, vomiting, diarrhea, abdominal pain and constipation. There could also be potential allergic reactions in those sensitive to the medication.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline (week 0) to study endpoint (week 10)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (week 0) to study endpoint (week 10)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Nicotine Reinstatement Duration
Change in Nicotine Self-Administration
Secondary study objectives
Change in Daily Cigarette Smoking
Other study objectives
Change in Body Weight
Change in Cigarette Craving
Body Weight Changes
+1 moreSide effects data
From 2020 Phase 4 trial • 104 Patients • NCT0418984821%
Nausea
12%
Decreased Appetite
100%
80%
60%
40%
20%
0%
Study treatment Arm
Overall Study
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: SemaglutideExperimental Treatment1 Intervention
Participants will receive semaglutide via subcutaneous injections at escalating doses (0.25mg to 1.0mg) over 9 weeks.
Group II: Sham/PlaceboPlacebo Group1 Intervention
Participants will receive sham subcutaneous injections over 9 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Semaglutide
2021
Completed Phase 4
~5160
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Tobacco Use Disorder include bupropion, nicotine replacement therapy (NRT), varenicline, and GLP-1 receptor agonists. Bupropion is an antidepressant that inhibits the reuptake of norepinephrine and dopamine, reducing withdrawal symptoms and the urge to smoke.
NRT provides a controlled dose of nicotine to ease withdrawal symptoms and reduce cravings. Varenicline is a selective nicotinic acetylcholine receptor agonist that reduces cravings and withdrawal symptoms by partially stimulating nicotine receptors and blocking nicotine from binding.
GLP-1 receptor agonists, like semaglutide, are being studied for their potential to reduce nicotine intake and prevent relapse by modulating reward pathways in the brain. Understanding these mechanisms is crucial for patients as it helps tailor treatment plans to individual needs, improving the chances of successful smoking cessation.
The Effects of Smoking Cessation on Diabetes Mellitus Patients.A review of tobacco use treatments in U.S. ethnic minority populations.A randomized trial of bupropion and/or nicotine gum as maintenance treatment for preventing smoking relapse.
The Effects of Smoking Cessation on Diabetes Mellitus Patients.A review of tobacco use treatments in U.S. ethnic minority populations.A randomized trial of bupropion and/or nicotine gum as maintenance treatment for preventing smoking relapse.
Find a Location
Who is running the clinical trial?
University of North Carolina, Chapel HillLead Sponsor
1,553 Previous Clinical Trials
4,292,962 Total Patients Enrolled
National Institute on Drug Abuse (NIDA)NIH
2,578 Previous Clinical Trials
3,286,935 Total Patients Enrolled
279 Trials studying Tobacco Use Disorder
49,578 Patients Enrolled for Tobacco Use Disorder
Christian Hendershot, PhDPrincipal InvestigatorUniversity of North Carolina, Chapel Hill
1 Previous Clinical Trials
111 Total Patients Enrolled
Media Library
Research Study Groups:
This trial has the following groups:- Group 1: Sham/Placebo
- Group 2: Semaglutide
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