Semaglutide for Post-Smoking Cessation Weight Management

Obesity Clinical Trial

Official title:

A Randomized Controlled Trial of Once-Weekly Semaglutide for Limiting Post-Smoking Cessation Weight Gain in Adult Smokers With Overweight/Obesity

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06173778
• Other study ID #: HSC-MS-23-0485
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: March 1, 2024
• Est. completion date: August 1, 2026

Study information

• Verified date: December 2023
• Source: The University of Texas Health Science Center, Houston
• Contact: Luba Yammine, PhD
• Phone: 713-486-2737
• Email: Luba.Yammine[@]uth.tmc.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This trial will examine the effect of semaglutide 2.4mg on changes in body weight, body composition, and peripheral and central mechanisms that control appetite, satiety, and food intake in the context of smoking cessation.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 197
• Est. completion date: August 1, 2026
• Est. primary completion date: July 1, 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Ability to provide informed consent before any study-related activity, willing to comply with al study procedures, and be available for the duration of the study.
• Body mass index (BMI) =30 kg/m2 or =27 kg/m2 with the presence of at least one of the following weight-related comorbidities (treated or untreated): hypertension (unless meets medical exclusion criterion 7), cardiovascular disease (unless meets medical exclusion criterion 6), dyslipidemia, or obstructive sleep apnea
• Have been smoking =5 cigarettes per day for at least 1 year (prior to screening) and provide positive cotinine test.
• Desire to quit smoking (defined as "intend to quit within one month")
• Agree (if the participant is female and of child-bearing potential) to use effective contraceptive methods, unless the participant's male partner(s) is surgically sterile (underwent vasectomy).
• Women of child-bearing potential must provide negative urine pregnancy tests prior to randomization.
• Normal cognitive restraint (assessed as cognitive restraint score of <4 from the Three Factor Eating Habits Questionnaire)
• Have a medical history and a brief physical examination demonstrating no clinically significant contraindications for study participation, in the judgment of the Study Physician and the Principal Investigator Exclusion Criteria: Medical Exclusions
• Personal or first-degree relative(s) history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN 2).
• Acute pancreatitis within the past 6 months prior to screening.
• History or presence of chronic pancreatitis.
• Type 1 or type 2 Diabetes Mellitus (previously diagnosed or indicated by HbA1C =48 mmol/mol (6.5%) as measured by central laboratory at screening).
• End stage renal disease (ESRD, previously diagnosed or indicated by estimated glomerular filtration rate (eGFR) value of eGFR < 15 ml/min/1.73 m2 as measured by central laboratory at screening).
• Any of the following: myocardial infarction, stroke, hospitalization for unstable angina or transient ischemic attack within the past 60 days prior to screening.
• Systolic blood pressure (SBP) >159 mmHg and/or diastolic blood pressure (DBP) >99 mmHg)
• History of malignant neoplasms within the past 5 years prior to screening. Basal and squamous cell skin cancer and any carcinoma in-situ are allowed.
• Severe gastrointestinal disease (i.e., severe gastroparesis).
• Known or suspected hypersensitivity to nicotine/nicotine patches; semaglutide, excipients, or related products.
• Women who are currently pregnant, or plan to become pregnant, or lactating, or of childbearing potential and are not using medically accepted forms of contraception.
• Have any illness or condition which in the opinion of the Principal Investigator and/or the Study Physician would preclude safe and/or successful completion of the study. Psychiatric / Substance Use Exclusions
• Psychoactive substance abuse or dependence (excluding nicotine dependence) within the past 3 months prior to screening (existing diagnosis or as determined by the structured interview).
• Urine drug test positive, before randomization, for any of the following substances:

1. benzodiazepines

2. cocaine

3. opioids

4. amphetamines

5. methamphetamine

6. buprenorphine

7. barbiturates

8. 3,4-methylenedioxy-methamphetamine (MDMA)

9. Tetrahydrocannabinol (THC)

• Psychotic or bipolar disorder, or mood disorder with psychotic features; or eating disorder (existing clinical diagnosis or as determined by the structured interview)
• Moderate to high risk for suicidality (as determined by the structured interview). Weight-Related Exclusions
• Previously undergone bariatric surgery
• Gained/lost =4.5 kg over the past 6 months (prior to screening)
• Currently enrolled in a behavioral weight management plan
• Uncontrolled thyroid disease (the criterion will be assessed at the Study Physician's and the Principal Investigator's discretion) Smoking-Related Exclusions -Currently using other combustible (e.g., cigars), other (e.g., chewing tobacco, snuff, snus) or alternative (e.g., electronic cigarettes) tobacco products Medication-Related Exclusions
• Currently using oral or injectable glucose lowering medications
• Currently using pharmacotherapy for smoking cessation (NRT, varenicline, or bupropion)
• Currently or recently (last 90 days prior to screening) taking medication used for weight management (i.e., orlistat, lorcaserin,vi naltrexone-bupropion, liraglutide, phentermine, topiramate, benzphetamine, diethylpropion, phendimetrazine)
• Currently or recently (within the past 14 days prior to screening) taking medication(s) known to impact appetite and/or weight (i.e., corticosteroids, excluding inhaled) General Exclusions
• Current, anticipated, or pending enrollment in another research study during this trial that could potentially affect participant safety and/or the study data/design as determined by the Principal Investigator and/or Study Physician.
• Not planning to live in the area for the duration of this trial.
• Surgery scheduled for the duration of the trial, except for minor surgical procedures, in opinion of the Principal Investigator and/or the Study Physician.
• Unable to communicate (read, write, and speak) fluently in English.

Related Conditions & MeSH terms

• Cigarette Smoking
• Obesity
• Overweight

Intervention

Drug:
• semaglutide 2.4mg
Semaglutide 2.4mg will be self-administered once a week under the surface of the skin and will be started at 0.24mg once a week for 4 weeks; in 4-week intervals, the dose will be increased until a dose of 2.4mg is reached
• Placebo
Non-active medication, self-administered
• Nicotine Replacement Therapy (NRT, nicotine patch)
Participants who smoke >10 cigarettes/day will use 21 mg patches for the first 6 weeks, 14 mg patches during weeks 7 and 8, and 7 mg patches during weeks 9 and 10. Participants who smoke 5-10 cigarettes per day will use 14 mg patches for the first 6 weeks and 7 mg patches for weeks 7-10.

Behavioral:
• Brief Smoking Cessation Counseling
Participants will receive weekly, manual-based individual smoking cessation counseling. Counseling will be provided by master's level clinicians.

Locations

Country	Name	City	State
United States	The University of Texas Health Science Center at Houston	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
The University of Texas Health Science Center, Houston

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Body Weight Percent		Baseline to Week 28
Secondary	Change in body weight as measured in kilograms (kg)		Baseline to Week 28
Secondary	Change in body fat mass as measured in kilograms (kg)		Baseline to Week 28
Secondary	Change in waist circumference as measured in centimeters(cm)		Baseline to Week 28