A Study of Brenipatide in Adults Who Quit Smoking Cigarettes and Want to Avoid Relapse
Eligible age
18–75 yrs
Accepts
All genders
Locations
12 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
This study evaluates the efficacy and safety of brenipatide when compared to placebo for reducing the risk of relapse to cigarette smoking in adults who have recently quit. Study participation will last approximately 34 weeks with up to 17 study visits, which includes a 2-week screening period, 24-week treatment period, 8-week safety follow-up period.
Sponsor: Eli Lilly and Company
You may qualify if…
- ✓ Have recently quit smoking and are motivated to stay quit from smoking
- ✓ Are reliable and willing to make themselves available for the duration of the study and attend required study visits and are willing and able to follow study procedures as required, such as self-inject study intervention
You may not qualify if…
- ✕ Have evidence of any substance use disorder within the past 180 days prior to screening, except mild alcohol use disorder, mild cannabis use disorder, or tobacco use disorder
- ✕ Have answered "yes" to either Question 4 or Question 5 on the "Suicidal Ideation" portion of the C-SSRS and the ideation occurred within the past 6 months, or have answered "yes" to any of the suicide-related behaviors on the "Suicidal Behavior" portion of the C-SSRS and the behavior occurred within the past 6 months
- ✕ Have severe chronic obstructive pulmonary disease, or any other clinically severe respiratory condition that in the investigator's opinion may pose a risk.
- ✕ Have participated in a clinical study and have received active treatment, or unknown if they received active treatment, within 90 days or 5 half-lives (whichever is longer) before screening
Where it's recruiting
Rogers
DeLand · Hollywood · Maitland · Miami
Woodstock
Dearborn
St Louis
Las Vegas
Rochester
North Charleston
Sioux Falls
Dallas · DeSoto · Houston
Newport News
Redmond
Source: ClinicalTrials.gov · NCT07223840 · last updated 2026-08-06