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Study identifier: NCT07223840 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study of Brenipatide in Adults Who Quit Smoking Cigarettes and Want to Avoid Relapse

Condition: Smoking  ·  Sponsor: Eli Lilly and Company

PhasePhase 2
Planned participants222
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

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.

This description comes directly from the study's public registry record.

Talk to the study team

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or  ·  1-317-615-4559  ·  LillyTrials@Lilly.com

Physicians interested in becoming principal investigators please contact  ·  clinical_inquiry_hub@lilly.com

Always discuss trial participation with your own doctor first.

Locations (27)

Woodland Research NorthwestRogers, Arkansas, United StatesRecruiting
Hillcrest Medical ResearchDeLand, Florida, United StatesActive Not Recruiting
TecTum ResearchHollywood, Florida, United StatesRecruiting
K2 Medical Research ORLANDOMaitland, Florida, United StatesRecruiting
GTL Medical & Research GroupMiami, Florida, United StatesRecruiting
North Georgia Clinical ResearchWoodstock, Georgia, United StatesRecruiting
Revival Research Institute, LLCDearborn, Michigan, United StatesRecruiting
Arch Clinical TrialsSt Louis, Missouri, United StatesRecruiting
Vector Clinical TrialsLas Vegas, Nevada, United StatesRecruiting
Rochester Clinical Research, LLCRochester, New York, United StatesRecruiting
Coastal Carolina Research CenterNorth Charleston, South Carolina, United StatesRecruiting
Circle Clinical ResearchSioux Falls, South Dakota, United StatesRecruiting

+ 15 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07223840