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A Multiple Dose Combination Study to Evaluate the Safety and Tolerability of Tirzepatide and LY3841136 in Overweight and Obese Participants
The main purpose of this study is to assess the safety and tolerability of LY3841136 when administered in combination with tirzepatide in overweight and obese patients. The study will last up to approximately 42 weeks.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Fortrea Clinical Research Unit
Daytona Beach, Florida, United States
Fortrea Clinical Research Unit
Dallas, Texas, United States
Fortrea Clinical Research Unit
Madison, Wisconsin, United States
Start Date
April 3, 2024
Primary Completion Date
September 29, 2025
Completion Date
September 29, 2025
Last Updated
October 15, 2025
96
ACTUAL participants
Tirzepatide
DRUG
LY3841136
DRUG
Placebo
DRUG
Lead Sponsor
Eli Lilly and Company
NCT07472881
NCT01143454
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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