Status and phase
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About
The main purpose of this study is to evaluate the efficacy and safety of retatrutide compared to tirzepatide in adults who have obesity. The study will last about 89 weeks.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Have a self-reported change in body weight >5 kilograms (kg) (11 pounds) within 90 days before screening.
Have a prior or planned surgical treatment for obesity.
Have a prior or planned endoscopic procedure and/or device-based therapy for obesity.
Have taken weight loss drugs, including over-the-counter medications, within 90 days prior to screening.
Have a family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN-2).
Have had within the past 90 days before screening:
Have New York Heart Association Functional Classification Class IV congestive heart failure.
Have a history of chronic or acute pancreatitis.
Primary purpose
Allocation
Interventional model
Masking
800 participants in 2 patient groups
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Central trial contact
There may be multiple sites in this clinical trial. 1-877-CTLILLY (1-877-285-4559) or
Data sourced from clinicaltrials.gov
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