Can a Two-Drug combo tip the scales against obesity?

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Are Japanese participants assigned male at birth (AMAB) or assigned female at birth (AFAB) who agree to contraception requirements or participants who are individuals not of childbearing potential (INOCBP). * Have a body mass index greater than or equal to (≥)25 kilograms per square meter (kg/m²) * Have had a stable weight for the 3 months prior to screening. Stable weight is defined as less than 5 percent (%) body weight change. Exclusion Criteria: * Have known allergies to related compounds of macupatide or eloralintide, or any components of the formulations. * Have a history of significant atopy, including severe allergic manifestations, or clinically significant multiple or severe drug allergies, or severe posttreatment hypersensitivity reactions. * Have a history or presence of psychiatric disorders, including a history of major depressive disorder or severe psychiatric disorders, within the last 3 years, that would present a safety risk or may significantly impair the participant's ability to comply with study procedures. * Have been diagnosed with Type 1 or Type 2 diabetes mellitus. * Have a history of chronic medical conditions involving the heart, liver, or kidneys. * Have a history of any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years. * Have a history or presence of a gastrointestinal (GI) disorder or previous surgery that impacts gastric emptying. * Have had or plan to have during the study, a device-based or surgical treatment use for obesity. * Have been treated, or plan to be treated, with prescription medications or other non approved drugs intended to promote weight loss, within 3 months prior to screening. * Are currently enrolled or have participated, within the last 30 days, in a clinical study involving an investigational product. If the previous investigational product has a long half-life, 5 half-lives or 30 days, whichever is longer, should have passed. * Have previously completed or withdrawn from this study or have previously received macupatide or eloralintide. * Have evidence of acute or chronic liver disease or pancreatic disease.