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NOT YET RECRUITING
NCT07765511
PHASE1

A Study of Macupatide (LY3532226) in Participants With Obesity or Overweight Without Type 2 Diabetes

Sponsor: Eli Lilly and Company

View on ClinicalTrials.gov

Summary

The main purpose of this study is to assess how well macupatide, when dosed alone and in combination with eloralintide, is tolerated and what side effects may occur in participants with obesity or overweight without Type 2 diabetes. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. For each participant, the study will last about 4 months and will include 2 stays in the Clinical Research Unit (CRU), each lasting 3-5 nights.

Official title: A Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Macupatide Monotherapy, and Macupatide in Combination With Eloralintide, in Japanese Participants With Obesity or Overweight Without Type 2 Diabetes.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-10

Completion Date

2027-06

Last Updated

2026-08-14

Healthy Volunteers

Yes

Interventions

DRUG

Macupatide

Administered SC

DRUG

Eloralintide

Administered SC

DRUG

Placebo

Administered SC

Locations (3)

Souseikai Fukuoka Mirai Hospital

Fukuoka, Japan

Sumida Hospital

Sumida-ku, Japan

Medical Corporation Houeikai Sekino Clinical Pharmacology Clinic

Toshima City, Japan