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NOT YET RECRUITING
NCT07790861
PHASE3

A Study of Orforglipron (LY3502970) in Chinese Participants With Obesity or Overweight and Weight-Related Health Problems

Sponsor: Eli Lilly and Company

View on ClinicalTrials.gov

Summary

The purpose of this study is to learn how well orforglipron works and how safe it is in Chinese adults with obesity or overweight and related health problems. Participation in this study will last about 53 weeks (about 1 year).

Official title: A Phase 3, Randomized, Double-Blind Study to Investigate the Efficacy and Safety of Once- Daily Oral Orforglipron Compared With Placebo in Chinese Adult Participants With Obesity or Overweight With Weight-Related Comorbidities

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

192

Start Date

2026-12

Completion Date

2028-03

Last Updated

2026-08-27

Healthy Volunteers

No

Interventions

DRUG

Orforglipron

Administered orally.

DRUG

Placebo

Administered orally.

Locations (13)

Sichuan Provincial People's Hospital

Chengdu, China

Zhujiang Hospital

Guangzhou, China

The first Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, China

Zhejiang Provincial People's Hospital

Hangzhou, China

The Fourth Affiliated Hospital of Harbin Medical University

Harbin, China

The Second People's Hospital of Hefei

Hefei, China

Jinan Central Hospital

Jinan, China

The First Affiliated Hospital of Henan University of Science &Technology

Luoyang Shi, China

Jiangxi Provincial People's Hospital

Nanchang, China

Nanjing First Hospital

Nanjing, China

The Second Affiliated Hospital of Nanjing Medical University

Nanjing, China

Jiangsu Province Hospital

Nanjing, China

Shanghai Sixth People's Hospital

Shanghai, China