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NCT07790861Not yet recruitingPhase 3

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

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

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

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).

Status (registry)
Not yet recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
192 (estimated)
First submitted
25 Aug 2026
Start date
Dec 2026
Primary completion date
Mar 2028
Lead sponsor
Eli Lilly and Company
Diseases
Obesity
NCT number
NCT07790861

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 192
  • From Dec 2026 to the primary completion date, Mar 2028
  • 13 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have a self-reported change in body weight \>5 kg within 90 days prior to screening
  • Had chronic or acute pancreatitis any time prior to screening

Other illness

  • Have type 1 diabetes (T1D), type 2 diabetes (T2D), or any other types of diabetes, history of ketoacidosis, or hyperosmolar state/coma
  • Have family (first-degree relative) or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2) syndrome

Who the study is looking for

  • Have body mass index (BMI) ≥28.0 kilograms per square meter (kg/m2) and \<30 kg/m2 or ≥24.0 kg/m2 and \<28 kg/m2, and at least 1 of the following weight-related comorbidities at screening:
    • hypertension
    • dyslipidemia
    • obstructive sleep apnea
    • Fatty liver
    • cardiovascular disease
  • Have a history of at least 1 self-reported unsuccessful dietary effort to lose body weight

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sichuan Provincial People's Hospital
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ChengduChinaUnknown status
Zhujiang Hospital
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GuangzhouChinaUnknown status
Zhejiang Provincial People's Hospital
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HangzhouChinaUnknown status
The First Affiliated Hospital Zhejiang University School of Medicine
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HangzhouChinaUnknown status
The Fourth Affiliated Hospital of Harbin Medical University
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HarbinChinaUnknown status
The Second People's Hospital of Hefei
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HefeiChinaUnknown status
Jinan Central Hospital
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JinanChinaUnknown status
The First Affiliated Hospital of Henan University of Science &Technology
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Luoyang ShiChinaUnknown status
Jiangxi Provincial People's Hospital
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NanchangChinaUnknown status
Jiangsu Province Hospital
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NanjingChinaUnknown status
Nanjing First Hospital
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NanjingChinaUnknown status
The Second Affiliated Hospital of Nanjing Medical University
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NanjingChinaUnknown status
Shanghai Sixth People's Hospital
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ShanghaiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.