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

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorEli Lilly and Company

About this trial

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).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

hypertension

dyslipidemia

obstructive sleep apnea

Fatty liver

Disqualifiers

Have type 1 diabetes (T1D), type 2 diabetes (T2D), or any other types of diabetes, history of ketoacidosis, or hyperosmolar state/coma

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

Have family (first-degree relative) or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2) syndrome

Trial design

Design model

Parallel

Treatments tested in this trial

  • Orforglipron

    Drug

    Administered orally.

  • Placebo

    Drug

    Administered orally.

Treatment groups

192 Participants
are divided into 2 treatment groups
Group A: OrforglipronExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Mean Percent Change From Baseline in Body Weight

Time frame
Baseline, Week 48

Secondary outcomes

1

Mean Change from Baseline in Waist Circumference

Time frame
Baseline, Week 48
2

Mean Change from Baseline in Body Mass Index (BMI)

Time frame
Baseline, Week 48
3

Mean Change from Baseline in Hemoglobin A1c (HbA1c)

Time frame
Baseline, Week 48
4

Mean Change from Baseline in Fasting Glucose

Time frame
Baseline, Week 48

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: