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NCT Number: NCT06704581

A Study of BGM0504 Injection in Participants with Obesity or Overweight

This is a multicenter, randomized, double-blind, placebo-controlled phase III validation clinical study in Chinese adult non-diabetic overweight or obese Participants. The main purpose is to evaluate the clinical efficacy of BGM0504 injection for 36 weeks of administration as an adjunct to diet, exercise, and behavioral interventions in overweight or obese non-diabetic adults in China for weight management, and to evaluate the clinical efficacy and safety of BGM0504 injection for 52 weeks of administration.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Peking University People's Hospital

Beijing, Beijing Municipality, 100044, China

Location status: Recruiting

Location contact

Chief physician, Peking University People's Hospital, PhD

CONTACT

[email protected]

8613910978815

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • A male or female aged 18 to 65 years inclusive at screening
  • BMI≥28 kg/m², or 24.0≤BMI<28.0 kg/m² and previous diagnosis with at least one of the following comorbidities: i. Prediabetes (impaired fasting blood glucose and/or impaired glucose tolerance), hypertension, nonalcoholic fatty liver disease, or one or more of these; ii. Joint pain with weight bearing; iii. Dyspnea caused by obesity or obstructive sleep apnea syndrome
  • Weight change < 5.0% (chief complaint) after diet and exercise control for at least 12 weeks before screening
  • Female participants who are not pregnant or lactating. Female participants with childbearing potential and their partners should use highly effective, medically accepted contraception, will not have pregnancy and fertility plan, and refrain from donating ovum until one month after the end of the study

Exclusion criteria

  • Diabetes mellitus
  • Known to be allergic to 3 or more kinds of foods or medications, or allergic to GLP-1 agonist, or have a severe allergic disease (asthma, urticaria, eczematous dermatitis, etc.) at screening
  • Has been treated with GLP-1 receptor agonists or similar drugs containing the same target, or drugs used for weight control in the three months prior to screening
  • Secondary disease or drug-induced obesity, including : elevated cortisol (e.g. Cushing's syndrome), obesity due to pituitary and hypothalamic damage, obesity due to diet drug reduction/discontinuation, etc.;
  • History of pancreatitis
  • Have the currently uncontrolled thyroid diseases with stable treatment dose and clinically significant abnormal results of thyroid function test occurred at screening
  • Previous history of moderate or severe depression, or PHQ-9 score ≥15, or history of other serious mental illness, or Any lifetime history of a suicide attempt

Treatment and study plan

5 mg BGM0504 injection

Drug

5mg BGM0504 injection administered subcutaneously (SC) once a week.

10 mg BGM0504 injection administered subcutaneously (SC) once a week

Drug

10mg BGM0504 injection administered subcutaneously (SC) once a week.

15 mg BGM0504 injection

Drug

15mg BGM0504 injection administered subcutaneously (SC) once a week.

BGM0504 placebo

Drug

BGM0504 placebo administered SC once a week.

Primary outcomes

  1. Percent Change from Baseline in Body Weight

    Time frame: Baseline,Week 36

    Change from baseline in body weight after 36 weeks of treatment

  2. Percentage of Participants Who Achieve≥5% Body Weight Reduction

    Time frame: Baseline,Week 36

    Percentage of Participants Who Achieve≥5% Body Weight Reduction

Secondary outcomes

  1. Percent Change From Baseline in Body Weight

    Time frame: Baseline, Week 52

    Percent Change from Baseline in Body Weight after 52weeks of treatment

  2. Change From Baseline in Body Weight

    Time frame: Baseline, Week36 and 52

    Change from baseline in body weight

  3. Percentage of Participants Who Achieve≥5% Body Weight Reduction

    Time frame: Baseline, Week 36 and 52

    Percentage of Participants Who Achieve≥5% Body Weight Reduction

  4. Percentage of Participants Who Achieve≥10% Body Weight Reduction

    Time frame: Baseline, Week 36 and 52

    Percentage of Participants Who Achieve≥10% Body Weight Reduction

  5. Percentage of Participants Who Achieve≥15%Body Weight Reduction

    Time frame: Baseline, Week 36 and 52

    Percentage of Participants Who Achieve≥15%Body Weight Reduction

  6. Percentage of Participants Who Achieve≥20% Body Weight Reduction

    Time frame: Baseline, Week 36 and 52

    Percentage of Participants Who Achieve≥20% Body Weight Reduction.

  7. Change From Baseline in Waist Circumference

    Time frame: Baseline, Week 36 and 52

    Change From Baseline in Waist Circumference after 52weeks of treatment.

  8. Change From Baseline in Body Mass Index (BMI)

    Time frame: Baseline, Week 36 and 52

    Change From Baseline in Body Mass Index (BMI) after 52weeks of treatment

  9. Change From Baseline in Fasting Glucose

    Time frame: Baseline, Week 36 and 52

    Change From Baseline in Fasting Glucose after 52weeks of treatment

  10. Change From Baseline in Hemoglobin A1c (HbA1c)

    Time frame: Baseline, Week 36 and 52

    Change From Baseline in Hemoglobin A1c (HbA1c) after 52weeks of treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

Ji,MD, chief physician, Peking University People's Hospital

CONTACT

[email protected]

13910978815

Sponsors and collaborators

Lead sponsor

BrightGene New Bio-Medical Technology(Wuxi) Co.Ltd.

Industry

Registry information

Official study title

A Multicenter, Randomized, Double-blind, Placebo-parallel Controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of BGM0504 Injection in Chinese Non-diabetes Participants with Overweight or Obese

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Nov 26, 2024
Registry last updated
Nov 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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