Peking University People's Hospital
Beijing, Beijing Municipality, 100044, China
Location status: Recruiting
NCT Number: NCT06704581
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.
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Phase 3
Beijing, Beijing Municipality, 100044, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
5mg BGM0504 injection administered subcutaneously (SC) once a week.
10mg BGM0504 injection administered subcutaneously (SC) once a week.
15mg BGM0504 injection administered subcutaneously (SC) once a week.
BGM0504 placebo administered SC once a week.
Time frame: Baseline,Week 36
Change from baseline in body weight after 36 weeks of treatment
Time frame: Baseline,Week 36
Percentage of Participants Who Achieve≥5% Body Weight Reduction
Time frame: Baseline, Week 52
Percent Change from Baseline in Body Weight after 52weeks of treatment
Time frame: Baseline, Week36 and 52
Change from baseline in body weight
Time frame: Baseline, Week 36 and 52
Percentage of Participants Who Achieve≥5% Body Weight Reduction
Time frame: Baseline, Week 36 and 52
Percentage of Participants Who Achieve≥10% Body Weight Reduction
Time frame: Baseline, Week 36 and 52
Percentage of Participants Who Achieve≥15%Body Weight Reduction
Time frame: Baseline, Week 36 and 52
Percentage of Participants Who Achieve≥20% Body Weight Reduction.
Time frame: Baseline, Week 36 and 52
Change From Baseline in Waist Circumference after 52weeks of treatment.
Time frame: Baseline, Week 36 and 52
Change From Baseline in Body Mass Index (BMI) after 52weeks of treatment
Time frame: Baseline, Week 36 and 52
Change From Baseline in Fasting Glucose after 52weeks of treatment
Time frame: Baseline, Week 36 and 52
Change From Baseline in Hemoglobin A1c (HbA1c) after 52weeks of treatment.
Contact information is provided by the study sponsor or research team.
BrightGene New Bio-Medical Technology(Wuxi) Co.Ltd.
Industry
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
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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