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NCT06973681CompletedPhase 2

A Study of BGM0504 Evaluating Weight Loss in Overweight or Obese Chinese Subjects

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Phase II Clinical Study to Evaluate the Safety, Tolerability, PK/PD Profile, and Efficacy of Multiple Doses of BGM0504 Injection in Overweight or Obese Subjects Without Diabetes

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

To assess the effect of BGM0504 injection versus placebo on weight loss in overweight or obese subjects after 24 weeks of treatment.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
120 (actual)
First submitted
14 May 2025
Start date
13 Oct 2023
Primary completion date
13 Sept 2024
Lead sponsor
BrightGene Bio-Medical Technology Co., Ltd.
Diseases
Obesity
NCT number
NCT06973681

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 120
  • From 13 Oct 2023 to the primary completion date, 13 Sept 2024
  • 1 site 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

  • Previous diagnosis of type 1 or type 2 diabetes mellitus;
  • Concomitant thyroid dysfunction that cannot be controlled at a stable drug dose atscreening, or clinically significant abnormalities in thyroid function test results at screening that require initiation of therapy;

Other illness

  • History of acute or chronic pancreatitis, or pancreatic injury;
  • History of thyroid C-cell carcinoma, MEN (multiple endocrine adenomatosis) 2A or 2B, or relevant family history;
  • Subjects with uncontrolled hypertension after treatment (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥ 100 mmHg at screening) or untreated blood pressure meeting the above criteria at screening;
  • At Screening, abdominal ultrasound indicated calculus gallbladder and polyps, or presence of clinical symptoms of gallbladder disease at Screening;

Other

  • Pregnant or breastfeeding women.

Who the study is looking for

  • BMI ≥ 28.0 kg/m2 or 24.0 ≤ BMI \< 28.0 kg/m2 with at least 1 weight-related comorbidity at screening visit;
  • Controlled by diet and exercise alone for at least 12 weeks prior to Screening with \<5.0% change in body weight and able to continue the original diet and exercise for weight control during the trial.

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
The Third Xiangya Hospital of Central South University
Coordinator of this site? Confirm its status
ChangshaChinaUnknown status

Related publications

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