A Study of BGM0504 in Early T2DM With Obesity
Condition(s) studied
Investigational drug(s) / intervention(s)
BGM0504: Administered as a subcutaneous injection once weekly for 52 weeks.
semaglutide: Administered as a subcutaneous injection once weekly for 52 weeks.
Study summary
This trial is conducted in China. The aim is to compare BGM0504 Injection 15 mg with semaglutide 1.0 mg in Chinese T2DM patients with obesity and inadequate control despite diet and exercise. Over 52 weeks of once weekly treatment, efficacy and safety are evaluated, including the rate of diabetes remission at 12 weeks after treatment discontinuation.
Eligibility
Primary outcome measure(s)
- Proportion of Participants Achieving HbA1c < 7.0% and Body Weight Reduction ≥ 10% from Baseline — Week 52
Composite endpoint assessing both glycemic control and weight loss.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Nanjing Drum Tower Hospital(The Affiliated Hospital of Nanjing University Medical School) | Nanjing | Jiangsu | Recruiting |
On this site
📄 Ozempic (semaglutide) drug profile →More BrightGene Bio-Medical Technology Co., Ltd. trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07743983 on ClinicalTrials.gov ↗ ← All trials in China