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Efficacy and Safety of Semaglutide Injection Vs WEGOVY® in Chinese Obese Patients
A Multicenter, Randomized, Open-label, Parallel-controlled Phase III Clinical Study Comparing the Efficacy and Safety of Semaglutide Injection and WEGOVY® in Chinese Obese Patients
Asset
Semaglutide
GLP-1 agonist
Listed sites
1
Recruiting sites
1
Enrollment
460
estimated
Study population
Obesity / overweight
Key I/E criterion
•BMI ≥28
Primary endpoint
•Body weight, % change
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
1. Male or female, aged ≥18 years and ≤75 years at the time of signing informed consent;
2. BMI ≥28 kg/m2;
3. A self-reported change in body weight no more than 5% within 90 days before screening.
Exclusion criteria
1. History of type 1 and type 2 diabetes;
2. Previous or planned (during the trial period) obesity treatment with surgery or a weight-loss device;
3. History or presence of chronic or acute pancreatitis;
4. Personal or first-degree relative(s) history of multiple endocrine neoplasia type 2 or medullary thyroid carcinoma;
5. A history or presence of suspected depression or other mental disorders;
6. Patient Health Questionnaire-9 score of ≥15 at screening
7. Uncontrolled hypertension, any of the following: myocardial infarction, stroke, hospitalisation for unstable angina, or transient ischaemic attack within the past 6 months prior to screening;
8. History of malignant neoplasms within the past 5 years prior to screening;
Endpoints (6)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Weight & body composition
3 endpointsThe percentage change in body weight from baseline to week 44
Time frame:week 44
Body weight, % change
percent change from baseline, improvement
The proportion of participants reaching a body weight loss of at least 5%, 10% and 15% at week 44
Time frame:week 44
≥15% weight-loss responders
threshold achievement, improvement
Change in waist circumference, body weight and BMI at week 44
Time frame:week 44
change from baseline, improvement
componentsWaist circumference, change, Body weight, absolute change (kg), BMI, change
Cardiometabolic biomarkers
1 endpointChange in blood pressure and lipids at week 44
Time frame:week 44
change from baseline, improvement
componentsSystolic BP, change, Diastolic BP, change, LDL-C, change, HDL-C, change, Triglycerides, change, Total cholesterol, change
Safety / tolerability / PK
2 endpointsAdverse events
Time frame:week 44
Treatment-emergent AEs (any)
event count, event
ADA and NAb
Time frame:week 44
Immunogenicity (ADA)
descriptive
componentsImmunogenicity (ADA)
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.