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RecruitingPhase 3

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

NCT IDNCT07036172
Org study IDHDM1702-301

Timeline

Milestones

Study start2025-01-03actual
Study first posted2025-06-25actual
Last update posted2025-06-25actual
Primary completion2026-04estimated (month precision)
Study completion2026-05estimated (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweight

Eligibility

Who can enroll

Minimum age18 Years
Maximum age75 Years
SexAll
Healthy volunteersNot accepted

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
Safety / tolerability / PK
2
Cardiometabolic biomarkers
1

Weight & body composition

3 endpoints
Primary/protocol endpoint

The percentage change in body weight from baseline to week 44

Time frame:week 44

Body weight, % change

percent change from baseline, improvement

Secondary/protocol endpoint

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

Secondary/protocol endpoint

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 endpoint
Secondary/protocol endpoint

Change 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 endpoints
Secondary/protocol endpoint

Adverse events

Time frame:week 44

Treatment-emergent AEs (any)

event count, event

Secondary/protocol endpoint

ADA and NAb

Time frame:week 44

Immunogenicity (ADA)

descriptive

componentsImmunogenicity (ADA)

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.