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RecruitingNCT07481747SURMOUNT-1Updated Mar 19, 2026

Efficacy and Safety of Tirzepatide Once Weekly Versus Placebo in Participants Who Are Either Obese or Overweight With Weight-Related Comorbidities (SURMOUNT-1)

A Phase 3 interventional study of Tirzepatide and Placebo in Obesity and Overweight (Without Type 2 Diabetes) With Weight-related Comorbidities, sponsored by Hudson Biotech. Recruiting at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-19.

Sponsored by Hudson Biotech · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Started Feb 2026; still recruiting 8 months later.
Phase
Phase 3
Study type
Interventional
Enrollment
2,539
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This Phase 3 study evaluates the efficacy and safety of once-weekly subcutaneous tirzepatide (a dual GIP and GLP-1 receptor agonist) at 5 mg, 10 mg, or 15 mg versus placebo, each used with a reduced-calorie diet and increased physical activity, in adults without type 2 diabetes who have obesity or are overweight with weight-related comorbidities. The primary efficacy assessment is at Week 72. Participants with prediabetes at randomization may continue in an additional long-term treatment period to assess progression to type 2 diabetes and longer-term weight outcomes.

Read the detailed description

After screening, eligible participants are randomized in a 1:1:1:1 ratio to receive tirzepatide 5 mg, 10 mg, 15 mg, or placebo once weekly by subcutaneous injection using an autoinjector. All participants receive lifestyle counseling focused on a reduced-calorie diet and increased physical activity. The main treatment period is 72 weeks. Participants identified with prediabetes at randomization can continue study treatment for up to 176 weeks (plus follow-up), allowing evaluation of longer-term weight management and time to onset/progression to type 2 diabetes. Safety is monitored throughout, including adverse events and laboratory testing.

02

Conditions studied

  • Obesity
  • Overweight (Without Type 2 Diabetes) With Weight-related Comorbidities

Keywords

  • Tirzepatide
  • LY3298176
  • dual incretin
  • GIP
  • GLP-1
  • obesity
  • overweight
  • weight management
  • placebo
  • randomized
  • double-blind
  • once-weekly
  • subcutaneous
  • lifestyle intervention
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,692 are open to participants now.

This study's planned enrollment of 2,539 is above the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Hudson Biotech is the lead sponsor of 8 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • BMI ≥30 kg/m², OR BMI ≥27 kg/m² with ≥1 weight-related comorbidity (e.g., hypertension, dyslipidemia, obstructive sleep apnea, cardiovascular disease)
  • History of at least one unsuccessful dietary effort to lose weight (self-reported)
  • Investigator judges participant capable and willing to self-inject (or have assistance), follow lifestyle advice, maintain a diary, and complete questionnaires
  • Age ≥18 years
  • Meets protocol contraception/pregnancy criteria (as applicable) and provides written informed consent

Exclusion criteria

Exclusion Criteria:

  • Type 1 or type 2 diabetes, history of ketoacidosis/hyperosmolar state, or screening labs diagnostic of diabetes
  • Recent significant weight change (>5 kg within 3 months prior to screening)
  • Prior/planned bariatric surgery; recent/ongoing endoscopic or device-based obesity therapies
  • Severe renal impairment (eGFR \<30 mL/min/1.73 m²)
  • Clinically significant gastric emptying abnormality or chronic use of drugs that directly affect GI motility
  • History of chronic or acute pancreatitis
  • Clinically significant thyroid abnormalities at screening (e.g., TSH outside protocol range) or anticipated need to initiate thyroid replacement during study
  • Obesity due to other endocrinologic disorders (e.g., Cushing syndrome) or monogenic/syndromic obesity (e.g., MC4R deficiency, Prader-Willi syndrome)
  • Significant unstable major depressive disorder/severe psychiatric disorder, lifetime suicide attempt, or concerning suicidality screening (PHQ-9/C-SSRS criteria)
  • Uncontrolled hypertension; recent major cardiovascular events; NYHA class IV heart failure
  • Active or significant liver disease or certain elevated liver tests at screening (per protocol thresholds)
  • Elevated calcitonin above protocol thresholds; personal/family history of medullary thyroid carcinoma or MEN2
  • Active/untreated malignancy or remission \<5 years (with specified exceptions)
  • Any other condition contraindicating GLP-1 receptor agonist therapy
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
2,539 participants (estimated)

Study arms

  • Experimental
    Arm 1: Tirzepatide 5 mg once weekly + lifestyle intervention

    Drug: Tirzepatide · Drug: Placebo · Behavioral: Reduced-calorie diet

  • Experimental
    Arm 2: Tirzepatide 10 mg once weekly + lifestyle intervention

    Drug: Tirzepatide · Drug: Placebo · Behavioral: Reduced-calorie diet

  • Experimental
    Arm 3: Tirzepatide 15 mg once weekly + lifestyle intervention

    Drug: Tirzepatide · Drug: Placebo · Behavioral: Reduced-calorie diet

  • Experimental
    Arm 4: Placebo once weekly + lifestyle intervention

    Drug: Tirzepatide · Drug: Placebo · Behavioral: Reduced-calorie diet

Interventions

  • DrugTirzepatide

    (once-weekly SC injection; doses 5/10/15 mg)

  • DrugPlacebo

    (once-weekly SC injection)

  • BehavioralReduced-calorie diet

    increased physical activity counseling

06

What researchers measure

Primary outcomes

  1. Mean percent change in body weight from randomization

    Time frame: 72 Weeks

  2. Percentage of participants achieving ≥5% body weight reduction from randomization

    Time frame: 72 Weeks

Secondary outcomes

  1. Mean change in body weight

    Mean change in body weight (kg) from randomization (pooled 10 mg and 15mg vs placebo)

    Time frame: 72 Weeks

  2. Changes in cardiometabolic measures in triglycerides

    Time frame: 72 weeks

07

Study locations

1 of 1 sites recruiting
  • Peking University Shenzhen Hospital
    Shenzhen, Guangdong 518036, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07481747
Lead sponsor
Hudson Biotech
Responsible party
Sponsor
First posted
Mar 19, 2026
Start date
Feb 2, 2026
Primary completion
Feb 14, 2027 (estimated)
Completion
Mar 17, 2028 (estimated)
Last update
Mar 19, 2026

Study contacts

Seni S Lu, Phd
Contact
Seni-Lu@beijing-biotech.com
+86 13076790030

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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