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.
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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
2,539
(once-weekly SC injection; doses 5/10/15 mg)
(once-weekly SC injection)
increased physical activity counseling
Peking University Shenzhen Hospital
Shenzhen, Guangdong, China
RECRUITINGMean percent change in body weight from randomization
Time frame: 72 Weeks
Percentage of participants achieving ≥5% body weight reduction from randomization
Time frame: 72 Weeks
Mean change in body weight
Mean change in body weight (kg) from randomization (pooled 10 mg and 15mg vs placebo)
Time frame: 72 Weeks
Changes in cardiometabolic measures in triglycerides
Time frame: 72 weeks
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