The main purpose of this study, performed under the master protocol W8M-MC-CWMM (NCT06143956), is to evaluate the effects of treatment with LY3549492 compared to placebo in adult participants with obesity or who are overweight with type 2 diabetes. Participation in the study will last about 11 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
1
Percent Change From Baseline in Body Weight
Percent change from baseline in body weight at Week 32. Body weight was intended to be measured in kilograms, and percent change was to be calculated relative to baseline.
Time frame: Baseline, Week 32
Change From Baseline in Body Weight
Change from baseline in body weight at Week 32. Body weight was intended to be measured in kilograms, and absolute change from baseline was to be calculated.
Time frame: Baseline, Week 32
Percentage of Participants Who Achieve ≥5% Body Weight Reduction
Percentage of participants who achieved at least 5% reduction in body weight from baseline to Week 32.
Time frame: Baseline, Week 32
Percentage of Participants Who Achieve ≥10% Body Weight Reduction
Percentage of participants who achieved at least 10% reduction in body weight from baseline to Week 32.
Time frame: Baseline, Week 32
Change From Baseline in Hemoglobin A1c (HbA1c)
Change from baseline in hemoglobin A1c (HbA1c) at Week 32. HbA1c was intended to be measured as a percentage and reflects average blood glucose levels over approximately 3 months.
Time frame: Baseline, Week 32
Pharmacokinetics (PK): Average Concentration of LY3549492
Average plasma concentration of LY3549492. Pharmacokinetic samples were intended to be collected at multiple timepoints, including pre-dose and post-dose intervals, to evaluate the pharmacokinetic profile of LY3549492 over time.
Time frame: Week 0 and Week 24 (6-18 hours post-dose); Weeks 3, 9, 15, and 18 (1-3 hours post-dose); Weeks 6 and 21 (3-6 hours post-dose); Week 12 (1-6 hours post-dose); and Weeks 30 and 32 (pre-dose).
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