The purpose of this study is to investigate the efficacy and safety of retatrutide compared with placebo in participants with Type 2 Diabetes and inadequate glycemic control. The study will last about 11 months and may include up to 11 visits.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
537
Administered SC.
Administered SC.
Change from Baseline in Hemoglobin A1c (HbA1c) (%)
Time frame: Baseline, Week 40
Percentage of Participants Who Achieve HbA1c < 7.0%
Time frame: Week 40
Percentage of Participants Who Achieve HbA1c ≤ 6.5%
Time frame: Week 40
Percentage of Participants Who Achieve HbA1c < 5.7%
Time frame: Week 40
Change from Baseline in Fasting Serum Glucose
Time frame: Baseline, Week 40
Percent Change from Baseline in Body Weight
Time frame: Baseline, Week 40
Change from Baseline in Body Weight
Time frame: Baseline, Week 40
Percentage of Participants Who Achieve Weight Reduction of ≥ 5%
Time frame: Week 40
Percentage of Participants Who Achieve Weight Reduction of ≥ 10%
Time frame: Week 40
Percentage of Participants Who Achieve Weight Reduction of ≥ 15%
Time frame: Week 40
Percentage of Participants Who Achieve HbA1c ≤ 6.5% and ≥ 10% Weight Reduction
Time frame: Week 40
Percent Change from Baseline in Triglycerides
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Time frame: Baseline, Week 40
Percent Change from Baseline in Non- High-Density Lipoprotein (HDL) Cholesterol
Time frame: Baseline, Week 40
Change from Baseline in Systolic Blood Pressure (SBP)
Time frame: Baseline, Week 40