About this trial
The purpose of this study is to see how well LY3938577 works and how safe it is compared to degludec in people with type 2 diabetes. Participation in the study will last about 26 weeks.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Have type 2 diabetes
Are receiving ≥20 units of basal insulin per day and ≤55 units/day and ≤1.5 units/kg/day at screening
Have hemoglobin A1c (HbA1c) 7.5% to 10.5% inclusive
Have a body mass index (BMI) of 20 or higher and less than 35 kilograms per square meter (kg/m2)
Disqualifiers
Have type 1 diabetes
Trial design
Parallel
Treatments tested in this trial
LY3938577
DrugAdministered SC
Degludec
DrugAdministered SC
Treatment groups
Trial outcomes
Primary outcomes
Change from Baseline in Glucose Time in Range Between 70 and 180 mg/dL Inclusive (Non-Inferiority Analysis)
Secondary outcomes
Change from Baseline in Glucose Time in Range Between 70 and 180 mg/dL Inclusive (Superiority Analysis)
Change from Baseline in Hemoglobin A1c (HbA1c)
Pharmacokinetics (PK): Average Concentration of LY3938577
Sponsors and contacts
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