Study detail
RecruitingPhase 2
A Phase 2, Randomized, Open-Label, Comparator-Controlled Trial to Evaluate the Efficacy and Safety of LY3938577 in Study Participants, With Type 2 Diabetes Previously Treated With Basal Insulin
Eli Lilly and Company
Summary
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
- Age range
- 18–70 years
- Sex
- All
- Healthy volunteers
- No
Detailed criteria
Inclusion Criteria: * 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) Exclusion Criteria: * Have type 1 diabetes
Interventions
- DrugLY3938577
Administered SC
- DrugDegludec
Administered SC
Locations (26)
- Tucson Clinical Research InstituteTucson, Arizona
- Encompass Clinical ResearchSpring Valley, California
- University Clinical Investigators, Inc.Tustin, California
- Tampa Bay Medical ResearchClearwater, Florida
- Encore Medical ResearchHollywood, Florida
- Clinical Research of Central FloridaLakeland, Florida