drugset / Trial / NCT04809220
A Study of Two Doses of Dulaglutide (LY2189265) in Japanese Patients With Type 2 Diabetes
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to evaluate the efficacy and safety of 2 doses of dulaglutide in Japanese participants with type 2 diabetes. The study duration is approximately 58 weeks.
Timeline
- Start
- 2021-04-13
- Primary completion
- 2022-10-01
- Completion
- 2023-04-26
Outcome
Met primary endpoint
registry analysis (superiority test); Dulaglutide 1.5 mg vs Dulaglutide 0.75 mg; p <.001; LS Mean Difference -0.29 (95% CI -0.43 to -0.14); Mixed Models Analysis NCT04809220 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Dulaglutide | Peptide | 0.75 mg | Subcutaneous |
| Subject | Dulaglutide | Peptide | 1.5 mg | Subcutaneous |