drugset / Trial / NCT03367377

A Study of LY3209590 in Participants With Type 2 Diabetes

NCT03367377

Phase 1 Completed 70 enrolled Eli Lilly and Company
RandomizedParallel-groupOpen-labelBasic science

Summary

This study will evaluate the safety and tolerability of LY3209590 when given by injection under the skin to participants with type 2 diabetes. It will also investigate how the body processes the study drug and the effect of the study drug on blood sugar levels. Information about any side effects will be documented. This study will last approximately 17 weeks, not including screening. Screening is required within 4 weeks prior to the start of the study.

Timeline

Start
2018-01-03
Primary completion
2018-10-03
Completion
2018-10-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Insulin Efsitora Alfa Protein / enzyme biologic Subcutaneous
Comparator insulin glargine Protein / enzyme biologic Subcutaneous