drugset / Trial / NCT01869959

A Study of LY2405319 in Participants With Type 2 Diabetes

NCT01869959 ↗

Phase 1 Completed 47 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The main purpose of this study was to evaluate the safety and tolerability of LY2405319. It was given as a daily injection under the skin to participants with type 2 diabetes mellitus (T2DM) for 28 days. This study determined how long the drug stays in the body and how it affects blood sugar levels. After screening, the study lasted about 2 months for each participant. Participants continued their prestudy regimen of diet and exercise alone or in combination with metformin.

Timeline

Start
2009-04
Primary completion
2009-06
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2405319 Unknown 3 mg Subcutaneous
Subject LY2405319 Unknown 10 mg Subcutaneous
Subject LY2405319 Unknown 20 mg Subcutaneous