drugset / Trial / NCT03449433

A Meal Test Study of LY900014 in Participants With Type 1 Diabetes Mellitus

NCT03449433

Phase 1 Completed 80 enrolled Eli Lilly and Company
RandomizedCrossoverDouble-blindBasic science

Summary

Two forms of insulin lispro (LY900014 and Humalog®) and two forms of insulin aspart (NovoRapid® and Fiasp®) will be given to trial participants with diabetes mellitus type 1 by injection under the skin. The study will assess how fast the active ingredient (insulin lispro or insulin aspart) gets into the blood stream and how long it takes the body to remove it. A test meal will be given to trial participants to assess the course of the blood sugar lowering effect of the investigational products. The safety and tolerability of LY900014 will also be assessed. Screening is required within 14 days prior to the lead in. For each participant, the study will last up to 91 days.

Timeline

Start
2018-03-15
Primary completion
2018-08-14
Completion
2018-08-14

Drugs

EvaluationDrugModalityDoseRoute
Comparator Insulin Lispro Protein / enzyme biologic Subcutaneous
Comparator insulin aspart Protein / enzyme biologic Subcutaneous