drugset / Trial / NCT05262387

A Study of LY900014 (Lyumjev) Versus Insulin Lispro (Humalog) in Participants With Type 1 Diabetes

NCT05262387

Phase 1 Completed 25 enrolled Eli Lilly and Company
RandomizedCrossoverDouble-blindBasic science

Summary

This study will be conducted in participants with type 1 diabetes mellitus on continuous subcutaneous insulin infusion (CSII) or pump therapy to evaluate the effect of LY900014 (Lyumjev) on blood sugar levels during exercise using different approaches on basal rate reduction and following a test meal compared to insulin lispro (Humalog). The study may last up to approximately 10 weeks and may include up to 7 visits.

Timeline

Start
2022-02-14
Primary completion
2023-03-07
Completion
2023-03-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Insulin Lispro Protein / enzyme biologic Subcutaneous
Subject Lyumjev Unknown Subcutaneous