drugset / Trial / NCT03433677

A Study of LY900014 and Insulin Lispro With an External Continuous Subcutaneous Insulin Infusion System in Adult Participants With Type 1 Diabetes

NCT03433677 ↗

Phase 3 Completed 49 enrolled Eli Lilly and Company
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to evaluate the compatibility and safety of LY900014 and insulin lispro with an external continuous subcutaneous insulin infusion system in adult participants with type 1 diabetes.

Timeline

Start
2018-02-21
Primary completion
2018-09-04
Completion
2018-09-04

Outcome

Missed primary endpoint

registry analysis (superiority test); Insulin Lispro (Humalog®) vs LY900014; p = 0.375 NCT03433677 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Insulin Lispro Protein / enzyme biologic 100 unknown Subcutaneous