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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Insulin Lispro | Protein / enzyme biologic | 100 unknown | Subcutaneous |