Type 1 Diabetes Mellitus Clinical Trial
Official title:
A Study to Evaluate the Pharmacokinetics and Glucodynamics of LY900014 Compared to Humalog in Children, Adolescents, and Adults With Type 1 Diabetes Mellitus
The purpose of this study is to compare LY900014 with insulin lispro (Humalog) in
participants with type 1 diabetes mellitus.
There are 2 parts to this study. Part A is investigating how the body processes LY900014 and
the effect of LY900014 on blood sugar levels compared to insulin lispro (Humalog) when study
treatment is given by subcutaneous injection. Part B of the study is investigating how the
body processes LY900014 and the effect of LY900014 on blood sugar levels compared to insulin
lispro (Humalog) when study treatment is given by continuous subcutaneous insulin infusion
(CSII) pump.
Screening is required within 28 days prior to the start of the study. For each participant,
the study will last about 40 days in each part.
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