A Study of How Insulin Peglispro (LY2605541) and Insulin Glargine Affect the Breakdown of Fat and Sugar in Type 1 Diabetics



Status:Completed
Conditions:Diabetes, Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 60
Updated:3/3/2019
Start Date:November 2013
End Date:October 2015

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Evaluation of the Effects of Insulin Peglispro (LY2605541) on Respiratory Quotient During Sleep and Response to Hyperinsulinemia Compared With That of Insulin Glargine in Patients With Type 1 Diabetes Mellitus

This is a two-period study of participants with type 1 diabetes mellitus (T1DM). In each
period, participants will receive once daily injections of stable dose LY2605541 or insulin
glargine for 28 to 35 days followed by procedures to look at how the body uses or stores fats
and sugars. Participants will continue to use meal time insulin throughout the study. Healthy
participants will also enroll in the study. They will not receive any study medication.


Inclusion Criteria:

Type 1 Diabetics:

- T1DM for more than 1 year with Hemoglobin A1c (HbA1c) of less than 9.5%

All Participants:

- Otherwise fit and healthy

- Non smoker

Exclusion Criteria:

Type 1 Diabetics:

- Taking medication or supplements other than insulin to control diabetes

- Suffered a hypoglycemic event in the last 12 months that required hospitalization or
have poor awareness of hypoglycemia

All Participants:

- Taking fibrates, thyroid replacement therapy, testosterone, beta blockers or systemic
corticosteroids
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