A Study of Lispro Formulations in Healthy Participants
Status:
Completed
Trial end date:
2015-09-01
Target enrollment:
Participant gender:
Summary
The purposes of this study are to determine:
- Part A
- How quickly your body absorbs, breaks down and gets rid of the different
formulations of insulin lispro compared to insulin lispro alone formulation.
- The safety of insulin lispro in different formulations and any side effects that
might be associated with it.
- Part B:
- How much insulin lispro from different dose ranges is found in the bloodstream
using a test insulin lispro formulation (selected from Part A).
- The safety of insulin lispro in different formulations and any side effects that
might be associated with it.
Participants may only enroll in one part. The study is expected to last up to 10 weeks for
each part.