drugset / Trial / NCT02342314
A Study of LY3143753 and LY3185643 in Healthy Participants
RandomizedParallel-groupDouble-blindBasic science
Summary
The study involves a single dose of LY3143753 or LY3185643, given as an injection into the abdomen. The study will evaluate the effects of the LY3143753 or LY3185643 on your body. The study is approximately 12 weeks for each participant, not including screening. Screening is required within 28 days prior to the start of the study. This study involves Part A (LY3143753) and Part B (LY3185643). Participants may only enroll in one part and at one dose level.
Timeline
- Start
- 2015-01
- Primary completion
- 2016-09
- Completion
- 2016-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | LY3143753 | Unknown | — | Subcutaneous |
| Subject | LY3185643 | Unknown | — | Subcutaneous |
| Comparator | rGlucagon | Unknown | — | Subcutaneous |
Indications
No indication recorded.