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| ID | Type | Description | Link |
|---|---|---|---|
| J2V-MC-GZLA | Other Identifier | Eli Lilly and Company |
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The main purpose of this study is to evaluate the safety and tolerability of the study drug known as LY3532226 in healthy participants. Blood tests will be performed to check how much LY3532226 gets into the bloodstream and how long it takes the body to eliminate it. This study will last approximately 8 weeks including screening period.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LY3532226 | Experimental | Single ascending doses of LY3532226 administered subcutaneously (SC). |
|
| Placebo | Placebo Comparator | Placebo administered SC. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LY3532226 | Drug | Administered SC. |
| |
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration | A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module | Baseline up to Week 8 |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3532226 | PK: Cmax of LY3532226 | Day 1 through Day 43 |
| PK: Area Under the Concentration Versus Time Curve (AUC) of LY3532226 | PK: AUC of LY3532226 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) | Eli Lilly and Company | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Lilly Centre for Clinical Pharmacology | Singapore | 138623 | Singapore |
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| Drug |
Administered SC. |
|
| Day 1 through Day 43 |
| PK: Time to Maximum Concentration (Tmax) of LY3532226 | PK: Tmax of LY3532226 | Day 1 through Day 43 |