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| ID | Type | Description | Link |
|---|---|---|---|
| J1A-MC-KDAE | Other Identifier | Eli Lilly and Company |
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The main purpose of this study is to evaluate the safety and tolerability of LY3462817 in healthy Japanese and non-Japanese participants. The study will also assess how fast LY3462817 gets into the blood stream and how long it takes the body to remove it. The study is open to healthy participants. The study will last up to approximately 12 weeks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LY3462817 - SC | Experimental | LY3462817 administered subcutaneously (SC) |
|
| LY3462817 - IV | Experimental | LY3462817 administered intravenously (IV) |
|
| Placebo - SC | Placebo Comparator | Placebo administered SC |
|
| Placebo - IV | Placebo Comparator | Placebo administered IV |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LY3462817 (SC) | Drug | Administered SC. |
| |
| Placebo (SC) |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants with One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration | A summary of TEAEs, SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module | Baseline through Week 12 |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3462817 | PK: AUC of LY3462817 | Predose on Day 1 through Day 85 |
| PK: Maximum Concentration (Cmax) of LY3462817 | PK: Cmax of LY3462817 |
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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 |
|---|---|---|---|---|---|---|
| Altasciences Clinical Los Angeles, Inc | Cypress | California | 90630 | United States |
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| Drug |
Administered SC. |
|
| LY3462817 (IV) | Drug | Administered IV. |
|
| Placebo (IV) | Drug | Administered IV. |
|
| Predose on Day 1 through Day 85 |