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| ID | Type | Description | Link |
|---|---|---|---|
| J1A-MC-KDAB | Other Identifier | Eli Lilly and Company |
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This study is being conducted to determine how safe and how well tolerated LY3462817 is when given intravenously (IV) (into a vein) and subcutaneously (SC) (just under the skin) to healthy participants. Blood tests will be done to check how much LY3462817 is in the bloodstream and how long the body takes to get rid of it. Each enrolled participant will receive 1 dose of LY3462817 or placebo. The study will last about 16 weeks, including screening.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LY3462817 - IV | Experimental | Escalating doses of LY3462817 administered as a single intravenous (IV) infusion in healthy participants |
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| Placebo | Placebo Comparator | Normal saline administered as a single IV infusion in healthy participants |
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| LY3462817 - SC | Experimental | Single dose of LY3462817 administered as subcutaneous (SC) injections in healthy participants |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LY3462817 IV | Biological | Administered IV |
| |
| LY3462817 SC |
| 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 | A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module | Baseline through to final follow-up at approximately Week 12 |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics: Maximum Concentration (Cmax) of LY3462817 | Pharmacokinetics: Cmax of LY3462817 | Baseline through to final follow-up at approximately Week 12 |
| Pharmacokinetics: Area Under the Concentration Versus Time Curve (AUC) 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 |
|---|---|---|---|---|---|---|
| Lilly Nus Centre for Clin Pharmacology | Singapore | 138623 | Singapore |
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| Biological |
Administered SC |
|
| Placebo | Drug | Administered IV |
|
Pharmacokinetics: AUC of LY3462817
| Baseline through to final follow-up at approximately Week 12 |