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| ID | Type | Description | Link |
|---|---|---|---|
| J5X-MC-YJAA | Other Identifier | Eli Lilly and Company |
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The purpose of this study is to evaluate safety and tolerability of LY4060874 in healthy participants.
Study participation may last up to 22 weeks and up to approximately 18 study visits.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LY4060874 (Part A Subcutaneous) | Experimental | Single ascending dose of LY4060874 administered subcutaneously (SC). |
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| LY4060874 (Part A Intravenous) | Experimental | Single ascending dose of LY4060874 administered intravenously (IV). |
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| LY4060874 (Part B) | Experimental | Multiple ascending doses of LY4060874 administered SC. |
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| LY4060874 (Part B Chinese) | Experimental | Multiple ascending doses of LY4060874 administered SC in Chinese participants. |
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| LY4060874 (Part C Japanese) | Experimental | Multiple ascending doses of LY4060874 administered SC in Japanese participants. |
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| Placebo (SC) | Placebo Comparator | Placebo administered SC in Part A, B, and C. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LY4060874 | Drug | Administered SC |
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| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) | Number of participants with one or more TEAEs and SAEs. | Baseline up to 22 Weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics (PK): Area Under the Concentration Versus Time (AUC) of LY4060874 | PK: Area Under the Concentration Versus Time (AUC) of LY4060874 | PK: Part A: Baseline up to 13 weeks; Part B and C: Baseline up to 18 weeks |
| PK: Maximum Observed Concentration of LY4060874 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| 1-877-CTLILLY (1-877-285-4559) or 3176154559 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 |
|---|---|---|---|---|---|---|
| Fortrea, Inc. | Dallas | Texas | 75247 | United States | ||
| Lilly Centre for Clinical Pharmacology |
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| Placebo (IV) | Placebo Comparator | Placebo administered IV in Part A. |
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| LY4060874 | Drug | Administered IV |
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| Placebo | Drug | Administered SC |
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| Placebo | Drug | Administered IV |
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PK: Cmax of LY4060874 |
| PK: Part A: Baseline up to 13 weeks; Part B and C: Baseline up to 18 weeks |
| Singapore |
| 138623 |
| Singapore |