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| ID | Type | Description | Link |
|---|---|---|---|
| I8H-MC-BDCJ | Other Identifier | Eli Lilly and Company | |
| 2020-003738-19 | EudraCT Number |
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The main purpose of this study is to look at the amount of the study drug, LY3209590, that gets into the blood stream and how long it takes the body to get rid of LY3209590 when given as different formulations. The tolerability of LY3209590 will also be evaluated and information about any side effects experienced will be collected. The study will last up to 142 days.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LY3209590 Lyophilized Formulation | Experimental | LY3209590 as lyophilized formulation administered subcutaneously (SC) in one of the two study periods. |
|
| LY3209590 Solution Formulation | Experimental | LY3209590 as solution formulation administered SC in one of the two study periods. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LY3209590 | Drug | Administered SC. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3209590 | PK: Cmax of LY3209590 | Predose on Day 1 through Day 65 |
| PK: Area Under the Concentration Versus Time Curve from Time Zero to Infinity (AUC[0-inf]) of LY3209590 | PK: AUC(0-inf) of LY3209590 | Predose on Day 1 through Day 65 |
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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 |
|---|---|---|---|---|---|---|
| Covance Clinical Research | Leeds | LS2 9LH | United Kingdom |
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