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| ID | Type | Description | Link |
|---|---|---|---|
| I9X-MC-MTAD | Other Identifier | Eli Lilly and Company |
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This study uses imaging to evaluate how LY3372689 binds to a protein in the brain. This study will be conducted in healthy participants and will last up to about 10 weeks. Screening must be completed within four weeks prior to enrollment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LY3372689 + [18F]LSN3316612 | Experimental | LY3372689 administered orally followed by [18F]LSN3316612 PET tracer administered intravenously (IV) approximately 24 hours later. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LY3372689 | Drug | Administered orally. |
| |
| [18F]LSN3316612 |
| Measure | Description | Time Frame |
|---|---|---|
| Percent O-GlcNAcase (OGA) Enzyme Occupancy (EO) | Percent OGA EO | Approximately 2 to 96 hours following the first dose |
| Percent OGA EO | Percent OGA EO | Approximately 2 to 96 hours following the last dose |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve During the Dosing Interval (AUC[0-tau]) of LY3372689 | PK: AUC(0-tau) of LY3372689 | Baseline through 24 hours |
| PK: Maximum Concentration (Cmax) of LY3372689 |
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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 |
|---|---|---|---|---|---|---|
| Institute for Neurodegenerative Disorders | New Haven | Connecticut | 06510 | United States |
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| Diagnostic Test |
Administered intravenously (IV). |
|
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PK: Cmax of LY3372689
| Baseline through 24 hours |