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This is a study to evaluate safety, tolerability, PK and PD effects of orally administered AZD8529 after single ascending doses
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental |
| |
| 2 | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AZD8529 | Drug | Oral |
| |
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| To assess the safety and tolerability of single dose administration of AZD8529 when given orally to healthy male subjects and female subjects of non-childbearing potential. | at each visit, at least daily, during the study. |
| Measure | Description | Time Frame |
|---|---|---|
| To characterize the pharmacokinetics of AZD8529 in plasma and urine. | Blood and urine samples will be taken during the study. | |
| To asses the effect of food on the safety and pharmacokinetic profile of AZD8529. | Safety assessments and blood and urine samples will be taken throughout the study. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sylvan J Hurewitz, MD | AstraZeneca Clinical Pharmacology Unit, US | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research Site | Philadelphia | Pennsylvania | United States |
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| ID | Term |
|---|---|
| C000608263 | AZD8529 |
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| Drug |
Oral |
|