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The aim of this study is to examine the safety and tolerability of a single dose of AZD9742 in elderly individuals.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Single dose of 750mg of intravenous AZD9742 in healthy elderly volunteers |
|
| 2 | Placebo Comparator | Sterile 5% dextrose solution |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AZD9742 | Drug | Sterile solution, 620 mg (20 mg/mL) in 50 mL vial with a fill volume of 31 mL |
| |
| Measure | Description | Time Frame |
|---|---|---|
| To assess the safety and tolerability of a single intravenous dose of AZD9742 in healthy elderly adults. | Adverse events, vital signs, electrocardiograms, telemetry, physical exams, and clinical laboratory assessments will be assessed prior to, during, and after treatment | The screening period is up to 28 days. Residential period will be a total of 5 days. Follow up will occur between 5 and 10 days after discharge. |
| Measure | Description | Time Frame |
|---|---|---|
| To evaluate the pharmacokinetics of a single intravenous dose of AZD9742 in healthy elderly volunteers | Blood and urine samples will be collected for the 4 days while in residence. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Billings W Billings, MD | Bio-Kinetic 1816 W. Mt Vernon, Springfield, MO 65802 | Principal Investigator |
| Colleen Jensen | AstraZeneca | Study Director |
| Brendan Smyth | AstraZeneca | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research Site | Springfield | Missouri | United States |
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| Placebo |
| Drug |
Sterile 5% dextrose solution |
|