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The purpose of this study is to evaluate the safety and tolerability of single doses of ILV-095 in healthy subjects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ILV-095 | Active Comparator | 6 SC single dose injections |
|
| Placebo | Placebo Comparator | Placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ILV-095 | Biological |
| ||
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Safety and tolerability will be evaluated from adverse events, physical examinations, vital sign measurements, cardiac rhythm monitoring, 12-lead ECGs, and clinical laboratory test results. | 3 weeks per group |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetic parameters | 3 weeks per group |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Medical Monitor | Wyeth is now a wholly owned subsidiary of Pfizer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Philadelphia | Pennsylvania | 19148 | United States |
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