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This is a randomized, placebo-controlled, ascending single dose study of KHK4827 to evaluate safety, tolerability, pharmacokinetics and pharmacodynamics of subcutaneous or intravenous administration of KHK4827 in healthy male subjects or moderate to severe psoriasis patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| KHK4827 | Experimental |
| |
| Placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Placebo | Drug |
| ||
| KHK4827 |
| Measure | Description | Time Frame |
|---|---|---|
| Safety |
|
| Measure | Description | Time Frame |
|---|---|---|
| Plasma KHK4827 concentrations and pharmacokinetic parameters | To assess PK parameters which include
| 16 time points up to 64 days |
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Inclusion Criteria:
Health volunteers
Psoriasis subjects
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Tokyo | Japan |
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| ID | Term |
|---|---|
| D011565 | Psoriasis |
| ID | Term |
|---|---|
| D017444 | Skin Diseases, Papulosquamous |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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| ID | Term |
|---|---|
| C571216 | brodalumab |
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