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The purpose of this study is to compare how the drug moves through the body following risankizumab subcutaneous (SC) and risankizumab intravenous (IV) doses.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Risankizumab Dose A | Experimental | Participants will receive Dose A of risankizumab via intravenous (IV) infusion. |
|
| Risankizumab Dose B | Experimental | Participants will receive Dose B of risankizumab via subcutaneous (SC) injection. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Risankizumab | Drug | Intravenous (IV) |
| |
| Risankizumab |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants with Adverse Events (AEs) | An AE is defined as any untoward medical occurrence in a patient or clinical investigation in which a participant is administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment. | Up to Approximately 155 Days |
| Maximum Observed Serum Concentration (Cmax) of Risankizumab | Cmax of Risankizumab. | Up to Approximately 155 Days |
| Time to Cmax (Tmax) of Risankizumab | Tmax of Risankizumab. | Up to Approximately 155 Days |
| Area Under the Serum Concentration-Time Curve (AUC) of Risankizumab | AUCt of Risankizumab. | Up to Approximately 155 Days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| ABBVIE CALL CENTER | Contact | 844-663-3742 | abbvieclinicaltrials@abbvie.com |
| Name | Affiliation | Role |
|---|---|---|
| ABBVIE INC. | AbbVie | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CenExel ACT- Anaheim Clinical Trials /ID# 281821 | Recruiting | Anaheim | California | 92801 | United States | |
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| ID | Term |
|---|---|
| C000601773 | risankizumab |
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| Drug |
Subcutaneous (SC) Injections |
|
| Cpmi /Id# 281783 |
| Recruiting |
| Miami |
| Florida |
| 33172 |
| United States |