Study to Assess Adverse Events When Subcutaneous Risankizumab Injection is Given to Adult Participants With Psoriasis in Real World Setting
NCT ID: NCT04799990
Last Updated: 2022-12-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2021-06-23
2022-03-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Risankizumab
Participants will receive risankizumab as prescribed by their physician.
Risankizumab
Subcutaneous Injection
Comparator Group 1
Participants will receive biologics other than interleukin (IL)-23 antagonists as prescribed by their physician.
Comparator 1
Subcutaneous or Intravenous Injection
Comparator Group 2
Participants will receive non-biologic systemic small molecules as prescribed by their physician.
Comparator 2
Oral, Opthalmic, Subcutaneous or Intravenous Injection
Interventions
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Risankizumab
Subcutaneous Injection
Comparator 1
Subcutaneous or Intravenous Injection
Comparator 2
Oral, Opthalmic, Subcutaneous or Intravenous Injection
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
18 Years
ALL
No
Sponsors
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AbbVie
INDUSTRY
Responsible Party
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Principal Investigators
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ABBVIE INC.
Role: STUDY_DIRECTOR
AbbVie
Countries
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Other Identifiers
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P16-772
Identifier Type: -
Identifier Source: org_study_id